Personal publications by the years
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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
 of Siberian Branch of Russian Academy of Sciences

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Personal publicalions (DB NIOCh)


2023

Reviews, articles

  1. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  2. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  3. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  4. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  5. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  6. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  7. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  8. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  9. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  10. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  11. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023, Advance Article, The article was first published on 29 Nov 2022 doi:10.1039/D2QM01046A, IF=8.682
  12. E.A. Chulanova, E.A. Radiush, Ya. Balmohammadi, J. Beckmann, S. Grabowsky, A.V. Zibarev
    New charge-transfer complexes of 1,2,5-chalcogenadiazoles with tetrathiafulvalenes† Check for updates
    CrystEngComm, 2023, Advance Article doi:10.1039/D2CE01385A, IF=3.756
  13. E.A. Chulanova, E.A. Radiush, Ya. Balmohammadi, J. Beckmann, S. Grabowsky, A.V. Zibarev
    New charge-transfer complexes of 1,2,5-chalcogenadiazoles with tetrathiafulvalenes† Check for updates
    CrystEngComm, 2023, Advance Article doi:10.1039/D2CE01385A, IF=3.756
  14. E.A. Chulanova, E.A. Radiush, Ya. Balmohammadi, J. Beckmann, S. Grabowsky, A.V. Zibarev
    New charge-transfer complexes of 1,2,5-chalcogenadiazoles with tetrathiafulvalenes† Check for updates
    CrystEngComm, 2023, Advance Article doi:10.1039/D2CE01385A, IF=3.756
  15. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
  16. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
  17. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
  18. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
  19. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.419
  20. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  21. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  22. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  23. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  24. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  25. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  26. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  27. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  28. E.N. Zapolotsky, S.P. Babailov, M.V. Kniazeva, Yu.V. Strelnikova, A.S. Ovsyannikov, A.T. Gubaidullin, S.E. Solovieva, I.S. Antipin, E.S. Fomin, I.P. Chuikov
    Synthesis, crystal structure and NMR-study new mononuclear paramagnetic Er (III) complex based on imine derivatives of thiacalix[4]arene
    Inorganica Chimica Acta, V.545, 24 January 2023, 121267 doi:10.1016/j.ica.2022.121267, IF=3.118
  29. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  30. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  31. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  32. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  33. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  34. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  35. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  36. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  37. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  38. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  39. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  40. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  41. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  42. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  43. L.N. Shishkina, O.Yu. Mazurkov, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, B.A. Selivanov, A.Ya. Tikhonov, S.G. Gamaley, G.G. Shimina, G.M. Sysoyeva, O.S. Taranov, E.D. Danilenko, A.P. Agafonov, R.A. Maksyutov
    Safety and Pharmacokinetics of the Substance of the Anti-Smallpox Drug NIOCH-14 after Oral Administration to Laboratory Animals
    Viruses 2023, 15(1), 205; doi:10.3390/v15010205, IF=5.817
  44. K. Sato, E. Bagryanskaya, M. Affronte, S. Hill
    A Special Issue of Applied Magnetic Resonance in Honor of Professor Takeji Takui on the Occasion of his 80th Birthday
    Applied Magnetic Resonance, (2023), Published 07 January 2023 doi:10.1007/s00723-022-01520-9, IF=0.973
  45. K. Sato, E. Bagryanskaya, M. Affronte, S. Hill
    A Special Issue of Applied Magnetic Resonance in Honor of Professor Takeji Takui on the Occasion of his 80th Birthday
    Applied Magnetic Resonance, (2023), Published 07 January 2023 doi:10.1007/s00723-022-01520-9, IF=0.973
  46. K. Sato, E. Bagryanskaya, M. Affronte, S. Hill
    A Special Issue of Applied Magnetic Resonance in Honor of Professor Takeji Takui on the Occasion of his 80th Birthday
    Applied Magnetic Resonance, (2023), Published 07 January 2023 doi:10.1007/s00723-022-01520-9, IF=0.973
  47. V.S. Moskaliuk, R.V. Kozhemyakina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E.A. Kulikova
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  48. V.S. Moskaliuk, R.V. Kozhemyakina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E.A. Kulikova
    On Associations between Fear-Induced Aggression, Bdnf Transcripts, and Serotonin Receptors in the Brains of Norway Rats: An Influence of Antiaggressive Drug TC-2153
    Int. J. Mol. Sci. 2023, 24(2), 983 doi:10.3390/ijms24020983, IF=6.208
  49. V.S. Moskaliuk, R.V. Kozhemyakina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E.A. Kulikova
    On Associations between Fear-Induced Aggression, Bdnf Transcripts, and Serotonin Receptors in the Brains of Norway Rats: An Influence of Antiaggressive Drug TC-2153
    Int. J. Mol. Sci. 2023, 24(2), 983 doi:10.3390/ijms24020983, IF=6.208
  50. V.S. Moskaliuk, R.V. Kozhemyakina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E.A. Kulikova
    On Associations between Fear-Induced Aggression, Bdnf Transcripts, and Serotonin Receptors in the Brains of Norway Rats: An Influence of Antiaggressive Drug TC-2153
    Int. J. Mol. Sci. 2023, 24(2), 983 doi:10.3390/ijms24020983, IF=6.208
  51. V.S. Moskaliuk, R.V. Kozhemyakina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E.A. Kulikova
    On Associations between Fear-Induced Aggression, Bdnf Transcripts, and Serotonin Receptors in the Brains of Norway Rats: An Influence of Antiaggressive Drug TC-2153
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  52. T.T. Efremova, S.V. Morozov, E.I. Chernyak, E.V. Chumanova
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  53. T.T. Efremova, S.V. Morozov, E.I. Chernyak, E.V. Chumanova
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  54. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
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  55. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
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  56. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
    Известия Академии наук. Серия химическая. 2023, № 1, стр. 248, IF=1.703
  57. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
    Известия Академии наук. Серия химическая. 2023, № 1, стр. 248, IF=1.703
  58. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
    Известия Академии наук. Серия химическая. 2023, № 1, стр. 248, IF=1.703
  59. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
    Известия Академии наук. Серия химическая. 2023, № 1, стр. 248, IF=1.703
  60. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
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  61. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
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  62. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
    Синтез конъюгатов (aR,7S)-колхицина с монотерпеноидами и изучение их биологиче ской активности
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  63. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
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  64. Е.С. Щегравина, С.Д. Усова, Д.С. Баев, Е.C. Можайцев, Д.Н. Щербаков, С.В. Беленькая, Е.А. Волосникова, В.Ю. Чиркова, Е.А. Шарлаева, Е.В. Свирщевская, И.П. Фонарева, А.Р. Ситдикова, Н.Ф. Салахутдинов, О.И. Яровая, А.Ю. Федоров
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  65. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
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  66. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
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  67. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
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  68. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
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  69. А.И. Далингер, Д.С. Баев, О.И. Яровая, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков, Н.Ф. Салахутдинов, С.З. Вацадзе
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  70. И.А. Заякин, А.Я. Акыева, М.А. Сыроешкин, И.Ю. Багрянская, Е.В. Третьяков, М.П. Егоров
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  71. И.А. Заякин, А.Я. Акыева, М.А. Сыроешкин, И.Ю. Багрянская, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и электрохимия нитронилнитроксилзамещенного 1,4-нафтохинона
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  72. И.А. Заякин, А.Я. Акыева, М.А. Сыроешкин, И.Ю. Багрянская, Е.В. Третьяков, М.П. Егоров
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  73. И.А. Заякин, А.Я. Акыева, М.А. Сыроешкин, И.Ю. Багрянская, Е.В. Третьяков, М.П. Егоров
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  74. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  75. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  76. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  77. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  78. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  79. P.A. Nikitina, E.I. Basanova, E.B. Nikolaenkova, I.A. Os'kina, O.A. Serova, N.I. Bormotov, L.N. Shishkina, V.P. Perevalov, A.Ya. Tikhonov
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  80. D.S. Baev, M.E. Blokhin, V.Yu. Chirkova, S.V. Belenkaya, O.A. Luzina, O.I. Yarovaya, N.F. Salakhutdinov, D.N. Shcherbakov
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  81. D.S. Baev, M.E. Blokhin, V.Yu. Chirkova, S.V. Belenkaya, O.A. Luzina, O.I. Yarovaya, N.F. Salakhutdinov, D.N. Shcherbakov
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  82. D.S. Baev, M.E. Blokhin, V.Yu. Chirkova, S.V. Belenkaya, O.A. Luzina, O.I. Yarovaya, N.F. Salakhutdinov, D.N. Shcherbakov
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  83. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, N. Valutsa, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation
    Pharmaceutics 2023, 15(1), 44; doi:10.3390/pharmaceutics15010044, IF=6.525
  84. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, N. Valutsa, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
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  85. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
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  86. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
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  87. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
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  88. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  89. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  90. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  91. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  92. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  93. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  94. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  95. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  96. E.S. Mozhaitsev, E.V. Suslov, D.A. Rastrepaeva, O.I. Yarovaya, S.S. Borisevich, E.M. Khamitov, D.S. Kolybalov, S.G. Arkhipov, N.I. Bormotov, L.N. Shishkina, O.A. Serova, R.V. Brunilin, A.A. Vernigora, M.B. Nawrozkij, A.P. Agafonov, R.A. Maksyutov, K.P. Volcho, N.F. Salakhutdinov
    Structure-Based Design, Synthesis, and Biological Evaluation of the Cage-Amide Derived Orthopox Virus Replication Inhibitors
    Viruses 2023, 15(1), 29 doi:10.3390/v15010029, IF=5.817
  97. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    Adducts of the Zinc Salt of Dinitramic Acid
    Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
  98. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    Adducts of the Zinc Salt of Dinitramic Acid
    Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
  99. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    Adducts of the Zinc Salt of Dinitramic Acid
    Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
  100. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    Adducts of the Zinc Salt of Dinitramic Acid
    Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
  101. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    Adducts of the Zinc Salt of Dinitramic Acid
    Materials 2023, 16(1), 70 doi:10.3390/ma16010070, IF=3.747
  102. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  103. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  104. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  105. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  106. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  107. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  108. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  109. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  110. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  111. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  112. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  113. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  114. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  115. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  116. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  117. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  118. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  119. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  120. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  121. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  122. Ya.V. Burgart, N.A. Elkina, E.V. Shchegolkov, O.P. Krasnykh, G.F. Makhaeva, G.A. Triandafilova, S.Yu. Solodnikov, N.P. Boltneva, E.V. Rudakova, N.V. Kovaleva, O.G. Serebryakova, M.V. Ulitko, S.S. Borisevich, N.A. Gerasimova, N.P. Evstigneeva, S.A. Kozlov, Yu.V. Korolkova, A.S. Minin, A.V. Belousova, E.S. Mozhaitsev, A.M. Klabukov, V.I. Saloutin
    Powerful Potential of Polyfluoroalkyl-Containing 4-Arylhydrazinylidenepyrazol-3-Ones for Pharmaceuticals
    Molecules 2023, 28(1), 59 doi:10.3390/molecules28010059, IF=4.927
  123. M.E. Mironov, T.V. Rybalova, M.A. Pokrovski, F. Emaminia, E.R. Gandalipov, A.G. Pokrovskii, E.E. Shults
    Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
    Steroids, V. 190, February 2023, 109133 doi:10.1016/j.steroids.2022.109133, IF=2.759
  124. M.E. Mironov, T.V. Rybalova, M.A. Pokrovski, F. Emaminia, E.R. Gandalipov, A.G. Pokrovskii, E.E. Shults
    Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
    Steroids, V. 190, February 2023, 109133 doi:10.1016/j.steroids.2022.109133, IF=2.759
  125. M.E. Mironov, T.V. Rybalova, M.A. Pokrovski, F. Emaminia, E.R. Gandalipov, A.G. Pokrovskii, E.E. Shults
    Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
    Steroids, V. 190, February 2023, 109133 doi:10.1016/j.steroids.2022.109133, IF=2.759
  126. M.E. Mironov, T.V. Rybalova, M.A. Pokrovski, F. Emaminia, E.R. Gandalipov, A.G. Pokrovskii, E.E. Shults
    Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
    Steroids, V. 190, February 2023, 109133 doi:10.1016/j.steroids.2022.109133, IF=2.759

2022

Reviews, articles

  1. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
    A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
    Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
  2. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
    A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
    Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
  3. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
    A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
    Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
  4. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
    A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
    Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
  5. N.P. Isaev, A.R. Melnikov, K.A. Lomanovich, M.V. Dugin, M.Yu. Ivanov, D.N. Polovyanenko, S.L. Veber, M.K. Bowman, E.G. Bagryanskaya
    A broadband pulse EPR spectrometer for high-throughput measurements in the X-band
    Journal of Magnetic Resonance Open, V. 14-15, June 2023, 100092 doi:10.1016/j.jmro.2022.100092
  6. O.I. Teplyakova, V.V. Fomenko, N.F. Salakhutdinov, N.G. Vlasenko
    Novochizol(TM) Seed Treatment: Effects On Germination, Growth And Development In Soft Spring Wheat
    Natural Products Chemistry & Research 2022, Vol.10, Issue 5, 1-4 doi:10.35248/naturalproducts.10.5.1-04
  7. O.I. Teplyakova, V.V. Fomenko, N.F. Salakhutdinov, N.G. Vlasenko
    Novochizol(TM) Seed Treatment: Effects On Germination, Growth And Development In Soft Spring Wheat
    Natural Products Chemistry & Research 2022, Vol.10, Issue 5, 1-4 doi:10.35248/naturalproducts.10.5.1-04
  8. I.E. Smirnova, E.V. Tret’yakova, D.S. Baev, O.B. Kazakova
    Synthetic modifications of abietane diterpene acids to potent antimicrobial agents
    Natural Product Research, Published Online: 27 Aug 2021 doi:10.1080/14786419.2021.1969566, IF=2.488
  9. I.E. Smirnova, E.V. Tret’yakova, D.S. Baev, O.B. Kazakova
    Synthetic modifications of abietane diterpene acids to potent antimicrobial agents
    Natural Product Research, Published Online: 27 Aug 2021 doi:10.1080/14786419.2021.1969566, IF=2.488
  10. I.E. Smirnova, E.V. Tret’yakova, D.S. Baev, O.B. Kazakova
    Synthetic modifications of abietane diterpene acids to potent antimicrobial agents
    Natural Product Research, Published Online: 27 Aug 2021 doi:10.1080/14786419.2021.1969566, IF=2.488
  11. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  12. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  13. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  14. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  15. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  16. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  17. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  18. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  19. N.A. Shekhovtsov, T.E. Kokina, K.A. Vinogradova, A.Y. Panarin, M.I. Rakhmanova, D.Y. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, V.P. Krivopalov, R. Czerwieniec, M.B. Bushuev
    Near-infrared emitting copper(I) complexes with a pyrazolylpyrimidine ligand: exploring relaxation pathways
    Dalton Trans., 2022, V. 51, N 7, Pp. 2898-2911 doi:10.1039/D1DT04325K, IF=4.569
  20. R.B. Seidakhmetova, A. Amanzhan, E.E. Shults, K.V. Goldaeva, S.M. Adekenov, D. Berillo
    Analgesic and Antidepressant Activity of 8-Substituted Harmine Derivatives
    Chemistry of Heterocyclic Compounds (2022), Published: 30 July 2022 doi:10.1007/s10593-022-03092-9, IF=1.49
  21. R.B. Seidakhmetova, A. Amanzhan, E.E. Shults, K.V. Goldaeva, S.M. Adekenov, D. Berillo
    Analgesic and Antidepressant Activity of 8-Substituted Harmine Derivatives
    Chemistry of Heterocyclic Compounds (2022), Published: 30 July 2022 doi:10.1007/s10593-022-03092-9, IF=1.49
  22. R.B. Seidakhmetova, A. Amanzhan, E.E. Shults, K.V. Goldaeva, S.M. Adekenov, D. Berillo
    Analgesic and Antidepressant Activity of 8-Substituted Harmine Derivatives
    Chemistry of Heterocyclic Compounds (2022), Published: 30 July 2022 doi:10.1007/s10593-022-03092-9, IF=1.49
  23. R.B. Seidakhmetova, A. Amanzhan, E.E. Shults, K.V. Goldaeva, S.M. Adekenov, D. Berillo
    Analgesic and Antidepressant Activity of 8-Substituted Harmine Derivatives
    Chemistry of Heterocyclic Compounds (2022), Published: 30 July 2022 doi:10.1007/s10593-022-03092-9, IF=1.49
  24. R.B. Seidakhmetova, A. Amanzhan, E.E. Shults, K.V. Goldaeva, S.M. Adekenov, D. Berillo
    Analgesic and Antidepressant Activity of 8-Substituted Harmine Derivatives
    Chemistry of Heterocyclic Compounds (2022), Published: 30 July 2022 doi:10.1007/s10593-022-03092-9, IF=1.49
  25. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  26. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  27. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  28. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  29. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  30. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  31. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  32. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  33. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  34. I. Zayakin, E. Tretyakov, A. Akyeva, M. Syroeshkin, Ju. Burykina, A. Dmitrenok, A. Korlyukov, D. Nasyrova, I. Bagryanskaya, D. Stass, V.P. Ananikov
    Overclocking nitronyl nitroxide gold derivatives in cross-coupling reactions
    Chemistry - A European Journal, First published: 19 October 2022 doi:10.1002/chem.202203118, IF=5.19
  35. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  36. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  37. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  38. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  39. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  40. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  41. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  42. D. Duvinage, F. Mostaghimi, M. Damrath, Ju. Spils, P. Komorr, D.S. Odintsov, M. Fedin, L.A. Shundrin, S. Mebs, J. Beckmann
    Synthesis and Single-Electron Oxidation of Bulky Bis(m-terphenyl)chalcogenides. The Quest for Kinetically Stabilized Radical Cations.
    Chemistry-A European Journal, First published: 23 November 2022 doi:10.1002/chem.202203498, IF=5.19
  43. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  44. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  45. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  46. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  47. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  48. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  49. M. V.Khvostov,N. V.Bulina,N. A.Zhukova,E. G.Morenkov,D. K.Rybin,S. V.Makarova,S. V.Leonov,V.S.Gorodov,V.Yu.Ulianitsky,T.G.Tolstikova
    A study on biological properties of titanium implants coated with multisubstituted hydroxyapatite
    Ceramics International, 48(23), с. 34780-34792 doi:10.1016/j.ceramint.2022.08.067, IF=5.532
  50. N.A. Shekhovtsov, A.A. Ryadun, V.F. Plyusnin, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    First 1-hydroxy-1H-imidazole-based ESIPT emitter with an O-H...O intramolecular hydrogen bond: ESIPT-triggered TICT and speciation in solution
    New J. Chem., 2022,46(47), 22804-22817 doi:10.1039/D2NJ04463C, IF=3.924
  51. N.A. Shekhovtsov, A.A. Ryadun, V.F. Plyusnin, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    First 1-hydroxy-1H-imidazole-based ESIPT emitter with an O-H...O intramolecular hydrogen bond: ESIPT-triggered TICT and speciation in solution
    New J. Chem., 2022,46(47), 22804-22817 doi:10.1039/D2NJ04463C, IF=3.924
  52. N.A. Shekhovtsov, A.A. Ryadun, V.F. Plyusnin, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    First 1-hydroxy-1H-imidazole-based ESIPT emitter with an O-H...O intramolecular hydrogen bond: ESIPT-triggered TICT and speciation in solution
    New J. Chem., 2022,46(47), 22804-22817 doi:10.1039/D2NJ04463C, IF=3.924
  53. N.A. Shekhovtsov, A.A. Ryadun, V.F. Plyusnin, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    First 1-hydroxy-1H-imidazole-based ESIPT emitter with an O-H...O intramolecular hydrogen bond: ESIPT-triggered TICT and speciation in solution
    New J. Chem., 2022,46(47), 22804-22817 doi:10.1039/D2NJ04463C, IF=3.924
  54. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
    Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
    Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
  55. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
    Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
    Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
  56. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  57. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  58. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  59. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  60. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  61. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  62. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  63. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  64. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  65. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  66. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  67. D.I. Dominskiy, O.G. Kharlanov, V.A. Trukhanov, A.Yu. Sosorev, N.I. Sorokina, M.S. Kazantsev, E.F. Lazneva, N.B. Gerasimova, V.S. Sobolev, A.S. Komolov, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Polarity Switching in Organic Electronic Devices via Terminal Substitution of Active-Layer Molecules
    ACS Applied Electronic Materials, 2022, 4, 12, 6345-6356 doi:10.1021/acsaelm.2c01481, IF=4.493
  68. A.S. Berezin, B. Selivanov, A. Danilenko, A. Sukhikh, A. Komarovskikh
    Manganese(II) Bromide Compound with Diprotonated 1-Hydroxy-2-(pyridin-2-yl)-4,5,6,7-tetrahydrobenzimidazole: Dual Emission and the Effect of Proton Transfers
    Inorganics 2022, 10(12), 245 doi:10.3390/inorganics10120245, IF=3.149
  69. A.S. Berezin, B. Selivanov, A. Danilenko, A. Sukhikh, A. Komarovskikh
    Manganese(II) Bromide Compound with Diprotonated 1-Hydroxy-2-(pyridin-2-yl)-4,5,6,7-tetrahydrobenzimidazole: Dual Emission and the Effect of Proton Transfers
    Inorganics 2022, 10(12), 245 doi:10.3390/inorganics10120245, IF=3.149
  70. A.S. Berezin, B. Selivanov, A. Danilenko, A. Sukhikh, A. Komarovskikh
    Manganese(II) Bromide Compound with Diprotonated 1-Hydroxy-2-(pyridin-2-yl)-4,5,6,7-tetrahydrobenzimidazole: Dual Emission and the Effect of Proton Transfers
    Inorganics 2022, 10(12), 245 doi:10.3390/inorganics10120245, IF=3.149
  71. A.S. Berezin, B. Selivanov, A. Danilenko, A. Sukhikh, A. Komarovskikh
    Manganese(II) Bromide Compound with Diprotonated 1-Hydroxy-2-(pyridin-2-yl)-4,5,6,7-tetrahydrobenzimidazole: Dual Emission and the Effect of Proton Transfers
    Inorganics 2022, 10(12), 245 doi:10.3390/inorganics10120245, IF=3.149
  72. V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
    Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
    Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
  73. V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
    Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
    Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
  74. V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
    Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
    Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
  75. V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
    Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
    Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
  76. V.V. Krisyuk, S.Urkasym. Kyzy, T.V. Rybalova, I.V. Korolkov, M.A. Grebenkina, A.N. Lavro
    Structure and Properties of Heterometallics Based on Lanthanides and Transition Metals with Methoxy-β-Diketonates
    Molecules 2022, 27(23), 8400 doi:10.3390/molecules27238400, IF=4.927
  77. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов
    Биоорганическая химия, 2022, N 7 doi:10.1134/S1068162022070147, IF=1.253
  78. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов
    Биоорганическая химия, 2022, N 7 doi:10.1134/S1068162022070147, IF=1.253
  79. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов
    Биоорганическая химия, 2022, N 7 doi:10.1134/S1068162022070147, IF=1.253
  80. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов
    Биоорганическая химия, 2022, N 7 doi:10.1134/S1068162022070147, IF=1.253
  81. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов
    Биоорганическая химия, 2022, N 7 doi:10.1134/S1068162022070147, IF=1.253
  82. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  83. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  84. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  85. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  86. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  87. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  88. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, М.А. Бондарева, А.А. Нефедов, В.Ю. Чиркова, Е.А. Шарлаева, С.В. Беленькая, Д.Н. Щербаков
    Состав липофильных компонентов эфирного экстракта рододендрона Адамса и активность против основной протеазы SARS COV 2
    Химия растительного сырья, 2022, № 4, c. 153-162. doi:10.14258/jcprm.20220411584
  89. M.P. Davydova, I.Yu. Bagryanskaya, E.H. Sadykov, A.V. Artem'ev
    A pyrimidine-derived diphosphine P-monoxide and a Ag(I) coordination polymer thereof: synthesis, structure, and luminescence
    Журнал структурной химии. 2022. Т. 63. № 12. С. 103553. doi:10.26902/JSC_id103553 (A PYRIMIDINE-DERIVED DIPHOSPHINE P-MONOXIDE AND A Ag(I) COORDINATION POLYMER THEREOF: SYNTHESIS, STRUCTURE, AND LUMINESCENCE/ M. P. Davydova, I. Yu. Bagryanskaya, E. H. Sadykov, A. V. Artem'ev// Journal of Structural Chemistry, 2022, V.63, N 12, pp 2020-2027 doi:10.1134/S0022476622120137), IF=1.004
  90. M.P. Davydova, I.Yu. Bagryanskaya, E.H. Sadykov, A.V. Artem'ev
    A pyrimidine-derived diphosphine P-monoxide and a Ag(I) coordination polymer thereof: synthesis, structure, and luminescence
    Журнал структурной химии. 2022. Т. 63. № 12. С. 103553. doi:10.26902/JSC_id103553 (A PYRIMIDINE-DERIVED DIPHOSPHINE P-MONOXIDE AND A Ag(I) COORDINATION POLYMER THEREOF: SYNTHESIS, STRUCTURE, AND LUMINESCENCE/ M. P. Davydova, I. Yu. Bagryanskaya, E. H. Sadykov, A. V. Artem'ev// Journal of Structural Chemistry, 2022, V.63, N 12, pp 2020-2027 doi:10.1134/S0022476622120137), IF=1.004
  91. M.P. Davydova, I.Yu. Bagryanskaya, E.H. Sadykov, A.V. Artem'ev
    A pyrimidine-derived diphosphine P-monoxide and a Ag(I) coordination polymer thereof: synthesis, structure, and luminescence
    Журнал структурной химии. 2022. Т. 63. № 12. С. 103553. doi:10.26902/JSC_id103553 (A PYRIMIDINE-DERIVED DIPHOSPHINE P-MONOXIDE AND A Ag(I) COORDINATION POLYMER THEREOF: SYNTHESIS, STRUCTURE, AND LUMINESCENCE/ M. P. Davydova, I. Yu. Bagryanskaya, E. H. Sadykov, A. V. Artem'ev// Journal of Structural Chemistry, 2022, V.63, N 12, pp 2020-2027 doi:10.1134/S0022476622120137), IF=1.004
  92. А.А. Мункуев, А.Ж. Шешковас, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов
    Оптимизация метода синтеза 2-адамантанкарбоновой кислоты
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 632-636. doi:10.15372/KhUR2022424 (OPTIMIZATION OF THE SYNTHESIS OF 2-ADAMANTANECARBOXYLIC ACID/ Munkuev A.A., Sheshkovas A.Zh., Suslov E.V., Volcho K.P., Salakhutdinov N.F.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 612-616. doi:10.15372/CSD2022424)
  93. Морозов С.В., Ширапова Г.С., Ермолаева О.А., Черняк Е.И., Ткачева Н.И., Батоев В.Б., Могнонов Д.М.
    Изучение поведения стойких органических загрязнителей в Байкал-Селенгинской экосистеме как элемент выполнения Стокгольмской конвенции
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 620-631. doi:10.15372/KhUR2022423 (STUDIES OF THE BEHAVIOUR OF PERSISTENT ORGANIC POLLUTANTS IN THE BAIKAL-SELENGA ECOSYSTEM AS AN ELEMENT OF THE IMPLEMENTATION OF THE STOCKHOLM CONVENTION/ Morozov S.V., Shirapova G.S., Ermolaeva O.A., Chernyak E.I., Tkacheva N.I., Batoev V.B., Mognonov D.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 600-611. doi:10.15372/CSD2022423)
  94. Морозов С.В., Ширапова Г.С., Ермолаева О.А., Черняк Е.И., Ткачева Н.И., Батоев В.Б., Могнонов Д.М.
    Изучение поведения стойких органических загрязнителей в Байкал-Селенгинской экосистеме как элемент выполнения Стокгольмской конвенции
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 620-631. doi:10.15372/KhUR2022423 (STUDIES OF THE BEHAVIOUR OF PERSISTENT ORGANIC POLLUTANTS IN THE BAIKAL-SELENGA ECOSYSTEM AS AN ELEMENT OF THE IMPLEMENTATION OF THE STOCKHOLM CONVENTION/ Morozov S.V., Shirapova G.S., Ermolaeva O.A., Chernyak E.I., Tkacheva N.I., Batoev V.B., Mognonov D.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 600-611. doi:10.15372/CSD2022423)
  95. Морозов С.В., Ширапова Г.С., Ермолаева О.А., Черняк Е.И., Ткачева Н.И., Батоев В.Б., Могнонов Д.М.
    Изучение поведения стойких органических загрязнителей в Байкал-Селенгинской экосистеме как элемент выполнения Стокгольмской конвенции
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 620-631. doi:10.15372/KhUR2022423 (STUDIES OF THE BEHAVIOUR OF PERSISTENT ORGANIC POLLUTANTS IN THE BAIKAL-SELENGA ECOSYSTEM AS AN ELEMENT OF THE IMPLEMENTATION OF THE STOCKHOLM CONVENTION/ Morozov S.V., Shirapova G.S., Ermolaeva O.A., Chernyak E.I., Tkacheva N.I., Batoev V.B., Mognonov D.M.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 600-611. doi:10.15372/CSD2022423)
  96. Е.С. Можайцев, А.А. Охина, К.Ю. Пономарев, А.Д. Рогачев, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
    N,N-замещенные биспидины как лиганды металлокомплексных катализаторов реакции этинилирования
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 615-619. doi:10.15372/KhUR2022422 (N,N-SUBSTITUTED BISPIDINES AS LIGANDS OF METAL COMPLEX CATALYSTS FOR THE ETHYNYLATION REACTION/ Mozhaitsev E.S., Okhina A.A., Ponomarev K.Yu., Rogachev A.D., Suslov E.V., Volcho K.P., Salakhutdinov N.F., Vatsadze S.Z.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 595-599. doi:10.15372/CSD2022422)
  97. Е.В. Карпова, Ю.С. Сотникова, А.В. Ластовка, А.В. Бауло, И.В. Сальникова
    Исследование домотканых культовых предметов хантов и манси конца XVIII века физико-химическими методами
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 605-614. doi:10.15372/KhUR2022421 (PHYSICOCHEMICAL INVESTIGATION OF HOMESPUN CULT OBJECTS OF THE KHANTY AND MANSI MADE AT THE END OF THE XVIII CENTURY/ Karpova E.V., Sotnikova Yu.S., Lastovka A.V., Baulo A.V., Salnikova I.V.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 585-594. doi:10.15372/CSD2022421)
  98. Е.В. Карпова, Ю.С. Сотникова, А.В. Ластовка, А.В. Бауло, И.В. Сальникова
    Исследование домотканых культовых предметов хантов и манси конца XVIII века физико-химическими методами
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 605-614. doi:10.15372/KhUR2022421 (PHYSICOCHEMICAL INVESTIGATION OF HOMESPUN CULT OBJECTS OF THE KHANTY AND MANSI MADE AT THE END OF THE XVIII CENTURY/ Karpova E.V., Sotnikova Yu.S., Lastovka A.V., Baulo A.V., Salnikova I.V.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 585-594. doi:10.15372/CSD2022421)
  99. Н.В. Басов, А.Д. Рогачев, Ю.С. Сотникова, Ю.В. Патрушев, А.Г. Покровский
    Исследование хроматографического поведения метаболитов из плазмы крови методом ВЭЖХ-МС/МС с использованием монолитной колонки с сорбентом на основе 1-винил-1,2,4-триазола
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 591-598. doi:10.15372/KhUR2022419 (INVESTIGATION OF THE CHROMATOGRAPHIC BEHAVIOUR OF METABOLITES FROM BLOOD PLASMA BY HPLC-MS/MS USING A MONOLITHIC COLUMN WITH A SORBENT BASED ON 1-VINYL-1,2,4-TRIAZOLE/ Basov N.V., Rogachev A.D., Sotnikova Yu.S., Patrushev Yu.V., Pokrovsky A.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 571-578. doi:10.15372/CSD2022419)
  100. Н.В. Басов, А.Д. Рогачев, Ю.С. Сотникова, Ю.В. Патрушев, А.Г. Покровский
    Исследование хроматографического поведения метаболитов из плазмы крови методом ВЭЖХ-МС/МС с использованием монолитной колонки с сорбентом на основе 1-винил-1,2,4-триазола
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 591-598. doi:10.15372/KhUR2022419 (INVESTIGATION OF THE CHROMATOGRAPHIC BEHAVIOUR OF METABOLITES FROM BLOOD PLASMA BY HPLC-MS/MS USING A MONOLITHIC COLUMN WITH A SORBENT BASED ON 1-VINYL-1,2,4-TRIAZOLE/ Basov N.V., Rogachev A.D., Sotnikova Yu.S., Patrushev Yu.V., Pokrovsky A.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 571-578. doi:10.15372/CSD2022419)
  101. Н.В. Басов, А.Д. Рогачев, Ю.С. Сотникова, Ю.В. Патрушев, А.Г. Покровский
    Исследование хроматографического поведения метаболитов из плазмы крови методом ВЭЖХ-МС/МС с использованием монолитной колонки с сорбентом на основе 1-винил-1,2,4-триазола
    Химия в интересах устойчивого развития. 2022. Т. 30. № 6. С. 591-598. doi:10.15372/KhUR2022419 (INVESTIGATION OF THE CHROMATOGRAPHIC BEHAVIOUR OF METABOLITES FROM BLOOD PLASMA BY HPLC-MS/MS USING A MONOLITHIC COLUMN WITH A SORBENT BASED ON 1-VINYL-1,2,4-TRIAZOLE/ Basov N.V., Rogachev A.D., Sotnikova Yu.S., Patrushev Yu.V., Pokrovsky A.G.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 571-578. doi:10.15372/CSD2022419)
  102. L. Politanskaya, B. Khasano, A. Potapov
    Synthetic approaches to fluorinated derivatives of 4-(vinylthio)pyridine
    Journal of Fluorine Chemistry, V. 264, December 2022, 110063 doi:10.1016/j.jfluchem.2022.110063, IF=2.226
  103. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  104. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  105. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  106. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  107. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  108. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  109. S.V. Cheresiz, A.A. Kononona, M. Skarnovich, A.N. Volkova, Yu.A. Poletaeva, F. Emaminia, O.V. Pyankov, E.E. Schultz, A.G. Pokrovsky
    An Amide Derivative of Betulonic Acid as a New Inhibitor of Sars-CoV-2 Spike Protein-Mediated Cell Entry and Sars-CoV-2 Infection
    Insight in Chem & Biochem. 2(2): 2022. ICBC. MS.ID.000535. doi:10.33552/ICBC.2022.02.000535
  110. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
    A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
    Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
  111. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
    A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
    Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
  112. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
    A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
    Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
  113. A. Kotlyarova, A.V. Podturkina, A.V. Pavlova, D.S. Gorina, A.V. Lastovka, O.V. Ardashov, A.D. Rogachev, A.E. Izyurov, A.B. Arefieva, A.V. Kulikov, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov, Yu. Sidorova
    A Newly Identified Monoterpenoid-Based Small Molecule Able to Support the Survival of Primary Cultured Dopamine Neurons and Alleviate MPTP-Induced Toxicity In Vivo
    Molecules 2022, 27(23), 8286; doi:10.3390/molecules27238286, IF=4.927
  114. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  115. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  116. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  117. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  118. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  119. E.O. Shestakova, S.G. Il'yasov, I.A. Shchurova, V.S. Glukhacheva, D.S. Il'yasov, E.E. Zhukov, A.O. Bryzgalov, T.G. Tolstikova, Yu.V. Gatilov
    Investigation of 1,4-Substituted 1,2,3-Triazole Derivatives as Antiarrhythmics: Synthesis, Structure, and Properties
    Pharmaceuticals 2022, 15(12), 1443 doi:10.3390/ph15121443, IF=5.215
  120. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  121. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  122. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  123. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  124. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  125. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  126. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  127. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  128. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  129. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  130. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  131. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  132. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  133. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  134. V.A. Ivanisenko, E.V. Gaisler, N.V. Basov, A.D. Rogachev, S.V. Cheresiz, T.V. Ivanisenko, P.S. Demenkov, E.L. Mishchenko, O.P. Khripko, Yu.I. Khripko, S.M. Voevoda, T.N. Karpenko, A.J. Velichko, M.I. Voevoda, N.A. Kolchanov, A.G. Pokrovsky
    Plasma metabolomics and gene regulatory networks analysis reveal the role of nonstructural SARS-CoV-2 viral proteins in metabolic dysregulation in COVID-19 patients
    Scientific Reports, 2022, V. 12, Article number: 19977 doi:10.1038/s41598-022-24170-0, IF=4.995
  135. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, M.S. Fedotova, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Study of Hypoglycemic Activity of Novel 9-N-alkyltetrahydroberberine Derivatives
    Int. J. Mol. Sci. 2022, 23(22), 14186 doi:10.3390/ijms232214186, IF=6.208
  136. E. Benassi, T. Vaganova, E. Malykhin, Yu. Gatilov, L. Nurtay, H. Fanc
    Intermolecular Interactions in the Crystalline Structure of Some Polyhalogenated Di– and Triamino Pyridines: Spectroscopical Perspectives
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, V. 281, 15 November 2022, 121632 doi:10.1016/j.saa.2022.121632, IF=4.83
  137. E. Benassi, T. Vaganova, E. Malykhin, Yu. Gatilov, L. Nurtay, H. Fanc
    Intermolecular Interactions in the Crystalline Structure of Some Polyhalogenated Di– and Triamino Pyridines: Spectroscopical Perspectives
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, V. 281, 15 November 2022, 121632 doi:10.1016/j.saa.2022.121632, IF=4.83
  138. E. Benassi, T. Vaganova, E. Malykhin, Yu. Gatilov, L. Nurtay, H. Fanc
    Intermolecular Interactions in the Crystalline Structure of Some Polyhalogenated Di– and Triamino Pyridines: Spectroscopical Perspectives
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, V. 281, 15 November 2022, 121632 doi:10.1016/j.saa.2022.121632, IF=4.83
  139. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  140. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  141. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  142. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  143. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  144. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  145. V.S. Glukhacheva, S.G. Il'yasov, E.O. Shestakova, E.E. Zhukov, D.S. Il'yasov, A.A. Minakova, I.V. Eltsov, A.A. Nefedov, A.M. Genaev
    Synthesis of Nitro- and Acetyl Derivatives of 3,7,10-Trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane
    Materials 2022, 15(23), 8320 doi:10.3390/ma15238320, IF=3.747
  146. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  147. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  148. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  149. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  150. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  151. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  152. A.S. Sokolova, O.I. Yarovaya, L.V. Kuzminykh, A.A. Shtro, A.M. Klabukov, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.S. Borisevich, E.M. Khamitov, N.F. Salakhutdinov
    Discovery of N-Containing (-)-Borneol Esters as Respiratory Syncytial Virus Fusion Inhibitors
    Pharmaceuticals 2022, 15(11), 1390 doi:10.3390/ph15111390, IF=5.215
  153. S.A. Dobrynin, M.M. Gulman, D.A. Morozov, I.F. Zhurko, A.I. Taratayko, Yu.S. Sotnikova, Yu.I. Glazachev, Yu.V. Gatilov, I.A. Kirilyuk
    Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides
    Molecules 2022, 27(21), 7626 doi:10.3390/molecules27217626, IF=4.927
  154. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  155. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  156. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  157. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  158. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  159. N.K. Korbozova, N.O. Kudrina, N.A. Zhukova, A.E. Grazhdannikov, I.V. Blavachinskaya, G.A. Seitimova, T.E. Kulmanov, T.G. Tolstikova, N.V. Terletskaya
    Antihypothyroid Effect of Salidroside
    Molecules 2022, 27(21), 7487 doi:10.3390/molecules27217487, IF=4.927
  160. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  161. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  162. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  163. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  164. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  165. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  166. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, S.N. Belogorodtsev, Ya.Sh. Schwartz
    Studies of the Specific Activity of Aerosolized Isoniazid against Tuberculosis in a Mouse Model
    Antibiotics 2022, 11(11), 1527 doi:10.3390/antibiotics11111527, IF=5.222
  167. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  168. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  169. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  170. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  171. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  172. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  173. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  174. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  175. D. Avgustinovich, A. Kizimenko, M. Marenina, M. Lvova, A. Kovner, I. Orlovskaya, L. Toporkova, E. Goiman, M. Tsyganov, D. Ponomarev
    Prolonged liver fluke infection combined with alcoholization: An experimental mouse model
    Experimental Parasitology, 2022, V. 242, November 2022, 108399 doi:10.1016/j.exppara.2022.108399, IF=2.131
  176. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
    Journal of Catalysis, 2022, V. 415, November 2022, Pp 12-18 doi:10.1016/j.jcat.2022.09.020, IF=8.46
  177. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
    Journal of Catalysis, 2022, V. 415, November 2022, Pp 12-18 doi:10.1016/j.jcat.2022.09.020, IF=8.46
  178. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
    Journal of Catalysis, 2022, V. 415, November 2022, Pp 12-18 doi:10.1016/j.jcat.2022.09.020, IF=8.46
  179. Д.С. Одинцов, И.К. Шундрина, А.А. Гисматулин, И.А. Азаров, Р.В. Андреев, В.А. Гриценко, Л.А. Шундрин
    Термостойкие полиимиды с электроноакцепторными пендантными группами тиоксантенонового ряда для запоминающих устройств резистивного типа с малым напряжением переключений
    Журнал структурной химии. 2022. Т. 63. № 11. С. 101782. doi: 10.26902/JSC_id101782 (HEAT-RESISTANT POLYIMIDES WITH ELECTRON-ACCEPTOR PENDANT GROUPS OF THE THIOXANTHENONE SERIES FOR RESISTIVE STORAGE DEVICES WITH A LOW SWITCHING VOLTAGE/ D. S. Odintsov, I. K. Shundrina, A. A. Gismatulin, I. A. Azarov, R. V. Andreev, V. A. Gritsenko & L. A. Shundrin// Journal of Structural Chemistry, 2022, V.63, N 11, pp 811-1819 doi:10.1134/S0022476622110117), IF=1.3
  180. Д.С. Одинцов, И.К. Шундрина, А.А. Гисматулин, И.А. Азаров, Р.В. Андреев, В.А. Гриценко, Л.А. Шундрин
    Термостойкие полиимиды с электроноакцепторными пендантными группами тиоксантенонового ряда для запоминающих устройств резистивного типа с малым напряжением переключений
    Журнал структурной химии. 2022. Т. 63. № 11. С. 101782. doi: 10.26902/JSC_id101782 (HEAT-RESISTANT POLYIMIDES WITH ELECTRON-ACCEPTOR PENDANT GROUPS OF THE THIOXANTHENONE SERIES FOR RESISTIVE STORAGE DEVICES WITH A LOW SWITCHING VOLTAGE/ D. S. Odintsov, I. K. Shundrina, A. A. Gismatulin, I. A. Azarov, R. V. Andreev, V. A. Gritsenko & L. A. Shundrin// Journal of Structural Chemistry, 2022, V.63, N 11, pp 811-1819 doi:10.1134/S0022476622110117), IF=1.3
  181. Д.С. Одинцов, И.К. Шундрина, А.А. Гисматулин, И.А. Азаров, Р.В. Андреев, В.А. Гриценко, Л.А. Шундрин
    Термостойкие полиимиды с электроноакцепторными пендантными группами тиоксантенонового ряда для запоминающих устройств резистивного типа с малым напряжением переключений
    Журнал структурной химии. 2022. Т. 63. № 11. С. 101782. doi: 10.26902/JSC_id101782 (HEAT-RESISTANT POLYIMIDES WITH ELECTRON-ACCEPTOR PENDANT GROUPS OF THE THIOXANTHENONE SERIES FOR RESISTIVE STORAGE DEVICES WITH A LOW SWITCHING VOLTAGE/ D. S. Odintsov, I. K. Shundrina, A. A. Gismatulin, I. A. Azarov, R. V. Andreev, V. A. Gritsenko & L. A. Shundrin// Journal of Structural Chemistry, 2022, V.63, N 11, pp 811-1819 doi:10.1134/S0022476622110117), IF=1.3
  182. L. Politanskaya, Ji.Wang, N.Troshkova, I.Chuikov, I. Bagryanskayaa
    One-pot synthesis of fluorinated 2-arylchroman-4-one derivatives from 2-(triisopropylsilyl)ethynylphenols and aromatic aldehydes
    Journal of Fluorine Chemistry V. 263, November 2022, 110045 doi:10.1016/j.jfluchem.2022.110045, IF=2.226
  183. A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
    Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
    Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
  184. A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
    Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
    Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
  185. A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
    Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
    Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
  186. A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
    Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
    Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
  187. A.V. Artem'ev, A.Yu. Baranov, A.S. Berezin, U.A. Lapteva, D.G. Samsonenko, I.Yu. Bagryanskaya
    Trigonal Planar Au@Ag3 Clusters Showing Exceptionally Fast and Efficient Phosphorescence in Violet to Deep-Blue Region
    Chemistry-A European Journal, 2022, V. 28, Iss. 60 , e202201563 doi:10.1002/chem.202201563, IF=5.02
  188. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  189. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  190. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  191. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  192. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  193. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  194. N. A. Shekhovtsov, E. B. Nikolaenkova, A. S. Berezin, V.F. Plyusnin, K. A. Vinogradova, D. Yu. Naumov, N. V. Pervukhina, A. Ya. Tikhonov, M. B. Bushuev
    Tuning ESIPT-coupled luminescence by expanding π-conjugation of a proton acceptor moiety in ESIPT-capable zinc(ii) complexes with 1-hydroxy-1H-imidazole-based ligands
    Dalton Trans., 2022, 51(16), 15166-15188 doi:10.1039/D2DT02460H, IF=4.569
  195. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  196. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  197. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  198. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  199. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  200. S.A. Stepanenko, D.M. Shivtsov, A.P. Koskin, I.P. Koskin, R.G. Kukushkin, P.M. Yeletsky, V.A. Yakovlev
    N-Heterocyclic Molecules as Potential Liquid Organic Hydrogen Carriers: Reaction Routes and Dehydrogenation Efficacy
    Catalysts 2022, 12(10), 1260; doi:10.3390/catal12101260, IF=4.5
  201. Д.А. Соколов, И.С. Иванова, С.В. Морозов, Т.Г. Пчельникова, Е.А. Солдатова
    ПОЛИЦИКЛИЧЕСКИЕ АРОМАТИЧЕСКИЕ УГЛЕВОДОРОДЫ В ТОРФЯНЫХ ОЛИГОТРОФНЫХ ПОЧВАХ СЕВЕРНЫХ ТЕРРИТОРИЙ ЗАПАДНОЙ СИБИРИ
    Почвоведение. 2022. № 10. С. 1228-1240. doi;10.31857/S0032180X22100148 (Eurasian Soil Science, 2022, V. 55, Pp. 1360-1370/ D.A. Sokolov, I.S. Ivanova, S.V. Morozov, T.G. Pchelnikova, E.A. Soldatova// Eurasian Soil Science doi:10.1134/S1064229322100143), IF=1.373
  202. Д.А. Соколов, И.С. Иванова, С.В. Морозов, Т.Г. Пчельникова, Е.А. Солдатова
    ПОЛИЦИКЛИЧЕСКИЕ АРОМАТИЧЕСКИЕ УГЛЕВОДОРОДЫ В ТОРФЯНЫХ ОЛИГОТРОФНЫХ ПОЧВАХ СЕВЕРНЫХ ТЕРРИТОРИЙ ЗАПАДНОЙ СИБИРИ
    Почвоведение. 2022. № 10. С. 1228-1240. doi;10.31857/S0032180X22100148 (Eurasian Soil Science, 2022, V. 55, Pp. 1360-1370/ D.A. Sokolov, I.S. Ivanova, S.V. Morozov, T.G. Pchelnikova, E.A. Soldatova// Eurasian Soil Science doi:10.1134/S1064229322100143), IF=1.373
  203. Д.А. Соколов, И.С. Иванова, С.В. Морозов, Т.Г. Пчельникова, Е.А. Солдатова
    ПОЛИЦИКЛИЧЕСКИЕ АРОМАТИЧЕСКИЕ УГЛЕВОДОРОДЫ В ТОРФЯНЫХ ОЛИГОТРОФНЫХ ПОЧВАХ СЕВЕРНЫХ ТЕРРИТОРИЙ ЗАПАДНОЙ СИБИРИ
    Почвоведение. 2022. № 10. С. 1228-1240. doi;10.31857/S0032180X22100148 (Eurasian Soil Science, 2022, V. 55, Pp. 1360-1370/ D.A. Sokolov, I.S. Ivanova, S.V. Morozov, T.G. Pchelnikova, E.A. Soldatova// Eurasian Soil Science doi:10.1134/S1064229322100143), IF=1.373
  204. Д.А. Соколов, И.С. Иванова, С.В. Морозов, Т.Г. Пчельникова, Е.А. Солдатова
    ПОЛИЦИКЛИЧЕСКИЕ АРОМАТИЧЕСКИЕ УГЛЕВОДОРОДЫ В ТОРФЯНЫХ ОЛИГОТРОФНЫХ ПОЧВАХ СЕВЕРНЫХ ТЕРРИТОРИЙ ЗАПАДНОЙ СИБИРИ
    Почвоведение. 2022. № 10. С. 1228-1240. doi;10.31857/S0032180X22100148 (Eurasian Soil Science, 2022, V. 55, Pp. 1360-1370/ D.A. Sokolov, I.S. Ivanova, S.V. Morozov, T.G. Pchelnikova, E.A. Soldatova// Eurasian Soil Science doi:10.1134/S1064229322100143), IF=1.373
  205. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  206. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  207. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  208. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  209. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  210. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  211. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  212. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  213. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  214. E. Khusnutdinova, Z. Galimova, A. Lobov, I. Baikova, O. Kazakova, Ha Nguyen Thi. Thu, N.V.. Tuyen, Yu. Gatilov, R. Csuk, I. Serbian, S. Hoenke
    Synthesis of messagenin and platanic acid chalcone derivatives and their biological potential
    Natural Product Research, 2022, V. 36 (20), Pp 5189-5198 doi:10.1080/14786419.2021.1922904, IF=2.488
  215. В.В. Шелковников, Д.И. Деревянко, Е.Ф. Пен
    Влияние термической пост-обработки на спектральные сдвиги фотополимерных отражательных голограмм и её использование для получения цветоделённых изображений
    Оптика и спектроскопия. 2022. Т. 130. № 10. С. 1559-1566. (EFFECT OF POST HEAT-TREATMENT ON SPECTRAL SHIFTS PHOTOPOLYMER REFLECTION HOLOGRAMS AND ITS USE FOR CREATING COLOR HOLOGRAMS/ SHELKOVNIKOV V.V., DEREVYANKO D. I., PEN E. F.// doi: 10.21883/OS.2022.10.53626.3795-22)
  216. Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya, A.V. Artem'ev
    1D CuI coordination polymers based on triphenylarsine and N,N'-ditopic co-ligands: synthesis, crystal structure and TADF properties
    Mendeleev Communications, 2022, 32(5), 649-651 doi:10.1016/j.mencom.2022.09.027, IF=1.837
  217. Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya, A.V. Artem'ev
    1D CuI coordination polymers based on triphenylarsine and N,N'-ditopic co-ligands: synthesis, crystal structure and TADF properties
    Mendeleev Communications, 2022, 32(5), 649-651 doi:10.1016/j.mencom.2022.09.027, IF=1.837
  218. Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya, A.V. Artem'ev
    1D CuI coordination polymers based on triphenylarsine and N,N'-ditopic co-ligands: synthesis, crystal structure and TADF properties
    Mendeleev Communications, 2022, 32(5), 649-651 doi:10.1016/j.mencom.2022.09.027, IF=1.837
  219. O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
    Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
    Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
  220. O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
    Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
    Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
  221. O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
    Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene
    Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
  222. O.I. Yarovaya, K.S. Kovaleva, S.S. Borisevich, T.V. Rybalova, Yu.V. Gatilov, E.O. Sinegubova, A.S. Volobueva, V.V. Zarubaev
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    Mendeleev Communications, 2022, 32(5), pp. 609-611 doi:10.1016/j.mencom.2022.09.013, IF=1.837
  223. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  224. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  225. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  226. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  227. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  228. D.I. Ivankin, N.S. Dyrkheeva, A.a L. Zakharenko, E.S. Ilina, T.O. Zarkov, J. Reynisson, O.A. Luzina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Monoterpene substituted thiazolidin-4-ones as novel TDP1 inhibitors: synthesis, biological evaluation and docking
    Bioorganic & Medicinal Chemistry Letters, V. 73, 1 October 2022, 128909 doi:10.1016/j.bmcl.2022.128909, IF=2.94
  229. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  230. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  231. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  232. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  233. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  234. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  235. A.S. Filimonov, O.I. Yarovaya, A.V. Zaykovskaya, N.B. Rudometova, D.N. Shcherbakov, V.Yu. Chirkova, D.S. Baev, S.S. Borisevich, O.A. Luzina, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    (+)-Usnic Acid and Its Derivatives as Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(10), 2154 doi:10.3390/v14102154, IF=5.817
  236. Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
    Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
    Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
  237. Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
    Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
    Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
  238. Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
    Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
    Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
  239. Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
    Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
    Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
  240. Ya.V. Demyanov, E.H. Sadykov, M.I. Rakhmanova, A.S. Novikov, I.Yu. Bagryanskaya, A.V. Artem'ev
    Tris(2-Pyridyl)Arsine as a New Platform for Design of Luminescent Cu(I) and Ag(I) Complexes
    Molecules 2022, 27(18), 6059 doi:10.3390/molecules27186059, IF=4.927
  241. A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    DFT insights into superelectrophilic activation of α,β-unsaturated nitriles and ketones in superacids
    Org. Biomol. Chem., 2022,20(34), 6799-6808 doi:10.1039/D2OB01141G, IF=3.89
  242. S. Wang, Ya.V. Zonov, V.M. Karpov, O.A. Luzina, T.V. Mezhenkova
    Carbonylation of Polyfluorinated 1-Arylalkan-1-ols and Diols in Superacids
    Molecules 2022, 27(24), 8757 doi:10.3390/molecules27248757, IF=4.927
  243. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  244. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  245. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  246. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  247. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  248. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
  249. Hu. Han, V.N. Kovtonyuk, Yu.V. Gatilov, R.V. Andreev
    Directed synthesis of isomeric polyfluorinated dinitrotetraoxacalixarenes and bicyclooxacalixarenes
    Journal of Fluorine Chemistry, 2022, V.261-262, 110022 doi:10.1016/j.jfluchem.2022.110022, IF=2.226
  250. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  251. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  252. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  253. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  254. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  255. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  256. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  257. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  258. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  259. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  260. S. Dragomanova, M. Lazarova, A. Munkuev, E. Suslov, K. Volcho, N. Salakhutdinov, A. Bibi, J. Reynisson, E. Tzvetanova, A. Alexandrova, A. Georgieva, D. Uzunova, M. Stefanova, R. Kalfin, L. Tancheva
    New Myrtenal-Adamantane Conjugates Alleviate Alzheimer’s-Type Dementia in Rat Model
    Molecules 2022, 27(17), 5456 doi:10.3390/molecules27175456, IF=4.927
  261. A.D. Kuimov, Ch.S. Becker, N.A. Shumilov, I.P. Koskin, A.A. Sonina, V.Yu. Komarov, I.K. Shundrina, M.S. Kazantsev
    Synthetic approach for the control of self-doping in luminescent organic semiconductors
    Mater. Chem. Front., 2022, V. 6, N 16, Pp. 2244-2255 doi:10.1039/D2QM00345G, IF=8.683
  262. M.D. Ganina, M.V. Tyurin, Ulz.T. Zhumatayeva, G.R. Lednev, S.V. Morozov, V.Yu. Kryukov
    Comparative Analysis of Epicuticular Lipids in Locusta migratoria and Calliptamus italicus: A Possible Role in Susceptibility to Entomopathogenic Fungi
    Insects 2022, 13(8), 736 doi:10.3390/insects13080736, IF=3.138
  263. M.D. Ganina, M.V. Tyurin, Ulz.T. Zhumatayeva, G.R. Lednev, S.V. Morozov, V.Yu. Kryukov
    Comparative Analysis of Epicuticular Lipids in Locusta migratoria and Calliptamus italicus: A Possible Role in Susceptibility to Entomopathogenic Fungi
    Insects 2022, 13(8), 736 doi:10.3390/insects13080736, IF=3.138
  264. M.D. Ganina, M.V. Tyurin, Ulz.T. Zhumatayeva, G.R. Lednev, S.V. Morozov, V.Yu. Kryukov
    Comparative Analysis of Epicuticular Lipids in Locusta migratoria and Calliptamus italicus: A Possible Role in Susceptibility to Entomopathogenic Fungi
    Insects 2022, 13(8), 736 doi:10.3390/insects13080736, IF=3.138
  265. M.D. Ganina, M.V. Tyurin, Ulz.T. Zhumatayeva, G.R. Lednev, S.V. Morozov, V.Yu. Kryukov
    Comparative Analysis of Epicuticular Lipids in Locusta migratoria and Calliptamus italicus: A Possible Role in Susceptibility to Entomopathogenic Fungi
    Insects 2022, 13(8), 736 doi:10.3390/insects13080736, IF=3.138
  266. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  267. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  268. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  269. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  270. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  271. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  272. A.A. Dokuchaeva, A.a B. Mochalova, T.P. Timchenko, K.S. Podolskaya, O.A. Pashkovskaya, E.V. Karpova, I.A. Ivanov, N.A. Filatova I. Yu Zhuravleva
    In Vivo Evaluation of PCL Vascular Grafts Implanted in Rat Abdominal Aorta
    Polymers 2022, 14(16), 3313 doi:10.3390/polym14163313, IF=4.967
  273. E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
    Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
    New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
  274. E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
    Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
    New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
  275. E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
    Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
    New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
  276. E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
    Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
    New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
  277. E.A. Radiush, E.A. Pritchina, E.A. Chulanova, A.A. Dmitriev, I. Yu Bagryanskaya, A.M-Z. Slawin, J. D. Woollins, N.P. Gritsan, A.V. Zibarev, N.A. Semenov
    Chalcogen-bonded donor–acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions Check for updates
    New J. Chem., 2022,46(30), 14490-14501 doi:10.1039/D2NJ02345H, IF=3.924
  278. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  279. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  280. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  281. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  282. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  283. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  284. L. G. Lavrenova,O. G. Shakirova,E. V. Korotaev,S.V. Trubina,A.Ya. Tikhonov,I. A. Os'kina,S. A. Petrov,K. Yu. Zhizhin,N. T. Kuznetsov
    High-Temperature Spin Crossover in Iron(II) Complexes with 2,6-Bis(1H-imidazol-2-yl)pyridine
    Molecules 2022, 27(16), 5093 doi:10.3390/molecules27165093, IF=4.927
  285. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  286. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  287. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  288. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  289. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  290. I.B. Ivshina, N.A. Luchnikova, P.Yu. Maltseva, I.V. Ilyina, K.P. Volcho, Yu.V. Gatilov, D.V. Korchagina, N.A. Kostrikina, V.V. Sorokin, A.L. Mulyukin, N.F. Salakhutdinov
    Biotransformation of (-)-Isopulegol by Rhodococcus rhodochrous
    Pharmaceuticals 2022, 15(8), 964; doi:10.3390/ph15080964, IF=5.215
  291. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  292. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  293. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  294. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  295. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  296. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  297. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  298. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  299. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bychinsky, V.A. Bobrov, A.E. Maltsev, V.D. Tikhova, L.V. Miroshnichenko, L.M. Kondratyeva, A.E. Kuzmina
    Biogeochemistry and element speciation in sapropel from freshwater Lake Dukhovoe (East Baikal region, Russia)
    Applied Geochemistry, 2022, V. 143,105384 doi:10.1016/j.apgeochem.2022.105384, IF=3.841
  300. N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
    Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
    Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
  301. N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
    Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
    Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
  302. N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
    Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
    Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
  303. N.S. Li-Zhulanov, I.V. Il'ina, A.Yu. Sidorenko, D.V. Korchagina, K.P. Volcho, V.E. Agabekov, N.F. Salakhutdinov
    Cascade transformation of 4-hydroxymethyl-2-carene into novel cage methanopyrano[4,3-b]thieno[3,2-g]benzofuran derivative
    Mendeleev Communications, V. 32, N 4, July-August 2022, Pp 443-445 doi:10.1016/j.mencom.2022.07.005, IF=1.837
  304. N.S. Li-Zhulanov, I.V. Il'ina, A.Yu. Sidorenko, D.V. Korchagina, K.P. Volcho, V.E. Agabekov, N.F. Salakhutdinov
    Cascade transformation of 4-hydroxymethyl-2-carene into novel cage methanopyrano[4,3-b]thieno[3,2-g]benzofuran derivative
    Mendeleev Communications, V. 32, N 4, July-August 2022, Pp 443-445 doi:10.1016/j.mencom.2022.07.005, IF=1.837
  305. S.I. Dikalov, A.E. Dikalova, I.A. Kirilyuk
    Coupling of phagocytic NADPH oxidase activity and mitochondrial superoxide production
    Frontiers in Cardiovascular Medicine, 2022, 9, 942736 doi:10.3389/fcvm.2022.942736, IF=5.846
  306. S.I. Dikalov, A.E. Dikalova, I.A. Kirilyuk
    Coupling of phagocytic NADPH oxidase activity and mitochondrial superoxide production
    Frontiers in Cardiovascular Medicine, 2022, 9, 942736 doi:10.3389/fcvm.2022.942736, IF=5.846
  307. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  308. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  309. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  310. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  311. Mingyang Han, Ivan Oleynik, Yanping Ma, Irina Oleynik, Gregory Solan, Xiang Hao, Wen-Hua Sun
    Modulating thermostability and productivity of benzhydryl-substituted bis(imino)pyridine-iron C2H4 polymerization catalysts through ortho-CnH2n-1 (n = 5, 6, 8, 12) ring size adjustment
    European Journal of Inorganic Chemistry, 2022, V. 2022, N 21, e202200224 doi:10.1002/ejic.202200224, IF=2.551
  312. V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
    Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
  313. V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
    Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
  314. V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
    Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
  315. V.V. Oreshko, K.S. Kovaleva, E.D. Mordvinova, O.I. Yarovaya, Yu.V. Gatilov, D.N. Shcherbakov, N.I. Bormotov, O.A. Serova, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and Antiviral Properties of Camphor-Derived Iminothiazolidine-4-Ones and 2,3-Dihydrothiazoles
    Molecules 2022, 27(15), 4761 doi:10.3390/molecules27154761, IF=4.927
  316. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  317. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  318. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  319. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  320. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  321. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  322. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  323. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  324. M. Babaev, E. Khusnutdinova, A. Lobov, Z. Galimova, A. Petrova, T. Rybalova, Thi Thu.Nguyen. Ha, C. Meyers, M. Prichard, O. Kazakova
    Allobetulone rearrangement to lαH,19βH-ursane triterpenoids with antiviral activity
    Natural Product Research, 2022, V. 36, N 13, Pp 3286-3296 doi:10.1080/14786419.2020.1855159, IF=2.488
  325. А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева, Л.Н. Захарова, А.В. Липеева, Э.Э. Шульц
    Антибактериальная активность производных пеуцеданина в отношении Staphylococcus aureus и Bacillus cereus
    Проблемы медицинской микологии. 2022. Т. 24. № 2. С. 67. (ВСЕРОССИЙСКИЙ КОНГРЕСС ПО МЕДИЦИНСКОЙ МИКРОБИОЛОГИИ, КЛИНИЧЕСКОЙ МИКОЛОГИИ И ИММУНОЛОГИИ-XXV КАШКИНСКИЕ ЧТЕНИЯ)
  326. А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева, Л.Н. Захарова, А.В. Липеева, Э.Э. Шульц
    Антибактериальная активность производных пеуцеданина в отношении Staphylococcus aureus и Bacillus cereus
    Проблемы медицинской микологии. 2022. Т. 24. № 2. С. 67. (ВСЕРОССИЙСКИЙ КОНГРЕСС ПО МЕДИЦИНСКОЙ МИКРОБИОЛОГИИ, КЛИНИЧЕСКОЙ МИКОЛОГИИ И ИММУНОЛОГИИ-XXV КАШКИНСКИЕ ЧТЕНИЯ)
  327. А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева, Л.Н. Захарова, А.В. Липеева, Э.Э. Шульц
    Антибактериальная активность производных пеуцеданина в отношении Staphylococcus aureus и Bacillus cereus
    Проблемы медицинской микологии. 2022. Т. 24. № 2. С. 67. (ВСЕРОССИЙСКИЙ КОНГРЕСС ПО МЕДИЦИНСКОЙ МИКРОБИОЛОГИИ, КЛИНИЧЕСКОЙ МИКОЛОГИИ И ИММУНОЛОГИИ-XXV КАШКИНСКИЕ ЧТЕНИЯ)
  328. А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева, Л.Н. Захарова, А.В. Липеева, Э.Э. Шульц
    Антибактериальная активность производных пеуцеданина в отношении Staphylococcus aureus и Bacillus cereus
    Проблемы медицинской микологии. 2022. Т. 24. № 2. С. 67. (ВСЕРОССИЙСКИЙ КОНГРЕСС ПО МЕДИЦИНСКОЙ МИКРОБИОЛОГИИ, КЛИНИЧЕСКОЙ МИКОЛОГИИ И ИММУНОЛОГИИ-XXV КАШКИНСКИЕ ЧТЕНИЯ)
  329. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  330. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  331. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  332. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  333. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  334. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  335. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  336. N.A. Shekhovtsov, K.A. Vinogradova, S.N. Vorobyova, A.S. Berezin, V.F. Plyusnin, D.Yu. Naumov, N.V. Pervukhina, E.B. Nikolaenkova, A.Ya. Tikhonov, M.B. Bushuev
    N-Hydroxy–N-oxide photoinduced tautomerization and excitation wavelength dependent luminescence of ESIPT-capable zinc(ii) complexes with a rationally designed 1-hydroxy-2,4-di(pyridin-2-yl)-1H-imidazole ESIPT-ligand
    Dalton Trans., 2022, V. 51, N 25, Pp 9818-9835 doi:10.1039/D2DT01232D, IF=4.569
  337. N.V. Terletskaya, N.K. Korbozova, A.E. Grazhdannikov, G.A. Seitimova, N.D. Meduntseva, N.O. Kudrina
    Accumulation of Secondary Metabolites of Rhodiola semenovii Boriss. In Situ in the Dynamics of Growth and Development
    Metabolites 2022, 12(7), 622 doi:10.3390/metabo12070622, IF=5.581
  338. N.V. Terletskaya, N.K. Korbozova, A.E. Grazhdannikov, G.A. Seitimova, N.D. Meduntseva, N.O. Kudrina
    Accumulation of Secondary Metabolites of Rhodiola semenovii Boriss. In Situ in the Dynamics of Growth and Development
    Metabolites 2022, 12(7), 622 doi:10.3390/metabo12070622, IF=5.581
  339. N.V. Terletskaya, N.K. Korbozova, A.E. Grazhdannikov, G.A. Seitimova, N.D. Meduntseva, N.O. Kudrina
    Accumulation of Secondary Metabolites of Rhodiola semenovii Boriss. In Situ in the Dynamics of Growth and Development
    Metabolites 2022, 12(7), 622 doi:10.3390/metabo12070622, IF=5.581
  340. N.V. Terletskaya, N.K. Korbozova, A.E. Grazhdannikov, G.A. Seitimova, N.D. Meduntseva, N.O. Kudrina
    Accumulation of Secondary Metabolites of Rhodiola semenovii Boriss. In Situ in the Dynamics of Growth and Development
    Metabolites 2022, 12(7), 622 doi:10.3390/metabo12070622, IF=5.581
  341. N.V. Terletskaya, N.K. Korbozova, A.E. Grazhdannikov, G.A. Seitimova, N.D. Meduntseva, N.O. Kudrina
    Accumulation of Secondary Metabolites of Rhodiola semenovii Boriss. In Situ in the Dynamics of Growth and Development
    Metabolites 2022, 12(7), 622 doi:10.3390/metabo12070622, IF=5.581
  342. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  343. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  344. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  345. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  346. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  347. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  348. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
  349. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  350. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  351. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  352. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  353. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  354. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  355. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  356. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  357. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  358. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
  359. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  360. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  361. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  362. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  363. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  364. G.C.Krieger Filho, F.Costa, G.F.Torraga Maria, P.Bufacchi, S.Trubachev, I.Shundrina, O.Korobeinichev
    Kinetic parameters and heat of reaction for forest fuels based on genetic algorithm optimization
    Thermochimica Acta, V. 713, July 2022, 179228 doi:10.1016/j.tca.2022.179228, IF=3.378
  365. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  366. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  367. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  368. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  369. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  370. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  371. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  372. A.Yu. Baranov, S.O. Slavova, A.S. Berezin, S.K. Petrovskii, D.G. Samsonenko, I.Yu. Bagryanskaya, V.P. Fedin, E.V. Grachova, A.V. Artem'ev
    Controllable Synthesis and Luminescence Behavior of Tetrahedral Au@Cu4 and Au@Ag4 Clusters Supported by tris(2-Pyridyl)phosphine
    Inorganic Chemistry, 2022, 61, 28, 10925-10933 doi:10.1021/acs.inorgchem.2c01474, IF=5.435
  373. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
    Известия Академии наук. Серия химическая. 2022. № 7. С. 1474-1482. (Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8), IF=1.704
  374. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
    Известия Академии наук. Серия химическая. 2022. № 7. С. 1474-1482. (Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8), IF=1.704
  375. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
    Известия Академии наук. Серия химическая. 2022. № 7. С. 1474-1482. (Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8), IF=1.704
  376. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
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  377. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
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  378. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
    Известия Академии наук. Серия химическая. 2022. № 7. С. 1474-1482. (Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8), IF=1.704
  379. П.А. Федюшин, А.Я. Акыева, М.А. Сыроешкин, Т.В. Рыбалова, Д.В. Стась, В.А. Королев, Е.В. Третьяков, М.П. Егоров
    Синтез, структура и свойства трет-бутилперфторбифенилнитроксила
    Известия Академии наук. Серия химическая. 2022. № 7. С. 1474-1482. (Synthesis, structure, and properties of tert-butyl perfluorobiphenyl nitroxide/ P.A. Fedyushin, A.Ya. Akyeva, M.A. Syroeshkin, T.V. Rybalova, D.V. Stass, V.A. Korolev, E.V. Tretyakov, M.P. Egorov// Russian Chemical Bulletin, 2022, V. 71, N 7, Pp 1474-1482 doi:10.1007/s11172-022-3553-8), IF=1.704
  380. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
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    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  381. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  382. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  383. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  384. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  385. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  386. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  387. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  388. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  389. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  390. Ia.S. Fomenko, M. Afewerki, M.I. Gongola, E.S. Vasilyev, L.S. Shu'pina, N.S. Ikonnikov, G.B. Shul'pin, D.G. Samsonenko, V.V. Yanshole, V.A. Nadolinny, A.N. Lavrov, A.V. Tkachev, A.L. Gushchin
    Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties
    Molecules 2022, 27(13), 4072 doi:10.3390/molecules27134072, IF=4.927
  391. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  392. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  393. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  394. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  395. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  396. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  397. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  398. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  399. O.I. Yarovaya, D.N. Shcherbakov, S.S. Borisevich, A.S. Sokolova, M.A. Gureev, E.M. Khamitov, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, A.D. Rogachev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Borneol Ester Derivatives as Entry Inhibitors of a Wide Spectrum of SARS-CoV-2 Viruses
    Viruses 2022, 14(6), 1295 doi:10.3390/v14061295, IF=5.818
  400. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  401. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  402. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  403. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  404. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  405. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  406. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  407. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  408. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  409. A. Sokolova, K.S. Kovaleva, S.O. Kuranov, N.I. Bormotov, S.S. Borisevich, O.I. Yarovaya, A. Zhukovets, O.A. Serova, M.B. Nawrozkij, A.A. Vernigora, A.V. Davidenko, E.M. Khamitov, R.Yu. Peshkov, L.N. Shishkina, R.A. Maksuytov, N.F. Salakhutdinov
    Design, synthesis and biological evaluation of novel (+)-сamphor and (-)-fenchone based derivatives as potent orthopoxviruses inhibitors
    ChemMedChem, 2022, V.17, N 12, e202100771 doi:10.1002/cmdc.202100771, IF=3.54
  410. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  411. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  412. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  413. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  414. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  415. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  416. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  417. V.V. Zarubaev, A.V. Garshinina, A.S. Volobueva, A.V. Slita, O.I. Yarovaya, V.V. Bykov, K.A. Leonov, V.S. Motov, V.A. Khazanov, N.F. Salakhutdinov
    Optimization of application schedule of camphecene, a novel anti-influenza compound, based on its pharmacokinetic characteristics
    Fundamental & Clinical Pharmacology, 2022, V.36, N 3, 2022, Pp 518-525 doi:10.1111/fcp.12750, IF=2.747
  418. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  419. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  420. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  421. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  422. Штро А.А., Галочкина А.В., Николаева Ю.В., Гаршинина А.В., Разгуляева Д.Н., Пономарев К.Ю., Можайцев Е.С., Суслов Е.В., Волчо К.П., Салахутдинов Н.Ф.
    Противовирусная активность производных адамантанов в отношении респираторно-синцитиального вируса
    Медицинский академический журнал. 2022. Т. 22. № 2. С. 115-123. doi:10.17816/MAJ108808
  423. S. Ketter, M. Dajka, O. Rogozhnikova, S.A. Dobrynin, V.M. Tormyshev, E.G. Bagryanskaya, B. Joseph
    In situ distance measurements in a membrane transporter using maleimide functionalized orthogonal spin labels and 5-pulse electron-electron double resonance spectroscopy
    Journal of Magnetic Resonance Open (companion title to the Journal of Magnetic Resonance), Volumes 10-11, June 2022, 100041 doi:10.1016/j.jmro.2022.100041
  424. S. Ketter, M. Dajka, O. Rogozhnikova, S.A. Dobrynin, V.M. Tormyshev, E.G. Bagryanskaya, B. Joseph
    In situ distance measurements in a membrane transporter using maleimide functionalized orthogonal spin labels and 5-pulse electron-electron double resonance spectroscopy
    Journal of Magnetic Resonance Open (companion title to the Journal of Magnetic Resonance), Volumes 10-11, June 2022, 100041 doi:10.1016/j.jmro.2022.100041
  425. S. Ketter, M. Dajka, O. Rogozhnikova, S.A. Dobrynin, V.M. Tormyshev, E.G. Bagryanskaya, B. Joseph
    In situ distance measurements in a membrane transporter using maleimide functionalized orthogonal spin labels and 5-pulse electron-electron double resonance spectroscopy
    Journal of Magnetic Resonance Open (companion title to the Journal of Magnetic Resonance), Volumes 10-11, June 2022, 100041 doi:10.1016/j.jmro.2022.100041
  426. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
  427. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
  428. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
  429. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
  430. S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
    Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
    Journal of Biomolecular Structure and Dynamics, 2022, V.40, N 12, Pp 5481-5492 doi:10.1080/07391102.2020.1871414, IF=5.235
  431. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  432. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  433. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  434. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  435. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.l. Laktionov
    Correction: Gostev et al. In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics. Polymers 2020, 12, 845
    Polymers 2022, 14(11), 2263; doi:10.3390/polym14112263, IF=4.967
  436. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
  437. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
  438. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
  439. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
  440. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
  441. M.A. Panfilov, T.Yu. Karogodina, Yao. Songyin, O.Yu. Karmatskih, A.Yu. Vorob'ev, I.S. Tretyakova, E.M. Glebov, A.E. Moskalensky
    Photophysical properties of BODIPYs with sterically-hindered nitrophenyls in meso-position
    Journal of Luminescence, V. 246, June 2022, 118837 doi:10.1016/j.jlumin.2022.118837, IF=4.171
  442. M.A. Panfilov, T.Yu. Karogodina, Yao. Songyin, O.Yu. Karmatskih, A.Yu. Vorob'ev, I.S. Tretyakova, E.M. Glebov, A.E. Moskalensky
    Photophysical properties of BODIPYs with sterically-hindered nitrophenyls in meso-position
    Journal of Luminescence, V. 246, June 2022, 118837 doi:10.1016/j.jlumin.2022.118837, IF=4.171
  443. M.A. Panfilov, T.Yu. Karogodina, Yao. Songyin, O.Yu. Karmatskih, A.Yu. Vorob'ev, I.S. Tretyakova, E.M. Glebov, A.E. Moskalensky
    Photophysical properties of BODIPYs with sterically-hindered nitrophenyls in meso-position
    Journal of Luminescence, V. 246, June 2022, 118837 doi:10.1016/j.jlumin.2022.118837, IF=4.171
  444. M.A. Panfilov, T.Yu. Karogodina, Yao. Songyin, O.Yu. Karmatskih, A.Yu. Vorob'ev, I.S. Tretyakova, E.M. Glebov, A.E. Moskalensky
    Photophysical properties of BODIPYs with sterically-hindered nitrophenyls in meso-position
    Journal of Luminescence, V. 246, June 2022, 118837 doi:10.1016/j.jlumin.2022.118837, IF=4.171
  445. M.A. Panfilov, T.Yu. Karogodina, Yao. Songyin, O.Yu. Karmatskih, A.Yu. Vorob'ev, I.S. Tretyakova, E.M. Glebov, A.E. Moskalensky
    Photophysical properties of BODIPYs with sterically-hindered nitrophenyls in meso-position
    Journal of Luminescence, V. 246, June 2022, 118837 doi:10.1016/j.jlumin.2022.118837, IF=4.171
  446. A.V. Artem'ev, A.Yu. Baranov, I.Yu. Bagryanskaya
    Trigonal planar clusters Ag@Ag3 supported by (2-PyCH2)3P ligands
    Inorganic Chemistry Communications, V. 140, June 2022, 109478 doi:10.1016/j.inoche.2022.109478, IF=3.428
  447. A.V. Artem'ev, A.Yu. Baranov, I.Yu. Bagryanskaya
    Trigonal planar clusters Ag@Ag3 supported by (2-PyCH2)3P ligands
    Inorganic Chemistry Communications, V. 140, June 2022, 109478 doi:10.1016/j.inoche.2022.109478, IF=3.428
  448. Е.Н. Заполоцкий, С.П. Бабайлов, И.П. Чуйков, В.В. Коковкин, О.Г. Шакирова
    Спин-кроссовер и температурная чувствительность парамагнитных химических сдвигов в спектрах ямр в водном растворе комплекса нафталинсульфоната железа(II) с трис(пиразол-1-ИЛ)метаном [FE(HC(PZ)3)2](C10H7SO3)2
    Журнал структурной химии. 2022. Т. 63. № 6. С. 789-795.... doi:10.2692.JSC_id93492 (SPIN CROSSOVER AND TEMPERATURE SENSITIVITY OF PARAMAGNETIC NMR CHEMICAL SHIFTS IN AN AQUEOUS SOLUTION OF THE IRON(II) NAPHTHALENESULFONATE COMPLEX WITH TRIS(PYRAZOL-1-YL)METHANE [Fe(HC(Pz)3)2](C10H7SO3)2/ E. N. Zapolotsky, S. P. Babailov, I. P. Chuykov, V. V. Kokovkin & O. G. Shakirova// Journal of Structural Chemistry, 2022, V. 63,Pp. 923-929 doi:10.1134/S0022476622060099), IF=1.004
  449. Е.Н. Заполоцкий, С.П. Бабайлов, И.П. Чуйков, В.В. Коковкин, О.Г. Шакирова
    Спин-кроссовер и температурная чувствительность парамагнитных химических сдвигов в спектрах ямр в водном растворе комплекса нафталинсульфоната железа(II) с трис(пиразол-1-ИЛ)метаном [FE(HC(PZ)3)2](C10H7SO3)2
    Журнал структурной химии. 2022. Т. 63. № 6. С. 789-795.... doi:10.2692.JSC_id93492 (SPIN CROSSOVER AND TEMPERATURE SENSITIVITY OF PARAMAGNETIC NMR CHEMICAL SHIFTS IN AN AQUEOUS SOLUTION OF THE IRON(II) NAPHTHALENESULFONATE COMPLEX WITH TRIS(PYRAZOL-1-YL)METHANE [Fe(HC(Pz)3)2](C10H7SO3)2/ E. N. Zapolotsky, S. P. Babailov, I. P. Chuykov, V. V. Kokovkin & O. G. Shakirova// Journal of Structural Chemistry, 2022, V. 63,Pp. 923-929 doi:10.1134/S0022476622060099), IF=1.004
  450. Е.Н. Заполоцкий, С.П. Бабайлов, И.П. Чуйков, В.В. Коковкин, О.Г. Шакирова
    Спин-кроссовер и температурная чувствительность парамагнитных химических сдвигов в спектрах ямр в водном растворе комплекса нафталинсульфоната железа(II) с трис(пиразол-1-ИЛ)метаном [FE(HC(PZ)3)2](C10H7SO3)2
    Журнал структурной химии. 2022. Т. 63. № 6. С. 789-795.... doi:10.2692.JSC_id93492 (SPIN CROSSOVER AND TEMPERATURE SENSITIVITY OF PARAMAGNETIC NMR CHEMICAL SHIFTS IN AN AQUEOUS SOLUTION OF THE IRON(II) NAPHTHALENESULFONATE COMPLEX WITH TRIS(PYRAZOL-1-YL)METHANE [Fe(HC(Pz)3)2](C10H7SO3)2/ E. N. Zapolotsky, S. P. Babailov, I. P. Chuykov, V. V. Kokovkin & O. G. Shakirova// Journal of Structural Chemistry, 2022, V. 63,Pp. 923-929 doi:10.1134/S0022476622060099), IF=1.004
  451. Е.Н. Заполоцкий, С.П. Бабайлов, И.П. Чуйков, В.В. Коковкин, О.Г. Шакирова
    Спин-кроссовер и температурная чувствительность парамагнитных химических сдвигов в спектрах ямр в водном растворе комплекса нафталинсульфоната железа(II) с трис(пиразол-1-ИЛ)метаном [FE(HC(PZ)3)2](C10H7SO3)2
    Журнал структурной химии. 2022. Т. 63. № 6. С. 789-795.... doi:10.2692.JSC_id93492 (SPIN CROSSOVER AND TEMPERATURE SENSITIVITY OF PARAMAGNETIC NMR CHEMICAL SHIFTS IN AN AQUEOUS SOLUTION OF THE IRON(II) NAPHTHALENESULFONATE COMPLEX WITH TRIS(PYRAZOL-1-YL)METHANE [Fe(HC(Pz)3)2](C10H7SO3)2/ E. N. Zapolotsky, S. P. Babailov, I. P. Chuykov, V. V. Kokovkin & O. G. Shakirova// Journal of Structural Chemistry, 2022, V. 63,Pp. 923-929 doi:10.1134/S0022476622060099), IF=1.004
  452. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  453. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  454. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  455. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  456. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  457. А.М. Чеплакова, В.С. Гусаров, Д.Г. Самсоненко, А.С. Виноградов, К.А. Коваленко, М.И. Рахманова, В.П. Федин
    Слоистые металл-органические координационные полимеры на основе бии трехъядерных кадмиевых блоков и октафторбифенил-4,4'-дикарбоксилат-анионов
    Журнал структурной химии. 2022. Т. 63. № 6. С. 761-770. doi:10.2692.JSC_id92420 (LAYERED METAL-ORGANIC COORDINATION POLYMERS BASED ON BI- AND TRINUCLEAR CADMIUM BLOCKS AND OCTAFLUOROBIPHENYL- 4,4'-DICARBOXYLATE ANIONS/ A. M. Cheplakova, V. S. Gusarov, D. G. Samsonenko, A. S. Vinogradov, K. A. Kovalenko, M. I. Rakhmanova & V. P. Fedin // Journal of Structural Chemistry, 2022, V. 63, Pp 95-904 doi:10.1134/S0022476622060063), IF=1.004
  458. Я.В. Зонов, С. Ван, Д.С. Голохвастова, В.М. Карпов, Т.В. Меженкова, Ю.В. Гатилов
    Восстановление перфторбензоциклоалкенонов и других полифторарилкетонов в спирты под действием LiBH4
    Журнал органической химии, Т. 58, N 6, Cc 619-631, doi:10.31857/S0514749222060040 (Reduction of Perfluorinated Benzocycloalkenones and Other Polyfluoroaryl Ketones to Alcohols with LiBH4/ S. Wang, D. S. Golokhvastova, Ya. V. Zonov, V. M. Karpov, T. V. Mezhenkova, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2022, V. 58, N 6, Pp 780-790 doi:10.1134/S1070428022060045), IF=0.862
  459. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  460. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  461. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  462. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  463. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  464. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  465. A.A. Munkuev, N.S. Dyrkheeva, T.E. Kornienko, E.S. Ilina, D.I. Ivankin, E.V. Suslov, D.V. Korchagina, Yu.V. Gatilov, A.L. Zakharenko, A.A. Malakhova, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Adamantane-Monoterpenoid Conjugates Linked via Heterocyclic Linkers Enhance the Cytotoxic Effect of Topotecan
    Molecules 2022, 27(11), 3374 doi:10.3390/molecules27113374, IF=4.927
  466. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  467. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  468. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  469. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  470. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  471. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
    Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
    Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
  472. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  473. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  474. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  475. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  476. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  477. A.S. Spitsyna, A.S. Poryvaev, N.E. Sannikova, A.A. Yazikova, I.A. Kirilyuk, S.A. Dobrynin, O.A. Chinak, M.V. Fedin, O.A. Krumkacheva
    Stability of ZIF-8 Nanoparticles in Most Common Cell Culture Media
    Molecules 2022, 27(10), 3240; doi:10.3390/molecules27103240, IF=4.927
  478. A.V. Markov, A.A. Ilyina, O.V. Salomatina, A.V. Sen'kova, A.A. Okhina, A.D. Rogachev, N.F. Salakhutdinov, M.A. Zenkova
    Novel Soloxolone Amides as Potent Anti-Glioblastoma Candidates: Design, Synthesis, In Silico Analysis and Biological Activities In Vitro and In Vivo
    Pharmaceuticals 2022, 15(5), 603; doi:10.3390/ph15050603, IF=5.215
  479. A.V. Markov, A.A. Ilyina, O.V. Salomatina, A.V. Sen'kova, A.A. Okhina, A.D. Rogachev, N.F. Salakhutdinov, M.A. Zenkova
    Novel Soloxolone Amides as Potent Anti-Glioblastoma Candidates: Design, Synthesis, In Silico Analysis and Biological Activities In Vitro and In Vivo
    Pharmaceuticals 2022, 15(5), 603; doi:10.3390/ph15050603, IF=5.215
  480. A.V. Markov, A.A. Ilyina, O.V. Salomatina, A.V. Sen'kova, A.A. Okhina, A.D. Rogachev, N.F. Salakhutdinov, M.A. Zenkova
    Novel Soloxolone Amides as Potent Anti-Glioblastoma Candidates: Design, Synthesis, In Silico Analysis and Biological Activities In Vitro and In Vivo
    Pharmaceuticals 2022, 15(5), 603; doi:10.3390/ph15050603, IF=5.215
  481. A.V. Markov, A.A. Ilyina, O.V. Salomatina, A.V. Sen'kova, A.A. Okhina, A.D. Rogachev, N.F. Salakhutdinov, M.A. Zenkova
    Novel Soloxolone Amides as Potent Anti-Glioblastoma Candidates: Design, Synthesis, In Silico Analysis and Biological Activities In Vitro and In Vivo
    Pharmaceuticals 2022, 15(5), 603; doi:10.3390/ph15050603, IF=5.215
  482. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, A.Yu. Dyrkach
    EPR Study of Accumulation and Toxic Effect of Iron and Copper During the Development of Solanum tuberosum L. in vitro
    Journal of Applied Spectroscopy, 2022, V. 89, № 2, Pp 288-295 doi:10.1007/s10812-022-01356-y, IF=0.816
  483. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, A.Yu. Dyrkach
    EPR Study of Accumulation and Toxic Effect of Iron and Copper During the Development of Solanum tuberosum L. in vitro
    Journal of Applied Spectroscopy, 2022, V. 89, № 2, Pp 288-295 doi:10.1007/s10812-022-01356-y, IF=0.816
  484. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, A.Yu. Dyrkach
    EPR Study of Accumulation and Toxic Effect of Iron and Copper During the Development of Solanum tuberosum L. in vitro
    Journal of Applied Spectroscopy, 2022, V. 89, № 2, Pp 288-295 doi:10.1007/s10812-022-01356-y, IF=0.816
  485. И.В. Сорокина, Н.А. Жукова, Ю.В. Мешкова, Д.С. Баев, Т.Г. Толстикова, М.А. Бакарев, Е.Л. Лушникова
    Моделирование доброкачественной гиперплазии предстательной железы у крыс высокой дозой тестостерона
    Бюллетень экспериментальной биологии и медицины. 2022. Т. 173. № 5. С. 656-663. (Modeling of benign prostatic hyperplasia in rats with a high dose of testosterone/ I. V. Sorokina, N.A. Zhukova, Yu.V. Meshkova, D.S. Baev, T.G. Tolstikova, M.A. Bakarev, E. L. Lushnikova// Bulletin of Experimental Biology and Medicine, 2022, doi:10.47056/0365-9615-2022-173-5-656-663 doi:10.1007/s10517-022-05613-0), IF=0.737
  486. И.В. Сорокина, Н.А. Жукова, Ю.В. Мешкова, Д.С. Баев, Т.Г. Толстикова, М.А. Бакарев, Е.Л. Лушникова
    Моделирование доброкачественной гиперплазии предстательной железы у крыс высокой дозой тестостерона
    Бюллетень экспериментальной биологии и медицины. 2022. Т. 173. № 5. С. 656-663. (Modeling of benign prostatic hyperplasia in rats with a high dose of testosterone/ I. V. Sorokina, N.A. Zhukova, Yu.V. Meshkova, D.S. Baev, T.G. Tolstikova, M.A. Bakarev, E. L. Lushnikova// Bulletin of Experimental Biology and Medicine, 2022, doi:10.47056/0365-9615-2022-173-5-656-663 doi:10.1007/s10517-022-05613-0), IF=0.737
  487. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  488. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  489. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  490. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  491. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  492. К.А. Виноградова, М.И. Рахманова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев, Н.В. Первухина, Д.Ю. Наумов, С.А. Мартынова
    Синтез, строение и фотолюминесценция комплексов цинка(II) и серебра(I) с 2-(3,5-диметил-1H-пиразол-1-ил)-4,6-дифенилпиримидином
    Координационная химия. 2022. Т. 48. № 5. С. 302-313. doi:10.31857/S0132344X22050097 (Synthesis, Structure, and Photoluminescence of Zinc(II) and Silver(I) Complexes with 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-4,6-Diphenylpyrimidine/ K. A. Vinogradova, M. I. Rakhmanova, E. B. Nikolaenkova, V. P. Krivopalov, M. B. Bushuev, N. V. Pervukhina, D. Yu. Naumov, S. A. Martynova// Russian Journal of Coordination Chemistry, 2022, V. 48, N 5, Pp 301-310 doi:10.1134/S1070328422050098), IF=1.814
  493. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
    A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
    Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
  494. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
    A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
    Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
  495. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
    A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
    Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
  496. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
    A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
    Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
  497. S.G. Il'yasov, V.S. Glukhacheva, D.S. Il'yasov, E.E. ZhukovaIli, V. Eltsov, Yu.V. Gatilov
    A novel energetic nickel coordination compound based on carbohydrazide and dinitramide
    Mendeleev Communications, V. 32, N 3, May–June 2022, Pp 344-346 doi:10.1016/j.mencom.2022.05.017, IF=1.837
  498. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  499. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  500. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  501. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  502. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  503. S.V. Dudkin, A.S. Chuprin, S.A. Belova, A.V. Vologzhanina, Yan.V. Zubavichus, P.M. Kaletina, I.K. Shundrina, E.G. Bagryanskaya, Yan.Z. Voloshin
    Hybrid iron(ii) phthalocyaninatoclathrochelates with a terminal reactive vinyl group and their organo-inorganic polymeric derivatives: synthetic approaches, X-ray structures and copolymerization with styrene
    Dalton Trans., 2022, V.,51, N 14, Pp 5645-5659 doi:10.1039/D1DT04187H, IF=4.569
  504. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  505. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  506. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  507. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  508. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  509. М.В. Кручинина, В.Н. Кручинин, А.А. Громов, М.В. Шашков, А.С. Соколова, И.Н. Яковина, А.А. Шестов
    Жирные кислоты мембран эритроцитов и сыворотки крови как биомаркеры для диагностики ранних стадий колоректального рака
    Сибирский онкологический журнал. 2022. Т. 21. № 2. С. 65-80. (Fatty acids of erythrocyte membranes and blood serum as biomarkers for early detection of colorectal cancer/ Kruchinina M.V., Kruchinin V.N., Gromov A.A., Shashkov M.V., Sokolova A.S., Yakovina I.N., Shestov A.A.// Siberian journal of oncology. 2022;21(2):65-80. (In Russ.) doi:10.21294/1814-4861-2022-21-2-65-80)
  510. Уркасым.кызы. С, Т.В. Рыбалова, В.Ю. Комаров, И.В. Корольков, В.В. Крисюк
    Летучие комплексы железа(III) с метоксизамещенным β-дикетонатом
    Журнал структурной химии. 2022. Т. 63. № 4. С. 425-434. doi:10.26902/JSC_id89894 (VOLATILE IRON(III) COMPLEXES WITH A METHOXY-SUBSTITUTED β-DIKETONATE/ S. Urkasym kyzy, T. V. Rybalova, V. Yu. Komarov, I. V. Korolkov, V. V. Krisyuk// Journal of Structural Chemistry, 2022, V. 63, № 4, Pp 524-533 doi:10.1134/S0022476622040035), IF=1.004
  511. Уркасым.кызы. С, Т.В. Рыбалова, В.Ю. Комаров, И.В. Корольков, В.В. Крисюк
    Летучие комплексы железа(III) с метоксизамещенным β-дикетонатом
    Журнал структурной химии. 2022. Т. 63. № 4. С. 425-434. doi:10.26902/JSC_id89894 (VOLATILE IRON(III) COMPLEXES WITH A METHOXY-SUBSTITUTED β-DIKETONATE/ S. Urkasym kyzy, T. V. Rybalova, V. Yu. Komarov, I. V. Korolkov, V. V. Krisyuk// Journal of Structural Chemistry, 2022, V. 63, № 4, Pp 524-533 doi:10.1134/S0022476622040035), IF=1.004
  512. Уркасым.кызы. С, Т.В. Рыбалова, В.Ю. Комаров, И.В. Корольков, В.В. Крисюк
    Летучие комплексы железа(III) с метоксизамещенным β-дикетонатом
    Журнал структурной химии. 2022. Т. 63. № 4. С. 425-434. doi:10.26902/JSC_id89894 (VOLATILE IRON(III) COMPLEXES WITH A METHOXY-SUBSTITUTED β-DIKETONATE/ S. Urkasym kyzy, T. V. Rybalova, V. Yu. Komarov, I. V. Korolkov, V. V. Krisyuk// Journal of Structural Chemistry, 2022, V. 63, № 4, Pp 524-533 doi:10.1134/S0022476622040035), IF=1.004
  513. Уркасым.кызы. С, Т.В. Рыбалова, В.Ю. Комаров, И.В. Корольков, В.В. Крисюк
    Летучие комплексы железа(III) с метоксизамещенным β-дикетонатом
    Журнал структурной химии. 2022. Т. 63. № 4. С. 425-434. doi:10.26902/JSC_id89894 (VOLATILE IRON(III) COMPLEXES WITH A METHOXY-SUBSTITUTED β-DIKETONATE/ S. Urkasym kyzy, T. V. Rybalova, V. Yu. Komarov, I. V. Korolkov, V. V. Krisyuk// Journal of Structural Chemistry, 2022, V. 63, № 4, Pp 524-533 doi:10.1134/S0022476622040035), IF=1.004
  514. A.I. Taratayko, Yu.I. Glazachev, I.V. Eltsov, E.I. Chernyak, I.A. Kirilyuk
    3,4-Unsubstituted 2-tert-Butyl-pyrrolidine-1-oxyls with Hydrophilic Functional Groups in the Side Chains
    Molecules 2022, 27(6), 1922 doi:10.3390/molecules27061922, IF=4.411
  515. A.I. Taratayko, Yu.I. Glazachev, I.V. Eltsov, E.I. Chernyak, I.A. Kirilyuk
    3,4-Unsubstituted 2-tert-Butyl-pyrrolidine-1-oxyls with Hydrophilic Functional Groups in the Side Chains
    Molecules 2022, 27(6), 1922 doi:10.3390/molecules27061922, IF=4.411
  516. A.I. Taratayko, Yu.I. Glazachev, I.V. Eltsov, E.I. Chernyak, I.A. Kirilyuk
    3,4-Unsubstituted 2-tert-Butyl-pyrrolidine-1-oxyls with Hydrophilic Functional Groups in the Side Chains
    Molecules 2022, 27(6), 1922 doi:10.3390/molecules27061922, IF=4.411
  517. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
  518. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
  519. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
  520. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
  521. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
  522. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  523. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  524. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  525. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  526. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  527. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  528. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  529. A.D. Mironova, M.A. Mikhaylov, A.M. Maksimov, K.A. Brylev, A.L. Gushchin, D.V. Stass, A.S. Novikov, I.V. Eltsov.P.A. Abramov, M.N. Sokolov
    Phosphorescent Complexes of {Mo6I8}4+ and {W6I8}4+ with Perfluorinated Aryl Thiolates featuring Unusual Molecular Structures
    European Journal of Inorganic Chemistry,V. 2022, N 7, March 9, 2022, e202100890 doi:10.1002/ejic.202100890, IF=2.551
  530. А.В. Харченко, С.Б. Цветовский, М.Л. Филипенко, В.В. Фоменко, В.В. Ступак
    Реакции электрической активности мозга животных на имплантаты различного типа, используемые для замещения дефектов твердой мозговой оболочки
    ПОЛИТРАВМА / POLYTRAUMA. 2022. № 1, С. 72-83. http://poly-trauma.ru/index.php/pt/article/view/329
  531. А.В. Харченко, С.Б. Цветовский, М.Л. Филипенко, В.В. Фоменко, В.В. Ступак
    Реакции электрической активности мозга животных на имплантаты различного типа, используемые для замещения дефектов твердой мозговой оболочки
    ПОЛИТРАВМА / POLYTRAUMA. 2022. № 1, С. 72-83. http://poly-trauma.ru/index.php/pt/article/view/329
  532. А.В. Харченко, С.Б. Цветовский, М.Л. Филипенко, В.В. Фоменко, В.В. Ступак
    Реакции электрической активности мозга животных на имплантаты различного типа, используемые для замещения дефектов твердой мозговой оболочки
    ПОЛИТРАВМА / POLYTRAUMA. 2022. № 1, С. 72-83. http://poly-trauma.ru/index.php/pt/article/view/329
  533. А.В. Харченко, С.Б. Цветовский, М.Л. Филипенко, В.В. Фоменко, В.В. Ступак
    Реакции электрической активности мозга животных на имплантаты различного типа, используемые для замещения дефектов твердой мозговой оболочки
    ПОЛИТРАВМА / POLYTRAUMA. 2022. № 1, С. 72-83. http://poly-trauma.ru/index.php/pt/article/view/329
  534. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  535. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  536. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  537. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  538. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  539. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  540. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
  541. M.M. Shmakov, S.A. Prikhod'ko, R.Yu. Peshkov, V.V. Bardin, N. Yu. Adonin
    Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols
    Molecular Catalysis, V. 521, March 2022, 112202 doi:10.1016/j.mcat.2022.112202, IF=5.089
  542. M.M. Shmakov, S.A. Prikhod'ko, R.Yu. Peshkov, V.V. Bardin, N. Yu. Adonin
    Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols
    Molecular Catalysis, V. 521, March 2022, 112202 doi:10.1016/j.mcat.2022.112202, IF=5.089
  543. M.M. Shmakov, S.A. Prikhod'ko, R.Yu. Peshkov, V.V. Bardin, N. Yu. Adonin
    Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols
    Molecular Catalysis, V. 521, March 2022, 112202 doi:10.1016/j.mcat.2022.112202, IF=5.089
  544. M.M. Shmakov, S.A. Prikhod'ko, R.Yu. Peshkov, V.V. Bardin, N. Yu. Adonin
    Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols
    Molecular Catalysis, V. 521, March 2022, 112202 doi:10.1016/j.mcat.2022.112202, IF=5.089
  545. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  546. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  547. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  548. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  549. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  550. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  551. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  552. A.D. Ivanova, E.V. Korotaev, V.Yu. Komarov, T.S. Sukhikh, S.V. Trubina, L.A. Sheludyakova, S.A. Petrov, A.Ya. Tikhonov, L.G. Lavrenova
    Spin crossover in iron(II) complexes with new ligand 2,6-bis(4,5-dimethyl-1H-imidazole-2-yl)pyridine
    Inorganica Chimica Acta, V. 532, 1 March 2022, 120746 doi:10.1016/j.ica.2021.120746, IF=3.118
  553. A.V. Shpatov, S.S. Zakharova, S.A. Popov
    Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles
    Chemistry of Natural Compounds, 2022, V. 58, N 2, Pp 290-296 doi:10.1007/s10600-022-03662-5, IF=0.83
  554. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  555. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  556. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  557. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  558. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  559. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, I.A. Krupnova, E.V. Pivovarova
    Acidic N-dealkylation in nitrotriazolium salts
    Mendeleev Communications, 2022, V. 32, N 2, Pp 215-217 doi:10.1016/j.mencom.2022.03.020, IF=1.837
  560. A.Yu. Makarov, Yu.M. Volkova, S.B. Zikirin, I.G. Irtegova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.A. Nefedov, A.V. Zibarev
    New 3,1,2,4-benzothiaselenadiazines, related π-heterocycles including Herz cations, radicals and molecular complexes, and Bunte salts
    New J. Chem., 2022, ,46(7), 3687-3696 doi:10.1039/D1NJ05979C, IF=3.925
  561. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  562. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  563. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  564. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  565. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  566. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  567. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  568. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  569. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
  570. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
    Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
    Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
  571. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
    Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
    Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
  572. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
    Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
    Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
  573. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
    Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
    Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
  574. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
  575. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
  576. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
  577. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
    Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
    European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
  578. I.Sh. Steinberg, E.V. Vasilyev, V.V. Shelkovnikov, I.Yu. Kargapolova
    Use of forbidden singlet-triplet electron transitions in photopolymer material for holographic recording with high intensity nanosecond laser pulses
    Optics Communications, V. 505, 15 February 2022, 127540 doi:10.1016/j.optcom.2021.127540, IF=2.335
  579. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  580. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  581. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  582. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  583. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  584. K.S. Ivanov, T. Riesebeck, A. Skolyapova, I. Liakisheva, M.S. Kazantsev, A.A. Sonina, R. Yu Peshkov, E.A. Mostovich
    P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones
    The Journal of Organic Chemistry, 2022, 87, 5, 2456-2469 doi:10.1021/acs.joc.1c02379, IF=4.198
  585. E. Benassi, T. Vaganova, E. Malykhin, H. Fan
    How do electron donating substituents affect the electronic structure, molecular topology, vibrational properties and intra- and intermolecular interactions of polyhalogenated pyridines?
    Phys. Chem. Chem. Phys., 2022, V.24, N 6, Pp. 4002-4021 doi:10.1039/D1CP05956D, IF=3.945
  586. E. Benassi, T. Vaganova, E. Malykhin, H. Fan
    How do electron donating substituents affect the electronic structure, molecular topology, vibrational properties and intra- and intermolecular interactions of polyhalogenated pyridines?
    Phys. Chem. Chem. Phys., 2022, V.24, N 6, Pp. 4002-4021 doi:10.1039/D1CP05956D, IF=3.945
  587. A. Paromov, I. Shchurova, A. Rogova, I. Bagryanskaya, D. Polovyanenko
    Acid-Catalyzed Condensation of Benzamide with Glyoxal, and Reaction Features
    Molecules 2022, 27(3), 1094 doi:10.3390/molecules27031094, IF=4.927
  588. A. Paromov, I. Shchurova, A. Rogova, I. Bagryanskaya, D. Polovyanenko
    Acid-Catalyzed Condensation of Benzamide with Glyoxal, and Reaction Features
    Molecules 2022, 27(3), 1094 doi:10.3390/molecules27031094, IF=4.927
  589. A. Paromov, I. Shchurova, A. Rogova, I. Bagryanskaya, D. Polovyanenko
    Acid-Catalyzed Condensation of Benzamide with Glyoxal, and Reaction Features
    Molecules 2022, 27(3), 1094 doi:10.3390/molecules27031094, IF=4.927
  590. T.A. Vaganova, E. Benassi, Yu.V. Gatilov, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Polyhalogenated aminobenzonitriles vs their co-crystals with 18-crown-6: amino group position as a tool to control crystal packing and solid-state fluorescence
    CrystEngComm, 2022, V. 24, N 5, Pp 987-1001 doi:10.1039/D1CE01469B, IF=3.756
  591. T.A. Vaganova, E. Benassi, Yu.V. Gatilov, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Polyhalogenated aminobenzonitriles vs their co-crystals with 18-crown-6: amino group position as a tool to control crystal packing and solid-state fluorescence
    CrystEngComm, 2022, V. 24, N 5, Pp 987-1001 doi:10.1039/D1CE01469B, IF=3.756
  592. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  593. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  594. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  595. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  596. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  597. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  598. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  599. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  600. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  601. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  602. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  603. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  604. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  605. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  606. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  607. A.A. O. Bashirzade, S.V. Cheresiz, A.S. Belova, A.V. Drobkov, A.D. Korotaeva, S. Azizi-Arani, A. Azimirad, E. Odle, Emma-Yanina.V. Gild, O.V. Ardashov, K.P. Volcho, D.V. Bozhko, V.O. Myrov, S.M. Kolchanova, A.I. Polovian, G.K. Galumov, N.F. Salakhutdinov, T.G. Amstislavskaya, A.V. Kalueff
    MPTP-Treated Zebrafish Recapitulate ‘Late-Stage’ Parkinson’s-like Cognitive Decline
    Toxics 2022, 10(2), 69; doi:10.3390/toxics10020069, IF=4.472
  608. D.N. Shcherbakov, G.Y. Galitsyn, T.P. Kukina, N.V. Panteleeva, O.I. Salnikova, P.V. Kolosov
    Prospects for comprehensive use of sea buckthorn of Novosibirsk selection
    AIP Conference Proceedings, 2022, 2390(1), 030085 doi:10.1063/5.0070159
  609. D.N. Shcherbakov, G.Y. Galitsyn, T.P. Kukina, N.V. Panteleeva, O.I. Salnikova, P.V. Kolosov
    Prospects for comprehensive use of sea buckthorn of Novosibirsk selection
    AIP Conference Proceedings, 2022, 2390(1), 030085 doi:10.1063/5.0070159
  610. D.N. Shcherbakov, G.Y. Galitsyn, T.P. Kukina, N.V. Panteleeva, O.I. Salnikova, P.V. Kolosov
    Prospects for comprehensive use of sea buckthorn of Novosibirsk selection
    AIP Conference Proceedings, 2022, 2390(1), 030085 doi:10.1063/5.0070159
  611. D.N. Shcherbakov, G.Y. Galitsyn, T.P. Kukina, N.V. Panteleeva, O.I. Salnikova, P.V. Kolosov
    Prospects for comprehensive use of sea buckthorn of Novosibirsk selection
    AIP Conference Proceedings, 2022, 2390(1), 030085 doi:10.1063/5.0070159
  612. D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, O.I. Salnikova, P.V. Kolosov
    Deodorized Distillate of Sunflower Oil as a Source of Kaurane Compounds
    AIP Conference Proceedings 2390(1), 030084, 2022. 030084-1–030084-5; doi:10.1063/5.0070161
  613. D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, O.I. Salnikova, P.V. Kolosov
    Deodorized Distillate of Sunflower Oil as a Source of Kaurane Compounds
    AIP Conference Proceedings 2390(1), 030084, 2022. 030084-1–030084-5; doi:10.1063/5.0070161
  614. D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, N.V. Panteleeva, T.V. Teplyakova, O.I. Salnikova
    GC-MS analysis of lipophilic Chaga mushroom constituents
    AIP Conference Proceedings, 2022, 2390(1), 030083 doi:10.1063/5.0070158
  615. D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, N.V. Panteleeva, T.V. Teplyakova, O.I. Salnikova
    GC-MS analysis of lipophilic Chaga mushroom constituents
    AIP Conference Proceedings, 2022, 2390(1), 030083 doi:10.1063/5.0070158
  616. D.N. Shcherbakov, T.P. Kukina, I.A. Elshin, N.V. Panteleeva, T.V. Teplyakova, O.I. Salnikova
    GC-MS analysis of lipophilic Chaga mushroom constituents
    AIP Conference Proceedings, 2022, 2390(1), 030083 doi:10.1063/5.0070158
  617. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  618. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  619. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  620. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  621. K. Kovaleva, O. Oleshko, O. Yarovaya, S. Cheresiz, A. Zakharenko, K. Ponomarev, O. Lavrik, A. Pokrovsky, N. Salakhutdinov
    Inhibition of the DNA repair enzyme TDP1 by the resin acid derivatives as a new way to increase the efficiency of glioblastoma chemotherapy
    AIP Conference Proceedings 2390, 020036 (2022) doi:10.1063/5.0069407
  622. Е.Ф. Пен, Н.Н. Вьюхина, П.Е. Твердохлеб, Е.В. Васильев, Д.И. Деревянко, В.В. Шелковников, С.И. Алиев
    Регистрация и анализ характеристик угловой селективности голограмм в фотополимерных материалах
    Приборы и техника эксперимента. 2022. № 2. С. 99-108. doi:10.31857/S0032816222020185 (Measurement and Analysis of the Angular Selectivity Characteristics of Holograms in Photopolymer Materials/ E. F. Pen, N. N. Vyukhina, P. E. Tverdokhleb, E. V. Vasiliev, D. I. Derevyanko, V. V. Shelkovnikov & S. I. Aliev// Instruments and Experimental Techniques, 2022, V.65, Pp 292-300 doi:10.1134/S0020441222020178), IF=0.573
  623. Е.Ф. Пен, Н.Н. Вьюхина, П.Е. Твердохлеб, Е.В. Васильев, Д.И. Деревянко, В.В. Шелковников, С.И. Алиев
    Регистрация и анализ характеристик угловой селективности голограмм в фотополимерных материалах
    Приборы и техника эксперимента. 2022. № 2. С. 99-108. doi:10.31857/S0032816222020185 (Measurement and Analysis of the Angular Selectivity Characteristics of Holograms in Photopolymer Materials/ E. F. Pen, N. N. Vyukhina, P. E. Tverdokhleb, E. V. Vasiliev, D. I. Derevyanko, V. V. Shelkovnikov & S. I. Aliev// Instruments and Experimental Techniques, 2022, V.65, Pp 292-300 doi:10.1134/S0020441222020178), IF=0.573
  624. Е.Ф. Пен, Н.Н. Вьюхина, П.Е. Твердохлеб, Е.В. Васильев, Д.И. Деревянко, В.В. Шелковников, С.И. Алиев
    Регистрация и анализ характеристик угловой селективности голограмм в фотополимерных материалах
    Приборы и техника эксперимента. 2022. № 2. С. 99-108. doi:10.31857/S0032816222020185 (Measurement and Analysis of the Angular Selectivity Characteristics of Holograms in Photopolymer Materials/ E. F. Pen, N. N. Vyukhina, P. E. Tverdokhleb, E. V. Vasiliev, D. I. Derevyanko, V. V. Shelkovnikov & S. I. Aliev// Instruments and Experimental Techniques, 2022, V.65, Pp 292-300 doi:10.1134/S0020441222020178), IF=0.573
  625. Е.Ф. Пен, Н.Н. Вьюхина, П.Е. Твердохлеб, Е.В. Васильев, Д.И. Деревянко, В.В. Шелковников, С.И. Алиев
    Регистрация и анализ характеристик угловой селективности голограмм в фотополимерных материалах
    Приборы и техника эксперимента. 2022. № 2. С. 99-108. doi:10.31857/S0032816222020185 (Measurement and Analysis of the Angular Selectivity Characteristics of Holograms in Photopolymer Materials/ E. F. Pen, N. N. Vyukhina, P. E. Tverdokhleb, E. V. Vasiliev, D. I. Derevyanko, V. V. Shelkovnikov & S. I. Aliev// Instruments and Experimental Techniques, 2022, V.65, Pp 292-300 doi:10.1134/S0020441222020178), IF=0.573
  626. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  627. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  628. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  629. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  630. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  631. M. Han, I.I. Oleynik, M. Liu, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    Ring size enlargement in an ortho-cycloalkyl-substituted bis(imino)pyridine-cobalt ethylene polymerization catalyst and its impact on performance and polymer properties
    Applied Organometalic Chemistry, V.36, N 2, February 2022, e6529 doi:10.1002/aoc.6529, IF=4.072
  632. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  633. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  634. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  635. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  636. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  637. I.Yu. Zhuravleva, E.V. Karpova, A.A. Dokuchaeva, E.V. Kuznetsova, S.V. Vladimirov, A.L. Ksenofontov, N.R. Nichay
    Bovine jugular vein conduit: What affects its elastomechanical properties and thermostability?
    Journal of Biomedical Materials Research Part A, 2022, V.110, N 2, Pp 394-408 doi:10.1002/jbm.a.37296, IF=4.854
  638. Yu.P. Ustimenko, A.M. Agafontsev, A.V. Tkachev
    Synthesis of chiral pinopyridines using catalysis by metal complexes
    Chemistry of Heterocyclic Compounds, 2022, V. 58, N 2-3, Pp 135-143 doi:10.1007/s10593-022-03066-x, IF=1.49
  639. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  640. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  641. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  642. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  643. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  644. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
  645. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  646. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  647. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  648. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  649. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  650. G.T. Sukhanov, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, I.А. Krupnova, K.K. Bosov, E.V. Pivovarova, V.I. Krasnov
    Energetic Materials Based on N-Substituted 4(5)-Nitro-1,2,3-Triazoles
    Materials 2022, 15(3), 1119 doi:10.3390/ma15031119, IF=3.748
  651. G.A. Selivanova, A.D. Skolyapova, J. Wang, E.V. Karpova, I. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov
    Azo dyes containing 1,3,4-thiadiazole fragment: synthesis, properties
    New J. Chem., 2022, 46(4), 1929-1942 doi:10.1039/D1NJ05084B, IF=3.925
  652. A.V. Artem'ev, Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya
    Pyridylarsine-based Cu(i) complexes showing TADF mixed with fast phosphorescence: a speeding-up emission rate using arsine ligands
    Dalton Trans., 2022, 51(3), 1048-1055 doi:10.1039/D1DT03759E, IF=4.569
  653. A.V. Artem'ev, Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya
    Pyridylarsine-based Cu(i) complexes showing TADF mixed with fast phosphorescence: a speeding-up emission rate using arsine ligands
    Dalton Trans., 2022, 51(3), 1048-1055 doi:10.1039/D1DT03759E, IF=4.569
  654. A.V. Artem'ev, Ya.V. Demyanov, M.I. Rakhmanova, I.Yu. Bagryanskaya
    Pyridylarsine-based Cu(i) complexes showing TADF mixed with fast phosphorescence: a speeding-up emission rate using arsine ligands
    Dalton Trans., 2022, 51(3), 1048-1055 doi:10.1039/D1DT03759E, IF=4.569
  655. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  656. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  657. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  658. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  659. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  660. A.A. Dokuchaeva, T.P. Timchenko, E.V. Karpova, S.V. Vladimirov, I.A. Soynov, I.Y. Zhuravleva
    Effects of Electrospinning Parameter Adjustment on the Mechanical Behavior of Poly-ε-caprolactone Vascular Scaffolds
    Polymers, 2022, 14(2), 349 doi:10.3390/polym14020349, IF=4.967
  661. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  662. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  663. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  664. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  665. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  666. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  667. E. Avdeeva, Ya. Reshetov, D. Domrachev, E. Gulina, S. Krivoshchekov, M. Shurupova, K. Brazovskii, M. Belousov
    Constituent composition of the essential oils from some species of the genus Saussurea DC
    Natural Product Research, 2022, V. 36, N 2, Pp 660-663 doi:10.1080/14786419.2020.1795655, IF=2.488
  668. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  669. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  670. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  671. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  672. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  673. S.P. Babailov, E.N.Zapolotsky, V.V. Kokovkin, O.G. Shakirova, I.V. Mironov, I.P. Chuikov, E.S. Fomin
    Switching of shifting and relaxational NMR-thermosensor properties of iron (II) tris-(pyrazol-1-yl) methane complexes due to spin-crossover
    Polyhedron, V. 212, 15 January 2022, 115611 doi:10.1016/j.poly.2021.115611, IF=2.975
  674. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  675. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  676. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  677. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  678. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  679. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  680. S.S. Borisevich, E.M. Khamitov, M.A. Gureev, O.I. Yarovaya, N.B. Rudometova, A.V. Zybkina, E.D. Mordvinova, D.N. Shcherbakov, R.A. Maksyutov, N.F. Salakhutdinov
    Simulation of Molecular Dynamics of SARS-CoV-2 S-Protein in the Presence of Multiple Arbidol Molecules: Interactions and Binding Mode Insights
    Viruses 2022, 14(1), 119 doi:10.3390/v14010119, IF=5.818
  681. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  682. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  683. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  684. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  685. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  686. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  687. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  688. D.P. Krut'ko, A.V. Medved'ko, K.A. Lyssenko, A.V. Churakov, A.I. Dalinger, M.A. Kalinin, A.O. Gudovannyy, K.Yu. Ponomarev, E.V. Suslov, S.Z. Vatsadze
    Bispidine Platform as a Tool for Studying Amide Configuration Stability
    Molecules 2022, 27(2), 430 doi:10.3390/molecules27020430, IF=4.927
  689. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  690. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  691. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  692. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  693. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  694. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  695. A.Yu. Sidorenko, Yu.M. Kurban, A.V. Kravtsova, I.V. I'ina, N.S. Li-Zhulanov, D.V. Korchagina, J.E. Sanchez-Velandia, A. Aho, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Clays catalyzed cascade Prins and Prins-Friedel-Crafts reactions for synthesis of terpenoid-derived polycyclic compounds
    Applied Catalysis A: General, V. 629, 5 January 2022, 118395 doi:10.1016/j.apcata.2021.118395, IF=5.723
  696. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  697. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  698. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  699. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  700. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  701. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  702. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  703. V.V. Fomenko, N.B. Rudometova, O.I. Yarovaya, A.D. Rogachev, A.A. Fando, A.V. Zaykovskaya, N.I. Komarova, D.N. Shcherbakov, O.V. Pyankov, A.G. Pokrovsky, L.I. Karpenko, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and In Vitro Study of Antiviral Activity of Glycyrrhizin Nicotinate Derivatives against HIV-1 Pseudoviruses and SARS-CoV-2 Viruses
    Molecules 2022, 27(1), 295 doi:10.3390/molecules27010295, IF=4.927
  704. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  705. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  706. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  707. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  708. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  709. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  710. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  711. E. Pashkina, V. Evseenko, N. Dumchenko, M. Zelikman, A. Aktanova, M. Bykova, M. Khvostov, A. Dushkin, V. Kozlov
    Preparation and Characterization of a Glycyrrhizic Acid-Based Drug Delivery System for Allergen-Specific Immunotherapy
    Nanomaterials 2022, 12(1), 148 doi:10.3390/nano12010148, IF=5.719
  712. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
  713. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
  714. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
  715. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
  716. I.Y. Zhuravleva, A.A. Dokuchaeva, E.V. Karpova, T.P. Timchenko, A.T. Titov, SvS. Shatskaya, Yu.F. Polienko
    Immobilized Bisphosphonates as Potential Inhibitors of Bioprosthetic Calcification: Effects on Various Xenogeneic Cardiovascular Tissues
    Biomedicines 2022, 10(1), 65 doi:10.3390/biomedicines10010065, IF=4.757
  717. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  718. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  719. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  720. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  721. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  722. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  723. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  724. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  725. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  726. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  727. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  728. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  729. D. Shcherbakov, D. Baev, M. Kalinin, A. Dalinger, V. Chirkova, S. Belenkaya, A. Khvostov, D. Krut'ko, A. Medved'ko, E. Volosnikova, E. Sharlaeva, D. Shanshin, T. Tolstikova, O. Yarovaya, R. Maksyutov, N. Salakhutdinov, S. Vatsadze
    Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors
    ACS Medicinal Chemistry Letters, 2022, 13, 1, 140-147 (Front Page) doi:10.1021/acsmedchemlett.1c00299, IF=4.632
  730. M.D. Semenova, S.A. Popov, E.E. Shul'ts, M. Turks
    Synthesis of New Ursane-Type Hybrids with Morpholinomethyl-, Dialkylamino-, and Hydroxyl-Substituted Azoles
    Chemistry of Natural Compoundsб 2022,58(1),Pp. 65-70 doi:10.1007/s10600-022-03597-x, IF=0.83
  731. Н.Э. Санникова, К.А. Жданова, А.С. Спицына, Н.А. Брагина, М.В. Федин, О.А. Крумкачева
    Исследование катионных порфиринов и их металлокомплексов методами ЭПР
    Координационная химия. 2022. Т. 48. № 1. С. 3-10. doi:10.31857/S0132344X22010030 (Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031), IF=1.814
  732. Н.Э. Санникова, К.А. Жданова, А.С. Спицына, Н.А. Брагина, М.В. Федин, О.А. Крумкачева
    Исследование катионных порфиринов и их металлокомплексов методами ЭПР
    Координационная химия. 2022. Т. 48. № 1. С. 3-10. doi:10.31857/S0132344X22010030 (Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031), IF=1.814
  733. Н.Э. Санникова, К.А. Жданова, А.С. Спицына, Н.А. Брагина, М.В. Федин, О.А. Крумкачева
    Исследование катионных порфиринов и их металлокомплексов методами ЭПР
    Координационная химия. 2022. Т. 48. № 1. С. 3-10. doi:10.31857/S0132344X22010030 (Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031), IF=1.814
  734. Н.Э. Санникова, К.А. Жданова, А.С. Спицына, Н.А. Брагина, М.В. Федин, О.А. Крумкачева
    Исследование катионных порфиринов и их металлокомплексов методами ЭПР
    Координационная химия. 2022. Т. 48. № 1. С. 3-10. doi:10.31857/S0132344X22010030 (Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031), IF=1.814
  735. Н.Э. Санникова, К.А. Жданова, А.С. Спицына, Н.А. Брагина, М.В. Федин, О.А. Крумкачева
    Исследование катионных порфиринов и их металлокомплексов методами ЭПР
    Координационная химия. 2022. Т. 48. № 1. С. 3-10. doi:10.31857/S0132344X22010030 (Study of Cationic Porphyrins and Their Metal Complexes by ESR Techniques/ N.E. Sannikova, K.A. Zhdanova, A.S. Spitsyna, N.A. Bragina, M.V. Fedin, O.A.Krumkacheva// Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2022, V. 48, N 1, Pp 1-8 doi:10.1134/S1070328422010031), IF=1.814
  736. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94
  737. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94
  738. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94
  739. V.V. Chernyshov, O.I. Yarovaya, Ia.L. Esaulkova, E. Sinegubova, S.S. Borisevich, I.I. Popadyuk, V.V. Zarubaev, N.F. Salakhutdinov
    Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
    Bioorganic & Medicinal Chemistry Letters, V. 55, 1 January 2022, 128465 doi:10.1016/j.bmcl.2021.128465, IF=2.94
  740. D.G. Trofimov, Yu.I. Glazachev, A.A. Gorodetsky, D.A. Komarov, T.V. Rybalova, I.A. Kirilyuk
    4-Dialkylamino-2,5-dihydroimidazol-1-oxyls with Functional Groups at the Position 2 and at the Exocyclic Nitrogen: The pH-Sensitive Spin Labels
    Gels 2022, 8(1),11 doi:10.3390/gels8010011, IF=4.432
  741. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
    New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
    Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
  742. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
    New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
    Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
  743. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
    New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
    Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
  744. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
    New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
    Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
  745. O.V. Salomatina, N.S. Dyrkheeva, I.I. Popadyuk, A.L. Zakharenko, E.S. Ilina, N.I. Komarova, J. Reynisson, N.F. Salakhutdinov, O.I. Lavrik, K.P. Volcho
    New Deoxycholic Acid Derived Tyrosyl-DNA Phosphodiesterase 1 Inhibitors Also Inhibit Tyrosyl-DNA Phosphodiesterase 2
    Molecules 2022, 27(1), 72 doi:10.3390/molecules27010072, IF=4.927
  746. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  747. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  748. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  749. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  750. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  751. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  752. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  753. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  754. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
    Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
    ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
  755. K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
    ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
    Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
  756. K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
    ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
    Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
  757. K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
    ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
    Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
  758. K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
    ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
    Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
  759. K.M. Turdybekov, S.A. Ivasenko, D.M. Turdybekov, A.S. Makhmutova, Yu.V. Gatilov, S.M. Adekenov
    ISOLATION AND STRUCTURE OF THE NEW SESQUITERPENE LACTONE 3-OXO-10β-HYDROXY-5,7&alpha(H),4,6β(H)-GUAI-1,11(13)-DIENE-6,12-OLIDE
    Bulletin of the Karaganda University. Chemistry Series. 2022. № 2 (106). С. 52-60. doi:10.31489/2022Ch2/2-22-8
  760. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  761. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  762. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  763. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  764. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  765. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  766. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  767. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  768. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  769. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  770. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
  771. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  772. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  773. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  774. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  775. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  776. Шиповалов А.В., Ванин А.Ф., Пьянков О.В., Багрянская Е.Г., Микоян В.Д., Ткачев Н.А., Асанбаева Н.А., Попкова В.Я.
    Противовирусная активность катионов нитрозония в отношении SARS-COV-2 на модели сирийского хомячка
    Биофизика. 2022. Т. 67. № 5. С. 969-981. doi:10.31857/S0006302922050 (Antiviral Activity of Nitrosonium Cations against SARS-CoV-2 on a Syrian Hamster Model/ A. V. Shipovalov, A. F. Vanin, O. V. Pyankov, E. G. Bagryanskaya, V. D. Mikoyan, N. A. Tkachev, N. A. Asanbaeva, V. Ya. Popkova// Biophysics, 2022, V. 67, N 5, pages785-795 doi:10.1134/S0006350922050165)
  777. Л.Н. Зибарева, Е.С. Филоненко, Е.И. Черняк, С.В. Морозов, О.А. Котельников
    Флавоноиды некоторых видов растений рода SILENE
    Химия растительного сырья. 2022. № 3. С. 109-118. doi:10.14258/jcprm.20220310592
  778. Л.Н. Зибарева, Е.С. Филоненко, Е.И. Черняк, С.В. Морозов, О.А. Котельников
    Флавоноиды некоторых видов растений рода SILENE
    Химия растительного сырья. 2022. № 3. С. 109-118. doi:10.14258/jcprm.20220310592
  779. Л.Н. Зибарева, Е.С. Филоненко, Е.И. Черняк, С.В. Морозов, О.А. Котельников
    Флавоноиды некоторых видов растений рода SILENE
    Химия растительного сырья. 2022. № 3. С. 109-118. doi:10.14258/jcprm.20220310592
  780. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  781. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  782. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  783. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  784. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  785. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  786. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667
  787. А.Д. Иванова, Л.Г. Лавренова, Е.В. Коротаев, С.В. Трубина, А.Я. Тихонов, В.В. Кривенцов, С.А. Петров, К.Ю. Жижин, Н.Т. Кузнецов
    ИССЛЕДОВАНИЕ СПИН-КРОССОВЕРА В КОМПЛЕКСАХ ЖЕЛЕЗА(II) С 2,6-БИС(4,5-ДИМЕТИЛ-1H-ИМИДАЗОЛ-2-ИЛ)ПИРИДИНОМ И КЛОЗО-БОРАТНЫМИ АНИОНАМИ
    Журнал неорганической химии. 2022. Т. 67. № 8. С. 1058-1069. doi:10.31857/S0044457X22080177 doi:10.1134/S0036023622080174, IF=1.667

2021

Reviews, articles

  1. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
  2. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
  3. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
  4. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
  5. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
  6. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  7. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  8. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  9. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  10. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  11. K.S. Kovaleva, O.I. Yarovaya, Yu.V. Gatilov, A.V. Slita, Ya.L. Esaulkova, V.V. Zarubaev, N.B. Rudometova, N.S. Shcherbakova, D.N. Shcherbakov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of N-Heterocyclic Hydrazine Derivatives of Camphor and Fenchone
    Chemistry of Heterocyclic Compounds (2021), 57, N. 4, Pp 455-461 doi:10.1007/s10593-021-02923-5, IF=1.277
  12. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  13. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  14. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  15. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  16. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  17. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  18. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  19. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  20. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  21. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  22. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
  23. D.S. Odintsov, I.K. Shundrina, D.E. Gorbunov, N.P. Gritsan, J. Beckmann, L.A. Shundrin
    Spectroelectrochemical study of the reduction of 2-methyl-9H-thioxanthene-9-one and its S,S-dioxide and electronic absorption spectra of their molecular ions
    Phys. Chem. Chem. Phys., 2021, 23(47), 26940-26947 doi:10.1039/D1CP04464H, IF=3.676
  24. D.S. Odintsov, I.K. Shundrina, D.E. Gorbunov, N.P. Gritsan, J. Beckmann, L.A. Shundrin
    Spectroelectrochemical study of the reduction of 2-methyl-9H-thioxanthene-9-one and its S,S-dioxide and electronic absorption spectra of their molecular ions
    Phys. Chem. Chem. Phys., 2021, 23(47), 26940-26947 doi:10.1039/D1CP04464H, IF=3.676
  25. D.S. Odintsov, I.K. Shundrina, D.E. Gorbunov, N.P. Gritsan, J. Beckmann, L.A. Shundrin
    Spectroelectrochemical study of the reduction of 2-methyl-9H-thioxanthene-9-one and its S,S-dioxide and electronic absorption spectra of their molecular ions
    Phys. Chem. Chem. Phys., 2021, 23(47), 26940-26947 doi:10.1039/D1CP04464H, IF=3.676
  26. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
    Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
    Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
  27. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
    Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
    Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
  28. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
    Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
    Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
  29. E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
    Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
    Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
  30. Н.И. Ткачева, С.В. Морозов, Е.В. Третьяков, А.В. Ткачев
    Обзор состояния (инвентаризация) стойких органических загрязнителей (СОЗ) в объектах окружающей среды Мурманской области
    Охрана окружающей среды и заповедное дело: электрон. журн. – 2021. - №3-4. – С. 106-127.
  31. T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
    Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
  32. T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
    Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
  33. T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
    Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
  34. T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
    Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
  35. T.M. Khomenko, A.A. Shtro, A.V. Galochkina, Yu.V. Nikolaeva, G.D. Petukhova, S.a S. Borisevich, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication
    Molecules 2021, 26(24), 7493 doi:10.3390/molecules26247493, IF=4.41
  36. I.V. Beregovaya, I.S. Tretyakova, V.I. Borovkov
    An Updated View of Primary Ionization Processes in Polar Liquids
    The Journal of Physical Chemistry Letters, 2021, 12, 47, 11573-11577 doi:10.1021/acs.jpclett.1c03388, IF=6.475
  37. I.V. Beregovaya, I.S. Tretyakova, V.I. Borovkov
    An Updated View of Primary Ionization Processes in Polar Liquids
    The Journal of Physical Chemistry Letters, 2021, 12, 47, 11573-11577 doi:10.1021/acs.jpclett.1c03388, IF=6.475
  38. S.S. Khutsishvili, T.V. Ganenko, B.G. Sukhov
    Formation and paramagnetic properties of manganese-containing bionanocomposites based on natural polysaccharide matrices
    Journal of Carbohydrate Chemistry,2021, V. 40, N 5, Pp 211-225 doi:10.1080/07328303.2021.1990314, IF=1.667
  39. S.S. Khutsishvili, T.V. Ganenko, B.G. Sukhov
    Formation and paramagnetic properties of manganese-containing bionanocomposites based on natural polysaccharide matrices
    Journal of Carbohydrate Chemistry,2021, V. 40, N 5, Pp 211-225 doi:10.1080/07328303.2021.1990314, IF=1.667
  40. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  41. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  42. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  43. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  44. M. Han, I.I. Oleynik, Ya. Ma, I.V. Oleynik, G.A. Solan, T. Liang, Wen-Hua. Sun
    &alpha,&alpha'-Bis (imino)-2,3:5,6-bis (pentamethylene)pyridines appended with benzhydryl and cycloalkyl substituents: Probing their effectiveness as tunable N,N,N-supports for cobalt ethylene polymerization catalysts
    Applied Organometallic Chemistry, V. 35, N 12, December 2021, e6429 doi:10.1002/aoc.6429, IF=4.105
  45. O. Yarovaya, A. Zaykovskaya, K. Kovaleva, O. Pyankov, N. Salakhutdinov
    Development and application of the cytopathic model of Hantaan viruses
    AIP Conference Proceedings 2388, 040021 (2021) doi:10.1063/5.0069403
  46. O. Yarovaya, A. Zaykovskaya, K. Kovaleva, O. Pyankov, N. Salakhutdinov
    Development and application of the cytopathic model of Hantaan viruses
    AIP Conference Proceedings 2388, 040021 (2021) doi:10.1063/5.0069403
  47. И.В. Паламарчук, З.Т. Шульгау, Ш.Д. Сергазы, А.М. Жуликеева, Ю.В. Гатилов, И.В. Кулаков
    Синтез, строение и гемореологическая активность пентазамещенного циклогексанола
    Журнал общей химии. 2021. Т. 91. № 12. С. 1954-1961. doi:10.31857/S0044460X21120155 (Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X), IF=0.867
  48. И.В. Паламарчук, З.Т. Шульгау, Ш.Д. Сергазы, А.М. Жуликеева, Ю.В. Гатилов, И.В. Кулаков
    Синтез, строение и гемореологическая активность пентазамещенного циклогексанола
    Журнал общей химии. 2021. Т. 91. № 12. С. 1954-1961. doi:10.31857/S0044460X21120155 (Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X), IF=0.867
  49. И.В. Паламарчук, З.Т. Шульгау, Ш.Д. Сергазы, А.М. Жуликеева, Ю.В. Гатилов, И.В. Кулаков
    Синтез, строение и гемореологическая активность пентазамещенного циклогексанола
    Журнал общей химии. 2021. Т. 91. № 12. С. 1954-1961. doi:10.31857/S0044460X21120155 (Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X), IF=0.867
  50. И.В. Паламарчук, З.Т. Шульгау, Ш.Д. Сергазы, А.М. Жуликеева, Ю.В. Гатилов, И.В. Кулаков
    Синтез, строение и гемореологическая активность пентазамещенного циклогексанола
    Журнал общей химии. 2021. Т. 91. № 12. С. 1954-1961. doi:10.31857/S0044460X21120155 (Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X), IF=0.867
  51. И.В. Паламарчук, З.Т. Шульгау, Ш.Д. Сергазы, А.М. Жуликеева, Ю.В. Гатилов, И.В. Кулаков
    Синтез, строение и гемореологическая активность пентазамещенного циклогексанола
    Журнал общей химии. 2021. Т. 91. № 12. С. 1954-1961. doi:10.31857/S0044460X21120155 (Synthesis, Structure, and Hemorheological Activity of Pentasubstituted Cyclohexanol/ I. V. Palamarchuk, Z. T. Shulgau, Sh. D. Sergazy, A. M. Zhulikeeva, Yu. V. Gatilov & I. V. Kulakov// Russian Journal of General Chemistry, 2021, V. 91, pp 2462–2468 doi:10.1134/S107036322112015X), IF=0.867
  52. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
    Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
  53. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
    Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
  54. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
    Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
  55. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
    Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
  56. Т.П. Кукина, Д.Н. Щербаков, А.В. Зыбкина, И.А. Елшин, В.О. Корсаков, О.И. Сальникова, П.В. Колосов, Ц. Сандаг, Д.А. Каракай, Е.Д. Мордвинова
    Влияние экстрагента на состав липофильных компонентов экстрактов корневища Rhodiola rosea L. и активность экстрактов.
    Химия растительного сырья. 2021. N 4. С. 307-317 doi:10.14258/jcprm.2021049872
  57. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  58. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
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  59. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  60. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  61. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  62. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  63. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  64. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  65. Е.С. Кобелева, Д.А. Невоструев, М.Н. Уваров, Д.Е. Уткин, В.А. Зиновьев, О.А. Гурова, М.С. Казанцев, К.М. Дегтяренко, А.В. Куликова, Л.В. Кулик
    Фторирование одностенных углеродных нанотрубок и их применение в органических фотовольтаических ячейках в качестве акцептора электрона
    Известия Академии наук. Серия химическая, 2021, № 12, 2427 (Fluorination of single-walled carbon nanotubes and their application in organic photovoltaic cells as an electron acceptor/ E. S. Kobeleva, D. A. Nevostruev, M. N. Uvarov, D. E. Utkin, V. A. Zinoviev, O. A. Gurova, M. S. Kazantzev, K. M. Degtyarenko, A. V. Kulikova & L. V. Kulik// Russian Chemical Bulletin, 2021, V. 70, N. 12, pp 2427-2433 doi:10.1007/s11172-021-3363-4), IF=1.222
  66. M.Yu. Petyuk, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    Dinuclear ReI complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties
    Mendeleev Communications, 2021, V. 31, N 6, Pp 810-812 doi:10.1016/j.mencom.2021.11.013, IF=1.786
  67. M.Yu. Petyuk, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    Dinuclear ReI complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties
    Mendeleev Communications, 2021, V. 31, N 6, Pp 810-812 doi:10.1016/j.mencom.2021.11.013, IF=1.786
  68. M.Yu. Petyuk, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    Dinuclear ReI complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties
    Mendeleev Communications, 2021, V. 31, N 6, Pp 810-812 doi:10.1016/j.mencom.2021.11.013, IF=1.786
  69. M.Yu. Petyuk, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    Dinuclear ReI complex based on 1,2,4,5-tetrakis(diphenylphosphino)- pyridine: synthesis and luminescence properties
    Mendeleev Communications, 2021, V. 31, N 6, Pp 810-812 doi:10.1016/j.mencom.2021.11.013, IF=1.786
  70. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
  71. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
  72. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
  73. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
  74. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  75. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  76. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  77. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  78. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  79. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  80. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  81. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  82. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  83. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  84. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  85. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  86. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  87. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  88. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  89. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  90. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  91. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  92. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  93. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  94. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  95. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  96. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  97. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  98. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  99. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  100. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  101. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  102. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
  103. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  104. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  105. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  106. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  107. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  108. E. Parman, M. Lokov, R. Jarviste, S. Tshepelevitsh, N.A. Semenov, E.A. Chulanova, G.E. Salnikov, D.O. Prima, Yu.G. Slizhov, I. Leito, A.V. Zibarev
    Acid-Base and Anion Binding Properties of Tetrafluorinated 1,3-Benzodiazole, 1,2,3-Benzotriazole and 2,1,3-Benzoselenadiazole
    ChemPhysChem, 2021, V. 22, N 22, Pp 2329-2335 doi:10.1002/cphc.202100475, IF=3.102
  109. S.F. Vasilevsky, O.L. Krivenko, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, I.V. Alabugin
    Cascade Transformations of 1-R-Ethynyl-9,10-anthraquinones with Amidines: Expanding Access to Isoaporphinoid Alkaloids
    Molecules 2021, 26(22), 6883 doi:10.3390/molecules26226883, IF=4.411
  110. S.F. Vasilevsky, O.L. Krivenko, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, I.V. Alabugin
    Cascade Transformations of 1-R-Ethynyl-9,10-anthraquinones with Amidines: Expanding Access to Isoaporphinoid Alkaloids
    Molecules 2021, 26(22), 6883 doi:10.3390/molecules26226883, IF=4.411
  111. S.F. Vasilevsky, O.L. Krivenko, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, I.V. Alabugin
    Cascade Transformations of 1-R-Ethynyl-9,10-anthraquinones with Amidines: Expanding Access to Isoaporphinoid Alkaloids
    Molecules 2021, 26(22), 6883 doi:10.3390/molecules26226883, IF=4.411
  112. A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
    Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
    Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
  113. A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
    Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
    Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
  114. A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
    Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
    Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
  115. A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
    Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
    Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
  116. A.V. Artem'ev, M.Yu. Petyuk, A.S. Berezin, A.L. Gushchin, M.N. Sokolov, I.Yu. Bagryanskaya
    Synthesis and study of Re(I) tricarbonyl complexes based on octachloro-1,10-phenanthroline: towards deep red-to-NIR emitters
    Polyhedron, V. 209, 15 November 2021, 115484 doi:10.1016/j.poly.2021.115484, IF=3.052
  117. A.A. Kuzhelev, D. Dai, V. Denysenkov, I.A. Kirilyuk, E.G. Bagryanskaya, T. F. Prisner
    Influence of Rotational Motion of Nitroxides on Overhauser Dynamic Nuclear Polarization: A Systematic Study at High Magnetic Fields
    The Journal of Physical Chemistry C, 2021, 125, 46, 25651–25659 doi:10.1021/acs.jpcc.1c06979, IF=4.125
  118. A.A. Kuzhelev, D. Dai, V. Denysenkov, I.A. Kirilyuk, E.G. Bagryanskaya, T. F. Prisner
    Influence of Rotational Motion of Nitroxides on Overhauser Dynamic Nuclear Polarization: A Systematic Study at High Magnetic Fields
    The Journal of Physical Chemistry C, 2021, 125, 46, 25651–25659 doi:10.1021/acs.jpcc.1c06979, IF=4.125
  119. A.A. Kuzhelev, D. Dai, V. Denysenkov, I.A. Kirilyuk, E.G. Bagryanskaya, T. F. Prisner
    Influence of Rotational Motion of Nitroxides on Overhauser Dynamic Nuclear Polarization: A Systematic Study at High Magnetic Fields
    The Journal of Physical Chemistry C, 2021, 125, 46, 25651–25659 doi:10.1021/acs.jpcc.1c06979, IF=4.125
  120. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
    Discovery of New Ginsenol-like Compounds with High Antiviral Activity
    Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
  121. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
    Discovery of New Ginsenol-like Compounds with High Antiviral Activity
    Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
  122. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
    Discovery of New Ginsenol-like Compounds with High Antiviral Activity
    Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
  123. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
    Discovery of New Ginsenol-like Compounds with High Antiviral Activity
    Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
  124. A.S. Volobueva, O.I. Yarovaya, M.V. Kireeva, S.S. Borisevich, K.S. Kovaleva, I.Ya. Mainagashev, Yu.V. Gatilov, M.G. Ilyina, V.V. Zarubaev, N.F. Salakhutdinov
    Discovery of New Ginsenol-like Compounds with High Antiviral Activity
    Molecules, 2021, 26(22), 6794 doi:10.3390/molecules26226794, IF=4.41
  125. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  126. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  127. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  128. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  129. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
  130. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
    Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
    International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
  131. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
    Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
    International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
  132. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
    Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
    International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
  133. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
    Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
    International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
  134. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
    Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
    Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
  135. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
    Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
    Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
  136. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
    Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
    Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
  137. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
    Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
    Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
  138. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  139. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  140. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  141. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  142. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  143. R.Zhang, M. Han, I.V. Oleynik, G.A. Solan, I. I. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    Boosting activity, thermostability, and lifetime of iron ethylene polymerization catalysts through gem-dimethyl substitution and incorporation of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, V.35, N 11, November 2021, e6376 doi:10.1002/aoc.6376, IF=4.105
  144. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecular Diversity, 2021, V. 25, N 4, Pp 2389-2397 doi:10.1007/s11030-020-10132-z, IF=2.229
  145. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecular Diversity, 2021, V. 25, N 4, Pp 2389-2397 doi:10.1007/s11030-020-10132-z, IF=2.229
  146. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecular Diversity, 2021, V. 25, N 4, Pp 2389-2397 doi:10.1007/s11030-020-10132-z, IF=2.229
  147. K. Kovaleva, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecular Diversity, 2021, V. 25, N 4, Pp 2389-2397 doi:10.1007/s11030-020-10132-z, IF=2.229
  148. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  149. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  150. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  151. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  152. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  153. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  154. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  155. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  156. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  157. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  158. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  159. O. Kazakova, L. Rubanik, A. Lobov, N. Poleshchuk, I. Baikova, Yu. Kapustina, A. Petrova, T. Korzun, T. Lopatina, A. Fedorova, T. Rybalova, D. Polovianenko, M. Mioc, C. Soica
    Synthesis of erythrodiol C-ring derivatives and their activity against Chlamydia trachomatis
    Steroids,V. 175, November 2021, 108912 doi:10.1016/j.steroids.2021.108912, IF=2.667
  160. O.N. Fedyaeva, S.V. Morozov, A.A. Vostrikova
    Supercritical water oxidation of chlorinated waste from pulp and paper mill
    Chemosphere, 2021, V. 238, 131239 doi:10.1016/j.chemosphere.2021.131239, IF=7
  161. O.N. Fedyaeva, S.V. Morozov, A.A. Vostrikova
    Supercritical water oxidation of chlorinated waste from pulp and paper mill
    Chemosphere, 2021, V. 238, 131239 doi:10.1016/j.chemosphere.2021.131239, IF=7
  162. В.Н. Кручинин, Д.С. Одинцов, Л.А. Шундрин, И.К. Шундрина, С.В. Рыхлицкий, Е.В. Спесивцев, В.А. Гриценко
    Оптические и электрохромные свойства тонких пленок амбиполяных полиимидов с пендантными группами на основе производных тоиксантенона
    Оптика и спектроскопия, 2021, N 11, стр. 1393 doi:10.21883/OS.2021.11.51638.2473-21, IF=0.891
  163. В.Н. Кручинин, Д.С. Одинцов, Л.А. Шундрин, И.К. Шундрина, С.В. Рыхлицкий, Е.В. Спесивцев, В.А. Гриценко
    Оптические и электрохромные свойства тонких пленок амбиполяных полиимидов с пендантными группами на основе производных тоиксантенона
    Оптика и спектроскопия, 2021, N 11, стр. 1393 doi:10.21883/OS.2021.11.51638.2473-21, IF=0.891
  164. В.Н. Кручинин, Д.С. Одинцов, Л.А. Шундрин, И.К. Шундрина, С.В. Рыхлицкий, Е.В. Спесивцев, В.А. Гриценко
    Оптические и электрохромные свойства тонких пленок амбиполяных полиимидов с пендантными группами на основе производных тоиксантенона
    Оптика и спектроскопия, 2021, N 11, стр. 1393 doi:10.21883/OS.2021.11.51638.2473-21, IF=0.891
  165. В.Н. Кручинин, Д.С. Одинцов, Л.А. Шундрин, И.К. Шундрина, С.В. Рыхлицкий, Е.В. Спесивцев, В.А. Гриценко
    Оптические и электрохромные свойства тонких пленок амбиполяных полиимидов с пендантными группами на основе производных тоиксантенона
    Оптика и спектроскопия, 2021, N 11, стр. 1393 doi:10.21883/OS.2021.11.51638.2473-21, IF=0.891
  166. S.A. Popov, C. Wang, Z. Qi, E.E. Shul'ts, M. Turks
    Synthesis and Antioxidant Activity of New N-Containing Hybrid Derivatives of Gallic and Ursolic Acids
    Chemistry of Natural Compounds, 2021, V. 57, N. 6, Pp. 1042-1046 doi:10.1007/s10600-021-03546-0, IF=0.809
  167. S.A. Popov, C. Wang, Z. Qi, E.E. Shul'ts, M. Turks
    Synthesis and Antioxidant Activity of New N-Containing Hybrid Derivatives of Gallic and Ursolic Acids
    Chemistry of Natural Compounds, 2021, V. 57, N. 6, Pp. 1042-1046 doi:10.1007/s10600-021-03546-0, IF=0.809
  168. S.A. Popov, C. Wang, Z. Qi, E.E. Shul'ts, M. Turks
    Synthesis and Antioxidant Activity of New N-Containing Hybrid Derivatives of Gallic and Ursolic Acids
    Chemistry of Natural Compounds, 2021, V. 57, N. 6, Pp. 1042-1046 doi:10.1007/s10600-021-03546-0, IF=0.809
  169. В.В. Шелковников, С.Л. Микерин, А.Э. Симанчук, П.А. Чубаков, С.В. Коротаев, Н.А. Орлова, В.Н. Бережная, И.Ю. Каргаполова, А.М. Максимов, Р.А. Ищенко, Н.Д. Рязанов
    Нелинейно-оптические свойства полифтортрифенилпиразолиндицианоизофороновых красителей в матрице поликарбоната
    Автометрия. 2021. Т. 57. № 6. С. 60-66. doi:10.15372/AUT20210606
  170. В.В. Шелковников, С.Л. Микерин, А.Э. Симанчук, П.А. Чубаков, С.В. Коротаев, Н.А. Орлова, В.Н. Бережная, И.Ю. Каргаполова, А.М. Максимов, Р.А. Ищенко, Н.Д. Рязанов
    Нелинейно-оптические свойства полифтортрифенилпиразолиндицианоизофороновых красителей в матрице поликарбоната
    Автометрия. 2021. Т. 57. № 6. С. 60-66. doi:10.15372/AUT20210606
  171. В.В. Шелковников, С.Л. Микерин, А.Э. Симанчук, П.А. Чубаков, С.В. Коротаев, Н.А. Орлова, В.Н. Бережная, И.Ю. Каргаполова, А.М. Максимов, Р.А. Ищенко, Н.Д. Рязанов
    Нелинейно-оптические свойства полифтортрифенилпиразолиндицианоизофороновых красителей в матрице поликарбоната
    Автометрия. 2021. Т. 57. № 6. С. 60-66. doi:10.15372/AUT20210606
  172. Д.И. Деревянко, Е.Ф. Пен, В.В. Шелковников, С.И. Алиев
    Тонкослойные голографические фотополимерные материалы с большим изменением показателя преломления
    Автометрия. 2021. Т. 57. № 6. С. 29-37. doi:10.15372/AUT20210603
  173. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  174. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  175. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  176. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  177. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  178. Г.Т. СУХАНОВ, Ю.В. ФИЛИППОВА, И.Ю. БАГРЯНСКАЯ, А.Г. СУХАНОВА, К.К. БОСОВ, И.А. КРУПНОВА, Е.В. ПИВОВАРОВА
    Синтез и свойства солей 1,3-диалкил-4-нитро-1,2,3-триазолия
    Химия в интересах устойчивого развития. 2021. Т. 29. № 6. С. 702-707. doi:10.15372/KhUR2021349
  179. Б.М. Урбагарова, В.В. Тараскин, Т.В. Елисафенко, Э.Э. Шульц, Е.А. Королюк, Л.Д. Раднаева
    Содержание основных действующих веществ в корнях природного и интродуцированного растения SAPOSHNIKOVIA DIVARICATA (TURCZ.) SCHISCHK
    Химия растительного сырья. 2021. № 3. С. 143-151 doi:10.14258/jcprm.2021039152
  180. Б.М. Урбагарова, В.В. Тараскин, Т.В. Елисафенко, Э.Э. Шульц, Е.А. Королюк, Л.Д. Раднаева
    Содержание основных действующих веществ в корнях природного и интродуцированного растения SAPOSHNIKOVIA DIVARICATA (TURCZ.) SCHISCHK
    Химия растительного сырья. 2021. № 3. С. 143-151 doi:10.14258/jcprm.2021039152
  181. Б.М. Урбагарова, В.В. Тараскин, Т.В. Елисафенко, Э.Э. Шульц, Е.А. Королюк, Л.Д. Раднаева
    Содержание основных действующих веществ в корнях природного и интродуцированного растения SAPOSHNIKOVIA DIVARICATA (TURCZ.) SCHISCHK
    Химия растительного сырья. 2021. № 3. С. 143-151 doi:10.14258/jcprm.2021039152
  182. Б.М. Урбагарова, В.В. Тараскин, Т.В. Елисафенко, Э.Э. Шульц, Е.А. Королюк, Л.Д. Раднаева
    Содержание основных действующих веществ в корнях природного и интродуцированного растения SAPOSHNIKOVIA DIVARICATA (TURCZ.) SCHISCHK
    Химия растительного сырья. 2021. № 3. С. 143-151 doi:10.14258/jcprm.2021039152
  183. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  184. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  185. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  186. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  187. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  188. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  189. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  190. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  191. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  192. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  193. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  194. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  195. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  196. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  197. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
  198. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  199. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  200. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  201. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  202. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  203. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  204. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
    The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
    J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
  205. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  206. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  207. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  208. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  209. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  210. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  211. R. Zhang, I.V. Oleynik, Ji. Li, G.A. Solan, Ya. Ma, Li. Jin, I.I. Oleynik, X. Hu, Wen-Hua. Sun
    Integrating ring-size adjustable cycloalkyl and benzhydryl groups as the steric protection in bis(arylimino)trihydroquinoline-cobalt catalysts for ethylene polymerization
    European Journal of Inorganic Chemistry, 2021, V.2021, N 38, , Pp 3956-3968 doi:10.1002/ejic.202100573, IF=2.523
  212. A. Zobnina, A. Moskalensky, A. Vorob'ev
    8-[4-(2-Hydroxypropane-2-yl)Phenyl]-1,3,4,4,5,7-Hexamethyl-4-Boron-3a,4a-Diaza-S-Indacene
    Molbank, 2021, 2021(4), M1286 doi:10.3390/M1286
  213. A. Zobnina, A. Moskalensky, A. Vorob'ev
    8-[4-(2-Hydroxypropane-2-yl)Phenyl]-1,3,4,4,5,7-Hexamethyl-4-Boron-3a,4a-Diaza-S-Indacene
    Molbank, 2021, 2021(4), M1286 doi:10.3390/M1286
  214. Yu.V. Khoroshunova,D. A. Morozov,A. I. Taratayko,S. A. Dobrynin,I. V. Eltsov,T. V. Rybalova,Yu. S. Sotnikova,D. N. Polovyanenko,N. B. Asanbaeva,I. A. Kirilyuk
    The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4
    Molecules 2021, 26(19), 6000 doi:10.3390/molecules26196000, IF=4.411
  215. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  216. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  217. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  218. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  219. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  220. Zh.S. Nurmaganbetov, V.A. Savelyev, Yu.V. Gatilov, O.A. Nurkenov, R.B. Seidakhmetova, Z.T. Shulgau, G.K. Mukusheva, S.D. Fazylov, E.E. Shults
    Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine
    Chemistry of Heterocyclic Compounds, 2021, V. 57, Pp 911-919 doi:10.1007/s10593-021-03000-7, IF=1.276
  221. A.O. Finke, V.G. Kartsev, E.E. Shults
    Synthesis of Alkaloid Sinomenine Derivatives Containing a Pyrimidine Substituent in Ring A
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N.9 , Pp 934-943 doi:10.1007/s10593-021-03003-4, IF=1.276
  222. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  223. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  224. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  225. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  226. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  227. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  228. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  229. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
  230. S.S. Khutsishvili, G.P. Aleksandrova, T.I. Vaku'skaya, B.G. Sukhov
    Structural and Magnetic Properties of Biocompatible Coated Magnetite Nanoparticles for Treating Antianemi (Revised May 2021)
    IEEE Transactions on Magnetics, 2021, V. 57, N 10, 5200309 doi:10.1109/TMAG.2021.3101904, IF=1.7
  231. S.S. Khutsishvili, G.P. Aleksandrova, T.I. Vaku'skaya, B.G. Sukhov
    Structural and Magnetic Properties of Biocompatible Coated Magnetite Nanoparticles for Treating Antianemi (Revised May 2021)
    IEEE Transactions on Magnetics, 2021, V. 57, N 10, 5200309 doi:10.1109/TMAG.2021.3101904, IF=1.7
  232. S.S. Khutsishvili, G.P. Aleksandrova, T.I. Vaku'skaya, B.G. Sukhov
    Structural and Magnetic Properties of Biocompatible Coated Magnetite Nanoparticles for Treating Antianemi (Revised May 2021)
    IEEE Transactions on Magnetics, 2021, V. 57, N 10, 5200309 doi:10.1109/TMAG.2021.3101904, IF=1.7
  233. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Stability study of the antiviral agent camphecene in dried blood spots at different temperatures
    Drug Testing and Analysis, V.13, N 10, October 2021, Pp 1797-1802 doi:10.1002/dta.3148, IF=3.345
  234. A.E. Moskalensky, T.Yu. Karogodina, A.Yu. Vorobev, S.G. Sokolovski
    Singlet oxygen luminescence detector based on low-cost InGaAs avalanche photodiode
    HardwareX, V. 10, October 2021, e00224 doi:10.1016/j.ohx.2021.e00224, IF=0.676
  235. A.E. Moskalensky, T.Yu. Karogodina, A.Yu. Vorobev, S.G. Sokolovski
    Singlet oxygen luminescence detector based on low-cost InGaAs avalanche photodiode
    HardwareX, V. 10, October 2021, e00224 doi:10.1016/j.ohx.2021.e00224, IF=0.676
  236. A.E. Moskalensky, T.Yu. Karogodina, A.Yu. Vorobev, S.G. Sokolovski
    Singlet oxygen luminescence detector based on low-cost InGaAs avalanche photodiode
    HardwareX, V. 10, October 2021, e00224 doi:10.1016/j.ohx.2021.e00224, IF=0.676
  237. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  238. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  239. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  240. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  241. V.P. Nikolin, N.A. Popova, V.I. Kaledin, O.A. Luzina, A.L. Zakharenko, N.F. Salakhutdinov, O.I. Lavrik
    The influence of an enamine usnic acid derivative (a tyrosyl-DNA phosphodiesterase 1 inhibitor) on the therapeutic effect of topotecan against transplanted tumors in vivo
    Clinical & Experimental Metastasis, 2021, 38, Pp 431-440 doi:10.1007/s10585-021-10113-y, IF=5.15
  242. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861
  243. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861
  244. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861
  245. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861
  246. E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
    Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
    Natural Product Research (Formerly Natural Product ), 2021, V. 35, N 21, Pp 3850-3858 doi:10.1080/14786419.2020.1744139, IF=2.861
  247. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  248. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  249. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  250. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  251. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  252. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  253. N.ikita A. Shekhovtsov, E.B. Nikolaenkova, A.S. Berezin, V.F. Plyusnin, K.A. Vinogradova, D.Yu. Naumov, N.V. Pervukhina, A.Ya. Tikhonov, M.B. Bushuev
    An 1-hydroxy-1H-imidazole ESIPT emitter demonstrating anti-Kasha fluorescence and direct excitation of a tautomeric form
    ChemPhysChem, 2021, V. 86, N 10, Pp 1436-1441 doi:10.1002/cplu.202100370, IF=3.102
  254. T. Skripkina, M. Belokozenko, S. Shatskaya, V. Tikhova, I. Lomovskiy
    Concentrating rare earth elements in brown coal humic acids by mechanochemical treatment Check for updates
    RSC Advances, 2021, V. 11, N 57, Pp 36016-36022 doi:10.1039/D1RA07228E, IF=3.361
  255. T. Skripkina, M. Belokozenko, S. Shatskaya, V. Tikhova, I. Lomovskiy
    Concentrating rare earth elements in brown coal humic acids by mechanochemical treatment Check for updates
    RSC Advances, 2021, V. 11, N 57, Pp 36016-36022 doi:10.1039/D1RA07228E, IF=3.361
  256. T. Skripkina, M. Belokozenko, S. Shatskaya, V. Tikhova, I. Lomovskiy
    Concentrating rare earth elements in brown coal humic acids by mechanochemical treatment Check for updates
    RSC Advances, 2021, V. 11, N 57, Pp 36016-36022 doi:10.1039/D1RA07228E, IF=3.361
  257. T. Skripkina, M. Belokozenko, S. Shatskaya, V. Tikhova, I. Lomovskiy
    Concentrating rare earth elements in brown coal humic acids by mechanochemical treatment Check for updates
    RSC Advances, 2021, V. 11, N 57, Pp 36016-36022 doi:10.1039/D1RA07228E, IF=3.361
  258. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  259. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  260. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  261. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  262. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  263. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  264. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  265. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  266. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
  267. S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
    A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
    Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
  268. S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
    A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
    Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
  269. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  270. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  271. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  272. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  273. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  274. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  275. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  276. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  277. S.A. Liakhov, I.A. Schepetkin, O.S. Karpenko, H.I. Duma, N.M. Haidarzhy, L.N. Kirpotina, A.R. Kovrizhina, A.I. Khlebnikov, I.Yu. Bagryanskaya, M.T. Quinn
    Novel c-Jun N-Terminal Kinase (JNK) Inhibitors with an 11H-Indeno[1,2-b]quinoxalin-11-one Scaffold
    Molecules 2021, 26(18), 5688 doi:10.3390/molecules26185688, IF=4.411
  278. Enrico. Benassi, T. Vaganova, E. Malykhin, Haiyan. Fan
    Impact of fluorination and chlorination on the electronic structure, topology and in-plane ring normal modes of pyridines† Check for updates
    Phys. Chem. Chem. Phys., 2021, V. 23, N. 34, Pp.18958-18974 doi:10.1039/D1CP02342J, IF=3.676
  279. Enrico. Benassi, T. Vaganova, E. Malykhin, Haiyan. Fan
    Impact of fluorination and chlorination on the electronic structure, topology and in-plane ring normal modes of pyridines† Check for updates
    Phys. Chem. Chem. Phys., 2021, V. 23, N. 34, Pp.18958-18974 doi:10.1039/D1CP02342J, IF=3.676
  280. S.S. Ovcherenko, O.A. Chinak, A.V. Chechushkov, S.A. Dobrynin, I.A. Kirilyuk, O.A. Krumkacheva, V.A. Richter, E.G. Bagryanskaya
    Uptake of Cell-Penetrating Peptide RL2 by Human Lung Cancer Cells: Monitoring by Electron Paramagnetic Resonance and Confocal Laser Scanning Microscopy
    Molecules 2021, 26(18), 5442 doi:10.3390/molecules26185442, IF=4.41
  281. S.S. Ovcherenko, O.A. Chinak, A.V. Chechushkov, S.A. Dobrynin, I.A. Kirilyuk, O.A. Krumkacheva, V.A. Richter, E.G. Bagryanskaya
    Uptake of Cell-Penetrating Peptide RL2 by Human Lung Cancer Cells: Monitoring by Electron Paramagnetic Resonance and Confocal Laser Scanning Microscopy
    Molecules 2021, 26(18), 5442 doi:10.3390/molecules26185442, IF=4.41
  282. S.S. Ovcherenko, O.A. Chinak, A.V. Chechushkov, S.A. Dobrynin, I.A. Kirilyuk, O.A. Krumkacheva, V.A. Richter, E.G. Bagryanskaya
    Uptake of Cell-Penetrating Peptide RL2 by Human Lung Cancer Cells: Monitoring by Electron Paramagnetic Resonance and Confocal Laser Scanning Microscopy
    Molecules 2021, 26(18), 5442 doi:10.3390/molecules26185442, IF=4.41
  283. D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
    One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
    The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
  284. D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
    One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
    The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
  285. D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
    One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
    The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
  286. D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
    One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
    The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
  287. D.S. Baranov, A.A. Popov, D.A. Nevostruev, A.A. Dmitriev, Yu.V. Gatilov, E.S. Kobeleva
    One-Pot Synthesis of 2-R-Naphtho[2,3-b]thiophene-4,9-diones via Cyclization of 2-(R-Ethynyl)-1,4-naphthoquinones with Na2S2O3
    The Journal of Organic Chemistry, 2021, V. 86, N. 17, Pp. 11361-11369 doi:10.1021/acs.joc.1c00852, IF=4.354
  288. O. Kazakova, E. Tret'yakova, D. Baev
    Evaluation of A-azepano-triterpenoids and related derivatives as antimicrobial and antiviral agents
    The Journal of Antibiotics, 2021, Vol. 74, N 9, Pp 559–573 doi: 10.1038/s41429-021-00448-9, IF=2.648
  289. O. Kazakova, E. Tret'yakova, D. Baev
    Evaluation of A-azepano-triterpenoids and related derivatives as antimicrobial and antiviral agents
    The Journal of Antibiotics, 2021, Vol. 74, N 9, Pp 559–573 doi: 10.1038/s41429-021-00448-9, IF=2.648
  290. I.V. Kulakov, I.V. Palamarchuk, E.B. Nikolaenkova, A.Ya. Tikhonov, Yu.V. Gatilov, A.S. Fisyuk
    Study of the cyclization of N-hydroxy- and N-methoxy-N-(2-oxoalkyl)amides
    Chemical Papers, 2021, V. 75, Pp 4517-4525 doi:10.1007/s11696-021-01673-0, IF=2.097
  291. I.V. Kulakov, I.V. Palamarchuk, E.B. Nikolaenkova, A.Ya. Tikhonov, Yu.V. Gatilov, A.S. Fisyuk
    Study of the cyclization of N-hydroxy- and N-methoxy-N-(2-oxoalkyl)amides
    Chemical Papers, 2021, V. 75, Pp 4517-4525 doi:10.1007/s11696-021-01673-0, IF=2.097
  292. I.V. Kulakov, I.V. Palamarchuk, E.B. Nikolaenkova, A.Ya. Tikhonov, Yu.V. Gatilov, A.S. Fisyuk
    Study of the cyclization of N-hydroxy- and N-methoxy-N-(2-oxoalkyl)amides
    Chemical Papers, 2021, V. 75, Pp 4517-4525 doi:10.1007/s11696-021-01673-0, IF=2.097
  293. В.С. Гусаров, А.М. Чеплакова, Д.Г. Самсоненко, А.С. Виноградов, В.П. Федин
    Синтез и кристаллическая структура металл-органических координационных полимеров на основе CD(II) и октафторбифенил-4,4'-дикарбоксилата
    Журнал неорганической химии. 2021. Т. 66. № 9. С. 1280-1286. doi:10.31857/S0044457X21090038 (Synthesis and Crystal Structure of Cadmium(II) Metal-Organic Coordination Polymers with Octafluorobiphenyl-4,4'-Dicarboxylate/ V. S. Gusarov, A. M. Cheplakova, D. G. Samsonenko, A. S. Vinogradov & V. P. Fedin// Russian Journal of Inorganic Chemistry, 2021, V. 66, N 9, Pp 1374-1379 doi:10.1134/S0036023621090035), IF=1.312
  294. В.С. Гусаров, А.М. Чеплакова, Д.Г. Самсоненко, А.С. Виноградов, В.П. Федин
    Синтез и кристаллическая структура металл-органических координационных полимеров на основе CD(II) и октафторбифенил-4,4'-дикарбоксилата
    Журнал неорганической химии. 2021. Т. 66. № 9. С. 1280-1286. doi:10.31857/S0044457X21090038 (Synthesis and Crystal Structure of Cadmium(II) Metal-Organic Coordination Polymers with Octafluorobiphenyl-4,4'-Dicarboxylate/ V. S. Gusarov, A. M. Cheplakova, D. G. Samsonenko, A. S. Vinogradov & V. P. Fedin// Russian Journal of Inorganic Chemistry, 2021, V. 66, N 9, Pp 1374-1379 doi:10.1134/S0036023621090035), IF=1.312
  295. В.С. Гусаров, А.М. Чеплакова, Д.Г. Самсоненко, А.С. Виноградов, В.П. Федин
    Синтез и кристаллическая структура металл-органических координационных полимеров на основе CD(II) и октафторбифенил-4,4'-дикарбоксилата
    Журнал неорганической химии. 2021. Т. 66. № 9. С. 1280-1286. doi:10.31857/S0044457X21090038 (Synthesis and Crystal Structure of Cadmium(II) Metal-Organic Coordination Polymers with Octafluorobiphenyl-4,4'-Dicarboxylate/ V. S. Gusarov, A. M. Cheplakova, D. G. Samsonenko, A. S. Vinogradov & V. P. Fedin// Russian Journal of Inorganic Chemistry, 2021, V. 66, N 9, Pp 1374-1379 doi:10.1134/S0036023621090035), IF=1.312
  296. В.С. Гусаров, А.М. Чеплакова, Д.Г. Самсоненко, А.С. Виноградов, В.П. Федин
    Синтез и кристаллическая структура металл-органических координационных полимеров на основе CD(II) и октафторбифенил-4,4'-дикарбоксилата
    Журнал неорганической химии. 2021. Т. 66. № 9. С. 1280-1286. doi:10.31857/S0044457X21090038 (Synthesis and Crystal Structure of Cadmium(II) Metal-Organic Coordination Polymers with Octafluorobiphenyl-4,4'-Dicarboxylate/ V. S. Gusarov, A. M. Cheplakova, D. G. Samsonenko, A. S. Vinogradov & V. P. Fedin// Russian Journal of Inorganic Chemistry, 2021, V. 66, N 9, Pp 1374-1379 doi:10.1134/S0036023621090035), IF=1.312
  297. Ya.V. Zonov, Siqi. Wanga, V.M. Karpov, T.V. Mezhenkova
    The aliphatic ring-opening and SNAr substitution in the reactions of perfluorobenzocycloalkenones with K2CO3 in water and methanol
    Journal of Fluorine Chemistry, 2021, V. 249, 109851 doi:10.1016/j.jfluchem.2021.109851, IF=2.05
  298. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    F- and OH-Containing Isopulegol-Derived Octahydro-2H-Chromenes as Agents against Influenza A Viru
    Med. Sci. Forum 2021, 7(1), 12. https://doi.org/10.3390/ECMS2021-10836 doi:10.3390/ECMS2021-10836
  299. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  300. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  301. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  302. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  303. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  304. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  305. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  306. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  307. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  308. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
  309. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  310. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  311. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  312. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  313. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  314. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  315. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  316. N.V. Bulina, D.K. Rybin, S.V. Makarova, D.V. Dudina, I.S. Batraev, A.V. Utkin, I.Yu. Prosanov, M.V. Khvostov, V.Yu. Ulianitsky
    Detonation Spraying of Hydroxyapatite on a Titanium Alloy Implant
    Materials 2021, 14(17), 4852 doi:10.3390/ma14174852, IF=3.622
  317. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
    Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
    The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
  318. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
    Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
    The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
  319. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
    Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
    The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
  320. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
    Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
    The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
  321. B.Y. Mladenova Kattnig, N.A. Chumakova, D.R. Kattnig, I.A. Grigor’ev, G. Grampp, A.I. Kokorin
    Influence of the Electric Charge of Spin Probes on Their Diffusion in Room-Temperature Ionic Liquids
    The Journal of Physical Chemistry B, 2021, V. 125, N 32, Pp. 9235–9243 doi:10.1021/acs.jpcb.1c02493, IF=2.99
  322. S.A. Popov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turksc
    Synthesis of water-soluble ester-linked ursolic acid-gallic acid hybrids with various hydrolytic stabilities
    Synthetic Communications, 2021, V.51, N 16, Pp 2466-2477 doi:10.1080/00397911.2021.1939057, IF=2.6
  323. S.A. Popov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turksc
    Synthesis of water-soluble ester-linked ursolic acid-gallic acid hybrids with various hydrolytic stabilities
    Synthetic Communications, 2021, V.51, N 16, Pp 2466-2477 doi:10.1080/00397911.2021.1939057, IF=2.6
  324. S.A. Popov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turksc
    Synthesis of water-soluble ester-linked ursolic acid-gallic acid hybrids with various hydrolytic stabilities
    Synthetic Communications, 2021, V.51, N 16, Pp 2466-2477 doi:10.1080/00397911.2021.1939057, IF=2.6
  325. D.O. Antonov, D.P. Tambasova, A.B. Shishmakov, I.A. Kirilyuk, E.G. Kovaleva
    Acidic and Electrosurface Properties of Binary TiO2–SiO2 Xerogels Using EPR of pH-Sensitive Nitroxides
    Gels, 2021, 7(3), 119 doi:10.3390/gels7030119, IF=4.702
  326. D.O. Antonov, D.P. Tambasova, A.B. Shishmakov, I.A. Kirilyuk, E.G. Kovaleva
    Acidic and Electrosurface Properties of Binary TiO2–SiO2 Xerogels Using EPR of pH-Sensitive Nitroxides
    Gels, 2021, 7(3), 119 doi:10.3390/gels7030119, IF=4.702
  327. D.O. Antonov, D.P. Tambasova, A.B. Shishmakov, I.A. Kirilyuk, E.G. Kovaleva
    Acidic and Electrosurface Properties of Binary TiO2–SiO2 Xerogels Using EPR of pH-Sensitive Nitroxides
    Gels, 2021, 7(3), 119 doi:10.3390/gels7030119, IF=4.702
  328. D.O. Antonov, D.P. Tambasova, A.B. Shishmakov, I.A. Kirilyuk, E.G. Kovaleva
    Acidic and Electrosurface Properties of Binary TiO2–SiO2 Xerogels Using EPR of pH-Sensitive Nitroxides
    Gels, 2021, 7(3), 119 doi:10.3390/gels7030119, IF=4.702
  329. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  330. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  331. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  332. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  333. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  334. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  335. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, G.G. Dultseva, S.V. An'kov, T.G. Tolstikova, V.L. Rusinov, V.N. Charushin
    An integrated aerosol setup for therapeutics and toxicological testing: generation techniques and measurement instrumentation
    Measurement, 2021, V. 181, Art. Num.109659 doi:10.1016/j.measurement.2021.109659, IF=3.927
  336. A.O. Finke, M.Y. Ravaeva, V.I. Krasnov, I.V. Cheretaev, E.N. Chuyan, D.S. Baev, E.E. Shults
    Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
    ChemistrySelect, 2021, V. 6,N 29, Pp 7391-7397 doi:10.1002/slct.202101790, IF=2.108
  337. A.O. Finke, M.Y. Ravaeva, V.I. Krasnov, I.V. Cheretaev, E.N. Chuyan, D.S. Baev, E.E. Shults
    Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
    ChemistrySelect, 2021, V. 6,N 29, Pp 7391-7397 doi:10.1002/slct.202101790, IF=2.108
  338. A.O. Finke, M.Y. Ravaeva, V.I. Krasnov, I.V. Cheretaev, E.N. Chuyan, D.S. Baev, E.E. Shults
    Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
    ChemistrySelect, 2021, V. 6,N 29, Pp 7391-7397 doi:10.1002/slct.202101790, IF=2.108
  339. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
  340. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
  341. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
  342. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
  343. N.S. Sirazhetdinova, V.A. Savelyev, D.S. Baev, T.S. Golubeva, L.S. Klimenko, T.G. Tolstikova, Ja. Ganbaatar, E.E. Shults
    Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives
    Medicinal Chemistry Research, 2021, V. 30, N. 8, Pp 1541-1556 doi:10.1007/s00044-021-02754-1, IF=1.965
  344. N.S. Sirazhetdinova, V.A. Savelyev, D.S. Baev, T.S. Golubeva, L.S. Klimenko, T.G. Tolstikova, Ja. Ganbaatar, E.E. Shults
    Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives
    Medicinal Chemistry Research, 2021, V. 30, N. 8, Pp 1541-1556 doi:10.1007/s00044-021-02754-1, IF=1.965
  345. N.S. Sirazhetdinova, V.A. Savelyev, D.S. Baev, T.S. Golubeva, L.S. Klimenko, T.G. Tolstikova, Ja. Ganbaatar, E.E. Shults
    Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives
    Medicinal Chemistry Research, 2021, V. 30, N. 8, Pp 1541-1556 doi:10.1007/s00044-021-02754-1, IF=1.965
  346. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  347. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  348. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  349. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  350. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  351. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  352. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  353. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  354. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  355. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  356. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  357. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  358. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  359. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  360. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  361. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  362. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  363. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  364. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  365. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  366. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  367. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  368. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  369. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  370. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  371. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  372. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  373. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  374. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  375. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  376. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  377. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  378. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  379. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  380. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  381. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  382. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  383. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  384. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  385. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  386. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  387. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  388. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  389. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  390. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
  391. R. A.Ishchenko,I. Yu.Kargapolova,N. А.Orlova,V.V.Shelkovnikov,A.М.Maksimov,N. D.Ryazanov,V.N.Berezhnaya,A.А.Chernonosov
    Polyfluorinated Triphenyl-4,5-Dihydro-1H-Pyrazoles with Dendroid Arylsulfanyl Moieties as Donor Blocks in Donor-Acceptor Chromophores
    Journal of Fluorine Chemistry, 2021, V. 248, 109841 doi:10.1016/j.jfluchem.2021.109841, IF=2.05
  392. M.D. Semenova, S.A. Popov, T.S. Golubeva, D.S. Baev, E.E. Shults, M. Turks
    Synthesis and Cytotoxicity of Sulfanyl, Sulfinyl and Sulfonyl Group Containing Ursane Conjugates with 1,3,4-Oxadiazoles and 1,2,4-Triazoles
    ChemistrySelectб 2021, V. 6, N 7, Pp 6472-6477, This article also appears in:Medicinal Chemistry & Drug Discovery doi:10.1002/slct.202101594, IF=2.109
  393. M.D. Semenova, S.A. Popov, T.S. Golubeva, D.S. Baev, E.E. Shults, M. Turks
    Synthesis and Cytotoxicity of Sulfanyl, Sulfinyl and Sulfonyl Group Containing Ursane Conjugates with 1,3,4-Oxadiazoles and 1,2,4-Triazoles
    ChemistrySelectб 2021, V. 6, N 7, Pp 6472-6477, This article also appears in:Medicinal Chemistry & Drug Discovery doi:10.1002/slct.202101594, IF=2.109
  394. T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
    Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
    CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
  395. T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
    Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
    CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
  396. T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
    Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
    CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
  397. T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
    Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
    CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
  398. T.A. Vaganova, Yu.V. Gatilov, S.E. Malykhin, D.P. Pishchur, M. Sukhov, B.A. Zakharov, E.V. Boldyreva, E.V. Malykhin
    Co-crystals of polyhalogenated diaminobenzonitriles with 18-crown-6: effect of fluorine on the stoichiometry and supramolecular structure
    CrystEngComm, 2021, V. 23, N 7, Pp 4767-4781 doi:10.1039/D1CE00530H, IF=3.545
  399. M. Panfilov, D. Chernova, I. Khalfina, A. Moskalensky, A. Vorob'ev
    Design and Synthesis of New Acridone-Based Nitric Oxide Fluorescent Probe
    Molecules 2021, 26(14), 4340 doi:10.3390/molecules26144340, IF=4.411
  400. M. Panfilov, D. Chernova, I. Khalfina, A. Moskalensky, A. Vorob'ev
    Design and Synthesis of New Acridone-Based Nitric Oxide Fluorescent Probe
    Molecules 2021, 26(14), 4340 doi:10.3390/molecules26144340, IF=4.411
  401. M. Panfilov, D. Chernova, I. Khalfina, A. Moskalensky, A. Vorob'ev
    Design and Synthesis of New Acridone-Based Nitric Oxide Fluorescent Probe
    Molecules 2021, 26(14), 4340 doi:10.3390/molecules26144340, IF=4.411
  402. M. Panfilov, D. Chernova, I. Khalfina, A. Moskalensky, A. Vorob'ev
    Design and Synthesis of New Acridone-Based Nitric Oxide Fluorescent Probe
    Molecules 2021, 26(14), 4340 doi:10.3390/molecules26144340, IF=4.411
  403. A.O. Bryzgalov, T.A. Yakovleva, L.V. Politanskaya, I.Yu. Bagryanskaya, T.G. Tolstikova
    Fluorinated 3,4-Dihydro-2H-1,4-Benzothiazin1,1-Dioxide Derivatives with Antiarrhythmic and Hypertensive Effects
    American Journal of Biomedical Science & Research, 2021,13(4),328-338 doi:10.34297/AJBSR.2021.13.001882
  404. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  405. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  406. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  407. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  408. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  409. E. A. Rudnitskaya, A. O. Burnyasheva, T. A. Kozlova, N. A. Muraleva, D. V. Telegina, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov & N. G. Kolosova
    Ambiguous Effects of Prolonged Dietary Supplementation with a Striatal-Enriched Protein Tyrosine Phosphatase Inhibitor, TC-2153, on a Rat Model of Sporadic Alzheimer’s Disease
    Neurochemical Journal, 2021, V. 15, N 3, Pp 292–301 doi:10.1134/S1819712421030090, IF=0.479
  410. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
    Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
    Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
  411. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
    Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
    Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
  412. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
    Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
    Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
  413. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
    Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
    Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
  414. A.S. Sokolova, O.I. Yarovaya, D.V. Baranova, A.V. Galochkina, A.A. Shtro, M.V. Kireeva, S.S. Borisevich, Y.V. Gatilov, V.V. Zarubaev, N.F. Salakhutdinov
    Quaternary ammonium salts based on (-)-borneol as effective inhibitors of influenza virus
    Archives of Virology, 2021, V. 166, N. 7, Pp 1965-1976 doi:10.1007/s00705-021-05102-1, IF=2.574
  415. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  416. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  417. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  418. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  419. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  420. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Уровни жирных кислот сыворотки крови и мембран эритроцитов могут быть использованы как биомаркеры для оценки тяжести НАЖБП
    Экспериментальная и клиническая гастроэнтерология. 2021. № 7 (191). С. 12-22. doi:10.31146/1682-8658-ecg-191-7-12-22
  421. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  422. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  423. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  424. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  425. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  426. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
  427. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  428. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  429. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  430. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  431. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  432. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  433. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  434. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, A.L. Zakharenko, E.S. Ilina, A.A. Malakhova, S.P. Medvedev, J. Reynisson, K.P. Volcho, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Monoterpenoids for Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibition
    Biomolecules, 2021, 11(7), 973 doi:10.3390/biom11070973, IF=4.81
  435. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
  436. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
  437. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
  438. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
  439. И.В. Егорова, В.В. Жидков, И.П. Гринишак, Н.А. Родионова, И.Ю. Багрянская, Н.В. Первухина
    Синтез и строение комплексных соединений сурьмы [(4-N,N-ME2C6H4)3MESB]I И [(4-N,N-ME2C6H4)3MESB]2[HG2I6]·2DMSO
    Журнал общей химии. 2021. Т. 91. № 7. С. 1100-1107. doi 10.31857/S0044460X2107009X (Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148), IF=0.868
  440. И.В. Егорова, В.В. Жидков, И.П. Гринишак, Н.А. Родионова, И.Ю. Багрянская, Н.В. Первухина
    Синтез и строение комплексных соединений сурьмы [(4-N,N-ME2C6H4)3MESB]I И [(4-N,N-ME2C6H4)3MESB]2[HG2I6]·2DMSO
    Журнал общей химии. 2021. Т. 91. № 7. С. 1100-1107. doi 10.31857/S0044460X2107009X (Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148), IF=0.868
  441. И.В. Егорова, В.В. Жидков, И.П. Гринишак, Н.А. Родионова, И.Ю. Багрянская, Н.В. Первухина
    Синтез и строение комплексных соединений сурьмы [(4-N,N-ME2C6H4)3MESB]I И [(4-N,N-ME2C6H4)3MESB]2[HG2I6]·2DMSO
    Журнал общей химии. 2021. Т. 91. № 7. С. 1100-1107. doi 10.31857/S0044460X2107009X (Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148), IF=0.868
  442. И.В. Егорова, В.В. Жидков, И.П. Гринишак, Н.А. Родионова, И.Ю. Багрянская, Н.В. Первухина
    Синтез и строение комплексных соединений сурьмы [(4-N,N-ME2C6H4)3MESB]I И [(4-N,N-ME2C6H4)3MESB]2[HG2I6]·2DMSO
    Журнал общей химии. 2021. Т. 91. № 7. С. 1100-1107. doi 10.31857/S0044460X2107009X (Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148), IF=0.868
  443. И.В. Егорова, В.В. Жидков, И.П. Гринишак, Н.А. Родионова, И.Ю. Багрянская, Н.В. Первухина
    Синтез и строение комплексных соединений сурьмы [(4-N,N-ME2C6H4)3MESB]I И [(4-N,N-ME2C6H4)3MESB]2[HG2I6]·2DMSO
    Журнал общей химии. 2021. Т. 91. № 7. С. 1100-1107. doi 10.31857/S0044460X2107009X (Synthesis and Structure of Antimony Complex Compounds [(4-N,N-Me2C6H4)3MeSb]I and [(4-N,N-Me2C6H4)3MeSb]2[Hg2I6]·2DMSO/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, N. А. Rodionova, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of General Chemistry, 2021, V. 91, N.7, Pp 1361-1367 doi:10.1134/S1070363221070148), IF=0.868
  444. S.M. Adekenov, A.S. Kishkentayeva, A.B. Khasenova, E.E. Shul'ts, Yu.V. Gatilov, I.Yu. Bagryanskaya
    New Arylhalo-Derivatives of Grosshe
    Chemistry of Natural Compounds, 2021, V. 57, N 7, Pp 685-690 doi:10.1007/s10600-021-03450-7, IF=0.809
  445. S.M. Adekenov, A.S. Kishkentayeva, A.B. Khasenova, E.E. Shul'ts, Yu.V. Gatilov, I.Yu. Bagryanskaya
    New Arylhalo-Derivatives of Grosshe
    Chemistry of Natural Compounds, 2021, V. 57, N 7, Pp 685-690 doi:10.1007/s10600-021-03450-7, IF=0.809
  446. S.M. Adekenov, A.S. Kishkentayeva, A.B. Khasenova, E.E. Shul'ts, Yu.V. Gatilov, I.Yu. Bagryanskaya
    New Arylhalo-Derivatives of Grosshe
    Chemistry of Natural Compounds, 2021, V. 57, N 7, Pp 685-690 doi:10.1007/s10600-021-03450-7, IF=0.809
  447. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  448. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  449. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  450. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  451. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  452. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  453. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  454. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  455. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  456. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  457. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  458. D.S. Baranov, D.A. Nevostruev, M.S. Kazantsev, V.A. Zinoviev, E.A. Zelentsova, A. A. Dmitriev, N.P. Gritsan, Yu.P. Tsentalovich, M. Kotova, J. Dureth, A. Sperlich, V. Dyakonov, L.V. Kulik
    Synthesis, Characterization and Photovoltaic Properties of Electron-Accepting (11-Oxoanthra[2,1-b]thiophen-6-ylidene)dipropanedinitrile-Based Molecules
    ChemistrySelect, 2021, V. 6, N 24, Pp. 6043-6049 doi:10.1002/slct.202101491, IF=2.109
  459. D.A. Sokolov, S.V. Morozov, E.V. Abakumov, V.A. Androkhanov
    Polycyclic Aromatic Hydrocarbons in Soils of Anthracite Deposit Dumps in Siberia
    Eurasian Soil Science, 2021, V. 54, N 6, Pp 875-887 doi:10.1134/S1064229321060120, IF=1.369
  460. D.A. Sokolov, S.V. Morozov, E.V. Abakumov, V.A. Androkhanov
    Polycyclic Aromatic Hydrocarbons in Soils of Anthracite Deposit Dumps in Siberia
    Eurasian Soil Science, 2021, V. 54, N 6, Pp 875-887 doi:10.1134/S1064229321060120, IF=1.369
  461. D.A. Sokolov, S.V. Morozov, E.V. Abakumov, V.A. Androkhanov
    Polycyclic Aromatic Hydrocarbons in Soils of Anthracite Deposit Dumps in Siberia
    Eurasian Soil Science, 2021, V. 54, N 6, Pp 875-887 doi:10.1134/S1064229321060120, IF=1.369
  462. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  463. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  464. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  465. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  466. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  467. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  468. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  469. A. Lipovka, A. Kharchenko, A. Dubovoy, M. Filipenko, V. Stupak, A. Mayorov, V. Fomenko, P. Geydt, D. Parshin
    The Effect of Adding Modified Chitosan on the Strength Properties of Bacterial Cellulose for Clinical Applications
    Polymers 2021, 13(12), 1995 doi:10.3390/polym13121995, IF=4.329
  470. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  471. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  472. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  473. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  474. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  475. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  476. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  477. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
  478. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  479. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  480. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  481. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  482. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  483. N.V. Terletskaya, N.K. Korbozova, N.O. Kudrina, T.N. Kobylina, M.S. Kurmanbayeva, N.D. Meduntseva, T.G. Tolstikova
    The Influence of Abiotic Stress Factors on the Morphophysiological and Phytochemical Aspects of the Acclimation of the Plant Rhodiola semenowii Boriss
    Plants, 2021, 10(6), 1196 doi:10.3390/plants10061196, IF=3.935
  484. A. Tkachev, N. Nekratova, N. Belousova, M. Shurupova, W. Letchamo
    Comparative GC-MS study of Schizonepeta multifida essential oil from Khakassia Republic shows potentials for nutraceuticals, flavor, and conservation
    Ukrainian Journal of Ecology, 2021, V.11, N ‏ ‏ 2, Pp 300-305 doi:10.15421/2021_114
  485. A. Tkachev, N. Nekratova, N. Belousova, M. Shurupova, W. Letchamo
    Comparative GC-MS study of Schizonepeta multifida essential oil from Khakassia Republic shows potentials for nutraceuticals, flavor, and conservation
    Ukrainian Journal of Ecology, 2021, V.11, N ‏ ‏ 2, Pp 300-305 doi:10.15421/2021_114
  486. A. Tkachev, N. Nekratova, N. Belousova, M. Shurupova, W. Letchamo
    Comparative GC-MS study of Schizonepeta multifida essential oil from Khakassia Republic shows potentials for nutraceuticals, flavor, and conservation
    Ukrainian Journal of Ecology, 2021, V.11, N ‏ ‏ 2, Pp 300-305 doi:10.15421/2021_114
  487. A. Tkachev, N. Nekratova, N. Belousova, M. Shurupova, W. Letchamo
    Comparative GC-MS study of Schizonepeta multifida essential oil from Khakassia Republic shows potentials for nutraceuticals, flavor, and conservation
    Ukrainian Journal of Ecology, 2021, V.11, N ‏ ‏ 2, Pp 300-305 doi:10.15421/2021_114
  488. Д.А. Соколов, С.В. Морозов, Е.В. Абакумов, В.А. Андроханов
    Полициклические ароматические углеводороды в почвах отвалов антрацитовых месторождений Сибири
    Почвоведение. 2021. № 6. С. 701-714. doi:10.31857/S0032180X21060125 (Polycyclic aromatic hydrocarbons in soils of anthracite deposit dumps in Siberia/ D.A. Sokolov , V.A. Androkhanov , S.V. Morozov , E.V.Abakumov// Eurasian Soil Science. 2021. Т. 54. № 6. С. 875-887. doi:10.1134/S1064229321060120), IF=1.369
  489. Д.А. Соколов, С.В. Морозов, Е.В. Абакумов, В.А. Андроханов
    Полициклические ароматические углеводороды в почвах отвалов антрацитовых месторождений Сибири
    Почвоведение. 2021. № 6. С. 701-714. doi:10.31857/S0032180X21060125 (Polycyclic aromatic hydrocarbons in soils of anthracite deposit dumps in Siberia/ D.A. Sokolov , V.A. Androkhanov , S.V. Morozov , E.V.Abakumov// Eurasian Soil Science. 2021. Т. 54. № 6. С. 875-887. doi:10.1134/S1064229321060120), IF=1.369
  490. Д.А. Соколов, С.В. Морозов, Е.В. Абакумов, В.А. Андроханов
    Полициклические ароматические углеводороды в почвах отвалов антрацитовых месторождений Сибири
    Почвоведение. 2021. № 6. С. 701-714. doi:10.31857/S0032180X21060125 (Polycyclic aromatic hydrocarbons in soils of anthracite deposit dumps in Siberia/ D.A. Sokolov , V.A. Androkhanov , S.V. Morozov , E.V.Abakumov// Eurasian Soil Science. 2021. Т. 54. № 6. С. 875-887. doi:10.1134/S1064229321060120), IF=1.369
  491. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  492. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  493. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  494. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  495. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  496. A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
    (+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
    ArchPharm, 2021, V.354, N 6, Art. Num. 2100038 doi:10.1002/ardp.202100038, IF=3.751
  497. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry. 2021. V.32. N3. P.1261-1267 doi:10.1007/s11224-021-01732-y, IF=1.887
  498. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry. 2021. V.32. N3. P.1261-1267 doi:10.1007/s11224-021-01732-y, IF=1.887
  499. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry. 2021. V.32. N3. P.1261-1267 doi:10.1007/s11224-021-01732-y, IF=1.887
  500. N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
    The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
    Structural Chemistry. 2021. V.32. N3. P.1261-1267 doi:10.1007/s11224-021-01732-y, IF=1.887
  501. И.Д. Иванов, К.И. Мосалев, А.В. Липеева, Э.Э. Шульц, В.А. Вавилин
    Исследование механизмов противовоспалительной и иммуномодулирующей активности соединений бетулиновой кислоты с фурокумаринами
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 6. С. 28-34. doi:10.30906/0869-2092-2021-84-6-28-34
  502. И.Д. Иванов, К.И. Мосалев, А.В. Липеева, Э.Э. Шульц, В.А. Вавилин
    Исследование механизмов противовоспалительной и иммуномодулирующей активности соединений бетулиновой кислоты с фурокумаринами
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 6. С. 28-34. doi:10.30906/0869-2092-2021-84-6-28-34
  503. И.Д. Иванов, К.И. Мосалев, А.В. Липеева, Э.Э. Шульц, В.А. Вавилин
    Исследование механизмов противовоспалительной и иммуномодулирующей активности соединений бетулиновой кислоты с фурокумаринами
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 6. С. 28-34. doi:10.30906/0869-2092-2021-84-6-28-34
  504. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  505. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  506. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  507. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  508. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  509. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  510. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  511. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  512. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
  513. И.В. Нечепуренко, И.Я. Майнагашев, А.А. Барабанов, С.А. Сергеев, Г.Д. Букатов, В.А. Захаров, М.А. Мацько, К.П. Волчо, Н.Ф. Салахутдинов
    Новый подход к синтезу диэтил-2,3-диизобутилсукцината - компонента титан-магниевых катализаторов полимеризации пропилена
    Журнал прикладной химии. 2021. Т. 94. № 6. С. 699-710. (DOI: 10.31857/S0044461821060037 ) (A New Approach to the Synthesis of Diethyl 2,3-Diisobutylsuccinate, a Component of Titanium–Magnesium Catalysts for Propylene Polymerization/ I.V. Nechepurenko, I.Ya. Mainagashev, A.A. Barabanov, S.A. Sergeev, G.D. Bukatov, V.A. Zakharov, M.A. Mats'ko, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Applied Chemistry, 2021, V. 94, N 6, Pp 715-725 doi:10.1134/S1070427221060033), IF=0.85
  514. И.В. Нечепуренко, И.Я. Майнагашев, А.А. Барабанов, С.А. Сергеев, Г.Д. Букатов, В.А. Захаров, М.А. Мацько, К.П. Волчо, Н.Ф. Салахутдинов
    Новый подход к синтезу диэтил-2,3-диизобутилсукцината - компонента титан-магниевых катализаторов полимеризации пропилена
    Журнал прикладной химии. 2021. Т. 94. № 6. С. 699-710. (DOI: 10.31857/S0044461821060037 ) (A New Approach to the Synthesis of Diethyl 2,3-Diisobutylsuccinate, a Component of Titanium–Magnesium Catalysts for Propylene Polymerization/ I.V. Nechepurenko, I.Ya. Mainagashev, A.A. Barabanov, S.A. Sergeev, G.D. Bukatov, V.A. Zakharov, M.A. Mats'ko, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Applied Chemistry, 2021, V. 94, N 6, Pp 715-725 doi:10.1134/S1070427221060033), IF=0.85
  515. И.В. Нечепуренко, И.Я. Майнагашев, А.А. Барабанов, С.А. Сергеев, Г.Д. Букатов, В.А. Захаров, М.А. Мацько, К.П. Волчо, Н.Ф. Салахутдинов
    Новый подход к синтезу диэтил-2,3-диизобутилсукцината - компонента титан-магниевых катализаторов полимеризации пропилена
    Журнал прикладной химии. 2021. Т. 94. № 6. С. 699-710. (DOI: 10.31857/S0044461821060037 ) (A New Approach to the Synthesis of Diethyl 2,3-Diisobutylsuccinate, a Component of Titanium–Magnesium Catalysts for Propylene Polymerization/ I.V. Nechepurenko, I.Ya. Mainagashev, A.A. Barabanov, S.A. Sergeev, G.D. Bukatov, V.A. Zakharov, M.A. Mats'ko, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Applied Chemistry, 2021, V. 94, N 6, Pp 715-725 doi:10.1134/S1070427221060033), IF=0.85
  516. И.В. Нечепуренко, И.Я. Майнагашев, А.А. Барабанов, С.А. Сергеев, Г.Д. Букатов, В.А. Захаров, М.А. Мацько, К.П. Волчо, Н.Ф. Салахутдинов
    Новый подход к синтезу диэтил-2,3-диизобутилсукцината - компонента титан-магниевых катализаторов полимеризации пропилена
    Журнал прикладной химии. 2021. Т. 94. № 6. С. 699-710. (DOI: 10.31857/S0044461821060037 ) (A New Approach to the Synthesis of Diethyl 2,3-Diisobutylsuccinate, a Component of Titanium–Magnesium Catalysts for Propylene Polymerization/ I.V. Nechepurenko, I.Ya. Mainagashev, A.A. Barabanov, S.A. Sergeev, G.D. Bukatov, V.A. Zakharov, M.A. Mats'ko, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Applied Chemistry, 2021, V. 94, N 6, Pp 715-725 doi:10.1134/S1070427221060033), IF=0.85
  517. И.В. Нечепуренко, И.Я. Майнагашев, А.А. Барабанов, С.А. Сергеев, Г.Д. Букатов, В.А. Захаров, М.А. Мацько, К.П. Волчо, Н.Ф. Салахутдинов
    Новый подход к синтезу диэтил-2,3-диизобутилсукцината - компонента титан-магниевых катализаторов полимеризации пропилена
    Журнал прикладной химии. 2021. Т. 94. № 6. С. 699-710. (DOI: 10.31857/S0044461821060037 ) (A New Approach to the Synthesis of Diethyl 2,3-Diisobutylsuccinate, a Component of Titanium–Magnesium Catalysts for Propylene Polymerization/ I.V. Nechepurenko, I.Ya. Mainagashev, A.A. Barabanov, S.A. Sergeev, G.D. Bukatov, V.A. Zakharov, M.A. Mats'ko, K.P. Volcho, N.F. Salakhutdinov// Russian Journal of Applied Chemistry, 2021, V. 94, N 6, Pp 715-725 doi:10.1134/S1070427221060033), IF=0.85
  518. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
    Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
    Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
  519. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
    Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
    Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
  520. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
    Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
    Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
  521. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
    Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
    Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
  522. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
    Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
    Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
  523. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
    Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
    Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
  524. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
    Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
    Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
  525. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
    Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
    Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
  526. A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
    Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
    Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.935
  527. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
  528. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
  529. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
  530. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
  531. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
    Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.706
  532. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  533. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  534. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  535. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  536. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  537. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  538. A. A. Munkuev,E. S. Mozhaitsev,A. A. Chepanova,E. V. Suslov,D. V. Korchagina,O. D. Zakharova,E. S. Ilina,N. S. Dyrkheeva,A. L. Zakharenko,J. Reynisson,K. P. Volcho,N. F. Salakhutdinov ,O. I. Lavrik
    Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments
    Molecules 2021, 26(11), 3128; doi:10.3390/molecules26113128, IF=4.411
  539. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  540. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  541. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  542. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  543. M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
    Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
    Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=3.125
  544. L. N. Grigor’eva,A. Ya. Tikhonov,K. A. Lomanovich,D. G. Mazhukin
    Stable Bicyclic Functionalized Nitroxides: The Synthesis of Derivatives of Aza-nortropinone–5-Methyl-3-oxo-6,8-diazabicyclo[3.2.1]-6-octene 8-oxyls
    Molecules 2021, 26(10), 3050 doi:10.3390/molecules26103050, IF=4.411
  545. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  546. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  547. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  548. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  549. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  550. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  551. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  552. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  553. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  554. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  555. O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
    Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.823
  556. A.G. Matveeva, V.N. Syryamina, V.M. Nekrasov, M.K. Bowman
    Non-uniform sampling in pulse dipolar spectroscopy by EPR: the redistribution of noise and the optimization of data acquisition
    Physical Chemistry Chemical Physics, 2021, V.,23, N 17, Pp 10335-10346 doi:10.1039/d1cp00705j, IF=3.676
  557. A.G. Matveeva, V.N. Syryamina, V.M. Nekrasov, M.K. Bowman
    Non-uniform sampling in pulse dipolar spectroscopy by EPR: the redistribution of noise and the optimization of data acquisition
    Physical Chemistry Chemical Physics, 2021, V.,23, N 17, Pp 10335-10346 doi:10.1039/d1cp00705j, IF=3.676
  558. A.G. Matveeva, V.N. Syryamina, V.M. Nekrasov, M.K. Bowman
    Non-uniform sampling in pulse dipolar spectroscopy by EPR: the redistribution of noise and the optimization of data acquisition
    Physical Chemistry Chemical Physics, 2021, V.,23, N 17, Pp 10335-10346 doi:10.1039/d1cp00705j, IF=3.676
  559. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  560. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  561. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  562. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  563. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  564. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  565. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  566. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021
  567. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  568. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  569. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  570. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  571. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  572. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  573. E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
    2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
    European Journal of Organic Chemistry,2021, V. 2021, N 17, Pp 2355-2361 doi:10.1002/ejoc.202100138, IF=3.021
  574. Е.В. Третьяков, А.М. Максимов, П.В. Никульшин, Т.В. Меженкова
    Эффективный подход к синтезу 2,3,4,5-тетрафторфенола
    Известия Академии наук. Серия химическая. 2021, Т. 70, N 5, С. 995-998 (An efficient approach to the synthesis of 2,3,4,5-tetrafluorophenol/ E.V. Tretyakov, A.M. Maksimov, P.V. Nikul’shin, T.V. Mezhenkova// Russian Chemical Bulletin, 2021, V, 70, N 5, Pp 995-998 doi:10.1007/s11172-021-3178-3), IF=1.222
  575. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  576. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  577. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  578. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  579. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  580. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  581. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  582. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  583. Кручинина М.В. , Светлова И.О. , Азгалдян А.В. , Осипенко М.Ф. , Валуйских Е.Ю. , Шашков М.В. , Соколова А.С. , Кручинин В.Н. , Яковина И.Н. , Осипенко И.В.
    Профиль жирных кислот мембран эритроцитов и сыворотки крови у пациентов с воспалительными заболеваниями кишечника в зависимости от стадии заболевания
    Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2021. № 5. С. 161-184.
  584. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  585. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  586. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  587. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  588. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  589. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  590. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  591. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  592. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  593. K. Kovaleva, O. Yarovaya, K. Ponomarev, S. Cheresiz, A. Azimirad, I. Chernyshova, A. Zakharenko, V. Konev, T. Khlebnikova, E. Mozhaytsev, E. Suslov, D. Nilov, V. Svedas, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Design, Synthesis, and Molecular Docking Study of New Tyrosyl-DNA Phosphodiesterase 1 (TDP1) Inhibitors Combining Resin Acids and Adamantane Moieties
    Pharmaceuticals 2021, 14(5), 422 doi:10.3390/ph14050422, IF=5.863
  594. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  595. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  596. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  597. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  598. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  599. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  600. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  601. А.С. Бобикова, В.С. Черепушкина, Т.Е. Миронова, В.Н. Афонюшкин, Н.А. Донченко, Е.В. Нефедова, Ян. Фуди, В.Ю. Коптев, В.В. Фоменко
    Изучение экспрессии функционально-значимых генов при терапии коронавирусной инфекции у цыплят
    Сибирский вестник сельскохозяйственной науки. 2021. Т. 51. № 5. С. 68-76 doi:10.26898/0370-8799-2021-5-8
  602. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  603. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  604. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  605. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  606. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  607. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  608. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  609. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, М.А. Скарнович, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Фармакокинетические показатели субстанци НИОХ-14 - нового противооспенного фармакологического вещества
    Экспериментальная и клиническая фармакология. 2021. Т. 84. № 5. С. 22-26. (Pharmacokinetic indicators of nioch-14 compound-new anti-smallpox substance/ O.Yu. Mazurkov, L.N. Shishkina, N.I. Bormotov, M.O. Skarnovich, O.A. Serova, N.A. Mazurkova, M.A. Skarnovich, A.A. Chernonosov, A.Ya.Tikhonov, B.A Selivanov.// Eksperimental'naya i Klinicheskaya Farmakologiya, 2021. V. 84. № 5. Pp. 22-26. doi:10.30906/0869-2092-2021-84-5-22-26)
  610. Потапов А. Г., Шундрина И. К.
    Влияние сомономеров на свойства сополиэфиров бутиленсукцината
    Высокомолекулярные соединения. Серия А. 2021. Т. 63. № 5. С. 301-306. (Influence of Comonomers on the Properties of Butylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2021, V. 63, N 5, Pp 465-470 doi:10.1134/S0965545X21050114), IF=1.206
  611. T. P. Kukina, D. N. Shcherbakov, V. O. Korsakov, I. A. Elshin, Ts. Sandag
    GC-MS analysis of lipophilic components of rhizomes of plant Rhodiola rosea L.
    AIP Conference Proceedings 2419, 020011 (2021).(INTERNATIONAL CONFERENCE ON FOOD SCIENCE AND BIOTECHNOLOGY (FSAB 2021), 20-20 April 2021, Ekaterinburg, Russia) doi:10.1063/5.0069867
  612. T. P. Kukina, D. N. Shcherbakov, V. O. Korsakov, I. A. Elshin, Ts. Sandag
    GC-MS analysis of lipophilic components of rhizomes of plant Rhodiola rosea L.
    AIP Conference Proceedings 2419, 020011 (2021).(INTERNATIONAL CONFERENCE ON FOOD SCIENCE AND BIOTECHNOLOGY (FSAB 2021), 20-20 April 2021, Ekaterinburg, Russia) doi:10.1063/5.0069867
  613. T. P. Kukina, D. N. Shcherbakov, V. O. Korsakov, I. A. Elshin, Ts. Sandag
    GC-MS analysis of lipophilic components of rhizomes of plant Rhodiola rosea L.
    AIP Conference Proceedings 2419, 020011 (2021).(INTERNATIONAL CONFERENCE ON FOOD SCIENCE AND BIOTECHNOLOGY (FSAB 2021), 20-20 April 2021, Ekaterinburg, Russia) doi:10.1063/5.0069867
  614. A.A. Sonina,Ch. S. Becker, A. D. Kuimov,I. K. Shundrina,V. Yu. Komarov,M.S. Kazantsev
    Alkyl-substituted bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophenes: weakening of intermolecular interactions and additive-assisted crystallization†
    CrystEngComm, 2021,V. 23, N 14, Pp 2654-2664 doi:10.1039/D0CE01794A, IF=3.545
  615. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  616. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  617. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  618. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  619. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  620. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  621. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  622. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  623. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  624. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  625. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  626. A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
    Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=4.411
  627. M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
    The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
    Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=4.527
  628. M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
    The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
    Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=4.527
  629. M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
    The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
    Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=4.527
  630. M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
    The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
    Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=4.527
  631. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  632. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  633. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  634. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  635. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  636. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  637. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  638. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  639. N.O. Vorozhtsov, O.I. Yarovaya, V.A. Roznyatovskii, B.N. Tarasevich, Yu.A. Kozlovskaya, A.I. Petkova, A.V. Slita, E.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov, E.K. Beloglazkina
    Synthesis and antiviral activity of novel 3-substituted pyrazolinium salts
    Chemistry of Heterocyclic Compounds, 2021, V. 57, N 4, Pp 432-441 doi:10.1007/s10593-021-02921-7, IF=1.277
  640. А.А. Коновалов, Е.В. Карпова, И.К. Шундрина, Е.П. Размахнин, И.В. Ельцов, Н.П. Гончаров
    Влияние аллельных вариантов ароматической алкогольдегидрогеназы CADIM на микроморфологические и химические показатели тканей у яровой мягкой пшеницы TRITICUM AESTIVUM L
    Прикладная биохимия и микробиология. 2021. Т. 57. № 4. С. 402-414. doi:10.31857/S0555109921040085 (Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086), IF=0.886
  641. А.А. Коновалов, Е.В. Карпова, И.К. Шундрина, Е.П. Размахнин, И.В. Ельцов, Н.П. Гончаров
    Влияние аллельных вариантов ароматической алкогольдегидрогеназы CADIM на микроморфологические и химические показатели тканей у яровой мягкой пшеницы TRITICUM AESTIVUM L
    Прикладная биохимия и микробиология. 2021. Т. 57. № 4. С. 402-414. doi:10.31857/S0555109921040085 (Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086), IF=0.886
  642. А.А. Коновалов, Е.В. Карпова, И.К. Шундрина, Е.П. Размахнин, И.В. Ельцов, Н.П. Гончаров
    Влияние аллельных вариантов ароматической алкогольдегидрогеназы CADIM на микроморфологические и химические показатели тканей у яровой мягкой пшеницы TRITICUM AESTIVUM L
    Прикладная биохимия и микробиология. 2021. Т. 57. № 4. С. 402-414. doi:10.31857/S0555109921040085 (Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086), IF=0.886
  643. А.А. Коновалов, Е.В. Карпова, И.К. Шундрина, Е.П. Размахнин, И.В. Ельцов, Н.П. Гончаров
    Влияние аллельных вариантов ароматической алкогольдегидрогеназы CADIM на микроморфологические и химические показатели тканей у яровой мягкой пшеницы TRITICUM AESTIVUM L
    Прикладная биохимия и микробиология. 2021. Т. 57. № 4. С. 402-414. doi:10.31857/S0555109921040085 (Effect of Allelic Variants of Aromatic Alcohol Dehydrogenase CADim on Micromorphological and Chemical Tissue Indices in the Spring Bread Wheat Triticum aestivum L./ A. A. Konovalov, E. V. Karpova, I. K. Shundrina, E. P. Razmakhnin, I. V. Eltsov, N. P. Goncharov// Applied Biochemistry and Microbiology, 2021, V. 57, N 4, Pp. 521-532 doi:10.1134/S0003683821040086), IF=0.886
  644. И.Е. Смирнова, Ю.В. Гатилов, И.Ю. Багрянская
    Синтез и молекулярная структура гидрокси- и оксимино-производных холлонгдиона
    Журнал органической химии. 2021. Т. 57. № 4. С. 592-596. DOI: 10.31857/S0514749221040169 (Synthesis and Molecular Structure of Hydroxy and Hydroxyimino Derivatives of Hollongdione/ I. E. Smirnova, Yu. V. Gatilov & I. Yu. Bagryanskaya// Russian Journal of Organic Chemistry, 2021, V. 57,N 4, Pp 671-674 doi:10.1134/S1070428021040266), IF=0.723
  645. С.В. Аньков, Т.Г. Толстикова, С.В. Валиулин, А.А. Онищук, М.С. Борисова, С.Н. Дубцов
    Сравнительная фармакокинетика аэрозольной и пероральной форм пиразинамида
    Химия в интересах устойчивого развития. 2021. Т. 29. № 2. С. 229-232. doi:10.15372/KhUR2021300 (COMPARATIVE PHARMACOKINETICS OF THE AEROSOL AND ORAL FORMS OF PYRAZINAMIDE/ An'kov S.V., Tolstikova T.G., Valiulin S.V., Onischuk A.A., Borisova M.S., Dubtsov S.N.// Chemistry for Sustainable Development. 2021. Т. 29. № 2. С. 224-228. doi:10.15372/CSD2021300)
  646. С.В. Аньков, Т.Г. Толстикова, С.В. Валиулин, А.А. Онищук, М.С. Борисова, С.Н. Дубцов
    Сравнительная фармакокинетика аэрозольной и пероральной форм пиразинамида
    Химия в интересах устойчивого развития. 2021. Т. 29. № 2. С. 229-232. doi:10.15372/KhUR2021300 (COMPARATIVE PHARMACOKINETICS OF THE AEROSOL AND ORAL FORMS OF PYRAZINAMIDE/ An'kov S.V., Tolstikova T.G., Valiulin S.V., Onischuk A.A., Borisova M.S., Dubtsov S.N.// Chemistry for Sustainable Development. 2021. Т. 29. № 2. С. 224-228. doi:10.15372/CSD2021300)
  647. С.В. Аньков, Т.Г. Толстикова, С.В. Валиулин, А.А. Онищук, М.С. Борисова, С.Н. Дубцов
    Сравнительная фармакокинетика аэрозольной и пероральной форм пиразинамида
    Химия в интересах устойчивого развития. 2021. Т. 29. № 2. С. 229-232. doi:10.15372/KhUR2021300 (COMPARATIVE PHARMACOKINETICS OF THE AEROSOL AND ORAL FORMS OF PYRAZINAMIDE/ An'kov S.V., Tolstikova T.G., Valiulin S.V., Onischuk A.A., Borisova M.S., Dubtsov S.N.// Chemistry for Sustainable Development. 2021. Т. 29. № 2. С. 224-228. doi:10.15372/CSD2021300)
  648. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  649. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  650. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  651. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  652. E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
    Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
    Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=4.411
  653. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  654. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  655. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  656. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  657. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  658. V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
    New Reaction Products of Acetylacetone with Semicarbazide Derivatives
    ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=3.512
  659. E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
    Bistricyclic aromatic enes annelated with nopinane fragment
    Tetrahedron, V.83, 12 March 2021, 131979 doi:10.1016/j.tet.2021.131979, IF=2.457
  660. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  661. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  662. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  663. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  664. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  665. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  666. Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
    Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
    Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=4.411
  667. E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
    First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
    Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=2.859
  668. E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
    First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
    Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=2.859
  669. E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
    First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
    Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=2.859
  670. M.A. Gromova, Yu.V. Kharitonov, T.C. Golubeva, E.E. Shults
    Macrocyclic peptide-diterpenoid conjugates by a sequential arylation/peptidecoupling/clickmacrocyclization procedure.
    Макрогетероциклы / Macroheterocycles 2021 14(3) 231-239. doi:10.6060/mhc210945s, IF=1.2
  671. A. Komarovskikh, A. Danilenko, A. Sukhikh, M. Syrokvashin, B. Selivanov
    Structure and EPR investigation of Cu(II) bifluoride complexes with zwitterionic N-hydroxyimidazole ligands
    Inorganica Chimica Acta, 2021, V. 517, 120187 doi:10.1016/j.ica.2020.120187, IF=2.545
  672. A. Komarovskikh, A. Danilenko, A. Sukhikh, M. Syrokvashin, B. Selivanov
    Structure and EPR investigation of Cu(II) bifluoride complexes with zwitterionic N-hydroxyimidazole ligands
    Inorganica Chimica Acta, 2021, V. 517, 120187 doi:10.1016/j.ica.2020.120187, IF=2.545
  673. A. Komarovskikh, A. Danilenko, A. Sukhikh, M. Syrokvashin, B. Selivanov
    Structure and EPR investigation of Cu(II) bifluoride complexes with zwitterionic N-hydroxyimidazole ligands
    Inorganica Chimica Acta, 2021, V. 517, 120187 doi:10.1016/j.ica.2020.120187, IF=2.545
  674. A. Komarovskikh, A. Danilenko, A. Sukhikh, M. Syrokvashin, B. Selivanov
    Structure and EPR investigation of Cu(II) bifluoride complexes with zwitterionic N-hydroxyimidazole ligands
    Inorganica Chimica Acta, 2021, V. 517, 120187 doi:10.1016/j.ica.2020.120187, IF=2.545
  675. А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
    Строение и стереохимия гидразонпроизводного гармина
    Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 (STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE/ A. Amanzhan, P. Zh. Zhanymkhanova, I. Yu. Bagryanskaya, E. E. Shults, A. Zh. Turmukhambetov, S. M. Adekenov// Journal of Structural Chemistry, V. 62, PP 491-495 doi:10.1134/S0022476621030161), IF=1.071
  676. А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
    Строение и стереохимия гидразонпроизводного гармина
    Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 (STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE/ A. Amanzhan, P. Zh. Zhanymkhanova, I. Yu. Bagryanskaya, E. E. Shults, A. Zh. Turmukhambetov, S. M. Adekenov// Journal of Structural Chemistry, V. 62, PP 491-495 doi:10.1134/S0022476621030161), IF=1.071
  677. А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
    Строение и стереохимия гидразонпроизводного гармина
    Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 (STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE/ A. Amanzhan, P. Zh. Zhanymkhanova, I. Yu. Bagryanskaya, E. E. Shults, A. Zh. Turmukhambetov, S. M. Adekenov// Journal of Structural Chemistry, V. 62, PP 491-495 doi:10.1134/S0022476621030161), IF=1.071
  678. А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
    Строение и стереохимия гидразонпроизводного гармина
    Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 (STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE/ A. Amanzhan, P. Zh. Zhanymkhanova, I. Yu. Bagryanskaya, E. E. Shults, A. Zh. Turmukhambetov, S. M. Adekenov// Journal of Structural Chemistry, V. 62, PP 491-495 doi:10.1134/S0022476621030161), IF=1.071
  679. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  680. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  681. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  682. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  683. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  684. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  685. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  686. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  687. A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
    Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
    Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.932
  688. I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
    Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
    New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.591
  689. I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
    Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
    New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.591
  690. I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
    Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
    New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.591
  691. A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
    Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
    Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=4.411
  692. A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
    Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
    Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=4.411
  693. A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
    Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
    Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=4.411
  694. M.V. Khvostov, A.A. Chernonosov, S.A. Borisov, M.S. Borisova, E.S. Meteleva, V.I. Evseenko, N.E. Polyakov, A.V. Dushkin, T.G. Tolstikova
    Study of supramolecular complex of nifedipine with arabinogalactan on Wistar and ISIAH rats
    Therapeutic Delivery. 2021. V.12. N2. P.119-131 doi:10.4155/tde-2020-0115
  695. M.V. Khvostov, A.A. Chernonosov, S.A. Borisov, M.S. Borisova, E.S. Meteleva, V.I. Evseenko, N.E. Polyakov, A.V. Dushkin, T.G. Tolstikova
    Study of supramolecular complex of nifedipine with arabinogalactan on Wistar and ISIAH rats
    Therapeutic Delivery. 2021. V.12. N2. P.119-131 doi:10.4155/tde-2020-0115
  696. M.V. Khvostov, A.A. Chernonosov, S.A. Borisov, M.S. Borisova, E.S. Meteleva, V.I. Evseenko, N.E. Polyakov, A.V. Dushkin, T.G. Tolstikova
    Study of supramolecular complex of nifedipine with arabinogalactan on Wistar and ISIAH rats
    Therapeutic Delivery. 2021. V.12. N2. P.119-131 doi:10.4155/tde-2020-0115
  697. M.V. Khvostov, A.A. Chernonosov, S.A. Borisov, M.S. Borisova, E.S. Meteleva, V.I. Evseenko, N.E. Polyakov, A.V. Dushkin, T.G. Tolstikova
    Study of supramolecular complex of nifedipine with arabinogalactan on Wistar and ISIAH rats
    Therapeutic Delivery. 2021. V.12. N2. P.119-131 doi:10.4155/tde-2020-0115
  698. M.V. Khvostov, A.A. Chernonosov, S.A. Borisov, M.S. Borisova, E.S. Meteleva, V.I. Evseenko, N.E. Polyakov, A.V. Dushkin, T.G. Tolstikova
    Study of supramolecular complex of nifedipine with arabinogalactan on Wistar and ISIAH rats
    Therapeutic Delivery. 2021. V.12. N2. P.119-131 doi:10.4155/tde-2020-0115
  699. О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
    Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
    Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// )
  700. О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
    Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
    Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// )
  701. О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
    Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
    Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// )
  702. О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
    Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
    Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// )
  703. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  704. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  705. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  706. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  707. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  708. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  709. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  710. Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
    Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
    Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi: 10.31857/S0026898421020051 (Antitumor Activity of the Combination of Topotecan and Tyrosyl-DNA-Phosphodiesterase 1 Inhibitor on Model Krebs-2 Mouse Ascite Carcinoma/ N. S. Dyrkheeva, A. L. Zakharenko, E. S. Novoselova, A. A. Chepanova, N. A. Popova, V. P. Nikolin, O. A. Luzina, N. F. Salakhutdinov, E. I. Ryabchikova, O. I. Lavrik// Molecular Biology, 2021, V 55, N 2, Pp 273-277 doi:10.1134/S0026893321020060), IF=1.374
  711. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, N.A. Orlova, I.A. Malakhov, V.N. Berezhnaya, E.D. Savina, Y.P. Tsentalovich
    Phototransformations of acrylamide derivatives of piperazine-substituted polyfluorinated chalcones
    Journal of Photochemistry and Photobiology A: Chemistry, 2021, V. 406, Art. Num. 112973 doi:10.1016/j.jphotochem.2020.112973, IF=2.668
  712. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, N.A. Orlova, I.A. Malakhov, V.N. Berezhnaya, E.D. Savina, Y.P. Tsentalovich
    Phototransformations of acrylamide derivatives of piperazine-substituted polyfluorinated chalcones
    Journal of Photochemistry and Photobiology A: Chemistry, 2021, V. 406, Art. Num. 112973 doi:10.1016/j.jphotochem.2020.112973, IF=2.668
  713. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  714. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  715. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  716. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  717. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  718. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  719. V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
    Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
    Chemistry of Heterocyclic Compoundsб 2021, V. 57, N. 2, Pp 187-198 doi:10.1007/s10593-021-02892-9, IF=1.277
  720. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
    Synthesis of pyrrole-ferrocene ensembles and their rearrangement into 2-(ferrocenylmethyl)-1,2-dihydro-3H-pyrrol-3-ones
    Journal of Organometallic Chemistry, 2021, V. 933, 121651 doi:10.1016/j.jorganchem.2020.121651, IF=2.369
  721. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
    Synthesis of pyrrole-ferrocene ensembles and their rearrangement into 2-(ferrocenylmethyl)-1,2-dihydro-3H-pyrrol-3-ones
    Journal of Organometallic Chemistry, 2021, V. 933, 121651 doi:10.1016/j.jorganchem.2020.121651, IF=2.369
  722. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
    Synthesis of pyrrole-ferrocene ensembles and their rearrangement into 2-(ferrocenylmethyl)-1,2-dihydro-3H-pyrrol-3-ones
    Journal of Organometallic Chemistry, 2021, V. 933, 121651 doi:10.1016/j.jorganchem.2020.121651, IF=2.369
  723. O.A. Tarasova, N.A. Nedolya, A.I. Albanov, I.Yu. Bagryanskaya, B.A. Trofimov
    Synthesis of pyrrole-ferrocene ensembles and their rearrangement into 2-(ferrocenylmethyl)-1,2-dihydro-3H-pyrrol-3-ones
    Journal of Organometallic Chemistry, 2021, V. 933, 121651 doi:10.1016/j.jorganchem.2020.121651, IF=2.369
  724. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  725. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  726. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  727. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  728. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  729. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  730. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  731. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  732. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.889
  733. B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
  734. B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
  735. B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
  736. Д.О. Васильева, С.С. Патрушев, Э.Э. Шульц, А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева
    Изучение антибактериальной активности бис-(11,13-дигидро-изоалантолактонов) с азотсодержащими линкерами in vitro
    Проблемы медицинской микологии. 2021. Т. 23. № 2. С. 77.
  737. Д.О. Васильева, С.С. Патрушев, Э.Э. Шульц, А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева
    Изучение антибактериальной активности бис-(11,13-дигидро-изоалантолактонов) с азотсодержащими линкерами in vitro
    Проблемы медицинской микологии. 2021. Т. 23. № 2. С. 77.
  738. Д.О. Васильева, С.С. Патрушев, Э.Э. Шульц, А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева
    Изучение антибактериальной активности бис-(11,13-дигидро-изоалантолактонов) с азотсодержащими линкерами in vitro
    Проблемы медицинской микологии. 2021. Т. 23. № 2. С. 77.
  739. Д.О. Васильева, С.С. Патрушев, Э.Э. Шульц, А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева
    Изучение антибактериальной активности бис-(11,13-дигидро-изоалантолактонов) с азотсодержащими линкерами in vitro
    Проблемы медицинской микологии. 2021. Т. 23. № 2. С. 77.
  740. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  741. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  742. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  743. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  744. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  745. Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
    Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
    Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.723
  746. L. Politanskaya, E. Tretyakov, Chanjuan. Xi
    Synthesis of polyfluorinated 4-hydroxyquinolin-2(1H)-ones based on the cyclization of 2-alkynylanilines with carbon dioxide
    Journal of Fluorine Chemistry, 2021, V. 242, 109720 doi:10.1016/j.jfluchem.2020.109720, IF=2.05
  747. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  748. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  749. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  750. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  751. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  752. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
    Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
    New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
  753. A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
    Org. Biomol. Chem., 2021, V. 19, N 4, Pp 866-872 doi:10.1039/D0OB01893G, IF=3.876
  754. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  755. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  756. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  757. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  758. H. Suo, I.V. Oleynik, I.I. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Post-functionalization of narrowly dispersed PE waxes generated using tuned N,N,N'-cobalt ethylene polymerization catalysts substituted with ortho-cycloalkyl groups
    Polymer, 2021, V. 213, 123294 doi:10.1016/j.polymer.2020.123294, IF=4.43
  759. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  760. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  761. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  762. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  763. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  764. V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=3.021
  765. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  766. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  767. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  768. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  769. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  770. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  771. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  772. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  773. E. S.Permyakova, P. V.Kiryukhantsev-Korneev,.A. Ponomarev, A. N.Sheveyko, S. A.Dobrynin, J. Polcak, P. V.Slukin, S.G.Ignatov, A.Manakhov, S.A.Kulinich, D. V.Shtansky
    Antibacterial activity of therapeutic agent-immobilized nanostructured TiCaPCON films against antibiotic-sensitive and antibiotic-resistant Escherichia coli strains
    Surface and Coatings Technology, 2021, Volume 405, 126538 doi:10.1016/j.surfcoat.2020.126538, IF=4.158
  774. S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
    Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
    Letters in Drug Design & Discovery, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15
  775. S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
    Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
    Letters in Drug Design & Discovery, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15
  776. S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
    Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
    Letters in Drug Design & Discovery, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15
  777. S.S. Patrushev, L.G. Burova, A.A. Shtro, T.V. Rybalova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, E.E. Shults
    Modifications of Isoalantolactone Leading to Effective Antibacterial and Antiviral Compounds
    Letters in Drug Design & Discovery, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15
  778. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
    Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
    Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.217
  779. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
    Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
    Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.217
  780. T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
    Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
    Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.217
  781. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  782. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  783. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  784. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  785. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  786. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  787. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  788. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  789. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  790. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
  791. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  792. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  793. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  794. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  795. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  796. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  797. O. V.Salomatina, I. I.Popadyuk, A. L.Zakharenko, O. D.Zakharova, A. A.Chepanova, N..S.Dyrkheeva, N.I.Komarova, J.Reynisson, R. O.Anarbaev, N. F.Salakhutdinov, O. I.Lavrik, K. P.Volcho
    Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: a synthesis, structure-activity relationship and molecular modeling study
    Steroids, V. 165, January 2021, 108771 doi:10.1016/j.steroids.2020.108771, IF=2.668
  798. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411
  799. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411
  800. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411
  801. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411
  802. A. Chubarov, A. Spitsyna, O. Krumkacheva, D. Mitin, D. Suvorov, V. Tormyshev, M. Fedin, M.K. Bowman, E. Bagryanskaya
    Reversible Dimerization of Human Serum Albumin
    Molecules 2021, 26(1), 108 doi:10.3390/molecules26010108, IF=4.411
  803. M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
    Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
    Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
  804. M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
    Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
    Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
  805. M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
    Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
    Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
  806. M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
    Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
    Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
  807. M. Yu.Petyuk, A. S.Berezin, A. L.Gushchin, I. Yu.Bagryanskaya, A. Yu.Baranov, A. V.Artem'ev
    Luminescent Re(I) scorpionates supported by tris(2-pyridyl)phosphine and its derivatives
    Inorganica Chimica Acta, 2021, V.516, 120136 doi:10.1016/j.ica.2020.120136, IF=2.545
  808. P. Alper, O.V. Salomatina, N.F. Salakhutdinov, E. Ulukaya, F. Ari
    Soloxolone methyl, as a 18&bi;H-glycyrrhetinic acid derivate, may result in endoplasmic reticulum stress to induce apoptosis in breast cancer cells
    Bioorganic & Medicinal Chemistry, 2021, V.30, 115963 doi:10.1016/j.bmc.2020.115963, IF=3.641
  809. P. Alper, O.V. Salomatina, N.F. Salakhutdinov, E. Ulukaya, F. Ari
    Soloxolone methyl, as a 18&bi;H-glycyrrhetinic acid derivate, may result in endoplasmic reticulum stress to induce apoptosis in breast cancer cells
    Bioorganic & Medicinal Chemistry, 2021, V.30, 115963 doi:10.1016/j.bmc.2020.115963, IF=3.641
  810. P. Alper, O.V. Salomatina, N.F. Salakhutdinov, E. Ulukaya, F. Ari
    Soloxolone methyl, as a 18&bi;H-glycyrrhetinic acid derivate, may result in endoplasmic reticulum stress to induce apoptosis in breast cancer cells
    Bioorganic & Medicinal Chemistry, 2021, V.30, 115963 doi:10.1016/j.bmc.2020.115963, IF=3.641
  811. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
  812. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
  813. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
  814. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
  815. I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
  816. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  817. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  818. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  819. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  820. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  821. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867
  822. Л.Г. Лавренова, А.А. Мищенко, И.В. Олейник, Е.В. Коротаев, А.Н. Лавров, М.А. Гребенкина, Л.А. Шелудякова, Л.С. Клюшова, И.И. Олейник
    Синтез и свойства координационных соединений железа(II) и меди(II) с 2,6-бис[1-(фенилимино)этил]пиридином
    Журнал общей химии. 2021. Т. 91. № 11. С. 1693-1703. doi:10.31857/S0044460X21110068 (Synthesis and Properties of Iron(II) and Copper(II) Coordination Compounds with 2,6-Bis[1-(phenylimino)ethyl]pyridine/ L. G. Lavrenova, A. A. Mishchenko, I. V. Oleynik, E. V. Korotaev, A. N. Lavrov, M. A. Grebenkina, L. A. Sheludyakova, L. S. Klyushova & I. I. Oleynik// Russian Journal of General Chemistry, 2021, V. 91, N 11, Pp 2167-2175 doi:10.1134/S1070363221110062), IF=0.867

2020

Reviews, articles

  1. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  2. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  3. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  4. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  5. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  6. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  7. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  8. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  9. S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
    Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
    Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=3.534
  10. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  11. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  12. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  13. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
  14. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
  15. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
  16. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
  17. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
  18. Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
    Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
    Биохимия. 2020. Т. 85. № 12. С. 1928-1938. DOI: 10.31857/S0320972520120155 (Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1/ D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova// Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159), IF=1.978
  19. Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
    Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
    Биохимия. 2020. Т. 85. № 12. С. 1928-1938. DOI: 10.31857/S0320972520120155 (Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1/ D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova// Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159), IF=1.978
  20. Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
    Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
    Биохимия. 2020. Т. 85. № 12. С. 1928-1938. DOI: 10.31857/S0320972520120155 (Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1/ D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova// Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159), IF=1.978
  21. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  22. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  23. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  24. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  25. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  26. N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
    Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426
  27. T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
    Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
  28. T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
    Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
  29. T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
    Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
  30. T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
    Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
  31. T.M. Khomenko, V.V. Zarubaev, M.V. Kireeva, A.S. Volobueva, A.V. Slita, S.S. Borisevich, D.V. Korchagina, N.I. Komarova, K.P. Volcho, N.F. Salakhutdinov
    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
    Bioorganic & Medicinal Chemistry Letters, 2020, V. 30, N 24, Art. Num. 127653 doi:10.1016/j.bmcl.2020.127653, IF=2.572
  32. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  33. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  34. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  35. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  36. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  37. A.V. Markov, K.V. Odarenko, A.V. Sen’kova, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova
    Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
    Molecules 2020, 25(24), 5925 doi:10.3390/molecules25245925, IF=3.266
  38. A.V. Markov, K.V. Odarenko, A.V. Sen’kova, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova
    Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
    Molecules 2020, 25(24), 5925 doi:10.3390/molecules25245925, IF=3.266
  39. A.V. Markov, K.V. Odarenko, A.V. Sen’kova, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova
    Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
    Molecules 2020, 25(24), 5925 doi:10.3390/molecules25245925, IF=3.266
  40. A.V. Markov, K.V. Odarenko, A.V. Sen’kova, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova
    Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
    Molecules 2020, 25(24), 5925 doi:10.3390/molecules25245925, IF=3.266
  41. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  42. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  43. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  44. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  45. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  46. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  47. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  48. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  49. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
    A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
    Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
  50. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
    Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
    Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
  51. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
    Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
    Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
  52. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
    Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
    Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
  53. P. Agback, A. Shernyukov, F. Dominguez, T. Agback, E.I. Frolova
    Novel NMR Assignment Strategy Reveals Structural Heterogeneity in Solution of the nsP3 HVD Domain of Venezuelan Equine Encephalitis Virus
    Molecules 2020, 25(24), 5824 doi:10.3390/molecules25245824, IF=3.266
  54. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  55. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  56. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  57. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  58. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  59. G.T. Sukhanov, I.А. Krupnova, Yu.V. Filippova, Yu.V. Gatilov, A.G. Sukhanova, K.K. Bosov, E.V. Pivovarova
    Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols
    Chemistry of Heterocyclic Compounds, 2020, V 56, Pp 1440–1448 doi:10.1007/s10593-020-02835-w, IF=1.519
  60. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  61. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  62. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  63. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  64. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  65. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  66. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  67. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  68. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  69. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
  70. M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shults
    Synthetic studies on tricyclic diterpenoids: convenient synthesis of 16-arylisopimaranes
    Monatshefte fur Chemie - Chemical Monthly, , 2020, V. 151, N 12, Pp. 1817 - 1827 doi:10.1007/s00706-020-02713-3, IF=1.348
  71. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  72. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  73. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  74. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  75. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  76. A.S. Sokolova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, N.S. Shcherbakova, A.V. Zaykovskaya, D.S. Baev, T.G. Tolstikova, D.N. Shcherbakov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
    Monoterpenoid-based inhibitors of filoviruses targeting the glycoprotein-mediated entry process
    European Journal of Medicinal Chemistry, 2020, V. 207, 112726 doi:10.1016/j.ejmech.2020.112726, IF=5.572
  77. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  78. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  79. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  80. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  81. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  82. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Н.В. Пантелеева, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, П.В. Колосов, Г.Ю. Галицын
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Биоорганическая химия, 2020, Т. 46, N 7, (Bioactive Components in Methyl tert-Butyl Ether Extract of Sea Buckthorn (Hippophae rhamnoides L.) Green Waste/ T. P. Kukina, D. N. Shcherbakov, K. V. Gensh, N. V. Panteleyeva, Ye. A. Tulysheva, O. I. Sal’nikova, A. Ye. Grazhdannikov, P. V. Kolosov, G. Yu. Galitsyn// Russian Journal of Bioorganic Chemistry, 2020, V. 46, N 7, Pp 1372-1377 doi:10.1134/S1068162020070067), IF=0.681
  83. A.M. Cheplakova, K.A. Kovalenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    A comparative study of perfluorinated and non-fluorinated UiO-67 in gas adsorption
    Journal of Porous Materials, 2020, V. 27, N 12, Pp 1773-1782 doi:10.1007/s10934-020-00941-w, IF=2.183
  84. A.M. Cheplakova, K.A. Kovalenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    A comparative study of perfluorinated and non-fluorinated UiO-67 in gas adsorption
    Journal of Porous Materials, 2020, V. 27, N 12, Pp 1773-1782 doi:10.1007/s10934-020-00941-w, IF=2.183
  85. A.M. Cheplakova, K.A. Kovalenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    A comparative study of perfluorinated and non-fluorinated UiO-67 in gas adsorption
    Journal of Porous Materials, 2020, V. 27, N 12, Pp 1773-1782 doi:10.1007/s10934-020-00941-w, IF=2.183
  86. K.P. Cheremnykh, V.A. Savelyev, S.A. Borisov, I.D. Ivanov, D.S. Baev, T.G. Tolstikova, V.A. Vavilin, E.E. Shults
    Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
    Molecules 2020, 25(23), 5578 doi:10.3390/molecules25235578, IF=3.266
  87. K.P. Cheremnykh, V.A. Savelyev, S.A. Borisov, I.D. Ivanov, D.S. Baev, T.G. Tolstikova, V.A. Vavilin, E.E. Shults
    Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
    Molecules 2020, 25(23), 5578 doi:10.3390/molecules25235578, IF=3.266
  88. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  89. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  90. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  91. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  92. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  93. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  94. A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556
  95. S. Kuranov, O. Luzina, M. Khvostov, D. Baev, D. Kuznetsova, N. Zhukova, P. Vassiliev, A. Kochetkov, T. Tolstikova, N. Salakhutdinov
    Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
    Pharmaceuticals 2020, 13(11), 404 doi:10.3390/ph13110404, IF=4.285
  96. S. Kuranov, O. Luzina, M. Khvostov, D. Baev, D. Kuznetsova, N. Zhukova, P. Vassiliev, A. Kochetkov, T. Tolstikova, N. Salakhutdinov
    Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
    Pharmaceuticals 2020, 13(11), 404 doi:10.3390/ph13110404, IF=4.285
  97. L.V. Politanskaya, P.A. Fedyushin, T.V. Rybalova, A.S. Bogomyakov, N.B. Asanbaeva, E.V. Tretyakov
    Fluorinated Organic Paramagnetic Building Blocks for Cross-Coupling Reactions
    Molecules 2020, 25(22), 5427 doi:10.3390/molecules25225427, IF=3.266
  98. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  99. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  100. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  101. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  102. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  103. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  104. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  105. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  106. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  107. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  108. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  109. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  110. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  111. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
  112. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  113. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  114. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  115. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  116. А. Чепанова, Н.С. Ли-Жуланов, Т.А. Кургина, А.Л. Захаренко, О.Д. Захарова, К.П. Волчо, Н.Ф. Салахутдинов, О.И. Лаврик
    Разработка ингибиторов tdpi на основе производных хроменов как потенциальных противораковых препаратов
    Гены и Клетки. 2020. Т. 15. № S3. С. 68-69.
  117. E.V. Vasilyev, V.V. Shelkovnikov, N.A. Orlova, I.Sh. Steinberg, V.A. Loskutov
    Single- and two-photon recording of holograms at combined cationic and free-radical polymerization photoinitiated by thioxanthenone derivatives
    Polymer Journal, 2020, V. 52, N 11, Pp 1279-1287 doi:10.1038/s41428-020-0381-2, IF=2.825
  118. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  119. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  120. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  121. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  122. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  123. H. Suo, Z. Li, I.V. Oleynik, Z. Wang, I.I. Oleynik, Y. Ma, Qi. Liu, W. Sun
    Achieving strictly linear polyethylenes by the NNN-Fe precatalysts finely tuned with different sizes of ortho-cycloalkyl substituents
    Applied Organometalic Chemistry, 2020, V. 34, N 11 , e5937 doi:10.1002/aoc.5937, IF=3.14
  124. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  125. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  126. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  127. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  128. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  129. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  130. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  131. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A
  132. S. Cherkasov, D. Parkhomenko, A. Genaev, G. Salnikov, M. Edeleva, D. Morozov, T. Rybalova, I. Kirilyuk, S.R-A. Marque, E. Bagryanskaya
    NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
    Molecules 2020, 25(21), 5080 doi:10.3390/molecules25215080, IF=3.266
  133. Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
    Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745
  134. Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
    Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745
  135. Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
    Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745
  136. Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
    Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745
  137. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  138. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  139. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  140. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  141. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  142. В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
    Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745
  143. Е.С. Можайцев, К.Ю. Пономарев, О.С. Патрушева, А.В. Медведько, А.И. Далингер, А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
    Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
    Журнал органической химии. 2020. Т. 56. № 11. С. 1768-1783 doi:10.31857/S0514749220110129. (Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123), IF=0.624
  144. Е.С. Можайцев, К.Ю. Пономарев, О.С. Патрушева, А.В. Медведько, А.И. Далингер, А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
    Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
    Журнал органической химии. 2020. Т. 56. № 11. С. 1768-1783 doi:10.31857/S0514749220110129. (Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123), IF=0.624
  145. Е.С. Можайцев, К.Ю. Пономарев, О.С. Патрушева, А.В. Медведько, А.И. Далингер, А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
    Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
    Журнал органической химии. 2020. Т. 56. № 11. С. 1768-1783 doi:10.31857/S0514749220110129. (Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123), IF=0.624
  146. L. Politanskaya, I. Bagryanskaya, E. Tretyakov, Ch. Xic
    Highly efficient synthesis of novel fluorinated 3-amino-2-mercaptobenzothiazole-2(3H)-thione derivatives
    Journal of Fluorine Chemistry, 2020, V.239, 109628 doi:10.1016/j.jfluchem.2020.109628, IF=2.322
  147. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  148. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  149. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  150. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  151. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  152. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  153. D. I. Derevyanko, V. V. Shelkovnikov, V. Y. Kovalskii, I.L. Zilberberg, S.I. Aliev, N. A. Orlova, V. D. Ugozhaev
    The Charge Transfer Complex Formed between the Components of Photopolymer Material as an Internal Sensitizer of Spectral Sensitivity
    ChemistrySelect, 2020, V. 5, N 38, Pp 11939-11947 doi:10.1002/slct.202002163, IF=1.81
  154. D. I. Derevyanko, V. V. Shelkovnikov, V. Y. Kovalskii, I.L. Zilberberg, S.I. Aliev, N. A. Orlova, V. D. Ugozhaev
    The Charge Transfer Complex Formed between the Components of Photopolymer Material as an Internal Sensitizer of Spectral Sensitivity
    ChemistrySelect, 2020, V. 5, N 38, Pp 11939-11947 doi:10.1002/slct.202002163, IF=1.81
  155. D. I. Derevyanko, V. V. Shelkovnikov, V. Y. Kovalskii, I.L. Zilberberg, S.I. Aliev, N. A. Orlova, V. D. Ugozhaev
    The Charge Transfer Complex Formed between the Components of Photopolymer Material as an Internal Sensitizer of Spectral Sensitivity
    ChemistrySelect, 2020, V. 5, N 38, Pp 11939-11947 doi:10.1002/slct.202002163, IF=1.81
  156. М.В. Кручинина, И.О. Светлова, С.А. Курилович, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 56-64. doi:10.31146/1682-8658-ecg-182-10-56-64
  157. М.В. Кручинина, И.О. Светлова, С.А. Курилович, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 56-64. doi:10.31146/1682-8658-ecg-182-10-56-64
  158. М.В. Кручинина, И.О. Светлова, С.А. Курилович, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 56-64. doi:10.31146/1682-8658-ecg-182-10-56-64
  159. М.В. Кручинина, И.О. Светлова, С.А. Курилович, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 56-64. doi:10.31146/1682-8658-ecg-182-10-56-64
  160. М.В. Кручинина, И.О. Светлова, С.А. Курилович, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 56-64. doi:10.31146/1682-8658-ecg-182-10-56-64
  161. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  162. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  163. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  164. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  165. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  166. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
    Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55
  167. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  168. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  169. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  170. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  171. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  172. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  173. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  174. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  175. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  176. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  177. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  178. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  179. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  180. T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
    Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
    Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677
  181. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
  182. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
  183. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
  184. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
  185. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
  186. S.A. Popov, M. D. Semenova, D. S. Baev, T. S. Frolova, E. E.Shults,Ch.Wang, M.Turks
    Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
    Steroids, 2020, V. 153, 108524 doi:10.1016/j.steroids.2019.108524, IF=1.948
  187. S.A. Popov, M. D. Semenova, D. S. Baev, T. S. Frolova, E. E.Shults,Ch.Wang, M.Turks
    Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
    Steroids, 2020, V. 153, 108524 doi:10.1016/j.steroids.2019.108524, IF=1.948
  188. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  189. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  190. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  191. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  192. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  193. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  194. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  195. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716
  196. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716
  197. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716
  198. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716
  199. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716
  200. A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
    2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
    Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
  201. A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
    2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
    Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
  202. А. Макубаева, Е.П. Романенко, С.М. Адекенов, А.В. Ткачев
    Компонентный состав и биологическая активность эфирного масла ligularia heterophylla rupr.
    Химия растительного сырья. 2020. № 3. С. 239-244. (COMPONENT COMPOSITION AND BIOLOGICAL ACTIVITY OF ESSENTIAL OIL OF LIGULARIA HETEROPHYLLA RUPR./ MAKUBAYEVA AIGERIM, ROMANENKO ELENA PETROVNA, ADEKENOV SERGAZY MYNZHASAROVICH, TKACHEV ALEKSEY VASIL'YEVICH// doi:10.14258/jcprm.2020038243)
  203. А. Макубаева, Е.П. Романенко, С.М. Адекенов, А.В. Ткачев
    Компонентный состав и биологическая активность эфирного масла ligularia heterophylla rupr.
    Химия растительного сырья. 2020. № 3. С. 239-244. (COMPONENT COMPOSITION AND BIOLOGICAL ACTIVITY OF ESSENTIAL OIL OF LIGULARIA HETEROPHYLLA RUPR./ MAKUBAYEVA AIGERIM, ROMANENKO ELENA PETROVNA, ADEKENOV SERGAZY MYNZHASAROVICH, TKACHEV ALEKSEY VASIL'YEVICH// doi:10.14258/jcprm.2020038243)
  204. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
    Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745
  205. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
    Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745
  206. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
    Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745
  207. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
    Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745
  208. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
    Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745
  209. Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
    Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745
  210. Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
    Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745
  211. Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
    Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
    Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745
  212. Н.Ф. Салахутдинов, С.С. Лаев, Д.С. Сергеевичев
    Модуляторы нарушения гемопоэза (обзор)
    Химия в интересах устойчивого развития. 2020. Т. 28. № 4. С. 343-365. (Modulators of hematopoiesis disorders (a review)/ Salakhutdinov N. F., Laev S. S., Sergeevichev D. S.// Chemistry for Sustainable Development, 2020, V. 28, N 4, Pp. 343-365 doi:10.15372/KhUR2020239)
  213. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  214. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  215. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  216. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  217. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  218. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  219. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  220. E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
    Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556
  221. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  222. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  223. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  224. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  225. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  226. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  227. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  228. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  229. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  230. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  231. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  232. V. Romanov, E. Tretyakov, G. Selivanova, J. Li, I. Bagryanskaya, A. Makarov, D. Luneau
    Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
    Crystals 2020, 10(9), 786 doi:10.3390/cryst10090786, IF=2.404
  233. V. Romanov, E. Tretyakov, G. Selivanova, J. Li, I. Bagryanskaya, A. Makarov, D. Luneau
    Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
    Crystals 2020, 10(9), 786 doi:10.3390/cryst10090786, IF=2.404
  234. V.N. Davydova, I.V. Sorokina, A.V. Volod’ko, E.V. Sokolova, M.S. Borisova, I.M. Yermak
    The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
    Mar. Drugs 2020, 18(9), 458 doi:10.3390/md18090458, IF=4.72
  235. V.N. Davydova, I.V. Sorokina, A.V. Volod’ko, E.V. Sokolova, M.S. Borisova, I.M. Yermak
    The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
    Mar. Drugs 2020, 18(9), 458 doi:10.3390/md18090458, IF=4.72
  236. V.N. Davydova, I.V. Sorokina, A.V. Volod’ko, E.V. Sokolova, M.S. Borisova, I.M. Yermak
    The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
    Mar. Drugs 2020, 18(9), 458 doi:10.3390/md18090458, IF=4.72
  237. V.N. Davydova, I.V. Sorokina, A.V. Volod’ko, E.V. Sokolova, M.S. Borisova, I.M. Yermak
    The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
    Mar. Drugs 2020, 18(9), 458 doi:10.3390/md18090458, IF=4.72
  238. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  239. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  240. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  241. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  242. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  243. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  244. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
    Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519
  245. А.Б. Санников, Е.В. Шайдаков, В.М. Емельяненко, Т.Г. Толстикова
    Экспериментальное клиническое исследование по использованию отечественного адгезива в облитерации варикозно измененных вен у человека
    Стационарозамещающие технологии: Амбулаторная хирургия. 2020. № 3-4. С. 113-123. doi:10.21518/1995-1477-2020-3-4-113-123
  246. А.Б. Санников, Е.В. Шайдаков, В.М. Емельяненко, Т.Г. Толстикова
    Экспериментальное клиническое исследование по использованию отечественного адгезива в облитерации варикозно измененных вен у человека
    Стационарозамещающие технологии: Амбулаторная хирургия. 2020. № 3-4. С. 113-123. doi:10.21518/1995-1477-2020-3-4-113-123
  247. А.Б. Санников, Е.В. Шайдаков, В.М. Емельяненко, Т.Г. Толстикова
    Экспериментальное клиническое исследование по использованию отечественного адгезива в облитерации варикозно измененных вен у человека
    Стационарозамещающие технологии: Амбулаторная хирургия. 2020. № 3-4. С. 113-123. doi:10.21518/1995-1477-2020-3-4-113-123
  248. A.A. Bogush, C. Dabu, V.D. Tikhova, J.K. Kim, L.C. Campos
    Biomass Ashes for Acid Mine Drainage Remediation
    Waste and Biomass Valorization, 2020, V. 11, N 7, Pp 4977-4989 doi:10.1007/s12649-019-00804-9, IF=2.851
  249. A.A. Bogush, C. Dabu, V.D. Tikhova, J.K. Kim, L.C. Campos
    Biomass Ashes for Acid Mine Drainage Remediation
    Waste and Biomass Valorization, 2020, V. 11, N 7, Pp 4977-4989 doi:10.1007/s12649-019-00804-9, IF=2.851
  250. A.A. Bogush, C. Dabu, V.D. Tikhova, J.K. Kim, L.C. Campos
    Biomass Ashes for Acid Mine Drainage Remediation
    Waste and Biomass Valorization, 2020, V. 11, N 7, Pp 4977-4989 doi:10.1007/s12649-019-00804-9, IF=2.851
  251. A.A. Bogush, C. Dabu, V.D. Tikhova, J.K. Kim, L.C. Campos
    Biomass Ashes for Acid Mine Drainage Remediation
    Waste and Biomass Valorization, 2020, V. 11, N 7, Pp 4977-4989 doi:10.1007/s12649-019-00804-9, IF=2.851
  252. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  253. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  254. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  255. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  256. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  257. S.G. Mamylov, T.S. Skripkina, V.D. Tikhova, A.L. Bychkov, O.I. Lomovsky
    Thermal analysis of mechanochemically activated humic acids of brown coal
    Journal of Physics: Conference Series 1675 (2020) 012093 doi:10.1088/1742-6596/1675/1/012093
  258. S.G. Mamylov, T.S. Skripkina, V.D. Tikhova, A.L. Bychkov, O.I. Lomovsky
    Thermal analysis of mechanochemically activated humic acids of brown coal
    Journal of Physics: Conference Series 1675 (2020) 012093 doi:10.1088/1742-6596/1675/1/012093
  259. S.G. Mamylov, T.S. Skripkina, V.D. Tikhova, A.L. Bychkov, O.I. Lomovsky
    Thermal analysis of mechanochemically activated humic acids of brown coal
    Journal of Physics: Conference Series 1675 (2020) 012093 doi:10.1088/1742-6596/1675/1/012093
  260. S.G. Mamylov, T.S. Skripkina, V.D. Tikhova, A.L. Bychkov, O.I. Lomovsky
    Thermal analysis of mechanochemically activated humic acids of brown coal
    Journal of Physics: Conference Series 1675 (2020) 012093 doi:10.1088/1742-6596/1675/1/012093
  261. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  262. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  263. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  264. S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
    3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
    Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
  265. S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
    3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
    Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
  266. S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
    3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
    Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
  267. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, Н.С. Сиражетдинова, В.А. Савельев, Э.Э. Шульц
    Антибактериальная активность азотсодержащих производных антрахинона в отношении STAPHYLOCOCCUS AUREUS
    Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 73.
  268. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, Н.С. Сиражетдинова, В.А. Савельев, Э.Э. Шульц
    Антибактериальная активность азотсодержащих производных антрахинона в отношении STAPHYLOCOCCUS AUREUS
    Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 73.
  269. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, Н.С. Сиражетдинова, В.А. Савельев, Э.Э. Шульц
    Антибактериальная активность азотсодержащих производных антрахинона в отношении STAPHYLOCOCCUS AUREUS
    Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 73.
  270. I. Zayakin, I. Bagryanskaya, D. Stass, M. Kazantsev, E. Tretyakov
    Synthesis and Structure of (Nitronyl Nitroxide-2-ido)(tert-butyldiphenylphosphine)gold(I) and -(Di(tert-butyl)phenylphosphine)gold(I) Derivatives; Their Comparative Study in the Cross-Coupling Reaction
    Crystals 2020, 10(9), 770 doi:10.3390/cryst10090770, IF=2.404
  271. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  272. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  273. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  274. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  275. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  276. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  277. O. Luzina, A. Filimonov, A. Zakharenko, A. Chepanova, O. Zakharova, E. Ilina, N. Dyrkheeva, G. Likhatskaya, N. Salakhutdinov, O. Lavrik
    Usnic Acid Conjugates with Monoterpenoids as Potent Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
    Journal of Natural Products, 2020, 83, 8, 2320–2329 doi:10.1021/acs.jnatprod.9b01089, IF=3.779
  278. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  279. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  280. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  281. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  282. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  283. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
    Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
    Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
  284. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
    Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
    Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
  285. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
    Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
    Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
  286. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
    Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
    Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
  287. А.Ю. Сидоренко, В.Е. Агабеков, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Получение хиральных изобензофуранов на основе 3-карена в присутствии галлуазитовых нанокатализаторов
    Доклады Национальной академии наук Беларуси. 2020. Т. 64. № 4. С. 426-430. doi:10.29235/1561-8323-2020-64-4-426-430
  288. А.Ю. Сидоренко, В.Е. Агабеков, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Получение хиральных изобензофуранов на основе 3-карена в присутствии галлуазитовых нанокатализаторов
    Доклады Национальной академии наук Беларуси. 2020. Т. 64. № 4. С. 426-430. doi:10.29235/1561-8323-2020-64-4-426-430
  289. А.Ю. Сидоренко, В.Е. Агабеков, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Получение хиральных изобензофуранов на основе 3-карена в присутствии галлуазитовых нанокатализаторов
    Доклады Национальной академии наук Беларуси. 2020. Т. 64. № 4. С. 426-430. doi:10.29235/1561-8323-2020-64-4-426-430
  290. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  291. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  292. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  293. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  294. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  295. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  296. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  297. Yu.I. Glazachev, A.A. Schlotgauer, V.A. Timoshnikov, P.A. Kononova, O.Yu. Selyutina, E.A. Shelepova, M.V. Zelikman, M.V. Khvostov, N.E. Polyakov
    Effect of Glycyrrhizic Acid and Arabinogalactan on the Membrane Potential of Rat Thymocytes Studied by Potential-Sensitive Fluorescent Probe
    The Journal of Membrane Biology, 2020, V. 253, Pp 343-356 doi:10.1007/s00232-020-00132-3, IF=1.876
  298. A.P. Koskin, R.V. Andreev, O.N. Primachenko, E.I. Shuvarakova, A.F. Bedilo
    Perfluorosulfonic acid polymer composites: Effect of the support and synthesis method on the acid and catalytic properties
    Molecular Catalysis, 2020, V. 492, 111006 doi:10.1016/j.mcat.2020.111006, IF=3.687
  299. A.P. Koskin, R.V. Andreev, O.N. Primachenko, E.I. Shuvarakova, A.F. Bedilo
    Perfluorosulfonic acid polymer composites: Effect of the support and synthesis method on the acid and catalytic properties
    Molecular Catalysis, 2020, V. 492, 111006 doi:10.1016/j.mcat.2020.111006, IF=3.687
  300. A.P. Koskin, R.V. Andreev, O.N. Primachenko, E.I. Shuvarakova, A.F. Bedilo
    Perfluorosulfonic acid polymer composites: Effect of the support and synthesis method on the acid and catalytic properties
    Molecular Catalysis, 2020, V. 492, 111006 doi:10.1016/j.mcat.2020.111006, IF=3.687
  301. A.P. Koskin, R.V. Andreev, O.N. Primachenko, E.I. Shuvarakova, A.F. Bedilo
    Perfluorosulfonic acid polymer composites: Effect of the support and synthesis method on the acid and catalytic properties
    Molecular Catalysis, 2020, V. 492, 111006 doi:10.1016/j.mcat.2020.111006, IF=3.687
  302. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
  303. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
  304. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
  305. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
  306. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  307. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  308. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  309. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  310. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  311. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  312. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  313. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  314. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  315. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  316. A.O. Zaykovskaya, N. Kumar, E.A. Kholkina, N.S. Li-Zhulanov, P. Maki-Arvela, A. Aho, J. Peltonen, M. Peurla, I. Heinma, B.T. Kusema, S. Streiff, D.Yu. Murzi
    Synthesis and physico-chemical characterization of Beta zeolite catalysts: Evaluation of catalytic properties in Prins cyclization of (–)-isopulegol
    Microporous and Mesoporous Materials, 2020, V. 302, 110236 doi:10.1016/j.micromeso.2020.110236, IF=4.157
  317. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  318. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  319. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  320. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  321. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  322. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  323. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  324. Деревянко Д.И., Басистый В.С., Шелковников В.В., Шундрина И.К., Бухтоярова А.Д., Сальников Г.Е., Бережная В.Н., Черноносов А.А.
    Гибридный фотополимерный материал на основе (8-акрилоил-1,4-дитиа-8-азаспиро[4.5]декан-2-ил)метил акрилата и тиол-силоксанового компонента для записи микроструктур: синтез, оптические и термомеханические свойства
    Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 5. С. 382-394. doi:10.31857/S2308113920050046 (Hybrid Photopolymer Material Based on (8-Acryloyl-1,4-dithia-8-azaspiro[4.5]decan-2-yl)methyl Acrylate and Thiol-Siloxane Component for Recording Microstructures: Synthesis and Optical and Thermomechanical Properties/ D. I. Derevyanko, V. S. Basistyi, V. V. Shelkovnikov, I. K. Shundrina, A. D. Bukhtoyarova, G. E. Sal’nikov, V. N. Berezhnaya & A. A. Chernonosov// Polymer Science, Series B, 2020, V.62, N 5, Pp 509-521 doi:10.1134/S1560090420050048), IF=0.976
  325. Н.А. Анисимова, Е.К. Слободчикова, М.Е. Иванова, Т.В. Рыбалова
    Взаимодействие 1-нитро-3,3,3-трибром- и 1-нитро-1,3,3,3-тетрабромпроп-1-енов с алифатическими диенами
    Журнал общей химии. 2020. Т. 90. № 8. С. 1173-1183.DOI: 10.31857/S0044460X2008003X (Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022), IF=0.716
  326. Н.А. Анисимова, Е.К. Слободчикова, М.Е. Иванова, Т.В. Рыбалова
    Взаимодействие 1-нитро-3,3,3-трибром- и 1-нитро-1,3,3,3-тетрабромпроп-1-енов с алифатическими диенами
    Журнал общей химии. 2020. Т. 90. № 8. С. 1173-1183.DOI: 10.31857/S0044460X2008003X (Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022), IF=0.716
  327. Н.А. Анисимова, Е.К. Слободчикова, М.Е. Иванова, Т.В. Рыбалова
    Взаимодействие 1-нитро-3,3,3-трибром- и 1-нитро-1,3,3,3-тетрабромпроп-1-енов с алифатическими диенами
    Журнал общей химии. 2020. Т. 90. № 8. С. 1173-1183.DOI: 10.31857/S0044460X2008003X (Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022), IF=0.716
  328. М.В. Киреева, О.И. Яровая, В.В. Зарубаев
    Ингибирующая активность каркасных соединений на основе кариофиллена в отношении гемагглютинина вируса гриппа А
    Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 86.
  329. М.В. Киреева, О.И. Яровая, В.В. Зарубаев
    Ингибирующая активность каркасных соединений на основе кариофиллена в отношении гемагглютинина вируса гриппа А
    Проблемы медицинской микологии. 2020. Т. 22. № 3. С. 86.
  330. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, E.V. Malykhin
    Polyfluorinated hydroxy and carboxy benzenes as a new type of H-donors for self-assembly with 18-crown-6 ether: synthesis, supramolecular structure and stability of co-crystals
    Journal of Fluorine Chemistry, 2020, V. 236, 109577 doi:10.1016/j.jfluchem.2020.109577, IF=2.332
  331. Yu.M. Volkova, A.Yu. Makarov, E.A. Pritchina, N.P. Gritsan, A.V. Zibarev
    Herz radicals: chemistry and materials science
    Mendeleev Commun., 2020, V. 30, N 4, Pp 385-394 doi:10.1016/j.mencom.2020.07.001, IF=1.694
  332. Yu.M. Volkova, A.Yu. Makarov, E.A. Pritchina, N.P. Gritsan, A.V. Zibarev
    Herz radicals: chemistry and materials science
    Mendeleev Commun., 2020, V. 30, N 4, Pp 385-394 doi:10.1016/j.mencom.2020.07.001, IF=1.694
  333. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  334. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  335. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  336. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  337. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  338. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  339. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  340. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  341. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  342. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  343. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  344. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  345. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  346. N. A. Muraleva ,N. A. Stefanova,N. G. Kolosova
    SkQ1 Suppresses the p38 MAPK Signaling Pathway Involved in Alzheimer's Disease-Like Pathology in OXYS Rats
    Antioxidants 2020, 9(8), 676 doi:10.3390/antiox9080676, IF=5.13
  347. N. A. Muraleva ,N. A. Stefanova,N. G. Kolosova
    SkQ1 Suppresses the p38 MAPK Signaling Pathway Involved in Alzheimer's Disease-Like Pathology in OXYS Rats
    Antioxidants 2020, 9(8), 676 doi:10.3390/antiox9080676, IF=5.13
  348. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
  349. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
  350. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
  351. E.A. Kulikova, O.S. Kozhevnikova, A.V. Kulikov, N.G. Kolosova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, D.V. Telegina
    Alterations of STEP46 and STEP61 Expression in the Rat Retina with Age and AMD-Like Retinopathy Development
    Int. J. Mol. Sci. 2020, 21(15), 5182 doi:10.3390/ijms21155182, IF=4.556
  352. V.I. Borovkov, P.A. Potashov, I.V. Beregovaya, L.N. Shchegoleva, Yu.N. Molin
    Primary Radical Cations in Irradiated Poly(isobutylene)
    The Journal of Physical Chemistry B, 2020, V. 124, N 32 , Pp 7059-7066 doi:10.1021/acs.jpcb.0c03280, IF=2.857
  353. V.I. Borovkov, P.A. Potashov, I.V. Beregovaya, L.N. Shchegoleva, Yu.N. Molin
    Primary Radical Cations in Irradiated Poly(isobutylene)
    The Journal of Physical Chemistry B, 2020, V. 124, N 32 , Pp 7059-7066 doi:10.1021/acs.jpcb.0c03280, IF=2.857
  354. V.I. Borovkov, P.A. Potashov, I.V. Beregovaya, L.N. Shchegoleva, Yu.N. Molin
    Primary Radical Cations in Irradiated Poly(isobutylene)
    The Journal of Physical Chemistry B, 2020, V. 124, N 32 , Pp 7059-7066 doi:10.1021/acs.jpcb.0c03280, IF=2.857
  355. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  356. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  357. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  358. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  359. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Changes in Amino Acid and Acylcarnitine Plasma Profiles for Distinguishing Patients with Multiple Sclerosis from Healthy Controls
    Multiple Sclerosis International, 2020, V. 2020, Art. Number 9010937 doi:10.1155/2020/9010937
  360. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  361. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  362. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  363. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  364. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  365. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  366. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  367. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Effect of bispidine containing monoterpenoid moieties on physical performance in mice
    2020 Cognitive Sciences, Genomics and Bioinformatics (CSGB), Novosibirsk, Russia, 2020, pp. 114-117 doi:10.1109/CSGB51356.2020.9214697
  368. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
  369. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
  370. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
  371. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
  372. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
  373. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  374. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  375. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  376. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  377. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  378. G. Audran, E.G. Bagryanskaya, S.R. A. Marque, P. Postnikov
    New Variants of Nitroxide Mediated Polymerization
    Polymers 2020, 12(7), 1481 doi:10.3390/polym12071481, IF=3.426
  379. G. Audran, E.G. Bagryanskaya, S.R. A. Marque, P. Postnikov
    New Variants of Nitroxide Mediated Polymerization
    Polymers 2020, 12(7), 1481 doi:10.3390/polym12071481, IF=3.426
  380. G. Audran, E.G. Bagryanskaya, S.R. A. Marque, P. Postnikov
    New Variants of Nitroxide Mediated Polymerization
    Polymers 2020, 12(7), 1481 doi:10.3390/polym12071481, IF=3.426
  381. А.Г. Сокол, А.А. Томиленко, Т.А. Бульбак, И.А. Сокол, П.А. Заикин, Н.В. Соболев
    Состав флюида восстановленной мантии по экспериментальным данным и результатам изучения флюидных включений в алмазах
    Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825 Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825, doi:10.15372/GiG2020103 (Composition of reduced mantle fluids: evidence from modeling experiments and fluid inclusions in natural diamond/ Sokol A.G., Tomilenko A.A., Bul'bak T.A., Sokol I.A., Zaikin P.A., Sobolev N.V// Russian geology and geophysics, 2020, V. 61, N 5-6, Pp 663-674 SI doi:10.15372/RGG2020103)
  382. А.Г. Сокол, А.А. Томиленко, Т.А. Бульбак, И.А. Сокол, П.А. Заикин, Н.В. Соболев
    Состав флюида восстановленной мантии по экспериментальным данным и результатам изучения флюидных включений в алмазах
    Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825 Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825, doi:10.15372/GiG2020103 (Composition of reduced mantle fluids: evidence from modeling experiments and fluid inclusions in natural diamond/ Sokol A.G., Tomilenko A.A., Bul'bak T.A., Sokol I.A., Zaikin P.A., Sobolev N.V// Russian geology and geophysics, 2020, V. 61, N 5-6, Pp 663-674 SI doi:10.15372/RGG2020103)
  383. А.Г. Сокол, А.А. Томиленко, Т.А. Бульбак, И.А. Сокол, П.А. Заикин, Н.В. Соболев
    Состав флюида восстановленной мантии по экспериментальным данным и результатам изучения флюидных включений в алмазах
    Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825 Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825, doi:10.15372/GiG2020103 (Composition of reduced mantle fluids: evidence from modeling experiments and fluid inclusions in natural diamond/ Sokol A.G., Tomilenko A.A., Bul'bak T.A., Sokol I.A., Zaikin P.A., Sobolev N.V// Russian geology and geophysics, 2020, V. 61, N 5-6, Pp 663-674 SI doi:10.15372/RGG2020103)
  384. А.Г. Сокол, А.А. Томиленко, Т.А. Бульбак, И.А. Сокол, П.А. Заикин, Н.В. Соболев
    Состав флюида восстановленной мантии по экспериментальным данным и результатам изучения флюидных включений в алмазах
    Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825 Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825, doi:10.15372/GiG2020103 (Composition of reduced mantle fluids: evidence from modeling experiments and fluid inclusions in natural diamond/ Sokol A.G., Tomilenko A.A., Bul'bak T.A., Sokol I.A., Zaikin P.A., Sobolev N.V// Russian geology and geophysics, 2020, V. 61, N 5-6, Pp 663-674 SI doi:10.15372/RGG2020103)
  385. А.Г. Сокол, А.А. Томиленко, Т.А. Бульбак, И.А. Сокол, П.А. Заикин, Н.В. Соболев
    Состав флюида восстановленной мантии по экспериментальным данным и результатам изучения флюидных включений в алмазах
    Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825 Геология и геофизика. 2020. Т. 61. № S5-6. С. 810-825, doi:10.15372/GiG2020103 (Composition of reduced mantle fluids: evidence from modeling experiments and fluid inclusions in natural diamond/ Sokol A.G., Tomilenko A.A., Bul'bak T.A., Sokol I.A., Zaikin P.A., Sobolev N.V// Russian geology and geophysics, 2020, V. 61, N 5-6, Pp 663-674 SI doi:10.15372/RGG2020103)
  386. A. Amanzhan, P.Zh. Zhanymkhanova, B. Aidanuly, E.E. Shults, A.Z. Turmukhambetov, S.M. Adekenov
    Synthesis and structure of hydrazone derivatives of harmine
    News of NAS RK. Series of Chemistry and technology, 2020, V. 3, N 441, Pp 88-95 doi:10.32014/2020.2518-1491.48
  387. A. Amanzhan, P.Zh. Zhanymkhanova, B. Aidanuly, E.E. Shults, A.Z. Turmukhambetov, S.M. Adekenov
    Synthesis and structure of hydrazone derivatives of harmine
    News of NAS RK. Series of Chemistry and technology, 2020, V. 3, N 441, Pp 88-95 doi:10.32014/2020.2518-1491.48
  388. A. Amanzhan, P.Zh. Zhanymkhanova, B. Aidanuly, E.E. Shults, A.Z. Turmukhambetov, S.M. Adekenov
    Synthesis and structure of hydrazone derivatives of harmine
    News of NAS RK. Series of Chemistry and technology, 2020, V. 3, N 441, Pp 88-95 doi:10.32014/2020.2518-1491.48
  389. A. Amanzhan, P.Zh. Zhanymkhanova, B. Aidanuly, E.E. Shults, A.Z. Turmukhambetov, S.M. Adekenov
    Synthesis and structure of hydrazone derivatives of harmine
    News of NAS RK. Series of Chemistry and technology, 2020, V. 3, N 441, Pp 88-95 doi:10.32014/2020.2518-1491.48
  390. A. Amanzhan, P.Zh. Zhanymkhanova, B. Aidanuly, E.E. Shults, A.Z. Turmukhambetov, S.M. Adekenov
    Synthesis and structure of hydrazone derivatives of harmine
    News of NAS RK. Series of Chemistry and technology, 2020, V. 3, N 441, Pp 88-95 doi:10.32014/2020.2518-1491.48
  391. Д.В. Пятрикас, Е.Л. Горбылева, А.В. Федяева, С.A. Захарова, А.В. Шпатов, С.А. Попов, Г.Б. Боровский
    Поиск биологически активных веществ природного происхождения на основе малополярных экстрактов хвойных
    Известия вузов. Прикладная химия и биотехнология. 2020. Т. 10. № 2 (33). С. 240-250. (Search for biologically active substances of natural origin based on low-polar conifer extracts/ D. V. Pyatrikas, E. L. Gorbyleva, A. V. Fedyaeva, S. S. Zakharova, A. V. Shpatov, S. A. Popov, G. B. Borovskii// Izvestiya Vuzov. Prikladnaya Khimiya i Biotekhnologiya doi:10.21285/2227-2925-2020-10-2-240-250)
  392. Д.В. Пятрикас, Е.Л. Горбылева, А.В. Федяева, С.A. Захарова, А.В. Шпатов, С.А. Попов, Г.Б. Боровский
    Поиск биологически активных веществ природного происхождения на основе малополярных экстрактов хвойных
    Известия вузов. Прикладная химия и биотехнология. 2020. Т. 10. № 2 (33). С. 240-250. (Search for biologically active substances of natural origin based on low-polar conifer extracts/ D. V. Pyatrikas, E. L. Gorbyleva, A. V. Fedyaeva, S. S. Zakharova, A. V. Shpatov, S. A. Popov, G. B. Borovskii// Izvestiya Vuzov. Prikladnaya Khimiya i Biotekhnologiya doi:10.21285/2227-2925-2020-10-2-240-250)
  393. Д.В. Пятрикас, Е.Л. Горбылева, А.В. Федяева, С.A. Захарова, А.В. Шпатов, С.А. Попов, Г.Б. Боровский
    Поиск биологически активных веществ природного происхождения на основе малополярных экстрактов хвойных
    Известия вузов. Прикладная химия и биотехнология. 2020. Т. 10. № 2 (33). С. 240-250. (Search for biologically active substances of natural origin based on low-polar conifer extracts/ D. V. Pyatrikas, E. L. Gorbyleva, A. V. Fedyaeva, S. S. Zakharova, A. V. Shpatov, S. A. Popov, G. B. Borovskii// Izvestiya Vuzov. Prikladnaya Khimiya i Biotekhnologiya doi:10.21285/2227-2925-2020-10-2-240-250)
  394. Д.В. Пятрикас, Е.Л. Горбылева, А.В. Федяева, С.A. Захарова, А.В. Шпатов, С.А. Попов, Г.Б. Боровский
    Поиск биологически активных веществ природного происхождения на основе малополярных экстрактов хвойных
    Известия вузов. Прикладная химия и биотехнология. 2020. Т. 10. № 2 (33). С. 240-250. (Search for biologically active substances of natural origin based on low-polar conifer extracts/ D. V. Pyatrikas, E. L. Gorbyleva, A. V. Fedyaeva, S. S. Zakharova, A. V. Shpatov, S. A. Popov, G. B. Borovskii// Izvestiya Vuzov. Prikladnaya Khimiya i Biotekhnologiya doi:10.21285/2227-2925-2020-10-2-240-250)
  395. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  396. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  397. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  398. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  399. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  400. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  401. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  402. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  403. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  404. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  405. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  406. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  407. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  408. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  409. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  410. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  411. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
  412. T.S. Khlebnicova, Yu.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.S. Frolova, D.S. Baev, T.G. Tolstikova
    Betulinic Acid-Azaprostanoid Hybrids: Synthesis and Pharmacological Evaluation as Anti-inflammatory Agents
    Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry, (Formerly Current Medicinal Chemistry - Anti-Inflammatory & Anti-Allergy Agents), 2020, V. 19, N 3, Pp 254-267 doi:10.2174/1871523018666190426152049
  413. T.S. Khlebnicova, Yu.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.S. Frolova, D.S. Baev, T.G. Tolstikova
    Betulinic Acid-Azaprostanoid Hybrids: Synthesis and Pharmacological Evaluation as Anti-inflammatory Agents
    Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry, (Formerly Current Medicinal Chemistry - Anti-Inflammatory & Anti-Allergy Agents), 2020, V. 19, N 3, Pp 254-267 doi:10.2174/1871523018666190426152049
  414. T.S. Khlebnicova, Yu.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.S. Frolova, D.S. Baev, T.G. Tolstikova
    Betulinic Acid-Azaprostanoid Hybrids: Synthesis and Pharmacological Evaluation as Anti-inflammatory Agents
    Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry, (Formerly Current Medicinal Chemistry - Anti-Inflammatory & Anti-Allergy Agents), 2020, V. 19, N 3, Pp 254-267 doi:10.2174/1871523018666190426152049
  415. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  416. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  417. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  418. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  419. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  420. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  421. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  422. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  423. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  424. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  425. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  426. L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
    Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
    Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762
  427. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  428. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  429. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  430. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  431. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  432. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  433. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  434. И.К. Шундрина, И.В. Олейник, В.И. Пастухов, Л.А. Шундрин, В.С. Черноносова, П.П. Лактионов
    Синтез полимеров уретанового типа с полидиметилсилоксановыми блоками для изготовления волокнистых матриксов методом электроформования
    Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 4. С. 306-314, doi: 10.31857/S2308113920040099 (Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090), IF=0.976
  435. И.К. Шундрина, И.В. Олейник, В.И. Пастухов, Л.А. Шундрин, В.С. Черноносова, П.П. Лактионов
    Синтез полимеров уретанового типа с полидиметилсилоксановыми блоками для изготовления волокнистых матриксов методом электроформования
    Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 4. С. 306-314, doi: 10.31857/S2308113920040099 (Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090), IF=0.976
  436. Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
    Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
    Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719
  437. Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
    Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
    Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719
  438. Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
    Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
    Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719
  439. A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
    Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp. 968-972 doi:10.1007/s10593-020-02760-y, IF=1.519
  440. A. M. Genaev, G. E. Salnikov, K.Yu. Koltunov
    Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 892-897 doi:10.1007/s10593-020-02749-7, IF=1.519
  441. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  442. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  443. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  444. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  445. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  446. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  447. О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
    Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774
  448. A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A new Сu(i) iodide complex showing deep-red luminescence
    Журнал структурной химии. 2020. Т. 61. № 7. С. 1131-1134. (doi:10.26902/JSC_id58729) (A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082), IF=0.745
  449. A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A new Сu(i) iodide complex showing deep-red luminescence
    Журнал структурной химии. 2020. Т. 61. № 7. С. 1131-1134. (doi:10.26902/JSC_id58729) (A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082), IF=0.745
  450. A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A new Сu(i) iodide complex showing deep-red luminescence
    Журнал структурной химии. 2020. Т. 61. № 7. С. 1131-1134. (doi:10.26902/JSC_id58729) (A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082), IF=0.745
  451. A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
    Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  452. A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
    Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  453. A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
    Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  454. В.Н. Ковтонюк, Х. Хань, Ю.В. Гатилов
    Синтез полифторированных тетраоксакаликс[4]аренов при взаимодействии пентафторнитробензола с резорцином, орцинолом и тетрафторрезорцином
    Журнал органической химии. 2020. Т. 56. № 7. С. 1030-1038. (Synthesis of polyfluorinated tetraoxacalix[4]arenes by the interaction of pentafluoronitrobenzene with resorcinol, orcinol, and tetrafluororesorcinol/ Kovtonyuk V. N., Han H., Gatilov Yu. V.// Russian Journal of Organic Chemistry, 2020 doi:10.31857/S0514749220070058), IF=0.751
  455. В.Н. Ковтонюк, Х. Хань, Ю.В. Гатилов
    Синтез полифторированных тетраоксакаликс[4]аренов при взаимодействии пентафторнитробензола с резорцином, орцинолом и тетрафторрезорцином
    Журнал органической химии. 2020. Т. 56. № 7. С. 1030-1038. (Synthesis of polyfluorinated tetraoxacalix[4]arenes by the interaction of pentafluoronitrobenzene with resorcinol, orcinol, and tetrafluororesorcinol/ Kovtonyuk V. N., Han H., Gatilov Yu. V.// Russian Journal of Organic Chemistry, 2020 doi:10.31857/S0514749220070058), IF=0.751
  456. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  457. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  458. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  459. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  460. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  461. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  462. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  463. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  464. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
    Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
    Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
  465. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
    Synthesis of Nitroxide Diradical Using a New Approach
    Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
  466. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
    Synthesis of Nitroxide Diradical Using a New Approach
    Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
  467. N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
    Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
    Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267
  468. N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
    Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
    Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267
  469. N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
    Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
    Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267
  470. N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
    Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
    Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267
  471. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
  472. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
  473. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
  474. Н.Э. Поляков, С.В. Валиулин, А.А. Онищук, Т.Г. Толстикова
    Новые подходы к повышению эффективности нестероидных противовоспалительных средств с использованием наноразмерных систем доставки
    Российский нейрохирургический журнал им. профессора А.Л. Поленова. 2020. Т. 12. № 2. С. 79-85. (NEW APPROACHES TO INCREASING THE EFFECTIVENESS OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS USING NANOSCALE DELIVERY SYSTEMS/ POLYAKOV N. E., VALIULIN S. V., ONISCHUK A. A., TOLSTIKOVA T. G.// )
  475. Н.Э. Поляков, С.В. Валиулин, А.А. Онищук, Т.Г. Толстикова
    Новые подходы к повышению эффективности нестероидных противовоспалительных средств с использованием наноразмерных систем доставки
    Российский нейрохирургический журнал им. профессора А.Л. Поленова. 2020. Т. 12. № 2. С. 79-85. (NEW APPROACHES TO INCREASING THE EFFECTIVENESS OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS USING NANOSCALE DELIVERY SYSTEMS/ POLYAKOV N. E., VALIULIN S. V., ONISCHUK A. A., TOLSTIKOVA T. G.// )
  476. Н.Э. Поляков, С.В. Валиулин, А.А. Онищук, Т.Г. Толстикова
    Новые подходы к повышению эффективности нестероидных противовоспалительных средств с использованием наноразмерных систем доставки
    Российский нейрохирургический журнал им. профессора А.Л. Поленова. 2020. Т. 12. № 2. С. 79-85. (NEW APPROACHES TO INCREASING THE EFFECTIVENESS OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS USING NANOSCALE DELIVERY SYSTEMS/ POLYAKOV N. E., VALIULIN S. V., ONISCHUK A. A., TOLSTIKOVA T. G.// )
  477. D.V. Spiryova, A.Yu. Vorobev, V.V. Klimontov, E.A. Koroleva, A.E. Moskalensky
    Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
    Biomedical Optics Express. 2020. V. 11. № 6. Pp. 3319-3330 doi:10.1364/BOE.392745, IF=3.91
  478. D.V. Spiryova, A.Yu. Vorobev, V.V. Klimontov, E.A. Koroleva, A.E. Moskalensky
    Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
    Biomedical Optics Express. 2020. V. 11. № 6. Pp. 3319-3330 doi:10.1364/BOE.392745, IF=3.91
  479. D.V. Spiryova, A.Yu. Vorobev, V.V. Klimontov, E.A. Koroleva, A.E. Moskalensky
    Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
    Biomedical Optics Express. 2020. V. 11. № 6. Pp. 3319-3330 doi:10.1364/BOE.392745, IF=3.91
  480. D.V. Spiryova, A.Yu. Vorobev, V.V. Klimontov, E.A. Koroleva, A.E. Moskalensky
    Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
    Biomedical Optics Express. 2020. V. 11. № 6. Pp. 3319-3330 doi:10.1364/BOE.392745, IF=3.91
  481. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  482. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  483. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  484. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  485. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  486. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  487. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  488. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  489. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
  490. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  491. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  492. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  493. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  494. S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
    Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
    Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567
  495. Полосьмак Н.В., Карпова Е.В., Амосов Е.В.
    Уникальная ткань с городища Джеты-Асар-2 (Восточное Приаралье) в контексте центрально-азиатской текстильной традиции
    Археология, этнография и антропология Евразии. 2020. Т. 48. № 3. С. 50-58. (An unusual fabric from Jety-Asar-2, Eastern Aral sea region, in the context of the central asian textile tradition/ POLOSMAK N.V., KARPOVA E.V., AMOSOV E.V.// doi:10.17746/1563-0102.2020.48.3.050-058)
  496. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  497. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  498. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  499. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  500. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  501. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
    Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202
  502. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  503. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  504. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  505. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  506. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  507. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  508. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  509. I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
    The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519
  510. V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
    Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 763-768 doi:10.1007/s10593-020-02728-y, IF=1.491
  511. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  512. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  513. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  514. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  515. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  516. А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
    Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
    Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048)
  517. M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
    A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
    Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745
  518. M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
    A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
    Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745
  519. M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
    A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
    Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745
  520. M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
    A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
    Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745
  521. M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
    Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
  522. M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
    Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
  523. M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
    Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
  524. L. A.Shundrin,I.A.Os'kina,I. G.Irtegova,A. F.Poveshchenko
    9H-Thioxanthen-9-one S,S-dioxide based redox active labels for electrochemical detection of DNA duplexes immobilized on Au electrodes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 296-298 doi:10.1016/j.mencom.2020.05.011, IF=1.694
  525. N.Yu. Adonin, V.V. Bardin
    Polyfluorinated arylboranes as catalysts in organic synthesis
    Mendeleev Communications, 2020, V. 30, N 3, Pp 262-272 doi:10.1016/j.mencom.2020.05.002, IF=1.694
  526. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  527. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  528. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  529. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  530. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  531. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  532. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
  533. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  534. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  535. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  536. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  537. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  538. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  539. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  540. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  541. A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
    Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
    Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556
  542. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  543. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  544. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  545. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  546. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  547. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  548. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  549. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  550. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  551. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  552. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  553. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  554. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  555. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  556. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  557. A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
    Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
    ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853
  558. А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
    Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
    Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216)
  559. А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
    Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
    Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216)
  560. А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
    Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
    Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216)
  561. А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
    Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
    Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216)
  562. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  563. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  564. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  565. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  566. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  567. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  568. M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
    High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
    Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174
  569. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
    Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
    ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
  570. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
    Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
    ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
  571. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
    Biophotonics approach for the study of leukocyte activation
    Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
  572. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
    Biophotonics approach for the study of leukocyte activation
    Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
  573. D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
    Biophotonics approach for the study of leukocyte activation
    Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325
  574. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  575. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  576. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  577. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  578. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  579. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  580. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  581. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  582. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  583. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  584. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
  585. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
  586. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
  587. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
  588. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  589. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  590. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  591. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  592. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  593. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  594. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  595. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  596. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  597. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  598. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  599. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  600. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  601. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  602. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
  603. D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
    Study of calcium signaling dynamics in single platelets using optical activation methods.
    Proceedings of SPIE, 2020, V. 11359, #113590U doi:10.1117/12.2559414
  604. D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
    Study of calcium signaling dynamics in single platelets using optical activation methods.
    Proceedings of SPIE, 2020, V. 11359, #113590U doi:10.1117/12.2559414
  605. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  606. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  607. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  608. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  609. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  610. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  611. M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
    Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52
  612. V.A. Logvinenko, V.P. Fadeeva, B.A. Selivanov, V.D. Tikhova, A.A. Nefedov, A.Ya. Tikhonov
    Thermal decomposition of several N,N'-bis(2-hydroxyiminoalkyl)-α,α'-dinitrones
    Journal of Thermal Analysis and Calorimetry, 2020, V. 140, N 2, Pp 685-693 doi:10.1007/s10973-019-08868-4, IF=2.731
  613. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  614. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  615. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  616. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  617. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  618. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  619. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  620. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  621. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  622. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
    Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
    Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
  623. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
    Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
    Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
  624. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
    Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
    Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
  625. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
    Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
    Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
  626. G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
    Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
    Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332
  627. D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
    Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
    Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
  628. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  629. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  630. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  631. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  632. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  633. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  634. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  635. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  636. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  637. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  638. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  639. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  640. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  641. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  642. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  643. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  644. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  645. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  646. Yu.S. Demidova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, A.A. Saraev, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Monoterpenoid Oximes Hydrogenation Over Platinum Catalysts
    Topics in Catalysis, 2020, V. 63, N 1-2, pages187-195 doi:10.1007/s11244-020-01234-x, IF=2.406
  647. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  648. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  649. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  650. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  651. А.В. Липеева, М.П. Долгих, Т.Г. Толстикова, Э.Э. Шульц
    Исследование растительных кумаринов. 18. конъюгаты кумаринов с лупановыми тритерпеноидами и 1,2,3-триазолами: синтез и противовоспалительная активность
    Биоорганическая химия. 2020. Т. 46. № 2. С. 115-123. DOI: 10.31857/S0132342320010194 (Study of Plant Coumarins. 18. Coumarin Conjugates with Lupane Triterpenoidsand 1,2,3-triazoles: Synthesis and Anti-inflammatory Activity/ Lipeeva A. V., Dolgikh М. Р., Tolstikova T. G., Shults E. E// Russian Journal of Bioorganic Chemistry, 2010, V. 46, N 2, Pp125-132 doi:10.1134/S1068162020010161), IF=0.682
  652. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  653. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  654. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  655. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  656. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  657. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  658. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  659. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  660. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  661. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  662. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  663. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  664. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  665. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  666. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  667. N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
    Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
    The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6
  668. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
  669. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  670. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  671. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  672. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  673. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  674. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  675. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  676. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  677. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  678. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  679. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  680. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
    Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
    Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
  681. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
    Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
    Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
  682. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
    Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
    Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
  683. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
    Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
    Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
  684. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
    Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
  685. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
    Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
    Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
  686. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
    Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
    Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
  687. A.D. Rogachev, D.V. Trebushat, A.N. Kudryashov, A.G. Pokrovsky
    Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
    Chromatographia, 2020, V. 83, N 2, pp 299-304 doi:10.1007/s10337-019-03835-5, IF=1.596
  688. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  689. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  690. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  691. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  692. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
    Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
    Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
  693. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
    Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
    Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
  694. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
    Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
    Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
  695. Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
    Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
    Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061
  696. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
    Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
    Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
  697. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
    Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
    Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
  698. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
    Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
    Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
  699. A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
    Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
    Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38
  700. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  701. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  702. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  703. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  704. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  705. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
  706. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
    Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
    Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
  707. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
    Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
    Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
  708. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  709. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  710. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  711. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  712. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  713. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  714. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  715. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  716. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  717. Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
    Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
    Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5
  718. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  719. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  720. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  721. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  722. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  723. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  724. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  725. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  726. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  727. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  728. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  729. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  730. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  731. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  732. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  733. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  734. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  735. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  736. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  737. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  738. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  739. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  740. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  741. A.Yu. Vorobev, A.E. Moskalensky
    Long-wavelength photoremovable protecting groups: On the way to in vivo application
    Computational and Structural Biotechnology Journal, 2020, V. 18, Pp 27-34 doi:10.1016/j.csbj.2019.11.007, IF=6.018
  742. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  743. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  744. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  745. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  746. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  747. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  748. Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
    Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
    Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109
  749. В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
    Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
    Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24)
  750. В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
    Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
    Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24)
  751. В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
    Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
    Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24)
  752. В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
    Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
    Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24)
  753. В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
    Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
    Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24)
  754. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174
  755. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174
  756. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174
  757. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174
  758. J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
    Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
    Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174
  759. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  760. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  761. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  762. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  763. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  764. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  765. E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
    Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
    Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073
  766. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
    Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
    Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
  767. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
    Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
    Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
  768. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
    Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
    Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
  769. В.В. Бардин, С.А. Приходько, М.М. Шмаков, А.Ю. Шабалин, Н.Ю. Адонин
    Синтез фторсодержащих арил(галоген)боранов из арил(фтор)боратов калия
    Журнал общей химии. 2020. Т. 90. № 1. С. 72-84 DOI:10.31857/S0044460X20010096 (Synthesis of Fluorine-Containing Aryl(halo)boranes from Potassium Aryl(fluoro)borates/ V. V. Bardin, S. A. Prikhod’ko, M. M. Shmakov, A. Yu. Shabalin & N. Yu. Adonin// Russian Journal of General Chemistry, 2020, V. 90, N 1 , Pp 50–61 doi:10.1134/S1070363220010089), IF=0.716
  770. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, С.А. Борисов, Т.Г. Толстикова, Д.Е. Семенов, М.А. Бакарев
    Простатотропное действие динатриевой соли глицирризиновой кислоты при моделировании доброкачественной гиперплазии предстательной железы
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 169. № 1. С. 124-129. (Prostatotropic action of glycyrrhizic acid disodium salt in modeling benign prostatic hyperplasia/ Nizomov S.A., Sorokina I.V., Zhukova N.A., Borisov S.A., Tolstikova T.G., Semenov D.E., Bakarev M.A.// Bulletin of Experimental Biology and Medicine, 2020, V. 169, N 1, Pp 114-118 doi:10.1007/s10517-020-04836-3), IF=0.775
  771. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, С.А. Борисов, Т.Г. Толстикова, Д.Е. Семенов, М.А. Бакарев
    Простатотропное действие динатриевой соли глицирризиновой кислоты при моделировании доброкачественной гиперплазии предстательной железы
    Бюллетень экспериментальной биологии и медицины. 2020. Т. 169. № 1. С. 124-129. (Prostatotropic action of glycyrrhizic acid disodium salt in modeling benign prostatic hyperplasia/ Nizomov S.A., Sorokina I.V., Zhukova N.A., Borisov S.A., Tolstikova T.G., Semenov D.E., Bakarev M.A.// Bulletin of Experimental Biology and Medicine, 2020, V. 169, N 1, Pp 114-118 doi:10.1007/s10517-020-04836-3), IF=0.775
  772. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
    Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
    Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
  773. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
    Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
    Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
  774. Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
    Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
    Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909)
  775. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
    Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
    Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
  776. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
    Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
    Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
  777. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
    Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
    Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
  778. С.А. Приходько, А.Ю. Шабалин, М.М. Шмаков, В.В. Бардин, Н.Ю. Адонин
    Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
    Известия Академии наук. Серия химическая. 2020. № 1. С. 17-31. (Ionic liquids with fluorine-containing anions as a new class of functional materials: features of the synthesis, physicochemical properties, and use/ S. A. Prikhod'ko, A. Yu. Shabalin, M. M. Shmakov, V. V. Bardin, N. Yu. Adonin// Russian Chemical Bulletin, 2020, V. 69, Pp 17–31 doi:10.1007/s11172-020-2719-5), IF=1.061
  779. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  780. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  781. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  782. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  783. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  784. Т.Е. Кокина, В.Ю. Комаров, Л.А. Глинская, С.Н. Бизяев, Л.А. Шелудякова, Ю.А. Еремина, Л.С. Клюшова, А.В. Ткачев
    Синтез, строение и цитотоксичность комплексов Pd(II) и Сu(II) с 1-терпенил-3-тиосемикарбазидами пинанового и пара-ментанового рядов
    Журнал структурной химии, 2020, т. 61, №1, стр.48, doi: 10.26902/JSC_id49663 (Synthesis, structure, and cytotoxicity of Pd(II) and Cu(II) complexes with 1-terpenyl-3-thiosemicarbazides of pinane and para-menthane series/ Kokina T.E., Komarov V. Yu., Glinskaya L.A., Bizyaev S.N., Sheludyakova L.A., Eremina Yu. A., Klyushova L.S., Tkachev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 1, Pp 44-56 doi:10.1134/S0022476620010059), IF=0.745
  785. L. Politanskaya, E. Tretyakov, Ch. Xi
    Synthesis of polyfluorinated o-hydroxyacetophenones - convenient precursors of 3-benzylidene-2-phenylchroman-4-ones
    Journal of Fluorine Chemistry, V. 229, January 2020, 109435 doi:10.1016/j.jfluchem.2019.109435, IF=2.332
  786. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
    Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
    Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209
  787. A.A. Okhina, A.D. Rogachev, O.I. Yarovaya, M.V. Khvostov, T.G. Tolstikova, A.G. Pokrovsky, V.A. Khazanov, N.F. Salakhutdinov
    Development and validation of an LC-MS/MS method for the quantitative analysis of the anti-influenza agent camphecene in rat plasma and its application to study the blood-to-plasma distribution of the agent
    Journal of Pharmaceutical and Biomedical Analysis, 2020, V. 180, 113039 doi:10.1016/j.jpba.2019.113039, IF=3.209
  788. D. Spiryova, A. Vorob'ev, A.E. Moskalensky
    Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
    Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621
  789. D. Spiryova, A. Vorob'ev, A.E. Moskalensky
    Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
    Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621

2019

Reviews, articles

  1. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  2. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  3. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  4. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  5. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  6. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  7. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  8. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
  9. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
  10. V.V. Bardin, N.Yu. Adonin
    The preparation of pentafluorophenyldihaloboranes from pentafluorophenylmercurials C6F5HgR and BX3: the dramatic dependence of the reaction direction on the ligand R
    Monatshefte für Chemie - Chemical Monthly, 2019, V.150, N 8, pp 1523-1531 doi:10.1007/s00706-019-02476-6, IF=1.501
  11. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  12. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  13. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  14. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  15. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  16. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
    Catalysis Letters, 2019, V. 149, N 12, pp 3454-3464 doi:10.1007/s10562-019-02958-6, IF=2.371
  17. S.V. Nikitin, J. Sanchez-Marquez, I.I. Oleynik, I. Oleynik, E.G. Bagryanskaya
    A screening DFT study of the para-substituent effect on local hyper-softness in bis(phenoxy-imine) titanium complexes to get insights about their catalytic activity in ethylene polymerization
    Molecular Catalysis, 2019, V. 469, Pp 57-67 doi:10.1016/j.mcat.2019.02.024, IF=2.938
  18. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
    Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
    The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
  19. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
    Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
    The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
  20. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  21. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  22. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  23. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  24. I. V. Beregovaya, L. N. Shchegoleva, D.A. Ovchinnikov, S.V. Blinkova, V.I. Borovkov, R.Andreev, V.A. Bagryansky, Yu.N. Molin
    Dimer Radical Anions of Polyfluoroarenes. Two More to a Small Family
    The Journal of Physical Chemistry A, 2019, 123, 51, 10968-10975 doi:10.1021/acs.jpca.9b09906, IF=2.641
  25. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
    Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
    Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
  26. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
    Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
    Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
  27. A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
    Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
    Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971
  28. A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
    Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
    Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147
  29. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  30. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  31. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  32. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  33. V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
    Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997
  34. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  35. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  36. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  37. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  38. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  39. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  40. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  41. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  42. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  43. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  44. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  45. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  46. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  47. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  48. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  49. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  50. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  51. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  52. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  53. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  54. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  55. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  56. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  57. Н.А. Панкрушина, О.И. Ломовский, Т.П. Шахтшнейдер
    Физическая активация процессов экстракции и органического синтеза
    Химия в интересах устойчивого развития. 2019. Т. 27. № 6. С. 704-715. (Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194)
  58. Н.А. Панкрушина, О.И. Ломовский, Т.П. Шахтшнейдер
    Физическая активация процессов экстракции и органического синтеза
    Химия в интересах устойчивого развития. 2019. Т. 27. № 6. С. 704-715. (Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194)
  59. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
    Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
    Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
  60. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
    Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
    Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
  61. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
    Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
    Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
  62. A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
    Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
    Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953
  63. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  64. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  65. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  66. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  67. O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
    Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447
  68. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
    Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
  69. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
    Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
  70. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
    Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
  71. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
    Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
  72. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
    Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052
  73. V.I. Borovkov, L.N. Shchegoleva
    Magnetic Resonance Characteristics of Negative Polarons in Neat Poly(3-hexyl-thiophene)
    Journal of Physical Chemistry C, 2019, 123, 46, 28058-28065 doi:10.1021/acs.jpcc.9b08331, IF=4.309
  74. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  75. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  76. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  77. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  78. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
    Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
    Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
  79. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
    Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
    Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
  80. A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
    Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
    Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789
  81. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
    Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
  82. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
    Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
  83. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  84. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  85. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  86. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  87. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  88. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  89. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  90. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  91. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  92. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  93. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  94. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  95. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  96. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
    Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
    UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453
  97. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
    Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
    Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
  98. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
    Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
    Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
  99. S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
    Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
    Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965
  100. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  101. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  102. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  103. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  104. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  105. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  106. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  107. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  108. N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
    Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
    Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937
  109. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  110. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  111. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  112. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  113. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  114. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  115. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  116. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  117. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  118. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  119. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  120. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  121. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  122. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  123. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  124. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  125. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  126. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  127. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  128. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  129. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  130. O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
    Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449
  131. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  132. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  133. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  134. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  135. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
    Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
    Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
  136. M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
    Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
    Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794
  137. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  138. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  139. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  140. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  141. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  142. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  143. А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
    Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
    Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794
  144. М.В. Хвостов, Т.Г. Толстикова, С.А. Борисов, А.В. Душкин
    Применение природных полисахаридов в фармацевтике
    Биоорганическая химия, 2019, том 45, № 6, с. 563-575 (doi:10.1134/S0132342319060241) (Application of Natural Polysaccharides in Pharmaceutics/ M.V. Khvostov, T.G. Tolstikova, S.A. Borisov, A.V. Dushkin// Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 438-450 doi:10.1134/S1068162019060219), IF=0.794
  145. Т.П. Кукина, И.В. Хан
    Липофильные компоненты мытников PEDICULARIS STRIATA PALLAS и PEDICULARIS FLAVA PALLAS
    Химия растительного сырья. 2019. № 4. С. 113-118. (Lipophilic constituents of pedicularis striata pallas и pedicularis flava pallas/ Kukina, T.P., Khan, I.V.// Khimiya Rastitel'nogo Syr'ya, Issue 4, 1 January 2020, Pages 113-118 doi:10.14258/jcprm.2019044952)
  146. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
    Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
    Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
  147. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
    Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
    Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
  148. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
    Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
    Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
  149. П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
    Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
    Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541
  150. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
    Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
  151. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
    Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
  152. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
    Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
  153. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
    Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
  154. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
    Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751
  155. L. Politanskaya, N. Troshkova, E. Tretyakov, Ch. Xi
    Synthesis of polyfluorinated bezofurans
    Journal of Fluorine Chemistry, Volume 227, November 2019, 109371 doi:10.1016/j.jfluchem.2019.109371, IF=2.055
  156. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
    Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
    Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
  157. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
    Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
    Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
  158. M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
    Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
    Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65
  159. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  160. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  161. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  162. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  163. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  164. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  165. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  166. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  167. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  168. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  169. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  170. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  171. A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
    Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59
  172. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
    Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
    ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
  173. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
    Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
    ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
  174. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
    A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
    ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
  175. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
    A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
    ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
  176. S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
    Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
    Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136
  177. S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
    Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
    Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136
  178. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  179. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  180. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  181. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  182. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  183. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  184. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  185. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  186. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  187. M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
    Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
    Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394
  188. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  189. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  190. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  191. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  192. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  193. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
    Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
  194. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
    Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
  195. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
    Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
  196. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
    Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907
  197. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
    Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
    Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
  198. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
    Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
    Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
  199. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
    Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
    Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
  200. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
    Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
    Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
  201. Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
    Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
    Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541
  202. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
    Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
    Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
  203. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
    Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
    Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
  204. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
    Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
    Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
  205. Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
    Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
    Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751
  206. В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
    Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
    Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751
  207. В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
    Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
    Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751
  208. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
    Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
    Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
  209. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
    Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
    Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
  210. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
    Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
    Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
  211. E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
    Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
    Mendeleev Commun., 2019, V. 29, N 5, Pp 584-586 doi:10.1016/j.mencom.2019.09.036, IF=2.01
  212. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  213. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  214. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  215. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  216. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  217. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  218. A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
    Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
    SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11
  219. A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
    Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
    SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11
  220. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
  221. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
  222. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
  223. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
  224. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
    CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
  225. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
    CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
  226. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
    Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
    MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
  227. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
    Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
    MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
  228. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
    Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
    MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
  229. A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
    Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
    MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649
  230. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  231. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  232. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  233. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  234. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  235. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  236. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  237. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  238. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  239. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  240. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  241. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  242. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  243. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  244. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  245. M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
    Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
    Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845
  246. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
    Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
  247. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
    Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
  248. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
    Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
  249. A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
    Oncotarget, 2019, V. 10, N 51, Pp 5267-5297 doi:10.18632/oncotarget.27085
  250. E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
    Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units
    Molecules 2019, 24(17), 3186 doi:10.3390/molecules24173186, IF=3.59
  251. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  252. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  253. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  254. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  255. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  256. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  257. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  258. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  259. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  260. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  261. E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
    The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
    IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544
  262. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  263. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  264. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  265. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  266. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  267. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  268. A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
    Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
    IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368
  269. E. Babaylova, A. Malygin, A. Gopanenko, D. Graifer, G. Karpova
    Tetrapeptide 60-63 of human ribosomal protein uS3 is crucial for translation initiation
    Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2019, V. 1862, N 9, 194411 doi:10.1016/j.bbagrm.2019.194411, IF=4.598
  270. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  271. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  272. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  273. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  274. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  275. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  276. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  277. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  278. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  279. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  280. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  281. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  282. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  283. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  284. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  285. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  286. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  287. K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
    Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
    Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256
  288. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  289. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  290. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  291. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  292. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  293. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  294. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  295. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  296. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  297. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  298. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  299. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  300. М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
    Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868
  301. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  302. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  303. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  304. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  305. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  306. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  307. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  308. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  309. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  310. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  311. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  312. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
    Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
    Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567
  313. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
    Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
    Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567
  314. О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
    Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
    Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567
  315. Т.П. Кукина, И.А. Елшин, О.И. Сальникова, И.В. Ельцов
    Алифатические и тритерпеновые продукты омыления эфирных экстрактов POPULUS NIGRA L
    Химия растительного сырья. 2019. № 3. С. 109-118. (Aliphatic and triterpenoic products of ether extracts saponification of POPULUS NIGRA L/ T. P. Kukina, I. A. Elshin , O. I. Salnikova , I. V. Eltsov// doi:10.14258/jcprm.2019034951)
  316. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  317. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  318. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  319. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  320. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  321. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  322. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  323. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  324. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  325. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  326. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
  327. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
    Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056
  328. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
    Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056
  329. B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
    Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056
  330. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
    Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
  331. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
    Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
  332. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
    Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
  333. D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
    Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
    IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052
  334. Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
    Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595
  335. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
    Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
    Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
  336. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
    Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
    Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
  337. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
    Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
    Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
  338. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
  339. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
  340. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
  341. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
  342. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  343. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  344. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  345. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  346. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  347. O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
    Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
    Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59
  348. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  349. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  350. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  351. K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
    Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
    Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035
  352. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
    The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
    Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
  353. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
    The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
    Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
  354. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
    The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
    Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
  355. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
    The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
    Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
  356. V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
    The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
    Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255
  357. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
    Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
    Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
  358. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
    Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
    Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
  359. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
    Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
    Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
  360. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
    Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
    Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
  361. V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
    Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
    Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255
  362. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  363. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  364. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  365. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  366. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  367. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
    Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148
  368. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  369. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  370. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  371. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  372. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  373. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  374. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  375. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  376. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  377. М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
    Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
    Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204
  378. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  379. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  380. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  381. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  382. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  383. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  384. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  385. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  386. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  387. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  388. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  389. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  390. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  391. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  392. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  393. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  394. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  395. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  396. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  397. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  398. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  399. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  400. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  401. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  402. Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
    Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
    Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541
  403. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
  404. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
  405. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
  406. A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
    Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
    Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59
  407. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  408. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  409. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  410. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  411. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  412. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  413. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  414. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  415. A. Ochkasova, M. Meschaninova, A. Venyaminova, A. Ivanov, D. Graifer, G. Karpova
    The human ribosome as a possible mRNA quality controller that recognizes the abasic site by protein uS3
    FEBS OPEN BIO, V. 9, Pp 163-163, Suppl. 1 Аннотация к встрече: P-11-010, WOS:000486972402108, IF=1.958
  416. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
    Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
    JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
  417. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
    Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
    JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
  418. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
    Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
    JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
  419. M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
    Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
    JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97
  420. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  421. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  422. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  423. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  424. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  425. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  426. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
  427. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  428. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  429. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  430. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  431. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  432. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  433. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  434. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  435. O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
    Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
    Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862
  436. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  437. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  438. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  439. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  440. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  441. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  442. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  443. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  444. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  445. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  446. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
    Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
  447. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
    Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
  448. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
    Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
  449. T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
    Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136
  450. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
    Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
    Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
  451. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
    Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
    Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
  452. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
    Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
    Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
  453. M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
    Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
    Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882)
  454. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
    Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
    Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
  455. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
    Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
    Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
  456. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
    Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
    Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
  457. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
    Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
    Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
  458. A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
    Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
    Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849
  459. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
    Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
    Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
  460. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
    Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
    Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
  461. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
    Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
    Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
  462. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
    Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
    Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129)
  463. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
    Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
    Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
  464. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
    Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
    Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
  465. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
    Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
    Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
  466. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
    Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
    Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
  467. Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
    Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
    Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636
  468. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  469. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  470. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  471. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  472. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  473. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  474. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  475. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  476. A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
    Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
    Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567
  477. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  478. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  479. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  480. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  481. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  482. A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
    Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
    Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705
  483. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
    Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
    Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
  484. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
    Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
    Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
  485. N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
    Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
    Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52
  486. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  487. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  488. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  489. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  490. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  491. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
    Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
    Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615
  492. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  493. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  494. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  495. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  496. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  497. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  498. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  499. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  500. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  501. D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
    Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
    Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629
  502. V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
    Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
    Journal of Soils and Sediments, 2019, V. 19, N 6, pp 2697-2707 doi:10.1007/s11368-018-2097-x, IF=2.669
  503. V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
    Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
    Journal of Soils and Sediments, 2019, V. 19, N 6, pp 2697-2707 doi:10.1007/s11368-018-2097-x, IF=2.669
  504. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
    Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
    Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
  505. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
    Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
    Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
  506. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
    Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
    Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
  507. T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
    Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
    Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929
  508. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  509. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  510. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  511. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  512. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  513. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  514. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  515. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
  516. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Д.Е. Семенов, А.Е. Просенко
    Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
    Бюллетень экспериментальной биологии и медицины. 2019. Т. 167. № 6. С. 772-776. (Morphological analysis of prostatotropic activity of (3,5-dimethyl-4-hydroxy) benzyltiodyododecan in the model of benign prostatic hyperplasia in rats/ S.A. Nizomov, I.V. Sorokina, N.A. Zhukova, T.G. Tolstikova, D.E. Semenov, A.E. Prosenko// Bulletin of Experimental Biology and Medicine, 2019, V. 167, N 6, pp 809-812 doi:10.1007/s10517-019-04628-4), IF=0.567
  517. С.А. Низомов, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Д.Е. Семенов, А.Е. Просенко
    Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
    Бюллетень экспериментальной биологии и медицины. 2019. Т. 167. № 6. С. 772-776. (Morphological analysis of prostatotropic activity of (3,5-dimethyl-4-hydroxy) benzyltiodyododecan in the model of benign prostatic hyperplasia in rats/ S.A. Nizomov, I.V. Sorokina, N.A. Zhukova, T.G. Tolstikova, D.E. Semenov, A.E. Prosenko// Bulletin of Experimental Biology and Medicine, 2019, V. 167, N 6, pp 809-812 doi:10.1007/s10517-019-04628-4), IF=0.567
  518. A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
    Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
    Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541
  519. A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
    Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
    Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541
  520. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
    Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
    J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
  521. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
    Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
    J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
  522. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  523. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  524. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  525. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  526. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  527. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  528. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
    Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
    International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213
  529. T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
    Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
    Journal of Antibiotics, 2019, V. 72, pp 590-599 doi:10.1038/s41429-019-0191-y, IF=2.446
  530. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
    Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
    Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
  531. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
    Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
    Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
  532. S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
    Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
    Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139
  533. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  534. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  535. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  536. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  537. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  538. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  539. T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
    Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
    Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802
  540. D. Stass, E. Tretyakov
    Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
    Magnetochemistry, 2019, 5(2), 32 (This article belongs to the Special Issue Controlling Molecular Nanomagnets) doi:10.3390/magnetochemistry5020032
  541. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  542. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  543. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  544. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  545. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  546. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  547. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  548. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  549. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  550. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  551. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
    Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
    Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
  552. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
    Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
    Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
  553. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
    Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
    Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
  554. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
    Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
    Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
  555. I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
    Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
    Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831
  556. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  557. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  558. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  559. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  560. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  561. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  562. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  563. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  564. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  565. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  566. P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
    Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
    Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372
  567. N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
    p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
    Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08
  568. N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
    p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
    Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08
  569. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  570. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  571. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  572. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  573. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  574. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  575. Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
    Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
    International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784
  576. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
  577. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
  578. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
  579. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
  580. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
  581. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  582. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  583. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  584. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  585. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  586. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  587. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  588. T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
    Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
    Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284
  589. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
    Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
  590. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
    Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
  591. И.В. Нечепуренко, Е.Д. Широкова, М.В. Хвостов, Т.С. Фролова, О.И. Синицина, А.М. Максимов, Р.А. Бредихин, Н.И. Комарова, Д.С. Фадеев, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014
  592. И.В. Нечепуренко, Е.Д. Широкова, М.В. Хвостов, Т.С. Фролова, О.И. Синицина, А.М. Максимов, Р.А. Бредихин, Н.И. Комарова, Д.С. Фадеев, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014
  593. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014
  594. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014
  595. А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014
  596. А.Г. Потапов, И.К. Шундрина
    Влияние алифатических диолов и дикарбоновых кислот на свойства сополиэфиров этиленсукцината
    Высокомолекулярные соединения. Серия А. 2019. Т. 61. № 5. С. 387-397. (DOI: 10.1134/S2308112019050146) (Effect of Aliphatic Diols and Dicarboxylic Acids on the Properties of Ethylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2019, V. 61, N 5, pp 544-554 doi:10.1134/S0965545X19050146), IF=0.984
  597. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
    О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
    Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751
  598. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
    О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
    Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751
  599. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
    О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
    Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751
  600. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
    О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
    Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751
  601. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
    О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
    Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751
  602. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  603. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  604. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  605. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  606. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  607. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  608. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  609. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  610. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  611. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  612. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  613. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  614. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  615. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  616. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  617. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  618. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  619. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  620. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  621. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  622. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  623. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  624. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  625. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  626. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  627. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  628. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  629. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  630. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  631. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  632. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  633. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  634. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  635. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  636. Л.В. ПОЛИТАНСКАЯ, Г.А. СЕЛИВАНОВА, Е.В. ПАНТЕЛЕЕВА, Е.В. ТРЕТЬЯКОВ, В.Е. ПЛАТОНОВ, П.В. НИКУЛЬШИН, А.С. ВИНОГРАДОВ, Я.В. ЗОНОВ, В.М. КАРПОВ, Т.В. МЕЖЕНКОВА, А.В. ВАСИЛЬЕВ, А.Б. КОЛДОБСКИЙ, О.С. ШИЛОВА, С.М. МОРОЗОВА, Я.В. БУРГАРТ, Е.В. ЩЕГОЛЬКОВ, В.И. САЛОУТИН, В.Б. СОКОЛОВ, А.Ю. АКСИНЕНКО, В.Г. НЕНАЙДЕНКО, М.Ю. МОСКАЛИК, В.В. АСТАХОВА, Б.А. ШАИНЯН, А.А. ТАБОЛИН, С.Л. ИОФФЕ, В.М. МУЗАЛЕВСКИЙ, Е.С. БАЛЕНКОВА, А.В. ШАСТИН, А.А. ТЮТЮНОВ, В.Э. БОЙКО, С.М. ИГУМНОВ, А.Д. ДИЛЬМАН, Н.Ю. АДОНИН, В.В. БАРДИН, С.М. МАСОУД, Д.В. ВОРОБЬЕВА, С.Н. ОСИПОВ, Э.В. НОСОВА, Г.Н. ЛИПУНОВА, В.Н. ЧАРУШИН, Д.О. ПРИМА, А.Г. МАКАРОВ, А.В. ЗИБАРЕВ, Б.А. ТРОФИМОВ, Л.Н. СОБЕНИНА, К.В. БЕЛЯЕВА, В.Я. СОСНОВСКИХ, Д.Л. ОБЫДЕННОВ, С.А. УСАЧЕВ
    Перспективные точки роста и вызовы фторорганической химии
    Успехи химии. 2019. Т. 88. № 5. С. 425-569. DOI:10.1070/RCR4871 (Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp), IF=4.612
  637. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  638. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  639. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  640. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  641. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  642. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  643. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  644. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  645. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  646. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  647. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  648. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  649. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  650. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  651. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  652. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  653. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  654. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  655. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  656. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  657. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  658. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  659. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  660. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  661. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  662. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  663. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  664. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  665. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  666. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  667. E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.V. Khvostov, N.E. Polyakov, O. Yu. Selyutina, T.G. Tolstikova, T.S. Frolova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
    Journal of Drug Delivery Science and Technology, V. 50, April 2019, Pp 66-77 doi:10.1016/j.jddst.2019.01.014, IF=2.606
  668. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  669. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  670. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  671. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  672. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  673. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
    CrystEngComm, 2019, V. 21, N 15, Pp 2524-2533 doi:10.1039/C9CE00073A, IF=3.382
  674. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
    CrystEngComm, 2019, V. 21, N 15, Pp 2524-2533 doi:10.1039/C9CE00073A, IF=3.382
  675. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
    CrystEngComm, 2019, V. 21, N 15, Pp 2524-2533 doi:10.1039/C9CE00073A, IF=3.382
  676. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
    CrystEngComm, 2019, V. 21, N 15, Pp 2524-2533 doi:10.1039/C9CE00073A, IF=3.382
  677. K.P. Cheremnykh, V.A. Savelyev, M.A. Pokrovskii, D.S. Baev, T.G. Tolstikova, A.G. Pokrovskii, E.E. Shults
    Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 545–558 doi:10.1007/s00044-019-02314-8, IF=1.72
  678. K.P. Cheremnykh, V.A. Savelyev, M.A. Pokrovskii, D.S. Baev, T.G. Tolstikova, A.G. Pokrovskii, E.E. Shults
    Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 545–558 doi:10.1007/s00044-019-02314-8, IF=1.72
  679. N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
    Effect of chiral polyhydrochromenes on cannabinoid system
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
  680. N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
    Effect of chiral polyhydrochromenes on cannabinoid system
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
  681. N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
    Effect of chiral polyhydrochromenes on cannabinoid system
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
  682. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, V.G. Shubin, H.S. Rzepa
    Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
    Org. Biomol. Chem., 2019, V. 17, N 15, pp 3781-3789 doi:10.1039/C9OB00607A, IF=3.49
  683. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  684. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  685. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  686. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  687. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  688. Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
    Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
    Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441
  689. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  690. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  691. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  692. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  693. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  694. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  695. J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
    Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
    Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06
  696. Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
    Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
    Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259
  697. Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
    Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
    Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259
  698. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  699. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  700. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  701. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  702. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  703. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  704. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  705. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  706. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  707. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
  708. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
    Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
    Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
  709. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
    Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
    Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
  710. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
    Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
    Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
  711. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
    Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
    Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
  712. D. V. Telegina, N.G. Kolosova, O. S. Kozhevnikova
    Immunohistochemical localization of NGF, BDNF, and their receptors in a normal and AMD-like rat retina
    BMC Medical Genomics, March 2019, 12(Supp. 2):48 (From 11th International Multiconference “Bioinformatics of Genome Regulation and StructureSystems Biology” - BGRSSB-2018 Novosibirsk, Russia. 20-25 August 2018) doi:10.1186/s12920-019-0493-8, IF=2.568
  713. D. V. Telegina, N.G. Kolosova, O. S. Kozhevnikova
    Immunohistochemical localization of NGF, BDNF, and their receptors in a normal and AMD-like rat retina
    BMC Medical Genomics, March 2019, 12(Supp. 2):48 (From 11th International Multiconference “Bioinformatics of Genome Regulation and StructureSystems Biology” - BGRSSB-2018 Novosibirsk, Russia. 20-25 August 2018) doi:10.1186/s12920-019-0493-8, IF=2.568
  714. Ju.A. Sidorova, K.P. Volcho, N.F. Salakhutdinov
    Neuroregeneration in Parkinson’s Disease: From Proteins to Small Molecules
    Current Neuropharmacology, 2019,V. 17 , N 3 , Pp. 268 - 287 doi:10.2174/1570159X16666180905094123, IF=4.568
  715. V. Morozov, E. Tretyakov
    Spin polarization in graphene nanoribbons functionalized with nitroxide
    Journal of Molecular Modeling, 2019, V.25, N 3, Article 58 doi:10.1007/s00894-019-3944-4, IF=1.335
  716. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  717. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  718. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  719. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  720. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  721. V.E. Evtushok, A.Yu. Vorob'ev
    Synthesis of pyrazolo- and [1,2,4]triazolo-[1,5-а]quinolin-9-ols by cycloaddition to 8-hydroxyquinoline N-imide
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 3, pp 229-234 doi:10.1007/s10593-019-02446-0, IF=1.492
  722. П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
    Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
    Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014
  723. П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
    Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
    Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014
  724. П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
    Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
    Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014
  725. П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
    Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
    Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014
  726. И.В. Береговая, Л.Н. Щеголева, В.И. Боровков, В.М. Карпов
    Анион-радикал перфторбензоциклобутена - структурно нежесткая частица
    Журнал структурной химии. 2019. Т. 60. № 3. С. 392-395. DOI:10.26902/JSC_id39468 (Perfluorobenzocyclobutene radical anion: A structurally flexible particle/ I.V. Beregovaya, L.N. Shchegoleva, V.I. Borovkov, V.M. Karpov// Journal of Structural Chemistry, 2019, V. 60, N 3, pp 373-376 doi:10.1134/S0022476619030041), IF=0.541
  727. Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
    Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
    Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751
  728. Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
    Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
    Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751
  729. D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
    Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
    ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716
  730. D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
    Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
    ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716
  731. D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
    Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
    ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716
  732. M. Edeleva, G. Audran, S. Marque, E. Bagryanskaya
    Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
    Materials, 2019, V. 12, N 5, Pp. 688-707 doi:10.3390/ma12050688, IF=2.972
  733. M. Edeleva, G. Audran, S. Marque, E. Bagryanskaya
    Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
    Materials, 2019, V. 12, N 5, Pp. 688-707 doi:10.3390/ma12050688, IF=2.972
  734. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
    Molecular receptors for recognition and sensing of nucleotides
    Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
  735. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
    Molecular receptors for recognition and sensing of nucleotides
    Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
  736. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
    Molecular receptors for recognition and sensing of nucleotides
    Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
  737. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
    Molecular receptors for recognition and sensing of nucleotides
    Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
  738. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  739. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  740. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  741. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  742. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  743. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  744. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  745. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  746. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  747. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  748. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  749. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  750. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  751. A.Kulikov,N.Sinyakova,E.Kulikova,N.Evglevsky,I.Kolotygin,K.Volcho,N.Salakhutdinov,V.Kulikov,A.Romaschenko,M.Moshkin
    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
    European Neuropsychopharmacology, V. 29, Supplement 1, 2019, Pp S198-S199, P.216 doi:10.1016/j.euroneuro.2018.11.330, IF=4.468
  752. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  753. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  754. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  755. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  756. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  757. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  758. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  759. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  760. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  761. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  762. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  763. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  764. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  765. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  766. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  767. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  768. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  769. M. Edeleva, D. Morozov, D. Parkhomenko, Yu. Polienko, A. Iurchenkova, I. Kirilyuk, E. Bagryanskaya
    Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization
    Chem. Commun., 2019,V. 55, N 2, Pp 190-193 doi:10.1039/C8CC08541B, IF=6.164
  770. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  771. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  772. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  773. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  774. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  775. K.A. Vinogradova, N.A. Shekhovtsov, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, I.V. Plokhikh, M.B. Bushuev
    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
    Inorganic Chemistry Communications, V. 100, February 2019, Pp 11-15 doi:10.1016/j.inoche.2018.12.002, IF=1.795
  776. Д.М. Могнонов, О.Ж. Аюрова, Д.Ш. Ширапов, С.В. Морозов, А.М. Мангадаев
    Оценка корректности результатов обращенной газовой хроматографии при определении термодинамической совместимости полимерных смесей
    Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (Evaluation of the correctness of the results reversed gas chromatography in determining thermodynamiccompatibility polymer blends/ Mognonov D. M., Ayurova O. Zh.1, Shirapov D. Sh., Morozov S.ergei V., Mangadaev A. M.// Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (in Russian) doi:10.17308/sorpchrom.2019.19/651)
  777. Д.М. Могнонов, О.Ж. Аюрова, Д.Ш. Ширапов, С.В. Морозов, А.М. Мангадаев
    Оценка корректности результатов обращенной газовой хроматографии при определении термодинамической совместимости полимерных смесей
    Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (Evaluation of the correctness of the results reversed gas chromatography in determining thermodynamiccompatibility polymer blends/ Mognonov D. M., Ayurova O. Zh.1, Shirapov D. Sh., Morozov S.ergei V., Mangadaev A. M.// Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (in Russian) doi:10.17308/sorpchrom.2019.19/651)
  778. Д.М. Могнонов, О.Ж. Аюрова, Д.Ш. Ширапов, С.В. Морозов, А.М. Мангадаев
    Оценка корректности результатов обращенной газовой хроматографии при определении термодинамической совместимости полимерных смесей
    Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (Evaluation of the correctness of the results reversed gas chromatography in determining thermodynamiccompatibility polymer blends/ Mognonov D. M., Ayurova O. Zh.1, Shirapov D. Sh., Morozov S.ergei V., Mangadaev A. M.// Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (in Russian) doi:10.17308/sorpchrom.2019.19/651)
  779. Д.М. Могнонов, О.Ж. Аюрова, Д.Ш. Ширапов, С.В. Морозов, А.М. Мангадаев
    Оценка корректности результатов обращенной газовой хроматографии при определении термодинамической совместимости полимерных смесей
    Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (Evaluation of the correctness of the results reversed gas chromatography in determining thermodynamiccompatibility polymer blends/ Mognonov D. M., Ayurova O. Zh.1, Shirapov D. Sh., Morozov S.ergei V., Mangadaev A. M.// Сорбционные и хроматографические процессы. 2019. Т. 19. № 1. С. 67-74. (in Russian) doi:10.17308/sorpchrom.2019.19/651)
  780. Д.И. Деревянко, Н.А. Орлова, В.В. Шелковников, И.К. Шундрина, Б.Г. Гольденберг, В.П. Корольков
    Формирование высокоаспектных микроструктур на тетраакрилат/акриламидных мономерах под действием синхротронного излучения
    Химия высоких энергий. 2019. Т. 53. № 2. С. 127-134. (Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048), IF=0.634
  781. Д.И. Деревянко, Н.А. Орлова, В.В. Шелковников, И.К. Шундрина, Б.Г. Гольденберг, В.П. Корольков
    Формирование высокоаспектных микроструктур на тетраакрилат/акриламидных мономерах под действием синхротронного излучения
    Химия высоких энергий. 2019. Т. 53. № 2. С. 127-134. (Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048), IF=0.634
  782. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  783. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  784. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  785. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  786. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  787. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  788. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  789. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  790. N. Dyrkheeva, O. Luzina, A. Filimonov, O. Zakharova, E. Ilina, A. Zakharenko, M. Kuprushkin, D. Nilov, I. Gushchina, V. Svedas, N. Salakhutdinov, O. Lavrik
    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
    Planta Medica, 2019, V. 85, N 2, Pp 103-111 doi:10.1055/a-0681-7069, IF=2.746
  791. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  792. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  793. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  794. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  795. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  796. С.В. Ларионов, М.И. Рахманова, Л.А. Глинская, Д.Ю. Наумов, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Комплексы Zn(II) с анионами тетрафтортерефталевой, октафторбифенил- 4,4'-дикарбоновой кислот и 1,10-фенантролином
    Журнал общей химии, 2019, Т. 89, N 2, Cc. 265-270, DOI: 10.1134/S0044460X1902015X (Zinc(II) Complexes with Tetrafluoroterephthalic and Octafluorobiphenyl-4,4'-dicarboxylic Acid Anions and 1,10-Phenanthroline/ S. V. Larionov, M. I. Rakhmanova, L. A. Glinskaya, D. Yu. Naumov, A. S. Vinogradov, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2019, V. 89, N 2, pp 261-265 doi:10.1134/S1070363219020154), IF=0.643
  797. С.В. Ларионов, М.И. Рахманова, Л.А. Глинская, Д.Ю. Наумов, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Комплексы Zn(II) с анионами тетрафтортерефталевой, октафторбифенил- 4,4'-дикарбоновой кислот и 1,10-фенантролином
    Журнал общей химии, 2019, Т. 89, N 2, Cc. 265-270, DOI: 10.1134/S0044460X1902015X (Zinc(II) Complexes with Tetrafluoroterephthalic and Octafluorobiphenyl-4,4'-dicarboxylic Acid Anions and 1,10-Phenanthroline/ S. V. Larionov, M. I. Rakhmanova, L. A. Glinskaya, D. Yu. Naumov, A. S. Vinogradov, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2019, V. 89, N 2, pp 261-265 doi:10.1134/S1070363219020154), IF=0.643
  798. С.В. Ларионов, М.И. Рахманова, Л.А. Глинская, Д.Ю. Наумов, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Комплексы Zn(II) с анионами тетрафтортерефталевой, октафторбифенил- 4,4'-дикарбоновой кислот и 1,10-фенантролином
    Журнал общей химии, 2019, Т. 89, N 2, Cc. 265-270, DOI: 10.1134/S0044460X1902015X (Zinc(II) Complexes with Tetrafluoroterephthalic and Octafluorobiphenyl-4,4'-dicarboxylic Acid Anions and 1,10-Phenanthroline/ S. V. Larionov, M. I. Rakhmanova, L. A. Glinskaya, D. Yu. Naumov, A. S. Vinogradov, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2019, V. 89, N 2, pp 261-265 doi:10.1134/S1070363219020154), IF=0.643
  799. С.В. Ларионов, М.И. Рахманова, Л.А. Глинская, Д.Ю. Наумов, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Комплексы Zn(II) с анионами тетрафтортерефталевой, октафторбифенил- 4,4'-дикарбоновой кислот и 1,10-фенантролином
    Журнал общей химии, 2019, Т. 89, N 2, Cc. 265-270, DOI: 10.1134/S0044460X1902015X (Zinc(II) Complexes with Tetrafluoroterephthalic and Octafluorobiphenyl-4,4'-dicarboxylic Acid Anions and 1,10-Phenanthroline/ S. V. Larionov, M. I. Rakhmanova, L. A. Glinskaya, D. Yu. Naumov, A. S. Vinogradov, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2019, V. 89, N 2, pp 261-265 doi:10.1134/S1070363219020154), IF=0.643
  800. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
    От 1,2,5-оксадиазоло[3,4-g]индолов к пирроло[2,3-f]хиноксалинам в одну препаративную стадию
    Журнал органической химии. 2019. Т. 55. № 2. С. 311-313. (From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage/ A.B. Budaev, A.V. Ivanov, O.V. Petrova, A.Ya. Tikhonov, V.A. Samsonov, L.N. Sobenina, B.A. Trofimov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 273-275 doi:10.1134/S1070428019020234), IF=0.751
  801. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
    От 1,2,5-оксадиазоло[3,4-g]индолов к пирроло[2,3-f]хиноксалинам в одну препаративную стадию
    Журнал органической химии. 2019. Т. 55. № 2. С. 311-313. (From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage/ A.B. Budaev, A.V. Ivanov, O.V. Petrova, A.Ya. Tikhonov, V.A. Samsonov, L.N. Sobenina, B.A. Trofimov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 273-275 doi:10.1134/S1070428019020234), IF=0.751
  802. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
    От 1,2,5-оксадиазоло[3,4-g]индолов к пирроло[2,3-f]хиноксалинам в одну препаративную стадию
    Журнал органической химии. 2019. Т. 55. № 2. С. 311-313. (From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage/ A.B. Budaev, A.V. Ivanov, O.V. Petrova, A.Ya. Tikhonov, V.A. Samsonov, L.N. Sobenina, B.A. Trofimov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 273-275 doi:10.1134/S1070428019020234), IF=0.751
  803. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
    От 1,2,5-оксадиазоло[3,4-g]индолов к пирроло[2,3-f]хиноксалинам в одну препаративную стадию
    Журнал органической химии. 2019. Т. 55. № 2. С. 311-313. (From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage/ A.B. Budaev, A.V. Ivanov, O.V. Petrova, A.Ya. Tikhonov, V.A. Samsonov, L.N. Sobenina, B.A. Trofimov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 273-275 doi:10.1134/S1070428019020234), IF=0.751
  804. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
    От 1,2,5-оксадиазоло[3,4-g]индолов к пирроло[2,3-f]хиноксалинам в одну препаративную стадию
    Журнал органической химии. 2019. Т. 55. № 2. С. 311-313. (From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage/ A.B. Budaev, A.V. Ivanov, O.V. Petrova, A.Ya. Tikhonov, V.A. Samsonov, L.N. Sobenina, B.A. Trofimov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 273-275 doi:10.1134/S1070428019020234), IF=0.751
  805. R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, T.V. Rybalova, E.V. Tretyakov
    Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles
    J. Org. Chem., 2019, 84 (2), pp 963-972 doi:10.1021/acs.joc.8b02904, IF=4.745
  806. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  807. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  808. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  809. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  810. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  811. A.B. Budaev, A.V. Ivanov, O.V. Petrova, V.A. Samsonov, I.A. Ushakov, A.Ya. Tikhonov, L.N. Sobenina, B.A. Trofimov
    1,2,5-Oxadiazolo[3,4-g]indoles via annelation of 6,7-dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one oxime with acetylene
    Mendeleev Communications, 2019, V. 29, N 1, Pp 53-54 doi:10.1016/j.mencom.2019.01.016, IF=2.01
  812. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  813. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  814. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  815. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  816. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  817. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  818. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  819. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  820. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  821. V.A. Sannikova, M.P. Davydova, P.S. Sherin, S.V. Babenko, V.V. Korolev, A.A. Stepanov, P.V. Nikul'shin, E.V. Kalneus, S.F. Vasilevsky, E. Benassi, A.R. Melnikov
    Determination of Hyperfine Coupling Constants of Fluorinated Diphenylacetylene Radical Anions by Magnetic Field-Affected Reaction Yield Spectroscopy
    J. Phys. Chem. A, 2019, 123 (2), pp 505-516 doi:10.1021/acs.jpca.8b10306, IF=2.641
  822. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  823. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  824. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  825. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  826. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  827. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  828. M.Y. Pakharukova, V.A. Samsonov, E.A. Serbina, V.A. Mordvinov
    A study of tribendimidine effects in vitro and in vivo on the liver fluke Opisthorchis felineus
    Parasites & Vectors, 2019, V.12, N 1, Art. Num 23 doi:10.1186/s13071-019-3288-z, IF=3.031
  829. M.Y. Pakharukova, V.A. Samsonov, E.A. Serbina, V.A. Mordvinov
    A study of tribendimidine effects in vitro and in vivo on the liver fluke Opisthorchis felineus
    Parasites & Vectors, 2019, V.12, N 1, Art. Num 23 doi:10.1186/s13071-019-3288-z, IF=3.031
  830. M.Y. Pakharukova, V.A. Samsonov, E.A. Serbina, V.A. Mordvinov
    A study of tribendimidine effects in vitro and in vivo on the liver fluke Opisthorchis felineus
    Parasites & Vectors, 2019, V.12, N 1, Art. Num 23 doi:10.1186/s13071-019-3288-z, IF=3.031
  831. D.I. Sharapa, A. Genaev, L. Cavallo, Yu. Minenkov
    A Robust and Cost-Efficient Scheme for Accurate Conformational Energies of Organic Molecules
    ChemPhysChem, 2019, V. 20, N 1, Pp 92-102 doi:10.1002/cphc.201801063, IF=3.077
  832. D.I. Sharapa, A. Genaev, L. Cavallo, Yu. Minenkov
    A Robust and Cost-Efficient Scheme for Accurate Conformational Energies of Organic Molecules
    ChemPhysChem, 2019, V. 20, N 1, Pp 92-102 doi:10.1002/cphc.201801063, IF=3.077
  833. D.I. Sharapa, A. Genaev, L. Cavallo, Yu. Minenkov
    A Robust and Cost-Efficient Scheme for Accurate Conformational Energies of Organic Molecules
    ChemPhysChem, 2019, V. 20, N 1, Pp 92-102 doi:10.1002/cphc.201801063, IF=3.077
  834. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  835. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  836. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  837. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  838. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  839. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  840. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  841. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  842. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  843. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  844. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  845. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  846. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  847. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  848. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  849. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  850. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  851. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  852. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  853. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  854. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
  855. С.В. Деревяшкин, Е.А. Соболева, В.В. Шелковников, А.И. Малышев, В.П. Корольков
    Маскирующие свойства структур на основе триакриламидного производного полифторхалкона при жидкостном и реактивном ионном травлении
    Микроэлектроника, 2019. №1, С. 16-30. (Masking Properties of Structures Based on a Triacrylamide Derivative of Polyfluorochalcone at Wet and Reactive Ion Etching/ S. V. Derevyashkin, E. A. Soboleva V. V. Shelkovnikov, A. I. Malyshev, V. P. Korolkov// Russian Microelectronics, 2019, V. 48, N 1, pp 13-27 doi:10.1134/S1063739719010037)
  856. С.В. Деревяшкин, Е.А. Соболева, В.В. Шелковников, А.И. Малышев, В.П. Корольков
    Маскирующие свойства структур на основе триакриламидного производного полифторхалкона при жидкостном и реактивном ионном травлении
    Микроэлектроника, 2019. №1, С. 16-30. (Masking Properties of Structures Based on a Triacrylamide Derivative of Polyfluorochalcone at Wet and Reactive Ion Etching/ S. V. Derevyashkin, E. A. Soboleva V. V. Shelkovnikov, A. I. Malyshev, V. P. Korolkov// Russian Microelectronics, 2019, V. 48, N 1, pp 13-27 doi:10.1134/S1063739719010037)
  857. Н.В. Полосьмак, С.С. Шацкая, М.В. Задорожный, Л.П. Кундо, Е.В. Карпова
    Результаты исследований золотых изделий из погребений Хунну Ноин-Ула (Монголия)
    Археология, этнография и антропология Евразии. 2019. Т. 47. № 1. С. 83-94. (The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094)
  858. Н.В. Полосьмак, С.С. Шацкая, М.В. Задорожный, Л.П. Кундо, Е.В. Карпова
    Результаты исследований золотых изделий из погребений Хунну Ноин-Ула (Монголия)
    Археология, этнография и антропология Евразии. 2019. Т. 47. № 1. С. 83-94. (The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094)
  859. Н.В. Полосьмак, С.С. Шацкая, М.В. Задорожный, Л.П. Кундо, Е.В. Карпова
    Результаты исследований золотых изделий из погребений Хунну Ноин-Ула (Монголия)
    Археология, этнография и антропология Евразии. 2019. Т. 47. № 1. С. 83-94. (The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094)
  860. Н.В. Полосьмак, С.С. Шацкая, М.В. Задорожный, Л.П. Кундо, Е.В. Карпова
    Результаты исследований золотых изделий из погребений Хунну Ноин-Ула (Монголия)
    Археология, этнография и антропология Евразии. 2019. Т. 47. № 1. С. 83-94. (The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094)
  861. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  862. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  863. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  864. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  865. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  866. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  867. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  868. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  869. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  870. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  871. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  872. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  873. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  874. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  875. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  876. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  877. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  878. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  879. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  880. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  881. A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, V.I. Kaledin, V.P. Nikolin, N.A. Popova, J. Patel, O.D. Zakharova, A.A. Chepanova, A. Zafar, J. Reynisson, E. Leung, I.K-H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel tyrosyl-DNA phosphodiesterase 1 inhibitors enhance the therapeutic impact of topoteсan on in vivo tumor models
    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
  882. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  883. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  884. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  885. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  886. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  887. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643
  888. M.A. Gromova, Yu.V. Kharitonov, M.A. Pokrovskii, I.Yu. Bagryanskaya, A.G. Pokrovskii, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes
    Chemistry of Natural Compounds, 2019, V. 55, N 1, pp 52-59 doi:10.1007/s10600-019-02613-x, IF=0.567
  889. M.A. Gromova, Yu.V. Kharitonov, M.A. Pokrovskii, I.Yu. Bagryanskaya, A.G. Pokrovskii, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes
    Chemistry of Natural Compounds, 2019, V. 55, N 1, pp 52-59 doi:10.1007/s10600-019-02613-x, IF=0.567
  890. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  891. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  892. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  893. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  894. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  895. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина, И.В. Ельцов, Н.В. Куратьева
    Комплексные соединения сурьмы: {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- и {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ ДМСО. Синтез и строение
    Журнал неорганической химии. 2019. Т. 64. № 1. С. 15-22. DOI:10.1134/S0044457X19010070 (Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078), IF=0.822
  896. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  897. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  898. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  899. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  900. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  901. Кукина Т.П., Щербаков Д.Н., Геньш К.В., Пантелеева Н.В., Тулышева Е.А., Сальникова О.И., Гражданников А.Е., Колосов П.В., Галицын Г.Ю.
    Биоактивные компоненты эфирного экстракта древесной зелени облепихи HIPPOPHAE RHAMNOIDES L
    Химия растительного сырья. 2019. № 1. С. 157-164. (Bioactive components of ethereal extract of wood greening sea buckthorn Hippophae rhamnoides L./ T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, N.V. Panteleyeva, E. A. Tulysheva, O.I. Sal'nikova, A.Ye. Grazhdannikov, P.V. Kolosov, G.Yu. Galitsyn// Khimiya Rastitel'nogo Syr'ya, 2019, N 1, Pp 157-164 doi:10.14258/jcprm.2019014340)
  902. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Реакции 1,4-нафтохинона и 5-гидрокси-1,4-нафтохинона с нингидрином
    Известия Академии наук. Серия химическая. 2019. № 1. С. 86-91. (Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8), IF=1.014
  903. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Реакции 1,4-нафтохинона и 5-гидрокси-1,4-нафтохинона с нингидрином
    Известия Академии наук. Серия химическая. 2019. № 1. С. 86-91. (Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8), IF=1.014
  904. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Реакции 1,4-нафтохинона и 5-гидрокси-1,4-нафтохинона с нингидрином
    Известия Академии наук. Серия химическая. 2019. № 1. С. 86-91. (Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8), IF=1.014
  905. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Реакции 1,4-нафтохинона и 5-гидрокси-1,4-нафтохинона с нингидрином
    Известия Академии наук. Серия химическая. 2019. № 1. С. 86-91. (Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8), IF=1.014
  906. Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
    Реакции 1,4-нафтохинона и 5-гидрокси-1,4-нафтохинона с нингидрином
    Известия Академии наук. Серия химическая. 2019. № 1. С. 86-91. (Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8), IF=1.014
  907. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  908. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  909. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  910. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  911. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  912. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
  913. P. Fedyushin, E. Panteleeva, I. Bagryanskaya, K. Maryunina, K. Inoue, D. Stass, E. Tretyakov
    An approach to fluorinated phthalonitriles containing a nitronyl nitroxide or iminonitroxide moiety
    Journal of Fluorine Chemistry, 2019, V. 217, Pp 1-7 doi:10.1016/j.jfluchem.2018.10.016, IF=2.055
  914. P. Fedyushin, E. Panteleeva, I. Bagryanskaya, K. Maryunina, K. Inoue, D. Stass, E. Tretyakov
    An approach to fluorinated phthalonitriles containing a nitronyl nitroxide or iminonitroxide moiety
    Journal of Fluorine Chemistry, 2019, V. 217, Pp 1-7 doi:10.1016/j.jfluchem.2018.10.016, IF=2.055
  915. P. Fedyushin, E. Panteleeva, I. Bagryanskaya, K. Maryunina, K. Inoue, D. Stass, E. Tretyakov
    An approach to fluorinated phthalonitriles containing a nitronyl nitroxide or iminonitroxide moiety
    Journal of Fluorine Chemistry, 2019, V. 217, Pp 1-7 doi:10.1016/j.jfluchem.2018.10.016, IF=2.055

2018

Reviews, articles

  1. D. Stass, E. Tretyakov
    Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
    Magnetochemistry, 2019, V.5, N 2, P 32-40 doi:10.3390/magnetochemistry5020032
  2. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  3. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  4. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  5. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  6. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  7. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  8. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
  9. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  10. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  11. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  12. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  13. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
    Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
    Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
  14. A.V. Artem'ev, I.Yu. Bagryanskaya
    [Cu4I73-]n: A novel 1-D iodocuprate aggregate
    Journal of Molecular Structure, 2018, V. 1173, Pp. 743-749 doi:10.1016/j.molstruc.2018.07.006, IF=2.011
  15. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  16. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  17. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  18. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  19. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  20. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  21. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  22. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  23. E.A. Kulikova, N.V. Khotskin, N.B. Illarionova, I.E. Sorokin, E.Y. Bazhenova, E.M. Kondaurova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, E. Ponimaskin, V.S. Naumenko, A.V. Kulikov
    Inhibitor of striatal-enriched protein tyrosine phosphatase, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), produces antidepressant-like effect and decreases functional activity and protein level of 5-HT2A receptor in the brain
    Neuroscience, 2018, V. 394, Pp 220-231 doi:10.1016/j.neuroscience.2018.10.031, IF=3.381
  24. O.A. Rakitin, A.V. Zibarev
    Focus Review Recent Progress in Synthesis and Applications of 5-Membered Chalcogen-Nitrogen π-Heterocycles with Three Heteroatoms
    Asian Journal of Organic Chemistry, 2018, V. 7, N 12, Pp 2397-2416 doi:10.1002/ajoc.201800536, IF=2.496
  25. Ch. Tantardini, S.G. Arkipov, K.A. Cherkashina, A.S. Kil'met'ev, E. V.Boldyreva
    Synthesis and crystal structure of a meloxicam co-crystal with benzoic acid
    Structural Chemistry, 2018, V. 29, N 6, pp 1867-1874 doi:10.1007/s11224-018-1166-5, IF=2.19
  26. Ch. Tantardini, S.G. Arkipov, K.A. Cherkashina, A.S. Kil'met'ev, E. V.Boldyreva
    Synthesis and crystal structure of a meloxicam co-crystal with benzoic acid
    Structural Chemistry, 2018, V. 29, N 6, pp 1867-1874 doi:10.1007/s11224-018-1166-5, IF=2.19
  27. Ch. Tantardini, S.G. Arkipov, K.A. Cherkashina, A.S. Kil'met'ev, E. V.Boldyreva
    Synthesis and crystal structure of a meloxicam co-crystal with benzoic acid
    Structural Chemistry, 2018, V. 29, N 6, pp 1867-1874 doi:10.1007/s11224-018-1166-5, IF=2.19
  28. Ch. Tantardini, S.G. Arkipov, K.A. Cherkashina, A.S. Kil'met'ev, E. V.Boldyreva
    Synthesis and crystal structure of a meloxicam co-crystal with benzoic acid
    Structural Chemistry, 2018, V. 29, N 6, pp 1867-1874 doi:10.1007/s11224-018-1166-5, IF=2.19
  29. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  30. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  31. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  32. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  33. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  34. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  35. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  36. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Эфиры и полиметиленэфиры пирокатехина и борной кислоты - синтез, структура
    Южно-Сибирский научный вестник, 2018, N 4(24), Cc 255-260 (Esthers and polymethylenesthers of pyrocatechine and boric acid - synthesis, structure/ M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy// S-SibSB, 2018, N 4 (24), Cc 255-260)
  37. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Эфиры и полиметиленэфиры пирокатехина и борной кислоты - синтез, структура
    Южно-Сибирский научный вестник, 2018, N 4(24), Cc 255-260 (Esthers and polymethylenesthers of pyrocatechine and boric acid - synthesis, structure/ M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy// S-SibSB, 2018, N 4 (24), Cc 255-260)
  38. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Эфиры и полиметиленэфиры пирокатехина и борной кислоты - синтез, структура
    Южно-Сибирский научный вестник, 2018, N 4(24), Cc 255-260 (Esthers and polymethylenesthers of pyrocatechine and boric acid - synthesis, structure/ M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy// S-SibSB, 2018, N 4 (24), Cc 255-260)
  39. М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
    Эфиры и полиметиленэфиры пирокатехина и борной кислоты - синтез, структура
    Южно-Сибирский научный вестник, 2018, N 4(24), Cc 255-260 (Esthers and polymethylenesthers of pyrocatechine and boric acid - synthesis, structure/ M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy// S-SibSB, 2018, N 4 (24), Cc 255-260)
  40. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  41. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  42. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  43. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  44. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  45. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  46. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  47. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  48. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  49. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane
    Org. Biomol. Chem., 2018, V.16, N 47, Pp 9129-9132 doi:10.1039/C8OB02653J, IF=3.423
  50. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane
    Org. Biomol. Chem., 2018, V.16, N 47, Pp 9129-9132 doi:10.1039/C8OB02653J, IF=3.423
  51. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  52. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  53. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  54. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  55. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  56. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Oxygen-induced leakage of spin polarization in Overhauser-enhanced magnetic resonance imaging: application for oximetry in tumors
    Journal of Magnetic Resonance, 2018, V. 297, Pp 42-50 doi:10.1016/j.jmr.2018.10.005, IF=2.586
  57. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  58. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  59. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  60. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  61. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  62. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  63. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  64. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  65. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  66. Yu.P. Ustimenko, A.M. Agafontsev, V.Yu. Komarov, A.V. Tkachev
    Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
    Mendeleev Communications, 2018, V. 28, N 6, Pp 584-586 doi:10.1016/j.mencom.2018.11.006, IF=2.098
  67. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
    Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
    Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
  68. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
    Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
    Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
  69. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
    Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
    Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
  70. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
    Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
    Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
  71. R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, E.V. Tretyakov
    Synthesis of 4'-alkyl-[1,1'-biphenyl]-2,3'-dicarbonitriles via dimerisation of phthalonitrile radical anion in liquid ammonia (18-10764UP)
    Arkivoc,2018, part vii, Pp 349-356 doi:10.24820/ark.5550190.p010.764, IF=1.47
  72. R. Ottenbacher, E. Talsi, T. Rybalova, K.P. Bryliakov
    Enantioselective Benzylic Hydroxylation of Arylalkanes with H2O2 in Fluorinated Alcohols in the Presence of Chiral Mn Aminopyridine Complexes
    ChemCatChem, 2018, V.10, N 22, Pp 5323-5330 doi:10.1002/cctc.201801476, IF=4.673
  73. R. Ottenbacher, E. Talsi, T. Rybalova, K.P. Bryliakov
    Enantioselective Benzylic Hydroxylation of Arylalkanes with H2O2 in Fluorinated Alcohols in the Presence of Chiral Mn Aminopyridine Complexes
    ChemCatChem, 2018, V.10, N 22, Pp 5323-5330 doi:10.1002/cctc.201801476, IF=4.673
  74. R. Ottenbacher, E. Talsi, T. Rybalova, K.P. Bryliakov
    Enantioselective Benzylic Hydroxylation of Arylalkanes with H2O2 in Fluorinated Alcohols in the Presence of Chiral Mn Aminopyridine Complexes
    ChemCatChem, 2018, V.10, N 22, Pp 5323-5330 doi:10.1002/cctc.201801476, IF=4.673
  75. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  76. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  77. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  78. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  79. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  80. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  81. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  82. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  83. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  84. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  85. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  86. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  87. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  88. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  89. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  90. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  91. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  92. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  93. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  94. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  95. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  96. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  97. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  98. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  99. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  100. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  101. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  102. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  103. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  104. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
  105. V.I. Borovkov, V.A. Bagryansky, G.A. Letyagin, I.V. Beregovaya, L.N. Shchegoleva, Y.N. Molin
    Manifestation of g-tensor anisotropy in the quantum beats of spin-correlated radical ion pairs
    Chemical Physics Letters, 2018, V. 712, Pages 208-213 doi:10.1016/j.cplett.2018.10.004, IF=1.685
  106. V.I. Borovkov, V.A. Bagryansky, G.A. Letyagin, I.V. Beregovaya, L.N. Shchegoleva, Y.N. Molin
    Manifestation of g-tensor anisotropy in the quantum beats of spin-correlated radical ion pairs
    Chemical Physics Letters, 2018, V. 712, Pages 208-213 doi:10.1016/j.cplett.2018.10.004, IF=1.685
  107. V.I. Borovkov, V.A. Bagryansky, G.A. Letyagin, I.V. Beregovaya, L.N. Shchegoleva, Y.N. Molin
    Manifestation of g-tensor anisotropy in the quantum beats of spin-correlated radical ion pairs
    Chemical Physics Letters, 2018, V. 712, Pages 208-213 doi:10.1016/j.cplett.2018.10.004, IF=1.685
  108. V.I. Borovkov, V.A. Bagryansky, G.A. Letyagin, I.V. Beregovaya, L.N. Shchegoleva, Y.N. Molin
    Manifestation of g-tensor anisotropy in the quantum beats of spin-correlated radical ion pairs
    Chemical Physics Letters, 2018, V. 712, Pages 208-213 doi:10.1016/j.cplett.2018.10.004, IF=1.685
  109. G.A. Selivanova, A.D. Skolyapova, R.I. Dralyuk, E.V. Karpova, I.K. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov, T.V. Basova, E.V. Tretyakov
    Solid-phase transitions of polymorphs of 4-(4-N,N-dialkylaminophenyl)azobiphenyl-2,3'4'-tricarbonitriles and their analogues
    Thermochimica Acta, 2018, V. 669, Pp 88-98 doi:10.1016/j.tca.2018.08.022, IF=2.188
  110. G.A. Selivanova, A.D. Skolyapova, R.I. Dralyuk, E.V. Karpova, I.K. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov, T.V. Basova, E.V. Tretyakov
    Solid-phase transitions of polymorphs of 4-(4-N,N-dialkylaminophenyl)azobiphenyl-2,3'4'-tricarbonitriles and their analogues
    Thermochimica Acta, 2018, V. 669, Pp 88-98 doi:10.1016/j.tca.2018.08.022, IF=2.188
  111. A.A. Kuzhelev, O.A. Krumkacheva, I.O. Timofeev, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya
    Electron-Spin Relaxation of Triarylmethyl Radicals in Glassy Trehalose
    Applied Magnetic Resonance, 2018, V. 49, N 11, pp 1171-1180 doi:10.1007/s00723-018-1023-0, IF=0.835
  112. A.A. Kuzhelev, O.A. Krumkacheva, I.O. Timofeev, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya
    Electron-Spin Relaxation of Triarylmethyl Radicals in Glassy Trehalose
    Applied Magnetic Resonance, 2018, V. 49, N 11, pp 1171-1180 doi:10.1007/s00723-018-1023-0, IF=0.835
  113. A.A. Kuzhelev, O.A. Krumkacheva, I.O. Timofeev, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya
    Electron-Spin Relaxation of Triarylmethyl Radicals in Glassy Trehalose
    Applied Magnetic Resonance, 2018, V. 49, N 11, pp 1171-1180 doi:10.1007/s00723-018-1023-0, IF=0.835
  114. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  115. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  116. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  117. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  118. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  119. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  120. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  121. V.V. Zarubaev, E.A. Pushkina, S.S. Borisevich, A.V. Galochkina, A.V. Garshinina, A.A. Shtro, A.A. Egorova, A.S. Sokolova, S.L. Khursan, O.I. Yarovaya, N.F. Salakhutdinov
    Selection of influenza virus resistant to the novel camphor-based antiviral camphecene results in loss of pathogenicity
    Virology, V. 524, November 2018, Pp 69-77 doi:10.1016/j.virol.2018.08.011, IF=3.374
  122. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  123. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  124. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  125. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  126. A.Yu. Sidorenko, I.V. Il'ina, A.V. Kravtsova, A. Aho, O.V. Ardashov, N.S. Li-Zhulanov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays
    Molecular Catalysis, 2018, V. 459, Pp 38-45 doi:10.1016/j.mcat.2018.07.025
  127. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  128. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  129. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  130. С.В. Деревяшкин, Е.А. Соболева, В.В. Шелковников, Е.В. Спесивцев
    Голографическая запись в микронных пленках на основе полифторхалконов
    Химия высоких энергий, 2018, Т. 52, №6. c. 507-514?\, DOI:10.1134/S0023119318060037 (Holographic Recording in Micron Films Based on Polyfluorochalcones/ S. V. Derevyashkin, E. A. Soboleva, V. V. Shelkovnikov, E. V. Spesivtsev// High Energy Chemistry, 2019, V. 53, N 1, pp 50-57 doi:10.1134/S0018143918060036), IF=0.737
  131. T.S. Khlebnikova, Yu.A. Piven', F.A. Lakhvich, T.S. Frolova, I.V. Sorokina, T.G. Tolstikova
    Synthesis and Cytotoxicity of Conjugates of Betulinic Acid and F-Containing 2-Acylcycloalkane-1,3-Diones
    Chemistry of Natural Compounds, 2018, V. 54, N 6, pp 1100-1105 doi:10.1007/s1060, IF=0.449
  132. T.S. Khlebnikova, Yu.A. Piven', F.A. Lakhvich, T.S. Frolova, I.V. Sorokina, T.G. Tolstikova
    Synthesis and Cytotoxicity of Conjugates of Betulinic Acid and F-Containing 2-Acylcycloalkane-1,3-Diones
    Chemistry of Natural Compounds, 2018, V. 54, N 6, pp 1100-1105 doi:10.1007/s1060, IF=0.449
  133. T.S. Khlebnikova, Yu.A. Piven', F.A. Lakhvich, T.S. Frolova, I.V. Sorokina, T.G. Tolstikova
    Synthesis and Cytotoxicity of Conjugates of Betulinic Acid and F-Containing 2-Acylcycloalkane-1,3-Diones
    Chemistry of Natural Compounds, 2018, V. 54, N 6, pp 1100-1105 doi:10.1007/s1060, IF=0.449
  134. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  135. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  136. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
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  137. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
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  138. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  139. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
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    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  140. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
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  141. Е.В. Колдышева, А.П. Меньщикова, Е.Л. Лушникова, Н.А. Попова, В.И. Каледин, В.П. Николин, А.Л. Захаренко, О.А. Лузина, Н.Ф. Салахутдинов, О.И. Лаврик
    Антиметастатическая активность комбинации топотекана и ингибитора тирозил-ДНК-фосфодиэстеразы 1 на модели карциномы легкого Льюис
    Бюллетень экспериментальной биологии и медицины 2018 г., том 166, № 11 ноябрь, р.609-615 (Antimetastatic Activity of Combined Topotecan and Tyrosyl-DNA Phosphodiesterase-1 Inhibitor on Modeled Lewis Lung Carcinoma/ E. V. Koldysheva, A. P. Men'shchikova, E. L. Lushnikova, N. A. Popova, V. I. Kaledin, V. P. Nikolin, A. L. Zakharenko, O. A. Luzina, N. F. Salakhutdinov, O. I. Lavrik// Bulletin of Experimental Biology and Medicine, March 2019, V. 166, N 5, pp 661-666 doi:10.1007/s10517-019-04413-3), IF=0.546
  142. Е.А. Чугунова, В.А. Самсонов, А.С. Газизов, А.Р. Бурилов, М.А. Пудовик, О.Г. Синяшин
    N-Оксиды 2H-бензимидазола: синтез, химические свойства и биологическая активность
    Известия Академии наук. Серия химическая, 2018, № 11,1955-1970 (2H-Benzimidazole N-oxides: synthesis, chemical properties, and biological activity/ E. A. Chugunova, V. A. Samsonov, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin// Russian Chemical Bulletin, 2018, V. 67, N 11, pp 1955-1970 doi:10.1007/s11172-018-2315-0), IF=0.781
  143. Е.А. Чугунова, В.А. Самсонов, А.С. Газизов, А.Р. Бурилов, М.А. Пудовик, О.Г. Синяшин
    N-Оксиды 2H-бензимидазола: синтез, химические свойства и биологическая активность
    Известия Академии наук. Серия химическая, 2018, № 11,1955-1970 (2H-Benzimidazole N-oxides: synthesis, chemical properties, and biological activity/ E. A. Chugunova, V. A. Samsonov, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin// Russian Chemical Bulletin, 2018, V. 67, N 11, pp 1955-1970 doi:10.1007/s11172-018-2315-0), IF=0.781
  144. Е.А. Чугунова, В.А. Самсонов, А.С. Газизов, А.Р. Бурилов, М.А. Пудовик, О.Г. Синяшин
    N-Оксиды 2H-бензимидазола: синтез, химические свойства и биологическая активность
    Известия Академии наук. Серия химическая, 2018, № 11,1955-1970 (2H-Benzimidazole N-oxides: synthesis, chemical properties, and biological activity/ E. A. Chugunova, V. A. Samsonov, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin// Russian Chemical Bulletin, 2018, V. 67, N 11, pp 1955-1970 doi:10.1007/s11172-018-2315-0), IF=0.781
  145. Е.А. Чугунова, В.А. Самсонов, А.С. Газизов, А.Р. Бурилов, М.А. Пудовик, О.Г. Синяшин
    N-Оксиды 2H-бензимидазола: синтез, химические свойства и биологическая активность
    Известия Академии наук. Серия химическая, 2018, № 11,1955-1970 (2H-Benzimidazole N-oxides: synthesis, chemical properties, and biological activity/ E. A. Chugunova, V. A. Samsonov, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin// Russian Chemical Bulletin, 2018, V. 67, N 11, pp 1955-1970 doi:10.1007/s11172-018-2315-0), IF=0.781
  146. Е.А. Чугунова, В.А. Самсонов, А.С. Газизов, А.Р. Бурилов, М.А. Пудовик, О.Г. Синяшин
    N-Оксиды 2H-бензимидазола: синтез, химические свойства и биологическая активность
    Известия Академии наук. Серия химическая, 2018, № 11,1955-1970 (2H-Benzimidazole N-oxides: synthesis, chemical properties, and biological activity/ E. A. Chugunova, V. A. Samsonov, A. S. Gazizov, A. R. Burilov, M. A. Pudovik, O. G. Sinyashin// Russian Chemical Bulletin, 2018, V. 67, N 11, pp 1955-1970 doi:10.1007/s11172-018-2315-0), IF=0.781
  147. Т.С. Скрипкина, А.Л. Бычков, В.Д. Тихова, О.И. Ломовский
    Твердофазные механохимические реакции гуминовых кислот бурого угля с перкарбонатом натрия
    Химия твердого топлива. 2018. № 6. С. 16-20. (Mechanochemical Solid-Phase Reactions of Humic Acids from Brown Coal with Sodium Percarbonate/ T. S. Skripkina, A. L. Bychkov, V. D. Tikhova, O. I. Lomovsky// Solid Fuel Chemistry, 2018, V. 52, IN 6, pp 356-360 doi:10.3103/S0361521918060101), IF=0.553
  148. Т.С. Скрипкина, А.Л. Бычков, В.Д. Тихова, О.И. Ломовский
    Твердофазные механохимические реакции гуминовых кислот бурого угля с перкарбонатом натрия
    Химия твердого топлива. 2018. № 6. С. 16-20. (Mechanochemical Solid-Phase Reactions of Humic Acids from Brown Coal with Sodium Percarbonate/ T. S. Skripkina, A. L. Bychkov, V. D. Tikhova, O. I. Lomovsky// Solid Fuel Chemistry, 2018, V. 52, IN 6, pp 356-360 doi:10.3103/S0361521918060101), IF=0.553
  149. Т.С. Скрипкина, А.Л. Бычков, В.Д. Тихова, О.И. Ломовский
    Твердофазные механохимические реакции гуминовых кислот бурого угля с перкарбонатом натрия
    Химия твердого топлива. 2018. № 6. С. 16-20. (Mechanochemical Solid-Phase Reactions of Humic Acids from Brown Coal with Sodium Percarbonate/ T. S. Skripkina, A. L. Bychkov, V. D. Tikhova, O. I. Lomovsky// Solid Fuel Chemistry, 2018, V. 52, IN 6, pp 356-360 doi:10.3103/S0361521918060101), IF=0.553
  150. А.П. Крысин, М.П. Долгих, Т.Г. Толстикова, Э.Э. Шульц, Л.М. Покровский
    Синтез и противовоспалительная активность тирозола и его структурных аналогов
    Химико-фармацевтический журнал, 2018, т. 52, № 11, С. 69-73. DOI: 10.30906/0023-1134-2018-52-11-69-73 (Synthesis and Anti-Inflammatory Activity of Tyrosol and Its Structural Analogs/ A.P. Krysin, T.G. Tolstikova, M.P., E.E. Shul'ts , L.M. Pokrovskii// Pharmaceutical Chemistry Journal, 2019, V. 52, N 11, pp 907-911 doi:10.1007/s11094-019-01924-1), IF=0.679
  151. А.М. Астахов, Д.В. Антишин, А.А. Нефёдов, Г.Е. Сальников, Э.С. Бука
    Нитримины. VII. реакция S,S'-диметил-N-нитроимидодитиокарбоната с щелочами. синтез S-метил-N-нитротиокарбамата и его солей
    Журнал органической химии. 2018. Т. 54. № 11. С. 1629-1633. ( DOI: 10.1134/S0514749218110031) (Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039), IF=0.654
  152. А.М. Астахов, Д.В. Антишин, А.А. Нефёдов, Г.Е. Сальников, Э.С. Бука
    Нитримины. VII. реакция S,S'-диметил-N-нитроимидодитиокарбоната с щелочами. синтез S-метил-N-нитротиокарбамата и его солей
    Журнал органической химии. 2018. Т. 54. № 11. С. 1629-1633. ( DOI: 10.1134/S0514749218110031) (Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039), IF=0.654
  153. А.М. Астахов, Д.В. Антишин, А.А. Нефёдов, Г.Е. Сальников, Э.С. Бука
    Нитримины. VII. реакция S,S'-диметил-N-нитроимидодитиокарбоната с щелочами. синтез S-метил-N-нитротиокарбамата и его солей
    Журнал органической химии. 2018. Т. 54. № 11. С. 1629-1633. ( DOI: 10.1134/S0514749218110031) (Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039), IF=0.654
  154. Н.А. Григорьева, И.Ю. Флейтлих, А.Я. Тихонов
    Экстракция серебра из солянокислых растворов дисульфидом бис(2,4,4-триметилпентил)дитио фосфиновой кислоты в смеси с алкилфенолами
    Цветные металлы, 2018, No. 11, 36-40 doi:10.17580/tsm.2018.11.05
  155. Н.А. Григорьева, И.Ю. Флейтлих, А.Я. Тихонов
    Экстракция серебра из солянокислых растворов дисульфидом бис(2,4,4-триметилпентил)дитио фосфиновой кислоты в смеси с алкилфенолами
    Цветные металлы, 2018, No. 11, 36-40 doi:10.17580/tsm.2018.11.05
  156. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  157. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  158. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  159. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  160. V.Yu. Kuksenok, V.V. Shtrykova, V.D. Filimonov, A.G. Druganov, A.A. Bondarev, K.S. Stankevich
    The determination of enantiomer composition of 1-((3-chlorophenyl)-(phenyl)methyl) amine and 1-((3-chlorophenyl)(phenyl)-methyl) urea (Galodif) by NMR spectroscopy, chiral HPLC, and polarimetry
    Chirality. 2018, V. 30, N 10 , Pp 1135-1143 doi:10.1002/chir.23005, IF=1.832
  161. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
    High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
    Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
  162. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
    High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
    Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
  163. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
    High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
    Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
  164. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
    High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
    Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
  165. A. Kuzhelev, D. Akhmetzyanov, V. Denysenkov, G. Shevelev, O. Krumkacheva, E. Bagryanskaya, T. Prisner
    High-frequency pulsed electron-electron double resonance spectroscopy on DNA duplexes using trityl tags and shaped microwave pulses
    Phys. Chem. Chem. Phys., 2018, V. 20, N 41, Pp 26140-26144 doi:10.1039/C8CP03951H, IF=3.905
  166. Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles
    Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles
    Mendeleev Communications, 2018, V. 28, N 5, Pp 453-460 doi:10.1016/j.mencom.2018.09.001, IF=2.098
  167. Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles
    Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles
    Mendeleev Communications, 2018, V. 28, N 5, Pp 453-460 doi:10.1016/j.mencom.2018.09.001, IF=2.098
  168. М.Д. Соколова, А.Ф. Федорова, М.Л. Давыдова, А.П. Крысин, Э.Э. Шульц, А.Р. Халдеева
    Изучение влияния малолетучих и нетоксичных функционализированных фенольных антиоксидантов на физико-механические свойства резин на основе БИКС-18
    Каучук и резина. 2018. Т. 77. № 5. С. 320-325.
  169. М.Д. Соколова, А.Ф. Федорова, М.Л. Давыдова, А.П. Крысин, Э.Э. Шульц, А.Р. Халдеева
    Изучение влияния малолетучих и нетоксичных функционализированных фенольных антиоксидантов на физико-механические свойства резин на основе БИКС-18
    Каучук и резина. 2018. Т. 77. № 5. С. 320-325.
  170. М.Д. Соколова, А.Ф. Федорова, М.Л. Давыдова, А.П. Крысин, Э.Э. Шульц, А.Р. Халдеева
    Изучение влияния малолетучих и нетоксичных функционализированных фенольных антиоксидантов на физико-механические свойства резин на основе БИКС-18
    Каучук и резина. 2018. Т. 77. № 5. С. 320-325.
  171. М.Д. Соколова, А.Ф. Федорова, М.Л. Давыдова, А.П. Крысин, Э.Э. Шульц, А.Р. Халдеева
    Изучение влияния малолетучих и нетоксичных функционализированных фенольных антиоксидантов на физико-механические свойства резин на основе БИКС-18
    Каучук и резина. 2018. Т. 77. № 5. С. 320-325.
  172. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  173. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  174. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  175. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  176. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  177. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  178. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  179. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  180. I.A. Orlovskaya, L.B. Toporkova, M.N. Lvova, I.V. Sorokina, A.V. Katokhin, G.B. Vishnivetskaya, E.V. Goiman, E.V. Kashina, T.G. Tolstikova, V.A. Mordvinov, D.F. Avgustinovich
    Social Defeat Stress Exacerbates the Blood Abnormalities in Opisthorchis felineus-infected mice
    Experimental Parasitology, 2018, V. 193, Pages 33-44 doi:10.1016/j.exppara.2018.08.004, IF=1.82
  181. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  182. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  183. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  184. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  185. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  186. R. Kong, X. Zhu, E.S. Meteleva, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, A.V. Dushkin, W. Su
    Atorvastatin calcium inclusion complexation with polysaccharide arabinogalactan and saponin disodium glycyrrhizate for increasing of solubility and bioavailability
    Drug Delivery and Translational Research, 2018, V 8, N 5, pp 1200-1213 doi:10.1007/s13346-018-0565-x, IF=3.394
  187. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  188. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  189. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  190. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  191. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  192. М.А. Цыганов, Г.Б. Вишнивецкая, Т.П. Кукина, И.В. Сорокина, М.Н. Львова, М.А. Проценко, Н.Е. Костина, Д.Ф. Августинович
    Исследование эффектов грибов Cantharellus cibarius на трематоду O. felineus и на хозяина паразита-инбредных мышей C57BL/6
    Вавиловский журнал генетики и селекции, 2018, Т. 22, N 7, Сс. 856-864 (Studyng the effects of Cantharellus cibarius fungi on Opisthorchis felineus trematode and on parasite host-C57BL/6 inbred mice/ M.A. Tsyganov, G.B. Vishnivetskaya, T.P. Kukina, I.V. Sorokina, M.N. Lvova, M.A. Protsenko, N.E. Kostina, D.F. Avgustinovich// VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, , 2018, V. 22, N 7, Pp. 856-864 doi:10.18699/VJ18.426)
  193. V.I. Anikeev, V.P. Sivcev, K.R. Valeev, K.P. Volcho, V.A. Sadykov, N.F. Salakhutdinov
    Highly selective reduction of nitroarenes by sc-isopropanol in the presence of zirconia in a flow reactor
    The Journal of Supercritical Fluids, V. 140, October 2018, Pp 233-237 doi:10.1016/j.supflu.2018.06.021, IF=3.122
  194. V.I. Anikeev, V.P. Sivcev, K.R. Valeev, K.P. Volcho, V.A. Sadykov, N.F. Salakhutdinov
    Highly selective reduction of nitroarenes by sc-isopropanol in the presence of zirconia in a flow reactor
    The Journal of Supercritical Fluids, V. 140, October 2018, Pp 233-237 doi:10.1016/j.supflu.2018.06.021, IF=3.122
  195. V.I. Anikeev, V.P. Sivcev, K.R. Valeev, K.P. Volcho, V.A. Sadykov, N.F. Salakhutdinov
    Highly selective reduction of nitroarenes by sc-isopropanol in the presence of zirconia in a flow reactor
    The Journal of Supercritical Fluids, V. 140, October 2018, Pp 233-237 doi:10.1016/j.supflu.2018.06.021, IF=3.122
  196. V.I. Anikeev, V.P. Sivcev, K.R. Valeev, K.P. Volcho, V.A. Sadykov, N.F. Salakhutdinov
    Highly selective reduction of nitroarenes by sc-isopropanol in the presence of zirconia in a flow reactor
    The Journal of Supercritical Fluids, V. 140, October 2018, Pp 233-237 doi:10.1016/j.supflu.2018.06.021, IF=3.122
  197. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
  198. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  199. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  200. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  201. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  202. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  203. Б.А. Селиванов, Н.И. Бормотов, Л.Н. Шишкина, Е.Ф. Беланов, О.А. Серова, А.С. Кабанов, О.Ю. Мазурков, А.Я. Тихонов
    Синтез и противовирусная активность полициклических N-амидоимидов на основе 4-оксатетрацикло[5.3.2.02,6.08,10]додец-11-ен-3,5-диона
    Хим.-фарм. журнал. 2018, Т. 52, No. 10, C. 3-7. (Synthesis and Antiviral Activity of Polycyclic N-Amidoimides Based on 4-Oxatetracyclo-[5.3.2.02, 6.08,10]Dodec-11-Ene-3,5-Dione/ B. A. Selivanov, N. I. Bormotov, L. N. Shishkina, E. F. Belanov, O. A. Serova, A. S. Kabanov, O. Yu. Mazurkov, A. Ya. Tikhonov// Pharmaceutical Chemistry Journal, 2019, V. 52, N 10, pp 820–824 doi:10.1007/s11094-019-1907-9), IF=0.679
  204. А.П. Крысин, А.А. Нефедов, Т.Я. Гаврикова, А.С. Кильметьев
    О реакции полисульфидов 2-трет-бутилфенола с каучуком и гептеном-1 в инертной атмосфере и на воздухе
    Химия в интересах устойчивого развития. 2018. Т. 26. № 4. С. 403-410. doi:10.15372/KhUR20180407
  205. S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
    Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
    J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
  206. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  207. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  208. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  209. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  210. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  211. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  212. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  213. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  214. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  215. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  216. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  217. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  218. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  219. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  220. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  221. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
  222. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and antiviral activity of camphor-based 1,3-thiazolidin-4-one and thiazole derivatives as Orthopoxvirus-reproduction inhibitors
    Med. Chem. Commun,, 2018, V. 9, N 10, Pp 1746-1753 doi:10.1039/C8MD00347E, IF=2.342
  223. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis and antiviral activity of camphor-based 1,3-thiazolidin-4-one and thiazole derivatives as Orthopoxvirus-reproduction inhibitors
    Med. Chem. Commun,, 2018, V. 9, N 10, Pp 1746-1753 doi:10.1039/C8MD00347E, IF=2.342
  224. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  225. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  226. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  227. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  228. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  229. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  230. N.S. Li-Zhulanov, A.L. Zakharenko, A.A. Chepanova, J. Patel, A. Zafar, K.P. Volcho, N.F. Salakhutdinov, J. Reynisson, I.K. H. Leung, O.I. Lavrik
    A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold
    Molecules 2018, 23(10), 2468; doi:10.3390/molecules23102468, IF=3.098
  231. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  232. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  233. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  234. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  235. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  236. A. Sidorenko, A. Kravtsova, A. Aho, I. Heinmaa, V. Agabekov, K. Volcho, N. Salakhutdinov, D. Murzin
    Acid-modified Halloysite Nanotubes as a Stereoselective Catalyst for Synthesis of 2H-Chromene Derivatives by the Reaction of Isopulegol with Aldehydes
    ChemCatChem, 2018, V. 10, N 18, Pp 3950-3954 doi:10.1002/cctc.201800974, IF=4.674
  237. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  238. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  239. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  240. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  241. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  242. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  243. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  244. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  245. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  246. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  247. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  248. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  249. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  250. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  251. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  252. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  253. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  254. A. Berezin, K. Vinogradova, V. Krivopalov, E. Nikolaenkova, V. Plyusnin, A. Kupryakov, N. Pervukhina, D. Naumov, M.B. Bushuev
    Excitation-wavelength-dependent emission and delayed fluorescence in a proton transfer system
    Chemistry - A European Journal, 2018, V. 24, N 49, Pp 12790-12795 doi:10.1002/chem.201802876, IF=5.16
  255. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  256. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  257. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  258. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  259. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  260. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  261. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  262. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  263. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  264. А.В. Ластовка, Е.Ю. Яковлева, В.Ф. Коллегов, В.П. Фадеева, Н.Ф. Салахутдинов
    Определение остаточных органических растворителей методом газовой хроматографии в субстанции (2R,4R,4AR,7R, 8AR)-4,7-диметил-2-(тиофен-2-ил)октагидро-2H-хромен-4-ол, обладающей анальгетической активностью
    Заводская лаборатория. Диагностика материалов. 2018. Т. 84. № 9. С. 13-20. doi:10.26896/1028-6861-2018-84-9-13-20
  265. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Discovery of a new class of inhibitors of Vaccinia virus based on (-)-borneol from Abies sibirica and (+)-camphor
    Chemistry & Biodiversity, 2018, V. 15, N 9, e1800153 doi:10.1002/cbdv.201800153, IF=1.617
  266. A.S. Sokolova, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, N.F. Salakhutdinov
    Discovery of a new class of inhibitors of Vaccinia virus based on (-)-borneol from Abies sibirica and (+)-camphor
    Chemistry & Biodiversity, 2018, V. 15, N 9, e1800153 doi:10.1002/cbdv.201800153, IF=1.617
  267. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
  268. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
  269. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
  270. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
  271. A.A. Kuzhelev, O.A. Krumkacheva, M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, V.M. Tormyshev, M. K Bowman, M.V. Fedin, E.G. Bagryanskaya
    Pulse EPR of Triarylmethyl Probes: New Approach for Investigation of Molecular Motions in Soft Matter
    J. Phys. Chem. B, 2018, 122 (36), pp 8624–8630 doi:10.1021/acs.jpcb.8b07714, IF=3.145
  272. Г.М. Байсаров, А.Р. Жуматаева, Г.К. Мукушева, Э.Э. Шульц, Р.Б. Сейдахметова, С.М. Адекенов
    Флавоноидные соединения ARTEMISIA GLABELLA KAR. ET KIR, синтезы на их основе и их биологическая активность
    Химия растительного сырья. 2018. № 3. С. 215-222.
  273. Г.М. Байсаров, А.Р. Жуматаева, Г.К. Мукушева, Э.Э. Шульц, Р.Б. Сейдахметова, С.М. Адекенов
    Флавоноидные соединения ARTEMISIA GLABELLA KAR. ET KIR, синтезы на их основе и их биологическая активность
    Химия растительного сырья. 2018. № 3. С. 215-222.
  274. Г.М. Байсаров, А.Р. Жуматаева, Г.К. Мукушева, Э.Э. Шульц, Р.Б. Сейдахметова, С.М. Адекенов
    Флавоноидные соединения ARTEMISIA GLABELLA KAR. ET KIR, синтезы на их основе и их биологическая активность
    Химия растительного сырья. 2018. № 3. С. 215-222.
  275. Г.М. Байсаров, А.Р. Жуматаева, Г.К. Мукушева, Э.Э. Шульц, Р.Б. Сейдахметова, С.М. Адекенов
    Флавоноидные соединения ARTEMISIA GLABELLA KAR. ET KIR, синтезы на их основе и их биологическая активность
    Химия растительного сырья. 2018. № 3. С. 215-222.
  276. Г.М. Байсаров, А.Р. Жуматаева, Г.К. Мукушева, Э.Э. Шульц, Р.Б. Сейдахметова, С.М. Адекенов
    Флавоноидные соединения ARTEMISIA GLABELLA KAR. ET KIR, синтезы на их основе и их биологическая активность
    Химия растительного сырья. 2018. № 3. С. 215-222.
  277. L.A. Shundrin, P.A. Avrorov, I.G. Irtegova, D.S. Odintsov, A.F. Poveshchenko
    Electrochemical reduction of 2,4-dimethyl(diethyl)-9-oxo-10-(4-heptoxyphenyl)-9H-thioxanthenium hexafluorophosphates and 2,4-dimethyl(diethyl)-9H-thioxanthene-9-ones
    Journal of Physical Organic Chemistry, 2018, V. 31, N 9, e3853 doi:10.1002/poc.3853, IF=1.591
  278. V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
    A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
    Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
  279. V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
    A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
    Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
  280. V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
    A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
    Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
  281. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  282. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  283. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  284. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  285. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  286. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  287. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  288. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  289. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  290. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  291. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  292. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  293. O. Zakharova, O. Luzina, A. Zakharenko, D. Sokolov, A. Filimonov, N. Dyrkheeva, A. Chepanova, E. Ilina, A. Ilyina, K. Klabenkova, B. Chelobanov, D. Stetsenko, A. Zafar, Ch. Eurtivong, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and evaluation of aryliden- and hetarylidenfuranone derivatives of usnic acid as highly potent Tdp1 inhibitors
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4470-4480 doi:10.1016/j.bmc.2018.07.039, IF=2.881
  294. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  295. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  296. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  297. S.O. Kuranov, I.P. Tsypysheva, M.V. Khvostov, L.F. Zainullina, S.S. Borisevich, Yu.V. Vakhitova, O.A. Luzina, N.F. Salakhutdinov
    Synthesis and evaluation of camphor and cytisine-based cyanopyrrolidines as DPP-IV inhibitors for the treatment of type 2 diabetes mellitus
    Bioorganic & Medicinal Chemistry, 2018, V. 26, N 15, Pp 4402-4409 doi:10.1016/j.bmc.2018.07.018, IF=2.881
  298. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  299. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  300. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  301. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  302. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  303. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  304. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  305. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  306. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  307. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  308. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  309. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  310. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  311. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  312. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  313. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  314. Y. Shuku, Y. Hirai, N.A. Semenov, E. Kadilenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin, K. Awaga
    3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(I) and [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Dalton Trans., 2018, V. 47, N 29, Pp 9897-9902 doi:10.1039/C8DT02214C, IF=4.98
  315. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, K.A. Vinogradova, Yu.V. Gatilov
    Hysteretic spin crossover in isomeric iron(II) complexes
    Dalton Trans., 2018, V. 47, N 29, Pp 9585-9591 doi:10.1039/C8DT02223B, IF=4.099
  316. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, K.A. Vinogradova, Yu.V. Gatilov
    Hysteretic spin crossover in isomeric iron(II) complexes
    Dalton Trans., 2018, V. 47, N 29, Pp 9585-9591 doi:10.1039/C8DT02223B, IF=4.099
  317. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  318. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  319. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  320. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  321. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  322. Ying-Zhao Ma, N. Pushkarevsky, T.S. Sukhikh, A.E. Galashov, A.G. Makarov, P.W. Roesky, S.N. Konchenko
    Steric influence and intermolecular interactions of formamidinate ligands in lanthanide (Sm, Yb) arylchalcogenolate complexes
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 29, Pp 3388-3396 doi:10.1002/ejic.201800201, IF=2.507
  323. T. Skripkina, A. Bychkov, V. Tikhova, B. Smolyakov, O. Lomovsky
    Mechanochemically oxidized brown coal and the effect of its application in polluted water
    Environmental Technology & Innovation, 2018, V. 11, Pp 74-82 doi:10.1016/j.eti.2018.04.010
  324. T. Skripkina, A. Bychkov, V. Tikhova, B. Smolyakov, O. Lomovsky
    Mechanochemically oxidized brown coal and the effect of its application in polluted water
    Environmental Technology & Innovation, 2018, V. 11, Pp 74-82 doi:10.1016/j.eti.2018.04.010
  325. T. Skripkina, A. Bychkov, V. Tikhova, B. Smolyakov, O. Lomovsky
    Mechanochemically oxidized brown coal and the effect of its application in polluted water
    Environmental Technology & Innovation, 2018, V. 11, Pp 74-82 doi:10.1016/j.eti.2018.04.010
  326. T. Skripkina, A. Bychkov, V. Tikhova, B. Smolyakov, O. Lomovsky
    Mechanochemically oxidized brown coal and the effect of its application in polluted water
    Environmental Technology & Innovation, 2018, V. 11, Pp 74-82 doi:10.1016/j.eti.2018.04.010
  327. L. Politanskaya, Z. Duan, I. Bagryanskaya, I. Eltsov, E. Tretyakov, Chanjuan. Xi
    Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
    Journal of Fluorine Chemistry, 2018, V. 212, Pp 130-136 doi:10.1016/j.jfluchem.2018.06.001, IF=1.879
  328. L. Politanskaya, Z. Duan, I. Bagryanskaya, I. Eltsov, E. Tretyakov, Chanjuan. Xi
    Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
    Journal of Fluorine Chemistry, 2018, V. 212, Pp 130-136 doi:10.1016/j.jfluchem.2018.06.001, IF=1.879
  329. L. Politanskaya, Z. Duan, I. Bagryanskaya, I. Eltsov, E. Tretyakov, Chanjuan. Xi
    Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
    Journal of Fluorine Chemistry, 2018, V. 212, Pp 130-136 doi:10.1016/j.jfluchem.2018.06.001, IF=1.879
  330. M.M. Shmakov, S.A. Prikhod'ko, V.V. Bardin, N.Yu. Adonin
    New approach to the generation of aryldifluoroboranes-prospective acid catalysts of organic reactions
    Mendeleev Communications, 2018, V. 28, N 4, Pp 369-371 doi:10.1016/j.mencom.2018.07.009, IF=2.098
  331. M.M. Shmakov, S.A. Prikhod'ko, V.V. Bardin, N.Yu. Adonin
    New approach to the generation of aryldifluoroboranes-prospective acid catalysts of organic reactions
    Mendeleev Communications, 2018, V. 28, N 4, Pp 369-371 doi:10.1016/j.mencom.2018.07.009, IF=2.098
  332. M.M. Shmakov, S.A. Prikhod'ko, V.V. Bardin, N.Yu. Adonin
    New approach to the generation of aryldifluoroboranes-prospective acid catalysts of organic reactions
    Mendeleev Communications, 2018, V. 28, N 4, Pp 369-371 doi:10.1016/j.mencom.2018.07.009, IF=2.098
  333. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  334. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  335. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  336. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  337. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  338. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  339. H. Suo, I.I. Oleynik, C.I. Bariashir, I.V. Oleynik, Z. Wang, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
    Strictly linear polyethylene using Co-catalysts chelated by fused bis(arylimino)pyridines: Probing ortho-cycloalkyl ring-size effects on molecular weight
    Polymer, 2018, V. 149, Pp 45-54 doi:10.1016/j.polymer.2018.06.066, IF=3.483
  340. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  341. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  342. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  343. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  344. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  345. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  346. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  347. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
  348. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  349. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  350. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  351. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  352. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  353. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  354. A.Yu. Sidorenko, A.V. Kravtsova, J. Warna, A. Aho, I. Heinmaa, I.V. Il'ina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays
    Molecular Catalysis, 2018, V. 453, Pp. 139-148 doi:10.1016/j.mcat.2018.05.007
  355. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  356. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  357. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  358. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  359. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  360. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  361. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  362. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  363. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  364. Е.С. Метелева, Ю.С. Чистяченко, Л.П. Сунцова, М.А. Цыганов, Г.Б. Вишнивецкая, Д.Ф. Августинович, М.В. Хвостов, Н.Э. Поляков, Т.Г. Толстикова, В.А. Мордвинов, А.В. Душкин, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных твердых композиций празиквантела и динатриевой соли глицирризиновой кислоты
    Doklady Biochemistry and Доклады Академии наук. 2018. Т. 481. № 6. С. 694-697.( DOI: 10.31857/S086956520002111-5) (Physicochemical Properties and Anti-Opisthorchosis Effect of Mechanochemically Synthesized Solid Compositions of Praziquantel with Glycyrrhizic Acid Disodium Salt/ E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, M.A. Tsyganov, G.B. Vishnivetskaya, D.F. Avgustinovich, M.V. Khvostov, N.E. Polyakov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov// Doklady Biochemistry and Biophysics, 2018, V. 481, N 1, pp 228-231 doi:10.1134/S1607672918040142), IF=0.61
  365. A.L. Zakharenko, E.S. Mozhaitsev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Synthesis and Inhibitory Properties of Imines Containing Monoterpenoid and Adamantane Fragments Against DNA Repair Enzyme Tyrosyl-DNA Phosphodiesterase 1 (Tdp1)
    Chemistry of Natural Compounds, 2018, V. 54, N 4, pp 672-676 doi:10.1007/s10600-018-2443-7, IF=0.449
  366. A.L. Zakharenko, E.S. Mozhaitsev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Synthesis and Inhibitory Properties of Imines Containing Monoterpenoid and Adamantane Fragments Against DNA Repair Enzyme Tyrosyl-DNA Phosphodiesterase 1 (Tdp1)
    Chemistry of Natural Compounds, 2018, V. 54, N 4, pp 672-676 doi:10.1007/s10600-018-2443-7, IF=0.449
  367. С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, А.В. Якиманский, А.А. Мартыненков, Н.А. Валишева
    Компактный амплитудный электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 4. С. 78-83. (Compact Amplitude Electro-Optic Modulator Based on Chromophore-Containing Polyimides/ S. L. Mikerin, A. I. Plekhanov, A. E. Simanchuk, A. V. Yakimanski, iA. A. Martynenkov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing,2018, V. 54, N 4, pp 385-389 doi:10.3103/S8756699018040106)
  368. С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, А.В. Якиманский, А.А. Мартыненков, Н.А. Валишева
    Компактный амплитудный электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 4. С. 78-83. (Compact Amplitude Electro-Optic Modulator Based on Chromophore-Containing Polyimides/ S. L. Mikerin, A. I. Plekhanov, A. E. Simanchuk, A. V. Yakimanski, iA. A. Martynenkov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing,2018, V. 54, N 4, pp 385-389 doi:10.3103/S8756699018040106)
  369. С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, А.В. Якиманский, А.А. Мартыненков, Н.А. Валишева
    Компактный амплитудный электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 4. С. 78-83. (Compact Amplitude Electro-Optic Modulator Based on Chromophore-Containing Polyimides/ S. L. Mikerin, A. I. Plekhanov, A. E. Simanchuk, A. V. Yakimanski, iA. A. Martynenkov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing,2018, V. 54, N 4, pp 385-389 doi:10.3103/S8756699018040106)
  370. С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, А.В. Якиманский, А.А. Мартыненков, Н.А. Валишева
    Компактный амплитудный электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 4. С. 78-83. (Compact Amplitude Electro-Optic Modulator Based on Chromophore-Containing Polyimides/ S. L. Mikerin, A. I. Plekhanov, A. E. Simanchuk, A. V. Yakimanski, iA. A. Martynenkov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing,2018, V. 54, N 4, pp 385-389 doi:10.3103/S8756699018040106)
  371. В.С. Шрамко, Я.В. Полонская, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Полиненасыщенные жирные кислоты и их ассоциации с параметрами окислительно-антиоксидантного потенциала крови и липопротеинассоциированной фосфолипазой А2 при коронарном атеросклерозе
    Бюллетень экспериментальной биологии и медицины. 2018. Т. 166. № 7. С. 14-17 (Polyunsaturated Fatty Acids and Their Correlations with Parameters of Oxidative/Antioxidant Potential of the Blood and Lipoprotein-Associated Phospholipase A2 in Coronary Atherosclerosis/ V. S. Shramko, YA. V. Polonskaya, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Yu. I. Ragino// Bulletin of Experimental Biology and Medicine, 2018, V. 166, N 1, pp 11-14 doi:10.1007/s10517-018-4277-5), IF=0.546
  372. В.С. Шрамко, Я.В. Полонская, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Полиненасыщенные жирные кислоты и их ассоциации с параметрами окислительно-антиоксидантного потенциала крови и липопротеинассоциированной фосфолипазой А2 при коронарном атеросклерозе
    Бюллетень экспериментальной биологии и медицины. 2018. Т. 166. № 7. С. 14-17 (Polyunsaturated Fatty Acids and Their Correlations with Parameters of Oxidative/Antioxidant Potential of the Blood and Lipoprotein-Associated Phospholipase A2 in Coronary Atherosclerosis/ V. S. Shramko, YA. V. Polonskaya, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Yu. I. Ragino// Bulletin of Experimental Biology and Medicine, 2018, V. 166, N 1, pp 11-14 doi:10.1007/s10517-018-4277-5), IF=0.546
  373. В.С. Шрамко, Я.В. Полонская, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Полиненасыщенные жирные кислоты и их ассоциации с параметрами окислительно-антиоксидантного потенциала крови и липопротеинассоциированной фосфолипазой А2 при коронарном атеросклерозе
    Бюллетень экспериментальной биологии и медицины. 2018. Т. 166. № 7. С. 14-17 (Polyunsaturated Fatty Acids and Their Correlations with Parameters of Oxidative/Antioxidant Potential of the Blood and Lipoprotein-Associated Phospholipase A2 in Coronary Atherosclerosis/ V. S. Shramko, YA. V. Polonskaya, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Yu. I. Ragino// Bulletin of Experimental Biology and Medicine, 2018, V. 166, N 1, pp 11-14 doi:10.1007/s10517-018-4277-5), IF=0.546
  374. В.С. Шрамко, Я.В. Полонская, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Полиненасыщенные жирные кислоты и их ассоциации с параметрами окислительно-антиоксидантного потенциала крови и липопротеинассоциированной фосфолипазой А2 при коронарном атеросклерозе
    Бюллетень экспериментальной биологии и медицины. 2018. Т. 166. № 7. С. 14-17 (Polyunsaturated Fatty Acids and Their Correlations with Parameters of Oxidative/Antioxidant Potential of the Blood and Lipoprotein-Associated Phospholipase A2 in Coronary Atherosclerosis/ V. S. Shramko, YA. V. Polonskaya, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Yu. I. Ragino// Bulletin of Experimental Biology and Medicine, 2018, V. 166, N 1, pp 11-14 doi:10.1007/s10517-018-4277-5), IF=0.546
  375. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  376. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  377. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  378. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  379. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  380. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  381. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  382. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
  383. L. Politanskaya, T. Rybalova, O. Zakharova, G. Nevinsky, E. Tretyakov
    p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their derivatives
    Journal of Fluorine Chemistry, 2018, V.211, Pp 129-140 doi:10.1016/j.jfluchem.2018.04.005, IF=1.879
  384. L. Politanskaya, T. Rybalova, O. Zakharova, G. Nevinsky, E. Tretyakov
    p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their derivatives
    Journal of Fluorine Chemistry, 2018, V.211, Pp 129-140 doi:10.1016/j.jfluchem.2018.04.005, IF=1.879
  385. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  386. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  387. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  388. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  389. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  390. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  391. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  392. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  393. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  394. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  395. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  396. И.В. Широких, Л.Г. Бурова, А.B. Липеева, Э.Э. Шульц
    Изучение антибактериальных свойств производных пеуцеданина в отношении staphylococcus sureus in vitro
    Сибирский медицинский вестник. 2018. № 2. С. 8-12.
  397. И.В. Широких, Л.Г. Бурова, А.B. Липеева, Э.Э. Шульц
    Изучение антибактериальных свойств производных пеуцеданина в отношении staphylococcus sureus in vitro
    Сибирский медицинский вестник. 2018. № 2. С. 8-12.
  398. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, А.В. Липеева, Э.Э. Шульц
    Иследование антимикробной активности кумариновых субстанций в отношении STAPHYLOCOCCUS AUREUS и PSEUDOMONAS AERUGINOSA
    Бактериология. 2018. Т. 3. № 2. С. 16-19. doi:10.20953/2500-1027-2018-2-16-19
  399. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, А.В. Липеева, Э.Э. Шульц
    Иследование антимикробной активности кумариновых субстанций в отношении STAPHYLOCOCCUS AUREUS и PSEUDOMONAS AERUGINOSA
    Бактериология. 2018. Т. 3. № 2. С. 16-19. doi:10.20953/2500-1027-2018-2-16-19
  400. А.Н. Евстропов, Л.Г. Бурова, И.В. Широких, А.В. Липеева, Э.Э. Шульц
    Иследование антимикробной активности кумариновых субстанций в отношении STAPHYLOCOCCUS AUREUS и PSEUDOMONAS AERUGINOSA
    Бактериология. 2018. Т. 3. № 2. С. 16-19. doi:10.20953/2500-1027-2018-2-16-19
  401. М.В. Кручинина, В.Н. Кручинин, Я.И. Прудникова, А.А. Громов, М.В. Шашков, А.С. Соколова
    Исследование уровня жирных кислот мембран эритроцитов и сыворотки крови у пациентов с колоректальным раком г. Новосибирска
    Успехи молекулярной онкологии. 2018. Т. 5. № 2. С. 50-61. (Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61)
  402. М.В. Кручинина, В.Н. Кручинин, Я.И. Прудникова, А.А. Громов, М.В. Шашков, А.С. Соколова
    Исследование уровня жирных кислот мембран эритроцитов и сыворотки крови у пациентов с колоректальным раком г. Новосибирска
    Успехи молекулярной онкологии. 2018. Т. 5. № 2. С. 50-61. (Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61)
  403. М.В. Кручинина, В.Н. Кручинин, Я.И. Прудникова, А.А. Громов, М.В. Шашков, А.С. Соколова
    Исследование уровня жирных кислот мембран эритроцитов и сыворотки крови у пациентов с колоректальным раком г. Новосибирска
    Успехи молекулярной онкологии. 2018. Т. 5. № 2. С. 50-61. (Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61)
  404. М.В. Кручинина, В.Н. Кручинин, Я.И. Прудникова, А.А. Громов, М.В. Шашков, А.С. Соколова
    Исследование уровня жирных кислот мембран эритроцитов и сыворотки крови у пациентов с колоректальным раком г. Новосибирска
    Успехи молекулярной онкологии. 2018. Т. 5. № 2. С. 50-61. (Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61)
  405. М.В. Кручинина, В.Н. Кручинин, Я.И. Прудникова, А.А. Громов, М.В. Шашков, А.С. Соколова
    Исследование уровня жирных кислот мембран эритроцитов и сыворотки крови у пациентов с колоректальным раком г. Новосибирска
    Успехи молекулярной онкологии. 2018. Т. 5. № 2. С. 50-61. (Study of the level of fatty acids in erythrocyte membranes and serum of patients with colorectal cancer in Novosibirsk/ M.V. Kruchinina, V.N. Kruchinin, Ya.I. Prudnikova, A.A. Gromov, M.V. Shashkov, A.S. Sokolova// doi:10.17650/2313-805X-2018-5-2-50-61)
  406. A.V. Karakulov, E.A. Karpova, V.G. Vasiliev
    Ecological and geographical variation of morphometric parameters and flavonoid composition of Rhododendron parvifolium
    Turczaninowia, 2018, V. 21, N 2, Pp 133-144 doi:10.14258/turczaninowia.21.2.14
  407. A.V. Karakulov, E.A. Karpova, V.G. Vasiliev
    Ecological and geographical variation of morphometric parameters and flavonoid composition of Rhododendron parvifolium
    Turczaninowia, 2018, V. 21, N 2, Pp 133-144 doi:10.14258/turczaninowia.21.2.14
  408. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  409. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  410. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  411. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  412. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  413. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  414. A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, A.N. Kruk, P.A. Zaikin, I.A. Sokol, Yu.V. Seryotkin, Yu.N. Palyanov
    The Fe-C-O-H-N system at 6.3-7.8 GPa and 1200-1400 °C: implications for deep carbon and nitrogen cycles
    Contributions to Mineralogy and Petrology, 2018, V.173, N 6, Article Number 47 doi:10.1007/s00410-018-1472-3, IF=3.626
  415. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина
    Диазид трис(2,6-диметоксифенил)сурьмы. синтез и строение
    Журнал неоранической химии, 2018, Т. 63, N 6, Сс. 745-749 (Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086), IF=0.709
  416. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина
    Диазид трис(2,6-диметоксифенил)сурьмы. синтез и строение
    Журнал неоранической химии, 2018, Т. 63, N 6, Сс. 745-749 (Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086), IF=0.709
  417. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина
    Диазид трис(2,6-диметоксифенил)сурьмы. синтез и строение
    Журнал неоранической химии, 2018, Т. 63, N 6, Сс. 745-749 (Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086), IF=0.709
  418. И.В. Егорова, В.В. Жидков, И.П. Гринишак, И.Ю. Багрянская, Н.В. Первухина
    Диазид трис(2,6-диметоксифенил)сурьмы. синтез и строение
    Журнал неоранической химии, 2018, Т. 63, N 6, Сс. 745-749 (Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086), IF=0.709
  419. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Содержание биологически активных полифенолов Lonicera Caerulea Subsp. Pallasii в природе и культуре
    Химия растительного сырья, 2018, N 2, Cc. 89-96 (The content of biologically active polyphenols Lonicera Caerulea Subsp. Pallasll in Natural Conditions and the introduction/ I.G. Boyarskikh, K.G. Vasiliev, T.A. Kukushkina// Khimiya Rastitel'nogo Syr'ya, 2018, N 2, Pp 89-96 doi:10.14258/jcprm.2018023452)
  420. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Содержание биологически активных полифенолов Lonicera Caerulea Subsp. Pallasii в природе и культуре
    Химия растительного сырья, 2018, N 2, Cc. 89-96 (The content of biologically active polyphenols Lonicera Caerulea Subsp. Pallasll in Natural Conditions and the introduction/ I.G. Boyarskikh, K.G. Vasiliev, T.A. Kukushkina// Khimiya Rastitel'nogo Syr'ya, 2018, N 2, Pp 89-96 doi:10.14258/jcprm.2018023452)
  421. С.В. Морозов, Г.С. Ширапова, Е.И. Черняк, Н.И. Ткачева, В.Б. Батоев, Д.М. Могнонов
    Стойкие органические загрязнители в экосистеме озера Байкал
    Химия в интересах устойчивого развития. 2018. Т. 26. № 3. С. 233-239. (Persistent Organic Pollutants in the Ecosystem of the Lake Baikal/ S.V. Morozov, G.S. Shirapova, E.I. Chernyak, N.I. Tkacheva, V.B. Batoev, D.M. Mognonov// doi:10.15372/KhUR20180301)
  422. С.В. Морозов, Г.С. Ширапова, Е.И. Черняк, Н.И. Ткачева, В.Б. Батоев, Д.М. Могнонов
    Стойкие органические загрязнители в экосистеме озера Байкал
    Химия в интересах устойчивого развития. 2018. Т. 26. № 3. С. 233-239. (Persistent Organic Pollutants in the Ecosystem of the Lake Baikal/ S.V. Morozov, G.S. Shirapova, E.I. Chernyak, N.I. Tkacheva, V.B. Batoev, D.M. Mognonov// doi:10.15372/KhUR20180301)
  423. С.В. Морозов, Г.С. Ширапова, Е.И. Черняк, Н.И. Ткачева, В.Б. Батоев, Д.М. Могнонов
    Стойкие органические загрязнители в экосистеме озера Байкал
    Химия в интересах устойчивого развития. 2018. Т. 26. № 3. С. 233-239. (Persistent Organic Pollutants in the Ecosystem of the Lake Baikal/ S.V. Morozov, G.S. Shirapova, E.I. Chernyak, N.I. Tkacheva, V.B. Batoev, D.M. Mognonov// doi:10.15372/KhUR20180301)
  424. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  425. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  426. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  427. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  428. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  429. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  430. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  431. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  432. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  433. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  434. G. Audran, E. Bagryanskaya, M. Edeleva, S. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    Coordination-Initiated Nitroxide-Mediated Polymerization (CI-NMP)
    Australian Journal of Chemistry, 2018, V. 71, N 5, Pp 334-340 doi:10.1071/CH17570, IF=1.059
  435. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  436. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  437. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  438. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  439. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  440. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  441. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  442. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  443. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  444. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  445. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  446. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  447. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  448. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  449. I. Duttagupta, N. Jugniot, G. Audran, J-M. Franconi, S.R-A. Marque, P. Massot, P. Mellet, E. Parzy, E. Thiaudiere, N. Vanthuyne
    Selective On/Off-Nitroxides as Radical Probes to Investigate Non-radical Enzymatic Activity by Electron Paramagnetic Resonance
    Chemistry - A European Journal, 2018, V. 24, N 30, Pp 7615-7619 doi:10.1002/chem.201800866, IF=5.16
  450. A.V. Artem'ev, E.P. Doronina, I.Yu. Bagryanskaya, L.V. Klyba
    Bis(dicyclohexylselenophosphinyl)selenide, [Cy2P(Se)]2Se: Synthesis, molecular structure and application for self-assembly of a tetrahedral Cu(I) cluster
    Journal of Molecular Structure, 2018, V. 1160, Pp 208-214 doi:10.1016/j.molstruc.2018.02.007, IF=2.011
  451. A.V. Artem'ev, E.P. Doronina, I.Yu. Bagryanskaya, L.V. Klyba
    Bis(dicyclohexylselenophosphinyl)selenide, [Cy2P(Se)]2Se: Synthesis, molecular structure and application for self-assembly of a tetrahedral Cu(I) cluster
    Journal of Molecular Structure, 2018, V. 1160, Pp 208-214 doi:10.1016/j.molstruc.2018.02.007, IF=2.011
  452. A.V. Artem'ev, E.P. Doronina, I.Yu. Bagryanskaya, L.V. Klyba
    Bis(dicyclohexylselenophosphinyl)selenide, [Cy2P(Se)]2Se: Synthesis, molecular structure and application for self-assembly of a tetrahedral Cu(I) cluster
    Journal of Molecular Structure, 2018, V. 1160, Pp 208-214 doi:10.1016/j.molstruc.2018.02.007, IF=2.011
  453. F. Gaston, N. Dupuy, S.R-A. Marque, D. Gigmes, S. Dorey
    Monitoring of the discoloration on γ-irradiated PE and EVA films to evaluate antioxidant stability
    JJOURNAL OF APPLIED POLYMER SCIENCE, 2018, V. 135, N 18, Pp 46114-46122 doi:10.1002/app.46114, IF=1.9
  454. F. Gaston, N. Dupuy, S.R-A. Marque, D. Gigmes, S. Dorey
    Monitoring of the discoloration on γ-irradiated PE and EVA films to evaluate antioxidant stability
    JJOURNAL OF APPLIED POLYMER SCIENCE, 2018, V. 135, N 18, Pp 46114-46122 doi:10.1002/app.46114, IF=1.9
  455. F. Gaston, N. Dupuy, S.R-A. Marque, D. Gigmes, S. Dorey
    Monitoring of the discoloration on γ-irradiated PE and EVA films to evaluate antioxidant stability
    JJOURNAL OF APPLIED POLYMER SCIENCE, 2018, V. 135, N 18, Pp 46114-46122 doi:10.1002/app.46114, IF=1.9
  456. F. Gaston, N. Dupuy, S.R-A. Marque, D. Gigmes, S. Dorey
    Monitoring of the discoloration on γ-irradiated PE and EVA films to evaluate antioxidant stability
    JJOURNAL OF APPLIED POLYMER SCIENCE, 2018, V. 135, N 18, Pp 46114-46122 doi:10.1002/app.46114, IF=1.9
  457. A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
    Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
    ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
  458. A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
    Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
    ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
  459. F. Gaston, N. Dupuy, S.R-A. Marque, S. Dorey
    Evaluation of multilayer film stability by Raman spectroscopy after gamma-irradiation sterilization process
    Vibrational Spectroscopy, 2018, V.96, Pp 52-59 doi:10.1016/j.vibspec.2018.03.002, IF=1.363
  460. F. Gaston, N. Dupuy, S.R-A. Marque, S. Dorey
    Evaluation of multilayer film stability by Raman spectroscopy after gamma-irradiation sterilization process
    Vibrational Spectroscopy, 2018, V.96, Pp 52-59 doi:10.1016/j.vibspec.2018.03.002, IF=1.363
  461. F. Gaston, N. Dupuy, S.R-A. Marque, S. Dorey
    Evaluation of multilayer film stability by Raman spectroscopy after gamma-irradiation sterilization process
    Vibrational Spectroscopy, 2018, V.96, Pp 52-59 doi:10.1016/j.vibspec.2018.03.002, IF=1.363
  462. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  463. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  464. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  465. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  466. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  467. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  468. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  469. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  470. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  471. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  472. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  473. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  474. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  475. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  476. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  477. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  478. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
    Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
    Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
  479. G. Audran, E.G. Bagryanskaya, I.Yu. Bagryanskaya, M. Edeleva, P. Kaletina, S.R-A. Marque, D. Parkhomenko, E.V. Tretyakov, S.I. Zhivetyeva
    The effect of the oxophilic Tb(III) cation on Csingle bond-ON bond homolysis in alkoxyamines
    Inorganic Chemistry Communications, 2018, V. 91, Pp 5-7 doi:10.1016/j.inoche.2018.02.019, IF=1.81
  480. A.A. Kuzhelev, O.A. Krumkacheva, G.Yu. Shevelev, M. Yulikov, M.V. Fedin, E.G. Bagryanskaya
    Room-temperature distance measurements using RIDME and the orthogonal spin labels trityl/nitroxide
    Phys. Chem. Chem. Phys., 2018, V. 20, N 15, Pp 10224-10230 doi:10.1039/C8CP01093E, IF=3.906
  481. A.A. Kuzhelev, O.A. Krumkacheva, G.Yu. Shevelev, M. Yulikov, M.V. Fedin, E.G. Bagryanskaya
    Room-temperature distance measurements using RIDME and the orthogonal spin labels trityl/nitroxide
    Phys. Chem. Chem. Phys., 2018, V. 20, N 15, Pp 10224-10230 doi:10.1039/C8CP01093E, IF=3.906
  482. A.A. Kuzhelev, O.A. Krumkacheva, G.Yu. Shevelev, M. Yulikov, M.V. Fedin, E.G. Bagryanskaya
    Room-temperature distance measurements using RIDME and the orthogonal spin labels trityl/nitroxide
    Phys. Chem. Chem. Phys., 2018, V. 20, N 15, Pp 10224-10230 doi:10.1039/C8CP01093E, IF=3.906
  483. A.A. Kuzhelev, O.A. Krumkacheva, G.Yu. Shevelev, M. Yulikov, M.V. Fedin, E.G. Bagryanskaya
    Room-temperature distance measurements using RIDME and the orthogonal spin labels trityl/nitroxide
    Phys. Chem. Chem. Phys., 2018, V. 20, N 15, Pp 10224-10230 doi:10.1039/C8CP01093E, IF=3.906
  484. S. Dikalov, Yu.F. Polienko, I. Kirilyuk
    Electron Paramagnetic Resonance Measurements of Reactive Oxygen Species by Cyclic Hydroxylamine Spin Probes
    Antioxidants & Redox Signaling, 2018, V. 28, N 15, Pp 1433-1444 doi:10.1089/ars.2017.7396, IF=6.53
  485. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  486. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  487. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  488. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  489. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  490. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  491. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  492. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  493. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  494. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
  495. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  496. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  497. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  498. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  499. А.С. Донченко, В.В. Фоменко, В.Г. Васильев, В.Н. Афонюшкин, Н.А. Донченко, Ю.Н. Козлова, В.Ю. Коптев
    Изучение антагонистической активности бактерий, подавляющей синтез феназинов Pseudomonas aereginosa
    Сибирский вестник сельскохозяйственной науки, 2018. Т. 48. №.5. С. 23-29. doi: 10.26898/0370-8799-2018-5-3 doi:10.26898/0370-8799-2018-5-3
  500. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, В.М. Берестовицкая, М.Е. Иванова
    Синтез и строение циклогексенов, функционализированных нитро- и трифтор(хлор)метильной группами
    Журнал общей химии. 2018. Т. 88. № 5. С. 738-746 (Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079), IF=0.658
  501. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, В.М. Берестовицкая, М.Е. Иванова
    Синтез и строение циклогексенов, функционализированных нитро- и трифтор(хлор)метильной группами
    Журнал общей химии. 2018. Т. 88. № 5. С. 738-746 (Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079), IF=0.658
  502. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, В.М. Берестовицкая, М.Е. Иванова
    Синтез и строение циклогексенов, функционализированных нитро- и трифтор(хлор)метильной группами
    Журнал общей химии. 2018. Т. 88. № 5. С. 738-746 (Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079), IF=0.658
  503. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, В.М. Берестовицкая, М.Е. Иванова
    Синтез и строение циклогексенов, функционализированных нитро- и трифтор(хлор)метильной группами
    Журнал общей химии. 2018. Т. 88. № 5. С. 738-746 (Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079), IF=0.658
  504. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, В.М. Берестовицкая, М.Е. Иванова
    Синтез и строение циклогексенов, функционализированных нитро- и трифтор(хлор)метильной группами
    Журнал общей химии. 2018. Т. 88. № 5. С. 738-746 (Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079), IF=0.658
  505. Е.В. Черкасова, Н.В. Первухина, Н.В. Куратьева, И.Ю. Багрянская, Т.Г. Черкасова
    Синтез и кристаллические структуры гекса(изотиоцианато)хроматов(III) комплексов некоторых лантаноидов(III) иттриевой группы и европия с никотиновой кислотой
    Журнал неорганической химии. 2018. Т. 63. № 5. С. 596-600 (doi:10.7868/S0044457X18050100) (Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X), IF=0.709
  506. Е.В. Черкасова, Н.В. Первухина, Н.В. Куратьева, И.Ю. Багрянская, Т.Г. Черкасова
    Синтез и кристаллические структуры гекса(изотиоцианато)хроматов(III) комплексов некоторых лантаноидов(III) иттриевой группы и европия с никотиновой кислотой
    Журнал неорганической химии. 2018. Т. 63. № 5. С. 596-600 (doi:10.7868/S0044457X18050100) (Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X), IF=0.709
  507. Е.В. Черкасова, Н.В. Первухина, Н.В. Куратьева, И.Ю. Багрянская, Т.Г. Черкасова
    Синтез и кристаллические структуры гекса(изотиоцианато)хроматов(III) комплексов некоторых лантаноидов(III) иттриевой группы и европия с никотиновой кислотой
    Журнал неорганической химии. 2018. Т. 63. № 5. С. 596-600 (doi:10.7868/S0044457X18050100) (Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X), IF=0.709
  508. Е.В. Черкасова, Н.В. Первухина, Н.В. Куратьева, И.Ю. Багрянская, Т.Г. Черкасова
    Синтез и кристаллические структуры гекса(изотиоцианато)хроматов(III) комплексов некоторых лантаноидов(III) иттриевой группы и европия с никотиновой кислотой
    Журнал неорганической химии. 2018. Т. 63. № 5. С. 596-600 (doi:10.7868/S0044457X18050100) (Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X), IF=0.709
  509. Г.Е. Сальников, А.М. Генаев, А.В. Шернюков, Ч. Чжу, Н.В. Ткаченко, К.Ю. Колтунов
    Конфигурационная стабильность 1,1’-би-2-нафтола в суперкислой среде HSO3F-SBF5-SO2ClF
    Журнал органической химии. 2018. Т. 54. № 5. С. 787-789 (Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214), IF=0.655
  510. Г.Е. Сальников, А.М. Генаев, А.В. Шернюков, Ч. Чжу, Н.В. Ткаченко, К.Ю. Колтунов
    Конфигурационная стабильность 1,1’-би-2-нафтола в суперкислой среде HSO3F-SBF5-SO2ClF
    Журнал органической химии. 2018. Т. 54. № 5. С. 787-789 (Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214), IF=0.655
  511. Г.Е. Сальников, А.М. Генаев, А.В. Шернюков, Ч. Чжу, Н.В. Ткаченко, К.Ю. Колтунов
    Конфигурационная стабильность 1,1’-би-2-нафтола в суперкислой среде HSO3F-SBF5-SO2ClF
    Журнал органической химии. 2018. Т. 54. № 5. С. 787-789 (Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214), IF=0.655
  512. M.M. Petrova, S.I. Zhivetyeva, E.V. Tretyakov
    Triplet Diradicals Derived From Quinone-Nitroxides: A Quantum-Chemical Study
    SDRP Journal of Computational Chemistry & Molecular Modelling, 2018, V: 2, N 2 doi:10.25177/JCCMM.2.2.5
  513. D.V. Spiryova, O.Yu. Karmatskih, A.Yu. Vorob'ev, A.E. Moskalensky
    Towards optical control of single blood platelet activation
    Серия книг: Proceedings of SPIE Том: 10717 Номер статьи: 1071722 ,Saratov Fall Meeting 2017: Laser Physics and Photonics XVIII; and Computational Biophysics and Analysis of Biomedical Data IV; 1071722 (2018) doi:10.1117/12.2305477
  514. D.V. Spiryova, O.Yu. Karmatskih, A.Yu. Vorob'ev, A.E. Moskalensky
    Towards optical control of single blood platelet activation
    Серия книг: Proceedings of SPIE Том: 10717 Номер статьи: 1071722 ,Saratov Fall Meeting 2017: Laser Physics and Photonics XVIII; and Computational Biophysics and Analysis of Biomedical Data IV; 1071722 (2018) doi:10.1117/12.2305477
  515. D.V. Spiryova, O.Yu. Karmatskih, A.Yu. Vorob'ev, A.E. Moskalensky
    Towards optical control of single blood platelet activation
    Серия книг: Proceedings of SPIE Том: 10717 Номер статьи: 1071722 ,Saratov Fall Meeting 2017: Laser Physics and Photonics XVIII; and Computational Biophysics and Analysis of Biomedical Data IV; 1071722 (2018) doi:10.1117/12.2305477
  516. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
  517. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
  518. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
  519. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
  520. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
  521. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  522. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  523. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  524. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  525. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  526. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  527. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  528. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  529. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  530. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  531. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  532. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  533. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  534. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  535. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  536. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  537. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  538. Т.Г. Толстикова, В.Н. Бабенко, И.Л. Коваленко, Д.А. Смагин, А.Г. Галямина, Н.Н. Кудрявцева, С.А. Борисов, Н.В. Тамкович
    Дифференциально экспрессирующиеся гены нейромедиаторных систем в дорсальном стриатуме самцов мышей с двигательными нарушениями
    Журнал высшей нервной деятельности им. И.П. Павлова, 2018, Т. 68, N 2, Сс. 227-249 (Differentially expressed neurotransmitter genes in the dorsal striatum of male mice with psychomotor disturbances/ D.A. Smagin, A.G. Galyamina, I.L. Kovalenko, V.N. Babenko, N.V. Tamkovich, S.A. Borisov, T.G. Tolstikova, N.N. Kudryavtseva// Zhurnal vysshei nervnoi deyatelnosti imeniI I P Pavlova, 2018, V. 68, N 2, Pp 227-249 doi:10.7868/S0044467718020089), IF=0.31
  539. I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
    Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
  540. I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
    Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
  541. I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
    Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
  542. I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
    Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
  543. V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
    A New Synthetic Route to Heteroanthracenes
    European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
  544. V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
    A New Synthetic Route to Heteroanthracenes
    European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
  545. V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
    A New Synthetic Route to Heteroanthracenes
    European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
  546. V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
    A New Synthetic Route to Heteroanthracenes
    European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
  547. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  548. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  549. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  550. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  551. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  552. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  553. V.Yu. Krukov, O.G. Tomilova, O.A. Luzina, O.N. Yaroslavtseva, Yu.B. Akhanaev, M.V. Tyurin, B.A. Duisembekov, N.F. Salakhutdinov, V.V. Glupov
    Effects of fluorine-containing usnic acid and fungus Beauveria bassiana on the survival and immune-physiological reactions of Colorado potato beetle larvae
    Pest Management Science, 2018, V. 74, N 3, Pp 598-606 doi:10.1002/ps.4741, IF=3.249
  554. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  555. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  556. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  557. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  558. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  559. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
    Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
  560. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  561. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  562. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  563. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  564. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  565. A.M. Cheplakova, K.A. Kovalenko, D.G. Samsonenko, V.A. Lazarenko, V.N. Khrustalev, A.S. Vinogradov, V.M. Karpov, V.E. Platonov, V.P. Fedin
    Metal-organic frameworks based on octafluorobiphenyl-4,4'-dicarboxylate: synthesis, crystal structure, and surface functionality
    Dalton Trans., 2018, V. 47, N 10, Pp. 3283-3297 doi:10.1039/C7DT04566B, IF=4.099
  566. I.O. Timofeev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Refining Spin–Spin Distance Distributions in Complex Biological Systems Using Multi-Gaussian Monte Carlo Analysis
    Applied Magnetic Resonance, 2018, V. 49, N 3, pp 265-276 doi:10.1007/s00723-017-0965-y, IF=0.835
  567. I.O. Timofeev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Refining Spin–Spin Distance Distributions in Complex Biological Systems Using Multi-Gaussian Monte Carlo Analysis
    Applied Magnetic Resonance, 2018, V. 49, N 3, pp 265-276 doi:10.1007/s00723-017-0965-y, IF=0.835
  568. I.O. Timofeev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Refining Spin–Spin Distance Distributions in Complex Biological Systems Using Multi-Gaussian Monte Carlo Analysis
    Applied Magnetic Resonance, 2018, V. 49, N 3, pp 265-276 doi:10.1007/s00723-017-0965-y, IF=0.835
  569. I.O. Timofeev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Refining Spin–Spin Distance Distributions in Complex Biological Systems Using Multi-Gaussian Monte Carlo Analysis
    Applied Magnetic Resonance, 2018, V. 49, N 3, pp 265-276 doi:10.1007/s00723-017-0965-y, IF=0.835
  570. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  571. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  572. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  573. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  574. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  575. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  576. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  577. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  578. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  579. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  580. Т.С. Фролова, С.Ж. Шарапов, О.И. Синицина, Т.Г. Толстикова, И.А. Григорьев, С.В. Морозов, Ю.В. Юшкова
    Новые ионные конъюгаты на основе a-токоферилсукцината как потенциальные цитотоксические агенты1
    Биоорганическая химия. 2018. Т. 44. № 3. С. 325-332. doi:10.7868/S0132342318030089, IF=0.838
  581. Т.С. Фролова, С.Ж. Шарапов, О.И. Синицина, Т.Г. Толстикова, И.А. Григорьев, С.В. Морозов, Ю.В. Юшкова
    Новые ионные конъюгаты на основе a-токоферилсукцината как потенциальные цитотоксические агенты1
    Биоорганическая химия. 2018. Т. 44. № 3. С. 325-332. doi:10.7868/S0132342318030089, IF=0.838
  582. Е.В. Третьяков, Т.В. Махнева, Л.В. Политанская, И.Ю. Багрянская, Д.В. Стась
    Молекулярная и кристаллическая структура 2-амино-полифторфенил-4,4,5,5-тетраметил-4,5-дигидро-1H-имидазол-3-оксид-1-оксилов
    Журнал структурной химии, 2018, Т.59, № 3, 2018, стр.712-719 (doi:10.26902/JSC20180328) (Molecular and Crystal Structure of 2-Amino-Polyfluorophenyl-4,4,5,5-Tetramethyl-4,5-Dihydro-1H-Imidazol- 3-Oxide-1-Oxyls/ E.V. Tretyakov, T.V. Makhneva, L.V. Politanskaya, I.Yu. Bagryanskaya, D.V. Stass// Journal of Structural Chemistry, 2018, V. 59, N 3, pp 689-696 doi:10.1134/S0022476618030289), IF=0.521
  583. S.I. Dikalov, A.E. Dikalova, D.A. Morozov, I.A. Kirilyuk
    Cellular accumulation and antioxidant activity of acetoxymethoxycarbonyl pyrrolidine nitroxides
    Free Radical Research, 2018, V. 52, N 3: International Conference on Electron Paramagnetic Resonance Spectroscopy and Imaging of Biological Systems (EPR-2017), Pp 339-350 doi:10.1080/10715762.2017.1390744, IF=3.038
  584. S.I. Dikalov, A.E. Dikalova, D.A. Morozov, I.A. Kirilyuk
    Cellular accumulation and antioxidant activity of acetoxymethoxycarbonyl pyrrolidine nitroxides
    Free Radical Research, 2018, V. 52, N 3: International Conference on Electron Paramagnetic Resonance Spectroscopy and Imaging of Biological Systems (EPR-2017), Pp 339-350 doi:10.1080/10715762.2017.1390744, IF=3.038
  585. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  586. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  587. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  588. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  589. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  590. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  591. D.S. Sergeevichev, A.A. Krasilnikova, A.G. Strelnikov, V.V. Fomenko, N.F. Salakhutdinov, A.B. Romanov, A.M. Karaskov, E.A. Pokushalov, J.S. Steinberg
    Globular chitosan prolongs the effective duration time and decreases the acute toxicity of botulinum neurotoxin after intramuscular injection in rats
    Toxicon, 2018, V. 143, Pp 90-95 doi:10.1016/j.toxicon.2018.01.013, IF=2.352
  592. A.V. Vorontsov, S.V. Tsybulya
    Influence of Nanoparticles Size on XRD Patterns for Small Monodisperse Nanoparticles of Cu0 and TiO2 Anatase
    Ind. Eng. Chem. Res., 2018, 57 (7), pp 2526-2536 doi:10.1021/acs.iecr.7b04480, IF=3.141
  593. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  594. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  595. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  596. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  597. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  598. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  599. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  600. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  601. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  602. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  603. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  604. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  605. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  606. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  607. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  608. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  609. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  610. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  611. A.A. Krasilnikova, D.S. Sergeevichev, V.V. Fomenko, A.A. Korobeynikov, M.B. Vasilyeva, A.S. Yunoshev, A.M. Karaskov, E.A. Pokushalov
    Globular chitosan treatment of bovine jugular veins: Evidence of anticalcification efficacy in the subcutaneous rat model
    Cardiovascular Pathology, V. 32, January-February 2018, Pp 1-7 doi:10.1016/j.carpath.2017.08.003, IF=2.496
  612. Е.Ф. Пен, В.В. Шелковников
    Особенности оптических свойств голографических структур на основе фотополимерных материалов
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 2. С. 9-15.
  613. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, I.P. Chuikov, E.V. Malykhin
    Controlled self-assembly of π-stacked/H-bonded 1D crystal structures from polyfluorinated arylamines and 18-crown-6 (2:1).Associate vs. co-former fluorescence properties
    CrystEngComm, 2018, V. 20, N 6, Pp 807-817 doi:10.1039/C7CE01851G, IF=3.304
  614. A.S. Berezin, K.A. Vinogradova, V.A. Nadolinny, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M.B. Bushuev
    Temperature- and excitation wavelength-dependent emission in a manganese(II) complex
    Dalton Trans., 2018, V. 47, N 5, Pp 1657-1665 doi:10.1039/C7DT04535B, IF=4.099
  615. A.S. Berezin, K.A. Vinogradova, V.A. Nadolinny, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M.B. Bushuev
    Temperature- and excitation wavelength-dependent emission in a manganese(II) complex
    Dalton Trans., 2018, V. 47, N 5, Pp 1657-1665 doi:10.1039/C7DT04535B, IF=4.099
  616. A.S. Berezin, K.A. Vinogradova, V.A. Nadolinny, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M.B. Bushuev
    Temperature- and excitation wavelength-dependent emission in a manganese(II) complex
    Dalton Trans., 2018, V. 47, N 5, Pp 1657-1665 doi:10.1039/C7DT04535B, IF=4.099
  617. A.S. Berezin, K.A. Vinogradova, V.A. Nadolinny, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M.B. Bushuev
    Temperature- and excitation wavelength-dependent emission in a manganese(II) complex
    Dalton Trans., 2018, V. 47, N 5, Pp 1657-1665 doi:10.1039/C7DT04535B, IF=4.099
  618. A.S. Berezin, K.A. Vinogradova, V.A. Nadolinny, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M.B. Bushuev
    Temperature- and excitation wavelength-dependent emission in a manganese(II) complex
    Dalton Trans., 2018, V. 47, N 5, Pp 1657-1665 doi:10.1039/C7DT04535B, IF=4.099
  619. K.P. Volcho, S.S. Laev, G.M. Ashraf, G. Aliev, N.F. Salakhutdinov
    Application of monoterpenoids and their derivatives for treatment of neurodegenerative disorders.
    Curr Med Chem., 2018, V. 25, N 39, Pp 5327 - 5346 doi:10.2174/0929867324666170112101837, IF=3.469
  620. K.P. Volcho, S.S. Laev, G.M. Ashraf, G. Aliev, N.F. Salakhutdinov
    Application of monoterpenoids and their derivatives for treatment of neurodegenerative disorders.
    Curr Med Chem., 2018, V. 25, N 39, Pp 5327 - 5346 doi:10.2174/0929867324666170112101837, IF=3.469
  621. A.O. Bryzgalov, T.G. Tolstikova, E.E. Shults, K.O. Petrova
    Natural Products as a Source of Antiarrhythmic Drugs
    Mini-Reviews in Medicinal Chemistry, 2018, V. 18, N 4, Pp 345 - 362 doi:10.2174/1389557516666161104144815, IF=2.645
  622. О.А. Логутенко, А.И. Титков, А.М. Воробьёв, И.К. Шундрина, Ю.М. Юхин, Н.З. Ляхов
    Синтез нано-частиц никеля восстановлением его солей модифицированным полиольным методом в присутствии полиакрилатов натрия с различной молекулярной массой
    Журнал общей химии, 2018, Т. 88, N 2, Сс. 311-318 (Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160), IF=0.658
  623. О.А. Логутенко, А.И. Титков, А.М. Воробьёв, И.К. Шундрина, Ю.М. Юхин, Н.З. Ляхов
    Синтез нано-частиц никеля восстановлением его солей модифицированным полиольным методом в присутствии полиакрилатов натрия с различной молекулярной массой
    Журнал общей химии, 2018, Т. 88, N 2, Сс. 311-318 (Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160), IF=0.658
  624. О.А. Логутенко, А.И. Титков, А.М. Воробьёв, И.К. Шундрина, Ю.М. Юхин, Н.З. Ляхов
    Синтез нано-частиц никеля восстановлением его солей модифицированным полиольным методом в присутствии полиакрилатов натрия с различной молекулярной массой
    Журнал общей химии, 2018, Т. 88, N 2, Сс. 311-318 (Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160), IF=0.658
  625. О.А. Логутенко, А.И. Титков, А.М. Воробьёв, И.К. Шундрина, Ю.М. Юхин, Н.З. Ляхов
    Синтез нано-частиц никеля восстановлением его солей модифицированным полиольным методом в присутствии полиакрилатов натрия с различной молекулярной массой
    Журнал общей химии, 2018, Т. 88, N 2, Сс. 311-318 (Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160), IF=0.658
  626. О.А. Логутенко, А.И. Титков, А.М. Воробьёв, И.К. Шундрина, Ю.М. Юхин, Н.З. Ляхов
    Синтез нано-частиц никеля восстановлением его солей модифицированным полиольным методом в присутствии полиакрилатов натрия с различной молекулярной массой
    Журнал общей химии, 2018, Т. 88, N 2, Сс. 311-318 (Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160), IF=0.658
  627. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions
    Mendeleev Communications, 2018, V. 28, N 1, Pp 27-28 doi:10.1016/j.mencom.2018.01.007, IF=2.098
  628. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions
    Mendeleev Communications, 2018, V. 28, N 1, Pp 27-28 doi:10.1016/j.mencom.2018.01.007, IF=2.098
  629. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  630. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  631. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  632. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  633. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  634. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  635. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  636. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
  637. Q. Zhang, N.E. Polyakov, Yu.S. Chistyachenko, M.V. Khvostov, T.S. Frolova, T.G. Tolstikova, A.V. Dushkin, W. Su
    Preparation of curcumin self-micelle solid dispersion with enhanced bioavailability and cytotoxic activity by mechanochemistry
    Drug Delivery, 2018, V. 25, N 1, P. 198-209 doi:10.1080/10717544.2017.1422298, IF=3.095
  638. Q. Zhang, N.E. Polyakov, Yu.S. Chistyachenko, M.V. Khvostov, T.S. Frolova, T.G. Tolstikova, A.V. Dushkin, W. Su
    Preparation of curcumin self-micelle solid dispersion with enhanced bioavailability and cytotoxic activity by mechanochemistry
    Drug Delivery, 2018, V. 25, N 1, P. 198-209 doi:10.1080/10717544.2017.1422298, IF=3.095
  639. Q. Zhang, N.E. Polyakov, Yu.S. Chistyachenko, M.V. Khvostov, T.S. Frolova, T.G. Tolstikova, A.V. Dushkin, W. Su
    Preparation of curcumin self-micelle solid dispersion with enhanced bioavailability and cytotoxic activity by mechanochemistry
    Drug Delivery, 2018, V. 25, N 1, P. 198-209 doi:10.1080/10717544.2017.1422298, IF=3.095
  640. Q. Zhang, N.E. Polyakov, Yu.S. Chistyachenko, M.V. Khvostov, T.S. Frolova, T.G. Tolstikova, A.V. Dushkin, W. Su
    Preparation of curcumin self-micelle solid dispersion with enhanced bioavailability and cytotoxic activity by mechanochemistry
    Drug Delivery, 2018, V. 25, N 1, P. 198-209 doi:10.1080/10717544.2017.1422298, IF=3.095
  641. Q. Zhang, N.E. Polyakov, Yu.S. Chistyachenko, M.V. Khvostov, T.S. Frolova, T.G. Tolstikova, A.V. Dushkin, W. Su
    Preparation of curcumin self-micelle solid dispersion with enhanced bioavailability and cytotoxic activity by mechanochemistry
    Drug Delivery, 2018, V. 25, N 1, P. 198-209 doi:10.1080/10717544.2017.1422298, IF=3.095
  642. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  643. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  644. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  645. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  646. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  647. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  648. E. Avdeeva, E. Shults, M. Skorokhodova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, E. Krasnov, M. Belousov
    Flavonol glycosides from Saussurea controversa and Their Efficiency in Experimental Osteomyelitis
    Planta Med Int Open, 2018, V. 5, N 1, : e24-e29 doi:10.1055/s-0044-100799
  649. A.M. Agafoncev, T.A. Shumilova, A.V. Tkachev
    Microwave Assisted Syntheses of 4-Amino-carane-3-ols from 3,4-Epoxycarane and Heterocyclic Amines
    Current microwawe chemistry, 2018, V. 5, N 1, Pp 54 - 61 doi:10.2174/2213335604666171129154210, IF=0.212
  650. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
  651. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
  652. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
  653. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
  654. A.V. Vorontsov, E.N. Kabachkov, I.L. Balikhin, E.N. Kurkin, V.N. Troitskii, P.G. Smirniotis
    Correlation of Surface Area with Photocatalytic Activity of TiO2
    Journal of Advanced Oxidation Technologies, 2018, V. 21, N 1, , Art Number 20170063 doi:10.26802/jaots.2017.0063, IF=0.901
  655. S. Dorey, F. Gaston, S.R-A. Marque, B. Bortolotti, N. Dupuy
    XPS analysis of PE and EVA samples irradiated at different γ-doses
    Applied Surface Science, 2018, V. 427, Pp 966-972 doi:10.1016/j.apsusc.2017.09.001, IF=4.439
  656. S. Dorey, F. Gaston, S.R-A. Marque, B. Bortolotti, N. Dupuy
    XPS analysis of PE and EVA samples irradiated at different γ-doses
    Applied Surface Science, 2018, V. 427, Pp 966-972 doi:10.1016/j.apsusc.2017.09.001, IF=4.439
  657. S. Dorey, F. Gaston, S.R-A. Marque, B. Bortolotti, N. Dupuy
    XPS analysis of PE and EVA samples irradiated at different γ-doses
    Applied Surface Science, 2018, V. 427, Pp 966-972 doi:10.1016/j.apsusc.2017.09.001, IF=4.439
  658. S. Dorey, F. Gaston, S.R-A. Marque, B. Bortolotti, N. Dupuy
    XPS analysis of PE and EVA samples irradiated at different γ-doses
    Applied Surface Science, 2018, V. 427, Pp 966-972 doi:10.1016/j.apsusc.2017.09.001, IF=4.439
  659. Деревянко Д.И., Корольков В.П., Шелковников В.В.
    Исследование механических свойств нового гибридного фотополимерного материала для фоторепликации
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 108-112. (STUDY OF MECHANICAL PROPERTIES OF A NEW HYBRID PHOTOPOLYMERIC MATERIAL FOR PHOTOREPLICATION/ D.I.Derevyanko, V.P.Korolkov, V.V.Shelkovnikov// )
  660. Микерин С.Л., Плеханов А.И., Симанчук А.Э., Якиманский А.В., Шелковников В.В., Валишева Н.А.
    Компактный планарный волноводный модулятор на основе электрооптических полимеров
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 95-100.
  661. Микерин С.Л., Плеханов А.И., Симанчук А.Э., Якиманский А.В., Шелковников В.В., Валишева Н.А.
    Компактный планарный волноводный модулятор на основе электрооптических полимеров
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 95-100.
  662. Микерин С.Л., Плеханов А.И., Симанчук А.Э., Якиманский А.В., Шелковников В.В., Валишева Н.А.
    Компактный планарный волноводный модулятор на основе электрооптических полимеров
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 95-100.
  663. Микерин С.Л., Плеханов А.И., Симанчук А.Э., Якиманский А.В., Шелковников В.В., Валишева Н.А.
    Компактный планарный волноводный модулятор на основе электрооптических полимеров
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 95-100.
  664. Микерин С.Л., Плеханов А.И., Симанчук А.Э., Якиманский А.В., Шелковников В.В., Валишева Н.А.
    Компактный планарный волноводный модулятор на основе электрооптических полимеров
    Интерэкспо Гео-Сибирь. 2018. Т. 5. № 1. С. 95-100.
  665. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  666. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  667. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  668. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  669. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  670. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  671. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  672. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  673. Avgustinovich D.F., Katokhin A.V., Kontsevaya G.V., Lvova M.N., Vishnivetskaya G.B., Kashina E.V., Marenina M.K., Maksimova G.A., Zav'yalov E.L., Mordvinov V.A.
    A comparative study of opistrorchis felineus (RIVOLTA, 1884) infection in inbred C57BL/6 AND outbred CD-1 mice
    Паразитология. 2018. Т. 52. № 1. С. 19-31
  674. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  675. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  676. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  677. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  678. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  679. М.В. Кручинина, А.А. Громов, Я.И. Прудникова, В.Н. Кручинин, М.В. Шашков, В.Н. Сидельников, А.С. Соколова, Н.Ф. Салахутдинов
    Изменения липидома при колоректальном раке
    Атеросклероз. 2018. Т. 14. № 1. С. 50-64 (CHANGES OF LIPIDOM IN COLORECTAL CANCER/ Kruchinina M.V., Gromov A.A., Prudnikova Ia.I., Kruchinin V.N., Shashkov M.V., Sidelnikov V.N., Sokolova A.S., Salakhutdinov N.F.// doi:10.15372/ATER20180107)
  680. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  681. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  682. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  683. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  684. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  685. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  686. G.Yu. Shevelev, E.L. Gulyak, A.A. Lomzov, A.A. Kuzhelev, O.A. Krumkacheva, M.S. Kupryushkin, V.M. Tormyshev, M.V. Fedin, E.G. Bagryanskaya, D. V. Pyshnyi
    A Versatile Approach to Attachment of Triarylmethyl Labels to DNA for Nanoscale Structural EPR Studies at Physiological Temperatures
    J. Phys. Chem. B, 2018, 122 (1), pp 137-143 doi:10.1021/acs.jpcb.7b10689, IF=3.146
  687. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  688. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  689. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  690. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  691. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  692. С.Н. Атутов, С.Л. Микерин, А.И. Плеханов, А.Э. Симанчук, В.А. Сорокин, А.В. Якиманский, Н.Н. Смирнов, Н.А. Валишева
    Планарный фазовый электрооптический модулятор на основе хромофорсодержащих полиимидов
    Автометрия. 2018. Т. 54. № 1. С. 46-53 (Planar Phase Electro-Optical Modulator Based on Chromophore-Doped Polyimides/ S. N. Atutov, S. L. Mikerin, A. I. Plekhanov, E.A. E. Simanchuk, V. A. Sorokin, A. V. Yakimansky, N. N. Smirnov, N. A. Valisheva// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 39-45 doi:10.3103/S8756699018010077)
  693. Е.Ф. Пен, В.В. Шелковников
    Сравнение дифракционной эффективности голографических отражательных решёток для различных схем записи в фотополимерном материале
    Автометрия. 2018. Т. 54. № 1. С. 3-9 (Comparison of the Diffraction Efficiency of Reflection Holographic Gratings for Different Recording Schemes in Photopolymer Materials/ E. F. Pen, V. V. Shelkovnikov// Optoelectronics, Instrumentation and Data Processing, 2018, V. 54, N 1, pp 1-6 doi:10.3103/S8756699018010016)
  694. Л.С. Константинова, Е.А. Князева, Ю.В. Гатилов, С.Г. Злотин, О.А. Ракитин
    Синтез и исследование структуры нитропроизводных 1-оксидов 2,1,3-бензотиадиазолов и их способности выделять NO
    Известия Академии наук. Серия химическая. 2018. № 1. С. 95-101 (Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6), IF=0.781
  695. Л.С. Константинова, Е.А. Князева, Ю.В. Гатилов, С.Г. Злотин, О.А. Ракитин
    Синтез и исследование структуры нитропроизводных 1-оксидов 2,1,3-бензотиадиазолов и их способности выделять NO
    Известия Академии наук. Серия химическая. 2018. № 1. С. 95-101 (Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6), IF=0.781
  696. Л.С. Константинова, Е.А. Князева, Ю.В. Гатилов, С.Г. Злотин, О.А. Ракитин
    Синтез и исследование структуры нитропроизводных 1-оксидов 2,1,3-бензотиадиазолов и их способности выделять NO
    Известия Академии наук. Серия химическая. 2018. № 1. С. 95-101 (Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6), IF=0.781
  697. Л.С. Константинова, Е.А. Князева, Ю.В. Гатилов, С.Г. Злотин, О.А. Ракитин
    Синтез и исследование структуры нитропроизводных 1-оксидов 2,1,3-бензотиадиазолов и их способности выделять NO
    Известия Академии наук. Серия химическая. 2018. № 1. С. 95-101 (Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6), IF=0.781
  698. Л.М. Горностаев, Т.А. Руковец, Е.В. Арнольд, Ю.Г. Халявина, Ю.В. Гатилов
    Оксимирование2-(К1-амино)-4-(К2-имино)-1(
    Журнал органической химии. 2018. Т. 54. № 1-12. С. 82-89. (Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062), IF=0.655
  699. Л.М. Горностаев, Т.А. Руковец, Е.В. Арнольд, Ю.Г. Халявина, Ю.В. Гатилов
    Оксимирование2-(К1-амино)-4-(К2-имино)-1(
    Журнал органической химии. 2018. Т. 54. № 1-12. С. 82-89. (Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062), IF=0.655
  700. Л.М. Горностаев, Т.А. Руковец, Е.В. Арнольд, Ю.Г. Халявина, Ю.В. Гатилов
    Оксимирование2-(К1-амино)-4-(К2-имино)-1(
    Журнал органической химии. 2018. Т. 54. № 1-12. С. 82-89. (Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062), IF=0.655
  701. Л.М. Горностаев, Т.А. Руковец, Е.В. Арнольд, Ю.Г. Халявина, Ю.В. Гатилов
    Оксимирование2-(К1-амино)-4-(К2-имино)-1(
    Журнал органической химии. 2018. Т. 54. № 1-12. С. 82-89. (Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062), IF=0.655
  702. Ю.А. Брылева, Л.А. Глинская, К.С. Маренин, А.С. Богомяков, Д.А. Пирязев, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(II) с хиральными лигандами, содержащими фрагменты монотерпеноидов и эфиров аминокислот
    Kоординационная химия, 2018, Том 44, № 1, С.28-37 (Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033), IF=0.674
  703. Ю.А. Брылева, Л.А. Глинская, К.С. Маренин, А.С. Богомяков, Д.А. Пирязев, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(II) с хиральными лигандами, содержащими фрагменты монотерпеноидов и эфиров аминокислот
    Kоординационная химия, 2018, Том 44, № 1, С.28-37 (Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033), IF=0.674
  704. Ю.А. Брылева, Л.А. Глинская, К.С. Маренин, А.С. Богомяков, Д.А. Пирязев, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(II) с хиральными лигандами, содержащими фрагменты монотерпеноидов и эфиров аминокислот
    Kоординационная химия, 2018, Том 44, № 1, С.28-37 (Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033), IF=0.674
  705. Ю.А. Брылева, Л.А. Глинская, К.С. Маренин, А.С. Богомяков, Д.А. Пирязев, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(II) с хиральными лигандами, содержащими фрагменты монотерпеноидов и эфиров аминокислот
    Kоординационная химия, 2018, Том 44, № 1, С.28-37 (Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033), IF=0.674
  706. Ю.А. Брылева, Л.А. Глинская, К.С. Маренин, А.С. Богомяков, Д.А. Пирязев, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(II) с хиральными лигандами, содержащими фрагменты монотерпеноидов и эфиров аминокислот
    Kоординационная химия, 2018, Том 44, № 1, С.28-37 (Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters/ Copper(II) Complexes with Chiral Ligands Containing Fragments of Monoterpenoids and Amino Acid Esters// Russian Journal of Coordination Chemistry, 2018, V. 44, N 2, pp 117-126 doi:10.1134/S1070328418020033), IF=0.674
  707. S. Dorey, F. Gaston, N. Dupuy, M. Barbaroux, S.R-A. Marque
    Reconciliation of pH, conductivity, total organic carbon with carboxylic acids detected by ion chromatography in solution after contact with multilayer films after γ-irradiation
    European Journal of Pharmaceutical Sciences, 2018, V. 117, Pages 216-226 doi:10.1016/j.ejps.2018.02.023, IF=3.466
  708. S. Dorey, F. Gaston, N. Dupuy, M. Barbaroux, S.R-A. Marque
    Reconciliation of pH, conductivity, total organic carbon with carboxylic acids detected by ion chromatography in solution after contact with multilayer films after γ-irradiation
    European Journal of Pharmaceutical Sciences, 2018, V. 117, Pages 216-226 doi:10.1016/j.ejps.2018.02.023, IF=3.466
  709. S. Dorey, F. Gaston, N. Dupuy, M. Barbaroux, S.R-A. Marque
    Reconciliation of pH, conductivity, total organic carbon with carboxylic acids detected by ion chromatography in solution after contact with multilayer films after γ-irradiation
    European Journal of Pharmaceutical Sciences, 2018, V. 117, Pages 216-226 doi:10.1016/j.ejps.2018.02.023, IF=3.466
  710. S. Dorey, F. Gaston, N. Dupuy, M. Barbaroux, S.R-A. Marque
    Reconciliation of pH, conductivity, total organic carbon with carboxylic acids detected by ion chromatography in solution after contact with multilayer films after γ-irradiation
    European Journal of Pharmaceutical Sciences, 2018, V. 117, Pages 216-226 doi:10.1016/j.ejps.2018.02.023, IF=3.466

2017

Reviews, articles

  1. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  2. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  3. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  4. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  5. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  6. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  7. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  8. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  9. R. Kong, X. Zhu, E.S. Meteleva, Yu.S. Chistyachenko, L.P. Suntsova, N.E. Polyakov, M.V. Khvostov, D.S. Baev, T.G. Tolstikova, J. Yu, A.V. Dushkin, W. Su
    Enhanced solubility and bioavailability of simvastatin by mechanochemically obtained complexes
    International Journal of Pharmaceutics, 2017, V. 534, N 1-2, Pp 108-118 doi:10.1016/j.ijpharm.2017.10.011, IF=3.648
  10. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  11. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  12. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  13. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  14. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  15. H. Suo, I.V. Oleynik, C. Huang, I.I. Oleynik, G.A. Solan, Ya. Ma, T.Liang. Wen-Hua. Sun
    ortho-Cycloalkyl substituted N,N'-diaryliminoacenaphthene-Ni(II) catalysts for polyethylene elastomers; exploring ring size and temperature effects
    Dalton Trans., 2017, V. 46, N 45, Pp 15684-15697 doi:10.1039/C7DT03362A, IF=4.28
  16. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  17. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  18. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  19. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  20. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  21. Шрамко В.С., Рагино Ю.И., Морозов С.В., Черняк Е.И., Чернявский А.М.
    Ненасыщенные жирные кислоты и липиднолипопротеиновые показатели у пациентов с коронарным атеросклерозом
    Комплексные проблемы сердечно-сосудистых заболеваний. 2017. Т. 6. № S4. С. 47.
  22. Шрамко В.С., Рагино Ю.И., Морозов С.В., Черняк Е.И., Чернявский А.М.
    Ненасыщенные жирные кислоты и липиднолипопротеиновые показатели у пациентов с коронарным атеросклерозом
    Комплексные проблемы сердечно-сосудистых заболеваний. 2017. Т. 6. № S4. С. 47.
  23. Шрамко В.С., Рагино Ю.И., Морозов С.В., Черняк Е.И., Чернявский А.М.
    Ненасыщенные жирные кислоты и липиднолипопротеиновые показатели у пациентов с коронарным атеросклерозом
    Комплексные проблемы сердечно-сосудистых заболеваний. 2017. Т. 6. № S4. С. 47.
  24. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  25. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  26. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  27. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  28. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  29. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  30. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  31. N.A. Vorotnikova, M.V. Edeleva, O.G. Kurskaya, K.A. Brylev, A.M. Shestopalov, Yu.V. Mironov, A.J. Sutherland, O.A. Efremova, M.A. Shestopalov
    One-pot synthesis of {Mo68}4+-doped polystyrene microspheres via a free-radical dispersion copolymerisation reaction
    Polymer international, 2017, V. 66, N 12, Pp 1906-1912 doi:10.1002/pi.5473, IF=2.69
  32. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  33. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  34. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  35. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  36. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  37. B. Epel, M. Krzykawska-Serda, V. Tormyshev, M.C. Maggio, E.D. Barth, C.A. Pelizzari, H.J. Halpern
    Spin Lattice Relaxation EPR pO2 Images May Direct the Location of Radiation Tumor Boosts to Enhance Tumor Cure
    , 2017, V. 75, N 3-4, pp 295-298 doi:10.1007/s12013-017-0825-2, IF=1.32
  38. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  39. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  40. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  41. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  42. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  43. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  44. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  45. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  46. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  47. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  48. A. Kononova, A. Sokolova, S. Cheresiz, O. Yarovaya, R. Nikitina, A. Chepurnov, A.G. Pokrovsky, N. Salakhutdonov
    N-Heterocyclic borneol derivatives as the inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry
    Med. Chem. Commun., 2017, V. 8, N 12, Pp 2233-2237 doi:10.1039/C7MD00424A, IF=2.608
  49. A.L. Bychkov, Al.I. Denkin, V.D. Tikhova, O.I. Lomovsky
    Prediction of higher heating values of plant biomass from ultimate analysis data
    Journal of Thermal Analysis and Calorimetry, , 2017, V. 130, N 3, pp 1399-1405 doi:10.1007/s10973-017-6350-0, IF=1.952
  50. A.L. Bychkov, Al.I. Denkin, V.D. Tikhova, O.I. Lomovsky
    Prediction of higher heating values of plant biomass from ultimate analysis data
    Journal of Thermal Analysis and Calorimetry, , 2017, V. 130, N 3, pp 1399-1405 doi:10.1007/s10973-017-6350-0, IF=1.952
  51. A.L. Bychkov, Al.I. Denkin, V.D. Tikhova, O.I. Lomovsky
    Prediction of higher heating values of plant biomass from ultimate analysis data
    Journal of Thermal Analysis and Calorimetry, , 2017, V. 130, N 3, pp 1399-1405 doi:10.1007/s10973-017-6350-0, IF=1.952
  52. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  53. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  54. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  55. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  56. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  57. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  58. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  59. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  60. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  61. A.S. Kondratyev, V.D. Shteingarts, V.V. Litvak, E.V. Tretyakov, A.V. Tkachev
    Domino reaction of (2-haloethyl)polyfluorophenyl sulfides, sulfoxides, and sulfones with ammonia or amines: one-pot synthesis of 3,4-dihydro-2H-1,4-benzothiazines polyfluorinated at the benzene ring and the corresponding 1-oxides and 1,1-dioxides
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 12, P 1350-1361 doi:10.1007/s10593-018-2217-y, IF=0.893
  62. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  63. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  64. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  65. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  66. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  67. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Необычная реакция 6,8-дихлор-3,3-диметил-7-нитро-3#-2,1,4-бензоксадиазин-4-оксида с 4-аминоморфолином
    Журнал общей химии. 2017. Т. 87. № 12. С. 2073-2075 (Unusual Reaction of 6,8-Dichloro-3,3-dimethyl-7-nitro-3H-2,1,4-benzoxadiazine 4-Oxide with 4-Aminomorpholine/ E. A. Chugunova, N. I. Akylbekov, M. R. Gaziev, V. A. Samsonov, A. B. Dobrynin, A. R. Burilov// doi:10.1134/S1070363217120222), IF=0.552
  68. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Необычная реакция 6,8-дихлор-3,3-диметил-7-нитро-3#-2,1,4-бензоксадиазин-4-оксида с 4-аминоморфолином
    Журнал общей химии. 2017. Т. 87. № 12. С. 2073-2075 (Unusual Reaction of 6,8-Dichloro-3,3-dimethyl-7-nitro-3H-2,1,4-benzoxadiazine 4-Oxide with 4-Aminomorpholine/ E. A. Chugunova, N. I. Akylbekov, M. R. Gaziev, V. A. Samsonov, A. B. Dobrynin, A. R. Burilov// doi:10.1134/S1070363217120222), IF=0.552
  69. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Необычная реакция 6,8-дихлор-3,3-диметил-7-нитро-3#-2,1,4-бензоксадиазин-4-оксида с 4-аминоморфолином
    Журнал общей химии. 2017. Т. 87. № 12. С. 2073-2075 (Unusual Reaction of 6,8-Dichloro-3,3-dimethyl-7-nitro-3H-2,1,4-benzoxadiazine 4-Oxide with 4-Aminomorpholine/ E. A. Chugunova, N. I. Akylbekov, M. R. Gaziev, V. A. Samsonov, A. B. Dobrynin, A. R. Burilov// doi:10.1134/S1070363217120222), IF=0.552
  70. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Необычная реакция 6,8-дихлор-3,3-диметил-7-нитро-3#-2,1,4-бензоксадиазин-4-оксида с 4-аминоморфолином
    Журнал общей химии. 2017. Т. 87. № 12. С. 2073-2075 (Unusual Reaction of 6,8-Dichloro-3,3-dimethyl-7-nitro-3H-2,1,4-benzoxadiazine 4-Oxide with 4-Aminomorpholine/ E. A. Chugunova, N. I. Akylbekov, M. R. Gaziev, V. A. Samsonov, A. B. Dobrynin, A. R. Burilov// doi:10.1134/S1070363217120222), IF=0.552
  71. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Необычная реакция 6,8-дихлор-3,3-диметил-7-нитро-3#-2,1,4-бензоксадиазин-4-оксида с 4-аминоморфолином
    Журнал общей химии. 2017. Т. 87. № 12. С. 2073-2075 (Unusual Reaction of 6,8-Dichloro-3,3-dimethyl-7-nitro-3H-2,1,4-benzoxadiazine 4-Oxide with 4-Aminomorpholine/ E. A. Chugunova, N. I. Akylbekov, M. R. Gaziev, V. A. Samsonov, A. B. Dobrynin, A. R. Burilov// doi:10.1134/S1070363217120222), IF=0.552
  72. N.V. Mamontova, E.I. Chernyak, E.V. Amosov, Yu.V. Gatilov, V.I. Vinogradova, S.F. Aripova, S.V. Morozov, I.A. Grigor'ev
    First Ionic Conjugates of Dihydroquercetin Monosuccinate with Amines
    Chemistry of Natural Compounds, 2017, V. 53, N 6, pp 1045-1051 doi:10.1007/s10600-017-2198-6, IF=0.46
  73. N.V. Mamontova, E.I. Chernyak, E.V. Amosov, Yu.V. Gatilov, V.I. Vinogradova, S.F. Aripova, S.V. Morozov, I.A. Grigor'ev
    First Ionic Conjugates of Dihydroquercetin Monosuccinate with Amines
    Chemistry of Natural Compounds, 2017, V. 53, N 6, pp 1045-1051 doi:10.1007/s10600-017-2198-6, IF=0.46
  74. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  75. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  76. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  77. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  78. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  79. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  80. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  81. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Получение новых производных 2я-бензимидазол 1,3- диоксида - аналогов ингибитора сепаразы (сепина-1)
    Журнал органической химии. 2017. Т. 53. № 12. С. 1860-1862., IF=0.602
  82. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Получение новых производных 2я-бензимидазол 1,3- диоксида - аналогов ингибитора сепаразы (сепина-1)
    Журнал органической химии. 2017. Т. 53. № 12. С. 1860-1862., IF=0.602
  83. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Получение новых производных 2я-бензимидазол 1,3- диоксида - аналогов ингибитора сепаразы (сепина-1)
    Журнал органической химии. 2017. Т. 53. № 12. С. 1860-1862., IF=0.602
  84. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Получение новых производных 2я-бензимидазол 1,3- диоксида - аналогов ингибитора сепаразы (сепина-1)
    Журнал органической химии. 2017. Т. 53. № 12. С. 1860-1862., IF=0.602
  85. Е.А. Чугунова, Н.И. Акылбеков, М.Р. Газиев, В.А. Самсонов, А.Б. Добрынин, А.Р. Бурилов
    Получение новых производных 2я-бензимидазол 1,3- диоксида - аналогов ингибитора сепаразы (сепина-1)
    Журнал органической химии. 2017. Т. 53. № 12. С. 1860-1862., IF=0.602
  86. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  87. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  88. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  89. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  90. A.V. Markov, A.V. Sen'kova, D. Warszycki, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
    Soloxolone methyl inhibits influenza virus replication and reduces virus-induced lung inflammation
    Scientific Reports, 2017, V. 7, Номер статьи 13968 doi:10.1038/s41598-017-14029-0, IF=4.258
  91. P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
    Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
    Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
  92. P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
    Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
    Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
  93. P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
    Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
    Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
  94. P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
    Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
    Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
  95. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  96. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  97. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  98. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  99. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  100. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  101. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  102. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  103. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  104. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  105. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  106. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  107. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  108. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  109. E.Y. Yakovleva, I.K. Shundrina
    Chromatographic adsorbents based on fluorinated polyimides supported on diatomite
    Advanced Materials and Technologies. 2017. № 4. С. 49-55 doi:10.17277/amt.2017.04.pp.049-055
  110. T. Kukina, I. Elshin, I. Eltsov
    Integration of “willow energy” with extraction technologies
    Ecology & Safety, Volume 11, 2017, pp. 299-306
  111. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  112. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  113. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  114. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  115. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  116. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  117. I.M. Yermak, N.P. Mischchenko, V.N. Davydova, V.P. Glazunov, D.V. Tarbeeva, A.O. Kravchenko, E.A. Pimenova, I.V. Sorokina
    Carrageenans-Sulfated Polysaccharides from Red Seaweeds as Matrices for the Inclusion of Echinochrome
    Marine drugs, 2017, V. 15 , N 11 , Art Number 337 doi:10.3390/md15110337, IF=3.503
  118. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
    Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
  119. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
    Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
  120. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
    Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
  121. I.I. Popadyuk, A.V. Markov, E.A. Morozova, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
    Steroids, 2017, V. 127, Pp 1-12 doi:10.1016/j.steroids.2017.08.016, IF=2.282
  122. А.Л. Иванов, О.Г. Сенаторова, М.М. Митасов, В.В. Антипов, М.Е. Страупенек, Н.Ю. Тормышева
    Кинетика охлаждения листовых деталей из алюминиевых сплавов при малодеформационной закалке в полимерной среде
    Металловедение и термическая обработка металлов. 2017. № 11 (749). С. 31-36. (The Kinetics of Cooling of Sheet Parts from Aluminum Alloys Under Low-Deformation Quenching in a Polymer Medium/ A.L. Ivanov, O.G. Senatorova, M.M. Mitasov, V.V. Antipov, M.E. Straupenek, N.Yu. Tormysheva// Metal Science and Heat Treatment, March 2018, V. 59, N 11-12, pp 703-708 doi:10.1007/s11041-018-0214-5), IF=0.247
  123. А.Л. Иванов, О.Г. Сенаторова, М.М. Митасов, В.В. Антипов, М.Е. Страупенек, Н.Ю. Тормышева
    Кинетика охлаждения листовых деталей из алюминиевых сплавов при малодеформационной закалке в полимерной среде
    Металловедение и термическая обработка металлов. 2017. № 11 (749). С. 31-36. (The Kinetics of Cooling of Sheet Parts from Aluminum Alloys Under Low-Deformation Quenching in a Polymer Medium/ A.L. Ivanov, O.G. Senatorova, M.M. Mitasov, V.V. Antipov, M.E. Straupenek, N.Yu. Tormysheva// Metal Science and Heat Treatment, March 2018, V. 59, N 11-12, pp 703-708 doi:10.1007/s11041-018-0214-5), IF=0.247
  124. А.Л. Иванов, О.Г. Сенаторова, М.М. Митасов, В.В. Антипов, М.Е. Страупенек, Н.Ю. Тормышева
    Кинетика охлаждения листовых деталей из алюминиевых сплавов при малодеформационной закалке в полимерной среде
    Металловедение и термическая обработка металлов. 2017. № 11 (749). С. 31-36. (The Kinetics of Cooling of Sheet Parts from Aluminum Alloys Under Low-Deformation Quenching in a Polymer Medium/ A.L. Ivanov, O.G. Senatorova, M.M. Mitasov, V.V. Antipov, M.E. Straupenek, N.Yu. Tormysheva// Metal Science and Heat Treatment, March 2018, V. 59, N 11-12, pp 703-708 doi:10.1007/s11041-018-0214-5), IF=0.247
  125. А.Л. Иванов, О.Г. Сенаторова, М.М. Митасов, В.В. Антипов, М.Е. Страупенек, Н.Ю. Тормышева
    Кинетика охлаждения листовых деталей из алюминиевых сплавов при малодеформационной закалке в полимерной среде
    Металловедение и термическая обработка металлов. 2017. № 11 (749). С. 31-36. (The Kinetics of Cooling of Sheet Parts from Aluminum Alloys Under Low-Deformation Quenching in a Polymer Medium/ A.L. Ivanov, O.G. Senatorova, M.M. Mitasov, V.V. Antipov, M.E. Straupenek, N.Yu. Tormysheva// Metal Science and Heat Treatment, March 2018, V. 59, N 11-12, pp 703-708 doi:10.1007/s11041-018-0214-5), IF=0.247
  126. A. Predtetchinsk, E. Predtechenskaya, I. Sorokina, A. Guzev
    Gender features of hyperprolactinemia as a protective factor in animal models of multiple sclerosis
    Multiple sclerosis journal, 2017, V. 23, Pp 769-769, Приложение: 3 Аннотация к встрече: EP1463 (7th Joint European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS)-Americas-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ACTRIMS), Paris, FRANCE, Oct 25-28, 2017) doi:10.1177/1352458517731285, IF=4.84
  127. A. Predtetchinsk, E. Predtechenskaya, I. Sorokina, A. Guzev
    Gender features of hyperprolactinemia as a protective factor in animal models of multiple sclerosis
    Multiple sclerosis journal, 2017, V. 23, Pp 769-769, Приложение: 3 Аннотация к встрече: EP1463 (7th Joint European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS)-Americas-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ACTRIMS), Paris, FRANCE, Oct 25-28, 2017) doi:10.1177/1352458517731285, IF=4.84
  128. A. Predtetchinsk, E. Predtechenskaya, I. Sorokina, A. Guzev
    Gender features of hyperprolactinemia as a protective factor in animal models of multiple sclerosis
    Multiple sclerosis journal, 2017, V. 23, Pp 769-769, Приложение: 3 Аннотация к встрече: EP1463 (7th Joint European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS)-Americas-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ACTRIMS), Paris, FRANCE, Oct 25-28, 2017) doi:10.1177/1352458517731285, IF=4.84
  129. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  130. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  131. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  132. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  133. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  134. G. Audran, R. Bikanga, P. Bremond, M. Edeleva, J.P. Joly, S-R.A. Marque, P. Nkolo, V. Roubaud
    How intramolecular hydrogen bonding (IHB) controls the C-ON bond homolysis in alkoxyamines
    Org. Biomol. Chem., 2017,15(39), 8425-8439 doi:10.1039/C7OB02223A, IF=3.563
  135. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    Way to Highly Emissive Materials: Increase of Rigidity by Introduction of a Furan Moiety in Co-Oligomers
    J. Phys. Chem. C, 2017, 121 (42), pp 23359-23369 doi:10.1021/acs.jpcc.7b08305, IF=4.535
  136. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  137. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  138. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  139. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  140. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  141. Ya.S. Fomenko, A.L. Gushchin, A.V. Tkachev, E.S. Vasilyev, P.A. Abramov, V.A. Nadolinny, M.M. Syrokvashin, M.N. Sokolov
    Fist oxidovanadium complexes containing chiral derivatives of dihydrophenanthroline and diazofluorene
    Polyhedron,2017, V. 135, Pp 96-100 doi:10.1016/j.poly.2017.07.003, IF=1.925
  142. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  143. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  144. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  145. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  146. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  147. M.P. Sartakov, N.V. Shpynova, I.D. Komissarov, Yu.M. Deryabina
    The Elemental Composition of Humic Acids of Sapropels: A Study for Lakes of the Upper and Middle Priobye, West Siberia
    International Journal of Ecology & Development, 2017, V. 32, N4 , Pp 138-144
  148. M.P. Sartakov, N.V. Shpynova, I.D. Komissarov, Yu.M. Deryabina
    The Elemental Composition of Humic Acids of Sapropels: A Study for Lakes of the Upper and Middle Priobye, West Siberia
    International Journal of Ecology & Development, 2017, V. 32, N4 , Pp 138-144
  149. M.P. Sartakov, N.V. Shpynova, I.D. Komissarov, Yu.M. Deryabina
    The Elemental Composition of Humic Acids of Sapropels: A Study for Lakes of the Upper and Middle Priobye, West Siberia
    International Journal of Ecology & Development, 2017, V. 32, N4 , Pp 138-144
  150. M.V. Trushin, R.G. Khamidullina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    The action of monoterpenoids with promising antiparkinsonian activity on fertility of Drosophila melanogaster
    Marmara Pharmaceutical Journal, 2017, V. 21, N 4, 2017, Pp 987-991 doi:10.12991/mpj.2017.29
  151. M.V. Trushin, R.G. Khamidullina, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    The action of monoterpenoids with promising antiparkinsonian activity on fertility of Drosophila melanogaster
    Marmara Pharmaceutical Journal, 2017, V. 21, N 4, 2017, Pp 987-991 doi:10.12991/mpj.2017.29
  152. A.G. Galyamina, D.A. Smagin, I.L. Kovalenko, T.G. Tolstikova, N.N. Kudryavtseva
    Psychomotor disturbances and changes in the expression of neurotransmitter genes in the dorsal striatum of aggressive and defeated male mice
    European Neuropsychopharmacology, 2017, V. 27, pp S677-S677, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31260-9, IF=4.238
  153. A.G. Galyamina, D.A. Smagin, I.L. Kovalenko, T.G. Tolstikova, N.N. Kudryavtseva
    Psychomotor disturbances and changes in the expression of neurotransmitter genes in the dorsal striatum of aggressive and defeated male mice
    European Neuropsychopharmacology, 2017, V. 27, pp S677-S677, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31260-9, IF=4.238
  154. A.G. Galyamina, D.A. Smagin, I.L. Kovalenko, T.G. Tolstikova, N.N. Kudryavtseva
    Psychomotor disturbances and changes in the expression of neurotransmitter genes in the dorsal striatum of aggressive and defeated male mice
    European Neuropsychopharmacology, 2017, V. 27, pp S677-S677, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31260-9, IF=4.238
  155. A.G. Galyamina, D.A. Smagin, I.L. Kovalenko, T.G. Tolstikova, N.N. Kudryavtseva
    Psychomotor disturbances and changes in the expression of neurotransmitter genes in the dorsal striatum of aggressive and defeated male mice
    European Neuropsychopharmacology, 2017, V. 27, pp S677-S677, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31260-9, IF=4.238
  156. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  157. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  158. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  159. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  160. E.A. Kulikova, N.B. Illarionova, K.P. Volcho, T.A. Khomenko, N.F. Salakhutdinov, N.V. Khotskin, E.Y. Bazhenova, A.V. Kulikov
    The effect of TC-2153, an inhibitor of striatal-enriched protein tyrosine phosphatase, on the 5-HT2A receptors
    European Neuropsychopharmacology, 2017, V. 27, pp S654-S654, S4 (30th Congress of the European-College-of-Neuropsychopharmacology (ECNP), Paris, France, Sep 02-05, 2017) doi:10.1016/S0924-977X(17)31224-5, IF=4.238
  161. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  162. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  163. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  164. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  165. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  166. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  167. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  168. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  169. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  170. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  171. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  172. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  173. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  174. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  175. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  176. M.B. Bushuev, K.A. Vinogradova, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Spin crossover in iron(II) hexafluorophosphate complexes with 2-(pyridin-2-yl)-4-(3,5-di-R-1H-pyrazol-1-yl)-6-methylpyrimidines
    Inorganica Chimica Acta, 2017, V. 467, Pp 238-243 doi:10.1016/j.ica.2017.08.006, IF=2.2
  177. M.B. Bushuev, K.A. Vinogradova, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Spin crossover in iron(II) hexafluorophosphate complexes with 2-(pyridin-2-yl)-4-(3,5-di-R-1H-pyrazol-1-yl)-6-methylpyrimidines
    Inorganica Chimica Acta, 2017, V. 467, Pp 238-243 doi:10.1016/j.ica.2017.08.006, IF=2.2
  178. M.B. Bushuev, K.A. Vinogradova, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Spin crossover in iron(II) hexafluorophosphate complexes with 2-(pyridin-2-yl)-4-(3,5-di-R-1H-pyrazol-1-yl)-6-methylpyrimidines
    Inorganica Chimica Acta, 2017, V. 467, Pp 238-243 doi:10.1016/j.ica.2017.08.006, IF=2.2
  179. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  180. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  181. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  182. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  183. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  184. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  185. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  186. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  187. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  188. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  189. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  190. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  191. Т.Е. Кокина, Л.А. Шелудякова, Ю.А. Еремина, Е.В. Воронцова, Л.А. Глинская, Д.А. Пирязев, Е.В. Лидер, А.В. Ткачев, С.В. Ларионов
    Комплексы Cu(I) и Pd(II) с тиосемикарбазонами (+)-камфоры и (-)-карвона: синтез, строение и цитотоксичность комплекса Pd(II)
    Журнал общей химии. 2017. Т. 87. № 10. С. 1674-1684 (Complexes of Cu(I) and Pd(II) with (+)-camphor and (-)-cavrone thiosemicarbazones: Synthesis, structure, and cytotoxicity of the Pd(II) complex/ T. E. Kokina, L. A. Sheludyakova, Yu. A. Eremina, E. V. Vorontsova, L. A. Glinskaya, D. A. Piryazev, E. V. Lider, A. V. Tkachev, S. V. Larionov// Russian Journal of General Chemistry, 2017, V. 87, N 10, pp 2332-2342 doi:10.1134/S1070363217100140), IF=0.552
  192. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников
    Исследование оптических методов формирования многоуровневого микрорельефа в тонких плёнках гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия. 2017. Т. 53. № 5. С. 57-65. (Study of the optical methods of formation of multilevel profile in the thin films of a hybrid photopolymer material based on thiol-siloxane and acrylate oligomers/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov// Optoelectronics, Instrumentation and Data Processing, 2017, V. 53, N 5, pp 466-473 doi:10.3103/S8756699017050065)
  193. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников
    Исследование оптических методов формирования многоуровневого микрорельефа в тонких плёнках гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия. 2017. Т. 53. № 5. С. 57-65. (Study of the optical methods of formation of multilevel profile in the thin films of a hybrid photopolymer material based on thiol-siloxane and acrylate oligomers/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov// Optoelectronics, Instrumentation and Data Processing, 2017, V. 53, N 5, pp 466-473 doi:10.3103/S8756699017050065)
  194. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  195. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  196. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  197. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  198. Ю.Н. Маляр, М.А. Михайленко, Н.А. Панкрушина, А.Н. Михеев, С.А. Кузнецова, Т.П. Шахтшнейдер
    Влияние микроволнового облучения на арабиногалактан и его взаимодействие с диацетатом бетулина
    Химия растительного сырья. 2017. № 4. С. 73-79
  199. E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
    Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
  200. E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
    Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
  201. E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
    Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
  202. E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
    Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
  203. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  204. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  205. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  206. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  207. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  208. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  209. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  210. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  211. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  212. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  213. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  214. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  215. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
  216. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  217. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  218. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  219. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  220. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  221. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  222. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  223. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  224. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
  225. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  226. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  227. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  228. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  229. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  230. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  231. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  232. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
    Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
    Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
  233. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  234. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  235. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  236. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  237. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  238. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  239. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  240. A. Romanov, A. Strelnikov, D. Sergeevichev, N. Salakhutdinov, V. Fomenko, V. Shabanov, D. Losik, I. Mikheenko, A. Karaskov, E. Pokushalov
    The influence of the new pharmaceutical composition containing botulinum toxin on different pharmacological models of heart rhythm disorders
    European Heart Journal. 38 (Supplement). 2017. P1711 (ESC Congress 2017, 26-30 August, Barcelona, Spain) doi:10.1093/eurheartj/ehx502.P1711, IF=0.896
  241. Yu.M. Deryabina, T.A. Kornakova, N.L. Bazhina, V.D. Tikhova
    Comparative Infrared Spectra Analysis of One Territory Soil Humic Acids by IR-EXPERT Computer System
    IInt. J. Green. Pharm. 2017 (Suppl); 11(3), pp S465-S469 (http://greenpharmacy.info/index.php/ijgp/article/view/1158) doi:10.22377/ijgp.v11i03.1158
  242. D.O. Prima, D.S. Baev, E.V. Vorontsova, T.S. Frolova, I.Yu. Bagryanskaya, Yu.G. Slizhov, T.G. Tolstikova, A.Yu. Makarov, A.V. Zibarev
    New cancer cells apoptosis agents: Fluorinated aza-heterocycles
    AIP Conference Proceedings, V. 1882, N 1, 020057 (2017) (Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications (PC IPCA’17), 23-26 May 2017, Tomsk, Russia) doi:10.1063/1.5001636
  243. D.O. Prima, D.S. Baev, E.V. Vorontsova, T.S. Frolova, I.Yu. Bagryanskaya, Yu.G. Slizhov, T.G. Tolstikova, A.Yu. Makarov, A.V. Zibarev
    New cancer cells apoptosis agents: Fluorinated aza-heterocycles
    AIP Conference Proceedings, V. 1882, N 1, 020057 (2017) (Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications (PC IPCA’17), 23-26 May 2017, Tomsk, Russia) doi:10.1063/1.5001636
  244. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  245. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  246. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  247. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  248. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  249. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  250. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  251. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  252. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  253. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  254. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  255. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  256. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  257. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  258. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  259. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  260. М.В. Кручинина, М.В. Паруликова, С.А. Курилович, А.А. Громов, В.М. Генералов, В.А. Рихтер, Д.В. Семенов, С.В. Морозов, А.С. Соколова, Н.Ф. Салахутдинов, М.В. Шашков, В.Н. Сидельников, В.Н. Кручинин
    Ассоциации функциональных параметров эритроцитов со структурой их мембран у мужчин г. новосибирска с атерогенными дислипидемиями и алкогольным поражением печени
    Атеросклероз. 2017. Т. 13. № 3. С. 5-13.
  261. Е.Ю. Яковлева, И.К. Шундрина, Е.Ю. Герасимов
    Высокотемпературные адсорбционные слои на основе фторированного полиимида и диатомитового носителя
    Журнал физической химии, 2017, V. 91, N 9, pp 1579-1587 (High-temperature adsorption layers based on fluoridated polyimide and diatomite carrier/ E.Yu. Yakovleva, I.K. Shundrina, E.Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2017, V. 91, N 9, pp 1797-1804 doi:10.1134/S0036024417090321)
  262. Е.Ю. Яковлева, И.К. Шундрина, Е.Ю. Герасимов
    Высокотемпературные адсорбционные слои на основе фторированного полиимида и диатомитового носителя
    Журнал физической химии, 2017, V. 91, N 9, pp 1579-1587 (High-temperature adsorption layers based on fluoridated polyimide and diatomite carrier/ E.Yu. Yakovleva, I.K. Shundrina, E.Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2017, V. 91, N 9, pp 1797-1804 doi:10.1134/S0036024417090321)
  263. D.O. Prima, E.V. Vorontsova, A.G. Makarov, A.Yu. Makarov, I.Yu. Bagryanskaya, T.F. Mikhailovskaya, Yu.G. Slizhov, A.V. Zibarev
    Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis
    Mendeleev Communications, 2017, V. 27, N 5, Pp 439-442 doi:10.1016/j.mencom.2017.09.002, IF=1.741
  264. D.O. Prima, E.V. Vorontsova, A.G. Makarov, A.Yu. Makarov, I.Yu. Bagryanskaya, T.F. Mikhailovskaya, Yu.G. Slizhov, A.V. Zibarev
    Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis
    Mendeleev Communications, 2017, V. 27, N 5, Pp 439-442 doi:10.1016/j.mencom.2017.09.002, IF=1.741
  265. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  266. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  267. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  268. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  269. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  270. D. Fedorishin, I. Sorokina, T. Tolstikova, A. Akulov, V. Glazacheva, N. Nemirovich-Danchenko, M. Khodanovich, V. Yarnykh
    Effects of insulin-like growth factor 1 on pathologic processes in the cuprizone model of multiple sclerosis
    Journal of Physics: Conference Series, 2017, V. 886, N 1, 012005 (3rd International Conference and Young Scientist School on Magnetic Resonance Imaging in Biomedical Research, MRIBiomed 2016; Novosibirsk; Russian Federation; 23 November 2016 до 26 November 2016; Код 130385) doi:10.1088/1742-6596/886/1/012005
  271. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  272. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  273. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  274. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  275. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  276. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  277. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  278. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  279. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  280. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  281. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453
  282. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453
  283. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453
  284. I.I. Popadyuk, A.V. Markov, V.O. Babich, O.V. Salomatina, E.B. Logashenko, M.A. Zenkova, N.F. Salakhutdinov
    Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: synthesis and evaluation of anti-proliferative activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 16, Pp 3755-3759 doi:10.1016/j.bmcl.2017.06.072, IF=2.453
  285. V. Shramko, S. Morozov, Ya. Polonskaya, E. Stakhneva, A. Chernyavskii, Yu. Ragino
    Serum content of saturated fatty acid in coronary atherosclerosis men
    Atherosclerosis, V. 263, August 2017, e222 (Poster session: lipidomics) doi:10.1016/j.atherosclerosis.2017.06.724
  286. V. Shramko, S. Morozov, Ya. Polonskaya, E. Stakhneva, A. Chernyavskii, Yu. Ragino
    Serum content of saturated fatty acid in coronary atherosclerosis men
    Atherosclerosis, V. 263, August 2017, e222 (Poster session: lipidomics) doi:10.1016/j.atherosclerosis.2017.06.724
  287. V. Shramko, S. Morozov, Ya. Polonskaya, E. Stakhneva, A. Chernyavskii, Yu. Ragino
    Serum content of saturated fatty acid in coronary atherosclerosis men
    Atherosclerosis, V. 263, August 2017, e222 (Poster session: lipidomics) doi:10.1016/j.atherosclerosis.2017.06.724
  288. V. Shramko, S. Morozov, Ya. Polonskaya, E. Stakhneva, A. Chernyavskii, Yu. Ragino
    Serum content of saturated fatty acid in coronary atherosclerosis men
    Atherosclerosis, V. 263, August 2017, e222 (Poster session: lipidomics) doi:10.1016/j.atherosclerosis.2017.06.724
  289. V. Shramko, S. Morozov, Ya. Polonskaya, E. Stakhneva, A. Chernyavskii, Yu. Ragino
    Serum content of saturated fatty acid in coronary atherosclerosis men
    Atherosclerosis, V. 263, August 2017, e222 (Poster session: lipidomics) doi:10.1016/j.atherosclerosis.2017.06.724
  290. A.V. Vorontsov, P.G. Smirniotis
    Benchmarking semiempirical and DFT methods for the interaction of thiophene and diethyl sulfide molecules with a Ti(OH)4(H2O) cluster
    Journal of Molecular Modeling, 2017, V. 23, N 8, NumArt 223 doi:10.1007/s00894-017-3392-y, IF=1.424
  291. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  292. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  293. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  294. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  295. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  296. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  297. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  298. G.A. Maksimova, M.Y. Pakharukova, E.V. Kashina, N.A. Zhukova, A.V. Kovner, M.N. Lvova, A.V. Katokhin, T.G. Tolstikova, B. Sripac, V.A. Mordvinov
    Effect of Opisthorchis felineus infection and dimethylnitrosamine administration on the induction of cholangiocarcinoma in Syrian hamsters
    Parasitology International, 2017, V. 66, N 4, Pp 458-463 doi:10.1016/j.parint.2015.10.002, IF=1.743
  299. С.А. Борисов, М.В. Хвостов, Т.Г. Толстикова, А.В. Душкин, Ю.С. Чистяченко
    Фармакодинамические исследования комплекса включения Полисахарида лиственницы арабиногалактана с напроксеном
    Сибирский научный медицинский журнал, ТОМ 37, № 4, 2017,С 19-25
  300. С.А. Борисов, М.В. Хвостов, Т.Г. Толстикова, А.В. Душкин, Ю.С. Чистяченко
    Фармакодинамические исследования комплекса включения Полисахарида лиственницы арабиногалактана с напроксеном
    Сибирский научный медицинский журнал, ТОМ 37, № 4, 2017,С 19-25
  301. V.T. Bauman, Ja. Ganbaatar, E.E. Shults
    Synthetic transformations of isoquinoline alkaloids: 1-(N-alkyl-1,2,3-triazol-4-yl)-6,18-endo-ethenodihydrothebainehydroquinones and triazolylnaphthohydroquinone-containing benzofuroazocines from thebaine
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 8, pp 913-919 doi:10.1007/s10593-017-2145-2, IF=0.893
  302. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  303. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  304. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  305. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  306. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  307. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  308. P. Nkolo, G. Audran, R. Bikanga, P. Bremond, S.R.A. Marque, V. Roubaud
    C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental
    Org. Biomol. Chem., 2016, 15(29), 6167-6176 doi:10.1039/c7ob01312d, IF=3.563
  309. P. Nkolo, G. Audran, R. Bikanga, P. Bremond, S.R.A. Marque, V. Roubaud
    C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental
    Org. Biomol. Chem., 2016, 15(29), 6167-6176 doi:10.1039/c7ob01312d, IF=3.563
  310. P. Nkolo, G. Audran, R. Bikanga, P. Bremond, S.R.A. Marque, V. Roubaud
    C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental
    Org. Biomol. Chem., 2016, 15(29), 6167-6176 doi:10.1039/c7ob01312d, IF=3.563
  311. P. Nkolo, G. Audran, R. Bikanga, P. Bremond, S.R.A. Marque, V. Roubaud
    C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental
    Org. Biomol. Chem., 2016, 15(29), 6167-6176 doi:10.1039/c7ob01312d, IF=3.563
  312. P. Nkolo, G. Audran, R. Bikanga, P. Bremond, S.R.A. Marque, V. Roubaud
    C-ON bond homolysis of alkoxyamines: when too high polarity is detrimental
    Org. Biomol. Chem., 2016, 15(29), 6167-6176 doi:10.1039/c7ob01312d, IF=3.563
  313. P. Nkolo, G. Audran, P. Bremond, R. Bikanga, S.R. A. Marque, V. Roubaud
    Impact of γ-irradiation, ageing and their interactions on multilayer films followed by AComDim
    Analytica Chimica Acta, 2017, V. 981, Pp 11-23 doi:10.1016/j.aca.2017.05.021, IF=4.949
  314. P. Nkolo, G. Audran, P. Bremond, R. Bikanga, S.R. A. Marque, V. Roubaud
    Impact of γ-irradiation, ageing and their interactions on multilayer films followed by AComDim
    Analytica Chimica Acta, 2017, V. 981, Pp 11-23 doi:10.1016/j.aca.2017.05.021, IF=4.949
  315. P. Nkolo, G. Audran, P. Bremond, R. Bikanga, S.R. A. Marque, V. Roubaud
    Impact of γ-irradiation, ageing and their interactions on multilayer films followed by AComDim
    Analytica Chimica Acta, 2017, V. 981, Pp 11-23 doi:10.1016/j.aca.2017.05.021, IF=4.949
  316. P. Nkolo, G. Audran, P. Bremond, R. Bikanga, S.R. A. Marque, V. Roubaud
    Impact of γ-irradiation, ageing and their interactions on multilayer films followed by AComDim
    Analytica Chimica Acta, 2017, V. 981, Pp 11-23 doi:10.1016/j.aca.2017.05.021, IF=4.949
  317. P. Nkolo, G. Audran, P. Bremond, R. Bikanga, S.R. A. Marque, V. Roubaud
    Impact of γ-irradiation, ageing and their interactions on multilayer films followed by AComDim
    Analytica Chimica Acta, 2017, V. 981, Pp 11-23 doi:10.1016/j.aca.2017.05.021, IF=4.949
  318. E.A. Kulikova, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Benzopentathiepine Derivative, 8-(Trifluoromethyl)-1,2,3,4,5-Benzopentathiepin-6-Amine Hydrochloride (TC-2153), as a Promising Anti-depressant of New Generation
    Letters in Drug Design & Discovery, 2017, V. 14, N 8, Pp 974-984 doi:10.2174/1570180814666161121112417, IF=1.169
  319. E.A. Kulikova, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Benzopentathiepine Derivative, 8-(Trifluoromethyl)-1,2,3,4,5-Benzopentathiepin-6-Amine Hydrochloride (TC-2153), as a Promising Anti-depressant of New Generation
    Letters in Drug Design & Discovery, 2017, V. 14, N 8, Pp 974-984 doi:10.2174/1570180814666161121112417, IF=1.169
  320. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, P.A. Avrorov, N.Yu. Selikhova, A.G. Makarov, A.Yu. Makarov, Yu.G. Slizhov, A.V. Zibarev
    Electrochemical properties and radical anions of carbocycle-fluorinated quinoxalines and their substituted derivatives
    Journal of Physical Organic Chemistry, 2017, V. 30, N 8, e3667 doi:10.1002/poc.3667, IF=1.335
  321. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, P.A. Avrorov, N.Yu. Selikhova, A.G. Makarov, A.Yu. Makarov, Yu.G. Slizhov, A.V. Zibarev
    Electrochemical properties and radical anions of carbocycle-fluorinated quinoxalines and their substituted derivatives
    Journal of Physical Organic Chemistry, 2017, V. 30, N 8, e3667 doi:10.1002/poc.3667, IF=1.335
  322. M.B. Bushuev, E.B. Nikolaenkova, V.P. Krivopalov
    Non-isothermal kinetics of spin crossover
    Phys Chem Chem Phys, 2017, V. 19, N 26, Pp 16955-16959 doi:10.1039/c7cp03442c, IF=4.123
  323. E. Chugunova, V. Samsonov, N. Akylbekov, D. Mazhukin
    Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinondioximes with ketones
    Tetrahedron, 2017, V. 73, N 27-28, Pp 3986-3992 doi:10.1016/j.tet.2017.05.078, IF=2.651
  324. E. Chugunova, V. Samsonov, N. Akylbekov, D. Mazhukin
    Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinondioximes with ketones
    Tetrahedron, 2017, V. 73, N 27-28, Pp 3986-3992 doi:10.1016/j.tet.2017.05.078, IF=2.651
  325. V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
    Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
    Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
  326. V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
    Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
    Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
  327. V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
    Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
    Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
  328. V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
    Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
    Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
  329. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  330. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  331. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  332. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  333. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  334. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  335. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  336. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  337. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  338. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  339. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  340. Н.А. Попова, Г.М. Сысоева, В.П. Николин, В.И. Каледин, Е.В. Третьяков, М.В. Еделева, С.М. Балахнин, Е.Л. Лушникова, G. Audran, С. Марк
    Сравнительное исследование токсичности алкоксиаминов in vitro и in vivo
    Бюллетень экспериментальной биологии и медицины, 2017, т. 164 (№ 7), 61-65. (Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6), IF=0.456
  341. Я.В. Полонская, В.С. Шрамко, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Баланс жирных кислот и их ассоциации с показателями липидного обмена и маркерами воспаления у мужчин с коронарным атеросклерозом
    Бюллетень экспериментальной биологии и медицины, 2017, Т.164, N 7, стр. 42-45 (Balance of Fatty Acids and Their Correlations with Parameters of Lipid Metabolism and Markers of Inflammation in Men with Coronary Atherosclerosis/ Ya. V. Polonskaya, V. S. Shramko, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Y. I. Ragino// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 33-35), IF=0.456
  342. Я.В. Полонская, В.С. Шрамко, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Баланс жирных кислот и их ассоциации с показателями липидного обмена и маркерами воспаления у мужчин с коронарным атеросклерозом
    Бюллетень экспериментальной биологии и медицины, 2017, Т.164, N 7, стр. 42-45 (Balance of Fatty Acids and Their Correlations with Parameters of Lipid Metabolism and Markers of Inflammation in Men with Coronary Atherosclerosis/ Ya. V. Polonskaya, V. S. Shramko, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Y. I. Ragino// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 33-35), IF=0.456
  343. Я.В. Полонская, В.С. Шрамко, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Баланс жирных кислот и их ассоциации с показателями липидного обмена и маркерами воспаления у мужчин с коронарным атеросклерозом
    Бюллетень экспериментальной биологии и медицины, 2017, Т.164, N 7, стр. 42-45 (Balance of Fatty Acids and Their Correlations with Parameters of Lipid Metabolism and Markers of Inflammation in Men with Coronary Atherosclerosis/ Ya. V. Polonskaya, V. S. Shramko, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Y. I. Ragino// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 33-35), IF=0.456
  344. Я.В. Полонская, В.С. Шрамко, С.В. Морозов, Е.И. Черняк, А.М. Чернявский, Ю.И. Рагино
    Баланс жирных кислот и их ассоциации с показателями липидного обмена и маркерами воспаления у мужчин с коронарным атеросклерозом
    Бюллетень экспериментальной биологии и медицины, 2017, Т.164, N 7, стр. 42-45 (Balance of Fatty Acids and Their Correlations with Parameters of Lipid Metabolism and Markers of Inflammation in Men with Coronary Atherosclerosis/ Ya. V. Polonskaya, V. S. Shramko, S. V. Morozov, E. I. Chernyak, A. M. Chernyavsky, Y. I. Ragino// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 33-35), IF=0.456
  345. T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
    Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
    Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
  346. T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
    Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
    Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
  347. T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
    Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
    Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
  348. T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
    Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
    Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
  349. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  350. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  351. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  352. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  353. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  354. O.V. Petrova, L.N. Sobenina, I.A. Ushakov, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov
    Multi-channel annulation of acetylene with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
    Mendeleev Communications, 2017, V. 27, N 4, J Pp 344-345 doi:10.1016/j.mencom.2017.07.007, IF=1.741
  355. T.M. Khomenko, V.V. Zarubaev, I.R. Orshanskaya, R.A. Kadyrova, V.A. Sannikova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-containing substituted coumarins
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 13, Pp 2920-2925 doi:10.1016/j.bmcl.2017.04.091, IF=2.453
  356. T.M. Khomenko, V.V. Zarubaev, I.R. Orshanskaya, R.A. Kadyrova, V.A. Sannikova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-containing substituted coumarins
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 13, Pp 2920-2925 doi:10.1016/j.bmcl.2017.04.091, IF=2.453
  357. T.M. Khomenko, V.V. Zarubaev, I.R. Orshanskaya, R.A. Kadyrova, V.A. Sannikova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-containing substituted coumarins
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 13, Pp 2920-2925 doi:10.1016/j.bmcl.2017.04.091, IF=2.453
  358. P. Nkolo, G.Audran, P. Bremond, R. Bikanga, S. R.A. Marque, V.Roubaud
    Hyperfine coupling constants of β-phosphorylated nitroxides: Subtle interplay between steric strain, hyperconjugation, and dipole-dipole interactions
    Tetrahedron, 2017, V. 73, N 23, Pp 3188-3201 doi:10.1016/j.tet.2017.04.027, IF=2.651
  359. P. Nkolo, G.Audran, P. Bremond, R. Bikanga, S. R.A. Marque, V.Roubaud
    Hyperfine coupling constants of β-phosphorylated nitroxides: Subtle interplay between steric strain, hyperconjugation, and dipole-dipole interactions
    Tetrahedron, 2017, V. 73, N 23, Pp 3188-3201 doi:10.1016/j.tet.2017.04.027, IF=2.651
  360. P. Nkolo, G.Audran, P. Bremond, R. Bikanga, S. R.A. Marque, V.Roubaud
    Hyperfine coupling constants of β-phosphorylated nitroxides: Subtle interplay between steric strain, hyperconjugation, and dipole-dipole interactions
    Tetrahedron, 2017, V. 73, N 23, Pp 3188-3201 doi:10.1016/j.tet.2017.04.027, IF=2.651
  361. P. Nkolo, G.Audran, P. Bremond, R. Bikanga, S. R.A. Marque, V.Roubaud
    Hyperfine coupling constants of β-phosphorylated nitroxides: Subtle interplay between steric strain, hyperconjugation, and dipole-dipole interactions
    Tetrahedron, 2017, V. 73, N 23, Pp 3188-3201 doi:10.1016/j.tet.2017.04.027, IF=2.651
  362. P. Nkolo, G.Audran, P. Bremond, R. Bikanga, S. R.A. Marque, V.Roubaud
    Hyperfine coupling constants of β-phosphorylated nitroxides: Subtle interplay between steric strain, hyperconjugation, and dipole-dipole interactions
    Tetrahedron, 2017, V. 73, N 23, Pp 3188-3201 doi:10.1016/j.tet.2017.04.027, IF=2.651
  363. О.Н. Шмендель, Д.Л. Прокушева, Д.В. Домрачев, В.В. Величко
    Анализ продукции «Багульника болотного побеги» различных производителей
    Фармация. 2017. Т. 66. № 4. С. 7-10.
  364. О.Н. Шмендель, Д.Л. Прокушева, Д.В. Домрачев, В.В. Величко
    Анализ продукции «Багульника болотного побеги» различных производителей
    Фармация. 2017. Т. 66. № 4. С. 7-10.
  365. О.Н. Шмендель, Д.Л. Прокушева, Д.В. Домрачев, В.В. Величко
    Анализ продукции «Багульника болотного побеги» различных производителей
    Фармация. 2017. Т. 66. № 4. С. 7-10.
  366. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  367. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  368. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  369. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  370. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  371. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  372. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  373. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  374. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  375. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  376. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  377. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  378. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  379. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  380. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  381. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  382. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  383. M.V. Khvostov, S.A. Borisov, T.G. Tolstikova, A.V. Dushkin, B.D. Tsyrenova, Yu.S. Chistyachenko, N.E. Polyakov, G.G. Dultseva, A.A. Onischuk, S.V. An’kov
    Supramolecular Complex of Ibuprofen with Larch Polysaccharide Arabinogalactan: Studies on Bioavailability and Pharmacokinetics
    European Journal of Drug Metabolism and Pharmacokinetics, 2017, V. 42, N 3, pp 431-440 doi:10.1007/s13318-016-0357-y, IF=1.399
  384. A.E. Paromov, S.V. Sysolyatin, Y.V. Gatilov
    An Acid-Catalyzed Cascade Synthesis of Oxaazatetracyclo [5.5.0.03,11.05,9]dodecane Derivatives
    Journal of Energetic Materials, 2017, V.35, N 3, Pp. 363-373 doi:10.1080/07370652.2016.1194499, IF=1.557
  385. A.E. Paromov, S.V. Sysolyatin, Y.V. Gatilov
    An Acid-Catalyzed Cascade Synthesis of Oxaazatetracyclo [5.5.0.03,11.05,9]dodecane Derivatives
    Journal of Energetic Materials, 2017, V.35, N 3, Pp. 363-373 doi:10.1080/07370652.2016.1194499, IF=1.557
  386. Т.В. Попова, Н.О. Карабинцева, Л.Н. Рачковская, Т.Г. Толстикова, А.А. Котлярова, А.Ю. Летягин
    Возможности создания полифункционального серебросодержащего препарата с детоксикационным эффектом
    Фармация и фармакология. 2017. Т. 5. № 3. С. 242-253. doi:10.19163/2307-9266-2017-5-3-243-253
  387. Т.В. Попова, Н.О. Карабинцева, Л.Н. Рачковская, Т.Г. Толстикова, А.А. Котлярова, А.Ю. Летягин
    Возможности создания полифункционального серебросодержащего препарата с детоксикационным эффектом
    Фармация и фармакология. 2017. Т. 5. № 3. С. 242-253. doi:10.19163/2307-9266-2017-5-3-243-253
  388. Т.В. Попова, Н.О. Карабинцева, Л.Н. Рачковская, Т.Г. Толстикова, А.А. Котлярова, А.Ю. Летягин
    Возможности создания полифункционального серебросодержащего препарата с детоксикационным эффектом
    Фармация и фармакология. 2017. Т. 5. № 3. С. 242-253. doi:10.19163/2307-9266-2017-5-3-243-253
  389. Т.В. Попова, Н.О. Карабинцева, Л.Н. Рачковская, Т.Г. Толстикова, А.А. Котлярова, А.Ю. Летягин
    Возможности создания полифункционального серебросодержащего препарата с детоксикационным эффектом
    Фармация и фармакология. 2017. Т. 5. № 3. С. 242-253. doi:10.19163/2307-9266-2017-5-3-243-253
  390. Т.В. Попова, Н.О. Карабинцева, Л.Н. Рачковская, Т.Г. Толстикова, А.А. Котлярова, А.Ю. Летягин
    Возможности создания полифункционального серебросодержащего препарата с детоксикационным эффектом
    Фармация и фармакология. 2017. Т. 5. № 3. С. 242-253. doi:10.19163/2307-9266-2017-5-3-243-253
  391. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
    Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
    Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
  392. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
    Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
    Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
  393. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
    Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
    Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
  394. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
    Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
    Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
  395. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  396. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  397. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  398. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  399. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  400. T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, Н.В. Куратьева, В.В. Медведев, Э.С. Татаринова, Е.В. Черкасова
    Гексафторосиликаты комплексов кобальта(II) с диметилсульфоксидом и диметилформамидом
    Журнал неоранической химии, 2017, V. 62, N 6, pp 776-781 (Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X), IF=0.787
  401. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  402. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  403. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  404. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  405. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  406. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  407. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  408. Б.А. Селиванов, А.Я. Тихонов, Е.Ф. Беланов, Н.И. Бормотов, А.С. Кабанов, О.Ю. Мазурков, О.А. Серова, Л.Н. Шишкина, А.П. Агафонов, А.Н. Сергеев
    Синтез и противовирусная активность 1-арил-3-{3,5-диоксо-4-азатетрацикло-[5.3.2.02,6.08,10]додец-11-ен-4-ил}мочевин
    Химико-фармацевтический журнал. 2017. Т. 51. № 6. С. 13-17. (Synthesis and Antiviral Activity of 1-Aryl-3-(3,5-Dioxo-4-Azatetracyclo-[5.3.2.02,6.08,10]Dodec-11-EN-4-YL)Ureas/ B. A. Selivanov, A. Y. Tikhonov, E. F. Belanov, N. I. Bormotov, A. S. Kabanov, O. Yu. Mazurkov, O. A. Serova, L. N. Shishkina, A. P. Agafonov, A. N. Sergeev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 6, pp 439-443 doi:10.1007/s11094-017-1629-9), IF=0.444
  409. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  410. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  411. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  412. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  413. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  414. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  415. G. Audran, R. Bikanga, P. Bremond, Jean-Patrick. Joly, S.R-A. Marque, P. Nkolo
    Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment
    J. Org. Chem., 2017, 82 (11), pp 5702-5709 doi:10.1021/acs.joc.7b00541, IF=4.848
  416. G. Audran, R. Bikanga, P. Bremond, Jean-Patrick. Joly, S.R-A. Marque, P. Nkolo
    Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment
    J. Org. Chem., 2017, 82 (11), pp 5702-5709 doi:10.1021/acs.joc.7b00541, IF=4.848
  417. G. Audran, R. Bikanga, P. Bremond, Jean-Patrick. Joly, S.R-A. Marque, P. Nkolo
    Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment
    J. Org. Chem., 2017, 82 (11), pp 5702-5709 doi:10.1021/acs.joc.7b00541, IF=4.848
  418. G. Audran, R. Bikanga, P. Bremond, Jean-Patrick. Joly, S.R-A. Marque, P. Nkolo
    Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment
    J. Org. Chem., 2017, 82 (11), pp 5702-5709 doi:10.1021/acs.joc.7b00541, IF=4.848
  419. G. Audran, R. Bikanga, P. Bremond, Jean-Patrick. Joly, S.R-A. Marque, P. Nkolo
    Normal, Leveled, and Enhanced Steric Effects in Alkoxyamines Carrying a β-Phosphorylated Nitroxyl Fragment
    J. Org. Chem., 2017, 82 (11), pp 5702-5709 doi:10.1021/acs.joc.7b00541, IF=4.848
  420. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  421. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  422. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  423. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  424. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  425. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  426. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  427. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  428. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  429. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  430. O.I. Artyushin, E.V. Sharova, N.M. Vinogradova, G.K. Genkina, A.A. Moiseeva, Z.S. Klemenkova, I.R. Orshanskaya, A.A. Shtro, R.A. Kadyrova, V.V. Zarubaev, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
    Synthesis of Camphecene Derivatives using Click Chemistry Methodology and Study of their Antiviral Activity
    Bioorganic & Medicinal Chemistry Letters, 2017, V.27, N 10, Pp 2181-2184 doi:10.1016/j.bmcl.2017.03.051, IF=2.453
  431. S.S. Patrushev, T.V. Rybalova, I. D. Ivanov, V.A. Vavilin, E.E. Shults
    Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines
    Tetrahedron, 2017, V. 73, N 19, Pp 2717-2726 In Press, Accepted Manuscript - Note to users doi:10.1016/j.tet.2017.03.016, IF=2.651
  432. S.S. Patrushev, T.V. Rybalova, I. D. Ivanov, V.A. Vavilin, E.E. Shults
    Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines
    Tetrahedron, 2017, V. 73, N 19, Pp 2717-2726 In Press, Accepted Manuscript - Note to users doi:10.1016/j.tet.2017.03.016, IF=2.651
  433. P.A. Zaikin, O.T. Dyan, D.V. Evtushok, A.N. Usoltsev, E.V. Karpova, G.I. Borodkin, V.G. Shubin
    Solvent-free Fluorination of Electron Rich Aromatic Compounds with F-TEDA-BF4 Reagent: Toward "Dry" Processes
    European Journal of Organic Chemistry, 2017, V. 2017, N 17, Pp 2469-2474 doi:10.1002/ejoc.201700179, IF=2.834
  434. P.A. Zaikin, O.T. Dyan, D.V. Evtushok, A.N. Usoltsev, E.V. Karpova, G.I. Borodkin, V.G. Shubin
    Solvent-free Fluorination of Electron Rich Aromatic Compounds with F-TEDA-BF4 Reagent: Toward "Dry" Processes
    European Journal of Organic Chemistry, 2017, V. 2017, N 17, Pp 2469-2474 doi:10.1002/ejoc.201700179, IF=2.834
  435. О.В. Федотова, И.В. Грехова, Ю.М. Дерябина, В.Д. Тихова
    Сравнительный анализ фракций при производстве гуминового препарата росток
    Аграрный вестник Урала, 2017, № 5 (159), С. 12.
  436. О.В. Федотова, И.В. Грехова, Ю.М. Дерябина, В.Д. Тихова
    Сравнительный анализ фракций при производстве гуминового препарата росток
    Аграрный вестник Урала, 2017, № 5 (159), С. 12.
  437. Т.В. Попова, Н.О. Карабинцева, Т.Г. Толстикова
    Исследование ассортимента лекарственных средств, применяемых в терапии острых кишечных инфекций
    Журнал научных статей Здоровье и образование в XXI веке. 2017. Т. 19. № 10. С. 356-358.
  438. Т.В. Попова, Н.О. Карабинцева, Т.Г. Толстикова
    Исследование ассортимента лекарственных средств, применяемых в терапии острых кишечных инфекций
    Журнал научных статей Здоровье и образование в XXI веке. 2017. Т. 19. № 10. С. 356-358.
  439. А.Б. Киселев, А.Ю. Овчинников, Т.Г. Толстикова, В.А. Чаукина, Н.А. Мирошниченко, Н.А. Жукова
    Транскутанная терапия назальной обструкции, сопровождающей интермиттирующий аллергический и острый инфекционный ринит
    Эффективная фармакотерапия. 2017. № 14. С. 8-12.
  440. А.Б. Киселев, А.Ю. Овчинников, Т.Г. Толстикова, В.А. Чаукина, Н.А. Мирошниченко, Н.А. Жукова
    Транскутанная терапия назальной обструкции, сопровождающей интермиттирующий аллергический и острый инфекционный ринит
    Эффективная фармакотерапия. 2017. № 14. С. 8-12.
  441. А.Б. Киселев, А.Ю. Овчинников, Т.Г. Толстикова, В.А. Чаукина, Н.А. Мирошниченко, Н.А. Жукова
    Транскутанная терапия назальной обструкции, сопровождающей интермиттирующий аллергический и острый инфекционный ринит
    Эффективная фармакотерапия. 2017. № 14. С. 8-12.
  442. А.Б. Киселев, А.Ю. Овчинников, Т.Г. Толстикова, В.А. Чаукина, Н.А. Мирошниченко, Н.А. Жукова
    Транскутанная терапия назальной обструкции, сопровождающей интермиттирующий аллергический и острый инфекционный ринит
    Эффективная фармакотерапия. 2017. № 14. С. 8-12.
  443. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  444. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  445. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  446. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  447. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, K.P. Volcho, E. Smolentseva, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Promoting effect of alcohols and formic acid on Au-catalyzed one-pot myrtenol amination
    Molecular Catalysis, 2017, V. 433, Pp 414-419 (Formerly known as Journal of Molecular Catalysis A: Chemical) doi:10.1016/j.mcat.2017.02.040, IF=4.211
  448. A.S. Sokolova, O.I. Yarovaya, M.D. Semenova, A.A. Shtro, I.R. Orshanskaya, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
    Med. Chem. Commun., 2017, 8(5), 960-963 doi:10.1039/C6MD00657D, IF=2.608
  449. A.S. Sokolova, O.I. Yarovaya, M.D. Semenova, A.A. Shtro, I.R. Orshanskaya, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
    Med. Chem. Commun., 2017, 8(5), 960-963 doi:10.1039/C6MD00657D, IF=2.608
  450. A.S. Sokolova, O.I. Yarovaya, M.D. Semenova, A.A. Shtro, I.R. Orshanskaya, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and in vitro study of novel borneol derivatives as potent inhibitors of the influenza A virus
    Med. Chem. Commun., 2017, 8(5), 960-963 doi:10.1039/C6MD00657D, IF=2.608
  451. В.И. Каледин, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Л.А. Богданова, Т.С. Морозкова, Д.Е. Семенов
    Усиление общетоксического и ослабление гепатотоксического действия диэтилнитрозамина при торможении его метаболизма у мышей
    Российский физиологический журнал им. И.М. Сеченова. 2017. Т. 103. № 5. С. 527-532.
  452. В.И. Каледин, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Л.А. Богданова, Т.С. Морозкова, Д.Е. Семенов
    Усиление общетоксического и ослабление гепатотоксического действия диэтилнитрозамина при торможении его метаболизма у мышей
    Российский физиологический журнал им. И.М. Сеченова. 2017. Т. 103. № 5. С. 527-532.
  453. В.И. Каледин, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Л.А. Богданова, Т.С. Морозкова, Д.Е. Семенов
    Усиление общетоксического и ослабление гепатотоксического действия диэтилнитрозамина при торможении его метаболизма у мышей
    Российский физиологический журнал им. И.М. Сеченова. 2017. Т. 103. № 5. С. 527-532.
  454. В.И. Каледин, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Л.А. Богданова, Т.С. Морозкова, Д.Е. Семенов
    Усиление общетоксического и ослабление гепатотоксического действия диэтилнитрозамина при торможении его метаболизма у мышей
    Российский физиологический журнал им. И.М. Сеченова. 2017. Т. 103. № 5. С. 527-532.
  455. A.Y. Shabalin, N.Y. Adonin, V.V. Bardin
    Substitution of fluorine in M[C6F5BF3] with organolithium compounds: Distinctions between O- and N-nucleophiles
    Beilstein Journal of Organic Chemistry, 2017, 13, с. 703-713 doi:10.3762/bjoc.13.69, IF=2.336
  456. A.Y. Shabalin, N.Y. Adonin, V.V. Bardin
    Substitution of fluorine in M[C6F5BF3] with organolithium compounds: Distinctions between O- and N-nucleophiles
    Beilstein Journal of Organic Chemistry, 2017, 13, с. 703-713 doi:10.3762/bjoc.13.69, IF=2.336
  457. Т.С. Фролова, А.В. Липеева, Д.С. Баев, Я.А. Цепилов, О.И. Синицына
    Апоптоз как основной механизм цитотоксического действия урсоловой и помоловой кислот в клетках глиомы
    Молекулярная биология. 2017. Т. 51. № 5. С. 809-816. (Apoptosis as the basic mechanism of cytotoxic action of ursolic and pomolic acids in glioma cells/ T. S. Frolova, A. V. Lipeeva, D. S. Baev, Y. A. Tsepilov, O. I. Sinitsyna// Molecular Biology, 2017, V. 51, N 5, pp 705-711 doi:10.1134/S0026893317050090), IF=0.799
  458. Т.С. Фролова, А.В. Липеева, Д.С. Баев, Я.А. Цепилов, О.И. Синицына
    Апоптоз как основной механизм цитотоксического действия урсоловой и помоловой кислот в клетках глиомы
    Молекулярная биология. 2017. Т. 51. № 5. С. 809-816. (Apoptosis as the basic mechanism of cytotoxic action of ursolic and pomolic acids in glioma cells/ T. S. Frolova, A. V. Lipeeva, D. S. Baev, Y. A. Tsepilov, O. I. Sinitsyna// Molecular Biology, 2017, V. 51, N 5, pp 705-711 doi:10.1134/S0026893317050090), IF=0.799
  459. S.S. Laev, N.F. Salakhutdinov, O.I. Lavrik
    Inhibitors of nuclease and redox activity of apurinic/apyrimidinic endonuclease 1/redox effector factor 1 (APE1/Ref-1)
    Bioorganic & Medicinal Chemistry, 2017, V. 25, N 9, Pp 2531-2544 doi:10.1016/j.bmc.2017.01.028, IF=2.93
  460. L.V. Saloutina, E.V. Tretyakov, P.A. Slepukhin, V.I. Saloutin, O.N. Chupakhin
    Synthesis of Cyclic Vicinal Trifluoromethylated Hydroxylamine and Nitrone Based on Perfluorodiacetyl
    Journal of Heterocyclic Chemistry, 2017, V. 54, N 3, Pp 1887-1890 doi:10.1002/jhet.2782, IF=0.893
  461. L.V. Saloutina, E.V. Tretyakov, P.A. Slepukhin, V.I. Saloutin, O.N. Chupakhin
    Synthesis of Cyclic Vicinal Trifluoromethylated Hydroxylamine and Nitrone Based on Perfluorodiacetyl
    Journal of Heterocyclic Chemistry, 2017, V. 54, N 3, Pp 1887-1890 doi:10.1002/jhet.2782, IF=0.893
  462. L.V. Saloutina, E.V. Tretyakov, P.A. Slepukhin, V.I. Saloutin, O.N. Chupakhin
    Synthesis of Cyclic Vicinal Trifluoromethylated Hydroxylamine and Nitrone Based on Perfluorodiacetyl
    Journal of Heterocyclic Chemistry, 2017, V. 54, N 3, Pp 1887-1890 doi:10.1002/jhet.2782, IF=0.893
  463. L.V. Saloutina, E.V. Tretyakov, P.A. Slepukhin, V.I. Saloutin, O.N. Chupakhin
    Synthesis of Cyclic Vicinal Trifluoromethylated Hydroxylamine and Nitrone Based on Perfluorodiacetyl
    Journal of Heterocyclic Chemistry, 2017, V. 54, N 3, Pp 1887-1890 doi:10.1002/jhet.2782, IF=0.893
  464. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  465. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  466. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  467. N.I. Belousova, D.V. Domrachev, N.S. Fursa, M.V. Belousov
    Composition of Essential Oil from Rhododendron caucasicum
    Chemistry of Natural Compounds, 2017, V. 53, N 3, pp 574-575 doi:10.1007/s10600-017-2054-8, IF=0.46
  468. N.I. Belousova, D.V. Domrachev, N.S. Fursa, M.V. Belousov
    Composition of Essential Oil from Rhododendron caucasicum
    Chemistry of Natural Compounds, 2017, V. 53, N 3, pp 574-575 doi:10.1007/s10600-017-2054-8, IF=0.46
  469. N.I. Belousova, D.V. Domrachev, N.S. Fursa, M.V. Belousov
    Composition of Essential Oil from Rhododendron caucasicum
    Chemistry of Natural Compounds, 2017, V. 53, N 3, pp 574-575 doi:10.1007/s10600-017-2054-8, IF=0.46
  470. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  471. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  472. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  473. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  474. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  475. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  476. Т.Е. Кокина, Л.А. Глинская, Е.С. Васильев, М.И. Рахманова, С.В. Макарова, Д.А. Пирязев, И.В. Корольков, А.В. Ткачёв, С.В. Ларионов
    Структура и фотолюминесценция комплексов zn(ii) и сd(ii) с хиральным бис-пиридином, содержащим фрагменты природного (-)-α-пинена
    Журнал структурной химии, 2017, Т. 58, N 5, Cc. 1032-1041 (Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene/ T.E. Kokina, L.A. Glinskaya, E.S. Vasiliev, M.I. Rakhmanova, S.V. Makarova, D.A. Piryazev, I.V. Korol'kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2017, V. 58, N 5, pp 994-1003 doi:10.1134/S0022476617050201), IF=0.472
  477. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, S.R.A. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    Zinc(II) Hexafluoroacetylacetonate Complexes of Alkoxyamines: NMR and Kinetic Investigations. First Step for a New Way to Prepare Hybrid Materials
    ChemistrySelect, 2017, V. 2, N 12, Pp 3584-3593 doi:10.1002/slct.201700678
  478. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  479. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  480. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  481. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  482. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  483. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  484. M. Yu. Khodanovich, I.V. Sorokina, V. Yu. Glazacheva, A.E. Akulov, N.M. Nemirovich-Danchenko, A.V. Romashchenko, T.G. Tolstikova, L.R. Mustafina, V.L. Yarnykh
    Histological validation of fast macromolecular proton fraction mapping as a quantitative myelin imaging method in the cuprizone demyelination model
    Scientific Reports, 2017, 7, Article number: 46686 doi:10.1038/srep46686, IF=4.258
  485. M.A. Voinov, C.T. Scheid, I.A. Kirilyuk, D.G. Trofimov, A.I. Smirnov
    IKMTSL-PTE, a Phospholipid-Based EPR Probe for Surface Electrostatic Potential of Biological Interfaces at Neutral pH: Effects of Temperature and Effective Dielectric Constant of the Solvent
    Journal of Physical Chemistry B, 2017, V. 121, N 11, Pp 2443-2453 doi:10.1021/acs.jpcb.7b00592, IF=3.177
  486. M.A. Voinov, C.T. Scheid, I.A. Kirilyuk, D.G. Trofimov, A.I. Smirnov
    IKMTSL-PTE, a Phospholipid-Based EPR Probe for Surface Electrostatic Potential of Biological Interfaces at Neutral pH: Effects of Temperature and Effective Dielectric Constant of the Solvent
    Journal of Physical Chemistry B, 2017, V. 121, N 11, Pp 2443-2453 doi:10.1021/acs.jpcb.7b00592, IF=3.177
  487. M.A. Voinov, C.T. Scheid, I.A. Kirilyuk, D.G. Trofimov, A.I. Smirnov
    IKMTSL-PTE, a Phospholipid-Based EPR Probe for Surface Electrostatic Potential of Biological Interfaces at Neutral pH: Effects of Temperature and Effective Dielectric Constant of the Solvent
    Journal of Physical Chemistry B, 2017, V. 121, N 11, Pp 2443-2453 doi:10.1021/acs.jpcb.7b00592, IF=3.177
  488. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  489. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  490. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  491. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  492. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  493. T.A. Vaganova, Y.V. Gatilov, S.E. Malykhin, D.P. Pishchur, Y.V. Larichev, V.I. Rodionov, E.V. Malykhin
    Design and supramolecular structure of crystal associates of polyfluoroarylenediamines and 18-crown-6 (2:1)
    Journal of Molecular Structure, V. 1133, 5 April 2017, P. 122-134 doi:10.1016/j.molstruc.2016.11.091, IF=1.753
  494. T.A. Vaganova, Y.V. Gatilov, S.E. Malykhin, D.P. Pishchur, Y.V. Larichev, V.I. Rodionov, E.V. Malykhin
    Design and supramolecular structure of crystal associates of polyfluoroarylenediamines and 18-crown-6 (2:1)
    Journal of Molecular Structure, V. 1133, 5 April 2017, P. 122-134 doi:10.1016/j.molstruc.2016.11.091, IF=1.753
  495. T.A. Vaganova, Y.V. Gatilov, S.E. Malykhin, D.P. Pishchur, Y.V. Larichev, V.I. Rodionov, E.V. Malykhin
    Design and supramolecular structure of crystal associates of polyfluoroarylenediamines and 18-crown-6 (2:1)
    Journal of Molecular Structure, V. 1133, 5 April 2017, P. 122-134 doi:10.1016/j.molstruc.2016.11.091, IF=1.753
  496. Киселев А.Б., Овчинников А.Ю., Толстикова Т.Г., Чаукина В.А., Мирошниченко Н.А., Жукова Н.А.
    Новый подход к ликвидации назальной обструкции при интермиттирующем аллергическом и остром инфекционном ринитах
    Российская оториноларингология. 2017. № 2 (87). С. 131-136
  497. Киселев А.Б., Овчинников А.Ю., Толстикова Т.Г., Чаукина В.А., Мирошниченко Н.А., Жукова Н.А.
    Новый подход к ликвидации назальной обструкции при интермиттирующем аллергическом и остром инфекционном ринитах
    Российская оториноларингология. 2017. № 2 (87). С. 131-136
  498. Киселев А.Б., Овчинников А.Ю., Толстикова Т.Г., Чаукина В.А., Мирошниченко Н.А., Жукова Н.А.
    Новый подход к ликвидации назальной обструкции при интермиттирующем аллергическом и остром инфекционном ринитах
    Российская оториноларингология. 2017. № 2 (87). С. 131-136
  499. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  500. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  501. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  502. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  503. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  504. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
    Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
  505. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  506. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  507. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  508. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  509. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  510. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  511. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  512. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  513. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  514. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  515. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  516. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  517. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  518. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  519. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  520. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  521. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  522. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  523. E.V. Svezhentseva, A.O. Solovieva, Y.A. Vorotnikov, O.G. Kurskaya, K.A. Brylev, A.R. Tsygankova, M.V. Edeleva, S.N. Gyrylova, N. Kitamura, O.A. Efremova, M.A. Shestopalov, Y.V. Mironov, A.M. Shestopalov
    Water-soluble hybrid materials based on {Mo6X8}4+ (X = Cl, Br, I) cluster complexes and sodium polystyrene sulfonate
    New Journal of Chemistry, 2017, V. 41, N 4, Pp 1670-1676 doi:10.1039/c6nj03469a, IF=3.269
  524. L. Bosco, T. Butscher, S.R.A. Marque
    β-Phosphorus Hyperfine Coupling Constant in Nitroxides: Conformational Effects in 6-Membered Ring Nitroxides
    Applied Magnetic Resonance, 2017, V. 48, N 4, pp 379-406 doi:10.1007/s00723-017-0867-z, IF=0.864
  525. L. Bosco, T. Butscher, S.R.A. Marque
    β-Phosphorus Hyperfine Coupling Constant in Nitroxides: Conformational Effects in 6-Membered Ring Nitroxides
    Applied Magnetic Resonance, 2017, V. 48, N 4, pp 379-406 doi:10.1007/s00723-017-0867-z, IF=0.864
  526. Е.А. Чугунова, Н.И. Акулбеков, В.А. Самсонов, С.А. Ситнов, А.Р. Бурилов
    Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring
    Журнал органической химии, 2017, Vol. 53, N. 4, pp. 628-629. (Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring/ E.A. Chugunova, N.I. Akylbekov, V.A. Samsonov, S.A. Sitnov, A.R. Burilov// Russian Journal of Organic Chemistry, 2017, V. 53, N 4, pp 637-638 doi:10.1134/S1070428017040273), IF=0.603
  527. Е.А. Чугунова, Н.И. Акулбеков, В.А. Самсонов, С.А. Ситнов, А.Р. Бурилов
    Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring
    Журнал органической химии, 2017, Vol. 53, N. 4, pp. 628-629. (Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring/ E.A. Chugunova, N.I. Akylbekov, V.A. Samsonov, S.A. Sitnov, A.R. Burilov// Russian Journal of Organic Chemistry, 2017, V. 53, N 4, pp 637-638 doi:10.1134/S1070428017040273), IF=0.603
  528. Е.А. Чугунова, Н.И. Акулбеков, В.А. Самсонов, С.А. Ситнов, А.Р. Бурилов
    Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring
    Журнал органической химии, 2017, Vol. 53, N. 4, pp. 628-629. (Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring/ E.A. Chugunova, N.I. Akylbekov, V.A. Samsonov, S.A. Sitnov, A.R. Burilov// Russian Journal of Organic Chemistry, 2017, V. 53, N 4, pp 637-638 doi:10.1134/S1070428017040273), IF=0.603
  529. Е.А. Чугунова, Н.И. Акулбеков, В.А. Самсонов, С.А. Ситнов, А.Р. Бурилов
    Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring
    Журнал органической химии, 2017, Vol. 53, N. 4, pp. 628-629. (Photochromism of 3H-2,1,4-benzoxadiazine 4-oxides with heterocyclic substituents on the benzene ring/ E.A. Chugunova, N.I. Akylbekov, V.A. Samsonov, S.A. Sitnov, A.R. Burilov// Russian Journal of Organic Chemistry, 2017, V. 53, N 4, pp 637-638 doi:10.1134/S1070428017040273), IF=0.603
  530. Т.Е. Кокина, Л.А. Глинская, К.С. Маренин, И.В. Корольков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Комплексы PdCl2 с оптически активными гибридными лигандами, построенными из молекул α-пинена и β-аланина
    Координационная химия. 2017. Т. 43. № 4. С. 212-221 (Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034), IF=0.541
  531. Т.Е. Кокина, Л.А. Глинская, К.С. Маренин, И.В. Корольков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Комплексы PdCl2 с оптически активными гибридными лигандами, построенными из молекул α-пинена и β-аланина
    Координационная химия. 2017. Т. 43. № 4. С. 212-221 (Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034), IF=0.541
  532. Т.Е. Кокина, Л.А. Глинская, К.С. Маренин, И.В. Корольков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Комплексы PdCl2 с оптически активными гибридными лигандами, построенными из молекул α-пинена и β-аланина
    Координационная химия. 2017. Т. 43. № 4. С. 212-221 (Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034), IF=0.541
  533. Т.Е. Кокина, Л.А. Глинская, К.С. Маренин, И.В. Корольков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Комплексы PdCl2 с оптически активными гибридными лигандами, построенными из молекул α-пинена и β-аланина
    Координационная химия. 2017. Т. 43. № 4. С. 212-221 (Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034), IF=0.541
  534. Т.Е. Кокина, Л.А. Глинская, К.С. Маренин, И.В. Корольков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Комплексы PdCl2 с оптически активными гибридными лигандами, построенными из молекул α-пинена и β-аланина
    Координационная химия. 2017. Т. 43. № 4. С. 212-221 (Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules/ T.E. Kokina, L.A. Glinskaya, K.S. Marenin, I.V. Korol'kov, D.Yu. Naumov, A.V. Tkachev, S.V. Larionov// Russian Journal of Coordination Chemistry, 2017, V. 43, N 4, pp 213-222 doi:10.1134/S1070328417030034), IF=0.541
  535. E.V. Tretyakov, P.A. Fedyushin, E.V. Panteleeva, D.V. Stass, I.Yu. Bagryanskaya, I.V. Beregovaya, A.S. Bogomyakov
    Substitution of a Fluorine Atom in Perfluorobenzonitrile by a Lithiated Nitronyl Nitroxide
    J. Org. Chem., 2017, 82 (8), pp 4179-4185 doi:10.1021/acs.joc.7b00144, IF=4.848
  536. E.V. Tretyakov, P.A. Fedyushin, E.V. Panteleeva, D.V. Stass, I.Yu. Bagryanskaya, I.V. Beregovaya, A.S. Bogomyakov
    Substitution of a Fluorine Atom in Perfluorobenzonitrile by a Lithiated Nitronyl Nitroxide
    J. Org. Chem., 2017, 82 (8), pp 4179-4185 doi:10.1021/acs.joc.7b00144, IF=4.848
  537. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, И.А. Викулина, К.О. Гусаченко, Д.И. Дудник
    Экспериментальное исследование голографических дифракционных ФПМ-ЖК-структур
    Доклады Томского государственного университета систем управления и радиоэлектроники. 2017. Т. 20. № 1. С. 29-32. doi:10.21293/1818-0442-2017-20-1-29-32
  538. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, И.А. Викулина, К.О. Гусаченко, Д.И. Дудник
    Экспериментальное исследование голографических дифракционных ФПМ-ЖК-структур
    Доклады Томского государственного университета систем управления и радиоэлектроники. 2017. Т. 20. № 1. С. 29-32. doi:10.21293/1818-0442-2017-20-1-29-32
  539. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, И.А. Викулина, К.О. Гусаченко, Д.И. Дудник
    Экспериментальное исследование голографических дифракционных ФПМ-ЖК-структур
    Доклады Томского государственного университета систем управления и радиоэлектроники. 2017. Т. 20. № 1. С. 29-32. doi:10.21293/1818-0442-2017-20-1-29-32
  540. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, И.А. Викулина, К.О. Гусаченко, Д.И. Дудник
    Экспериментальное исследование голографических дифракционных ФПМ-ЖК-структур
    Доклады Томского государственного университета систем управления и радиоэлектроники. 2017. Т. 20. № 1. С. 29-32. doi:10.21293/1818-0442-2017-20-1-29-32
  541. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, И.А. Викулина, К.О. Гусаченко, Д.И. Дудник
    Экспериментальное исследование голографических дифракционных ФПМ-ЖК-структур
    Доклады Томского государственного университета систем управления и радиоэлектроники. 2017. Т. 20. № 1. С. 29-32. doi:10.21293/1818-0442-2017-20-1-29-32
  542. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  543. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  544. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  545. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  546. М.В. Кручинина, Я.И. Прудникова, В.Н. Кручинин, В.А. Володин, М.В. Шашков, А.С. Соколова
    Возможности неинвазивной диагностики колоректального рака методами хроматографии и RAMAN-спектроскопии
    Гастроэнтерология Санкт-Петербурга, 2017. № 1. С. 86-86
  547. A.G. Matveeva, Yu.V. Yushkova, S.V. Morozov, I.A. Grygor'ev, S.A. Dzuba
    Multi-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency DomainMulti-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency Domain
    Zeitschrift fur Physikalische Chemie, 2017б V. 231, N 3, Pp 671-688 doi:10.1515/zpch-2016-0830, IF=1.327
  548. A.G. Matveeva, Yu.V. Yushkova, S.V. Morozov, I.A. Grygor'ev, S.A. Dzuba
    Multi-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency DomainMulti-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency Domain
    Zeitschrift fur Physikalische Chemie, 2017б V. 231, N 3, Pp 671-688 doi:10.1515/zpch-2016-0830, IF=1.327
  549. M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
    Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
    CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
  550. M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
    Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
    CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
  551. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  552. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  553. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  554. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  555. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  556. E.S. Stoyanov, A.S. Nizovtsev
    Stabilization of carbocations CHБ3+, C2H5+, i-C3H7+, tert-Bu+, and cyclo-pentyl+ in solid phases: experimental data versus calculations
    Phys. Chem. Chem. Phys., 2017, 19(10), 7270-7279 doi:10.1039/C6CP06839A, IF=4.123
  557. A.S. Sokolova, O.I. Yarovaya, A.A. Shtro, M.S. Borisova, E.A. Morozova, T.G. Tolstikova, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and biological activity of heterocyclic borneol derivatives
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 371-377 doi:10.1007/s10593-017-2063-3, IF=0.893
  558. A.S. Sokolova, O.I. Yarovaya, A.A. Shtro, M.S. Borisova, E.A. Morozova, T.G. Tolstikova, V.V. Zarubaev, N.F. Salakhutdinov
    Synthesis and biological activity of heterocyclic borneol derivatives
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 371-377 doi:10.1007/s10593-017-2063-3, IF=0.893
  559. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
    Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
  560. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
    Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
  561. K.S. Kovaleva, O.I. Yarovaya, A.V. Shernyukov, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, N.F. Salakhutdinov
    Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 3, pp 364-370 doi:10.1007/s10593-017-2058-0, IF=0.893
  562. A.I. Kokorin, B.Y. Mladenova-Kattnig, I.A. Grigor'ev, G. Grampp
    Unexpected Features of the Intramolecular Spin Exchange in Imidazoline Nitroxide Biradicals Dissolved in Ionic Liquids
    Applied Magnetic Resonance, 2017, V. 48, N 3, Pp 287-296 doi:10.1007/s00723-016-0858-5, IF=0.864
  563. A.I. Kokorin, B.Y. Mladenova-Kattnig, I.A. Grigor'ev, G. Grampp
    Unexpected Features of the Intramolecular Spin Exchange in Imidazoline Nitroxide Biradicals Dissolved in Ionic Liquids
    Applied Magnetic Resonance, 2017, V. 48, N 3, Pp 287-296 doi:10.1007/s00723-016-0858-5, IF=0.864
  564. A.I. Kokorin, B.Y. Mladenova-Kattnig, I.A. Grigor'ev, G. Grampp
    Unexpected Features of the Intramolecular Spin Exchange in Imidazoline Nitroxide Biradicals Dissolved in Ionic Liquids
    Applied Magnetic Resonance, 2017, V. 48, N 3, Pp 287-296 doi:10.1007/s00723-016-0858-5, IF=0.864
  565. S.M. Adekenov, Zh.R. Shaimerdenova, Yu.V. Gatilov, G.A. Atazhanova
    Two New Sesquiterpene Lactones from Artemisia halophila
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 284-289 doi:10.1007/s10600-017-1971-x, IF=0.46
  566. S.M. Adekenov, Zh.R. Shaimerdenova, Yu.V. Gatilov, G.A. Atazhanova
    Two New Sesquiterpene Lactones from Artemisia halophila
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 284-289 doi:10.1007/s10600-017-1971-x, IF=0.46
  567. S.M. Adekenov, Zh.R. Shaimerdenova, Yu.V. Gatilov, G.A. Atazhanova
    Two New Sesquiterpene Lactones from Artemisia halophila
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 284-289 doi:10.1007/s10600-017-1971-x, IF=0.46
  568. E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46
  569. E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46
  570. E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46
  571. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
  572. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
  573. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
  574. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
  575. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
  576. Н.И. Ткачева, С.В. Морозов, В.В. Ломиворотов, И.А. Григорьев
    Органические соединения - доноры сероводорода - с кардиопротекторными свойствами (обзор)
    Химико-фармацевтический журнал. 2017. Т. 51. № 3. С. 3-12. (Organic Hydrogen Sulfide Donor Compounds with Cardioprotective Properties (Review)/ N. I. Tkacheva, S. V. Morozov, B. B. Lomivorotov, I. A. Grigor'ev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 3, pp 165-174 doi:10.1007/s11094-017-1576-5), IF=0.444
  577. T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
    Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
    Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
  578. T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
    Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
    Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
  579. T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
    Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
    Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
  580. T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
    Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
    Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
  581. А.В. Тихомирова, И.Ю. Багрянская, Н.В. Первухина, Т.Г. Черкасова
    Синтез и кристаллическая структура гексаиододимеркурата(II) комплекса кобальта(ii) с ε-капролактамом
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 193-196 (Cobalt(II) hexaiododimercurate(II) complex with ε-caprolactam: Synthesis and crystal structure/ A.V. Tikhomirova, I.Yu. Bagryanskaya, N.V. Pervukhina, T.G. Cherkasova// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 187-190 doi:10.1134/S0036023617020206), IF=0.787
  582. А.В. Тихомирова, И.Ю. Багрянская, Н.В. Первухина, Т.Г. Черкасова
    Синтез и кристаллическая структура гексаиододимеркурата(II) комплекса кобальта(ii) с ε-капролактамом
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 193-196 (Cobalt(II) hexaiododimercurate(II) complex with ε-caprolactam: Synthesis and crystal structure/ A.V. Tikhomirova, I.Yu. Bagryanskaya, N.V. Pervukhina, T.G. Cherkasova// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 187-190 doi:10.1134/S0036023617020206), IF=0.787
  583. А.В. Тихомирова, И.Ю. Багрянская, Н.В. Первухина, Т.Г. Черкасова
    Синтез и кристаллическая структура гексаиододимеркурата(II) комплекса кобальта(ii) с ε-капролактамом
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 193-196 (Cobalt(II) hexaiododimercurate(II) complex with ε-caprolactam: Synthesis and crystal structure/ A.V. Tikhomirova, I.Yu. Bagryanskaya, N.V. Pervukhina, T.G. Cherkasova// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 187-190 doi:10.1134/S0036023617020206), IF=0.787
  584. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, А.Л. Ворнаков, Е.В. Черкасова, Н.В. Куратьева
    Синтез и кристаллическая структура двойного комплексного соединения [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 188-192 (Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X), IF=0.787
  585. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, А.Л. Ворнаков, Е.В. Черкасова, Н.В. Куратьева
    Синтез и кристаллическая структура двойного комплексного соединения [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 188-192 (Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X), IF=0.787
  586. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, А.Л. Ворнаков, Е.В. Черкасова, Н.В. Куратьева
    Синтез и кристаллическая структура двойного комплексного соединения [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 188-192 (Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X), IF=0.787
  587. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, А.Л. Ворнаков, Е.В. Черкасова, Н.В. Куратьева
    Синтез и кристаллическая структура двойного комплексного соединения [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 188-192 (Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X), IF=0.787
  588. Т.Г. Черкасова, И.Ю. Багрянская, Н.В. Первухина, А.Л. Ворнаков, Е.В. Черкасова, Н.В. Куратьева
    Синтез и кристаллическая структура двойного комплексного соединения [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4
    Журнал неорганической химии. 2017. Т. 62. № 2. С. 188-192 (Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X), IF=0.787
  589. D.I. Derevyanko, V.V. Shelkovnikov, N.A. Orlova, B.G. Goldenberg, A.G. Lemzyakov, V.P. Korolkov
    Fabrication of High-aspect-ratio Microstructures for LIGA-technology by Sinchrotron Radiation Polymerisation of Thetetraacrylate Monomer
    Physics Procedia, 2017, V 86, Pp 122-126 (International Conference on Photonics of Nano- and Bio-Structures, PNBS-2015, 19-20 June 2015, Vladivostok, Russia and the International Conference on Photonics of Nano- and Micro-Structures, PNMS-2015, 7-11 September 2015, Tomsk, Russia.) doi:10.1016/j.phpro.2017.01.032
  590. D.I. Derevyanko, V.V. Shelkovnikov, N.A. Orlova, B.G. Goldenberg, A.G. Lemzyakov, V.P. Korolkov
    Fabrication of High-aspect-ratio Microstructures for LIGA-technology by Sinchrotron Radiation Polymerisation of Thetetraacrylate Monomer
    Physics Procedia, 2017, V 86, Pp 122-126 (International Conference on Photonics of Nano- and Bio-Structures, PNBS-2015, 19-20 June 2015, Vladivostok, Russia and the International Conference on Photonics of Nano- and Micro-Structures, PNMS-2015, 7-11 September 2015, Tomsk, Russia.) doi:10.1016/j.phpro.2017.01.032
  591. D.I. Derevyanko, V.V. Shelkovnikov, N.A. Orlova, B.G. Goldenberg, A.G. Lemzyakov, V.P. Korolkov
    Fabrication of High-aspect-ratio Microstructures for LIGA-technology by Sinchrotron Radiation Polymerisation of Thetetraacrylate Monomer
    Physics Procedia, 2017, V 86, Pp 122-126 (International Conference on Photonics of Nano- and Bio-Structures, PNBS-2015, 19-20 June 2015, Vladivostok, Russia and the International Conference on Photonics of Nano- and Micro-Structures, PNMS-2015, 7-11 September 2015, Tomsk, Russia.) doi:10.1016/j.phpro.2017.01.032
  592. G.Audran, E. Bagryanskaya, M. Edeleva, S.R. A. Marque, T. Yamasaki
    Dual-initiator alkoxyamines with an N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl) nitroxide moiety for preparation of block co-polymers
    RSC Adv., 2017, V. 7, N 9, Pp 4993-5001 doi:10.1039/C6RA27231B, IF=3.108
  593. G.Audran, E. Bagryanskaya, M. Edeleva, S.R. A. Marque, T. Yamasaki
    Dual-initiator alkoxyamines with an N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl) nitroxide moiety for preparation of block co-polymers
    RSC Adv., 2017, V. 7, N 9, Pp 4993-5001 doi:10.1039/C6RA27231B, IF=3.108
  594. A.S. Sokolova, О.I. Yarovaya, D.S. Baev, А.V. Shernyukov, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
    European Journal of Medicinal Chemistry, 2017, V. 127, Pp 661-670 doi:10.1016/j.ejmech.2016.10.035, IF=4.519
  595. A.S. Sokolova, О.I. Yarovaya, D.S. Baev, А.V. Shernyukov, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
    Aliphatic and alicyclic camphor imines as effective inhibitors of influenza virus H1N1
    European Journal of Medicinal Chemistry, 2017, V. 127, Pp 661-670 doi:10.1016/j.ejmech.2016.10.035, IF=4.519
  596. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
  597. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
  598. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
  599. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
  600. Л.Г. Бурова, И.В. Широких, С.С. Патрушев, Т.Г. Толстикова, Э.Э. Шульц
    Взаимосвязь структура-антибактериальная активность в ряду производных изоалантолактона
    Фундаментальная и клиническая медицина. 2017. Т. 2. № 1. С. 28-34.
  601. Л.Г. Бурова, И.В. Широких, С.С. Патрушев, Т.Г. Толстикова, Э.Э. Шульц
    Взаимосвязь структура-антибактериальная активность в ряду производных изоалантолактона
    Фундаментальная и клиническая медицина. 2017. Т. 2. № 1. С. 28-34.
  602. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  603. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  604. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  605. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  606. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  607. M.Yu. Ivanov, S.A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Influence of C2-Methylation of Imidazolium Based Ionic Liquids on Photoinduced Spin Dynamics of the Dissolved ZnTPP Studied by Time-Resolved EPR
    Zeitschrift für Physikalische Chemie, Zeitschrift für Physikalische Chemie, 2017, V. 231, N 2, Pp 391-404 doi:10.1515/zpch-2016-0820, IF=1.327
  608. M.Yu. Ivanov, S.A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Influence of C2-Methylation of Imidazolium Based Ionic Liquids on Photoinduced Spin Dynamics of the Dissolved ZnTPP Studied by Time-Resolved EPR
    Zeitschrift für Physikalische Chemie, Zeitschrift für Physikalische Chemie, 2017, V. 231, N 2, Pp 391-404 doi:10.1515/zpch-2016-0820, IF=1.327
  609. M.Yu. Ivanov, S.A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Influence of C2-Methylation of Imidazolium Based Ionic Liquids on Photoinduced Spin Dynamics of the Dissolved ZnTPP Studied by Time-Resolved EPR
    Zeitschrift für Physikalische Chemie, Zeitschrift für Physikalische Chemie, 2017, V. 231, N 2, Pp 391-404 doi:10.1515/zpch-2016-0820, IF=1.327
  610. M.Yu. Ivanov, S.A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Influence of C2-Methylation of Imidazolium Based Ionic Liquids on Photoinduced Spin Dynamics of the Dissolved ZnTPP Studied by Time-Resolved EPR
    Zeitschrift für Physikalische Chemie, Zeitschrift für Physikalische Chemie, 2017, V. 231, N 2, Pp 391-404 doi:10.1515/zpch-2016-0820, IF=1.327
  611. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  612. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  613. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  614. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  615. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  616. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  617. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  618. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  619. I.D. Markova, N.E. Polyakov, O.Yu. Selyutina, L.G. Fedenok, K.Yu. Fedotov, I.A. Slepneva, T.V. Leshina, A.G. Pokrovsky, N.V. Vasilieva, L.M. Weiner
    Light-Stimulated Generation of Free Radicals by Quinones-Chelators
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 369-389 doi:10.1515/zpch-2016-0831, IF=1.327
  620. Ю.П. Зернов, Т.В. Кобзева, Т.Ю. Дранова, Д.В. Стась, А.А. Алексеев, А.А. Нефедов
    Люминофоры светящегося гриба NEONOTHOPANUS NAMBI
    Биофизика. 2017. Т. 62. № 2. С. 340-346. (Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300)
  621. Ю.П. Зернов, Т.В. Кобзева, Т.Ю. Дранова, Д.В. Стась, А.А. Алексеев, А.А. Нефедов
    Люминофоры светящегося гриба NEONOTHOPANUS NAMBI
    Биофизика. 2017. Т. 62. № 2. С. 340-346. (Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300)
  622. Ю.П. Зернов, Т.В. Кобзева, Т.Ю. Дранова, Д.В. Стась, А.А. Алексеев, А.А. Нефедов
    Люминофоры светящегося гриба NEONOTHOPANUS NAMBI
    Биофизика. 2017. Т. 62. № 2. С. 340-346. (Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300)
  623. Ю.П. Зернов, Т.В. Кобзева, Т.Ю. Дранова, Д.В. Стась, А.А. Алексеев, А.А. Нефедов
    Люминофоры светящегося гриба NEONOTHOPANUS NAMBI
    Биофизика. 2017. Т. 62. № 2. С. 340-346. (Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300)
  624. Ю.П. Зернов, Т.В. Кобзева, Т.Ю. Дранова, Д.В. Стась, А.А. Алексеев, А.А. Нефедов
    Люминофоры светящегося гриба NEONOTHOPANUS NAMBI
    Биофизика. 2017. Т. 62. № 2. С. 340-346. (Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300)
  625. A.V. Shpatov, S.A. Popov, O.I. Salnikova, T.P. Kukina, E.N. Shmidt, B.H. Um
    Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and P. sibirica Du Tour)
    Chemistry & Biodiversity, 2017, V. 14, N 2, Article number e1600203 doi:10.1002/cbdv.201600203, IF=1.44
  626. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Оценка эффективности действия нового местного гемостатического ванкомицин-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сиб. мед. журнал.-2017. - Т. 32, № 1. - С. 108-111.
  627. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Оценка эффективности действия нового местного гемостатического ванкомицин-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сиб. мед. журнал.-2017. - Т. 32, № 1. - С. 108-111.
  628. A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
    Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
    Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
  629. A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
    Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
    Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
  630. A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
    Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
    Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
  631. A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
    Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
    Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
  632. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  633. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  634. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  635. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  636. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  637. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  638. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  639. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  640. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  641. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  642. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  643. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  644. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  645. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  646. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  647. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  648. Р.З. Сагдеев, С.Е. Толстиков, С.В. Фокин, И.В. Обшарова, С.В. Туманов, С.Л. Вебер, Г.В. Романенко, А.С. Богомяков, М.В. Федин, Е.В. Третьяков, М. Халкроу, В.И. Овчаренко
    Синтез и исследование комплекса CuII с нитроксилом - аналога «прыгающих» кристаллов
    Известия Академии наук. Серия химическая. 2017. № 2. С. 222-230. (Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y), IF=0.528
  649. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  650. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  651. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  652. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  653. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  654. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  655. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  656. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  657. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  658. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  659. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  660. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  661. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  662. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  663. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  664. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  665. S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, M.T. Gamer, R.T. Boere, P.W. Roesky, A.V. Zibarev, S.N. Konchenko
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
  666. Yu.M. Volkova, A.Yu. Makarov, S.B. Zikirin, A.M. Genaev, I.Yu. Bagryanskaya, A.V. Zibarev
    3,1,2,4-Benzothiaselenadiazine and related heterocycles: synthesis and transformation into Herz-type radicals
    Mendeleev Communications, 2017, V. 27, N 1, Pp 19-22 doi:10.1016/j.mencom.2017.01.005, IF=1.741
  667. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  668. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  669. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  670. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  671. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  672. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  673. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  674. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  675. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  676. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
    Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
  677. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
    Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
  678. Н.И. Ткачева, С.В. Морозов, Е.М. Стахнёва, Б.С. Шрамко, Ю.И. Рагино
    Хроматографическое определение содержания жирных кислот в различных биологических средах при атеросклеротических повреждениях
    Атеросклероз и дислипидемии. 2017. № 1 (26). С. 17-28.
  679. Н.И. Ткачева, С.В. Морозов, Е.М. Стахнёва, Б.С. Шрамко, Ю.И. Рагино
    Хроматографическое определение содержания жирных кислот в различных биологических средах при атеросклеротических повреждениях
    Атеросклероз и дислипидемии. 2017. № 1 (26). С. 17-28.
  680. Н.И. Ткачева, С.В. Морозов, Е.М. Стахнёва, Б.С. Шрамко, Ю.И. Рагино
    Хроматографическое определение содержания жирных кислот в различных биологических средах при атеросклеротических повреждениях
    Атеросклероз и дислипидемии. 2017. № 1 (26). С. 17-28.
  681. E. Karpova, A. Nefedov, V. Mamatyuk, N. Polosmak, L. Kundo
    Multi-analytical approach (SEM-EDS, FTIR, Py-GC/MS) to characterize the lacquer objects from Xiongnu burial complex (Noin-Ula, Mongolia)
    Microchemical Journal, Volume 130, January 2017, Pages 336-344 doi:10.1016/j.microc.2016.10.013, IF=3.33
  682. E. Karpova, A. Nefedov, V. Mamatyuk, N. Polosmak, L. Kundo
    Multi-analytical approach (SEM-EDS, FTIR, Py-GC/MS) to characterize the lacquer objects from Xiongnu burial complex (Noin-Ula, Mongolia)
    Microchemical Journal, Volume 130, January 2017, Pages 336-344 doi:10.1016/j.microc.2016.10.013, IF=3.33
  683. E.E. Shults, M.M. Shakirov, M.A. Pokrovsky, T.N. Petrova, A.G. Pokrovsky, P.G. Gorovoy
    Phenolic compounds from Glycyrrhiza pallidiflora Maxim and their cytotoxic activity
    Natural Product Research, 2017, V. 31,N 4, Pp 445-452 doi:10.1080/14786419.2016.1188094, IF=1.827
  684. E.E. Shults, M.M. Shakirov, M.A. Pokrovsky, T.N. Petrova, A.G. Pokrovsky, P.G. Gorovoy
    Phenolic compounds from Glycyrrhiza pallidiflora Maxim and their cytotoxic activity
    Natural Product Research, 2017, V. 31,N 4, Pp 445-452 doi:10.1080/14786419.2016.1188094, IF=1.827
  685. E.E. Shults, M.M. Shakirov, M.A. Pokrovsky, T.N. Petrova, A.G. Pokrovsky, P.G. Gorovoy
    Phenolic compounds from Glycyrrhiza pallidiflora Maxim and their cytotoxic activity
    Natural Product Research, 2017, V. 31,N 4, Pp 445-452 doi:10.1080/14786419.2016.1188094, IF=1.827
  686. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  687. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  688. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  689. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  690. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  691. I.L. Simakova, Yu.S. Demidova, M. Estrada, S. Beloshapkin, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, A. Simakov
    Gold catalyzed one-pot myrtenol amination: Effect of catalyst redox activationOriginal Research Article
    Сatalysis Today, V. 279, Part 1, 1 January 2017, Pages 63-70 doi:10.1016/j.cattod.2016.01.044, IF=4.636
  692. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  693. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  694. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  695. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  696. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  697. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  698. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  699. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  700. M. Stekrova, P. Maki-Arvela, E. Leino, K.M. Valkaj, K. Eranen, A. Aho, A. Smeds, N. Kumar, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Two-step synthesis of monoterpenoid dioxinols exhibiting analgesic activity from isopulegol and benzaldehyde over heterogeneous catalysts
    Catalysis Today, Catalysis Today, V. 279, Part 1, 1 January 2017, Pp 56-62 doi:10.1016/j.cattod.2016.03.046, IF=4.636
  701. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова
    Первый российский комплексный гемостатик
    Наука из первых рук. 2017. Т. 73. № 1. С. 84-89.
  702. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова
    Первый российский комплексный гемостатик
    Наука из первых рук. 2017. Т. 73. № 1. С. 84-89.
  703. А.Г. Стрельников, Н.Ф. Салахутдинов
    Ботокс для сердца
    Наука из первых рук. 2017. Т. 73. № 1. С. 66-71.
  704. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
  705. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
  706. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
  707. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
  708. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  709. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  710. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  711. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  712. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  713. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  714. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  715. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  716. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  717. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  718. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  719. B.M. Urbagarova, V.V. Taraskin, E.E. Shul'ts, L.D. Radnaeva, O.A. Anenkhonov, Zh. Ganbaatar, N.B. Boldanova
    Biologically Active Compounds from the Lipid Fraction of Saposhnikovia divaricata
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 138-140 doi:10.1007/s10600-017-1928-0, IF=0.46
  720. Yu.V. Kharitonov, M.M. Shakirov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. XXXV.* Synthesis and Cytotoxicity of Macroheterocyclic Compounds Based on Lambertianic Acid
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 77-82 doi:10.1007/s10600-017-1915-5, IF=0.46
  721. Yu.V. Kharitonov, M.M. Shakirov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. XXXV.* Synthesis and Cytotoxicity of Macroheterocyclic Compounds Based on Lambertianic Acid
    Chemistry of Natural Compounds, January 2017, V. 53, N 1, pp 77-82 doi:10.1007/s10600-017-1915-5, IF=0.46
  722. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  723. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  724. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  725. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  726. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  727. А.Л. Захаренко, О.А. Лузина, Д.Н. Соколов, О.Д. Захарова, М.Е. Рахманова, А.А. Чепанова, Н.С. Дырхеева, О.И. Лаврик, Н.Ф. Салахутдинов
    Производные усниновой кислоты как эффективные ингибиторы тирозил-ДНК-фосфодиэстеразы 1
    Биоорганическая химия. 2017. Т. 43. № 1. С. 97-104. (Usnic acid derivatives are effective inhibitors of tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, O.A. Luzina, D.N. Sokolov, O.D. Zakharova, M.E. Rakhmanova, A.A. Chepanova, N.S. Dyrkheeva, O.I. Lavrik, N.F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, January 2017, Volume 43, Issue 1, pp 84-90 doi:10.1134/S1068162017010125), IF=0.689
  728. Л.Н. Зибарева, О.В. Волкова, С.В. Морозов, Е.И. Черняк
    Фитоэкдистероиды корней SILENE FRIVALDSZKYANA HAMPE
    Химия растительного сырья. 2017. № 1. С. 71-75
  729. Л.Н. Зибарева, О.В. Волкова, С.В. Морозов, Е.И. Черняк
    Фитоэкдистероиды корней SILENE FRIVALDSZKYANA HAMPE
    Химия растительного сырья. 2017. № 1. С. 71-75
  730. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Ю.В. Гатилов
    Соли нитросемикарбазона фурфурола
    Известия Академии наук. Серия химическая. 2017. № 1. С. 83-85 (Furfural nitrosemicarbazone salts/ V. S. Glukhacheva, S. G. Il'yasov, G. V. Sakovich, Yu. V. Gatilov// Russian Chemical Bulletin, January 2017, V. 66, N 1, pp 83-85 doi:10.1007/s11172-017-1703-1), IF=0.528
  731. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Ю.В. Гатилов
    Соли нитросемикарбазона фурфурола
    Известия Академии наук. Серия химическая. 2017. № 1. С. 83-85 (Furfural nitrosemicarbazone salts/ V. S. Glukhacheva, S. G. Il'yasov, G. V. Sakovich, Yu. V. Gatilov// Russian Chemical Bulletin, January 2017, V. 66, N 1, pp 83-85 doi:10.1007/s11172-017-1703-1), IF=0.528
  732. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Ю.В. Гатилов
    Соли нитросемикарбазона фурфурола
    Известия Академии наук. Серия химическая. 2017. № 1. С. 83-85 (Furfural nitrosemicarbazone salts/ V. S. Glukhacheva, S. G. Il'yasov, G. V. Sakovich, Yu. V. Gatilov// Russian Chemical Bulletin, January 2017, V. 66, N 1, pp 83-85 doi:10.1007/s11172-017-1703-1), IF=0.528
  733. О.В. Петрова, Л.Н. Собенина, А.Б. Будаев, А.В. Иванов, В.А. Самсонов, А.Я. Тихонов, Б.А. Трофимов
    Образование 1-аминофеназина из оксима 3,4-дигидрофеназин-1(2н)-она в системе ацетилен-КОН-ДСМО
    Журнал органической химии, 2017, V. 53, N 1, pp 151-153 (Formation of 1-aminophenazine from 3,4-dihydrophenazin-1(2H)-one oxime in the system acetylene-KOH-DMSO/ O.V. Petrova, L.N. Sobenina, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov// Russian Journal of Organic Chemistry, January 2017, V. 53, N 1, pp 150-152 doi:10.1134/S1070428017010316), IF=0.603
  734. О.В. Петрова, Л.Н. Собенина, А.Б. Будаев, А.В. Иванов, В.А. Самсонов, А.Я. Тихонов, Б.А. Трофимов
    Образование 1-аминофеназина из оксима 3,4-дигидрофеназин-1(2н)-она в системе ацетилен-КОН-ДСМО
    Журнал органической химии, 2017, V. 53, N 1, pp 151-153 (Formation of 1-aminophenazine from 3,4-dihydrophenazin-1(2H)-one oxime in the system acetylene-KOH-DMSO/ O.V. Petrova, L.N. Sobenina, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov// Russian Journal of Organic Chemistry, January 2017, V. 53, N 1, pp 150-152 doi:10.1134/S1070428017010316), IF=0.603
  735. О.В. Петрова, Л.Н. Собенина, А.Б. Будаев, А.В. Иванов, В.А. Самсонов, А.Я. Тихонов, Б.А. Трофимов
    Образование 1-аминофеназина из оксима 3,4-дигидрофеназин-1(2н)-она в системе ацетилен-КОН-ДСМО
    Журнал органической химии, 2017, V. 53, N 1, pp 151-153 (Formation of 1-aminophenazine from 3,4-dihydrophenazin-1(2H)-one oxime in the system acetylene-KOH-DMSO/ O.V. Petrova, L.N. Sobenina, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov// Russian Journal of Organic Chemistry, January 2017, V. 53, N 1, pp 150-152 doi:10.1134/S1070428017010316), IF=0.603
  736. О.В. Петрова, Л.Н. Собенина, А.Б. Будаев, А.В. Иванов, В.А. Самсонов, А.Я. Тихонов, Б.А. Трофимов
    Образование 1-аминофеназина из оксима 3,4-дигидрофеназин-1(2н)-она в системе ацетилен-КОН-ДСМО
    Журнал органической химии, 2017, V. 53, N 1, pp 151-153 (Formation of 1-aminophenazine from 3,4-dihydrophenazin-1(2H)-one oxime in the system acetylene-KOH-DMSO/ O.V. Petrova, L.N. Sobenina, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov// Russian Journal of Organic Chemistry, January 2017, V. 53, N 1, pp 150-152 doi:10.1134/S1070428017010316), IF=0.603
  737. О.В. Петрова, Л.Н. Собенина, А.Б. Будаев, А.В. Иванов, В.А. Самсонов, А.Я. Тихонов, Б.А. Трофимов
    Образование 1-аминофеназина из оксима 3,4-дигидрофеназин-1(2н)-она в системе ацетилен-КОН-ДСМО
    Журнал органической химии, 2017, V. 53, N 1, pp 151-153 (Formation of 1-aminophenazine from 3,4-dihydrophenazin-1(2H)-one oxime in the system acetylene-KOH-DMSO/ O.V. Petrova, L.N. Sobenina, A.B. Budaev, A.V. Ivanov, V.A. Samsonov, A.Ya. Tikhonov, B.A. Trofimov// Russian Journal of Organic Chemistry, January 2017, V. 53, N 1, pp 150-152 doi:10.1134/S1070428017010316), IF=0.603
  738. Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
    Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
  739. Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
    Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
  740. Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
    Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
  741. Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
    Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
  742. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  743. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  744. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  745. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  746. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  747. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19
  748. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895
  749. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895
  750. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895
  751. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895
  752. E. Valdman, I. Kapitsa, Е. Ivanova, T. Voronina, O. Ardashov, K. Volcho, V. Khazanov, N. Salakhutdinov
    Evolution of anti-parkinsonian activity of monoterpenoid (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in various in vivo models
    European Journal of Pharmacology, 2017, V. 815, Pp 351-363 doi:10.1016/j.ejphar.2017.09.022, IF=2.895
  753. A.A. Kuzhelev, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, R.K. Strizhakov, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Radicals: An EPR Study of 13C Hyperfine Coupling Constants
    Zeitschrift für Physikalische Chemie, 2017, V. 231, N 4, Pp.777-794 doi:10.1515/zpch-2016-0811, IF=1.327
  754. A.A. Kuzhelev, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, R.K. Strizhakov, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Radicals: An EPR Study of 13C Hyperfine Coupling Constants
    Zeitschrift für Physikalische Chemie, 2017, V. 231, N 4, Pp.777-794 doi:10.1515/zpch-2016-0811, IF=1.327

2016

Reviews, articles

  1. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  2. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  3. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  4. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  5. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  6. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  7. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  8. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  9. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  10. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  11. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  12. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  13. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  14. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  15. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  16. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  17. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  18. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  19. B.A. Knyazev, E.G. Bagryanskaya, E.N. Chesnokov, Yu.Yu. Chopova, V.V. Gerasimov, Ya.V. Getmanov, B.G. Goldenberg, G.N. Kulipanov, A.S. Kozlov, V.V. Kubarev, A.K. Nikitin, V.S. Pavelyev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Sheglov, S.S. Serednyakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser as a User Facility
    Physics Procedia, 2016, V. 84, Pp 27-34 (Proceedings of the International Conference "Synchrotron and Free electron laser Radiation: generation and application" (SFR-2016), July 4 - 7, 2016, Novosibirsk, Russia) doi:10.1016/j.phpro.2016.11.006
  20. T.S. Khlebnicova, Y.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: synthesis and biological evaluation as potential anti-inflammatory agents
    Известия Национальной академии наук Беларуси. Серия химических наук. Минск. “Беларуская навука.” 2016. C. 81-82.
  21. T.S. Khlebnicova, Y.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: synthesis and biological evaluation as potential anti-inflammatory agents
    Известия Национальной академии наук Беларуси. Серия химических наук. Минск. “Беларуская навука.” 2016. C. 81-82.
  22. T.S. Khlebnicova, Y.A. Piven, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
    Fluorine-containing lupane triterpenoid acid derivatives: synthesis and biological evaluation as potential anti-inflammatory agents
    Известия Национальной академии наук Беларуси. Серия химических наук. Минск. “Беларуская навука.” 2016. C. 81-82.
  23. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  24. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  25. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  26. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  27. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  28. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  29. В.В. Шелковников, Г.А. Любас, С.В. Коротаев, Т.Н. Копылова, Е.Н. Тельминов, Р.М. Гадиров, Е.Н. Никонова, С.Ю. Никонов, Т.А. Солодова, В.А. Новиков
    Lasing of a Solid-State Active Element Based on Anodized Генерация лазерного излучения твердотельным активным элементом на основе плёнки анодированного оксида алюминия, активированной родамином 6Ж
    Изв. Вузов. Физика, 2016, Т. 59, N 12, Сс. 11-16 (Lasing of a Solid-State Active Element Based on Anodized Aluminum Oxide Film Doped with Rhodamine 6G/ V.V. Shelkovnikov, G.A. Lyubas, S.V. Korotaev, T.N. Kopylova, E.N. Tel'minov, R.M. Gadirov, E.N. Nikonova, S.Yu. Nikonov, T.A. Solodova, V.A. Novikov// Russian Physics Journal, April 2017, V.59, N 12, pp 1989-1995 doi:10.1007/s11182-017-1005-y), IF=0.666
  30. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, N.F. Salakhutdinov
    Derivatives of usnic acid inhibit broad range of influenza viruses and protect mice from lethal influenza infection
    Antivir Chem Chemotherapy, V.24, N 3-4, August 2015, pp. 92-98, Published March 27, 2016 doi:10.1177/2040206616636992
  31. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, N.F. Salakhutdinov
    Derivatives of usnic acid inhibit broad range of influenza viruses and protect mice from lethal influenza infection
    Antivir Chem Chemotherapy, V.24, N 3-4, August 2015, pp. 92-98, Published March 27, 2016 doi:10.1177/2040206616636992
  32. G. Audran, L. Bosco, P. Bremond, T. Butscher, S.R.A. Marque, S. Viel
    Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides
    ChemPhysChem, 2016. V. 17, N 23, Pp 3954-3963 doi:10.1002/cphc.201600647, IF=3.138
  33. G. Audran, L. Bosco, P. Bremond, T. Butscher, S.R.A. Marque, S. Viel
    Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides
    ChemPhysChem, 2016. V. 17, N 23, Pp 3954-3963 doi:10.1002/cphc.201600647, IF=3.138
  34. G. Audran, L. Bosco, P. Bremond, T. Butscher, S.R.A. Marque, S. Viel
    Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides
    ChemPhysChem, 2016. V. 17, N 23, Pp 3954-3963 doi:10.1002/cphc.201600647, IF=3.138
  35. G. Audran, L. Bosco, P. Bremond, T. Butscher, S.R.A. Marque, S. Viel
    Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides
    ChemPhysChem, 2016. V. 17, N 23, Pp 3954-3963 doi:10.1002/cphc.201600647, IF=3.138
  36. G. Audran, L. Bosco, P. Bremond, T. Butscher, S.R.A. Marque, S. Viel
    Intramolecular Hydrogen Bond Reverting the Solvent Effect on Phosphorus Hyperfine Coupling Constants of β-Phosphorylated Nitroxides
    ChemPhysChem, 2016. V. 17, N 23, Pp 3954-3963 doi:10.1002/cphc.201600647, IF=3.138
  37. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.141 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  38. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.141 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  39. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.141 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  40. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
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  41. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
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  42. D. Sergeevichev, V. Fomenko, A. Dokuchaeva, E. Chepeleva, A. Korobeynikov, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Preventing Calcification and Improving Biomechanical Issues of Vein Tissues Using Chitosan
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  43. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  44. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  45. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  46. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  47. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
    Tissue Engineering: Part A. 2016. Vol.22, Suppl.1, S.46 DOI: 10.1089/ ten.tea.2016.5000.abstracts (conference TERMIS - Americas Conference and Exhibition, San Diego, CA, DEC 11-14, 2016), IF=3.891
  48. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  49. Sergeevichev, V. Fomenko, A. Strelnikov, A. Dokuchaeva, A. Korobeynikov, E. Chepeleva, N. Salakhutdinov, E. Pokushalov, A. Karaskov
    Denervation Properties of Botullinum Neurotoxin Type A in Complex with Chitozan
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  50. Н.В. Полосьмак, Е.А. Карпова
    Фрагменты гобеленов из 22-го кургана могильника Ноин-Ула (начало I века н.э.)
    Археология, этнография и антропология Евразии, 2016, Т. 44 № 4 , С.76-82 (Remains of tapestry from a Xiongnu (Early 1st Century AD) Burial in Mound 22 at Noin-Ula/ N.V. Polosmak, E.A. Karpova// ARCHAEOLOGY ETHNOLOGY AND ANTHROPOLOGY OF EURASIA,, 2016, V/. 44 № 4 , Pp.76-82 doi:10.17746/1563-0110.2016.44.4.076-082)
  51. А.А. Bogush, V.G. Voronin, V.D. Tikhova, G.N. Anoshin
    Acid Rock Drainage Remediation and Element Removal Using a Peat-Humic Agent with Subsequent Thermal Treatment of the Metal-Organic Residue.
    Mine Water and the Environment Journal, December 2016, V. 35, N 4, pp 536-546 doi:10.1007/s10230-015-0380-2, IF=0.864
  52. А.А. Bogush, V.G. Voronin, V.D. Tikhova, G.N. Anoshin
    Acid Rock Drainage Remediation and Element Removal Using a Peat-Humic Agent with Subsequent Thermal Treatment of the Metal-Organic Residue.
    Mine Water and the Environment Journal, December 2016, V. 35, N 4, pp 536-546 doi:10.1007/s10230-015-0380-2, IF=0.864
  53. А.А. Bogush, V.G. Voronin, V.D. Tikhova, G.N. Anoshin
    Acid Rock Drainage Remediation and Element Removal Using a Peat-Humic Agent with Subsequent Thermal Treatment of the Metal-Organic Residue.
    Mine Water and the Environment Journal, December 2016, V. 35, N 4, pp 536-546 doi:10.1007/s10230-015-0380-2, IF=0.864
  54. А.Р. Таркова, С.В. Морозов, Н.И. Ткачева, В.И. Родионов, И.А. Григорьев, А.М. Чернявский
    Оценка гемостатических свойств нового местного антибиотик-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сибирский научный медицинский журнал, 2016, т.36, № 6, 12-17
  55. А.Р. Таркова, С.В. Морозов, Н.И. Ткачева, В.И. Родионов, И.А. Григорьев, А.М. Чернявский
    Оценка гемостатических свойств нового местного антибиотик-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сибирский научный медицинский журнал, 2016, т.36, № 6, 12-17
  56. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  57. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  58. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  59. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  60. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  61. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  62. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  63. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  64. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  65. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  66. O.A. Efremova, Yu.A. Vorotnikov, K.A. Brylev, N.A. Vorotnikova, I.N. Novozhilov, N.V. Kuratieva, M.V. Edeleva, D.M. Benoit, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov, A.J. Sutherland
    Octahedral molybdenum cluster complexes with aromatic sulfonate ligands
    Dalton Trans., 2016,45, 15427-15435 doi:10.1039/C6DT02863B, IF=4.177
  67. C. Tantardini, S.G. Arkhipov, K.A. Cherkashina, A.S. Kil'met'ev, E.V. Boldyreva
    Crystal structure of a 2:1 co-crystal of meloxicam with acetylendicarboxylic acid
    Acta Crystallographica Section E, CRYSTALLOGRAPHIC COMMUNICATIONS, 2016, Том: 72 Стр.: 1856-1859 doi:10.1107/S2056989016018909
  68. C. Tantardini, S.G. Arkhipov, K.A. Cherkashina, A.S. Kil'met'ev, E.V. Boldyreva
    Crystal structure of a 2:1 co-crystal of meloxicam with acetylendicarboxylic acid
    Acta Crystallographica Section E, CRYSTALLOGRAPHIC COMMUNICATIONS, 2016, Том: 72 Стр.: 1856-1859 doi:10.1107/S2056989016018909
  69. C. Tantardini, S.G. Arkhipov, K.A. Cherkashina, A.S. Kil'met'ev, E.V. Boldyreva
    Crystal structure of a 2:1 co-crystal of meloxicam with acetylendicarboxylic acid
    Acta Crystallographica Section E, CRYSTALLOGRAPHIC COMMUNICATIONS, 2016, Том: 72 Стр.: 1856-1859 doi:10.1107/S2056989016018909
  70. C. Tantardini, S.G. Arkhipov, K.A. Cherkashina, A.S. Kil'met'ev, E.V. Boldyreva
    Crystal structure of a 2:1 co-crystal of meloxicam with acetylendicarboxylic acid
    Acta Crystallographica Section E, CRYSTALLOGRAPHIC COMMUNICATIONS, 2016, Том: 72 Стр.: 1856-1859 doi:10.1107/S2056989016018909
  71. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  72. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  73. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  74. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  75. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  76. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  77. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  78. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  79. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  80. С.В. Ларионов, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексных соединений Eu(III), содержащих анионы перфтор-3-метилбензойной кислоты
    Журнал общей химии 2016. Т. 86. № 12. С. 2045-2049 (Synthesis and photoluminescence of Eu(III) complex compounds containing anions of perfluoro-3-methylbenzoic acid/ S. V. Larionov, M. I. Rakhmanova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, December 2016, Volume 86, Issue 12, pp 2677-2681 doi:10.1134/S1070363216120173), IF=0.481
  81. С.В. Ларионов, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексных соединений Eu(III), содержащих анионы перфтор-3-метилбензойной кислоты
    Журнал общей химии 2016. Т. 86. № 12. С. 2045-2049 (Synthesis and photoluminescence of Eu(III) complex compounds containing anions of perfluoro-3-methylbenzoic acid/ S. V. Larionov, M. I. Rakhmanova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, December 2016, Volume 86, Issue 12, pp 2677-2681 doi:10.1134/S1070363216120173), IF=0.481
  82. S.I. Zhivetyeva, O.D. Zakharova, L.P. Ovchinnikova, D.S. Baev, I.Yu. Bagryanskaya, V.D. Shteingarts, T.G. Tolstikova, G.A. Nevinsky, E.V. Tretyakov
    Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
    Journal of Fluorine Chemistry, V. 192, Part A, December 2016, Pp 68-77 doi:10.1016/j.jfluchem.2016.10.014, IF=2.213
  83. S.I. Zhivetyeva, O.D. Zakharova, L.P. Ovchinnikova, D.S. Baev, I.Yu. Bagryanskaya, V.D. Shteingarts, T.G. Tolstikova, G.A. Nevinsky, E.V. Tretyakov
    Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
    Journal of Fluorine Chemistry, V. 192, Part A, December 2016, Pp 68-77 doi:10.1016/j.jfluchem.2016.10.014, IF=2.213
  84. S.I. Zhivetyeva, O.D. Zakharova, L.P. Ovchinnikova, D.S. Baev, I.Yu. Bagryanskaya, V.D. Shteingarts, T.G. Tolstikova, G.A. Nevinsky, E.V. Tretyakov
    Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
    Journal of Fluorine Chemistry, V. 192, Part A, December 2016, Pp 68-77 doi:10.1016/j.jfluchem.2016.10.014, IF=2.213
  85. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  86. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  87. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  88. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  89. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  90. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  91. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  92. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  93. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  94. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  95. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  96. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  97. A.Zakharenko, O. Luzina, O.Koval, D. Nilov, I. Gushchina, N. Dyrkheeva, V. Svedas, N. Salakhutdinov, O. Lavrik
    Tyrosyl-DNA phosphodiesterase 1 inhibitors: usnic acid enamines enhance the cytotoxic effect of camptothecin
    J. Nat. Prod., 2016, 79 (11), pp 2961-2967 doi:10.1021/acs.jnatprod.6b00979, IF=3.661
  98. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  99. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  100. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  101. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  102. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  103. M.A. Gilinsky, T.P. Johnston, N.A. Zhukova, N.I. Dubrovina, T.V. Latysheva, S.E. Naumenko, R.A. Sukhovershin
    Methylated arginine analogues: their potential role in atherosclerosis and cognition using the poloxamer-407-induced mouse model of dyslipidemia
    Canadian Journal of Physiology and Pharmacology, 2016, V. 94, N 11, Pp 1122-1131 doi:10.1139/cjpp-2016-0104, IF=1.703
  104. G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva
    Trityl-based alkoxyamines as NMP controllers and spin-labels
    Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A, IF=5.687
  105. G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva
    Trityl-based alkoxyamines as NMP controllers and spin-labels
    Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A, IF=5.687
  106. G. Audran, E. Bagryanskaya, I. Bagryanskaya, P. Bremond, M. Edeleva, S.R. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    C-ON bond homolysis of alkoxyamines triggered by paramagnetic copper(II) salts
    Inorg. Chem. Front., 2016,3, 1464-1472 doi:10.1039/C6QI00277C, IF=4.532
  107. G. Audran, E. Bagryanskaya, I. Bagryanskaya, P. Bremond, M. Edeleva, S.R. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    C-ON bond homolysis of alkoxyamines triggered by paramagnetic copper(II) salts
    Inorg. Chem. Front., 2016,3, 1464-1472 doi:10.1039/C6QI00277C, IF=4.532
  108. M.V. Fedin, G. Yu. Shevelev, D. V. Pyshnyi, V.M. Tormyshev, G. Jeschke, M. Yulikov, E.G. Bagryanskaya
    Interaction of Triarylmethyl Radical with DNA Termini Revealed by Orientation-Selective W-band Double Electron-Electron Resonance Spectroscopy
    Phys. Chem. Chem. Phys., 2016,18(42), 29549-29554l doi:10.1039/C6CP05904J, IF=4.448
  109. M.V. Fedin, G. Yu. Shevelev, D. V. Pyshnyi, V.M. Tormyshev, G. Jeschke, M. Yulikov, E.G. Bagryanskaya
    Interaction of Triarylmethyl Radical with DNA Termini Revealed by Orientation-Selective W-band Double Electron-Electron Resonance Spectroscopy
    Phys. Chem. Chem. Phys., 2016,18(42), 29549-29554l doi:10.1039/C6CP05904J, IF=4.448
  110. M.V. Fedin, G. Yu. Shevelev, D. V. Pyshnyi, V.M. Tormyshev, G. Jeschke, M. Yulikov, E.G. Bagryanskaya
    Interaction of Triarylmethyl Radical with DNA Termini Revealed by Orientation-Selective W-band Double Electron-Electron Resonance Spectroscopy
    Phys. Chem. Chem. Phys., 2016,18(42), 29549-29554l doi:10.1039/C6CP05904J, IF=4.448
  111. M.V. Fedin, G. Yu. Shevelev, D. V. Pyshnyi, V.M. Tormyshev, G. Jeschke, M. Yulikov, E.G. Bagryanskaya
    Interaction of Triarylmethyl Radical with DNA Termini Revealed by Orientation-Selective W-band Double Electron-Electron Resonance Spectroscopy
    Phys. Chem. Chem. Phys., 2016,18(42), 29549-29554l doi:10.1039/C6CP05904J, IF=4.448
  112. M.V. Fedin, G. Yu. Shevelev, D. V. Pyshnyi, V.M. Tormyshev, G. Jeschke, M. Yulikov, E.G. Bagryanskaya
    Interaction of Triarylmethyl Radical with DNA Termini Revealed by Orientation-Selective W-band Double Electron-Electron Resonance Spectroscopy
    Phys. Chem. Chem. Phys., 2016,18(42), 29549-29554l doi:10.1039/C6CP05904J, IF=4.448
  113. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  114. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  115. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  116. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  117. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  118. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  119. O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
  120. O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
  121. O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
  122. O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
  123. S.S. Laev, N.F. Salakhutdinov, O.I. Lavrik
    Tyrosyl-DNA phosphodiesterase inhibitors: Progress and potential
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5017-5027 doi:10.1016/j.bmc.2016.09.045, IF=2.923
  124. М.А. Баженова, В.Д. Тихова, В.П. Фадеева
    Определение бора в органических соединениях атомно-эмиссионным способом
    Журнал аналитической химии, 2016, Т. 71, N. 11, С. 1145-1151. (Determination of Boron in Organic Compounds by Microwave Plasma-Atomic Emission Spectrometry/ M.A. Bazhenov, V.D. Tikhova, V.P. Fadeeva// Journal of Analytical Chemistry, 2016, Vol. 71, No. 11, pp. 1089-1095. doi:10.1134/S1061934816090033), IF=0.694
  125. N.A. Pankrushina, K.B. Rakhmetali
    Synthesis of lappaconitine N-oxide under microwave activation
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N 11, pp 970-972 doi:10.1007/s10593-017-1995-y, IF=0.814
  126. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  127. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  128. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  129. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  130. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  131. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  132. Е.А. Чугунова, Н.И. Акылбеков, Н.В. Гаврилов, В.А. Самсонов, С.А. Ситнов, А.Б. Добрынин, М.А. Пудовик, А.Р. Бурилов
    Синтез новых 3н-бензо[1,2,5]оксадиазин-4-оксидов, содержащих гетероциклические фрагменты в бензольном кольце
    Журнал общей химии, 2016, Т. 86, N 11, pp 1908-1910 (Synthesis of new 3H-benzo[1,2,5]oxadiazine-4-oxides with heterocyclic moieties in the benzene ring/ E.A. Chugunova, N.I. Akylbekov, N.V. Gavrilov, V.A. Samsonov, S.A. Sitnov, A.B. Dobrynin, M.A. Pudovik, A.R. Burilov// Russian Journal of General Chemistry, November 2016, Volume 86, Issue 11, pp 2548-2550 doi:10.1134/S1070363216110232), IF=0.481
  133. S.V. Nikitin, V.V. Nikitin, I.I. Oleynik, I.V. Oleynik, E.G. Bagryanskaya
    Activity of phenoxy-imine titanium catalysts in ethylene polymerization: A quantum chemical approach
    Journal of Molecular Catalysis A: Chemical, V. 423, November 2016, Pp 285-292 doi:10.1016/j.molcata.2016.07.010, IF=3.957
  134. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
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    European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
  135. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
    Antioxidant and antitumor activity of trolox, trolox succinate, an α-tocopheryl succinate conjugates with nitroxides
    European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
  136. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
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    European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
  137. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
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    European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
  138. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  139. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  140. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  141. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  142. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  143. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  144. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  145. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  146. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  147. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  148. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  149. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
  150. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
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    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  151. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  152. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  153. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  154. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  155. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  156. I.V. Sorokina, T.G. Tolstikova, A.V. Volod'ko, I.M. Yermak
    Modification of Biological Properties of k-Carrageenan in Polyionic Complexes with Chitosan
    Achievements in the Life Sciences,2016, V. 10, Supplement, Page S51 (http://www.sciencedirect.com/science/article/pii/S2078152016301900) doi:10.1016/j.als.2016.12.050
  157. I.V. Sorokina, T.G. Tolstikova, A.V. Volod'ko, I.M. Yermak
    Modification of Biological Properties of k-Carrageenan in Polyionic Complexes with Chitosan
    Achievements in the Life Sciences,2016, V. 10, Supplement, Page S51 (http://www.sciencedirect.com/science/article/pii/S2078152016301900) doi:10.1016/j.als.2016.12.050
  158. A.A. Onischuk, T.G. Tolstikova, S.V. An'kov, A.M. Baklanov, S.V. Valiulin, M.V. Khvostov, I.V. Sorokina, G.G. Dultseva, N.A. Zhukova
    Ibuprofen, Indomethacin and Diclofenac Sodium Nanoaerosol: Generation, Inhalation Delivery and Biological Effects in Mice and Rats
    Journal of Aerosol Science, V. 100, October 2016, Pp 164-177 doi:10.1016/j.jaerosci.2016.05.005, IF=2.278
  159. A.A. Onischuk, T.G. Tolstikova, S.V. An'kov, A.M. Baklanov, S.V. Valiulin, M.V. Khvostov, I.V. Sorokina, G.G. Dultseva, N.A. Zhukova
    Ibuprofen, Indomethacin and Diclofenac Sodium Nanoaerosol: Generation, Inhalation Delivery and Biological Effects in Mice and Rats
    Journal of Aerosol Science, V. 100, October 2016, Pp 164-177 doi:10.1016/j.jaerosci.2016.05.005, IF=2.278
  160. A.A. Onischuk, T.G. Tolstikova, S.V. An'kov, A.M. Baklanov, S.V. Valiulin, M.V. Khvostov, I.V. Sorokina, G.G. Dultseva, N.A. Zhukova
    Ibuprofen, Indomethacin and Diclofenac Sodium Nanoaerosol: Generation, Inhalation Delivery and Biological Effects in Mice and Rats
    Journal of Aerosol Science, V. 100, October 2016, Pp 164-177 doi:10.1016/j.jaerosci.2016.05.005, IF=2.278
  161. A.A. Onischuk, T.G. Tolstikova, S.V. An'kov, A.M. Baklanov, S.V. Valiulin, M.V. Khvostov, I.V. Sorokina, G.G. Dultseva, N.A. Zhukova
    Ibuprofen, Indomethacin and Diclofenac Sodium Nanoaerosol: Generation, Inhalation Delivery and Biological Effects in Mice and Rats
    Journal of Aerosol Science, V. 100, October 2016, Pp 164-177 doi:10.1016/j.jaerosci.2016.05.005, IF=2.278
  162. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, Н.П. Гончаров, Е.Я. Кондратенко
    Хромосомная локализация гена быстромигрирующего изофермента ароматической алкогольдегидрогеназы AADH1F (CAD1F) у мягкой пшеницы TRITICUM AESTIVUM L.
    Генетика, 2016, Т. 52, Т 10, С. 1222-1228 doi:10.1134/S1022795416080056
  163. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, Н.П. Гончаров, Е.Я. Кондратенко
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    Генетика, 2016, Т. 52, Т 10, С. 1222-1228 doi:10.1134/S1022795416080056
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  165. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
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  166. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
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  167. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
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  168. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
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  173. M.Y. Ivanov, V.A. Nadolinny, E.G. Bagryanskay, Yu.A. Grishin, M.V. Fedin, S.L. Veber
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  174. Р.Ю. Пешков, Ван Чуньянь, Е.В. Пантелеева, Е.В. Третьяков, В.Д. Штейнгарц
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    Известия Академии наук. Серия химическая, 2016, № 10, C. 2330-2436 (Synthesis of 4-(ω-X-alkyl)benzonitriles (X=1,3-dioxan-2-yl, CN, (CO2Et) by the reaction of terephthalonitrile dianion with ω-X-alkyl bromides in liquid ammonia/ R. Yu. Peshkov, Chynyan Wang, E. V. Panteleeva, E. V. Tretyakov, V. D. Shteingarts// Russian Chemical Bulletin, 2016, V. 65, N 10, pp 2430-2436 doi:10.1007/s11172-016-1602-x), IF=0.579
  175. В.В. Бардин, Н.Ю. Адонин
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    Журнал органической химии, 2016, Т. 52, N 10, Cтр. 1400-1407 (Reactions of aromatic compounds with xenon difluoride/ V. V. Bardin, N. Yu. Adonin// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1400-1407 doi:10.1134/S1070428016100055), IF=0.759
  176. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Е.В. Стукань, И.Ю. Багрянская, В.М. Берестовицкая
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    Журнал органической химии, 2016, Т. 52, N 10, Cтр. 11391-1396 (1-Bromo-3,3,3-trifluoro-1-nitropropene: Synthesis and reaction with phenyl azide/ N. A. AnisimovaEmail authorE. K. SlobodchikovaA. A. KuzhaevaE. V. Stukan’I. Yu. BagryanskayaV. M. Berestovitskaya// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1379-1384 doi:10.1134/S1070428016100018), IF=0.759
  177. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Е.В. Стукань, И.Ю. Багрянская, В.М. Берестовицкая
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  178. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Е.В. Стукань, И.Ю. Багрянская, В.М. Берестовицкая
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  180. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Е.В. Стукань, И.Ю. Багрянская, В.М. Берестовицкая
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  181. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  182. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  183. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  184. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  185. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  186. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
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  187. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  188. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  189. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  190. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  191. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  192. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Complementary-addressed site-directed spin labeling of long natural RNAs
    Nucl. Acids Res. (19 September 2016), 44(16): 7935-7943. doi:10.1093/nar/gkw516, IF=9.201
  193. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Complementary-addressed site-directed spin labeling of long natural RNAs
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  194. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Complementary-addressed site-directed spin labeling of long natural RNAs
    Nucl. Acids Res. (19 September 2016), 44(16): 7935-7943. doi:10.1093/nar/gkw516, IF=9.201
  195. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
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  196. B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
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    Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
  197. B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
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    Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
  198. B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
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    Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
  199. Т.С. Фролова, Д.С. Баев, О.И. Синицына
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    Успехи современной науки и образования. 2016. Т. 4. № 9. С. 14-18.
  200. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  201. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
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    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  202. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  203. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  204. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  205. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  206. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  207. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  208. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  209. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  210. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  211. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  212. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  213. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  214. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  215. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  216. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  217. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  218. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  219. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  220. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  221. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  222. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  223. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  224. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  225. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  226. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  227. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  228. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  229. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  230. H. Chen, A.G. Maryasov, O. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M. Bowman
    Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
    Phys. Chem. Chem. Phys., 2016,18, 24954-24965 doi:10.1039/C6CP02649D, IF=4.448
  231. H. Chen, A.G. Maryasov, O. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M. Bowman
    Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
    Phys. Chem. Chem. Phys., 2016,18, 24954-24965 doi:10.1039/C6CP02649D, IF=4.448
  232. H. Chen, A.G. Maryasov, O. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M. Bowman
    Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
    Phys. Chem. Chem. Phys., 2016,18, 24954-24965 doi:10.1039/C6CP02649D, IF=4.448
  233. А.В. Бабина, В.А. Лавриненко, О.И. Яровая, Н.Ф. Салахутдинов
    Действие нового противовирусного агента камфецина на поведение мышей
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 9. С. 329-332. (Effect of New Antiviral Agent Camphecin on Behavior of Mice/ A. V. Babina, V. A. Lavrinenko, O. I. Yarovaya, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, January 2017, V. 162, N 3, pp 346-348 doi:10.1007/s10517-017-3612-6), IF=0.448
  234. А.В. Бабина, В.А. Лавриненко, О.И. Яровая, Н.Ф. Салахутдинов
    Действие нового противовирусного агента камфецина на поведение мышей
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 9. С. 329-332. (Effect of New Antiviral Agent Camphecin on Behavior of Mice/ A. V. Babina, V. A. Lavrinenko, O. I. Yarovaya, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, January 2017, V. 162, N 3, pp 346-348 doi:10.1007/s10517-017-3612-6), IF=0.448
  235. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    Ti-Salalen Mediated Asymmetric Epoxidation of Olefins with H2O2: Effect of Ligand on the Catalytic Performance, and Insight into the Oxidation Mechanism
    Journal of Molecular Catalysis A: Chemical, 2016, V. 421, 2016, Pages 131-137 doi:10.1016/j.molcata.2016.05.019, IF=3.957
  236. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    Ti-Salalen Mediated Asymmetric Epoxidation of Olefins with H2O2: Effect of Ligand on the Catalytic Performance, and Insight into the Oxidation Mechanism
    Journal of Molecular Catalysis A: Chemical, 2016, V. 421, 2016, Pages 131-137 doi:10.1016/j.molcata.2016.05.019, IF=3.957
  237. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  238. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  239. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  240. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  241. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  242. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  243. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  244. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  245. P. Maki-Arvela, M. Barsukova, I. Winberg, A. Smeds, J. Hemming, K. Eranen, A. Torozova, A. Aho, K. Volcho, D.Yu. Murzin
    Unprecedented Selective Heterogeneously Catalysed “Green” Oxidation of Betulin to Biologically Active Compounds using Synthetic Air and Supported Ru Catalysts
    CHEMISTRYSELECT, V. 1, N 13, August 16, 2016, Pp 3866-3869 doi:10.1002/slct.201600731
  246. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева, И.А. Григорьев, В.И. Родионов
    Экспериментальная оценка гемостатической активности нового антибиотик-содержащего средства местного действия на основе окисленной целлюлозы
    Современная медицина: актуальные вопросы. 2016. № 8 (50). С. 19-26.
  247. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева, И.А. Григорьев, В.И. Родионов
    Экспериментальная оценка гемостатической активности нового антибиотик-содержащего средства местного действия на основе окисленной целлюлозы
    Современная медицина: актуальные вопросы. 2016. № 8 (50). С. 19-26.
  248. F. Gaston, N. Dupuy, S. R.A. Marque, M. Barbaroux, S. Dorey
    One year monitoring by FTIR of γ-irradiated multilayer film PE/EVOH/PE
    Radiation Physics and Chemistry, V. 125, August 2016, Pp 115-121 doi:10.1016/j.radphyschem.2016.03.010, IF=1.207
  249. F. Gaston, N. Dupuy, S. R.A. Marque, M. Barbaroux, S. Dorey
    One year monitoring by FTIR of γ-irradiated multilayer film PE/EVOH/PE
    Radiation Physics and Chemistry, V. 125, August 2016, Pp 115-121 doi:10.1016/j.radphyschem.2016.03.010, IF=1.207
  250. F. Gaston, N. Dupuy, S. R.A. Marque, M. Barbaroux, S. Dorey
    One year monitoring by FTIR of γ-irradiated multilayer film PE/EVOH/PE
    Radiation Physics and Chemistry, V. 125, August 2016, Pp 115-121 doi:10.1016/j.radphyschem.2016.03.010, IF=1.207
  251. F. Gaston, N. Dupuy, S. R.A. Marque, M. Barbaroux, S. Dorey
    One year monitoring by FTIR of γ-irradiated multilayer film PE/EVOH/PE
    Radiation Physics and Chemistry, V. 125, August 2016, Pp 115-121 doi:10.1016/j.radphyschem.2016.03.010, IF=1.207
  252. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  253. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  254. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  255. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  256. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  257. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  258. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  259. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  260. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
  261. T.N. Drebushchak, V.A. Drebushchak, N.A. Pankrushina, E.V. Boldyreva
    Single-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamide
    CrystEngComm, 2016,18, 5736-5743 doi:10.1039/C6CE00764C, IF=3.848
  262. T.N. Drebushchak, V.A. Drebushchak, N.A. Pankrushina, E.V. Boldyreva
    Single-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamide
    CrystEngComm, 2016,18, 5736-5743 doi:10.1039/C6CE00764C, IF=3.848
  263. T.N. Drebushchak, V.A. Drebushchak, N.A. Pankrushina, E.V. Boldyreva
    Single-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamide
    CrystEngComm, 2016,18, 5736-5743 doi:10.1039/C6CE00764C, IF=3.848
  264. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  265. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  266. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  267. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  268. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  269. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
  270. Е.Л. Лушникова, Е.В. Колдышева, Т.Г. Толстикова, И.В. Сорокина, Е.И. Южик, М.М. Мжельская, М.Г. Клинникова
    Кардиотоксический и дислипидемический эффект доксорубицина и амида бетулоновой кислоты
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 8. С. 247-252. (Cardiotoxic and Dyslipidemic Effects of Doxorubicin and Betulinic Acid Amide/ M. G. Klinnikova, E. L. Lushnikova, E. V. Koldysheva, T. G. Tolstikova, I. V. Sorokina, E. I. Yuzhik, M. M. Mzhelskaya// Bulletin of Experimental Biology and Medicine,, 2016, V. 162, N 2, pp 277-282 doi:10.1007/s10517-016-3594-9), IF=0.448
  271. Е.Л. Лушникова, Е.В. Колдышева, Т.Г. Толстикова, И.В. Сорокина, Е.И. Южик, М.М. Мжельская, М.Г. Клинникова
    Кардиотоксический и дислипидемический эффект доксорубицина и амида бетулоновой кислоты
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 8. С. 247-252. (Cardiotoxic and Dyslipidemic Effects of Doxorubicin and Betulinic Acid Amide/ M. G. Klinnikova, E. L. Lushnikova, E. V. Koldysheva, T. G. Tolstikova, I. V. Sorokina, E. I. Yuzhik, M. M. Mzhelskaya// Bulletin of Experimental Biology and Medicine,, 2016, V. 162, N 2, pp 277-282 doi:10.1007/s10517-016-3594-9), IF=0.448
  272. Е.Л. Лушникова, Е.В. Колдышева, Т.Г. Толстикова, И.В. Сорокина, Е.И. Южик, М.М. Мжельская, М.Г. Клинникова
    Кардиотоксический и дислипидемический эффект доксорубицина и амида бетулоновой кислоты
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 8. С. 247-252. (Cardiotoxic and Dyslipidemic Effects of Doxorubicin and Betulinic Acid Amide/ M. G. Klinnikova, E. L. Lushnikova, E. V. Koldysheva, T. G. Tolstikova, I. V. Sorokina, E. I. Yuzhik, M. M. Mzhelskaya// Bulletin of Experimental Biology and Medicine,, 2016, V. 162, N 2, pp 277-282 doi:10.1007/s10517-016-3594-9), IF=0.448
  273. Е.Л. Лушникова, Е.В. Колдышева, Т.Г. Толстикова, И.В. Сорокина, Е.И. Южик, М.М. Мжельская, М.Г. Клинникова
    Кардиотоксический и дислипидемический эффект доксорубицина и амида бетулоновой кислоты
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 8. С. 247-252. (Cardiotoxic and Dyslipidemic Effects of Doxorubicin and Betulinic Acid Amide/ M. G. Klinnikova, E. L. Lushnikova, E. V. Koldysheva, T. G. Tolstikova, I. V. Sorokina, E. I. Yuzhik, M. M. Mzhelskaya// Bulletin of Experimental Biology and Medicine,, 2016, V. 162, N 2, pp 277-282 doi:10.1007/s10517-016-3594-9), IF=0.448
  274. Е.Л. Лушникова, Е.В. Колдышева, Т.Г. Толстикова, И.В. Сорокина, Е.И. Южик, М.М. Мжельская, М.Г. Клинникова
    Кардиотоксический и дислипидемический эффект доксорубицина и амида бетулоновой кислоты
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 162. № 8. С. 247-252. (Cardiotoxic and Dyslipidemic Effects of Doxorubicin and Betulinic Acid Amide/ M. G. Klinnikova, E. L. Lushnikova, E. V. Koldysheva, T. G. Tolstikova, I. V. Sorokina, E. I. Yuzhik, M. M. Mzhelskaya// Bulletin of Experimental Biology and Medicine,, 2016, V. 162, N 2, pp 277-282 doi:10.1007/s10517-016-3594-9), IF=0.448
  275. T.G. Tolstikova, M.V. Khvostov, N.A. Zhukova, N.V. Shikina, Ismagilov
    Synthesis and safety evaluation of gold nanoparticles in the in vivo experiment
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 555-560. doi:10.15372/KhUR20160416
  276. T.G. Tolstikova, M.V. Khvostov, N.A. Zhukova, N.V. Shikina, Ismagilov
    Synthesis and safety evaluation of gold nanoparticles in the in vivo experiment
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 555-560. doi:10.15372/KhUR20160416
  277. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Polyaromatic hydrocarbons in the vicinity of the major highways of Novosibirsk
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 491-497 doi:10.15372/KhUR20160409
  278. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Polyaromatic hydrocarbons in the vicinity of the major highways of Novosibirsk
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 491-497 doi:10.15372/KhUR20160409
  279. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Polyaromatic hydrocarbons in the vicinity of the major highways of Novosibirsk
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 491-497 doi:10.15372/KhUR20160409
  280. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Organic carbon in the city territories of the south of West Siberia
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 483-489 doi:10.15372/KhUR20160408
  281. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Organic carbon in the city territories of the south of West Siberia
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 483-489 doi:10.15372/KhUR20160408
  282. V.F. Raputa, V.V. Kokovkin, S.V. Morozov, T.V. Yaroslavtseva
    Organic carbon in the city territories of the south of West Siberia
    Химия в интересах устойчивого развития. 2016. Т. 24. № 4. С. 483-489 doi:10.15372/KhUR20160408
  283. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Selective one-pot carvone oxime hydrogenation over titania supported gold catalyst as a novel approach for dihydrocarvone synthesis
    Journal of Molecular Catalysis A: Chemical, V. 420, August 2016, Pp 142-148 doi:10.1016/j.molcata.2016.04.013, IF=3.957
  284. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Selective one-pot carvone oxime hydrogenation over titania supported gold catalyst as a novel approach for dihydrocarvone synthesis
    Journal of Molecular Catalysis A: Chemical, V. 420, August 2016, Pp 142-148 doi:10.1016/j.molcata.2016.04.013, IF=3.957
  285. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Selective one-pot carvone oxime hydrogenation over titania supported gold catalyst as a novel approach for dihydrocarvone synthesis
    Journal of Molecular Catalysis A: Chemical, V. 420, August 2016, Pp 142-148 doi:10.1016/j.molcata.2016.04.013, IF=3.957
  286. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, K.P. Volcho, N.F. Salakhutdinov, I.L. Simakova, D.Yu. Murzin
    Selective one-pot carvone oxime hydrogenation over titania supported gold catalyst as a novel approach for dihydrocarvone synthesis
    Journal of Molecular Catalysis A: Chemical, V. 420, August 2016, Pp 142-148 doi:10.1016/j.molcata.2016.04.013, IF=3.957
  287. R.Yu. Peshkov, E.V. Panteleeva, W. Chunyan, E.V. Tretyakov, V.D. Shteingarts
    One-pot synthesis of 4'-alkyl-4-cyanobiaryls on the basis of the terephthalonitrile dianion and neutral aromatic nitrile cross-coupling
    Beilstein Journal of Organic Chemistry, 2016, V.12, Pp 1577-1584 doi:10.3762/bjoc.12.153, IF=2.697
  288. A.G. Potapov, I.K. Shundrina
    The influence of different fillers on mechanical and physical properties of high-molecular-weight biodegradable aliphatic polyesters
    Polymer Science Series A, July 2016, V. 58, N 4, pp 585-592 doi:10.1134/S0965545X1604012X, IF=0.759
  289. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  290. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  291. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  292. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  293. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  294. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  295. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  296. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  297. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  298. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  299. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  300. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  301. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  302. F. Gaston, N. Dupuy, S. R. A. Marquе, M. Barbaroux, S. Dorey
    FTIR study of ageing of γ-irradiated biopharmaceutical EVA based film
    Polymer Degradation and Stability, V. 129, July 2016, Pp 19-25 doi:10.1016/j.polymdegradstab.2016.03.040, IF=3.119
  303. F. Gaston, N. Dupuy, S. R. A. Marquе, M. Barbaroux, S. Dorey
    FTIR study of ageing of γ-irradiated biopharmaceutical EVA based film
    Polymer Degradation and Stability, V. 129, July 2016, Pp 19-25 doi:10.1016/j.polymdegradstab.2016.03.040, IF=3.119
  304. F. Gaston, N. Dupuy, S. R. A. Marquе, M. Barbaroux, S. Dorey
    FTIR study of ageing of γ-irradiated biopharmaceutical EVA based film
    Polymer Degradation and Stability, V. 129, July 2016, Pp 19-25 doi:10.1016/j.polymdegradstab.2016.03.040, IF=3.119
  305. F. Gaston, N. Dupuy, S. R. A. Marquе, M. Barbaroux, S. Dorey
    FTIR study of ageing of γ-irradiated biopharmaceutical EVA based film
    Polymer Degradation and Stability, V. 129, July 2016, Pp 19-25 doi:10.1016/j.polymdegradstab.2016.03.040, IF=3.119
  306. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  307. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  308. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  309. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  310. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  311. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  312. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  313. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  314. N.A. Vorotnikova, O.A. Efremova, A.R. Tsygankova, K.A. Brylev, M.V. Edeleva, O.G. Kurskaya, A.J. Sutherland, A.M. Shestopalov, Yu.V. Mironov, M.A. Shestopalov
    Characterization and cytotoxicity studies of thiol-modified polystyrene microbeads doped with [(mo6x8)(no3)6]2-) (x=cl, br, i)
    Polymers for Advanced Technologies, 2016, V. 27, N 7, Pp 922-928 doi:10.1002/pat.3749, IF=1.822
  315. E.M. Osnitsky, M.P. Sartakov, E.A. Zarov, Yu.M. Deryabina
    Elemental Composition of the Humic Acids in the High-Moor Peats of the Western Siberia Taiga Zone.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 6. Pp. 3104-3113
  316. E.M. Osnitsky, M.P. Sartakov, E.A. Zarov, Yu.M. Deryabina
    Elemental Composition of the Humic Acids in the High-Moor Peats of the Western Siberia Taiga Zone.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 6. Pp. 3104-3113
  317. E.M. Osnitsky, M.P. Sartakov, E.A. Zarov, Yu.M. Deryabina
    Elemental Composition of the Humic Acids in the High-Moor Peats of the Western Siberia Taiga Zone.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 6. Pp. 3104-3113
  318. A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
    Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
    J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
  319. A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
    Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
    J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
  320. A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
    Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
    J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
  321. A.A. Gorodetsky, I.A. Kirilyuk, V.V. Khramtsov, D.A. Komarov
    Functional electron paramagnetic resonance imaging of ischemic rat heart: Monitoring of tissue oxygenation and pH
    Magnetic Resonance in Medicine, 2016,V. 76, N 1, Pp 350-358 doi:10.1002/mrm.25867, IF=3.782
  322. М.П. Сартаков, И.Д. Комиссаров, Ю.М. Дерябина
    Исследование электронных спектров поглощения гуминовых кислот торфов среднетаежной зоны Западной Сибири
    Вестник Красноярского государственного аграрного университета. 2016. № 7 (118). С. 48-55. (The research of electronic spectrum absorbtion of peats’ humic acids of Western Siberia middle Taiga Zone/ M.P. Sartakov, I.D. Komissarov, Yu.M. Deryabina// Вестник Красноярского государственного аграрного университета. 2016. № 7 (118). С. 48-55.)
  323. М.П. Сартаков, И.Д. Комиссаров, Ю.М. Дерябина
    Исследование электронных спектров поглощения гуминовых кислот торфов среднетаежной зоны Западной Сибири
    Вестник Красноярского государственного аграрного университета. 2016. № 7 (118). С. 48-55. (The research of electronic spectrum absorbtion of peats’ humic acids of Western Siberia middle Taiga Zone/ M.P. Sartakov, I.D. Komissarov, Yu.M. Deryabina// Вестник Красноярского государственного аграрного университета. 2016. № 7 (118). С. 48-55.)
  324. В.П. Чубаков, П.А. Чубаков, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Люминесцентное детектирование паров первичных алифатических аминов в низких концентрациях хромофорами пирилоцианинового ряда
    Российские нанотехнологии. 2016. Т. 11. № 7-8. С. 30-34 (Luminescence detection of vapors of primary aliphatic amines at low concentrations using pyrylocyanine chromophores/ V.P. Chubakov, P.A. Chubakov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov// Nanotechnologies in Russia, July 2016, V. 11, N 7, pp 407-413 doi:10.1134/S1995078016040054)
  325. В.П. Чубаков, П.А. Чубаков, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Люминесцентное детектирование паров первичных алифатических аминов в низких концентрациях хромофорами пирилоцианинового ряда
    Российские нанотехнологии. 2016. Т. 11. № 7-8. С. 30-34 (Luminescence detection of vapors of primary aliphatic amines at low concentrations using pyrylocyanine chromophores/ V.P. Chubakov, P.A. Chubakov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov// Nanotechnologies in Russia, July 2016, V. 11, N 7, pp 407-413 doi:10.1134/S1995078016040054)
  326. В.П. Чубаков, П.А. Чубаков, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Люминесцентное детектирование паров первичных алифатических аминов в низких концентрациях хромофорами пирилоцианинового ряда
    Российские нанотехнологии. 2016. Т. 11. № 7-8. С. 30-34 (Luminescence detection of vapors of primary aliphatic amines at low concentrations using pyrylocyanine chromophores/ V.P. Chubakov, P.A. Chubakov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov// Nanotechnologies in Russia, July 2016, V. 11, N 7, pp 407-413 doi:10.1134/S1995078016040054)
  327. А.Я. Болсуновский, О.И. Синицына, Т.С. Фролова, Е.А. Васюнина, Д.В. Дементьев
    Оценка генотоксичности малых доз гамма-излучения с помощью SOS-хромотеста и теста Эймса
    Доклады Академии Наук, 2015, т. 269, N 6, Стр. 742-745 (Genotoxicity assessment of low-level doses of gamma radiation with the SOS chromotest and the Ames test/ A. Ya. Bolsunovsky, O. I. Sinitsyna, T. S. Frolova, E. A. Vasyunina, D. V. Dementyev// Doklady Biochemistry and Biophysics, July 2016, V. 469, N 1, pp 309-312 doi:10.1134/S1607672916040190), IF=0.393
  328. А.Я. Болсуновский, О.И. Синицына, Т.С. Фролова, Е.А. Васюнина, Д.В. Дементьев
    Оценка генотоксичности малых доз гамма-излучения с помощью SOS-хромотеста и теста Эймса
    Доклады Академии Наук, 2015, т. 269, N 6, Стр. 742-745 (Genotoxicity assessment of low-level doses of gamma radiation with the SOS chromotest and the Ames test/ A. Ya. Bolsunovsky, O. I. Sinitsyna, T. S. Frolova, E. A. Vasyunina, D. V. Dementyev// Doklady Biochemistry and Biophysics, July 2016, V. 469, N 1, pp 309-312 doi:10.1134/S1607672916040190), IF=0.393
  329. А.Я. Болсуновский, О.И. Синицына, Т.С. Фролова, Е.А. Васюнина, Д.В. Дементьев
    Оценка генотоксичности малых доз гамма-излучения с помощью SOS-хромотеста и теста Эймса
    Доклады Академии Наук, 2015, т. 269, N 6, Стр. 742-745 (Genotoxicity assessment of low-level doses of gamma radiation with the SOS chromotest and the Ames test/ A. Ya. Bolsunovsky, O. I. Sinitsyna, T. S. Frolova, E. A. Vasyunina, D. V. Dementyev// Doklady Biochemistry and Biophysics, July 2016, V. 469, N 1, pp 309-312 doi:10.1134/S1607672916040190), IF=0.393
  330. А.Я. Болсуновский, О.И. Синицына, Т.С. Фролова, Е.А. Васюнина, Д.В. Дементьев
    Оценка генотоксичности малых доз гамма-излучения с помощью SOS-хромотеста и теста Эймса
    Доклады Академии Наук, 2015, т. 269, N 6, Стр. 742-745 (Genotoxicity assessment of low-level doses of gamma radiation with the SOS chromotest and the Ames test/ A. Ya. Bolsunovsky, O. I. Sinitsyna, T. S. Frolova, E. A. Vasyunina, D. V. Dementyev// Doklady Biochemistry and Biophysics, July 2016, V. 469, N 1, pp 309-312 doi:10.1134/S1607672916040190), IF=0.393
  331. Л.С. Клименко, Н.С. Сиражетдинова, В.А. Савельев, Т.П. Мартьянов, Д.В. Корчагин
    Фотохимическая циклоконденсация 2-азидо-1-арилтиоантрахинонов с фенолами
    Известия Академии наук. Серия химическая. 2016. № 7. С. 1814-1819. (Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols/ L. S. Klimenko, S. Sirazhetdinova, V. A. Savel'ev, T. P. Martyanov, D. V. Korchagin// Russian Chemical Bulletin, 2016, V. 65, N 7, pp 1814-1819 doi:10.1007/s11172-016-1515-8), IF=0.578
  332. Л.С. Клименко, Н.С. Сиражетдинова, В.А. Савельев, Т.П. Мартьянов, Д.В. Корчагин
    Фотохимическая циклоконденсация 2-азидо-1-арилтиоантрахинонов с фенолами
    Известия Академии наук. Серия химическая. 2016. № 7. С. 1814-1819. (Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols/ L. S. Klimenko, S. Sirazhetdinova, V. A. Savel'ev, T. P. Martyanov, D. V. Korchagin// Russian Chemical Bulletin, 2016, V. 65, N 7, pp 1814-1819 doi:10.1007/s11172-016-1515-8), IF=0.578
  333. Л.С. Клименко, Н.С. Сиражетдинова, В.А. Савельев, Т.П. Мартьянов, Д.В. Корчагин
    Фотохимическая циклоконденсация 2-азидо-1-арилтиоантрахинонов с фенолами
    Известия Академии наук. Серия химическая. 2016. № 7. С. 1814-1819. (Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols/ L. S. Klimenko, S. Sirazhetdinova, V. A. Savel'ev, T. P. Martyanov, D. V. Korchagin// Russian Chemical Bulletin, 2016, V. 65, N 7, pp 1814-1819 doi:10.1007/s11172-016-1515-8), IF=0.578
  334. Л.С. Клименко, Н.С. Сиражетдинова, В.А. Савельев, Т.П. Мартьянов, Д.В. Корчагин
    Фотохимическая циклоконденсация 2-азидо-1-арилтиоантрахинонов с фенолами
    Известия Академии наук. Серия химическая. 2016. № 7. С. 1814-1819. (Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols/ L. S. Klimenko, S. Sirazhetdinova, V. A. Savel'ev, T. P. Martyanov, D. V. Korchagin// Russian Chemical Bulletin, 2016, V. 65, N 7, pp 1814-1819 doi:10.1007/s11172-016-1515-8), IF=0.578
  335. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  336. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  337. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  338. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  339. D.S. Baranov, Y.V. Gatilov
    Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines
    Mendeleev Communications, 2016, V. 26, N 4, Pp 282-284 doi:10.1016/j.mencom.2016.07.004, IF=1.404
  340. A.A. Lomzov, E.A. Sviridov, A.V. Shernuykov, G.Yu. Shevelev, D.V. Pyshnyi, E.G. Bagryanskaya
    A Study of a DNA Duplex by Nuclear Magnetic Resonance (NMR) and Molecular Dynamics Simulations. Validation of Pulsed Dipolar Electron Paramagnetic Resonance Distance Measurements using Triarylmethyl-Based Spin Labels
    J. Phys. Chem. B, 2016, 120 (23), pp 5125-5133 doi:10.1021/acs.jpcb.6b03193, IF=3.187
  341. A.A. Lomzov, E.A. Sviridov, A.V. Shernuykov, G.Yu. Shevelev, D.V. Pyshnyi, E.G. Bagryanskaya
    A Study of a DNA Duplex by Nuclear Magnetic Resonance (NMR) and Molecular Dynamics Simulations. Validation of Pulsed Dipolar Electron Paramagnetic Resonance Distance Measurements using Triarylmethyl-Based Spin Labels
    J. Phys. Chem. B, 2016, 120 (23), pp 5125-5133 doi:10.1021/acs.jpcb.6b03193, IF=3.187
  342. A.A. Lomzov, E.A. Sviridov, A.V. Shernuykov, G.Yu. Shevelev, D.V. Pyshnyi, E.G. Bagryanskaya
    A Study of a DNA Duplex by Nuclear Magnetic Resonance (NMR) and Molecular Dynamics Simulations. Validation of Pulsed Dipolar Electron Paramagnetic Resonance Distance Measurements using Triarylmethyl-Based Spin Labels
    J. Phys. Chem. B, 2016, 120 (23), pp 5125-5133 doi:10.1021/acs.jpcb.6b03193, IF=3.187
  343. A.A. Kuzhelev, G. Yu. Shevelev, O.A. Krumkacheva, V.M. Tormyshev, D.V. Pyshnyi, M.V. Fedin, E.G. Bagryanskaya
    Saccharides as Prospective Immobilizers of Nucleic Acids for Room-Temperature Structural EPR Studies
    J. Phys. Chem. Lett., 2016, V. 7, N 12, pp 2544-2548 doi:10.1021/acs.jpclett.6b01024, IF=8.538
  344. A.A. Kuzhelev, G. Yu. Shevelev, O.A. Krumkacheva, V.M. Tormyshev, D.V. Pyshnyi, M.V. Fedin, E.G. Bagryanskaya
    Saccharides as Prospective Immobilizers of Nucleic Acids for Room-Temperature Structural EPR Studies
    J. Phys. Chem. Lett., 2016, V. 7, N 12, pp 2544-2548 doi:10.1021/acs.jpclett.6b01024, IF=8.538
  345. A.A. Kuzhelev, G. Yu. Shevelev, O.A. Krumkacheva, V.M. Tormyshev, D.V. Pyshnyi, M.V. Fedin, E.G. Bagryanskaya
    Saccharides as Prospective Immobilizers of Nucleic Acids for Room-Temperature Structural EPR Studies
    J. Phys. Chem. Lett., 2016, V. 7, N 12, pp 2544-2548 doi:10.1021/acs.jpclett.6b01024, IF=8.538
  346. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
    First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
    Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
  347. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
    First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
    Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
  348. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
    First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
    Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
  349. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  350. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  351. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  352. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  353. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  354. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  355. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  356. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  357. L.N. Rachkovskaya, T.V. Popova, A. Yu. Letyagin, T.G. Tolstikova, M.A. Korolyov, N. Bogdanchikova, A.N. Pestryakov, A.A. Kotlyarova, V. Burmistrov, V.I. Konenkov
    Silver containing sorbents: Physicochemical and biological properties
    Resource-Efficient Technologies, 2016, V. 2, N 2, Pages 43-49 doi:10.1016/j.reffit.2016.06.001
  358. M.P. Sartakov, Y.M. Deryabina, N. Komissarov
    Elemental analysis of humic acids in peat resources of Khantymansiysk Autonomous region - Ygra
    International Journal of Pharmacy and Technology, 2016, V. 8, N 2, Pp 14244-14255
  359. M.P. Sartakov, Y.M. Deryabina, N. Komissarov
    Elemental analysis of humic acids in peat resources of Khantymansiysk Autonomous region - Ygra
    International Journal of Pharmacy and Technology, 2016, V. 8, N 2, Pp 14244-14255
  360. E. Karpova, V. Vasiliev, V. Mamatyuk, N. Polosmak, L. Kundo
    Xiongnu burial complex: A study of ancient textiles from the 22nd Noin-Ula barrow (Mongolia, first century AD)
    Journal of Archaeological Science, V. 70, June 2016, Pp 15-22 doi:10.1016/j.jas.2016.04.001, IF=2.255
  361. E. Karpova, V. Vasiliev, V. Mamatyuk, N. Polosmak, L. Kundo
    Xiongnu burial complex: A study of ancient textiles from the 22nd Noin-Ula barrow (Mongolia, first century AD)
    Journal of Archaeological Science, V. 70, June 2016, Pp 15-22 doi:10.1016/j.jas.2016.04.001, IF=2.255
  362. M.V. Khvostov, T.G. Tolstikova, S.A. Borisov, N.A. Zhukova, A.V. Dushkin, Yu.S. Chistyachenko, N.E. Polyakov
    Improving the Efficiency and Safety of Aspirin by Complexation with the Natural Polysaccharide Arabinogalactan
    Current Drug Delivery, 2016, V. 13, N 4, Pp 582-589 doi:10.2174/1567201812666150605104944, IF=1.445
  363. M.V. Khvostov, T.G. Tolstikova, S.A. Borisov, N.A. Zhukova, A.V. Dushkin, Yu.S. Chistyachenko, N.E. Polyakov
    Improving the Efficiency and Safety of Aspirin by Complexation with the Natural Polysaccharide Arabinogalactan
    Current Drug Delivery, 2016, V. 13, N 4, Pp 582-589 doi:10.2174/1567201812666150605104944, IF=1.445
  364. M.V. Khvostov, T.G. Tolstikova, S.A. Borisov, N.A. Zhukova, A.V. Dushkin, Yu.S. Chistyachenko, N.E. Polyakov
    Improving the Efficiency and Safety of Aspirin by Complexation with the Natural Polysaccharide Arabinogalactan
    Current Drug Delivery, 2016, V. 13, N 4, Pp 582-589 doi:10.2174/1567201812666150605104944, IF=1.445
  365. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
    Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  366. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
    Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  367. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
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    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  368. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
    Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  369. E.V. Sharova, G.K. Genkina, N.M. Vinogradova, O.I. Artyushin, O.I. Yarovaya, V.K. Brel
    Phosphorylation of natural productsCytisine, anabasine, and camphor using click chemistry methodology
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2016, V. 191, N 11-12, Pp 1556-1557 (21st International Conference on Phosphorus Chemistry (ICPC-2016),Kazan, RUSSIA, JUN 05-10, 2016 doi:10.1080/10426507.2016.1213257, IF=0.722
  370. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
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    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  371. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  372. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  373. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  374. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  375. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  376. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  377. T.S. Sukhikh, D. A. Bashirov, D. Ogienko, N. Kuratieva, P. S. Sherin, M.I. Rakhmanova, E. A. Chulanova, N. P. Gritsan, S.N.Konchenko, A. V. Zibarev
    Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds
    RSC Adv., 2016, 6(50), 43901-43910 doi:10.1039/C6RA06547C, IF=3.289
  378. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  379. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  380. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  381. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  382. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  383. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  384. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  385. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  386. Yu.A. Vorotnikov, O.A. Efremova, N.A. Vorotnikova, K.A. Brylev, M.V. Edeleva, A.R. Tsygankova, A.I. Smolentsev, N. Kitamura, Yu.V. Mironov, M.A. Shestopalov
    On the synthesis and characterisation of luminescent hybrid particles: Mo6 metal cluster complex/SiO2
    RSC Adv., 2016,6(49), 43367-43375 doi:10.1039/C6RA04321F, IF=3.289
  387. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников, О.Б. Витрик, А.Ю. Жижченко
    Исследование оптических и термооптических характеристик гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия, 2016, N 2, стр. 88-96 (10.15372/AUT20160211) (Study of optical and thermo-optical properties of a hybrid photopolymer material based on thiol-siloxane and tetraacrylate oligomer/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov, O. B. Vitrick, A. Yu. Zhizhchenko// Optoelectronics, Instrumentation and Data Processing, March 2016, V. 52, N 2, pp 180-186 doi:10.3103/S8756699016020114)
  388. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников, О.Б. Витрик, А.Ю. Жижченко
    Исследование оптических и термооптических характеристик гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия, 2016, N 2, стр. 88-96 (10.15372/AUT20160211) (Study of optical and thermo-optical properties of a hybrid photopolymer material based on thiol-siloxane and tetraacrylate oligomer/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov, O. B. Vitrick, A. Yu. Zhizhchenko// Optoelectronics, Instrumentation and Data Processing, March 2016, V. 52, N 2, pp 180-186 doi:10.3103/S8756699016020114)
  389. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников, О.Б. Витрик, А.Ю. Жижченко
    Исследование оптических и термооптических характеристик гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия, 2016, N 2, стр. 88-96 (10.15372/AUT20160211) (Study of optical and thermo-optical properties of a hybrid photopolymer material based on thiol-siloxane and tetraacrylate oligomer/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov, O. B. Vitrick, A. Yu. Zhizhchenko// Optoelectronics, Instrumentation and Data Processing, March 2016, V. 52, N 2, pp 180-186 doi:10.3103/S8756699016020114)
  390. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников, О.Б. Витрик, А.Ю. Жижченко
    Исследование оптических и термооптических характеристик гибридного фотополимерного материала на основе тиол-силоксановых и акрилатных олигомеров
    Автометрия, 2016, N 2, стр. 88-96 (10.15372/AUT20160211) (Study of optical and thermo-optical properties of a hybrid photopolymer material based on thiol-siloxane and tetraacrylate oligomer/ N. G. Mironnikov, V. P. Korolkov, D. I. Derevyanko, V. V. Shelkovnikov, O. B. Vitrick, A. Yu. Zhizhchenko// Optoelectronics, Instrumentation and Data Processing, March 2016, V. 52, N 2, pp 180-186 doi:10.3103/S8756699016020114)
  391. С.О. Вечкапова, Т.А. Запара, Е.А. Морозова, А.Л. Проскура, Э.Э. Шульц, Т.Г. Толстикова, А.С. Ратушняк
    Амид ламбертиановой кислоты подавляет гиперактивацию ионотропных глутаматных рецепторов, но не синаптическую потенциацию в срезах гиппокампа
    Бюллетень экспериментальной биологии и медицины. 2016. № 6. С. 736-739. (Amide of Lambertian Acid Suppresses Hyperactivation of Inotropic Glutamate Receptors, but not Synaptic Potentiation in Hippocampal Sections/ S. O. Vechkapova, T. A. Zapara, E. A. Morozova, A. L. Proskura, E. E. Schul'ts, T. G. Tolstikova, A. S. Ratushnyak// Bulletin of Experimental Biology and Medicine doi:10.1007/s10517-016-3509-9), IF=0.448
  392. С.О. Вечкапова, Т.А. Запара, Е.А. Морозова, А.Л. Проскура, Э.Э. Шульц, Т.Г. Толстикова, А.С. Ратушняк
    Амид ламбертиановой кислоты подавляет гиперактивацию ионотропных глутаматных рецепторов, но не синаптическую потенциацию в срезах гиппокампа
    Бюллетень экспериментальной биологии и медицины. 2016. № 6. С. 736-739. (Amide of Lambertian Acid Suppresses Hyperactivation of Inotropic Glutamate Receptors, but not Synaptic Potentiation in Hippocampal Sections/ S. O. Vechkapova, T. A. Zapara, E. A. Morozova, A. L. Proskura, E. E. Schul'ts, T. G. Tolstikova, A. S. Ratushnyak// Bulletin of Experimental Biology and Medicine doi:10.1007/s10517-016-3509-9), IF=0.448
  393. С.О. Вечкапова, Т.А. Запара, Е.А. Морозова, А.Л. Проскура, Э.Э. Шульц, Т.Г. Толстикова, А.С. Ратушняк
    Амид ламбертиановой кислоты подавляет гиперактивацию ионотропных глутаматных рецепторов, но не синаптическую потенциацию в срезах гиппокампа
    Бюллетень экспериментальной биологии и медицины. 2016. № 6. С. 736-739. (Amide of Lambertian Acid Suppresses Hyperactivation of Inotropic Glutamate Receptors, but not Synaptic Potentiation in Hippocampal Sections/ S. O. Vechkapova, T. A. Zapara, E. A. Morozova, A. L. Proskura, E. E. Schul'ts, T. G. Tolstikova, A. S. Ratushnyak// Bulletin of Experimental Biology and Medicine doi:10.1007/s10517-016-3509-9), IF=0.448
  394. С.О. Вечкапова, Т.А. Запара, Е.А. Морозова, А.Л. Проскура, Э.Э. Шульц, Т.Г. Толстикова, А.С. Ратушняк
    Амид ламбертиановой кислоты подавляет гиперактивацию ионотропных глутаматных рецепторов, но не синаптическую потенциацию в срезах гиппокампа
    Бюллетень экспериментальной биологии и медицины. 2016. № 6. С. 736-739. (Amide of Lambertian Acid Suppresses Hyperactivation of Inotropic Glutamate Receptors, but not Synaptic Potentiation in Hippocampal Sections/ S. O. Vechkapova, T. A. Zapara, E. A. Morozova, A. L. Proskura, E. E. Schul'ts, T. G. Tolstikova, A. S. Ratushnyak// Bulletin of Experimental Biology and Medicine doi:10.1007/s10517-016-3509-9), IF=0.448
  395. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  396. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  397. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  398. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  399. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  400. Н.И. Иванова, П.А. Волков, К.О. Храпова, Л.И. Ларина, И.Ю. Багрянская, Н.К. Гусарова, Б.А. Трофимов
    Реакция (диарилфосфорил)(арил)метанолов с алкилпропиолатами. регио- и стереоселективный синтез функциональных виниловых эфиров
    Журнал органической химии. 2016. Т. 52. № 6. С. 788-792. (Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026), IF=0.759
  401. M.B. Bushuev, D.P. Pishchur, E.B. Nikolaenkova, V.P. Krivopalov
    Compensation effects and relation between the activation energy of spin transition and the hysteresis loop width for an iron(II) complex
    Phys. Chem. Chem. Phys., 2016,18(25), 16690-16699 doi:10.1039/C6CP01892K, IF=4.448
  402. M.B. Bushuev, D.P. Pishchur, E.B. Nikolaenkova, V.P. Krivopalov
    Compensation effects and relation between the activation energy of spin transition and the hysteresis loop width for an iron(II) complex
    Phys. Chem. Chem. Phys., 2016,18(25), 16690-16699 doi:10.1039/C6CP01892K, IF=4.448
  403. E.V. Tretyakov, R.Yu. Peshkov, E.V. Panteleeva, A.S. Scrypnik, D.V. Stass, G.V. Romanenko, V.I. Ovcharenko
    Addition of Cyanomethyl Anion to the Cyano Group of 2-Cyano-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl, a Nitronyl Nitroxide
    Tetrahedron Letters, V. 57, N 21, 25 May 2016, Pp 2327-2330 doi:10.1016/j.tetlet.2016.04.070, IF=2.346
  404. E.V. Tretyakov, R.Yu. Peshkov, E.V. Panteleeva, A.S. Scrypnik, D.V. Stass, G.V. Romanenko, V.I. Ovcharenko
    Addition of Cyanomethyl Anion to the Cyano Group of 2-Cyano-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl, a Nitronyl Nitroxide
    Tetrahedron Letters, V. 57, N 21, 25 May 2016, Pp 2327-2330 doi:10.1016/j.tetlet.2016.04.070, IF=2.346
  405. E.V. Tretyakov, R.Yu. Peshkov, E.V. Panteleeva, A.S. Scrypnik, D.V. Stass, G.V. Romanenko, V.I. Ovcharenko
    Addition of Cyanomethyl Anion to the Cyano Group of 2-Cyano-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl, a Nitronyl Nitroxide
    Tetrahedron Letters, V. 57, N 21, 25 May 2016, Pp 2327-2330 doi:10.1016/j.tetlet.2016.04.070, IF=2.346
  406. E.V. Tretyakov, R.Yu. Peshkov, E.V. Panteleeva, A.S. Scrypnik, D.V. Stass, G.V. Romanenko, V.I. Ovcharenko
    Addition of Cyanomethyl Anion to the Cyano Group of 2-Cyano-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl, a Nitronyl Nitroxide
    Tetrahedron Letters, V. 57, N 21, 25 May 2016, Pp 2327-2330 doi:10.1016/j.tetlet.2016.04.070, IF=2.346
  407. Yu.F. Polienko, O.A. Snytnikova, V.V. Yanshole, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev, Yu.P. Tsentalovich
    Effect of the spacer length and nitroxide sterical shielding upon photostability of spin-labeled kynurenines
    Journal of Photochemistry and Photobiology A: Chemistry, V.322-323, 15 May-1 June 2016, Pp 76-84 doi:10.1016/j.jphotochem.2016.03.007, IF=2.476
  408. Yu.F. Polienko, O.A. Snytnikova, V.V. Yanshole, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev, Yu.P. Tsentalovich
    Effect of the spacer length and nitroxide sterical shielding upon photostability of spin-labeled kynurenines
    Journal of Photochemistry and Photobiology A: Chemistry, V.322-323, 15 May-1 June 2016, Pp 76-84 doi:10.1016/j.jphotochem.2016.03.007, IF=2.476
  409. Yu.F. Polienko, O.A. Snytnikova, V.V. Yanshole, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev, Yu.P. Tsentalovich
    Effect of the spacer length and nitroxide sterical shielding upon photostability of spin-labeled kynurenines
    Journal of Photochemistry and Photobiology A: Chemistry, V.322-323, 15 May-1 June 2016, Pp 76-84 doi:10.1016/j.jphotochem.2016.03.007, IF=2.476
  410. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  411. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  412. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  413. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  414. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  415. L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
    Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
  416. L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
    Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
  417. L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
    Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
  418. A.S. Poryvaev, A.M. Sheveleva, D.I. Kolokolov, A.G. Stepanov, E.G. Bagryanskaya, M.V. Fedin
    Mobility and Reactivity of 4-Substituted TEMPO Derivatives in Metal-Organic Framework MIL-53(Al)
    J. Phys. Chem. C, 2016, 120 (19), pp 10698-10704 doi:10.1021/acs.jpcc.6b02966, IF=4.508
  419. A.S. Poryvaev, A.M. Sheveleva, D.I. Kolokolov, A.G. Stepanov, E.G. Bagryanskaya, M.V. Fedin
    Mobility and Reactivity of 4-Substituted TEMPO Derivatives in Metal-Organic Framework MIL-53(Al)
    J. Phys. Chem. C, 2016, 120 (19), pp 10698-10704 doi:10.1021/acs.jpcc.6b02966, IF=4.508
  420. A.S. Poryvaev, A.M. Sheveleva, D.I. Kolokolov, A.G. Stepanov, E.G. Bagryanskaya, M.V. Fedin
    Mobility and Reactivity of 4-Substituted TEMPO Derivatives in Metal-Organic Framework MIL-53(Al)
    J. Phys. Chem. C, 2016, 120 (19), pp 10698-10704 doi:10.1021/acs.jpcc.6b02966, IF=4.508
  421. A.S. Poryvaev, A.M. Sheveleva, D.I. Kolokolov, A.G. Stepanov, E.G. Bagryanskaya, M.V. Fedin
    Mobility and Reactivity of 4-Substituted TEMPO Derivatives in Metal-Organic Framework MIL-53(Al)
    J. Phys. Chem. C, 2016, 120 (19), pp 10698-10704 doi:10.1021/acs.jpcc.6b02966, IF=4.508
  422. A.S. Poryvaev, A.M. Sheveleva, D.I. Kolokolov, A.G. Stepanov, E.G. Bagryanskaya, M.V. Fedin
    Mobility and Reactivity of 4-Substituted TEMPO Derivatives in Metal-Organic Framework MIL-53(Al)
    J. Phys. Chem. C, 2016, 120 (19), pp 10698-10704 doi:10.1021/acs.jpcc.6b02966, IF=4.508
  423. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  424. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  425. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  426. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  427. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  428. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  429. А.Ф. Повещенко, О.В. Повещенко, А.О. Соловьева, К.Э. Зубарева, Т.В. Миллер, М.А. Шестопалов, Л.А. Шундрин, В.И. Коненков
    Мезенхимальные стволовые клетки и пептиды: роль и значение в механизмах молекулярной таргетной терапии
    Молекулярная медицина, 2016, Т.14(5), С.15-21. (http://molmed.rusvrach.ru/ru/node/2286)
  430. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  431. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  432. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  433. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  434. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  435. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  436. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  437. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  438. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  439. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  440. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  441. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  442. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  443. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  444. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  445. O.Yu. Mazurkov, A.S. Kabanov, L.N. Shishkina, A.A. Sergeev, M.O. Skarnovich, N.I. Bormotov, M.A. Skarnovich, A.S. Ovchinnikova, K.A. Titova, D.O. Galahova, L.E. Bulychev, A.A. Sergeev, O.S. Taranov, B.A. Selivanov, A.Y. Tikhonov, E.L. Zavjalov, A.P. Agafonov, A.N. Sergeev
    New effective chemically synthesized anti-smallpox compound NIOCH-14
    J. Gen. Virol., 2016, V. 97, N 5, Pp: 1229-1239 doi:10.1099/jgv.0.000422, IF=3.191
  446. M.P. Sartakov, E.D. Lapshina, E.M. Osnitsky, E.A. Zarov, Yu.M. Deryabina
    The Thermal Stability Comparative Analysis of Humic Acids in the Sphagnous Peat of the Western Siberia Taiga Zone Raised Bogs.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 5. Pp. 1311-1320
  447. M.P. Sartakov, E.D. Lapshina, E.M. Osnitsky, E.A. Zarov, Yu.M. Deryabina
    The Thermal Stability Comparative Analysis of Humic Acids in the Sphagnous Peat of the Western Siberia Taiga Zone Raised Bogs.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 5. Pp. 1311-1320
  448. M.P. Sartakov, E.D. Lapshina, E.M. Osnitsky, E.A. Zarov, Yu.M. Deryabina
    The Thermal Stability Comparative Analysis of Humic Acids in the Sphagnous Peat of the Western Siberia Taiga Zone Raised Bogs.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 5. Pp. 1311-1320
  449. M.P. Sartakov, E.D. Lapshina, E.M. Osnitsky, E.A. Zarov, Yu.M. Deryabina
    The Thermal Stability Comparative Analysis of Humic Acids in the Sphagnous Peat of the Western Siberia Taiga Zone Raised Bogs.
    Research Journal of Pharmaceutical, Biological and Chemical Sciences. 2016. V. 7. N 5. Pp. 1311-1320
  450. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  451. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  452. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  453. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  454. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  455. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  456. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  457. И.Ю. Журавлева, Е.В. Карпова, Е.В. Кузнецова, А.С. Юношев, А.А. Коробейников, Т.П. Тимченко, Н.Р. Ничай, И.А. Сойнов, А.В. Горбатых
    Клапаносодержащий ксеновенозный кондуит: terra incognita или tabula rasa?
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 90-101. (Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101)
  458. А.А. Котлярова, А.Ю. Летягин, Т.Г. Толстикова, Н.П. Бгатова, Л.Н. Рачковская
    Влияние литийсодержащей композиции на этанол-индуцированные изменения в печени и мозге лабораторных мышей
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 29-34 (The effect of a lithium-containing composition on ethanol-induced changes in liver and brain within the experiments on mice/ Kotlyarova, A.Yu. Letyagin, T.G. Tolstikova, N.P. Bgatova, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 29-34)
  459. А.А. Котлярова, А.Ю. Летягин, Т.Г. Толстикова, Н.П. Бгатова, Л.Н. Рачковская
    Влияние литийсодержащей композиции на этанол-индуцированные изменения в печени и мозге лабораторных мышей
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 29-34 (The effect of a lithium-containing composition on ethanol-induced changes in liver and brain within the experiments on mice/ Kotlyarova, A.Yu. Letyagin, T.G. Tolstikova, N.P. Bgatova, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 29-34)
  460. А.А. Котлярова, А.Ю. Летягин, Т.Г. Толстикова, Н.П. Бгатова, Л.Н. Рачковская
    Влияние литийсодержащей композиции на этанол-индуцированные изменения в печени и мозге лабораторных мышей
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 29-34 (The effect of a lithium-containing composition on ethanol-induced changes in liver and brain within the experiments on mice/ Kotlyarova, A.Yu. Letyagin, T.G. Tolstikova, N.P. Bgatova, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 29-34)
  461. А.А. Котлярова, А.Ю. Летягин, Т.Г. Толстикова, Н.П. Бгатова, Л.Н. Рачковская
    Влияние литийсодержащей композиции на этанол-индуцированные изменения в печени и мозге лабораторных мышей
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 29-34 (The effect of a lithium-containing composition on ethanol-induced changes in liver and brain within the experiments on mice/ Kotlyarova, A.Yu. Letyagin, T.G. Tolstikova, N.P. Bgatova, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 29-34)
  462. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская
    Исследование аллергогенных свойств нового серебросодержащего тонкодисперсного сорбента
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 24-28. (Research of the allergenic properties of new silver containing finely particulate sorbent/ T.V. Popova, T.G. Tolstikova, A.Yu. Letyagin, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 24-28)
  463. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская
    Исследование аллергогенных свойств нового серебросодержащего тонкодисперсного сорбента
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 24-28. (Research of the allergenic properties of new silver containing finely particulate sorbent/ T.V. Popova, T.G. Tolstikova, A.Yu. Letyagin, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 24-28)
  464. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская
    Исследование аллергогенных свойств нового серебросодержащего тонкодисперсного сорбента
    Сибирский научный медицинский журнал. 2016. Т. 36. № 2. С. 24-28. (Research of the allergenic properties of new silver containing finely particulate sorbent/ T.V. Popova, T.G. Tolstikova, A.Yu. Letyagin, L.N. Rachkovskaya// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 24-28)
  465. А.М. Чернявский, А.Р. Таркова, Т.М. Рузматов, С.В. Морозов, И.А. Григорьев
    Инфекции в кардиохирургии
    Хирургия. Журнал им. Н.И. Пирогова. 2016. № 5. С. 64-68.
  466. А.М. Чернявский, А.Р. Таркова, Т.М. Рузматов, С.В. Морозов, И.А. Григорьев
    Инфекции в кардиохирургии
    Хирургия. Журнал им. Н.И. Пирогова. 2016. № 5. С. 64-68.
  467. А.М. Чернявский, А.Р. Таркова, Т.М. Рузматов, С.В. Морозов, И.А. Григорьев
    Инфекции в кардиохирургии
    Хирургия. Журнал им. Н.И. Пирогова. 2016. № 5. С. 64-68.
  468. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  469. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  470. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  471. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  472. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  473. M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev
    Структура пламени сверхвысокомолекулярного полиэтилена в противотоке воздуха
    Физика горения и взрыва, 2016, Т. 52, N 3, С. 8-22 (DOI:10.15372/FGV20160302) (Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023), IF=0.604
  474. И.П. Жураковский, Т.Г. Толстикова, И.В. Сорокина, Н.А. Жукова, М.П. Борисова, И.О. Маринкин, А.И. Аутеншлюс
    Эффективность применения β-аланинамида бетулоновой кислоты при стафиллококковом остеомиелите у крыс Вистар
    Современные проблемы науки и образования. -2016. - № 5. (Электронный журнал) URL: https://www.science-education.ru/ru/article/view?id=25172.
  475. И.П. Жураковский, Т.Г. Толстикова, И.В. Сорокина, Н.А. Жукова, М.П. Борисова, И.О. Маринкин, А.И. Аутеншлюс
    Эффективность применения β-аланинамида бетулоновой кислоты при стафиллококковом остеомиелите у крыс Вистар
    Современные проблемы науки и образования. -2016. - № 5. (Электронный журнал) URL: https://www.science-education.ru/ru/article/view?id=25172.
  476. И.П. Жураковский, Т.Г. Толстикова, И.В. Сорокина, Н.А. Жукова, М.П. Борисова, И.О. Маринкин, А.И. Аутеншлюс
    Эффективность применения β-аланинамида бетулоновой кислоты при стафиллококковом остеомиелите у крыс Вистар
    Современные проблемы науки и образования. -2016. - № 5. (Электронный журнал) URL: https://www.science-education.ru/ru/article/view?id=25172.
  477. И.П. Жураковский, Т.Г. Толстикова, И.В. Сорокина, Н.А. Жукова, М.П. Борисова, И.О. Маринкин, А.И. Аутеншлюс
    Эффективность применения β-аланинамида бетулоновой кислоты при стафиллококковом остеомиелите у крыс Вистар
    Современные проблемы науки и образования. -2016. - № 5. (Электронный журнал) URL: https://www.science-education.ru/ru/article/view?id=25172.
  478. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  479. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  480. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  481. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  482. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
  483. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
  484. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
  485. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
  486. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  487. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  488. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  489. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  490. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  491. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  492. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  493. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  494. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  495. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  496. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  497. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  498. G. Audran, L. Bosco, P. Nkolo, R. Bikanga, P. Bremond, T. Butscher, S.R. A. Marque
    The β-phosphorus hyperfine coupling constant in nitroxides: 6. Solvent effects in non-cyclic nitroxides
    Organic & Biomolecular Chemistry, 2016,14 (15), 3729-3743 doi:10.1039/C6OB00359A, IF=3.559
  499. В.В. Шелковников, Е.В. Васильев, В.В. Русских, Л.В. Эктова, В.Н. Бережная, Е.Ф. Пен
    Свойства монохромных и двухцветных голограмм в слоистых фотополимерных материалах
    Автометрия. 2016. Т. 52. № 4. С. 107-117. (Monochrome and two-color holograms in layered photopolymer materials/ V. V. Shelkovnikov, E. V. Vasil'ev, V. V. Russkikh, L. V. Ektova, V. N. Berezhnaya, E. F. Pen// Optoelectronics, Instrumentation and Data Processing, 2016, V. 52, N 4, pp 404-412 doi:10.3103/S8756699016040130)
  500. Д.Е. Семенов, Н.А. Жукова, Т.Г. Толстикова, И.В. Сорокина, Е.Л. Лушникова
    Особенности течения паразитарной инвазии, вызванной opisthorchis felineus, у золотистых хомяков
    Бюллетень экспериментальной биологии и медицины. 2016. Т. 161. № 4. С. 468-474. (Specific Features of Progression of the Parasitic Invasion, caused by Opisthorchis felineus, in Golden Hamsters/ D. E. Semenov, N. A. Zhukova, T. G. Tolstikova, I. V. Sorokina, E. L. Lushnikova// Bulletin of Experimental Biology and Medicine, 2016, V. 161, N 4, Pp 481-486 doi:10.1007/s10517-016-3443-x), IF=0.448
  501. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  502. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  503. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  504. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  505. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  506. M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
    Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
  507. G. Audran, P. Bremond, J.-P. Joly, S.R. A. Marque, T. Yamasaki
    C-ON bond homolysis in alkoxyamines. Part 12: the effect of the para-substituent in the 1-phenylethyl fragment
    Org. Biomol. Chem., 2016, 14, 3574-3583 doi:10.1039/C6OB00384B, IF=3.559
  508. G. Audran, P. Bremond, J.-P. Joly, S.R. A. Marque, T. Yamasaki
    C-ON bond homolysis in alkoxyamines. Part 12: the effect of the para-substituent in the 1-phenylethyl fragment
    Org. Biomol. Chem., 2016, 14, 3574-3583 doi:10.1039/C6OB00384B, IF=3.559
  509. G. Audran, P. Bremond, J.-P. Joly, S.R. A. Marque, T. Yamasaki
    C-ON bond homolysis in alkoxyamines. Part 12: the effect of the para-substituent in the 1-phenylethyl fragment
    Org. Biomol. Chem., 2016, 14, 3574-3583 doi:10.1039/C6OB00384B, IF=3.559
  510. G. Audran, P. Bremond, J.-P. Joly, S.R. A. Marque, T. Yamasaki
    C-ON bond homolysis in alkoxyamines. Part 12: the effect of the para-substituent in the 1-phenylethyl fragment
    Org. Biomol. Chem., 2016, 14, 3574-3583 doi:10.1039/C6OB00384B, IF=3.559
  511. E.I. Chernyak, Yu.V. Yushkova, S.V. Pavlushin, S.O. Nikolenko, V.V. Martem'yanov, S.V. Morozov
    Dynamics of Biologically Active Compound Contents from Betula pendula Leaves During Early Leaf Development
    Chemistry of Natural Compounds, 2016, V. 52, N 2, Pp 193-198 doi:10.1007/s10600-016-1592-9, IF=0.472
  512. E.I. Chernyak, Yu.V. Yushkova, S.V. Pavlushin, S.O. Nikolenko, V.V. Martem'yanov, S.V. Morozov
    Dynamics of Biologically Active Compound Contents from Betula pendula Leaves During Early Leaf Development
    Chemistry of Natural Compounds, 2016, V. 52, N 2, Pp 193-198 doi:10.1007/s10600-016-1592-9, IF=0.472
  513. E.I. Chernyak, Yu.V. Yushkova, S.V. Pavlushin, S.O. Nikolenko, V.V. Martem'yanov, S.V. Morozov
    Dynamics of Biologically Active Compound Contents from Betula pendula Leaves During Early Leaf Development
    Chemistry of Natural Compounds, 2016, V. 52, N 2, Pp 193-198 doi:10.1007/s10600-016-1592-9, IF=0.472
  514. M.E. Mironov, M.A. Pokrovsky, Yu.V. Kharitonov, M.M. Shakirov, A.G. Pokrovsky, E.E. Shults
    Furanolabdanoid–based 1,2,4-oxadiazoles: Synthesis and cytotoxic activity
    CHEMISTRYSELECT, V. 1, N 3, March 2016, Pp: 417-424 doi:10.1002/slct.201600042
  515. M.E. Mironov, M.A. Pokrovsky, Yu.V. Kharitonov, M.M. Shakirov, A.G. Pokrovsky, E.E. Shults
    Furanolabdanoid–based 1,2,4-oxadiazoles: Synthesis and cytotoxic activity
    CHEMISTRYSELECT, V. 1, N 3, March 2016, Pp: 417-424 doi:10.1002/slct.201600042
  516. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  517. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  518. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  519. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  520. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
    New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
    Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
  521. G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
    X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
    Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
  522. G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
    X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
    Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
  523. G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
    X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
    Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
  524. G. Audran, P.l. Bremond, S. R. A. Marque, T. Yamasaki
    C-ON Bond Homolysis of Alkoxyamines, Part 11: Activation of the Nitroxyl Fragment
    J. Org. Chem., 2016, 81 (5), pp 1981-1988 doi:10.1021/acs.joc.5b02790, IF=4.784
  525. G. Audran, P.l. Bremond, S. R. A. Marque, T. Yamasaki
    C-ON Bond Homolysis of Alkoxyamines, Part 11: Activation of the Nitroxyl Fragment
    J. Org. Chem., 2016, 81 (5), pp 1981-1988 doi:10.1021/acs.joc.5b02790, IF=4.784
  526. G. Audran, P.l. Bremond, S. R. A. Marque, T. Yamasaki
    C-ON Bond Homolysis of Alkoxyamines, Part 11: Activation of the Nitroxyl Fragment
    J. Org. Chem., 2016, 81 (5), pp 1981-1988 doi:10.1021/acs.joc.5b02790, IF=4.784
  527. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
  528. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
  529. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
  530. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
  531. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
  532. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  533. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  534. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  535. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  536. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  537. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  538. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  539. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  540. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
  541. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
  542. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
  543. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская, В.А. Бурмистров
    Экспериментальное исследование показателей гемодинамики при парентеральном введении серебросодержащего тонкодисперсного сорбента
    Химико-фармацевтический журнал, 2016, Т. 50, № 3, С. 16-19. (Experimental Study of the Biocompatibility of Soft Tissues and a Finely Dispersed Sorbent Containing Silver/ T. V. Popova, T. G. Tolstikova, A. Yu. Letyagin, L. N. Rachkovskaya, V. A. Burmistrov// Pharmaceutical Chemistry Journal, 2016, V. 50, N 3, pp 152-155), IF=0.46
  544. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская, В.А. Бурмистров
    Экспериментальное исследование показателей гемодинамики при парентеральном введении серебросодержащего тонкодисперсного сорбента
    Химико-фармацевтический журнал, 2016, Т. 50, № 3, С. 16-19. (Experimental Study of the Biocompatibility of Soft Tissues and a Finely Dispersed Sorbent Containing Silver/ T. V. Popova, T. G. Tolstikova, A. Yu. Letyagin, L. N. Rachkovskaya, V. A. Burmistrov// Pharmaceutical Chemistry Journal, 2016, V. 50, N 3, pp 152-155), IF=0.46
  545. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская, В.А. Бурмистров
    Экспериментальное исследование показателей гемодинамики при парентеральном введении серебросодержащего тонкодисперсного сорбента
    Химико-фармацевтический журнал, 2016, Т. 50, № 3, С. 16-19. (Experimental Study of the Biocompatibility of Soft Tissues and a Finely Dispersed Sorbent Containing Silver/ T. V. Popova, T. G. Tolstikova, A. Yu. Letyagin, L. N. Rachkovskaya, V. A. Burmistrov// Pharmaceutical Chemistry Journal, 2016, V. 50, N 3, pp 152-155), IF=0.46
  546. Т.В. Попова, Т.Г. Толстикова, А.Ю. Летягин, Л.Н. Рачковская, В.А. Бурмистров
    Экспериментальное исследование показателей гемодинамики при парентеральном введении серебросодержащего тонкодисперсного сорбента
    Химико-фармацевтический журнал, 2016, Т. 50, № 3, С. 16-19. (Experimental Study of the Biocompatibility of Soft Tissues and a Finely Dispersed Sorbent Containing Silver/ T. V. Popova, T. G. Tolstikova, A. Yu. Letyagin, L. N. Rachkovskaya, V. A. Burmistrov// Pharmaceutical Chemistry Journal, 2016, V. 50, N 3, pp 152-155), IF=0.46
  547. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  548. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  549. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  550. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  551. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  552. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  553. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  554. D.V. Trukhin, O.Yu. Rogozhnikova, T.I. Troitskaya, V.G. Vasiliev, M.l K. Bowman, V.M. Tormyshev
    Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals
    Synlett, 2016, 27(06), Pp 893-899 doi:10.1055/s-0035-1561299, IF=2.322
  555. D.S. Baranov, D.S. Fadeev
    Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones
    Mendeleev Communications, V. 26, N 2, March-April 2016, Pp 174- 176 doi:10.1016/j.mencom.2016.03.032, IF=1.404
  556. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  557. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  558. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  559. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  560. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  561. E.S. Stoyanov, S.E. Malykhin
    Carbon monoxide protonation in condensed phases and bonding to surface superacidic Bronsted centers
    Phys. Chem. Chem. Phys., 2016,18(6), 4871-4880 doi:10.1039/C5CP07441J, IF=4.448
  562. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  563. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  564. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  565. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  566. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  567. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  568. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  569. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  570. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  571. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  572. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, K. Kabitaev, S.R-A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere, S. Viel
    β-Phosphorus hyperfine coupling constant in nitroxides: 5. Solvent effect
    RSC Adv., 2016,6(7), 5653-5670 doi:10.1039/C5RA23521A, IF=3.289
  573. O.D. Zakharova, L.P. Ovchinnikova, S.I. Zhivetyeva, L.I. Goryunov, V.D. Shteingarts, E.V. Tretyakov, G.A. Nevinsky
    Synthesis and Evaluation of Cytotoxicity and Antioxidant Properties of Polyfluorinated Phosphorus-containing 1,4-Benzoquinones and 1,4-Naphthoquinones
    Adv. Res., 2016, 6(6), 1-12 doi:10.9734/AIR/2016/24265
  574. O.D. Zakharova, L.P. Ovchinnikova, S.I. Zhivetyeva, L.I. Goryunov, V.D. Shteingarts, E.V. Tretyakov, G.A. Nevinsky
    Synthesis and Evaluation of Cytotoxicity and Antioxidant Properties of Polyfluorinated Phosphorus-containing 1,4-Benzoquinones and 1,4-Naphthoquinones
    Adv. Res., 2016, 6(6), 1-12 doi:10.9734/AIR/2016/24265
  575. O.D. Zakharova, L.P. Ovchinnikova, S.I. Zhivetyeva, L.I. Goryunov, V.D. Shteingarts, E.V. Tretyakov, G.A. Nevinsky
    Synthesis and Evaluation of Cytotoxicity and Antioxidant Properties of Polyfluorinated Phosphorus-containing 1,4-Benzoquinones and 1,4-Naphthoquinones
    Adv. Res., 2016, 6(6), 1-12 doi:10.9734/AIR/2016/24265
  576. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников
    Оптические методы формирования многоуровневого микрорельефа в тонких пленках гибридного фотополимерного материала «ГИБРИМЕР-ТАТС»
    Интерэкспо Гео-Сибирь. 2016. Т. 5. № 2. С. 15-19.
  577. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко, В.В. Шелковников
    Оптические методы формирования многоуровневого микрорельефа в тонких пленках гибридного фотополимерного материала «ГИБРИМЕР-ТАТС»
    Интерэкспо Гео-Сибирь. 2016. Т. 5. № 2. С. 15-19.
  578. M.K. Fomina, D.F. Avgustinovich, T.G. Tolstikova
    Studies of the Effects of a Complex of Buspirone with Glycyrrhyzic Acid on the Behavior of Mice during Formation of an Anxious-Depressive State
    Neuroscience and Behavioral Physiology, 2016, V. 46, N 2, pp 153-159 doi:10.1007/s11055-015-0212-7
  579. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  580. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  581. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  582. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  583. М.Е. Рахманова, О.А. Лузина, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Синтез цианэтильных производных усниновой кислоты и их цитотоксическая активность
    Известия Академии наук. Серия химическая. 2016. № 2. С. 566-569 (Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives/ M. E. RakhmanovaO. A. LuzinaEmail authorM. A. PokrovskiiA. G. PokrovskiiN. F. Salakhutdinov// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 566-569 doi:10.1007/s11172-016-1338-7), IF=0.578
  584. М.Е. Рахманова, О.А. Лузина, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Синтез цианэтильных производных усниновой кислоты и их цитотоксическая активность
    Известия Академии наук. Серия химическая. 2016. № 2. С. 566-569 (Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives/ M. E. RakhmanovaO. A. LuzinaEmail authorM. A. PokrovskiiA. G. PokrovskiiN. F. Salakhutdinov// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 566-569 doi:10.1007/s11172-016-1338-7), IF=0.578
  585. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Т.Г. Толстикова, А.О. Брызгалов, Н.В. Плешкова
    Синтез, свойства и применение 4-нитросемикарбазонов
    Известия Академии наук. Серия химическая. 2016. № 2. С. 550-560 (Synthesis, properties, and application of 4-nitrosemicarbazones/ V. S. Glukhacheva,S. G. Il'yasov, G. V. Sakovich, T. G. Tolstikova, A. O. Bryzgalov, N. V. Pleshkova// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 550-560 doi:10.1007/s11172-016-1336-9), IF=0.578
  586. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Т.Г. Толстикова, А.О. Брызгалов, Н.В. Плешкова
    Синтез, свойства и применение 4-нитросемикарбазонов
    Известия Академии наук. Серия химическая. 2016. № 2. С. 550-560 (Synthesis, properties, and application of 4-nitrosemicarbazones/ V. S. Glukhacheva,S. G. Il'yasov, G. V. Sakovich, T. G. Tolstikova, A. O. Bryzgalov, N. V. Pleshkova// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 550-560 doi:10.1007/s11172-016-1336-9), IF=0.578
  587. В.С. Глухачева, С.Г. Ильясов, Г.В. Сакович, Т.Г. Толстикова, А.О. Брызгалов, Н.В. Плешкова
    Синтез, свойства и применение 4-нитросемикарбазонов
    Известия Академии наук. Серия химическая. 2016. № 2. С. 550-560 (Synthesis, properties, and application of 4-nitrosemicarbazones/ V. S. Glukhacheva,S. G. Il'yasov, G. V. Sakovich, T. G. Tolstikova, A. O. Bryzgalov, N. V. Pleshkova// Russian Chemical Bulletin, February 2016, V. 65, N 2, pp 550-560 doi:10.1007/s11172-016-1336-9), IF=0.578
  588. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  589. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  590. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  591. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  592. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  593. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  594. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  595. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  596. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  597. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  598. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  599. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  600. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  601. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  602. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  603. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  604. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  605. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  606. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  607. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  608. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  609. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  610. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  611. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  612. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  613. Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
    Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
    Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875
  614. Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
    Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
    Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875
  615. Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
    Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
    Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875
  616. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  617. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  618. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  619. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  620. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  621. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  622. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  623. T.A. Korolenko, T.P. Johnston, F.V. Tuzikov, N.A. Tuzikova, A.B. Pupyshev, V.K. Spiridonov, N.V. Goncharova, I.V. Maiborodin, N.A. Zhukova
    Early-stage atherosclerosis in poloxamer 407-induced hyperlipidemic mice: pathological features and changes in the lipid composition of serum lipoprotein fractions and subfractions
    Lipids in Health and Disease, 15:16, 22 January 2016 doi:10.1186/s12944-016-0186-7, IF=2.137
  624. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, H.S. Rzepa, V.G. Shubin
    Noncatalytic bromination of benzene: A combined computational and experimental study
    Journal of Computational Chemistry, V. 37, N 2, 15 January 2016, Pp 210-225 doi:10.1002/jcc.23985, IF=3.648
  625. K.A. Vinogradova, V.P. Krivopalov, E. B. Nikolaenkova, N. V. Pervukhina, D.Yu. Naumov, E.G. Boguslavsky, M.B. Bushuev
    Mixed-valence copper(I,II) complexes with 4-(1H-pyrazol-1-yl)-6-R-pyrimidines: from ionic structures to coordination polymers
    Dalton Trans., 2016, 45 (2), 515-524 doi:10.1039/C5DT04005A, IF=4.177
  626. K.A. Vinogradova, V.P. Krivopalov, E. B. Nikolaenkova, N. V. Pervukhina, D.Yu. Naumov, E.G. Boguslavsky, M.B. Bushuev
    Mixed-valence copper(I,II) complexes with 4-(1H-pyrazol-1-yl)-6-R-pyrimidines: from ionic structures to coordination polymers
    Dalton Trans., 2016, 45 (2), 515-524 doi:10.1039/C5DT04005A, IF=4.177
  627. K.A. Vinogradova, V.P. Krivopalov, E. B. Nikolaenkova, N. V. Pervukhina, D.Yu. Naumov, E.G. Boguslavsky, M.B. Bushuev
    Mixed-valence copper(I,II) complexes with 4-(1H-pyrazol-1-yl)-6-R-pyrimidines: from ionic structures to coordination polymers
    Dalton Trans., 2016, 45 (2), 515-524 doi:10.1039/C5DT04005A, IF=4.177
  628. K.A. Vinogradova, V.P. Krivopalov, E. B. Nikolaenkova, N. V. Pervukhina, D.Yu. Naumov, E.G. Boguslavsky, M.B. Bushuev
    Mixed-valence copper(I,II) complexes with 4-(1H-pyrazol-1-yl)-6-R-pyrimidines: from ionic structures to coordination polymers
    Dalton Trans., 2016, 45 (2), 515-524 doi:10.1039/C5DT04005A, IF=4.177
  629. K.A. Vinogradova, V.P. Krivopalov, E. B. Nikolaenkova, N. V. Pervukhina, D.Yu. Naumov, E.G. Boguslavsky, M.B. Bushuev
    Mixed-valence copper(I,II) complexes with 4-(1H-pyrazol-1-yl)-6-R-pyrimidines: from ionic structures to coordination polymers
    Dalton Trans., 2016, 45 (2), 515-524 doi:10.1039/C5DT04005A, IF=4.177
  630. Т.В. Попова, Т.Г. Толстикова, Л.Н. Рачковская
    Исследование нового пористого носителя в серебросодержащей композиции на модели фарминдуцированных язв желудка и двенадцатиперстной кишки
    Интер-медикал 2016, Т..17, N 1 , с.56-59
  631. Т.В. Попова, Т.Г. Толстикова, Л.Н. Рачковская
    Исследование нового пористого носителя в серебросодержащей композиции на модели фарминдуцированных язв желудка и двенадцатиперстной кишки
    Интер-медикал 2016, Т..17, N 1 , с.56-59
  632. Г.А. Селиванова, Е.В. Амосов, В.Г. Васильев, Е.А. Лукьянец, Е.В. Третьяков, В.Д. Штейнгарц
    Синтез с микроволновым содействием цинковых комплексов фталоцианинов из азосоединений на основе аминотрициандифенила
    Макрогетероциклы, 2016, 9(1), 80-88 (Microwave-Assisted Synthesis of Phthalocyanine Zinc Complexes Derived from Aminotricyanobiphenyl-Based Azo Dyes/ G.A. Selivanova, E. V. Amosov, V. G. Vasilyev, E. A. Lukyanets, E. V. Tretyakov, V.D. Shteingarts// Macroheterocycles 2016 9(1) 80-88 doi:10.6060/mhc151192s), IF=0.804
  633. Г.А. Селиванова, Е.В. Амосов, В.Г. Васильев, Е.А. Лукьянец, Е.В. Третьяков, В.Д. Штейнгарц
    Синтез с микроволновым содействием цинковых комплексов фталоцианинов из азосоединений на основе аминотрициандифенила
    Макрогетероциклы, 2016, 9(1), 80-88 (Microwave-Assisted Synthesis of Phthalocyanine Zinc Complexes Derived from Aminotricyanobiphenyl-Based Azo Dyes/ G.A. Selivanova, E. V. Amosov, V. G. Vasilyev, E. A. Lukyanets, E. V. Tretyakov, V.D. Shteingarts// Macroheterocycles 2016 9(1) 80-88 doi:10.6060/mhc151192s), IF=0.804
  634. B. Epel, G. Redler, V. Tormyshev, H.J. Halpern
    Towards Human Oxygen Images with Electron Paramagnetic Resonance Imaging
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part VII, pp 363-369 doi:10.1007/978-1-4939-3023-4_45, IF=1.952
  635. B. Epel, G. Redler, V. Tormyshev, H.J. Halpern
    Towards Human Oxygen Images with Electron Paramagnetic Resonance Imaging
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part VII, pp 363-369 doi:10.1007/978-1-4939-3023-4_45, IF=1.952
  636. B. Epel, G. Redler, V. Tormyshev, H.J. Halpern
    Towards Human Oxygen Images with Electron Paramagnetic Resonance Imaging
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part VII, pp 363-369 doi:10.1007/978-1-4939-3023-4_45, IF=1.952
  637. B. Epel, G. Redler, C. Pelizzari, V.M. Tormyshev, H.J. Halpern
    Approaching Oxygen-Guided Intensity-Modulated Radiation Therapy
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part IV, pp 185-193 doi:10.1007/978-1-4939-3023-4_23, IF=1.952
  638. B. Epel, G. Redler, C. Pelizzari, V.M. Tormyshev, H.J. Halpern
    Approaching Oxygen-Guided Intensity-Modulated Radiation Therapy
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part IV, pp 185-193 doi:10.1007/978-1-4939-3023-4_23, IF=1.952
  639. B. Epel, G. Redler, C. Pelizzari, V.M. Tormyshev, H.J. Halpern
    Approaching Oxygen-Guided Intensity-Modulated Radiation Therapy
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part IV, pp 185-193 doi:10.1007/978-1-4939-3023-4_23, IF=1.952
  640. B. Epel, G. Redler, C. Pelizzari, V.M. Tormyshev, H.J. Halpern
    Approaching Oxygen-Guided Intensity-Modulated Radiation Therapy
    Oxygen Transport to Tissue XXXVII, V.876 of the series Advances in Experimental Medicine and Biolog, Part IV, pp 185-193 doi:10.1007/978-1-4939-3023-4_23, IF=1.952
  641. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  642. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  643. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  644. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  645. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  646. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  647. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  648. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  649. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  650. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  651. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    nZ,(n + 4)Z-Dienoic fatty acids: a new method for the synthesis and inhibitory action on topoisomerase I and IIα
    Medicinal Chemistry Research, 2016, V. 25, N 1, pp 30-39 doi:10.1007/s00044-015-1446-1, IF=1.435
  652. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  653. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  654. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  655. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  656. S.P. Babailov, I.P. Chuikov, A.I. Kruppa
    Activation Energies of Intermolecular Dynamics in Ethylenediaminetetraacetate Complexes with Lanthanides: An Effect of the “Gadolinium Break”
    Inorganica Chimica Acta, V. 439, 1 January 2016, Pp 117-122 doi:10.1016/j.ica.2015.10.009, IF=1.917
  657. S.P. Babailov, I.P. Chuikov, A.I. Kruppa
    Activation Energies of Intermolecular Dynamics in Ethylenediaminetetraacetate Complexes with Lanthanides: An Effect of the “Gadolinium Break”
    Inorganica Chimica Acta, V. 439, 1 January 2016, Pp 117-122 doi:10.1016/j.ica.2015.10.009, IF=1.917
  658. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unusual transformations of aliphatic nitro compounds in a flow reactor in high-pressure isopropanol on alumina. Part 2. Formation of esters
    The Journal of Supercritical Fluids, V. 107, January 2016, Pages 179-181 doi:10.1016/j.supflu.2015.08.007, IF=2.578
  659. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unusual transformations of aliphatic nitro compounds in a flow reactor in high-pressure isopropanol on alumina. Part 2. Formation of esters
    The Journal of Supercritical Fluids, V. 107, January 2016, Pages 179-181 doi:10.1016/j.supflu.2015.08.007, IF=2.578
  660. И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
    Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
    Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150
  661. И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
    Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
    Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150
  662. И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
    Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
    Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150
  663. Е.Ф. Пен, И.А. Зарубин, В.В. Шелковников, Е.В. Васильев
    Методика определения параметров усадки голографических фотополимерных материалов
    Автометрия, 2016, Т. 52,. № 1, С. 60-69. (Method for determining the shrinkage parameters of holographic photopolymer materials/ E.F. Pen, I.A. Zarubin, V.V. Shelkovnikov, E.V. Vasil'ev.// Optoelectronics, Instrumentation and Data Processing, 2016. V. 52. № 1. Pp 60-69. doi:10.3103/S8756699016010088)
  664. Е.Ф. Пен, И.А. Зарубин, В.В. Шелковников, Е.В. Васильев
    Методика определения параметров усадки голографических фотополимерных материалов
    Автометрия, 2016, Т. 52,. № 1, С. 60-69. (Method for determining the shrinkage parameters of holographic photopolymer materials/ E.F. Pen, I.A. Zarubin, V.V. Shelkovnikov, E.V. Vasil'ev.// Optoelectronics, Instrumentation and Data Processing, 2016. V. 52. № 1. Pp 60-69. doi:10.3103/S8756699016010088)
  665. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408
  666. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408
  667. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408
  668. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408
  669. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408
  670. K.S. Kovaleva, A.A. Kononova, V.A. Korobeynikov, S.V. Cheresiz, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, O.I. Yarovaya, A.G. Pokrovsky, N.F. Salakhutdinov
    Cytotoxic and Antiviral Properties of Novel Dehydroabietylamine Salts
    Med Chem (Los Angeles) 6:10, 642-646 doi:10.4172/2161-0444.1000408

2015

Reviews, articles

  1. I. A. Kirilyuk, A. A. Bobko, S. V. Semenov, D. A. Komarov, I. G. Irtegova, I. A. Grigor'ev, E. G. Bagryanskaya
    The effect of sterical shielding on the redox properties of imidazoline and imidazolidine nitroxides
    J. Org. Chem., 2015, 80 (18), pp 9118-9125 doi:10.1021/acs.joc.5b01494, IF=4.721
  2. I. A. Kirilyuk, A. A. Bobko, S. V. Semenov, D. A. Komarov, I. G. Irtegova, I. A. Grigor'ev, E. G. Bagryanskaya
    The effect of sterical shielding on the redox properties of imidazoline and imidazolidine nitroxides
    J. Org. Chem., 2015, 80 (18), pp 9118-9125 doi:10.1021/acs.joc.5b01494, IF=4.721
  3. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  4. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  5. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  6. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  7. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  8. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
  9. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  10. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  11. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  12. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  13. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  14. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  15. M. Stekrova, P. Maki-Arvela, N. Kumar, E. Behravesh, A. Aho, Q. Balme, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Prins cyclization: Synthesis of compounds with tetrahydropyran moiety over heterogeneous catalysts
    Journal of Molecular Catalysis A: Chemical, V. 410, 15 December 2015, P 260-270 doi:10.1016/j.molcata.2015.09.021, IF=3.615
  16. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  17. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  18. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  19. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  20. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  21. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  22. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Doubly Spin-Labeled RNA as an EPR Reporter for Studying Multicomponent Supramolecular AssembliesOriginal Research Article
    Biophysical Journal, V. 109, N 12, 15 December 2015, Pp 2637-2643 doi:10.1016/j.bpj.2015.10.042, IF=3.971
  23. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов, Н.И. Кравченко
    Эффективность различных форм местных гемостатических материалов на основе окисленной целлюлозы в эксперименте
    Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59. (Efficacy of different forms of local hemostatic materials based on oxidize cellulose in the experiment/ A.R. Tarkova, A.M. Chernyavskiy, I.A. Grigor'ev, S.V. Morozov, V.I. Rodionov, N.I. Kravchenko// Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59.(in Russian))
  24. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов, Н.И. Кравченко
    Эффективность различных форм местных гемостатических материалов на основе окисленной целлюлозы в эксперименте
    Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59. (Efficacy of different forms of local hemostatic materials based on oxidize cellulose in the experiment/ A.R. Tarkova, A.M. Chernyavskiy, I.A. Grigor'ev, S.V. Morozov, V.I. Rodionov, N.I. Kravchenko// Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59.(in Russian))
  25. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов, Н.И. Кравченко
    Эффективность различных форм местных гемостатических материалов на основе окисленной целлюлозы в эксперименте
    Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59. (Efficacy of different forms of local hemostatic materials based on oxidize cellulose in the experiment/ A.R. Tarkova, A.M. Chernyavskiy, I.A. Grigor'ev, S.V. Morozov, V.I. Rodionov, N.I. Kravchenko// Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59.(in Russian))
  26. M.P. Sartakov, Y.M. Deryabina, N.V. Chuhareva
    Thermodynamical stability and element composition peat humic acids Khanty-Mansiysk district
    Research Journal of Pharmaceutical, Biological and Chemical Sciences, 2015, V. 6, N 5, Pp 1589-1593
  27. M.P. Sartakov, Y.M. Deryabina, N.V. Chuhareva
    Thermodynamical stability and element composition peat humic acids Khanty-Mansiysk district
    Research Journal of Pharmaceutical, Biological and Chemical Sciences, 2015, V. 6, N 5, Pp 1589-1593
  28. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  29. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  30. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  31. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  32. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  33. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  34. Z. Sun, E. Yue, M. Qu, I.V. Oleynik, I.I. Oleynik, K. Li, T. Liang, W. Zhang, Wen-Hua. Sun
    8-(2-Cycloalkylphenylimino)-5,6,7-trihydroquinolylnickel halides: polymerizing ethylene to highly branched and lower molecular weight polyethylenes
    Inorg. Chem. Front., 2015,2(3), 223-227 doi:10.1039/c4qi00162a
  35. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  36. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  37. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  38. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  39. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  40. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  41. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  42. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  43. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  44. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  45. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  46. Yu.S. Chistyachenko, E.S. Meteleva, M.Y. Pakharukova, A.V. Katokhin, M.V. Khvostov, A.I. Varlamova, I.I. Glamazdin, S.S. Khalikov, N.E. Polyakov, I.A. Arkhipov, T.G. Tolstikova, V.A. Mordvinov, A.V. Dushkin, N.Z. Lyakhov
    A Physicochemical and Pharmacological Study of the Newly Synthesized Complex of Albendazole and the Polysaccharide Arabinogalactan from Larch Wood
    Current Drug Delivery, 2015, V. 12, N 5, Pp 477-490 doi:10.2174/1567201812666150518094739, IF=1.478
  47. V.V. Shelkovnikov, L.V. Ektova, N.A. Orlova, L.N. Ogneva, D.I. Derevyanko, I.K. Shundrina, G.E. Salnikov, L.V. Yanshole
    Synthesis and thermomechanical properties of hybrid photopolymer films based on the thiol-siloxane and acrylate oligomers
    Journal of Materials Science, December 2015, V. 50, N 23, pp 7544-7556 doi:10.1007/s10853-015-9265-9, IF=2.371
  48. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  49. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  50. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  51. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  52. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  53. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  54. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  55. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  56. A. Torozova, P. Maki-Arvela, N. Kumar, A. Aho, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, K.P. Volcho, N.F. Salakhutdinov, D.Y. Murzin
    Isomerization of verbenol oxide to a diol with para-menthane structure exhibiting anti-Parkinson activity
    Reaction Kinetics, Mechanisms and Catalysis, 2015, V. 116, N 2, pp 299-314 doi:10.1007/s11144-015-0903-7, IF=1.169
  57. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  58. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  59. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  60. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  61. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  62. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  63. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  64. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  65. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  66. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  67. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  68. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  69. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  70. G. Audran, L. Bosco, P. Bremond, T. Butscher, J-M. Franconi, S.R. A. Marque, P. Mellet, E. Parzy, M. Santelli, E. Thiaudiere
    The β-phosphorus hyperfine coupling constant in nitroxide: part 3: titration of water by electron paramagnetic resonance
    Org. Biomol. Chem., 2015,13(48), 11393-11400 doi:10.1039/C5OB01867F, IF=3.562
  71. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
  72. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
  73. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
  74. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
  75. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
  76. A.A. Kuzhelev, D.V. Trukhin, O.A. Krumkacheva, R.K. Strizhakov, O.Yu. Rogozhnikova, T.I. Troitskaya, M.V. Fedin, V.M. Tormyshev, E. G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Triarylmethyl Radicals at the X- and Q-Bands
    J. Phys. Chem. B, 2015, 119 (43), pp 13630-13640 doi:10.1021/acs.jpcb.5b03027, IF=3.302
  77. A.A. Kuzhelev, D.V. Trukhin, O.A. Krumkacheva, R.K. Strizhakov, O.Yu. Rogozhnikova, T.I. Troitskaya, M.V. Fedin, V.M. Tormyshev, E. G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Triarylmethyl Radicals at the X- and Q-Bands
    J. Phys. Chem. B, 2015, 119 (43), pp 13630-13640 doi:10.1021/acs.jpcb.5b03027, IF=3.302
  78. E.G. Kovaleva, L.S. Molochnikov, V.A. Osipova, D.P. Stepanova, V.A. Reznikov
    Electrosurface Properties of Nanostructured Silica Assessed by EPR of Molecular pH Labels
    Applied Magnetic Resonance, December 2015, V. 46, N 12, pp 1367-1382 doi:10.1007/s00723-015-0704-1, IF=1.167
  79. E.G. Kovaleva, L.S. Molochnikov, V.A. Osipova, D.P. Stepanova, V.A. Reznikov
    Electrosurface Properties of Nanostructured Silica Assessed by EPR of Molecular pH Labels
    Applied Magnetic Resonance, December 2015, V. 46, N 12, pp 1367-1382 doi:10.1007/s00723-015-0704-1, IF=1.167
  80. E.G. Kovaleva, L.S. Molochnikov, V.A. Osipova, D.P. Stepanova, V.A. Reznikov
    Electrosurface Properties of Nanostructured Silica Assessed by EPR of Molecular pH Labels
    Applied Magnetic Resonance, December 2015, V. 46, N 12, pp 1367-1382 doi:10.1007/s00723-015-0704-1, IF=1.167
  81. E.G. Kovaleva, L.S. Molochnikov, V.A. Osipova, D.P. Stepanova, V.A. Reznikov
    Electrosurface Properties of Nanostructured Silica Assessed by EPR of Molecular pH Labels
    Applied Magnetic Resonance, December 2015, V. 46, N 12, pp 1367-1382 doi:10.1007/s00723-015-0704-1, IF=1.167
  82. И.В. Ильина, М.А. Покровский, О.С. Михальченко, Д.В. Корчагина, К.П. Волчо, А.Г. Покровский, Н.Ф. Салахутдинов
    Синтез и цитотоксическая активность замещенных гексагидро-2 H-4,6-(эпоксиметано)хромен-8(5 H)-онов, получаемых из (-)-вербенона
    Известия Академии наук. Серия химическая, 2015, № 9, С. 2257. (Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone/ I. V. Il'ina, M. A. Pokrovsky, O. S. Mikhalchenko, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 64, N 9, pp 2257-2260 doi:10.1007/s11172-015-1148-3), IF=0.481
  83. И.В. Ильина, М.А. Покровский, О.С. Михальченко, Д.В. Корчагина, К.П. Волчо, А.Г. Покровский, Н.Ф. Салахутдинов
    Синтез и цитотоксическая активность замещенных гексагидро-2 H-4,6-(эпоксиметано)хромен-8(5 H)-онов, получаемых из (-)-вербенона
    Известия Академии наук. Серия химическая, 2015, № 9, С. 2257. (Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone/ I. V. Il'ina, M. A. Pokrovsky, O. S. Mikhalchenko, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 64, N 9, pp 2257-2260 doi:10.1007/s11172-015-1148-3), IF=0.481
  84. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, И.С. Крюковская, Ю.В. Гатилов
    Превращения 2-алкиламино-1,4-нафтохинонов при действии нитрующей смеси в уксусной кислоте
    Журнал органической химии. 2015. Т. 51. № 12. С. 1767-1771. (Transformations of 2-alkylamino-1,4-naphthoquinones under the action of nitrating mixture in acetic acid/ L. M. Gornostaev , E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, I. S. Kryukovskaya, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2015, V.51, N 12, pp 1733-1738 doi:10.1134/S107042801512012X), IF=0.657
  85. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, И.С. Крюковская, Ю.В. Гатилов
    Превращения 2-алкиламино-1,4-нафтохинонов при действии нитрующей смеси в уксусной кислоте
    Журнал органической химии. 2015. Т. 51. № 12. С. 1767-1771. (Transformations of 2-alkylamino-1,4-naphthoquinones under the action of nitrating mixture in acetic acid/ L. M. Gornostaev , E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, I. S. Kryukovskaya, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2015, V.51, N 12, pp 1733-1738 doi:10.1134/S107042801512012X), IF=0.657
  86. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, И.С. Крюковская, Ю.В. Гатилов
    Превращения 2-алкиламино-1,4-нафтохинонов при действии нитрующей смеси в уксусной кислоте
    Журнал органической химии. 2015. Т. 51. № 12. С. 1767-1771. (Transformations of 2-alkylamino-1,4-naphthoquinones under the action of nitrating mixture in acetic acid/ L. M. Gornostaev , E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, I. S. Kryukovskaya, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2015, V.51, N 12, pp 1733-1738 doi:10.1134/S107042801512012X), IF=0.657
  87. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, И.С. Крюковская, Ю.В. Гатилов
    Превращения 2-алкиламино-1,4-нафтохинонов при действии нитрующей смеси в уксусной кислоте
    Журнал органической химии. 2015. Т. 51. № 12. С. 1767-1771. (Transformations of 2-alkylamino-1,4-naphthoquinones under the action of nitrating mixture in acetic acid/ L. M. Gornostaev , E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, I. S. Kryukovskaya, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2015, V.51, N 12, pp 1733-1738 doi:10.1134/S107042801512012X), IF=0.657
  88. Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, И.С. Крюковская, Ю.В. Гатилов
    Превращения 2-алкиламино-1,4-нафтохинонов при действии нитрующей смеси в уксусной кислоте
    Журнал органической химии. 2015. Т. 51. № 12. С. 1767-1771. (Transformations of 2-alkylamino-1,4-naphthoquinones under the action of nitrating mixture in acetic acid/ L. M. Gornostaev , E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, I. S. Kryukovskaya, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2015, V.51, N 12, pp 1733-1738 doi:10.1134/S107042801512012X), IF=0.657
  89. E.A. Kulikova, E.Y. Bazhenova, N.K. Popova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
    Letters in Drug Design & Discovery, 2015, V. 12, N 10, Pp 833 - 836 doi:10.2174/1570180812666150522221634, IF=0.769
  90. E.A. Kulikova, E.Y. Bazhenova, N.K. Popova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
    Letters in Drug Design & Discovery, 2015, V. 12, N 10, Pp 833 - 836 doi:10.2174/1570180812666150522221634, IF=0.769
  91. E.A. Kulikova, E.Y. Bazhenova, N.K. Popova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
    Letters in Drug Design & Discovery, 2015, V. 12, N 10, Pp 833 - 836 doi:10.2174/1570180812666150522221634, IF=0.769
  92. E.A. Kulikova, E.Y. Bazhenova, N.K. Popova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov
    Effect of Acute Administration of 8-(Trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine Hydrochloride (TC-2153) on Biogenic Amines Metabolism in Mouse Brain
    Letters in Drug Design & Discovery, 2015, V. 12, N 10, Pp 833 - 836 doi:10.2174/1570180812666150522221634, IF=0.769
  93. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  94. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  95. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  96. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  97. A.S. Sokolova, О.I. Yarovaya, А.V. Shernyukov, Yu.V. Gatilov, Yu.V. Razumova, V.V. Zarubaev, T.S. Tretiak, А.G. Pokrovsky, O.I. Kiselev, N.F. Salakhutdinov
    Discovery of a new class of antiviral compounds: Camphor imine derivatives
    European Journal of Medicinal Chemistry, V. 105, 13 November 2015, Pp 263-273 doi:10.1016/j.ejmech.2015.10.010, IF=3.447
  98. О.Г. Сенаторова, И.Ф. Михайлова, А.Л. Иванов, М.М. Митасов, В.В. Сидельников
    Малодеформационная закалка алюминиевых сплавов в полимерных средах
    МЕТАЛЛОВЕДЕНИЕ И ТЕРМИЧЕСКАЯ ОБРАБОТКА МЕТАЛЛОВ, 2015, N 11, C. 33-36 (Low-distortion quenching of aluminum alloys in polymer media/ O.G. Senatorova, I.F. Mikhailova, A.L. Ivanov, M.M. Mitasov, V.V. Sidel'nikov// Metal Science and Heat Treatment, Metal Science and Heat Treatment, March 2016, V. 57, N 11, pp 669-672 doi:10.1007/s11041-016-9940-8)
  99. О.Г. Сенаторова, И.Ф. Михайлова, А.Л. Иванов, М.М. Митасов, В.В. Сидельников
    Малодеформационная закалка алюминиевых сплавов в полимерных средах
    МЕТАЛЛОВЕДЕНИЕ И ТЕРМИЧЕСКАЯ ОБРАБОТКА МЕТАЛЛОВ, 2015, N 11, C. 33-36 (Low-distortion quenching of aluminum alloys in polymer media/ O.G. Senatorova, I.F. Mikhailova, A.L. Ivanov, M.M. Mitasov, V.V. Sidel'nikov// Metal Science and Heat Treatment, Metal Science and Heat Treatment, March 2016, V. 57, N 11, pp 669-672 doi:10.1007/s11041-016-9940-8)
  100. О.Г. Сенаторова, И.Ф. Михайлова, А.Л. Иванов, М.М. Митасов, В.В. Сидельников
    Малодеформационная закалка алюминиевых сплавов в полимерных средах
    МЕТАЛЛОВЕДЕНИЕ И ТЕРМИЧЕСКАЯ ОБРАБОТКА МЕТАЛЛОВ, 2015, N 11, C. 33-36 (Low-distortion quenching of aluminum alloys in polymer media/ O.G. Senatorova, I.F. Mikhailova, A.L. Ivanov, M.M. Mitasov, V.V. Sidel'nikov// Metal Science and Heat Treatment, Metal Science and Heat Treatment, March 2016, V. 57, N 11, pp 669-672 doi:10.1007/s11041-016-9940-8)
  101. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  102. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  103. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  104. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  105. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  106. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  107. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  108. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  109. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  110. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  111. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  112. H.J. Arabshahi, M. Rensburg, L.I. Pilkington, C.Y. Jeon, M. Song, L. Gridel, E. Leung, D. Barker, M. Vuica-Ross, K.P. Volcho, A.L. Zakharenko, O.I. Lavrik, J. Reynisson
    A synthesis, in silico, in vitro and in vivo study of thieno[2,3-b]pyridine anticancer analogues
    MedChemComm, 2015, V. 6, N 11, Pp 1987-1997 doi:10.1039/c5md00245a, IF=2.494
  113. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  114. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  115. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  116. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  117. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  118. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  119. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  120. A.V. Artem'ev, S.F. Malysheva, N.A. Belogorlova, N.I. Protzuk, A.I. Albanov, I.Yu. Bagryanskaya, E.Yu. Schmidt, N.K. Gusarova, B.A. Trofimov
    An Expedient Access to γ-Ketophosphine Chalcogenides via the Chemo- and Regioselective Addition of Secondary Phosphine Chalcogenides to β,γ-Ethylenic Ketones
    HETEROATOM CHEMISTRY, V. 26, N 6, 2015, Pp 455-462 doi:10.1002/hc.21281, IF=1.75
  121. E.V. Suslov, K.Yu. Ponomarev, A.D. Rogachev, M.A. Pokrovsky, A.G. Pokrovsky, M.B. Pykhtina, A.B. Beklemishev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Compounds Combining Aminoadamantane and Monoterpene Moieties: Cytotoxicity and Mutagenic Effects
    Medicinal Chemistry, V. 11, N 7, Pp 629 - 635 doi:10.2174/1573406411666150518110053, IF=1.363
  122. E.V. Suslov, K.Yu. Ponomarev, A.D. Rogachev, M.A. Pokrovsky, A.G. Pokrovsky, M.B. Pykhtina, A.B. Beklemishev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Compounds Combining Aminoadamantane and Monoterpene Moieties: Cytotoxicity and Mutagenic Effects
    Medicinal Chemistry, V. 11, N 7, Pp 629 - 635 doi:10.2174/1573406411666150518110053, IF=1.363
  123. E.V. Suslov, K.Yu. Ponomarev, A.D. Rogachev, M.A. Pokrovsky, A.G. Pokrovsky, M.B. Pykhtina, A.B. Beklemishev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Compounds Combining Aminoadamantane and Monoterpene Moieties: Cytotoxicity and Mutagenic Effects
    Medicinal Chemistry, V. 11, N 7, Pp 629 - 635 doi:10.2174/1573406411666150518110053, IF=1.363
  124. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
    Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
    PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
  125. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
    Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
    PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
  126. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
    Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
    PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
  127. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
    Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
    PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
  128. А. Л. Захаренко, К. Ю. Пономарев, Е. В. Суслов, Д. В. Корчагина, К. П. Волчо, И. А. Васильева, Н. Ф. Салахутдинов, О. И. Лаврик
    Ингибиторные свойства азотсодержащих монотерпеноидных производных адамантана в отношении тирозил-днк-фосфодиэстеразы 1
    Биоорганическая химия, 2015, Т. 41, № 6, С. 731-736. (Inhibitory properties of nitrogen-containing adamantane derivatives with monoterpenoid fragments against tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, K.U. Ponomarev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, I.A. Vasil'eva, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, November 2015, V. 41, N 6, pp 657-662 doi:10.1134/S1068162015060199), IF=0.535
  129. А. Л. Захаренко, К. Ю. Пономарев, Е. В. Суслов, Д. В. Корчагина, К. П. Волчо, И. А. Васильева, Н. Ф. Салахутдинов, О. И. Лаврик
    Ингибиторные свойства азотсодержащих монотерпеноидных производных адамантана в отношении тирозил-днк-фосфодиэстеразы 1
    Биоорганическая химия, 2015, Т. 41, № 6, С. 731-736. (Inhibitory properties of nitrogen-containing adamantane derivatives with monoterpenoid fragments against tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, K.U. Ponomarev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, I.A. Vasil'eva, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, November 2015, V. 41, N 6, pp 657-662 doi:10.1134/S1068162015060199), IF=0.535
  130. А. Л. Захаренко, К. Ю. Пономарев, Е. В. Суслов, Д. В. Корчагина, К. П. Волчо, И. А. Васильева, Н. Ф. Салахутдинов, О. И. Лаврик
    Ингибиторные свойства азотсодержащих монотерпеноидных производных адамантана в отношении тирозил-днк-фосфодиэстеразы 1
    Биоорганическая химия, 2015, Т. 41, № 6, С. 731-736. (Inhibitory properties of nitrogen-containing adamantane derivatives with monoterpenoid fragments against tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, K.U. Ponomarev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, I.A. Vasil'eva, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, November 2015, V. 41, N 6, pp 657-662 doi:10.1134/S1068162015060199), IF=0.535
  131. А. Л. Захаренко, К. Ю. Пономарев, Е. В. Суслов, Д. В. Корчагина, К. П. Волчо, И. А. Васильева, Н. Ф. Салахутдинов, О. И. Лаврик
    Ингибиторные свойства азотсодержащих монотерпеноидных производных адамантана в отношении тирозил-днк-фосфодиэстеразы 1
    Биоорганическая химия, 2015, Т. 41, № 6, С. 731-736. (Inhibitory properties of nitrogen-containing adamantane derivatives with monoterpenoid fragments against tyrosyl-DNA phosphodiesterase 1/ A.L. Zakharenko, K.U. Ponomarev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, I.A. Vasil'eva, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, November 2015, V. 41, N 6, pp 657-662 doi:10.1134/S1068162015060199), IF=0.535
  132. С.П. Бабайлов, П.А. Стабников, Н.В. Куратьева, П.В. Никульшин, С.А. Громилов
    Кристаллическая структура пентафторацетанилида
    Журнал структурной химии, 2015, Т. 56, No. 6, pp. 1256-1259 (Crystal structure of pentafluoroacetanilide/ S. P. Babailov, P. A. Stabnikov, N. V. Kuratieva, P. V. Nikulshin, S. A. Gromilov// Journal of Structural Chemistry, November 2015, V. 56, N 6, pp 1201-1204 doi:10.1134/S002247661506030X), IF=0.508
  133. С.П. Бабайлов, П.А. Стабников, Н.В. Куратьева, П.В. Никульшин, С.А. Громилов
    Кристаллическая структура пентафторацетанилида
    Журнал структурной химии, 2015, Т. 56, No. 6, pp. 1256-1259 (Crystal structure of pentafluoroacetanilide/ S. P. Babailov, P. A. Stabnikov, N. V. Kuratieva, P. V. Nikulshin, S. A. Gromilov// Journal of Structural Chemistry, November 2015, V. 56, N 6, pp 1201-1204 doi:10.1134/S002247661506030X), IF=0.508
  134. С.П. Бабайлов, П.А. Стабников, Н.В. Куратьева, П.В. Никульшин, С.А. Громилов
    Кристаллическая структура пентафторацетанилида
    Журнал структурной химии, 2015, Т. 56, No. 6, pp. 1256-1259 (Crystal structure of pentafluoroacetanilide/ S. P. Babailov, P. A. Stabnikov, N. V. Kuratieva, P. V. Nikulshin, S. A. Gromilov// Journal of Structural Chemistry, November 2015, V. 56, N 6, pp 1201-1204 doi:10.1134/S002247661506030X), IF=0.508
  135. С.П. Бабайлов, П.А. Стабников, Н.В. Куратьева, П.В. Никульшин, С.А. Громилов
    Кристаллическая структура пентафторацетанилида
    Журнал структурной химии, 2015, Т. 56, No. 6, pp. 1256-1259 (Crystal structure of pentafluoroacetanilide/ S. P. Babailov, P. A. Stabnikov, N. V. Kuratieva, P. V. Nikulshin, S. A. Gromilov// Journal of Structural Chemistry, November 2015, V. 56, N 6, pp 1201-1204 doi:10.1134/S002247661506030X), IF=0.508
  136. Р.А. Бредихин, А.М. Максимов, Ю.В. Гатилов, В.В. Киреенков, В.Е. Платонов
    Реакции полифторбензолтиолов с полигалогенметанами и их производными в щелочной среде
    Журнал органической химии. 2015. Т. 51. № 11. С. 1582-1590 (Reactions of polyfluorobenzenethiols with polyhalomethanes and their derivatives in an alkaline medium/ Bredikhin R.A., Maksimov A.M., Gatilov Y.V., Kireenkov V.V., Platonov, V.E.// Russian Journal of Organic Chemistry, V. 51, N 11, 2015, Pp 1551-1559 doi:10.1134/S1070428015110068), IF=0.657
  137. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  138. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  139. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  140. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  141. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  142. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  143. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  144. В.А. Мордвинов, М.Ю. Пахарукова, А.В. Катохин, А.В. Душкин, Ю.С. Чистяченко, А.И. Белоусов, М.В. Хвостов, Н.А. Жукова, С.С. Халиков, Т.Г. Толстикова, Н.З. Ляхов
    Сибирский описторхоз. биология, распространенность и разработка новых препаратов для его лечения
    Химия в интересах устойчивого развития. 2015. Т. 23. № 5. С. 579-584. (Siberian Opisthorchosis. Biology, Distribution and Development of New Preparations for Its Treatment/ MORDVINOV V.A., PAKHARUKOVA M. YU., KATOKHIN A.V., DUSHKIN A.V., CHISTYACHENKO YU. S., BELOUSOV A.I., KHVOSTOV M.V., ZHUKOVA N.A., KHALIKOV S.S., TOLSTIKOVA T.G., LYAKHOV N.Z.// doi:10.15372/KhUR20150511)
  145. М.П. Сартаков, Н.В. Шпынова, Ю.М. Дерябина, И.Д. Комиссаров
    Элементный состав гуминовых кислот сапропелей Среднего Приобья и юга Обь-Иртышского бассейна Западной Сибири.
    Химия в интересах устойчивого развития. 2015. №5. С.523-526 (Elemental Composition of Humic Acids in Sapropel of the Middle Ob Region and the South of the Ob-Irtysh Basin in West Siberia/ SARTAKOV M.P., SHPYNOVA N.V., DERYABINA YU. M., KOMISSAROV I.D.// Chemistry for Sustainable Development, 2015. №5. С.523-526 doi:10.15372/KhUR20150503)
  146. М.П. Сартаков, Н.В. Шпынова, Ю.М. Дерябина, И.Д. Комиссаров
    Элементный состав гуминовых кислот сапропелей Среднего Приобья и юга Обь-Иртышского бассейна Западной Сибири.
    Химия в интересах устойчивого развития. 2015. №5. С.523-526 (Elemental Composition of Humic Acids in Sapropel of the Middle Ob Region and the South of the Ob-Irtysh Basin in West Siberia/ SARTAKOV M.P., SHPYNOVA N.V., DERYABINA YU. M., KOMISSAROV I.D.// Chemistry for Sustainable Development, 2015. №5. С.523-526 doi:10.15372/KhUR20150503)
  147. М.П. Сартаков, Н.В. Шпынова, Ю.М. Дерябина, И.Д. Комиссаров
    Элементный состав гуминовых кислот сапропелей Среднего Приобья и юга Обь-Иртышского бассейна Западной Сибири.
    Химия в интересах устойчивого развития. 2015. №5. С.523-526 (Elemental Composition of Humic Acids in Sapropel of the Middle Ob Region and the South of the Ob-Irtysh Basin in West Siberia/ SARTAKOV M.P., SHPYNOVA N.V., DERYABINA YU. M., KOMISSAROV I.D.// Chemistry for Sustainable Development, 2015. №5. С.523-526 doi:10.15372/KhUR20150503)
  148. I.V. Kulakov, E.B. Nikolaenkova, Yu.V. Gatilov, A.Ya. Tikhonov, A.S. Fisyuk
    Synthesis of 1-hydroxy-1,5-dihydro-2H-pyrrol-2-ones or 1-hydroxy-1,6-dihydropyridine-2,5-diones from N-hydroxy-N-(2-oxoalkyl)amides
    Tetrahedron Letters, V. 56, N 44, 28 October 2015, Pp 5980-5981 doi:10.1016/j.tetlet.2015.09.030, IF=2.378
  149. I.V. Kulakov, E.B. Nikolaenkova, Yu.V. Gatilov, A.Ya. Tikhonov, A.S. Fisyuk
    Synthesis of 1-hydroxy-1,5-dihydro-2H-pyrrol-2-ones or 1-hydroxy-1,6-dihydropyridine-2,5-diones from N-hydroxy-N-(2-oxoalkyl)amides
    Tetrahedron Letters, V. 56, N 44, 28 October 2015, Pp 5980-5981 doi:10.1016/j.tetlet.2015.09.030, IF=2.378
  150. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, G.V. Romanenko, V.I. Ovcharenko
    Spatial distribution of phases during gradual magnetostructural transitions in copper(II)–nitroxide based molecular magnets
    Dalton Trans., 2015,44, 18823-18830 doi:10.1039/C5DT03441H, IF=4.197
  151. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, G.V. Romanenko, V.I. Ovcharenko
    Spatial distribution of phases during gradual magnetostructural transitions in copper(II)–nitroxide based molecular magnets
    Dalton Trans., 2015,44, 18823-18830 doi:10.1039/C5DT03441H, IF=4.197
  152. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, G.V. Romanenko, V.I. Ovcharenko
    Spatial distribution of phases during gradual magnetostructural transitions in copper(II)–nitroxide based molecular magnets
    Dalton Trans., 2015,44, 18823-18830 doi:10.1039/C5DT03441H, IF=4.197
  153. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, G.V. Romanenko, V.I. Ovcharenko
    Spatial distribution of phases during gradual magnetostructural transitions in copper(II)–nitroxide based molecular magnets
    Dalton Trans., 2015,44, 18823-18830 doi:10.1039/C5DT03441H, IF=4.197
  154. Д.И. Деревянко, В.В. Шелковников, В.П. Корольков, В.Н. Бережная, Н.А. Орлова, Л.Н. Огнева, В.А. Лоскутов, Н.Г. Миронников
    Исследование оптических методов формирования многоуровневого дифракционного микрорельефа на пленках гибридного фотополимерного материала «Гибример-42»
    В сборнике: Голография. Наука и практика Сборник трудов. 2015. С. 147-149.
  155. Д.И. Деревянко, В.В. Шелковников, В.П. Корольков, В.Н. Бережная, Н.А. Орлова, Л.Н. Огнева, В.А. Лоскутов, Н.Г. Миронников
    Исследование оптических методов формирования многоуровневого дифракционного микрорельефа на пленках гибридного фотополимерного материала «Гибример-42»
    В сборнике: Голография. Наука и практика Сборник трудов. 2015. С. 147-149.
  156. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова
    Полиморфизм ферментов лигнификации у растений: функциональное значение и прикладные аспекты
    Успехи современной биологии. 2015. Т. 135. № 5. С. 496-513. (Polymorphism of Lignification Enzymes in Plants: the Functional Importance and Applied Aspects/ A.A. Konovalov, I.K. Shundrina, E.V. Karpova// Biology Bulletin Reviews, March 2016, V.6, N 2, pp 149-163 doi:10.1134/S2079086416020031)
  157. Т.С. Фролова, О.И. Синицына, В.И. Каледин
    Мутагенная активность в тесте Эймса четырех аминоазосоединений с различной канцерогенностью для печени крыс
    Биофизика. 2015. Т. 60. № 5. С. 990-994. (Mutagenic Activity of Four Aminoazo Compounds with Different Carcinogenicity for Rat Liver in the Ames Test/ T.S. Frolova, O.I Sinitsyna, V.I. Kaledin// Biophysics, 2015, V. 60, N 5, Pp 990-994 doi:10.1134/S000635091505005X)
  158. Т.С. Фролова, О.И. Синицына, В.И. Каледин
    Мутагенная активность в тесте Эймса четырех аминоазосоединений с различной канцерогенностью для печени крыс
    Биофизика. 2015. Т. 60. № 5. С. 990-994. (Mutagenic Activity of Four Aminoazo Compounds with Different Carcinogenicity for Rat Liver in the Ames Test/ T.S. Frolova, O.I Sinitsyna, V.I. Kaledin// Biophysics, 2015, V. 60, N 5, Pp 990-994 doi:10.1134/S000635091505005X)
  159. А.Г. Шушарин, М.С. Бирюкова, М.П. Половинка, Н.А. Жукова, Т.Г. Толстикова
    Исследование дегенеративных процессов в головке бедренной кости крыс на фоне длительной алкогольной интоксикации
    Сибирский научный медицинский журнал. 2015. Т. 35. № 4. С. 4-8. (Investigation of degenerative processes in the femoral head of rats with prolonged alcohol intoxication/ A.G. Shusharin, M.S. Biruykova, M.P. Polovinka, N.A. Zhukova, T.G. Tolstikova// The Siberian Scientific Medical Journal, 2015, V. 35, № 4, Pp 4-8)
  160. А.Г. Шушарин, М.С. Бирюкова, М.П. Половинка, Н.А. Жукова, Т.Г. Толстикова
    Исследование дегенеративных процессов в головке бедренной кости крыс на фоне длительной алкогольной интоксикации
    Сибирский научный медицинский журнал. 2015. Т. 35. № 4. С. 4-8. (Investigation of degenerative processes in the femoral head of rats with prolonged alcohol intoxication/ A.G. Shusharin, M.S. Biruykova, M.P. Polovinka, N.A. Zhukova, T.G. Tolstikova// The Siberian Scientific Medical Journal, 2015, V. 35, № 4, Pp 4-8)
  161. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  162. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  163. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  164. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  165. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  166. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин, И.Ю. Тямина
    Каталитический синтез диоксинола с обезболивающим эффектом
    Научно-технический вестник Поволжья. 2015. № 5. С. 88-90. (CATALYTIC SYNTHESIS OF DIOXINOL WITH ANTICONVULSANT ACTIVITY/ A.S. Torozova, E.M. Sulman, P.V. Sinitsyna, P. Maki-Arvela, K.P. Volcho, D.Yu., Murzin, I. Yu. Tiamina// Научно-технический вестник Поволжья. 2015. № 5. С. 88-90.)
  167. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  168. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  169. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  170. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  171. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  172. Т.Г. Толстикова, В.А. Мордвинов, Г.А. Максимова, М.Ю. Пахарукова, Е.В. Кашина, Н.А. Жукова, М.Н. Львова, М.В. Хвостов, Д.С. Баев, А.В. Катохин
    Морфофункциональные и биохимические показатели у золотистых хомячков при развитии холангиокарциномы, ассоциированной с описторхозом
    Вавиловский журнал генетики и селекции. 2015;19 (4): 466-473 (doi:10.18699/VJ15.062) (The morphofunctional and biochemical characteristics of opisthorchiasis-associated cholangiocarcinoma in a Syrian hamster model/ G. A. Maksimova , M. Y. Pakharukova, E. V. Kashina, N. A. Zhukova, M. N. Lvova, M. V. Khvostov, D. S. Baev, A. V. Katokhin, T. G. Tolstikova, V. A. Mordvinov// Russian Journal of Genetics: Applied Research, June 2016, V. 6, N 4, pp 454-462, doi:10.1134/S2079059716040134 doi:10.1134/S2079059716040134)
  173. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  174. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  175. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  176. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  177. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  178. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  179. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  180. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  181. Z. Sun, F. Huang, M. Qu, E. Yue, I.V. Oleynik, I.I. Oleynik, Y. Zeng, T. Liang, K. Li, W. Zhang, Wen-Hua. Sun
    Targeting polyethylene waxes: 9-(2-cycloalkylphenylimino)-5,6,7,8-tetrahydrocycloheptapyridylnickel halides and their use as catalysts for ethylene polymerization
    RSC Adv., 2015, V. 5, N. 93, Pp 77913-77921 doi:10.1039/C5RA15806K, IF=3.839
  182. G. Audran, M.B. Ibanou, P. Bremond, J-P. Joly, S.R. Marque
    Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents
    RSC Adv., 2015, V.5, N 93, Pp 76660-76665 doi:10.1039/C5RA13899J, IF=3.839
  183. G. Audran, M.B. Ibanou, P. Bremond, J-P. Joly, S.R. Marque
    Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents
    RSC Adv., 2015, V.5, N 93, Pp 76660-76665 doi:10.1039/C5RA13899J, IF=3.839
  184. G. Audran, M.B. Ibanou, P. Bremond, J-P. Joly, S.R. Marque
    Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents
    RSC Adv., 2015, V.5, N 93, Pp 76660-76665 doi:10.1039/C5RA13899J, IF=3.839
  185. G. Audran, M.B. Ibanou, P. Bremond, J-P. Joly, S.R. Marque
    Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents
    RSC Adv., 2015, V.5, N 93, Pp 76660-76665 doi:10.1039/C5RA13899J, IF=3.839
  186. K.S. Taletskiy, V.I. Borovkov, L.N. Schegoleva, I.V. Beregovaya, A.I. Taratayko, Y.N. Molin
    Radical Cationic Pathway for the Decay of Ionized Glyme Molecules in Liquid Solution
    Journal of Physical Chemistry B, 2015, V. 119, N 45, Pages 14472-14478 doi:10.1021/acs.jpcb.5b06086, IF=3.302
  187. K.S. Taletskiy, V.I. Borovkov, L.N. Schegoleva, I.V. Beregovaya, A.I. Taratayko, Y.N. Molin
    Radical Cationic Pathway for the Decay of Ionized Glyme Molecules in Liquid Solution
    Journal of Physical Chemistry B, 2015, V. 119, N 45, Pages 14472-14478 doi:10.1021/acs.jpcb.5b06086, IF=3.302
  188. K.S. Taletskiy, V.I. Borovkov, L.N. Schegoleva, I.V. Beregovaya, A.I. Taratayko, Y.N. Molin
    Radical Cationic Pathway for the Decay of Ionized Glyme Molecules in Liquid Solution
    Journal of Physical Chemistry B, 2015, V. 119, N 45, Pages 14472-14478 doi:10.1021/acs.jpcb.5b06086, IF=3.302
  189. M.Yu. Ivanov, S.L. Veber S. A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Probing Microenvironment in Ionic Liquids by Time-Resolved EPR of Photoexcited Triplets
    J. Phys. Chem. B, 2015, 119 (42), pp 13440-13449 doi:10.1021/acs.jpcb.5b06792, IF=3.302
  190. M.Yu. Ivanov, S.L. Veber S. A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Probing Microenvironment in Ionic Liquids by Time-Resolved EPR of Photoexcited Triplets
    J. Phys. Chem. B, 2015, 119 (42), pp 13440-13449 doi:10.1021/acs.jpcb.5b06792, IF=3.302
  191. M.Yu. Ivanov, S.L. Veber S. A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Probing Microenvironment in Ionic Liquids by Time-Resolved EPR of Photoexcited Triplets
    J. Phys. Chem. B, 2015, 119 (42), pp 13440-13449 doi:10.1021/acs.jpcb.5b06792, IF=3.302
  192. M.Yu. Ivanov, S.L. Veber S. A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Probing Microenvironment in Ionic Liquids by Time-Resolved EPR of Photoexcited Triplets
    J. Phys. Chem. B, 2015, 119 (42), pp 13440-13449 doi:10.1021/acs.jpcb.5b06792, IF=3.302
  193. M.Yu. Ivanov, S.L. Veber S. A. Prikhod'ko, N.Yu. Adonin, E.G. Bagryanskaya, M.V. Fedin
    Probing Microenvironment in Ionic Liquids by Time-Resolved EPR of Photoexcited Triplets
    J. Phys. Chem. B, 2015, 119 (42), pp 13440-13449 doi:10.1021/acs.jpcb.5b06792, IF=3.302
  194. Т.Е. Кокина, Л.А. Глинская, Н.Б. Горшков, Н.В. Куратьева, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Строение соединений [Pd2(H2L1)Cl4] и [Pd2(H2L1)Cl4]•0,5CH2Cl2 с хиральным бис-α-сульфанилоксимом - производным природного монотерпеноида (+)-3-карена(H2L1)
    Журнал структурной химии, 2015, V. 56, N 5, pp 978-984 (Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145), IF=0.508
  195. Т.Е. Кокина, Л.А. Глинская, Н.Б. Горшков, Н.В. Куратьева, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Строение соединений [Pd2(H2L1)Cl4] и [Pd2(H2L1)Cl4]•0,5CH2Cl2 с хиральным бис-α-сульфанилоксимом - производным природного монотерпеноида (+)-3-карена(H2L1)
    Журнал структурной химии, 2015, V. 56, N 5, pp 978-984 (Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145), IF=0.508
  196. Т.Е. Кокина, Л.А. Глинская, Н.Б. Горшков, Н.В. Куратьева, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Строение соединений [Pd2(H2L1)Cl4] и [Pd2(H2L1)Cl4]•0,5CH2Cl2 с хиральным бис-α-сульфанилоксимом - производным природного монотерпеноида (+)-3-карена(H2L1)
    Журнал структурной химии, 2015, V. 56, N 5, pp 978-984 (Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145), IF=0.508
  197. Т.Е. Кокина, Л.А. Глинская, Н.Б. Горшков, Н.В. Куратьева, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Строение соединений [Pd2(H2L1)Cl4] и [Pd2(H2L1)Cl4]•0,5CH2Cl2 с хиральным бис-α-сульфанилоксимом - производным природного монотерпеноида (+)-3-карена(H2L1)
    Журнал структурной химии, 2015, V. 56, N 5, pp 978-984 (Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145), IF=0.508
  198. Т.Е. Кокина, Л.А. Глинская, Н.Б. Горшков, Н.В. Куратьева, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Строение соединений [Pd2(H2L1)Cl4] и [Pd2(H2L1)Cl4]•0,5CH2Cl2 с хиральным бис-α-сульфанилоксимом - производным природного монотерпеноида (+)-3-карена(H2L1)
    Журнал структурной химии, 2015, V. 56, N 5, pp 978-984 (Structure of [Pd2(H2L1)Cl4] and [Pd2(H2L1)Cl4]•0,5CH2Cl2 compounds with chiral bis-α-sulfanyl oxime, a derivative of natural monoterpenoid (+)-3-carene (H2L1)/ T.E. Kokina, L.A. Glinskaya, N.B. Gorshkov, N.V. Kuratieva, I.V. Korol’kov, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2015, V. 56, N 5, pp 919-925 doi:10.1134/S0022476615050145), IF=0.508
  199. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  200. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  201. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  202. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  203. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  204. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  205. Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, Л.А. Шелудякова, Н.В. Куратьева, П.Е. Плюснин, М.И. Рахманова, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов Cu(II) и Ag(I) с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α -пинена
    Координационная химия. 2015. Т. 41. № 10. С. 604. (Copper(II) and silver(I) complexes with chiral N-substituted aminoacetic acid derivatives containing the natural monoterpenes (+)-3-carene and (-)-α-pinene: Synthesis and structures/ T. E. Kokina , A. M. Agafontsev, K. S. Marenin, L. A. Glinskaya, L. A. Sheludyakova, N. V. Kurat'eva, P. E. Plyusnin, M. I. Rakhmanova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2015, V. 41, N 10, pp 658-663 doi:10.1134/S1070328415100024), IF=0.484
  206. L. V. Politanskaya, I. P. Chuikov, E. V. Tretyakov, V. D. Shteingarts, L. P. Ovchinnikova, O. D. Zakharova, G. A. Nevinsky
    An effective two-step synthesis, fluorescent properties, antioxidant activity and cytotoxicity evaluation of benzene-fluorinated 2,2-dimethyl-2,3-dihydro-1H-quinolin-4-ones
    Journal of Fluorine Chemistry, V. 178, October 2015, Pp 142-153 doi:10.1016/j.jfluchem.2015.07.006, IF=1.947
  207. L. V. Politanskaya, I. P. Chuikov, E. V. Tretyakov, V. D. Shteingarts, L. P. Ovchinnikova, O. D. Zakharova, G. A. Nevinsky
    An effective two-step synthesis, fluorescent properties, antioxidant activity and cytotoxicity evaluation of benzene-fluorinated 2,2-dimethyl-2,3-dihydro-1H-quinolin-4-ones
    Journal of Fluorine Chemistry, V. 178, October 2015, Pp 142-153 doi:10.1016/j.jfluchem.2015.07.006, IF=1.947
  208. L. V. Politanskaya, I. P. Chuikov, E. V. Tretyakov, V. D. Shteingarts, L. P. Ovchinnikova, O. D. Zakharova, G. A. Nevinsky
    An effective two-step synthesis, fluorescent properties, antioxidant activity and cytotoxicity evaluation of benzene-fluorinated 2,2-dimethyl-2,3-dihydro-1H-quinolin-4-ones
    Journal of Fluorine Chemistry, V. 178, October 2015, Pp 142-153 doi:10.1016/j.jfluchem.2015.07.006, IF=1.947
  209. O.V. Ardashov, Yu. S. Demidova, D.V. Korchagina, K.P. Volcho, I.L. Simakova, N.F. Salakhutdinov
    The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid
    Helvetica Chimica Acta, V. 98, N 10, Pp 1442-1455 doi:10.1002/hlca.201500125, IF=1.138
  210. O.V. Ardashov, Yu. S. Demidova, D.V. Korchagina, K.P. Volcho, I.L. Simakova, N.F. Salakhutdinov
    The First Synthesis of (4S,5R,6R)-5,6-Dihydroxy-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic Acid
    Helvetica Chimica Acta, V. 98, N 10, Pp 1442-1455 doi:10.1002/hlca.201500125, IF=1.138
  211. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatuyk, N.V. Pleshkova, D.S. Fadeev, I. V. Alabugin
    Reaction of α,β-alkynylketones with β-amino alcohols: pseudoephedrine- assisted cleavage of triple bond via formal internal redox process
    Mendeleev Communications, V. 25, N 5, 2015, Pp 377-379 doi:10.1016/j.mencom.2015.09.021, IF=1.34
  212. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatuyk, N.V. Pleshkova, D.S. Fadeev, I. V. Alabugin
    Reaction of α,β-alkynylketones with β-amino alcohols: pseudoephedrine- assisted cleavage of triple bond via formal internal redox process
    Mendeleev Communications, V. 25, N 5, 2015, Pp 377-379 doi:10.1016/j.mencom.2015.09.021, IF=1.34
  213. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatuyk, N.V. Pleshkova, D.S. Fadeev, I. V. Alabugin
    Reaction of α,β-alkynylketones with β-amino alcohols: pseudoephedrine- assisted cleavage of triple bond via formal internal redox process
    Mendeleev Communications, V. 25, N 5, 2015, Pp 377-379 doi:10.1016/j.mencom.2015.09.021, IF=1.34
  214. P.P. Chapala, M.V. Bermeshev, V.G. Lakhtin, A.M. Genaev, A.N. Tavtorkin, E.Sh. Finkelshtein
    [2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
    Mendeleev Communications, V.25, N 5, 2015, Pp 344-345 doi:10.1016/j.mencom.2015.09.008, IF=1.34
  215. P.P. Chapala, M.V. Bermeshev, V.G. Lakhtin, A.M. Genaev, A.N. Tavtorkin, E.Sh. Finkelshtein
    [2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
    Mendeleev Communications, V.25, N 5, 2015, Pp 344-345 doi:10.1016/j.mencom.2015.09.008, IF=1.34
  216. P.P. Chapala, M.V. Bermeshev, V.G. Lakhtin, A.M. Genaev, A.N. Tavtorkin, E.Sh. Finkelshtein
    [2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
    Mendeleev Communications, V.25, N 5, 2015, Pp 344-345 doi:10.1016/j.mencom.2015.09.008, IF=1.34
  217. P.P. Chapala, M.V. Bermeshev, V.G. Lakhtin, A.M. Genaev, A.N. Tavtorkin, E.Sh. Finkelshtein
    [2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
    Mendeleev Communications, V.25, N 5, 2015, Pp 344-345 doi:10.1016/j.mencom.2015.09.008, IF=1.34
  218. P.P. Chapala, M.V. Bermeshev, V.G. Lakhtin, A.M. Genaev, A.N. Tavtorkin, E.Sh. Finkelshtein
    [2σ + 2σ + 2π]-Cycloaddition of quadricyclane to partially methylated chlorosilylalkenes
    Mendeleev Communications, V.25, N 5, 2015, Pp 344-345 doi:10.1016/j.mencom.2015.09.008, IF=1.34
  219. E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, I.Yu. Bagryanskaya, N.P. Gritsan, A.V. Zibarev
    Novel long-lived π-heterocyclic radical anion: a hybrid of 1,2,5-thiadiazo- and 1,2,3-dithiazolidyls
    Mendeleev Communications, V. 25, N 5, September-October 2015, Pp 336-338 doi:10.1016/j.mencom.2015.09.005, IF=1.34
  220. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов
    Исследование местных гемостатических средств с целью профилактики осложнений срединной стернотомии в эксперименте
    В сборнике: Современные аспекты диагностики и лечения в кардиохирургии Материалы научно-практической конференции с международным участием. 2015. С. 78-80.
  221. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов
    Исследование местных гемостатических средств с целью профилактики осложнений срединной стернотомии в эксперименте
    В сборнике: Современные аспекты диагностики и лечения в кардиохирургии Материалы научно-практической конференции с международным участием. 2015. С. 78-80.
  222. L. Politanskaya, V. Shteingarts, E. Tretyakov, A. Potapov
    The p-toluenesulfonic acid-catalyzed transformation of polyfluorinated 2-alkynylanilines to 2-aminoarylketones and indoles
    Tetrahedron Letters, V. 56, N 39, 23 September 2015, Pp 5328-5332 doi:10.1016/j.tetlet.2015.07.078, IF=2.378
  223. Д.Е. Семенов, Н.А. Жукова, Т.Г. Толстикова, И.В. Сорокина, М.С. Бирюкова, Е.П. Иванова
    Патоморфогенез токсических поражений печени, индуцированных полихимиотерапией и тетрахлорметаном и их коррекция тритерпеновыми производными
    В книге: ФУНДАМЕНТАЛЬНЫЕ АСПЕКТЫ КОМПЕНСАТОРНО-ПРИСПОСОБИТЕЛЬНЫХ ПРОЦЕССОВ МОЛЕКУЛЯРНО-КЛЕТОЧНЫЕ И МЕДИКО-ЭКОЛОГИЧЕСКИЕ ПРОБЛЕМЫ КОМПЕНСАЦИИ И ПРИСПОСОБЛЕНИЯ. Федеральное государственное бюджетное научное учреждение «Научно-исследовательский институт экспериментальной и клинической медицины». Ответственный редактор: академик РАН, доктор медицинских наук, профессор В.А. Шкурупий. Новосибирск, 2015. С. 259-260.
  224. Е.А. Морозова, Т.Г. Толстикова, А.А. Старостенко, Т.Н. Быстрова
    Исследование хронической токсичности декстразида
    В книге: ФУНДАМЕНТАЛЬНЫЕ АСПЕКТЫ КОМПЕНСАТОРНО-ПРИСПОСОБИТЕЛЬНЫХ ПРОЦЕССОВ МОЛЕКУЛЯРНО-КЛЕТОЧНЫЕ И МЕДИКО-ЭКОЛОГИЧЕСКИЕ ПРОБЛЕМЫ КОМПЕНСАЦИИ И ПРИСПОСОБЛЕНИЯ. Федеральное государственное бюджетное научное учреждение «Научно-исследовательский институт экспериментальной и клинической медицины». Ответственный редактор: академик РАН, доктор медицинских наук, профессор В.А. Шкурупий. Новосибирск, 2015. С. 176-177.
  225. Е.А. Морозова, Т.Г. Толстикова, А.А. Старостенко, Т.Н. Быстрова
    Исследование хронической токсичности декстразида
    В книге: ФУНДАМЕНТАЛЬНЫЕ АСПЕКТЫ КОМПЕНСАТОРНО-ПРИСПОСОБИТЕЛЬНЫХ ПРОЦЕССОВ МОЛЕКУЛЯРНО-КЛЕТОЧНЫЕ И МЕДИКО-ЭКОЛОГИЧЕСКИЕ ПРОБЛЕМЫ КОМПЕНСАЦИИ И ПРИСПОСОБЛЕНИЯ. Федеральное государственное бюджетное научное учреждение «Научно-исследовательский институт экспериментальной и клинической медицины». Ответственный редактор: академик РАН, доктор медицинских наук, профессор В.А. Шкурупий. Новосибирск, 2015. С. 176-177.
  226. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  227. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  228. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  229. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  230. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  231. M.N. Timofeeva, V.N. Panchenko, A. Gil, S.V. Zakusin, V. V. Krupskaya, K.P. Volcho, M.A. Vicente
    Effect of structure and acidity of acid modified clay materials on synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
    Catalysis Communications, 2015, V. 69, , Pp 234-238 doi:10.1016/j.catcom.2015.07.005, IF=3.698
  232. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, В.В. Шелковников
    Экспериментальное исследование формирования и считывания неоднородных голографических ФПМ-ЖК структур
    Ученые записки физического факультета Московского университета. 2015. № 4. С. 154304.
  233. А.О. Семкин, С.Н. Шарангович, Е.В. Васильев, В.В. Шелковников
    Экспериментальное исследование формирования и считывания неоднородных голографических ФПМ-ЖК структур
    Ученые записки физического факультета Московского университета. 2015. № 4. С. 154304.
  234. E. Bagryanskaya, H. Lee, Cz. Rudowicz, H. Ohta
    Modern Trends in the Development of EPR/ESR
    Applied Magnetic Resonance, September 2015, V. 46, N 9, pp 965-966 doi:10.1007/s00723-015-0719-7, IF=1.167
  235. E. Bagryanskaya, H. Lee, Cz. Rudowicz, H. Ohta
    Modern Trends in the Development of EPR/ESR
    Applied Magnetic Resonance, September 2015, V. 46, N 9, pp 965-966 doi:10.1007/s00723-015-0719-7, IF=1.167
  236. E. Bagryanskaya, H. Lee, Cz. Rudowicz, H. Ohta
    Modern Trends in the Development of EPR/ESR
    Applied Magnetic Resonance, September 2015, V. 46, N 9, pp 965-966 doi:10.1007/s00723-015-0719-7, IF=1.167
  237. I.V. Nechepurenko, U.A. Boyarskikh, M.V. Khvostov, D.S. Baev, N.I. Komarova, M.L. Filipenko, T.G. Tolstikova, N.F. Salakhutdinov
    Hypolipidemic Berberine Derivatives with a Reduced Aromatic Ring C
    Chemistry of Natural Compounds, 2015, V 51, N 5, pp 916-922 doi:10.1007/s10600-015-1447-9, IF=0.509
  238. I.V. Nechepurenko, U.A. Boyarskikh, M.V. Khvostov, D.S. Baev, N.I. Komarova, M.L. Filipenko, T.G. Tolstikova, N.F. Salakhutdinov
    Hypolipidemic Berberine Derivatives with a Reduced Aromatic Ring C
    Chemistry of Natural Compounds, 2015, V 51, N 5, pp 916-922 doi:10.1007/s10600-015-1447-9, IF=0.509
  239. С.В. Аньков, Т.Г. Толстикова, А.А. Онищук, М.В. Хвостов, И.В. Сорокина, А.М. Бакланов, В.М. Фомин, В.В. Болдырев
    Анальгетический эффект наноаэрозольной формы некоторых нестероидных противовоспалительных препаратов
    Химико-фармацевтический журнал. 2015. Т. 49. № 10. С. 37-39. (Analgesic Effect of Several Nonsteroidal Anti-Inflammatory Drug Nanoaerosols/ S. V. An'kov, T. G. Tolstikova , A. A. Onishchuk, M. V. Khvostov, I. V. Sorokina, A. M. Baklanov, V. M. Fomin, V. V. Boldyrev// Pharmaceutical Chemistry Journal, 2016, V. 49, N 10, pp 680-682 doi:10.1007/s11094-016-1352-y), IF=0.451
  240. С.В. Аньков, Т.Г. Толстикова, А.А. Онищук, М.В. Хвостов, И.В. Сорокина, А.М. Бакланов, В.М. Фомин, В.В. Болдырев
    Анальгетический эффект наноаэрозольной формы некоторых нестероидных противовоспалительных препаратов
    Химико-фармацевтический журнал. 2015. Т. 49. № 10. С. 37-39. (Analgesic Effect of Several Nonsteroidal Anti-Inflammatory Drug Nanoaerosols/ S. V. An'kov, T. G. Tolstikova , A. A. Onishchuk, M. V. Khvostov, I. V. Sorokina, A. M. Baklanov, V. M. Fomin, V. V. Boldyrev// Pharmaceutical Chemistry Journal, 2016, V. 49, N 10, pp 680-682 doi:10.1007/s11094-016-1352-y), IF=0.451
  241. С.В. Аньков, Т.Г. Толстикова, А.А. Онищук, М.В. Хвостов, И.В. Сорокина, А.М. Бакланов, В.М. Фомин, В.В. Болдырев
    Анальгетический эффект наноаэрозольной формы некоторых нестероидных противовоспалительных препаратов
    Химико-фармацевтический журнал. 2015. Т. 49. № 10. С. 37-39. (Analgesic Effect of Several Nonsteroidal Anti-Inflammatory Drug Nanoaerosols/ S. V. An'kov, T. G. Tolstikova , A. A. Onishchuk, M. V. Khvostov, I. V. Sorokina, A. M. Baklanov, V. M. Fomin, V. V. Boldyrev// Pharmaceutical Chemistry Journal, 2016, V. 49, N 10, pp 680-682 doi:10.1007/s11094-016-1352-y), IF=0.451
  242. С.В. Аньков, Т.Г. Толстикова, А.А. Онищук, М.В. Хвостов, И.В. Сорокина, А.М. Бакланов, В.М. Фомин, В.В. Болдырев
    Анальгетический эффект наноаэрозольной формы некоторых нестероидных противовоспалительных препаратов
    Химико-фармацевтический журнал. 2015. Т. 49. № 10. С. 37-39. (Analgesic Effect of Several Nonsteroidal Anti-Inflammatory Drug Nanoaerosols/ S. V. An'kov, T. G. Tolstikova , A. A. Onishchuk, M. V. Khvostov, I. V. Sorokina, A. M. Baklanov, V. M. Fomin, V. V. Boldyrev// Pharmaceutical Chemistry Journal, 2016, V. 49, N 10, pp 680-682 doi:10.1007/s11094-016-1352-y), IF=0.451
  243. А.Н. Ляпунов, Е.П. Безуглая, Н.А. Ляпунов, И.А. Кирилюк
    Исследование гелей с карбомерами методами ротационной вискозиметрии и спиновых зондов
    Химико-фармацевтический журнал. 2015. Т. 49. № 9. С. 51-56. (Studies of Carbomer Gels Using Rotational Viscometry and Spin Probes/ A. N. Lyapunov, E. P. Bezuglaya, N. A. Lyapunov, I. A. Kirilyuk// Pharmaceutical Chemistry Journal, 2015, V. 49, N 9, pp 639-644 doi:10.1007/s11094-015-1344-3), IF=0.451
  244. А.Н. Ляпунов, Е.П. Безуглая, Н.А. Ляпунов, И.А. Кирилюк
    Исследование гелей с карбомерами методами ротационной вискозиметрии и спиновых зондов
    Химико-фармацевтический журнал. 2015. Т. 49. № 9. С. 51-56. (Studies of Carbomer Gels Using Rotational Viscometry and Spin Probes/ A. N. Lyapunov, E. P. Bezuglaya, N. A. Lyapunov, I. A. Kirilyuk// Pharmaceutical Chemistry Journal, 2015, V. 49, N 9, pp 639-644 doi:10.1007/s11094-015-1344-3), IF=0.451
  245. А.Н. Ляпунов, Е.П. Безуглая, Н.А. Ляпунов, И.А. Кирилюк
    Исследование гелей с карбомерами методами ротационной вискозиметрии и спиновых зондов
    Химико-фармацевтический журнал. 2015. Т. 49. № 9. С. 51-56. (Studies of Carbomer Gels Using Rotational Viscometry and Spin Probes/ A. N. Lyapunov, E. P. Bezuglaya, N. A. Lyapunov, I. A. Kirilyuk// Pharmaceutical Chemistry Journal, 2015, V. 49, N 9, pp 639-644 doi:10.1007/s11094-015-1344-3), IF=0.451
  246. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  247. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  248. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  249. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  250. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  251. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  252. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  253. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  254. L.S. Konstantinova, I.E. Bobkova, Yu.V. Nelyubina, E.A. Chulanova, I.G. Irtegova, N.V. Vasilieva, P.S. Camacho, S.E. Ashbrook, G. Hua, A.M. Z. Slawin, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    [1,2,5]Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selena­diazole and Generation of Persistent Radical Anions
    European Journal of Organic Chemistry, V. 2015, N 25, pages 5585-5593, September 2015 doi:10.1002/ejoc.201500742, IF=3.65
  255. E.S. Stoyanov, G.D. Gomes
    tert-Butyl Carbocation in Condensed Phases: Stabilization via Hyperconjugation, Polarization, and Hydrogen Bonding
    JOURNAL OF PHYSICAL CHEMISTRY A, V. 119, N 32, Pp 8619-8629 doi:10.1021/acs.jpca.5b04657, IF=2.693
  256. Yu.V. Patrushev, E.Y. Yakovleva, I.K. Shundrina, D.P. Ivanov, T.S. Glazneva
    The properties of capillary columns with sorbents based on poly-(1-trimethylsilyl-1-propyne) modified with nitrous oxide
    Journal of Chromatography A, V. 1406, 7 August 2015, Pages 291-298 doi:10.1016/j.chroma.2015.06.013, IF=4.169
  257. Yu.V. Patrushev, E.Y. Yakovleva, I.K. Shundrina, D.P. Ivanov, T.S. Glazneva
    The properties of capillary columns with sorbents based on poly-(1-trimethylsilyl-1-propyne) modified with nitrous oxide
    Journal of Chromatography A, V. 1406, 7 August 2015, Pages 291-298 doi:10.1016/j.chroma.2015.06.013, IF=4.169
  258. Yu.V. Patrushev, E.Y. Yakovleva, I.K. Shundrina, D.P. Ivanov, T.S. Glazneva
    The properties of capillary columns with sorbents based on poly-(1-trimethylsilyl-1-propyne) modified with nitrous oxide
    Journal of Chromatography A, V. 1406, 7 August 2015, Pages 291-298 doi:10.1016/j.chroma.2015.06.013, IF=4.169
  259. Yu.V. Patrushev, E.Y. Yakovleva, I.K. Shundrina, D.P. Ivanov, T.S. Glazneva
    The properties of capillary columns with sorbents based on poly-(1-trimethylsilyl-1-propyne) modified with nitrous oxide
    Journal of Chromatography A, V. 1406, 7 August 2015, Pages 291-298 doi:10.1016/j.chroma.2015.06.013, IF=4.169
  260. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  261. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  262. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  263. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  264. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  265. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  266. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    lsoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
    ACS Catal., 2015, 5 (8), pp 4673-4679 doi:10.1021/acscatal.5b01212, IF=9.312
  267. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    lsoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
    ACS Catal., 2015, 5 (8), pp 4673-4679 doi:10.1021/acscatal.5b01212, IF=9.312
  268. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  269. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  270. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  271. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  272. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  273. V.A. D'yakonov, L.U. Dzhemileva, A.A. Makarov, A.R. Mulyukova, D.S. Baev, E.K. Khusnutdinova, T.G. Tolstikova, U.M. Dzhemilev
    11-Phenylundeca-5Z,9Z-dienoic Acid: Stereoselective Synthesis and Dual Topoisomerase I/IIα Inhibition
    CURRENT CANCER DRUG TARGETS, 2015, V. 15, N 6, Pp 504-510 doi:10.2174/1568009615666150506093155, IF=3.522
  274. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  275. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  276. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  277. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  278. V.V. Zarubaev, A.V. Garshinina, T.S. Tretiak, V.A. Fedorova, A.A. Shtro, A.S. Sokolova, O.I. Yarovaya, N.F. Salakhutdinov
    Broad range of inhibiting action of novel camphor-based compound with anti-hemagglutinin activity against influenza viruses in vitro and in vivo
    Antiviral Research, V. 120, 2015, Pp 126-133 doi:10.1016/j.antiviral.2015.06.004, IF=3.938
  279. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
    Synthesis and biological activity of novel deoxycholic acid derivatives
    Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792
  280. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
    Synthesis and biological activity of novel deoxycholic acid derivatives
    Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792
  281. I.I. Popadyuk, A.V. Markov, O.V. Salomatina, E.B. Logashenko, A.V. Shernyukov, M.A. Zenkova, N.F. Salakhutdinov
    Synthesis and biological activity of novel deoxycholic acid derivatives
    Bioorganic & Medicinal Chemistry, V. 23, N 15, 2015, Pp 5022-5034 doi:10.1016/j.bmc.2015.05.012, IF=2.792
  282. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unique shortening of carbon chain during reduction of aliphatic nitro compounds to amines in the presence of supercritical isopropanol on alumina
    The Journal of Supercritical Fluids, V.103, 2015, Pp 101-104 doi:10.1016/j.supflu.2015.04.029, IF=2.371
  283. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Unique shortening of carbon chain during reduction of aliphatic nitro compounds to amines in the presence of supercritical isopropanol on alumina
    The Journal of Supercritical Fluids, V.103, 2015, Pp 101-104 doi:10.1016/j.supflu.2015.04.029, IF=2.371
  284. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  285. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  286. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  287. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  288. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  289. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  290. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  291. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  292. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  293. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  294. N.A. Pushkarevsky, N.A. Semenov, A.A. Dmitriev, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, B.E. Bode, N.P. Gritsan, L.S. Konstantinova, J.D. Woollins, O.A. Rakitin, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2015, 54 (14), pp 7007-7013 doi:10.1021/acs.inorgchem.5b01033, IF=4.762
  295. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  296. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  297. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  298. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  299. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  300. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.M. Efimov, T. Ruuholas, V.V. Glupov
    Asynchrony between host plant and insects-defoliator within a tritrophic system: The role of herbivore innate immunity
    PLos ONE. 2015, Vol. 10. No. 6 Article Number e0130988 doi:10.1371/journal.pone.0130988, IF=3.234
  301. A.V. Lipeeva, M.A. Pokrovsky, D.S. Baev, M.M. Shakirov, I.Y. Bagryanskaya, T.G. Tolstikova, A.G. Pokrovsky, E.E. Shults
    Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity
    European Journal of Medicinal Chemistry, V.100, 2015, Pp 119-128 doi:10.1016/j.ejmech.2015.05.016, IF=3.447
  302. Д.И. Деревянко, В.В. Шелковников, В.Н. Бережная, В.А. Лоскутов, Н.А. Орлова, Л.Н. Огнева, Н.Г. Миронников, В.П. Корольков
    Гибридный материал на основе силоксансодержащих тиольных и акрилатных олигомеров для записи дифракционных структур и его термооптические свойства
    ИЗВЕСТИЯ ВОЛГОГРАДСКОГО ГОСУДАРСТВЕННОГО ТЕХНИЧЕСКОГО УНИВЕРСИТЕТА, 2015, № 7, 82-85
  303. Д.И. Деревянко, В.В. Шелковников, В.Н. Бережная, В.А. Лоскутов, Н.А. Орлова, Л.Н. Огнева, Н.Г. Миронников, В.П. Корольков
    Гибридный материал на основе силоксансодержащих тиольных и акрилатных олигомеров для записи дифракционных структур и его термооптические свойства
    ИЗВЕСТИЯ ВОЛГОГРАДСКОГО ГОСУДАРСТВЕННОГО ТЕХНИЧЕСКОГО УНИВЕРСИТЕТА, 2015, № 7, 82-85
  304. Д.В. Белик, А.С. Емцев, А.В. Шумейко, М.В. Хвостов
    Магнитоэлектрическая система для стимуляции гемопоэза при снижении количества клеток крови и возрастных изменениях объема красного костного мозга
    Биотехносфера. 2015. № 3 (39). С. 20-24. (Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow/ Belik D.V., Emtsev A.S., Schumeyko A.V., Khvostov M.V.// )
  305. Д.В. Белик, А.С. Емцев, А.В. Шумейко, М.В. Хвостов
    Магнитоэлектрическая система для стимуляции гемопоэза при снижении количества клеток крови и возрастных изменениях объема красного костного мозга
    Биотехносфера. 2015. № 3 (39). С. 20-24. (Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow/ Belik D.V., Emtsev A.S., Schumeyko A.V., Khvostov M.V.// )
  306. Д.В. Белик, А.С. Емцев, А.В. Шумейко, М.В. Хвостов
    Магнитоэлектрическая система для стимуляции гемопоэза при снижении количества клеток крови и возрастных изменениях объема красного костного мозга
    Биотехносфера. 2015. № 3 (39). С. 20-24. (Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow Magnetoelectric system for stimulation of hematopoiesis at decrease in quantity of blood cells and age changes of volume of red marrow/ Belik D.V., Emtsev A.S., Schumeyko A.V., Khvostov M.V.// )
  307. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  308. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  309. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  310. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  311. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  312. O.B. Bekker, D.N. Sokolov, O.A. Luzina, N.I. Komarova, Yu.V. Gatilov, S.N. Andreevskaya, T.G. Smirnova, D.A. Maslov, L.N. Chernousova, N.F. Salakhutdinov, V.N. Danilenko
    Synthesis and activity of (+)-usnic acid and (-)-usnic acid derivatives containing 1,3-thiazole cycle against Mycobacterium tuberculosis
    Medicinal Chemistry Research, 2015, V. 24, N 7, pp 2926-2938 doi:10.1007/s00044-015-1348-2, IF=1.401
  313. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  314. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  315. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  316. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  317. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  318. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, М.И. Рахманова, П.Е. Плюснин, А.С. Виноградов, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез октафторбифенил-4,4'-дикарбоновой кислоты и фотолюминесцирующих соединений на ее основе
    Журнал общей химии. 2015. Т. 85. № 7. С. 1092-1098., IF=0.477
  319. M.O. Korotkikh, N.A. Pankrushina, O.I. Sal'nikova, A.E. Sonnikova
    Alkaloids from the New Species Papaver kuvajevii
    Chemistry of Natural Compounds, July 2015, Volume 51, Issue 4, pp 803-804 doi:10.1007/s10600-015-1418-1, IF=0.509
  320. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509
  321. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509
  322. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509
  323. O.A. Luzina, D.N. Sokolov, M.A. Pokrovskii, A.G. Pokrovskii, O.B. Bekker, V.N. Danilenko, N.F. Salakhutdinov
    Synthesis and Biological Activity of Usnic Acid Enamine Derivatives
    Chemistry of Natural Compounds, July 2015, V. 51, N 4, pp 646-651 doi:10.1007/s10600-015-1376-7, IF=0.509
  324. I.I. Barabanov, A.V. Polukhin, V.V. Korolev, L.V. Kuibida, A.A. Nefedov
    Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene
    Mendeleev Communications, V. 25, N 4, July-August 2015, Pp 260-261 doi:10.1016/j.mencom.2015.07.008, IF=1.154
  325. I.I. Barabanov, A.V. Polukhin, V.V. Korolev, L.V. Kuibida, A.A. Nefedov
    Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene
    Mendeleev Communications, V. 25, N 4, July-August 2015, Pp 260-261 doi:10.1016/j.mencom.2015.07.008, IF=1.154
  326. I.I. Barabanov, A.V. Polukhin, V.V. Korolev, L.V. Kuibida, A.A. Nefedov
    Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene
    Mendeleev Communications, V. 25, N 4, July-August 2015, Pp 260-261 doi:10.1016/j.mencom.2015.07.008, IF=1.154
  327. I.I. Barabanov, A.V. Polukhin, V.V. Korolev, L.V. Kuibida, A.A. Nefedov
    Novel covalently linked pyrene–aryl azide systems: synthesis of 1-(4-azidobenzoyloxy)pyrene
    Mendeleev Communications, V. 25, N 4, July-August 2015, Pp 260-261 doi:10.1016/j.mencom.2015.07.008, IF=1.154
  328. T.S. Frolova, O.D. Zakharova, Y.F. Polienko, Y.V. Yushkova, E.I. Chernyak, S.V. Morozov, O.I. Sinitsina, I.A. Grigor’ev, G.A. Nevinsky
    Conjugates of trolox and alpha-tocopheryl succinate with nitroxides: Synthesis, antioxidant and antitumor activity
    International Journal of Medicine and Pharmaceutical Sciences. 2015. Vol. 5. No. 3. P. 9-24.
  329. T.S. Frolova, O.D. Zakharova, Y.F. Polienko, Y.V. Yushkova, E.I. Chernyak, S.V. Morozov, O.I. Sinitsina, I.A. Grigor’ev, G.A. Nevinsky
    Conjugates of trolox and alpha-tocopheryl succinate with nitroxides: Synthesis, antioxidant and antitumor activity
    International Journal of Medicine and Pharmaceutical Sciences. 2015. Vol. 5. No. 3. P. 9-24.
  330. T.S. Frolova, O.D. Zakharova, Y.F. Polienko, Y.V. Yushkova, E.I. Chernyak, S.V. Morozov, O.I. Sinitsina, I.A. Grigor’ev, G.A. Nevinsky
    Conjugates of trolox and alpha-tocopheryl succinate with nitroxides: Synthesis, antioxidant and antitumor activity
    International Journal of Medicine and Pharmaceutical Sciences. 2015. Vol. 5. No. 3. P. 9-24.
  331. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  332. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  333. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  334. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  335. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  336. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  337. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  338. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  339. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  340. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  341. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  342. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  343. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  344. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  345. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  346. G.N. Kulipanov, E.G. Bagryanskaya, E.N. Chesnokov, Y.Y. Choporova, V.V. Gerasimov, Y.V. Getmanov, S.L. Kiselev, B.A. Knyazev, V.V. Kubarev, S.E. Peltek, V.M. Popik, T.V. Salikova, M.A. Scheglov, S.S. Seredniakov, O.A. Shevchenko, A.N. Skrinsky, S.L. Veber, N.A. Vinokurov
    Novosibirsk Free Electron Laser-Facility Description and Recent Experiments
    Terahertz Science and Technology, IEEE Transactions on, 2015, Vol. 5, N 5, pp. 798 - 809 doi:10.1109/TTHZ.2015.2453121, IF=2.177
  347. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  348. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  349. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  350. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  351. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  352. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  353. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  354. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  355. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  356. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  357. O. B. Shevelev, A.E. Akulov, A. S. Dotsenko, G. V. Kontsevaya, M. A. Zolotykh, L.A. Gerlinskaya, S. G. Veprev, T. N. Goryachkovskaya., N. A. Zhukova, N. A. Kolchanov, S. E. Pel'tek,M. P. Moshkin
    Neurometabolic Effect of Altaian Fungus Ganoderma lucidum (Reishi Mushroom) in Rats Under Moderate Alcohol Consumption
    Alcoholism: Clinical and Experimental Research, 2015, V. 39, N 7, pp 1128-1136. doi:10.1111/acer.12758, IF=3.205
  358. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, С.В. Блинкова, Г.А. Летягин, В.А. Багрянский, Ю.Н. Молин
    Времяразрешенный магнитный эффект как метод изучения ион-радикальных пар с быстрой эволюцией спинового состояния
    Доклады Академии Наук (Физ.химия), 2015, Т. 462, № 2, Сс. 178-181 (Time-resolved magnetic field effect as a method of studying radical pairs with rapid evolution of spin state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, S. V. Blinkova, G. A. Letyagin, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, May 2015, Volume 462, Issue 1, pp 103-106 doi:10.1134/S0012501615050024), IF=0.586
  359. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, С.В. Блинкова, Г.А. Летягин, В.А. Багрянский, Ю.Н. Молин
    Времяразрешенный магнитный эффект как метод изучения ион-радикальных пар с быстрой эволюцией спинового состояния
    Доклады Академии Наук (Физ.химия), 2015, Т. 462, № 2, Сс. 178-181 (Time-resolved magnetic field effect as a method of studying radical pairs with rapid evolution of spin state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, S. V. Blinkova, G. A. Letyagin, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, May 2015, Volume 462, Issue 1, pp 103-106 doi:10.1134/S0012501615050024), IF=0.586
  360. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, С.В. Блинкова, Г.А. Летягин, В.А. Багрянский, Ю.Н. Молин
    Времяразрешенный магнитный эффект как метод изучения ион-радикальных пар с быстрой эволюцией спинового состояния
    Доклады Академии Наук (Физ.химия), 2015, Т. 462, № 2, Сс. 178-181 (Time-resolved magnetic field effect as a method of studying radical pairs with rapid evolution of spin state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, S. V. Blinkova, G. A. Letyagin, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, May 2015, Volume 462, Issue 1, pp 103-106 doi:10.1134/S0012501615050024), IF=0.586
  361. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, С.В. Блинкова, Г.А. Летягин, В.А. Багрянский, Ю.Н. Молин
    Времяразрешенный магнитный эффект как метод изучения ион-радикальных пар с быстрой эволюцией спинового состояния
    Доклады Академии Наук (Физ.химия), 2015, Т. 462, № 2, Сс. 178-181 (Time-resolved magnetic field effect as a method of studying radical pairs with rapid evolution of spin state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, S. V. Blinkova, G. A. Letyagin, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, May 2015, Volume 462, Issue 1, pp 103-106 doi:10.1134/S0012501615050024), IF=0.586
  362. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, С.В. Блинкова, Г.А. Летягин, В.А. Багрянский, Ю.Н. Молин
    Времяразрешенный магнитный эффект как метод изучения ион-радикальных пар с быстрой эволюцией спинового состояния
    Доклады Академии Наук (Физ.химия), 2015, Т. 462, № 2, Сс. 178-181 (Time-resolved magnetic field effect as a method of studying radical pairs with rapid evolution of spin state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, S. V. Blinkova, G. A. Letyagin, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, May 2015, Volume 462, Issue 1, pp 103-106 doi:10.1134/S0012501615050024), IF=0.586
  363. Н.А. Жукова, Т.Г. Толстикова, И.В. Сорокина, М.П. Бирюкова, Д.Е. Семенов
    Патоморфология поражений печени различного генеза и их коррекция бетулоновой кислотой и ее амидом
    В сборнике: НОВЫЕ ИНФОРМАЦИОННЫЕ ТЕХНОЛОГИИ В МЕДИЦИНЕ, БИОЛОГИИ, ФАРМАКОЛОГИИ И ЭКОЛОГИИ материалы Международной конференции: Весенняя сессия. Под редакцией Е.Л. Глориозова. 2015. С. 251-263.
  364. Н.А. Жукова, Т.Г. Толстикова, И.В. Сорокина, М.П. Бирюкова, Д.Е. Семенов
    Патоморфология поражений печени различного генеза и их коррекция бетулоновой кислотой и ее амидом
    В сборнике: НОВЫЕ ИНФОРМАЦИОННЫЕ ТЕХНОЛОГИИ В МЕДИЦИНЕ, БИОЛОГИИ, ФАРМАКОЛОГИИ И ЭКОЛОГИИ материалы Международной конференции: Весенняя сессия. Под редакцией Е.Л. Глориозова. 2015. С. 251-263.
  365. С.В. Аньков, Т.Г. Толстикова, А.А. Онищук, Н.А. Жукова, М.В. Хвостов
    Токсико-фармакологические свойства наноаэрозольной формы нестероидных противовоспалительных средств
    В сборнике: НОВЫЕ ИНФОРМАЦИОННЫЕ ТЕХНОЛОГИИ В МЕДИЦИНЕ, БИОЛОГИИ, ФАРМАКОЛОГИИ И ЭКОЛОГИИ материалы Международной конференции: Весенняя сессия. Под редакцией Е.Л. Глориозова. 2015. С. 239-244.
  366. А.И. Говди, И.В. Сорокина, Д.С. Баев, А.О. Брызгалов, Т.Г. Толстикова, Г.А. Толстиков, С.Ф. Василевский
    Ацетиленовые производные амида бетулоновой кислоты - новая группа соединений, обладающих спазмолитической активностью
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1327. (Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity/ A. I. Govdi, I. V. Sorokina, D. S. Baev, A. O. Bryzgalov, T. G. Tolstikova, G. A. Tolstikov, S. F. Vasilevsky// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1327-1334 doi:10.1007/s11172-015-1013-4), IF=0.481
  367. А.И. Говди, И.В. Сорокина, Д.С. Баев, А.О. Брызгалов, Т.Г. Толстикова, Г.А. Толстиков, С.Ф. Василевский
    Ацетиленовые производные амида бетулоновой кислоты - новая группа соединений, обладающих спазмолитической активностью
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1327. (Acetylenic derivatives of betulonic acid amide as a new type of compounds possessing spasmolytic activity/ A. I. Govdi, I. V. Sorokina, D. S. Baev, A. O. Bryzgalov, T. G. Tolstikova, G. A. Tolstikov, S. F. Vasilevsky// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1327-1334 doi:10.1007/s11172-015-1013-4), IF=0.481
  368. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  369. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  370. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  371. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  372. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  373. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  374. И.П. Поздняков, Н.М. Сторожок, Н.П. Медяник, С.А. Креков, В.Е. Борисенко, А.П. Крысин, В.Ф. Плюснин, В.П. Гривин
    Фотохимия n-замещенных амидов салициловой кислоты
    Известия Академии наук. Серия химическая. 2015. № 6. С. 1319. (Photochemistry of N-substituted salicylic acid amides/ I. P. Pozdnyakov, N. M. Storozhok , N. P. Medyanik, S. A. Krekov, V. E. Borisenko, A. P. Krysin, V. F. Plyusnin, V. P. Grivin// Russian Chemical Bulletin, 2015, V. 64, N 6, pp 1319-1326 doi:10.1007/s11172-015-1012-5), IF=0.481
  375. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  376. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  377. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  378. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  379. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  380. V. A. D'yakonov, L.U. Dzhemileva , A.A. Makarov, A. R. Mulukova, D. S. Baev, E. K. Khusnutdinova., T. G. Tolstikova , U. M. Dzhemilev
    Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and II alpha inhibitory activity
    Bioorganic & Medicinal Chemistry Letters, V. 25, N 11, 2015, Pp 2405-2408 doi:10.1016/j.bmcl.2015.04.011, IF=2.42
  381. Д.И. Деревянко, В.В. Шелковников, Л.В. Эктова, Н.А. Орлова, Л.Н. Огнева, В.А. Лоскутов, Н.Г. Миронников, В.П. Корольков
    Механические и термооптические свойства силоксансодержащих тиольных и акрилатных олигомеров. получение дифракционных структур на их основе
    В книге: Олигомеры-2015 сборник тезисов докладов V Международной конференции-школы по химии и физикохимии олигомеров. отв. редактор М. П. Березин. Волгоград, 2015. С. 138.
  382. Д.И. Деревянко, В.В. Шелковников, Л.В. Эктова, Н.А. Орлова, Л.Н. Огнева, В.А. Лоскутов, Н.Г. Миронников, В.П. Корольков
    Механические и термооптические свойства силоксансодержащих тиольных и акрилатных олигомеров. получение дифракционных структур на их основе
    В книге: Олигомеры-2015 сборник тезисов докладов V Международной конференции-школы по химии и физикохимии олигомеров. отв. редактор М. П. Березин. Волгоград, 2015. С. 138.
  383. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  384. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  385. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  386. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  387. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  388. G.K. Mukusheva, P.Zh. Zhanymkhanova, A.Sh. Turysbaeva, M.A. Pokrovskii, M.M. Shakirov, A.G. Pokrovskii, E.E. Shul’ts, S.M. Adekenov
    Synthesis and Cytotoxicity of Pinostrobin Hydrazone Derivatives
    Chemistry of Natural Compounds, 2015, V. 51, N 3, pp 464-471 doi:10.1007/s10600-015-1316-6, IF=0.509
  389. M. Sartakov, Y. Deryabina, I. Komissarov
    Thermodynamic stability and chemical composition of humic acids of peat of the Khanty-Mansi area
    Proceedings of the XIV International Academic Congress " Fundamental and Applied Studies in the Modern World "(United Kingdom, Oxford, 23-25 May 2015) . “Oxford University Press”, 2015.
  390. M. Sartakov, Y. Deryabina, I. Komissarov
    Thermodynamic stability and chemical composition of humic acids of peat of the Khanty-Mansi area
    Proceedings of the XIV International Academic Congress " Fundamental and Applied Studies in the Modern World "(United Kingdom, Oxford, 23-25 May 2015) . “Oxford University Press”, 2015.
  391. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  392. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  393. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  394. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  395. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  396. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  397. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov, A.G. Mal'kina, B.A. Trofimov
    Reaction of 1-substituted benzimidazoles with acylacetylenes and water: ring-opening versus ring-expansion and isotopic effect of deuterium
    Tetrahedron, 2015, V. 71, N 19, Pp 2891-2899 doi:10.1016/j.tet.2015.03.056, IF=2.641
  398. V. V. Bardin, A. Yu. Shabalin, N. Yu. Adonin
    Weakly nucleophilic potassium aryltrifluoroborates in palladium-catalyzed Suzuki-Miyaura reactions: relative reactivity of K[4-RC6F4BF3] and the role of silver-assistance in acceleration of transmetallation
    Beilstein J. Org. Chem. 2015, 11, 608-616. doi:10.3762/bjoc.11.68, IF=2.762
  399. V. V. Bardin, A. Yu. Shabalin, N. Yu. Adonin
    Weakly nucleophilic potassium aryltrifluoroborates in palladium-catalyzed Suzuki-Miyaura reactions: relative reactivity of K[4-RC6F4BF3] and the role of silver-assistance in acceleration of transmetallation
    Beilstein J. Org. Chem. 2015, 11, 608-616. doi:10.3762/bjoc.11.68, IF=2.762
  400. Yu.S. Chistyachenko, A.V. Dushkin, N.E. Polyakov, M.V. Khvostov, T.G. Tolstikova, G.A. Tolstikov, N.Z. Lyakhov
    Polysaccharide arabinogalactan from larch Larix sibirica as carrier for molecules of salicylic and acetylsalicylic acid: preparation, physicochemical and pharmacological study
    Drug Delivery, 2015, Vol. 22, No. 3 , Pages 400-407 doi:10.3109/10717544.2014.884655, IF=2.558
  401. Yu.S. Chistyachenko, A.V. Dushkin, N.E. Polyakov, M.V. Khvostov, T.G. Tolstikova, G.A. Tolstikov, N.Z. Lyakhov
    Polysaccharide arabinogalactan from larch Larix sibirica as carrier for molecules of salicylic and acetylsalicylic acid: preparation, physicochemical and pharmacological study
    Drug Delivery, 2015, Vol. 22, No. 3 , Pages 400-407 doi:10.3109/10717544.2014.884655, IF=2.558
  402. Yu.S. Chistyachenko, A.V. Dushkin, N.E. Polyakov, M.V. Khvostov, T.G. Tolstikova, G.A. Tolstikov, N.Z. Lyakhov
    Polysaccharide arabinogalactan from larch Larix sibirica as carrier for molecules of salicylic and acetylsalicylic acid: preparation, physicochemical and pharmacological study
    Drug Delivery, 2015, Vol. 22, No. 3 , Pages 400-407 doi:10.3109/10717544.2014.884655, IF=2.558
  403. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  404. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  405. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  406. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  407. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  408. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  409. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  410. A. Zakharenko, T.Khomenko, S. Zhukova, O. Koval, O. Zakharova, R. Anarbaev, N. Lebedeva, D.Korchagina, N. Komarova, V.Vasiliev, J.Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    Synthesis and biological evaluation of novel tyrosyl-DNA phosphodiesterase 1 inhibitors with a benzopentathiepine moiety
    Bioorganic & Medicinal Chemistry, V. 23, N 9, 2015, Pp 2044-2052 doi:10.1016/j.bmc.2015.03.020, IF=2.793
  411. A. M. Sheveleva, I. K. Shundrina, S. L. Veber, A. D. Buhtojarova, V. V. Russkih, V. V. Shelkovnikov, M. V. Fedin, E. G. Bagryanskaya
    Inherent Microporosity and Photostability of Fluoroacrylic Polymer Films Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    Applied Magnetic Resonance, 2015, V.46, N 5, pp 523-540 doi:10.1007/s00723-014-0640-5, IF=1.167
  412. A. M. Sheveleva, I. K. Shundrina, S. L. Veber, A. D. Buhtojarova, V. V. Russkih, V. V. Shelkovnikov, M. V. Fedin, E. G. Bagryanskaya
    Inherent Microporosity and Photostability of Fluoroacrylic Polymer Films Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    Applied Magnetic Resonance, 2015, V.46, N 5, pp 523-540 doi:10.1007/s00723-014-0640-5, IF=1.167
  413. A. M. Sheveleva, I. K. Shundrina, S. L. Veber, A. D. Buhtojarova, V. V. Russkih, V. V. Shelkovnikov, M. V. Fedin, E. G. Bagryanskaya
    Inherent Microporosity and Photostability of Fluoroacrylic Polymer Films Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    Applied Magnetic Resonance, 2015, V.46, N 5, pp 523-540 doi:10.1007/s00723-014-0640-5, IF=1.167
  414. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  415. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  416. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  417. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  418. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  419. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  420. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  421. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  422. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  423. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  424. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  425. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  426. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, Т.Ю. Полякова, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, Н.И. Суслов, А.М. Дыгай
    Участие цамф- и ikk-зависимых сигнальных путей в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 601-604. (Role of cAMP- and IKK-2-Dependent Signaling Pathways in Functional Stimulation of Mesenchymal Progenitor Cells with Alkaloid Songorine/ G. N. Zyuz’kov , V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, T. Yu. Polyakova, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shul’ts, L. A. Stavrova, Ya. V. Burmina, N. I. Suslov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 642-645 doi:10.1007/s10517-015-3036-0), IF=0.358
  427. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  428. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  429. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  430. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  431. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  432. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  433. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  434. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Э.Э. Шульц, Г.Н. Зюзьков, С.Г. Аксиненко, О.Г. Афанасьева, А.В. Крапивин, Т.Г. Харина
    Анксиолитическая активность дитерпенового алкалоида зонгорина
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 5. С. 577-579. (Anxiolytic Activity of Diterpene Alkaloid Songorine/ Yu. V. Nesterova , T. N. Povet'eva, N. I. Suslov, E. E. Shults, G. N. Ziuz’kov, S. G. Aksinenko, O. G. Afanas’eva, A. V. Krapivin, T. G. Kharina// Bulletin of Experimental Biology and Medicine, September 2015, V. 159, N 5, pp 620-622 doi:10.1007/s10517-015-3029-z), IF=0.358
  435. Г.А. Толстиков, А.Г. Толстиков, Т.Г. Толстикова
    Берёза лечила и будет лечить
    В сборнике: Береза Сборник статей. РОССИЙСКАЯ АКАДЕМИЯ НАУК; Институт лингвистических исследований; Санкт-Петербургский научный центр. Санкт-Петербург, 2015. С. 83-126.
  436. Г.А. Толстиков, А.Г. Толстиков, Т.Г. Толстикова
    Берёза лечила и будет лечить
    В сборнике: Береза Сборник статей. РОССИЙСКАЯ АКАДЕМИЯ НАУК; Институт лингвистических исследований; Санкт-Петербургский научный центр. Санкт-Петербург, 2015. С. 83-126.
  437. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, V.I. Ovcharenko
    Electron paramagnetic resonance of switchable copper-nitroxide-based molecular magnets: An indispensable tool for intriguing systems
    Coordination Chemistry Reviews, 2015, V. 289–290, Pp 341-356, Special Issue: SI doi:10.1016/j.ccr.2014.11.015, IF=12.239
  438. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, V.I. Ovcharenko
    Electron paramagnetic resonance of switchable copper-nitroxide-based molecular magnets: An indispensable tool for intriguing systems
    Coordination Chemistry Reviews, 2015, V. 289–290, Pp 341-356, Special Issue: SI doi:10.1016/j.ccr.2014.11.015, IF=12.239
  439. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, V.I. Ovcharenko
    Electron paramagnetic resonance of switchable copper-nitroxide-based molecular magnets: An indispensable tool for intriguing systems
    Coordination Chemistry Reviews, 2015, V. 289–290, Pp 341-356, Special Issue: SI doi:10.1016/j.ccr.2014.11.015, IF=12.239
  440. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  441. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  442. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  443. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  444. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  445. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  446. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  447. M. Bermeshev, P. Chapala, V. Lakhtin, A. Genaev, M. Filatova, A. Peregudov, K. Utegenov, N. Ustynyuk, E. Finkelshtein
    Experimental and Theoretical Study of [2 σ+2 σ+2 π]-Cycloaddition of Quadricyclane and Ethylenes Containing Three Silyl-Groups
    Silicon , 2015б V. 7, N 2, Pp: 117-126, SI doi:10.1007/s12633-014-9263-6, IF=1.069
  448. Д.В. Белик, А.В. Шумейко, А.С. Емцев, М.В. Хвостов
    Биотехническая система для стимуляции гемопоэза при сниженном количестве клеток крови и возрастных изменениях объема красного костного мозга
    Научные исследования и разработки молодых ученых. 2015. № 4. С. 78-83.
  449. Д.В. Белик, А.В. Шумейко, А.С. Емцев, М.В. Хвостов
    Биотехническая система для стимуляции гемопоэза при сниженном количестве клеток крови и возрастных изменениях объема красного костного мозга
    Научные исследования и разработки молодых ученых. 2015. № 4. С. 78-83.
  450. Д.В. Белик, А.В. Шумейко, А.С. Емцев, М.В. Хвостов
    Биотехническая система для стимуляции гемопоэза при сниженном количестве клеток крови и возрастных изменениях объема красного костного мозга
    Научные исследования и разработки молодых ученых. 2015. № 4. С. 78-83.
  451. A.E. Dikalova, I.A. Kirilyuk, S.I. Dikalov
    Antihypertensive effect of mitochondria-targeted proxyl nitroxides
    Redox Biology, V. 4, 2015, Pp 355-362 doi:10.1016/j.redox.2014.12.012
  452. A.E. Dikalova, I.A. Kirilyuk, S.I. Dikalov
    Antihypertensive effect of mitochondria-targeted proxyl nitroxides
    Redox Biology, V. 4, 2015, Pp 355-362 doi:10.1016/j.redox.2014.12.012
  453. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  454. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  455. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  456. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  457. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  458. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  459. Ю.И. Рагино, В.А. Вавилин, Е.М. Стахнева, Н.Ф. Салахутдинов, О.Г. Сафронова, А.Б. Шинтяпина, В.В. Ляхович, Ю.П. Никитин
    Влияние симваглизина на экспрессию и ингибирование 3-гидрокси-3-метилглутарил коэнзим а редуктазы в печени крыс
    Атеросклероз. 2015. Т. 11. № 2. С. 14-19. (INFLUENCE OF simvaglyzin ON expression AND INHIBITION of HMG-CoA reductase in rats liver/ Yu.I. Ragino, V.A. Vavilin, E.M. Stakhneva, N.F. Salakhutdinov, O.G. Safronova, A.B. Shintyapina, V.V. Lyakhovich, Yu.P. Nikitin// Атеросклероз. 2015. Т. 11. № 2. С. 14-19.)
  460. S. Yu. Kurbakova, I. V. Il'ina, O. S. Mikhalchenko, M. A. Pokrovsky, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov
    The short way to chiral compounds with hexahydrofluoreno[9,1-bc]furan framework: Synthesis and cytotoxic activity
    Bioorganic & Medicinal Chemistry, V. 23, N 7, 2015, Pp 1472-1480. doi:10.1016/j.bmc.2015.02.013, IF=2.793
  461. S. Yu. Kurbakova, I. V. Il'ina, O. S. Mikhalchenko, M. A. Pokrovsky, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov
    The short way to chiral compounds with hexahydrofluoreno[9,1-bc]furan framework: Synthesis and cytotoxic activity
    Bioorganic & Medicinal Chemistry, V. 23, N 7, 2015, Pp 1472-1480. doi:10.1016/j.bmc.2015.02.013, IF=2.793
  462. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  463. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  464. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  465. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  466. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  467. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  468. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, O.V. Vysotskaya, O. A. Tarasova, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Dual reactivity of secondary phosphines and their chalcogenides towards 1-(vinyloxy)alkylferrocenes: the switch between α- and β-addition
    Tetrahedron, 2015, V. 71, N 13, Pp 1998-2003 doi:10.1016/j.tet.2015.02.011, IF=2.641
  469. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, I.A. Belousova, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.V. Glupov
    Leaf surface lipophilic compounds as one of the factors of silver birch chemical defense against larvae of gypsy moth
    PLos ONE. 2015, Vol. 10. No. 3, Article Number: e0121917 doi:10.1371/journal.pone.0121917, IF=3.234
  470. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, I.A. Belousova, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.V. Glupov
    Leaf surface lipophilic compounds as one of the factors of silver birch chemical defense against larvae of gypsy moth
    PLos ONE. 2015, Vol. 10. No. 3, Article Number: e0121917 doi:10.1371/journal.pone.0121917, IF=3.234
  471. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, I.A. Belousova, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.V. Glupov
    Leaf surface lipophilic compounds as one of the factors of silver birch chemical defense against larvae of gypsy moth
    PLos ONE. 2015, Vol. 10. No. 3, Article Number: e0121917 doi:10.1371/journal.pone.0121917, IF=3.234
  472. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, I.A. Belousova, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.V. Glupov
    Leaf surface lipophilic compounds as one of the factors of silver birch chemical defense against larvae of gypsy moth
    PLos ONE. 2015, Vol. 10. No. 3, Article Number: e0121917 doi:10.1371/journal.pone.0121917, IF=3.234
  473. V.V. Martemyanov, S.V. Pavlushin, I.M. Dubovskiy, I.A. Belousova, Yu.V. Yushkova, S.V. Morosov, E.I. Chernyak, V.V. Glupov
    Leaf surface lipophilic compounds as one of the factors of silver birch chemical defense against larvae of gypsy moth
    PLos ONE. 2015, Vol. 10. No. 3, Article Number: e0121917 doi:10.1371/journal.pone.0121917, IF=3.234
  474. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  475. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  476. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  477. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  478. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  479. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  480. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  481. T.S. Sukhikh, D.A. Bashirov, N.V. Kuratieva, A.I. Smolentsev, A.S. Bogomyakov, V.A. Burilov, A.R. Mustafina, A.V. Zibarev, S.N. Konchenko
    New NIR-emissive tetranuclear Er(III) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
    Dalton Trans., 2015, 44(12), 5727-5734 doi:10.1039/C4DT03878A, IF=4.197
  482. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  483. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  484. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  485. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  486. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  487. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  488. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  489. S.L. Veber, E.A. Suturina, M.V. Fedin, K.N. Boldyrev, K.Y. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, N.P. Gritsan, E.G. Bagryanskaya
    FTIR Study of Thermally Induced Magnetostructural Transitions in Breathing Crystals
    Inorg. Chem., 2015, 54 (7), pp 3446-3455 doi:10.1021/ic5031153, IF=4.762
  490. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, E.V. Tretyakov, E.M. Zueva, V.I. Ovcharenko
    One-electron electrochemical oxidation and reduction of the first C(sp2)-coupled nitronyl nitroxide diradical
    Tetrahedron Letters, V. 56, N 10, 4 March 2015, Pp. 1207-1210. doi:10.1016/j.tetlet.2015.01.134, IF=2.379
  491. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, E.V. Tretyakov, E.M. Zueva, V.I. Ovcharenko
    One-electron electrochemical oxidation and reduction of the first C(sp2)-coupled nitronyl nitroxide diradical
    Tetrahedron Letters, V. 56, N 10, 4 March 2015, Pp. 1207-1210. doi:10.1016/j.tetlet.2015.01.134, IF=2.379
  492. L.A. Shundrin, I.G. Irtegova, N.V. Vasilieva, E.V. Tretyakov, E.M. Zueva, V.I. Ovcharenko
    One-electron electrochemical oxidation and reduction of the first C(sp2)-coupled nitronyl nitroxide diradical
    Tetrahedron Letters, V. 56, N 10, 4 March 2015, Pp. 1207-1210. doi:10.1016/j.tetlet.2015.01.134, IF=2.379
  493. В.Д. Тихова, Т.Ф. Богданова, М.И. Дергачёва, В.П. Фадеева, Е.В. Каллас
    Сравнительный анализ гуминовых кислот палеопочв хакасии с использованием компьютерной программы ИК-ЭКСПЕРТ
    Теоретическая и прикладная экология. 2015. № 1. С. 24-27. (A comparative analysis of humic acids from Khakassia paleosols using ir-expert computer program/ Tikhova V.D., Bogdanova T.F., Dergacheva M.I., Fadeeva V.P., Kallas E.V.// Теоретическая и прикладная экология. 2015. № 1. С. 24-27.)
  494. В.Д. Тихова, Т.Ф. Богданова, М.И. Дергачёва, В.П. Фадеева, Е.В. Каллас
    Сравнительный анализ гуминовых кислот палеопочв хакасии с использованием компьютерной программы ИК-ЭКСПЕРТ
    Теоретическая и прикладная экология. 2015. № 1. С. 24-27. (A comparative analysis of humic acids from Khakassia paleosols using ir-expert computer program/ Tikhova V.D., Bogdanova T.F., Dergacheva M.I., Fadeeva V.P., Kallas E.V.// Теоретическая и прикладная экология. 2015. № 1. С. 24-27.)
  495. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective carvone hydrogenation to dihydrocarvone over titania supported gold catalyst
    Catalysis Today, Volume 241, Part B, 1 March 2015, Pages 189-194 doi:10.1016/j.cattod.2014.03.053, IF=3.893
  496. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective carvone hydrogenation to dihydrocarvone over titania supported gold catalyst
    Catalysis Today, Volume 241, Part B, 1 March 2015, Pages 189-194 doi:10.1016/j.cattod.2014.03.053, IF=3.893
  497. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective carvone hydrogenation to dihydrocarvone over titania supported gold catalyst
    Catalysis Today, Volume 241, Part B, 1 March 2015, Pages 189-194 doi:10.1016/j.cattod.2014.03.053, IF=3.893
  498. Yu.S. Demidova, E.V. Suslov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective carvone hydrogenation to dihydrocarvone over titania supported gold catalyst
    Catalysis Today, Volume 241, Part B, 1 March 2015, Pages 189-194 doi:10.1016/j.cattod.2014.03.053, IF=3.893
  499. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252
  500. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252
  501. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252
  502. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252
  503. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252
  504. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  505. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  506. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  507. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  508. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  509. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  510. E. G. Bagryanskaya, P. Bremond, T. Butscher, S. R. A. Marque, D. Parkhomenko, V. Roubaud, D. Siri, S. Viel
    Hydrogen-Bonding Effects for the C-ON Bond Homolysis and Reformation Reactions of Alkoxyamines
    Macromolecular Chemistry and Physics, V.216, N 5, pp 475-488, March 2015 doi:10.1002/macp.201400438, IF=2.616
  511. E.V. Suslov, D.V. Korchagina, M.A. Pokrovskii, A.G. Pokrovskii, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Cytotoxic Activity of Aza-Michael Reaction Products from Ethyl Sorbate and Heterocyclic Amines
    Chemistry of Natural Compounds, March 2015, Volume 51, Issue 2, pp 296-301 doi:10.1007/s10600-015-1264-1, IF=0.509
  512. E.V. Suslov, D.V. Korchagina, M.A. Pokrovskii, A.G. Pokrovskii, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Cytotoxic Activity of Aza-Michael Reaction Products from Ethyl Sorbate and Heterocyclic Amines
    Chemistry of Natural Compounds, March 2015, Volume 51, Issue 2, pp 296-301 doi:10.1007/s10600-015-1264-1, IF=0.509
  513. Н.А. Семенов, А.В. Лончаков, Н.П. Грицан, А.В. Зибарев
    Донорно-акцепторная координация анионов атомами халькогенов 1,2,5-халькогенадиазолов
    Известия Академии наук. Серия химическая. 2015. № 3. С. 499-510 (Donor-acceptor coordination of anions by chalcogen atoms of 1,2,5-chalcogenadiazoles/ N. A. Semenov, A. V. Lonchakov, N. P. Gritsan , A. V. Zibarev// Russian Chemical Bulletin, 2015, V. 64, N 3, pp 499-510 doi:10.1007/s11172-015-0893-7), IF=0.481
  514. Н.А. Семенов, А.В. Лончаков, Н.П. Грицан, А.В. Зибарев
    Донорно-акцепторная координация анионов атомами халькогенов 1,2,5-халькогенадиазолов
    Известия Академии наук. Серия химическая. 2015. № 3. С. 499-510 (Donor-acceptor coordination of anions by chalcogen atoms of 1,2,5-chalcogenadiazoles/ N. A. Semenov, A. V. Lonchakov, N. P. Gritsan , A. V. Zibarev// Russian Chemical Bulletin, 2015, V. 64, N 3, pp 499-510 doi:10.1007/s11172-015-0893-7), IF=0.481
  515. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  516. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  517. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  518. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  519. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  520. С.В. Ларионов, Т.Е. Кокина, Л.И. Мячина, Л.А. Глинская, М.И. Рахманова, Д.Ю. Наумов, А.В. Ткачев, А.М. Агафонцев
    Комплексы хлоридов Pd(II) и Zn(II) с α-аминооксимом - производным природного монотерпеноида (+)-3-карена, cодержащим фрагмент антрацена
    Координационная химия, 2015, Т. 41, N 3, стр. 144-150. (Complexes of Pd(II) and Zn(II) chlorides with anthracene-containing &aplha;-amino oxime derived from the naturally occurring monoterpenoid (+)-3-carene/ S. V. Larionov, T. E. Kokina, L. I. Myachina, L. A. Glinskaya, M. I. Rakhmanova, D. Yu. Naumov, A. V. Tkachev, A. M. Agafontsev// Russian Journal of Coordination Chemistry, March 2015, Volume 41, Issue 3, pp 162-168 doi:10.1134/S1070328415030070), IF=0.484
  521. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, D.S. Fadeev, Yu.V. Gatilov, A.A. Stepanov, N.V. Vasilieva, I.V. Alabugin
    Conformational Flexibility of Fused Tetracenedione Propellers Obtained from One-Pot Reductive Dimerization of Acetylenic Quinones
    J. Org. Chem., 2015, 80 (3), pp 1618-1631 doi:10.1021/jo502543b, IF=4.721
  522. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, D.S. Fadeev, Yu.V. Gatilov, A.A. Stepanov, N.V. Vasilieva, I.V. Alabugin
    Conformational Flexibility of Fused Tetracenedione Propellers Obtained from One-Pot Reductive Dimerization of Acetylenic Quinones
    J. Org. Chem., 2015, 80 (3), pp 1618-1631 doi:10.1021/jo502543b, IF=4.721
  523. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, D.S. Fadeev, Yu.V. Gatilov, A.A. Stepanov, N.V. Vasilieva, I.V. Alabugin
    Conformational Flexibility of Fused Tetracenedione Propellers Obtained from One-Pot Reductive Dimerization of Acetylenic Quinones
    J. Org. Chem., 2015, 80 (3), pp 1618-1631 doi:10.1021/jo502543b, IF=4.721
  524. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  525. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  526. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  527. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  528. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  529. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  530. M.N. Timofeeva, K.P. Volcho, O.S. Mikhalchenko, V.N. Panchenko, V.V. Krupskaya, S.V. Tsybulya, A. Gil, M.A. Vicente, N.F. Salakhutdinov
    Synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol over acid modified montmorillonite clays: Effect of acidity on the Prins cyclization
    Journal of Molecular Catalysis A: Chemical, V. 398 Pp 26-34 doi:10.1016/j.molcata.2014.11.016, IF=3.615
  531. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Antioxidant Activity and Cytotoxicity of Polyfluorinated 1, 4- Naphthoquinones with Alkylating Functions in the Quinone Moiety
    International Journal of Medicine and Pharmaceutical Sciences (IJMPS), 2015, V.5, N 1, Pp. 11-20 (Paper ID=IJMPSFEB20151)
  532. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Antioxidant Activity and Cytotoxicity of Polyfluorinated 1, 4- Naphthoquinones with Alkylating Functions in the Quinone Moiety
    International Journal of Medicine and Pharmaceutical Sciences (IJMPS), 2015, V.5, N 1, Pp. 11-20 (Paper ID=IJMPSFEB20151)
  533. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Antioxidant Activity and Cytotoxicity of Polyfluorinated 1, 4- Naphthoquinones with Alkylating Functions in the Quinone Moiety
    International Journal of Medicine and Pharmaceutical Sciences (IJMPS), 2015, V.5, N 1, Pp. 11-20 (Paper ID=IJMPSFEB20151)
  534. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  535. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  536. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  537. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  538. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  539. L.S. Konstantinova, E.A. Knyazeva, A.A. Nefyodov, P.S. Camacho, Sh.E. M. Ashbrook, J.D. Woollins, A.V. Zibarev, O.A. Rakitin
    Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles
    Tetrahedron Letters, V. 56, N 9, 25 February 2015, Pp 1107-1110. doi:10.1016/j.tetlet.2015.01.106, IF=2.379
  540. В.П. Сивцев, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, В.И. Аникеев
    Восстановление нитротолуолов в сверхкритическом изопропаноле в реакторе проточного типа в присутствии Al2O3
    Журнал физической химии. 2015. Т. 89. № 2. С. 220-224. (Reduction of nitrotoluenes in supercritical isopropanol over Al2O3/ V. P. Sivcev, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov, V. I. Anikeev// Russian Journal of Physical Chemistry A, February 2015, Volume 89, Issue 2, pp 202-206 doi:10.1134/S0036024415020314), IF=0.562
  541. А.С. Торозова, Э.М. Cульман, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Исследование мезопористых структур МСМ-41 и МСМ-48 в синтезе биологически активного вещества для лечения болезни Паркинсона
    Вестник Тверского государственного университета. Серия: Химия. 2015. № 2. С. 31-37.
  542. А.С. Торозова, Э.М. Cульман, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Исследование мезопористых структур МСМ-41 и МСМ-48 в синтезе биологически активного вещества для лечения болезни Паркинсона
    Вестник Тверского государственного университета. Серия: Химия. 2015. № 2. С. 31-37.
  543. А.С. Торозова, Э.М. Cульман, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Исследование мезопористых структур МСМ-41 и МСМ-48 в синтезе биологически активного вещества для лечения болезни Паркинсона
    Вестник Тверского государственного университета. Серия: Химия. 2015. № 2. С. 31-37.
  544. А.С. Торозова, Э.М. Cульман, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Исследование мезопористых структур МСМ-41 и МСМ-48 в синтезе биологически активного вещества для лечения болезни Паркинсона
    Вестник Тверского государственного университета. Серия: Химия. 2015. № 2. С. 31-37.
  545. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Гемостатический материал местного действия на основе окисленной целлюлозы
    Сибирский научный медицинский журнал. 2015, Т. 35. № 2. С. 11-15. (Local hemostatic agent based on oxidized cellulose/ A.R. Tarkova, A.M. Chernyavskiy, S.V. Morozov, I.A. Grigor’ev, N.I. Tkacheva, V.I. Rodionov// The Siberian Scientific Medical Journal, 2015, V. 35, № 2, Pp 11-15)
  546. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Гемостатический материал местного действия на основе окисленной целлюлозы
    Сибирский научный медицинский журнал. 2015, Т. 35. № 2. С. 11-15. (Local hemostatic agent based on oxidized cellulose/ A.R. Tarkova, A.M. Chernyavskiy, S.V. Morozov, I.A. Grigor’ev, N.I. Tkacheva, V.I. Rodionov// The Siberian Scientific Medical Journal, 2015, V. 35, № 2, Pp 11-15)
  547. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
  548. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
  549. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
  550. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
  551. G. K. Mukusheva, A. V. Lipeeva, P. Zh. Zhanymkhanova, E. E. Shults, Yu. V. Gatilov, M. M. Shakirov, S. M. Adekenov
    The flavanone pinostrobin in the synthesis of coumarin-chalcone hybrids with a triazole linker
    Chemistry of Heterocyclic Compounds, 2015, V. 51, N 2, pp 146-152 doi:10.1007/s10593-015-1672-y, IF=0.621
  552. G. K. Mukusheva, A. V. Lipeeva, P. Zh. Zhanymkhanova, E. E. Shults, Yu. V. Gatilov, M. M. Shakirov, S. M. Adekenov
    The flavanone pinostrobin in the synthesis of coumarin-chalcone hybrids with a triazole linker
    Chemistry of Heterocyclic Compounds, 2015, V. 51, N 2, pp 146-152 doi:10.1007/s10593-015-1672-y, IF=0.621
  553. G. K. Mukusheva, A. V. Lipeeva, P. Zh. Zhanymkhanova, E. E. Shults, Yu. V. Gatilov, M. M. Shakirov, S. M. Adekenov
    The flavanone pinostrobin in the synthesis of coumarin-chalcone hybrids with a triazole linker
    Chemistry of Heterocyclic Compounds, 2015, V. 51, N 2, pp 146-152 doi:10.1007/s10593-015-1672-y, IF=0.621
  554. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  555. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  556. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  557. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  558. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  559. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  560. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  561. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  562. A. Torozova, P. Maki-Arvela, A. Aho, N. Kumar, A. Smeds, M. Peurla, R. Sjoholm, I. Heinmaa, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Heterogeneous catalysis for transformation of biomass derived compounds beyond fuels: Synthesis of monoterpenoid dioxinols with analgesic activity
    Journal of Molecular Catalysis A: Chemical, Volume 397, February 2015, Pages 48-55 doi:10.1016/j.molcata.2014.10.023, IF=3.615
  563. Yu.P. Bogza, A.L. Katsiel’, A.N. Sharypova, T.G. Tolstikova, A.S. Fisyuk
    Synthesis and Biological Activity of 4H-Thieno[3,2-c]Chromene Derivatives
    Chemistry of Heterocyclic Compounds, March 2015, Volume 50, Issue 12, pp 1712-1718 doi:10.1007/s10593-015-1642-4, IF=0.621
  564. Yu.P. Bogza, A.L. Katsiel’, A.N. Sharypova, T.G. Tolstikova, A.S. Fisyuk
    Synthesis and Biological Activity of 4H-Thieno[3,2-c]Chromene Derivatives
    Chemistry of Heterocyclic Compounds, March 2015, Volume 50, Issue 12, pp 1712-1718 doi:10.1007/s10593-015-1642-4, IF=0.621
  565. Yu.P. Bogza, A.L. Katsiel’, A.N. Sharypova, T.G. Tolstikova, A.S. Fisyuk
    Synthesis and Biological Activity of 4H-Thieno[3,2-c]Chromene Derivatives
    Chemistry of Heterocyclic Compounds, March 2015, Volume 50, Issue 12, pp 1712-1718 doi:10.1007/s10593-015-1642-4, IF=0.621
  566. Yu.P. Bogza, A.L. Katsiel’, A.N. Sharypova, T.G. Tolstikova, A.S. Fisyuk
    Synthesis and Biological Activity of 4H-Thieno[3,2-c]Chromene Derivatives
    Chemistry of Heterocyclic Compounds, March 2015, Volume 50, Issue 12, pp 1712-1718 doi:10.1007/s10593-015-1642-4, IF=0.621
  567. M.B. Bushuev, Yu.V. Gatilov, V.P. Krivopalov, O.P. Shkurko
    Tetra- and polynuclear cadmium(II) complexes with 3,5-bis(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine. Synthesis, polymorphism, lone pair-π interactions and luminescence
    Inorganica Chimica Acta, 2015, V. 425, pp. 182-188 doi:10.1016/j.ica.2014.10.017, IF=2.046
  568. Н.Г. Миронников, Д.И. Деревянко, В.П. Корольков, В.В. Шелковников
    Сканирующая лазерная запись на пленках гибридного фотополимерного материала на основе тиол-силоксан-акрилатных олигомеров
    В сборнике: IV Международная конференция по фотонике и информационной оптике Сборник научных трудов. Москва, 2015. С. 88-89.
  569. Н.Г. Миронников, Д.И. Деревянко, В.П. Корольков, В.В. Шелковников
    Сканирующая лазерная запись на пленках гибридного фотополимерного материала на основе тиол-силоксан-акрилатных олигомеров
    В сборнике: IV Международная конференция по фотонике и информационной оптике Сборник научных трудов. Москва, 2015. С. 88-89.
  570. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  571. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  572. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  573. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  574. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  575. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  576. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  577. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  578. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  579. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  580. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  581. A. Torozova, P. Maki-Arvela, N.D. Shcherban, N. Kumar, A. Aho, M. Stekrova, K. Maduna Valkaj, P. Sinitsyna, S.M. Filonenko, P.S. Yaremov, V.G. Ilyin, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Effect of acidity and texture of micro-, mesoporous and hybrid micromesoporous materials on the synthesis of paramenthanic diol exhibiting anti-Parkinson activity
    Catalysis, Structure & Reactivity, Volume 1, Issue 3, 2015, pages 146-154 doi:10.1179/2055075815Y.0000000009
  582. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  583. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  584. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  585. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  586. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  587. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  588. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  589. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  590. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  591. А.С. Кабанов, Л.Н. Шишкина, О.Ю. Мазурков, М.О. Скарнович, Н.И. Бормотов, О.А. Серова, Ал.А. Сергеев, Ар.А. Сергеев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Оценка лечебно-профилактической эффективности химического соединения НИОХ-14 в отношении вируса эктромелии in vivo
    Журнал микробиологии, эпидемиологии и иммунобиологии, 2015, (1), 58 - 65 (Evaluation of therapeutic-prophylactic effectiveness of chemical compound NIOC-14 against ectromelia virus in vivo/ Kabanov, A.S., Shishkina, L.N., Mazurkov, O.Yu., Skarnovich, M.O., Bormotov, N.I., Serova, O.A., Sergeev, Al.A., Sergeev, Ar.A., Selivanov, B.A., Tikhonov, A.Ya., Agafonov, A.P., Sergeev, A.N.// Journal of the microbiology, epidemiology and immunobiology, 2015,(1), pp 58-65)
  592. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко
    Исследование механических и термооптических свойств нового гибридного фотополимерного материала
    Интерэкспо Гео-Сибирь. 2015. Т. 5. № 1. С. 59-64.
  593. Н.Г. Миронников, В.П. Корольков, Д.И. Деревянко
    Исследование механических и термооптических свойств нового гибридного фотополимерного материала
    Интерэкспо Гео-Сибирь. 2015. Т. 5. № 1. С. 59-64.
  594. Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, В.А. Мордвинов
    Роль opisthorchis felineus в индукции рака желчных протоков
    Паразитология. 2015. Т. 49. № 1. С. 3-11.
  595. Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, В.А. Мордвинов
    Роль opisthorchis felineus в индукции рака желчных протоков
    Паразитология. 2015. Т. 49. № 1. С. 3-11.
  596. Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, В.А. Мордвинов
    Роль opisthorchis felineus в индукции рака желчных протоков
    Паразитология. 2015. Т. 49. № 1. С. 3-11.
  597. Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, В.А. Мордвинов
    Роль opisthorchis felineus в индукции рака желчных протоков
    Паразитология. 2015. Т. 49. № 1. С. 3-11.
  598. Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, В.А. Мордвинов
    Роль opisthorchis felineus в индукции рака желчных протоков
    Паразитология. 2015. Т. 49. № 1. С. 3-11.
  599. A.I. Govdi, N.V. Sokolova, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, V.I. Mamatyuk, D.S. Fadeev, S.F. Vasilevsky, V.G. Nenajdenko
    Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
    MedChemComm, 2015, V.6, N 1, pp. 230-238. doi:10.1039/c4md00236a, IF=2.495
  600. A.I. Govdi, N.V. Sokolova, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, V.I. Mamatyuk, D.S. Fadeev, S.F. Vasilevsky, V.G. Nenajdenko
    Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
    MedChemComm, 2015, V.6, N 1, pp. 230-238. doi:10.1039/c4md00236a, IF=2.495
  601. A.I. Govdi, N.V. Sokolova, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, V.I. Mamatyuk, D.S. Fadeev, S.F. Vasilevsky, V.G. Nenajdenko
    Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
    MedChemComm, 2015, V.6, N 1, pp. 230-238. doi:10.1039/c4md00236a, IF=2.495
  602. A.I. Govdi, N.V. Sokolova, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, V.I. Mamatyuk, D.S. Fadeev, S.F. Vasilevsky, V.G. Nenajdenko
    Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
    MedChemComm, 2015, V.6, N 1, pp. 230-238. doi:10.1039/c4md00236a, IF=2.495
  603. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  604. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  605. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  606. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  607. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  608. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  609. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  610. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  611. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  612. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  613. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  614. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
  615. И.Г. Боярских, О.В. Чанкина, А.И. Сысо, В.Г. Васильев
    Тренды содержания химических элементов в листьях LONICERA CAERULEA (CAPRIFOLIACEAE) в связи с их вторичным метаболизмом в природных популяциях горного алтая
    Известия Российской академии наук. Серия физическая. 2015. Т. 79. № 1. С. 106. (Trends in the content of chemical elements in leaves of Lonicers Caerulea (Caprifoliaceae) in connection with their secondary metabolism in the natural populations of the Altai Mountains/ I. G. Boyarskikh, O. V. Chankina, A. I. Syso, V. G. Vasiliev// Bulletin of the Russian Academy of Sciences: Physics, January 2015, Volume 79, Issue 1, pp 94-97 doi:10.3103/S1062873815010086)
  616. И.Г. Боярских, О.В. Чанкина, А.И. Сысо, В.Г. Васильев
    Тренды содержания химических элементов в листьях LONICERA CAERULEA (CAPRIFOLIACEAE) в связи с их вторичным метаболизмом в природных популяциях горного алтая
    Известия Российской академии наук. Серия физическая. 2015. Т. 79. № 1. С. 106. (Trends in the content of chemical elements in leaves of Lonicers Caerulea (Caprifoliaceae) in connection with their secondary metabolism in the natural populations of the Altai Mountains/ I. G. Boyarskikh, O. V. Chankina, A. I. Syso, V. G. Vasiliev// Bulletin of the Russian Academy of Sciences: Physics, January 2015, Volume 79, Issue 1, pp 94-97 doi:10.3103/S1062873815010086)
  617. И.Г. Боярских, О.В. Чанкина, А.И. Сысо, В.Г. Васильев
    Тренды содержания химических элементов в листьях LONICERA CAERULEA (CAPRIFOLIACEAE) в связи с их вторичным метаболизмом в природных популяциях горного алтая
    Известия Российской академии наук. Серия физическая. 2015. Т. 79. № 1. С. 106. (Trends in the content of chemical elements in leaves of Lonicers Caerulea (Caprifoliaceae) in connection with their secondary metabolism in the natural populations of the Altai Mountains/ I. G. Boyarskikh, O. V. Chankina, A. I. Syso, V. G. Vasiliev// Bulletin of the Russian Academy of Sciences: Physics, January 2015, Volume 79, Issue 1, pp 94-97 doi:10.3103/S1062873815010086)
  618. Душкин А.В., Чистяченко Ю.С., Комаров Д.А., Хвостов М.В., Толстикова Т.Г., Журко И.Ф., Кирилюк И.А., Григорьев И.А., Ляхов Н.З.
    О механизме увеличения мембранной проницаемости веществ из их межмолекулярных комплексов с полисахаридом арабиногалактаном из лиственниц larches Larix sibirica и Larix gmelinii
    Доклады Академии наук (БИОХИМИЯ, БИОФИЗИКА, МОЛЕКУЛЯРНАЯ БИОЛОГИЯ), , Т. 460, No. 1, Стр. 107-110. (About the mechanism of membrane permeability enhancement by substances in their intermolecular complexes with polysaccharide arabinogalactan from larches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, D. A. Komarov, M. V. Khvostov, T. G. Tolstikova, I. F. Zhurko, I. A. Kirilyuk, I. A. Grigor’ev, N. Z. Lyakhov// Doklady Biochemistry and Biophysics, January 2015, Volume 460, Issue 1, pp 9-12 doi:10.1134/S1607672915010020), IF=0.343
  619. Душкин А.В., Чистяченко Ю.С., Комаров Д.А., Хвостов М.В., Толстикова Т.Г., Журко И.Ф., Кирилюк И.А., Григорьев И.А., Ляхов Н.З.
    О механизме увеличения мембранной проницаемости веществ из их межмолекулярных комплексов с полисахаридом арабиногалактаном из лиственниц larches Larix sibirica и Larix gmelinii
    Доклады Академии наук (БИОХИМИЯ, БИОФИЗИКА, МОЛЕКУЛЯРНАЯ БИОЛОГИЯ), , Т. 460, No. 1, Стр. 107-110. (About the mechanism of membrane permeability enhancement by substances in their intermolecular complexes with polysaccharide arabinogalactan from larches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, D. A. Komarov, M. V. Khvostov, T. G. Tolstikova, I. F. Zhurko, I. A. Kirilyuk, I. A. Grigor’ev, N. Z. Lyakhov// Doklady Biochemistry and Biophysics, January 2015, Volume 460, Issue 1, pp 9-12 doi:10.1134/S1607672915010020), IF=0.343
  620. Душкин А.В., Чистяченко Ю.С., Комаров Д.А., Хвостов М.В., Толстикова Т.Г., Журко И.Ф., Кирилюк И.А., Григорьев И.А., Ляхов Н.З.
    О механизме увеличения мембранной проницаемости веществ из их межмолекулярных комплексов с полисахаридом арабиногалактаном из лиственниц larches Larix sibirica и Larix gmelinii
    Доклады Академии наук (БИОХИМИЯ, БИОФИЗИКА, МОЛЕКУЛЯРНАЯ БИОЛОГИЯ), , Т. 460, No. 1, Стр. 107-110. (About the mechanism of membrane permeability enhancement by substances in their intermolecular complexes with polysaccharide arabinogalactan from larches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, D. A. Komarov, M. V. Khvostov, T. G. Tolstikova, I. F. Zhurko, I. A. Kirilyuk, I. A. Grigor’ev, N. Z. Lyakhov// Doklady Biochemistry and Biophysics, January 2015, Volume 460, Issue 1, pp 9-12 doi:10.1134/S1607672915010020), IF=0.343
  621. Е.А. Куликова, М.А. Тихонова, К.П. Волчо, Т.М. Хоменко, Н.Ф. Салахутдинов, А.В. Куликов, Н.К. Попова
    Сравнение поведенческих эффектов флуоксетина, имипрамина и нового психотропного препарата ТС-2153 у мышей, различающихся по наследственной предрасположенности к каталепсии
    Журнал высшей нервной деятельности им. И.П. Павлова. 2015. Т. 65. № 1. С. 105-112 (Comparison of Behavioral Effects of Fluoxetine, Imipramine and New Psychotropic Drug TC-2153 on Mice with Hereditary Predisposition to Catalepsy/ E. A. Kulikova , M. A.Nikhonova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA , 2015, V.65, N 1, Pp. 105-112 doi:10.7868/S0044467715010050)
  622. Е.А. Куликова, М.А. Тихонова, К.П. Волчо, Т.М. Хоменко, Н.Ф. Салахутдинов, А.В. Куликов, Н.К. Попова
    Сравнение поведенческих эффектов флуоксетина, имипрамина и нового психотропного препарата ТС-2153 у мышей, различающихся по наследственной предрасположенности к каталепсии
    Журнал высшей нервной деятельности им. И.П. Павлова. 2015. Т. 65. № 1. С. 105-112 (Comparison of Behavioral Effects of Fluoxetine, Imipramine and New Psychotropic Drug TC-2153 on Mice with Hereditary Predisposition to Catalepsy/ E. A. Kulikova , M. A.Nikhonova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA , 2015, V.65, N 1, Pp. 105-112 doi:10.7868/S0044467715010050)
  623. Е.А. Куликова, М.А. Тихонова, К.П. Волчо, Т.М. Хоменко, Н.Ф. Салахутдинов, А.В. Куликов, Н.К. Попова
    Сравнение поведенческих эффектов флуоксетина, имипрамина и нового психотропного препарата ТС-2153 у мышей, различающихся по наследственной предрасположенности к каталепсии
    Журнал высшей нервной деятельности им. И.П. Павлова. 2015. Т. 65. № 1. С. 105-112 (Comparison of Behavioral Effects of Fluoxetine, Imipramine and New Psychotropic Drug TC-2153 on Mice with Hereditary Predisposition to Catalepsy/ E. A. Kulikova , M. A.Nikhonova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA , 2015, V.65, N 1, Pp. 105-112 doi:10.7868/S0044467715010050)
  624. Е.А. Куликова, М.А. Тихонова, К.П. Волчо, Т.М. Хоменко, Н.Ф. Салахутдинов, А.В. Куликов, Н.К. Попова
    Сравнение поведенческих эффектов флуоксетина, имипрамина и нового психотропного препарата ТС-2153 у мышей, различающихся по наследственной предрасположенности к каталепсии
    Журнал высшей нервной деятельности им. И.П. Павлова. 2015. Т. 65. № 1. С. 105-112 (Comparison of Behavioral Effects of Fluoxetine, Imipramine and New Psychotropic Drug TC-2153 on Mice with Hereditary Predisposition to Catalepsy/ E. A. Kulikova , M. A.Nikhonova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA , 2015, V.65, N 1, Pp. 105-112 doi:10.7868/S0044467715010050)
  625. Yu.V. Zagurskaya, V.G. Vasil’ev, A.L. Bogatyrev, I.I. Bayandina, T.P. Kukina
    Flavonoids and Hydroxycinnamic Acids from Leonurus quinquelobatus
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 156-157 doi:10.1007/s10600-015-1227-6, IF=0.509
  626. Yu.V. Zagurskaya, V.G. Vasil’ev, A.L. Bogatyrev, I.I. Bayandina, T.P. Kukina
    Flavonoids and Hydroxycinnamic Acids from Leonurus quinquelobatus
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 156-157 doi:10.1007/s10600-015-1227-6, IF=0.509
  627. Yu.V. Zagurskaya, V.G. Vasil’ev, A.L. Bogatyrev, I.I. Bayandina, T.P. Kukina
    Flavonoids and Hydroxycinnamic Acids from Leonurus quinquelobatus
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 156-157 doi:10.1007/s10600-015-1227-6, IF=0.509
  628. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509
  629. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509
  630. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509
  631. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509
  632. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  633. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  634. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  635. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  636. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  637. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  638. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  639. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  640. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  641. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  642. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  643. Г.Н. Зюзьков, В.В. Жданов, Л.А. Мирошниченко, Е.В. Удут, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, Л.А. Ставрова, Я.В. Бурмина, А.М. Дыгай
    Участие PI3K, МАРK ERK1/2 и р38 в стимуляции функций мезенхимных клеток–предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2015. Т. 159. № 1. С. 67-70. (Involvement of PI3K, MAPK ERK1/2 and p38 in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, L. A. Miroshnichenko, E. V. Udut, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. V. Udut, T. G. Tolstikova, E. E. Shults, L. A. Stavrova, Ya. V. Burmina, A. M. Dygai// Bulletin of Experimental Biology and Medicine, 2015, V. 159, N 1, pp 58-61 doi:10.1007/s10517-015-2889-6), IF=0.358
  644. С.Ф. Василевский, Д.С. Баранов, А.И. Говди, И.В. Сорокина, Т.Г. Толстикова
    Синтез и противовоспалительная активность пропаргиламиновых производных нафтохинонлевопимаровой кислоты
    Биоорганическая химия. 2015. Т. 41. № 1. С. 97-101. (The synthesis and anti-inflammatory activity of propargylamino derivatives of naphthoquinonlevopimaric acid/ S. F. Vasilevsky, D. S. Baranov, A. I. Govdi, I. V. Sorokina, T. G. Tolstikova// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 83-86 doi:10.1134/S1068162015010148), IF=0.535
  645. С.Ф. Василевский, Д.С. Баранов, А.И. Говди, И.В. Сорокина, Т.Г. Толстикова
    Синтез и противовоспалительная активность пропаргиламиновых производных нафтохинонлевопимаровой кислоты
    Биоорганическая химия. 2015. Т. 41. № 1. С. 97-101. (The synthesis and anti-inflammatory activity of propargylamino derivatives of naphthoquinonlevopimaric acid/ S. F. Vasilevsky, D. S. Baranov, A. I. Govdi, I. V. Sorokina, T. G. Tolstikova// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 83-86 doi:10.1134/S1068162015010148), IF=0.535
  646. С.Ф. Василевский, Д.С. Баранов, А.И. Говди, И.В. Сорокина, Т.Г. Толстикова
    Синтез и противовоспалительная активность пропаргиламиновых производных нафтохинонлевопимаровой кислоты
    Биоорганическая химия. 2015. Т. 41. № 1. С. 97-101. (The synthesis and anti-inflammatory activity of propargylamino derivatives of naphthoquinonlevopimaric acid/ S. F. Vasilevsky, D. S. Baranov, A. I. Govdi, I. V. Sorokina, T. G. Tolstikova// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 83-86 doi:10.1134/S1068162015010148), IF=0.535
  647. М.П. Давыдова, И.В. Сорокина, Т.Г. Толстикова, В.И. Маматюк, Д.С. Фадеев, С.Ф. Василевский
    Синтез новых аналогов комбретастатина A-4 и изучение их противовоспалительной активности
    Биоорганическая химия. 2015. Т. 41. № 1. С. 82-89. (Synthesis of new combretastatin A-4 analogues and study of their anti-inflammatory activity/ M. P. Davydova, I. V. Sorokina, T. G. Tolstikova, V. I. Mamatyuk, D. S. Fadeev, S. F. Vasilevsky// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 70-76 doi:10.1134/S1068162015010033), IF=0.535
  648. М.П. Давыдова, И.В. Сорокина, Т.Г. Толстикова, В.И. Маматюк, Д.С. Фадеев, С.Ф. Василевский
    Синтез новых аналогов комбретастатина A-4 и изучение их противовоспалительной активности
    Биоорганическая химия. 2015. Т. 41. № 1. С. 82-89. (Synthesis of new combretastatin A-4 analogues and study of their anti-inflammatory activity/ M. P. Davydova, I. V. Sorokina, T. G. Tolstikova, V. I. Mamatyuk, D. S. Fadeev, S. F. Vasilevsky// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 70-76 doi:10.1134/S1068162015010033), IF=0.535
  649. Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, А.Я. Тихонов, В.А. Рябинин, А.Н. Синяков
    Синтез нуклеозидов, содержащих фотолабильную 2-(2-нитрофенил)пропоксикарбонильную группу
    Журнал органической химии. 2015. Т. 51. № 1. С. 142-144. (Synthesis of nucleosides containing a photolabile 2-(2-nitrophenyl)propoxycarbonyl group/ E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, A. Ya. Tikhonov, V. A. Ryabinin, A. N. Sinyakov// Russian Journal of Organic Chemistry, January 2015, Volume 51, Issue 1, pp 141-144 doi:10.1134/S1070428015010297), IF=0.658
  650. Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, А.Я. Тихонов, В.А. Рябинин, А.Н. Синяков
    Синтез нуклеозидов, содержащих фотолабильную 2-(2-нитрофенил)пропоксикарбонильную группу
    Журнал органической химии. 2015. Т. 51. № 1. С. 142-144. (Synthesis of nucleosides containing a photolabile 2-(2-nitrophenyl)propoxycarbonyl group/ E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, A. Ya. Tikhonov, V. A. Ryabinin, A. N. Sinyakov// Russian Journal of Organic Chemistry, January 2015, Volume 51, Issue 1, pp 141-144 doi:10.1134/S1070428015010297), IF=0.658
  651. Н.И. Белоусова, Н.А. Некратова, А.В. Ткачев, М.Н. Шурупова
    Эфирное масло Shizonepeta multifida (Республика Хакасия)
    в Кн. «Лекарственные растения: фундаментальные и прикладные проблемы». Новосибирск: Золотой колос, 2015 (ISBN 978-5-94477-170-4) - С. 59-63.
  652. Н.И. Белоусова, Н.А. Некратова, А.В. Ткачев, М.Н. Шурупова
    Эфирное масло Shizonepeta multifida (Республика Хакасия)
    в Кн. «Лекарственные растения: фундаментальные и прикладные проблемы». Новосибирск: Золотой колос, 2015 (ISBN 978-5-94477-170-4) - С. 59-63.
  653. Н.И. Белоусова, Н.А. Некратова, А.В. Ткачев, М.Н. Шурупова
    Эфирное масло Shizonepeta multifida (Республика Хакасия)
    в Кн. «Лекарственные растения: фундаментальные и прикладные проблемы». Новосибирск: Золотой колос, 2015 (ISBN 978-5-94477-170-4) - С. 59-63.
  654. E. Chugunova, V. Samsonov, T. Gerasimova, T. Rybalova, I. Bagryanskaya
    Synthesis and some properties of 2H-benzimidazole 1,3-dioxides
    Tetrahedron, V. 71, N 39, 30 September 2015, Pp 7233-7244 doi:10.1016/j.tet.2015.03.096, IF=2.641
  655. E. Chugunova, V. Samsonov, T. Gerasimova, T. Rybalova, I. Bagryanskaya
    Synthesis and some properties of 2H-benzimidazole 1,3-dioxides
    Tetrahedron, V. 71, N 39, 30 September 2015, Pp 7233-7244 doi:10.1016/j.tet.2015.03.096, IF=2.641
  656. Фролова Т.С., Кукина Т.П., Синицина О.И.
    Генотоксические и мутагенные свойства бетулиновой и бетулоновой кислот
    Биоорганическая химия. 2015. Т. 41. № 4. С. 462-467. (Genotoxic and mutagenic properties of synthetic betulinic acid and betulonic acid/ T. S. Frolova, T. P. Kukina, O. I. Sinitsyna// Russian Journal of Bioorganic Chemistry, July 2015, V. 41, N 4, pp 409-413 doi:10.1134/S1068162015040056), IF=0.535

2014

Reviews, articles

  1. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  2. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  3. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  4. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  5. А.С. Торозова, Э.М. Сульман, П.В. Синицына, П. Мяки-Арвела, К.П. Волчо, Д.Ю. Мурзин
    Применение цеолитов в процессе превращения эпоксида вербенола с образованием биологически активного вещества с обезболивающим эффектом
    В книге: Ресурсо- и энергосберегающие технологии в химической и нефтехимической промышленности VII Международная конференция Российского химического общества имени Д.И. Менделеева, посвященная 100-летию со дня рождения Л.А. Костандова. Редакционная коллегия: А.Ю. Цивадзе, Е.Г. Винокуров, Н.Р. Косинова, Н.Н. Кулов. 2015. С. 88-90.
  6. G.Zh. Baisalova, N.A. Pankrushina, D.V. Domrachev, O.I. Salnikova, R.Sh. Erkassov
    Volatile Constituents of Halimodendron halodendron Voss. Growing in Kazakhstan
    Journal of Essential Oil Bearing Plants, 2014, V.. 17, N 5, P. 886-890. doi:10.1080/0972060X.2014.935074, IF=0.187
  7. G.Zh. Baisalova, N.A. Pankrushina, D.V. Domrachev, O.I. Salnikova, R.Sh. Erkassov
    Volatile Constituents of Halimodendron halodendron Voss. Growing in Kazakhstan
    Journal of Essential Oil Bearing Plants, 2014, V.. 17, N 5, P. 886-890. doi:10.1080/0972060X.2014.935074, IF=0.187
  8. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, O.I. Kiselev, N.F. Salakhutdinov
    Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
    Bioorganic & Medicinal Chemistry, V. 22, N 24, 15 December 2014, Pp 6826-6836. doi:10.1016/j.bmc.2014.10.033, IF=2.95
  9. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, O.I. Kiselev, N.F. Salakhutdinov
    Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
    Bioorganic & Medicinal Chemistry, V. 22, N 24, 15 December 2014, Pp 6826-6836. doi:10.1016/j.bmc.2014.10.033, IF=2.95
  10. A.A. Shtro, V.V. Zarubaev, O.A. Luzina, D.N. Sokolov, O.I. Kiselev, N.F. Salakhutdinov
    Novel derivatives of usnic acid effectively inhibiting reproduction of influenza A virus
    Bioorganic & Medicinal Chemistry, V. 22, N 24, 15 December 2014, Pp 6826-6836. doi:10.1016/j.bmc.2014.10.033, IF=2.95
  11. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  12. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  13. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  14. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  15. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  16. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  17. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  18. A.A. Onischuk, T.G. Tolstikova, A.M. Baklanov, M.V. Khvostov, I.V. Sorokina, N.A. Zhukova, S.V. An’kov, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin, G. Steven Huang
    Generation, inhalation delivery and anti-hypertensive effect of nisoldipine nanoaerosol
    J. Aerosol Science, 2014 , V. 78, P. 41-54. doi:10.1016/j.jaerosci.2014.08.004, IF=2.704
  19. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  20. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  21. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  22. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  23. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  24. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  25. Ю.С. Чистяченко, А.В. Душкин, М.В. Хвостов, Н.А. Жукова, Т.Г. Толстикова, А.И. Белоусов, М.Ю. Пахарукова, А.В. Катохин, В.А. Мордвинов, С.С. Халиков
    Перспективный противоописторхозный препарат на основе албендазола
    Теория и практика борьбы с паразитарными болезнями. 2014. № 15. С. 339-342., 2014, 15, 339-342
  26. I. Il’ina, O. Mikhalchenko, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov, E. Pokushalov
    Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
    Medicinal Chemistry Research, 2014, V. 23, N 12, pp 5063-5073 doi:10.1007/s00044-014-1071-4, IF=1.402
  27. Т.С. Морозкова, Л.А. Богданова, Д.Е. Семенов, Н.А. Жукова, Н.А. Попова
    Мыши линии PT/Y чувствительны к ингибирующему глюкокортикоидную индукцию тирозинаминотрансферазы и гепатоканцерагенному действию орто-аминоазотолуола
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 12. С. 757-761. (PT/Y Mice Are Sensitive to the Inhibitory Effect of o-Aminoazotoluene on Glucocorticoid Induction of Tyrosine Aminotransferase and Its Hepatocarcinogenic Effect/ T. S. Morozkova, L. A. Bogdanova, D. E. Semenov, N. A. Zhukova, N. A. Popova// Bulletin of Experimental Biology and Medicine, April 2015, V. 158, N 6, pp 789-793 doi:10.1007/s10517-015-2863-3), IF=0.365
  28. Т.С. Морозкова, Л.А. Богданова, Д.Е. Семенов, Н.А. Жукова, Н.А. Попова
    Мыши линии PT/Y чувствительны к ингибирующему глюкокортикоидную индукцию тирозинаминотрансферазы и гепатоканцерагенному действию орто-аминоазотолуола
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 12. С. 757-761. (PT/Y Mice Are Sensitive to the Inhibitory Effect of o-Aminoazotoluene on Glucocorticoid Induction of Tyrosine Aminotransferase and Its Hepatocarcinogenic Effect/ T. S. Morozkova, L. A. Bogdanova, D. E. Semenov, N. A. Zhukova, N. A. Popova// Bulletin of Experimental Biology and Medicine, April 2015, V. 158, N 6, pp 789-793 doi:10.1007/s10517-015-2863-3), IF=0.365
  29. Т.С. Морозкова, Л.А. Богданова, Д.Е. Семенов, Н.А. Жукова, Н.А. Попова
    Мыши линии PT/Y чувствительны к ингибирующему глюкокортикоидную индукцию тирозинаминотрансферазы и гепатоканцерагенному действию орто-аминоазотолуола
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 12. С. 757-761. (PT/Y Mice Are Sensitive to the Inhibitory Effect of o-Aminoazotoluene on Glucocorticoid Induction of Tyrosine Aminotransferase and Its Hepatocarcinogenic Effect/ T. S. Morozkova, L. A. Bogdanova, D. E. Semenov, N. A. Zhukova, N. A. Popova// Bulletin of Experimental Biology and Medicine, April 2015, V. 158, N 6, pp 789-793 doi:10.1007/s10517-015-2863-3), IF=0.365
  30. Т.С. Морозкова, Л.А. Богданова, Д.Е. Семенов, Н.А. Жукова, Н.А. Попова
    Мыши линии PT/Y чувствительны к ингибирующему глюкокортикоидную индукцию тирозинаминотрансферазы и гепатоканцерагенному действию орто-аминоазотолуола
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 12. С. 757-761. (PT/Y Mice Are Sensitive to the Inhibitory Effect of o-Aminoazotoluene on Glucocorticoid Induction of Tyrosine Aminotransferase and Its Hepatocarcinogenic Effect/ T. S. Morozkova, L. A. Bogdanova, D. E. Semenov, N. A. Zhukova, N. A. Popova// Bulletin of Experimental Biology and Medicine, April 2015, V. 158, N 6, pp 789-793 doi:10.1007/s10517-015-2863-3), IF=0.365
  31. Л.Н. Мазалов, А.Д. Федоренко, Н.А. Крючкова, Ю.П. Диков, Ю.Ф. Полиенко, И.А. Григорьев
    Рентгеноспектральное и рентгеноэлектронное изучение электронного строения парамагнитных и диамагнитных производных 3-имидазолина
    Журнал структурной химии, 2014, 55(6), 1100-1113 (X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079), IF=0.5
  32. Л.Н. Мазалов, А.Д. Федоренко, Н.А. Крючкова, Ю.П. Диков, Ю.Ф. Полиенко, И.А. Григорьев
    Рентгеноспектральное и рентгеноэлектронное изучение электронного строения парамагнитных и диамагнитных производных 3-имидазолина
    Журнал структурной химии, 2014, 55(6), 1100-1113 (X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079), IF=0.5
  33. Л.Н. Мазалов, А.Д. Федоренко, Н.А. Крючкова, Ю.П. Диков, Ю.Ф. Полиенко, И.А. Григорьев
    Рентгеноспектральное и рентгеноэлектронное изучение электронного строения парамагнитных и диамагнитных производных 3-имидазолина
    Журнал структурной химии, 2014, 55(6), 1100-1113 (X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079), IF=0.5
  34. Л.Н. Мазалов, А.Д. Федоренко, Н.А. Крючкова, Ю.П. Диков, Ю.Ф. Полиенко, И.А. Григорьев
    Рентгеноспектральное и рентгеноэлектронное изучение электронного строения парамагнитных и диамагнитных производных 3-имидазолина
    Журнал структурной химии, 2014, 55(6), 1100-1113 (X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079), IF=0.5
  35. Л.М. Горностаев, Ю.Г. Халявина, Т.И. Лаврикова, Ю.В. Гатилов, Г.А. Сташина, С.И. Фирганг
    Превращение 2-алкиламино-1,4-нафтохинонов в 2-алкил-4,5-диоксонафто[2,1- D][1,3]оксазол-4-оксимы под действием нитрозилсерной кислоты
    Журнал органической химии. 2014. Т. 50. № 12. С. 1832-1838. (Transformation of 2-alkylamino-1,4-naphthoquinones into 2-alkylnaphtho[2,1-d][1,3]oxazole-4,5-dione 4-oximes by the action of nitrosylsulfuric acid/ L. M. Gornostaev, Yu. G. Khalyavina, T. I. Lavrikova, Yu. V. Gatilov, G. A. Stashina, S. I. Firgang// Russian Journal of Organic Chemistry, December 2014, V. 50, N 12, pp 1814-1820 doi:10.1134/S1070428014120173), IF=0.675
  36. Л.М. Горностаев, Ю.Г. Халявина, Т.И. Лаврикова, Ю.В. Гатилов, Г.А. Сташина, С.И. Фирганг
    Превращение 2-алкиламино-1,4-нафтохинонов в 2-алкил-4,5-диоксонафто[2,1- D][1,3]оксазол-4-оксимы под действием нитрозилсерной кислоты
    Журнал органической химии. 2014. Т. 50. № 12. С. 1832-1838. (Transformation of 2-alkylamino-1,4-naphthoquinones into 2-alkylnaphtho[2,1-d][1,3]oxazole-4,5-dione 4-oximes by the action of nitrosylsulfuric acid/ L. M. Gornostaev, Yu. G. Khalyavina, T. I. Lavrikova, Yu. V. Gatilov, G. A. Stashina, S. I. Firgang// Russian Journal of Organic Chemistry, December 2014, V. 50, N 12, pp 1814-1820 doi:10.1134/S1070428014120173), IF=0.675
  37. Л.М. Горностаев, Ю.Г. Халявина, Т.И. Лаврикова, Ю.В. Гатилов, Г.А. Сташина, С.И. Фирганг
    Превращение 2-алкиламино-1,4-нафтохинонов в 2-алкил-4,5-диоксонафто[2,1- D][1,3]оксазол-4-оксимы под действием нитрозилсерной кислоты
    Журнал органической химии. 2014. Т. 50. № 12. С. 1832-1838. (Transformation of 2-alkylamino-1,4-naphthoquinones into 2-alkylnaphtho[2,1-d][1,3]oxazole-4,5-dione 4-oximes by the action of nitrosylsulfuric acid/ L. M. Gornostaev, Yu. G. Khalyavina, T. I. Lavrikova, Yu. V. Gatilov, G. A. Stashina, S. I. Firgang// Russian Journal of Organic Chemistry, December 2014, V. 50, N 12, pp 1814-1820 doi:10.1134/S1070428014120173), IF=0.675
  38. Л.М. Горностаев, Ю.Г. Халявина, Т.И. Лаврикова, Ю.В. Гатилов, Г.А. Сташина, С.И. Фирганг
    Превращение 2-алкиламино-1,4-нафтохинонов в 2-алкил-4,5-диоксонафто[2,1- D][1,3]оксазол-4-оксимы под действием нитрозилсерной кислоты
    Журнал органической химии. 2014. Т. 50. № 12. С. 1832-1838. (Transformation of 2-alkylamino-1,4-naphthoquinones into 2-alkylnaphtho[2,1-d][1,3]oxazole-4,5-dione 4-oximes by the action of nitrosylsulfuric acid/ L. M. Gornostaev, Yu. G. Khalyavina, T. I. Lavrikova, Yu. V. Gatilov, G. A. Stashina, S. I. Firgang// Russian Journal of Organic Chemistry, December 2014, V. 50, N 12, pp 1814-1820 doi:10.1134/S1070428014120173), IF=0.675
  39. Л.М. Горностаев, Ю.Г. Халявина, Т.И. Лаврикова, Ю.В. Гатилов, Г.А. Сташина, С.И. Фирганг
    Превращение 2-алкиламино-1,4-нафтохинонов в 2-алкил-4,5-диоксонафто[2,1- D][1,3]оксазол-4-оксимы под действием нитрозилсерной кислоты
    Журнал органической химии. 2014. Т. 50. № 12. С. 1832-1838. (Transformation of 2-alkylamino-1,4-naphthoquinones into 2-alkylnaphtho[2,1-d][1,3]oxazole-4,5-dione 4-oximes by the action of nitrosylsulfuric acid/ L. M. Gornostaev, Yu. G. Khalyavina, T. I. Lavrikova, Yu. V. Gatilov, G. A. Stashina, S. I. Firgang// Russian Journal of Organic Chemistry, December 2014, V. 50, N 12, pp 1814-1820 doi:10.1134/S1070428014120173), IF=0.675
  40. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращение перекисных продуктов озонолиза (S)-(-)-лимонена в системе HCl-метанол
    Журнал органической химии. 2014. Т. 50. № 12. С. 1765-1767. (Transformation of peroxide products of (S)-(-)-limonene ozonolysis in the system HCl-methanol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, December 2014, V. 50, IN 12, pp 1746-1748 doi:10.1134/S1070428014120045), IF=0.675
  41. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращение перекисных продуктов озонолиза (S)-(-)-лимонена в системе HCl-метанол
    Журнал органической химии. 2014. Т. 50. № 12. С. 1765-1767. (Transformation of peroxide products of (S)-(-)-limonene ozonolysis in the system HCl-methanol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, December 2014, V. 50, IN 12, pp 1746-1748 doi:10.1134/S1070428014120045), IF=0.675
  42. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращение перекисных продуктов озонолиза (S)-(-)-лимонена в системе HCl-метанол
    Журнал органической химии. 2014. Т. 50. № 12. С. 1765-1767. (Transformation of peroxide products of (S)-(-)-limonene ozonolysis in the system HCl-methanol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, December 2014, V. 50, IN 12, pp 1746-1748 doi:10.1134/S1070428014120045), IF=0.675
  43. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращение перекисных продуктов озонолиза (S)-(-)-лимонена в системе HCl-метанол
    Журнал органической химии. 2014. Т. 50. № 12. С. 1765-1767. (Transformation of peroxide products of (S)-(-)-limonene ozonolysis in the system HCl-methanol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, December 2014, V. 50, IN 12, pp 1746-1748 doi:10.1134/S1070428014120045), IF=0.675
  44. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращение перекисных продуктов озонолиза (S)-(-)-лимонена в системе HCl-метанол
    Журнал органической химии. 2014. Т. 50. № 12. С. 1765-1767. (Transformation of peroxide products of (S)-(-)-limonene ozonolysis in the system HCl-methanol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, December 2014, V. 50, IN 12, pp 1746-1748 doi:10.1134/S1070428014120045), IF=0.675
  45. N.Yu. Adonin, A.Yu. Shabalin, V.V. Bardin
    Hydrodeboration of potassium polyfluoroaryl(fluoro)borates with alcohols
    Journal of Fluorine Chemistry, V. 168, 2014, Pp 111-120 doi:10.1016/j.jfluchem.2014.09.016, IF=1.952
  46. N.Yu. Adonin, A.Yu. Shabalin, V.V. Bardin
    Hydrodeboration of potassium polyfluoroaryl(fluoro)borates with alcohols
    Journal of Fluorine Chemistry, V. 168, 2014, Pp 111-120 doi:10.1016/j.jfluchem.2014.09.016, IF=1.952
  47. A.N. Antimonova, N.I. Petrenko, M.M. Shakirov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shul’ts
    Synthesis and Cytotoxic Activity of Lupane Triterpenoids Containing 1,3,4-Oxadiazoles
    Chemistry of Natural Compounds, 2014, V. 50, N 6, pp 1016-1023 doi:10.1007/s10600-014-1150-2, IF=0.5
  48. A.N. Antimonova, N.I. Petrenko, M.M. Shakirov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shul’ts
    Synthesis and Cytotoxic Activity of Lupane Triterpenoids Containing 1,3,4-Oxadiazoles
    Chemistry of Natural Compounds, 2014, V. 50, N 6, pp 1016-1023 doi:10.1007/s10600-014-1150-2, IF=0.5
  49. А.С. Торозова, В.П. Молчанов, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Каталитическая изомеризация эпоксида вербенола с использованием цеолитов
    Научно-технический вестник Поволжья. 2014. № 5. С. 77-80.
  50. А.С. Торозова, В.П. Молчанов, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Каталитическая изомеризация эпоксида вербенола с использованием цеолитов
    Научно-технический вестник Поволжья. 2014. № 5. С. 77-80.
  51. А.С. Торозова, В.П. Молчанов, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Каталитическая изомеризация эпоксида вербенола с использованием цеолитов
    Научно-технический вестник Поволжья. 2014. № 5. С. 77-80.
  52. А.С. Торозова, В.П. Молчанов, П. Мяки-Арвела, К.П. Волчо, Н.Ф. Салахутдинов, Д.Ю. Мурзин
    Каталитическая изомеризация эпоксида вербенола с использованием цеолитов
    Научно-технический вестник Поволжья. 2014. № 5. С. 77-80.
  53. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, А.А. Нефедов, Н.П. Гончаров
    Наследование и фенотипическое проявление функционального и нулевого аллелей ароматической алкогольдегидрогеназы (cad) у диплоидных пшениц
    Генетика. 2014. Т. 50. № 11. С. 1310. (Inheritance and phenotype expression of functional and null alleles of aromatic alcohol dehydrogenase (CAD) in diploid wheats/ A. A. Konovalov, I. K. Shundrina, E. V. Karpova, A. A. Nefedov, N. P. Goncharov// Russian Journal of Genetics, November 2014, V. 50, N 11, pp 1161-1168. doi:10.1134/S1022795414110052), IF=0.409
  54. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, А.А. Нефедов, Н.П. Гончаров
    Наследование и фенотипическое проявление функционального и нулевого аллелей ароматической алкогольдегидрогеназы (cad) у диплоидных пшениц
    Генетика. 2014. Т. 50. № 11. С. 1310. (Inheritance and phenotype expression of functional and null alleles of aromatic alcohol dehydrogenase (CAD) in diploid wheats/ A. A. Konovalov, I. K. Shundrina, E. V. Karpova, A. A. Nefedov, N. P. Goncharov// Russian Journal of Genetics, November 2014, V. 50, N 11, pp 1161-1168. doi:10.1134/S1022795414110052), IF=0.409
  55. А.Н. Кораблев, Н.А. Попова, Т.Г. Толстикова, А.А. Ходаков, Е.В. Предтеченская
    Влияние амида бетулоновой кислоты на ремиелинизациюпри купризон-индуцированной демиелинизации у мышей
    Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32. (Betamid influence on remyelination in cuprizone-induced demyelination in mice/ A.N. Korablev, N.A. Popova, T.G. Tolstikova, A.A. Khodakov, E.V. Predtechenskaya// Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32.(In Russian))
  56. А.Н. Кораблев, Н.А. Попова, Т.Г. Толстикова, А.А. Ходаков, Е.В. Предтеченская
    Влияние амида бетулоновой кислоты на ремиелинизациюпри купризон-индуцированной демиелинизации у мышей
    Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32. (Betamid influence on remyelination in cuprizone-induced demyelination in mice/ A.N. Korablev, N.A. Popova, T.G. Tolstikova, A.A. Khodakov, E.V. Predtechenskaya// Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32.(In Russian))
  57. А.Н. Кораблев, Н.А. Попова, Т.Г. Толстикова, А.А. Ходаков, Е.В. Предтеченская
    Влияние амида бетулоновой кислоты на ремиелинизациюпри купризон-индуцированной демиелинизации у мышей
    Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32. (Betamid influence on remyelination in cuprizone-induced demyelination in mice/ A.N. Korablev, N.A. Popova, T.G. Tolstikova, A.A. Khodakov, E.V. Predtechenskaya// Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32.(In Russian))
  58. А.Н. Кораблев, Н.А. Попова, Т.Г. Толстикова, А.А. Ходаков, Е.В. Предтеченская
    Влияние амида бетулоновой кислоты на ремиелинизациюпри купризон-индуцированной демиелинизации у мышей
    Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32. (Betamid influence on remyelination in cuprizone-induced demyelination in mice/ A.N. Korablev, N.A. Popova, T.G. Tolstikova, A.A. Khodakov, E.V. Predtechenskaya// Вестник Уральской медицинской академической науки. 2014. № 3. С. 31-32.(In Russian))
  59. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  60. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  61. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  62. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  63. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  64. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  65. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  66. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
    Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
    Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
  67. Т.А. Брусенцева, А.А. Филиппов, В.М. Фомин, Е.В. Малыхин, Т.А. Ваганова
    Влияние природы нанодисперсного наполнителя на механические свойства эпоксиангидридных полимерных композитов
    Российские нанотехнологии. 2014. Т. 9. № 11-12. С. 35-40. (Influence of the nanosized filler nature on the mechanical properties of epoxy-anhydride polymer composites/ T. A. Brusentseva, A. A. Filippov, V. M. Fomin, E. V. Malykhin, T. A. Vaganova// Nanotechnologies in Russia, November 2014, Volume 9, Issue 11-12, pp 638-644 doi:10.1134/S1995078014060068)
  68. Т.А. Брусенцева, А.А. Филиппов, В.М. Фомин, Е.В. Малыхин, Т.А. Ваганова
    Влияние природы нанодисперсного наполнителя на механические свойства эпоксиангидридных полимерных композитов
    Российские нанотехнологии. 2014. Т. 9. № 11-12. С. 35-40. (Influence of the nanosized filler nature on the mechanical properties of epoxy-anhydride polymer composites/ T. A. Brusentseva, A. A. Filippov, V. M. Fomin, E. V. Malykhin, T. A. Vaganova// Nanotechnologies in Russia, November 2014, Volume 9, Issue 11-12, pp 638-644 doi:10.1134/S1995078014060068)
  69. Т.А. Брусенцева, А.А. Филиппов, В.М. Фомин, Е.В. Малыхин, Т.А. Ваганова
    Влияние природы нанодисперсного наполнителя на механические свойства эпоксиангидридных полимерных композитов
    Российские нанотехнологии. 2014. Т. 9. № 11-12. С. 35-40. (Influence of the nanosized filler nature on the mechanical properties of epoxy-anhydride polymer composites/ T. A. Brusentseva, A. A. Filippov, V. M. Fomin, E. V. Malykhin, T. A. Vaganova// Nanotechnologies in Russia, November 2014, Volume 9, Issue 11-12, pp 638-644 doi:10.1134/S1995078014060068)
  70. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  71. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  72. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  73. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  74. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  75. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  76. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  77. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  78. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  79. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  80. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  81. Г.Н. Зюзьков, В.В. Жданов, Е.В. Удут, Л.А. Мирошниченко, А.В. Чайковский, Е.В. Симанина, М.Г. Данилец, М.Ю. Минакова, В.П. Демкин, В.В. Удут, Т.Г. Толстикова, Э.Э. Шульц, В.И. Агафонов, А.М. Дыгай
    Роль NF-KB/IKK-зависимого сигналинга в стимуляции функций мезенхимных клеток-предшественников алкалоидом зонгорином
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 11. С. 572-575. (Role of NF-κB/IKK-Dependent Signaling in Functional Stimulation of Mesenchymal Progenitor Cells by Alkaloid Songorine/ G. N. Zyuz’kov, V. V. Zhdanov, E. V. Udut, L. A. Miroshnichenko, A. V. Chaikovskii, E. V. Simanina, M. G. Danilets, M. Yu. Minakova, V. P. Demkin, V. V. Udut, T. G. Tolstikova, E. E. Shults, V. I. Agafonov, A. M. Dygai// Bulletin of Experimental Biology and Medicine, March 2015, V. 158, N 5, pp 624-627 doi:10.1007/s10517-015-2822-z), IF=0.365
  82. Г.Ю. Ишмуратов, В.А. Выдрина, Ю.А. Галкина, М.П. Яковлева, Р.Р. Муслухов, Г.А. Толстиков
    Варианты новой реакции в химии алюминийорганических соединений
    Журнал органической химии. 2014. Т. 50. № 11. С. 1714-1717. (Versions of new reaction in the chemistry of organoaluminum compounds/ G. Yu. Ishmuratov, V. A. Vydrina, Yu. A. Galkina, M. P. Yakovleva, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1704-1707 doi:10.1134/S1070428014110311), IF=0.675
  83. Г.Ю. Ишмуратов, В.А. Выдрина, Ю.А. Галкина, М.П. Яковлева, Р.Р. Муслухов, Г.А. Толстиков
    Варианты новой реакции в химии алюминийорганических соединений
    Журнал органической химии. 2014. Т. 50. № 11. С. 1714-1717. (Versions of new reaction in the chemistry of organoaluminum compounds/ G. Yu. Ishmuratov, V. A. Vydrina, Yu. A. Galkina, M. P. Yakovleva, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1704-1707 doi:10.1134/S1070428014110311), IF=0.675
  84. Г.Ю. Ишмуратов, В.А. Выдрина, Ю.А. Галкина, М.П. Яковлева, Р.Р. Муслухов, Г.А. Толстиков
    Варианты новой реакции в химии алюминийорганических соединений
    Журнал органической химии. 2014. Т. 50. № 11. С. 1714-1717. (Versions of new reaction in the chemistry of organoaluminum compounds/ G. Yu. Ishmuratov, V. A. Vydrina, Yu. A. Galkina, M. P. Yakovleva, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1704-1707 doi:10.1134/S1070428014110311), IF=0.675
  85. Г.Ю. Ишмуратов, В.А. Выдрина, Ю.А. Галкина, М.П. Яковлева, Р.Р. Муслухов, Г.А. Толстиков
    Варианты новой реакции в химии алюминийорганических соединений
    Журнал органической химии. 2014. Т. 50. № 11. С. 1714-1717. (Versions of new reaction in the chemistry of organoaluminum compounds/ G. Yu. Ishmuratov, V. A. Vydrina, Yu. A. Galkina, M. P. Yakovleva, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1704-1707 doi:10.1134/S1070428014110311), IF=0.675
  86. Г.Ю. Ишмуратов, В.А. Выдрина, Ю.А. Галкина, М.П. Яковлева, Р.Р. Муслухов, Г.А. Толстиков
    Варианты новой реакции в химии алюминийорганических соединений
    Журнал органической химии. 2014. Т. 50. № 11. С. 1714-1717. (Versions of new reaction in the chemistry of organoaluminum compounds/ G. Yu. Ishmuratov, V. A. Vydrina, Yu. A. Galkina, M. P. Yakovleva, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1704-1707 doi:10.1134/S1070428014110311), IF=0.675
  87. И.И. Олейник, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. XVII. синтез метоксизамещенных (N-арил)салицилальдиминов, содержащих ω-алкенилоксигруппу, и комплексов дихлорида титана(IV) на их основе
    Журнал органической химии. 2014. Т. 50. № 11. С. 1581-1588. (Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XVII. Synthesis of methoxy-substituted (p-aryl)salicylaldimines containing ω-alkenyloxy group, and their complexes with titanium(IV) dichloride/ I. I. Oleinik, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, November 2014, V. 50, N 11, pp 1565-1572 doi:10.1134/S1070428014110050), IF=0.675
  88. T.A. Vaganova, T.A. Brusentseva, A.A. Filippov, E.V. Malykhin
    Synthesis and characterization of epoxy-anhydride polymers modified by polyfluoroaromatic oligoimides
    Journal of Polymer Research, October 2014, V. 21, N 11, Art. 588. doi:10.1007/s10965-014-0588-z, IF=1.896
  89. T.A. Vaganova, T.A. Brusentseva, A.A. Filippov, E.V. Malykhin
    Synthesis and characterization of epoxy-anhydride polymers modified by polyfluoroaromatic oligoimides
    Journal of Polymer Research, October 2014, V. 21, N 11, Art. 588. doi:10.1007/s10965-014-0588-z, IF=1.896
  90. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  91. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  92. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  93. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  94. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  95. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  96. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  97. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  98. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  99. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  100. E. Sokol, O. Kozmenko, S. Smirnov, I. Sokol, S. Novikova, A. Tomilenko, S. Kokh, T. Ryazanova, V. Reutsky, T. Bul’bak, Ye. Vapnik, M. Deyak
    Geochemical assessment of hydrocarbon migration phenomena: Case studies from the south-western margin of the Dead Sea Basin
    Journal of Asian Earth Sciences, V. 93, 2014, Pp 211-228. doi:10.1016/j.jseaes.2014.07.023, IF=2.831
  101. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  102. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  103. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  104. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  105. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  106. A.V. Artem'ev, V.A. Shagun, N.K. Gusarova, C.W. Liub, J.H. Liao, Yu.V. Gatilov, B.A. Trofimov
    DFT study and dynamic NMR evidence for cis-trans conformational isomerism in square planar Ni(II) thioselenophosphinate, Ni(SeSPPh2)(2)
    Journal of Organometallic Chemistry, 2014, V. 768, Pp 151-156. doi:10.1016/j.jorganchem.2014.06.013, IF=2.302
  107. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  108. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  109. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  110. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  111. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  112. R.K. Strizhakov, E.V. Tretyakov, A.S. Medvedeva, V.V. Novokshonov, V.G. Vasiliev, V.I. Ovcharenko, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
    Permethyl-β-Cyclodextrin Spin-Labeled with Nitronyl Nitroxide: Synthesis and EPR Study
    Applied Magnetic Resonance, October 2014, V.45, N 10, pp 1087-1098. doi:10.1007/s00723-014-0591-x, IF=1.151
  113. E.V. Zaytseva, A.V. Shernyukov, A.M. Genaev, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
    New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments
    ARKIVOC, 2014, (vi) 10-24. http://www.arkat-usa.org/get-file/51547/ doi:10.3998/ark.5550190.p008.808, IF=1.75
  114. G.T. Sukhanov, G.V. Sakovich, Yu.V. Filippova, I.Yu. Bagryanskaya, A.G. Sukhanova
    Regioselective quaternization of N-alkyl-4-nitro- 1,2,3-triazoles in ButOH–HClO4 system
    Mendeleev Communications, V. 24, N 5, September–October 2014, Pp. 280-282 doi:10.1016/j.mencom.2014.09.011, IF=1.154
  115. G.T. Sukhanov, G.V. Sakovich, Yu.V. Filippova, I.Yu. Bagryanskaya, A.G. Sukhanova
    Regioselective quaternization of N-alkyl-4-nitro- 1,2,3-triazoles in ButOH–HClO4 system
    Mendeleev Communications, V. 24, N 5, September–October 2014, Pp. 280-282 doi:10.1016/j.mencom.2014.09.011, IF=1.154
  116. G.T. Sukhanov, G.V. Sakovich, Yu.V. Filippova, I.Yu. Bagryanskaya, A.G. Sukhanova
    Regioselective quaternization of N-alkyl-4-nitro- 1,2,3-triazoles in ButOH–HClO4 system
    Mendeleev Communications, V. 24, N 5, September–October 2014, Pp. 280-282 doi:10.1016/j.mencom.2014.09.011, IF=1.154
  117. G.T. Sukhanov, G.V. Sakovich, Yu.V. Filippova, I.Yu. Bagryanskaya, A.G. Sukhanova
    Regioselective quaternization of N-alkyl-4-nitro- 1,2,3-triazoles in ButOH–HClO4 system
    Mendeleev Communications, V. 24, N 5, September–October 2014, Pp. 280-282 doi:10.1016/j.mencom.2014.09.011, IF=1.154
  118. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  119. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  120. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  121. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  122. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  123. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  124. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  125. P.A. Volkov, N.N. Pogodaeva, N.I. Ivanova, K.O. Khrapova, L.I. Larina, B.G. Sukhov, Yu.V. Gatilov, N.K. Gusarova, B.A. Trofimov
    Reaction of hydroxyflavones with secondary phosphine chalcogenides in the CCl4/Et3N system: synthesis of a new family of phosphorylated flavonoids
    Tetrahedron Letters, 2014, V. 55, N 35, Pp 4927-4929. doi:10.1016/j.tetlet.2014.07.016, IF=2.391
  126. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  127. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  128. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  129. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  130. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  131. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  132. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
  133. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  134. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  135. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  136. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  137. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  138. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  139. B.A. Trofimov, L.A. Oparina, O.A. Tarasova, A.V. Artem'ev, V.B. Kobychev, Yu.V. Gatilov, A.I. Albanov, N.K. Gusarova
    Tuneable superbase-catalyzed vinylation of α-hydroxyalkylferrocenes with alkynes
    Tetrahedron, 2014, V.70, N 35, P. 5954-5960. doi:10.1016/j.tet.2014.06.010, IF=2.816
  140. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  141. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  142. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  143. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  144. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  145. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, N.V. Vasilieva, I.G. Irtegova, Yu.V. Nelyubina, I.Yu. Bagryanskaya, L.A. Shundrin, Z.Yu. Sosnovskaya, A.V. Zibarev, O.A. Rakitin
    1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties
    Tetrahedron, 2014, V.70, N 35, P. 5558-5568. doi:10.1016/j.tet.2014.06.096, IF=2.816
  146. В.С. Глухачева, С.Г. Ильясов, Т.Г. Толстикова
    Новые биологически активные вещества на основе арилнитропроизводных мочевин
    Южно-Сибирский научный вестник. 2014. № 4 (8). С. 15-17.
  147. В.С. Глухачева, С.Г. Ильясов, Т.Г. Толстикова
    Новые биологически активные вещества на основе арилнитропроизводных мочевин
    Южно-Сибирский научный вестник. 2014. № 4 (8). С. 15-17.
  148. Ю.В. Загурская, В.Г. Васильев, А.Л. Богатырев, И.И. Баяндина
    Состав фенольных соединений сырьевой части Leonurus Quinquelobatus Gilib. из различных регионов западной сибири
    Вестник Кемеровского государственного университета. 2014. № 4-3. С. 232-236. (PHENOLIC COMPOUNDS COMPOSITION OF LEONURUS QUINQUELOBATUS GILIB. HERB FROM DIFFERENT REGIONS OF WESTERN SIBERIA/ Zagurskaya Yulia V., Vasiliev Vladimir G., Bogatyrev Aleksey L., Bayandina Irina I.// )
  149. Ю.В. Загурская, В.Г. Васильев, А.Л. Богатырев, И.И. Баяндина
    Состав фенольных соединений сырьевой части Leonurus Quinquelobatus Gilib. из различных регионов западной сибири
    Вестник Кемеровского государственного университета. 2014. № 4-3. С. 232-236. (PHENOLIC COMPOUNDS COMPOSITION OF LEONURUS QUINQUELOBATUS GILIB. HERB FROM DIFFERENT REGIONS OF WESTERN SIBERIA/ Zagurskaya Yulia V., Vasiliev Vladimir G., Bogatyrev Aleksey L., Bayandina Irina I.// )
  150. Ю.В. Загурская, В.Г. Васильев, А.Л. Богатырев, И.И. Баяндина
    Состав фенольных соединений сырьевой части Leonurus Quinquelobatus Gilib. из различных регионов западной сибири
    Вестник Кемеровского государственного университета. 2014. № 4-3. С. 232-236. (PHENOLIC COMPOUNDS COMPOSITION OF LEONURUS QUINQUELOBATUS GILIB. HERB FROM DIFFERENT REGIONS OF WESTERN SIBERIA/ Zagurskaya Yulia V., Vasiliev Vladimir G., Bogatyrev Aleksey L., Bayandina Irina I.// )
  151. Д.Е. Семенов, Н.А. Жукова, Е.П. Иванова, И.В. Сорокина, Д.С. Баев, Г.И. Непомнящих, Т.Г. Толстикова, М.С. Бирюкова
    Гепатопротекторные свойства амида бетулоновой кислоты и гептрала при токсическом поражении печени тетрахлорметаном в сочетании с этанолом
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 9. С. 320-326. (Hepatoprotective Properties of Betulonic Acid Amide and Heptral in Toxic Liver Injury Induced by Carbon Tetrachloride in Combination with Ethanol/ D. E. Semenov, N. A. Zhukova, E. P. Ivanova, I. V. Sorokina, D. S. Baiev, G. I. Nepomnyashchikh, T. G. Tolstikova, M. S. Biryukova// Bulletin of Experimental Biology and Medicine, January 2015, V. 158, N 3, pp 336-341 doi:10.1007/s10517-015-2756-5), IF=0.365
  152. Д.Е. Семенов, Н.А. Жукова, Е.П. Иванова, И.В. Сорокина, Д.С. Баев, Г.И. Непомнящих, Т.Г. Толстикова, М.С. Бирюкова
    Гепатопротекторные свойства амида бетулоновой кислоты и гептрала при токсическом поражении печени тетрахлорметаном в сочетании с этанолом
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 9. С. 320-326. (Hepatoprotective Properties of Betulonic Acid Amide and Heptral in Toxic Liver Injury Induced by Carbon Tetrachloride in Combination with Ethanol/ D. E. Semenov, N. A. Zhukova, E. P. Ivanova, I. V. Sorokina, D. S. Baiev, G. I. Nepomnyashchikh, T. G. Tolstikova, M. S. Biryukova// Bulletin of Experimental Biology and Medicine, January 2015, V. 158, N 3, pp 336-341 doi:10.1007/s10517-015-2756-5), IF=0.365
  153. А.Н. Синяков, Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, В.А. Самсонов, А.Я. Тихонов, М.Ю. Палаткина, Д.Е. Зайцев
    Фотогенератор трихлоруксусной кислоты - перспективный детритилирующий агент для микрочипового олигонуклеотидного синтеза
    Биоорганическая химия. 2014. Т. 40. № 5. С. 636-638. (Photogenerator of trichloroacetic acid as a promising detritylation agent for oligonucleotide microarray synthesis/ A. N. Sinyakov, E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, V. A. Samsonov, A. Y. Tikhonov, M. Yu. Palatkina, D. E. Zaytsev// Russian Journal of Bioorganic Chemistry, 2014, V. 40, N 5, pp 586-588. doi:10.1134/S1068162014050124), IF=0.623
  154. А.Н. Синяков, Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, В.А. Самсонов, А.Я. Тихонов, М.Ю. Палаткина, Д.Е. Зайцев
    Фотогенератор трихлоруксусной кислоты - перспективный детритилирующий агент для микрочипового олигонуклеотидного синтеза
    Биоорганическая химия. 2014. Т. 40. № 5. С. 636-638. (Photogenerator of trichloroacetic acid as a promising detritylation agent for oligonucleotide microarray synthesis/ A. N. Sinyakov, E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, V. A. Samsonov, A. Y. Tikhonov, M. Yu. Palatkina, D. E. Zaytsev// Russian Journal of Bioorganic Chemistry, 2014, V. 40, N 5, pp 586-588. doi:10.1134/S1068162014050124), IF=0.623
  155. А.Н. Синяков, Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, В.А. Самсонов, А.Я. Тихонов, М.Ю. Палаткина, Д.Е. Зайцев
    Фотогенератор трихлоруксусной кислоты - перспективный детритилирующий агент для микрочипового олигонуклеотидного синтеза
    Биоорганическая химия. 2014. Т. 40. № 5. С. 636-638. (Photogenerator of trichloroacetic acid as a promising detritylation agent for oligonucleotide microarray synthesis/ A. N. Sinyakov, E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, V. A. Samsonov, A. Y. Tikhonov, M. Yu. Palatkina, D. E. Zaytsev// Russian Journal of Bioorganic Chemistry, 2014, V. 40, N 5, pp 586-588. doi:10.1134/S1068162014050124), IF=0.623
  156. Е.А. Морозова, Т.А. Запара, А.С. Ратушняк, С.О. Вечкапова, Т.Г. Толстикова, Э.Э. Шульц
    К механизму анальгетической активности высокоэффективных анальгетиков нового структурного типа: эксперименты in vitro
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 289-293. (About the Mechanism of Analgesic Activity of Highly Efficient Analgesics of the New Structural Type: in vitro Experiments/ E.A. Morozova, T.A. Zapara, A.S.Ratushnyak, S.O.Vechkapova, T.G. Tolstikova, E.E. Shults// Chemistry for Sustainable Development, 2014. Т. 22. № 3. С. 289-293. (in russian))
  157. Е.А. Морозова, Т.А. Запара, А.С. Ратушняк, С.О. Вечкапова, Т.Г. Толстикова, Э.Э. Шульц
    К механизму анальгетической активности высокоэффективных анальгетиков нового структурного типа: эксперименты in vitro
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 289-293. (About the Mechanism of Analgesic Activity of Highly Efficient Analgesics of the New Structural Type: in vitro Experiments/ E.A. Morozova, T.A. Zapara, A.S.Ratushnyak, S.O.Vechkapova, T.G. Tolstikova, E.E. Shults// Chemistry for Sustainable Development, 2014. Т. 22. № 3. С. 289-293. (in russian))
  158. Е.А. Морозова, Т.А. Запара, А.С. Ратушняк, С.О. Вечкапова, Т.Г. Толстикова, Э.Э. Шульц
    К механизму анальгетической активности высокоэффективных анальгетиков нового структурного типа: эксперименты in vitro
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 289-293. (About the Mechanism of Analgesic Activity of Highly Efficient Analgesics of the New Structural Type: in vitro Experiments/ E.A. Morozova, T.A. Zapara, A.S.Ratushnyak, S.O.Vechkapova, T.G. Tolstikova, E.E. Shults// Chemistry for Sustainable Development, 2014. Т. 22. № 3. С. 289-293. (in russian))
  159. A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, V.S. Malkov, I.Yu. Bagryanskaya, Y.V. Gatilov, A.S. Knyazev, Yu.G. Slizhov, A.V. Zibarev
    New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds
    Journal of Fluorine Chemistry, 2014, V. 165, Pp 123–131. doi:10.1016/j.jfluchem.2014.06.019, IF=1.952
  160. A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, V.S. Malkov, I.Yu. Bagryanskaya, Y.V. Gatilov, A.S. Knyazev, Yu.G. Slizhov, A.V. Zibarev
    New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds
    Journal of Fluorine Chemistry, 2014, V. 165, Pp 123–131. doi:10.1016/j.jfluchem.2014.06.019, IF=1.952
  161. A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, V.S. Malkov, I.Yu. Bagryanskaya, Y.V. Gatilov, A.S. Knyazev, Yu.G. Slizhov, A.V. Zibarev
    New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds
    Journal of Fluorine Chemistry, 2014, V. 165, Pp 123–131. doi:10.1016/j.jfluchem.2014.06.019, IF=1.952
  162. A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, V.S. Malkov, I.Yu. Bagryanskaya, Y.V. Gatilov, A.S. Knyazev, Yu.G. Slizhov, A.V. Zibarev
    New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds
    Journal of Fluorine Chemistry, 2014, V. 165, Pp 123–131. doi:10.1016/j.jfluchem.2014.06.019, IF=1.952
  163. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  164. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  165. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  166. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  167. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  168. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  169. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
  170. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
  171. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
  172. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
  173. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
  174. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
  175. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  176. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  177. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  178. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  179. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  180. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  181. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  182. E. Lork, V.G. Vasiliev, S.N. Konchenko, J. Beckmann, N.P. Gritsan, A.V. Zibarev, N.A. Semenov, A.V. Lonchakov, N.A. Pushkarevsky, E.A. Suturina, V.V. Korolev
    Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
    Organometallics, 2014, 33 (16), pp 4302-4314. doi:10.1021/om5006403, IF=4.252
  183. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева
    Разработка гемостатического материала на основе окисленной целлюлозы.
    Международный научный журнал «Educatio». 2014. № 6, ч. 4. С. 38-41.
  184. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева
    Разработка гемостатического материала на основе окисленной целлюлозы.
    Международный научный журнал «Educatio». 2014. № 6, ч. 4. С. 38-41.
  185. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова, Н.И. Ткачева
    Контроль локального гемостаза с помощью препаратов окисленной целлюлозы
    Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75 (Local hemostasis control by using of oxidized cellulose drugs/ A.M. Cherniavskii, I.A. Grigor'ev, S.V. Morozov, A.R. Tarkova, N.I. Tkacheva// Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75)
  186. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова, Н.И. Ткачева
    Контроль локального гемостаза с помощью препаратов окисленной целлюлозы
    Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75 (Local hemostasis control by using of oxidized cellulose drugs/ A.M. Cherniavskii, I.A. Grigor'ev, S.V. Morozov, A.R. Tarkova, N.I. Tkacheva// Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75)
  187. О.А. Рабина, Е.Н. Степанова
    Идентификация и обнаружение фальсификации растительных масел методом хроматографии
    Вестник Сибирского университета потребительской кооперации. 2014. № 1 (8). С. 98-101. (Detection of Vegetable Oil Adulteration Using the Method of Chromatography/ O.A. Rabina, E.N. Stepanova// Siberian University of Consumer Cooperation. 2014. № 1 (8). С. 98-101.(in russian).)
  188. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  189. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  190. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  191. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  192. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  193. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  194. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, E.A. Chulanova, I.V. Yushina, N.P. Gritsan, S.N. Konchenko, A.V. Zibarev
    Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
    RSC Adv., 2014, V. 4, N 54, 28309-28316. doi:10.1039/c4ra03342f, IF=3.707
  195. E.V. Zaitseva, A.V. Shernyukov, S.A. Amitina, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
    Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups
    Chemistry of Heterocyclic Compounds, November 2014, V. 50, N 8, pp 1113-1125. doi:10.1007/s10593-014-1571-7, IF=0.698
  196. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  197. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  198. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  199. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  200. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  201. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  202. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
  203. R. K. Strizhakov, L. A. Shundrin, N. G. Kolosova, N. A. Stefanova, E. U. Fursova, V. I. Ovcharenko, E. G. Bagryanskaya
    Nitronyl Nitroxides as a Spin Probe in EPR Tomography In Vivo
    Applied Magnetic Resonance, 2014, V. 45, N 8, pp 743-758. doi:10.1007/s00723-014-0555-1, IF=1.151
  204. R. K. Strizhakov, L. A. Shundrin, N. G. Kolosova, N. A. Stefanova, E. U. Fursova, V. I. Ovcharenko, E. G. Bagryanskaya
    Nitronyl Nitroxides as a Spin Probe in EPR Tomography In Vivo
    Applied Magnetic Resonance, 2014, V. 45, N 8, pp 743-758. doi:10.1007/s00723-014-0555-1, IF=1.151
  205. R. K. Strizhakov, L. A. Shundrin, N. G. Kolosova, N. A. Stefanova, E. U. Fursova, V. I. Ovcharenko, E. G. Bagryanskaya
    Nitronyl Nitroxides as a Spin Probe in EPR Tomography In Vivo
    Applied Magnetic Resonance, 2014, V. 45, N 8, pp 743-758. doi:10.1007/s00723-014-0555-1, IF=1.151
  206. R. K. Strizhakov, L. A. Shundrin, N. G. Kolosova, N. A. Stefanova, E. U. Fursova, V. I. Ovcharenko, E. G. Bagryanskaya
    Nitronyl Nitroxides as a Spin Probe in EPR Tomography In Vivo
    Applied Magnetic Resonance, 2014, V. 45, N 8, pp 743-758. doi:10.1007/s00723-014-0555-1, IF=1.151
  207. S.i F. Vasilevsky, M.P. Davydova, D.N. Tomilin, L.N. Sobenina, V.I. Mamatuyk, N.V. Pleshkova
    Peculiarities of the cascade cleavage of the polarized C≡C-fragment in α-ketoacetylenes on reaction with ethylene diamine
    ARKIVOС, 2014, V. 2014, Part (v), pp. 132 - 144. doi:10.3998/ark.5550190.p008.663, IF=1.75
  208. S.i F. Vasilevsky, M.P. Davydova, D.N. Tomilin, L.N. Sobenina, V.I. Mamatuyk, N.V. Pleshkova
    Peculiarities of the cascade cleavage of the polarized C≡C-fragment in α-ketoacetylenes on reaction with ethylene diamine
    ARKIVOС, 2014, V. 2014, Part (v), pp. 132 - 144. doi:10.3998/ark.5550190.p008.663, IF=1.75
  209. S.i F. Vasilevsky, M.P. Davydova, D.N. Tomilin, L.N. Sobenina, V.I. Mamatuyk, N.V. Pleshkova
    Peculiarities of the cascade cleavage of the polarized C≡C-fragment in α-ketoacetylenes on reaction with ethylene diamine
    ARKIVOС, 2014, V. 2014, Part (v), pp. 132 - 144. doi:10.3998/ark.5550190.p008.663, IF=1.75
  210. S.i F. Vasilevsky, M.P. Davydova, D.N. Tomilin, L.N. Sobenina, V.I. Mamatuyk, N.V. Pleshkova
    Peculiarities of the cascade cleavage of the polarized C≡C-fragment in α-ketoacetylenes on reaction with ethylene diamine
    ARKIVOС, 2014, V. 2014, Part (v), pp. 132 - 144. doi:10.3998/ark.5550190.p008.663, IF=1.75
  211. M.A. Timoshenko, A.B. Ayusheev, Yu.V. Kharitonov, M.M. Shakirov, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. XXXIV.* Preparation of Carboxyl Derivatives of Isopimaric Acid
    Chemistry of Natural Compounds, October 2014, Volume 50, Issue 4, pp 673-680. doi:10.1007/s10600-014-1050-5, IF=0.5
  212. Д.Ф. Августинович, М.К. Фомина, Е.В. Суслов, Т.Г. Толстикова, К.П. Волчо, Н.Ф. Салахутдинов
    Исследование влияния производных 2-аминоадамантана на поведение мышей в модернизированном тесте "свет--темнота"
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 158. № 8. С. 177-182. (Effect of 2-Aminoadamantane Derivatives on Behavior of Mice in a Modified Light/Dark Test/ D. F. Avgustinovich, M. K. Fomina, E. V. Suslov, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov// Bulletin of Experimental Biology and Medicine, December 2014, V. 158, N 2, pp 213-218 doi:10.1007/s10517-014-2725-4), IF=0.365
  213. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в уксусной кислоте
    Журнал органической химии. 2014. Т. 50. № 8. С. 1095-1101. (Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 8, pp 1075-1081. doi:10.1134/S1070428014080016), IF=0.675
  214. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в уксусной кислоте
    Журнал органической химии. 2014. Т. 50. № 8. С. 1095-1101. (Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 8, pp 1075-1081. doi:10.1134/S1070428014080016), IF=0.675
  215. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в уксусной кислоте
    Журнал органической химии. 2014. Т. 50. № 8. С. 1095-1101. (Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 8, pp 1075-1081. doi:10.1134/S1070428014080016), IF=0.675
  216. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в уксусной кислоте
    Журнал органической химии. 2014. Т. 50. № 8. С. 1095-1101. (Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 8, pp 1075-1081. doi:10.1134/S1070428014080016), IF=0.675
  217. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в уксусной кислоте
    Журнал органической химии. 2014. Т. 50. № 8. С. 1095-1101. (Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 8, pp 1075-1081. doi:10.1134/S1070428014080016), IF=0.675
  218. S.I. Zhivetyeva, L.I. Goryunov, I.Yu. Bagryanskaya, J. Grobe, V.D. Shteingarts, E.U. Wurthwein
    Phosphinodefluorination of polyfluorobenzenes by silylphosphines Ph(R)PSiMe3 (R = Me, Ph): Further experimental and computational evidences for the concerted A(N)D(N) mechanism of aromatic nucleophilic substitution
    Journal of Fluorine Chemistry, 2014, V. 164, Pp. 58-69. doi:10.1016/j.jfluchem.2014.04.012, IF=1.952
  219. S.I. Zhivetyeva, L.I. Goryunov, I.Yu. Bagryanskaya, J. Grobe, V.D. Shteingarts, E.U. Wurthwein
    Phosphinodefluorination of polyfluorobenzenes by silylphosphines Ph(R)PSiMe3 (R = Me, Ph): Further experimental and computational evidences for the concerted A(N)D(N) mechanism of aromatic nucleophilic substitution
    Journal of Fluorine Chemistry, 2014, V. 164, Pp. 58-69. doi:10.1016/j.jfluchem.2014.04.012, IF=1.952
  220. N.M. Troshkova, L.I. Goryunov, V.D. Shteingarts, O.D. Zakharova, L.P. Ovchinnikova, G.A. Nevinsky
    Synthesis and cytotoxicity evaluation of polyfluorinated 1,4-naphthoquinones containing amino acid substituents
    Journal of Fluorine Chemistry, 2014, V.164, Pp 18-26. doi:10.1016/j.jfluchem.2014.04.014, IF=1.952
  221. N.M. Troshkova, L.I. Goryunov, V.D. Shteingarts, O.D. Zakharova, L.P. Ovchinnikova, G.A. Nevinsky
    Synthesis and cytotoxicity evaluation of polyfluorinated 1,4-naphthoquinones containing amino acid substituents
    Journal of Fluorine Chemistry, 2014, V.164, Pp 18-26. doi:10.1016/j.jfluchem.2014.04.014, IF=1.952
  222. N.M. Troshkova, L.I. Goryunov, V.D. Shteingarts, O.D. Zakharova, L.P. Ovchinnikova, G.A. Nevinsky
    Synthesis and cytotoxicity evaluation of polyfluorinated 1,4-naphthoquinones containing amino acid substituents
    Journal of Fluorine Chemistry, 2014, V.164, Pp 18-26. doi:10.1016/j.jfluchem.2014.04.014, IF=1.952
  223. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  224. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  225. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  226. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  227. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  228. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
  229. L.N. Zibareva, A.A. Seliverstova, A. Suksamrarn, S.V. Morozov, E.I. Chernyak
    Phytoecdysteroids from the Aerial Part of Silene colpophylla
    Chemistry of Natural Compounds, July 2014, V. 50, N 3, pp 571-572 doi:10.1007/s10600-014-1021-x, IF=0.5
  230. L.N. Zibareva, A.A. Seliverstova, A. Suksamrarn, S.V. Morozov, E.I. Chernyak
    Phytoecdysteroids from the Aerial Part of Silene colpophylla
    Chemistry of Natural Compounds, July 2014, V. 50, N 3, pp 571-572 doi:10.1007/s10600-014-1021-x, IF=0.5
  231. L.N. Zibareva, A.A. Seliverstova, A. Suksamrarn, S.V. Morozov, E.I. Chernyak
    Phytoecdysteroids from the Aerial Part of Silene colpophylla
    Chemistry of Natural Compounds, July 2014, V. 50, N 3, pp 571-572 doi:10.1007/s10600-014-1021-x, IF=0.5
  232. N. V. Kosheleva, E. I. Chernyak, S. V. Morozov, V. I. Vinogradova, Sh. Sh. Sagdullaev, N. D. Abdullaev, I. A. Grigor’ev
    Synthesis of the First Dihydroquercetin-Cytisine Conjugates
    Chemistry of Natural Compounds, 2014, V. 50, N 3, pp 443-445. doi:10.1007/s10600-014-0982-0, IF=0.5
  233. N. V. Kosheleva, E. I. Chernyak, S. V. Morozov, V. I. Vinogradova, Sh. Sh. Sagdullaev, N. D. Abdullaev, I. A. Grigor’ev
    Synthesis of the First Dihydroquercetin-Cytisine Conjugates
    Chemistry of Natural Compounds, 2014, V. 50, N 3, pp 443-445. doi:10.1007/s10600-014-0982-0, IF=0.5
  234. N. V. Kosheleva, E. I. Chernyak, S. V. Morozov, V. I. Vinogradova, Sh. Sh. Sagdullaev, N. D. Abdullaev, I. A. Grigor’ev
    Synthesis of the First Dihydroquercetin-Cytisine Conjugates
    Chemistry of Natural Compounds, 2014, V. 50, N 3, pp 443-445. doi:10.1007/s10600-014-0982-0, IF=0.5
  235. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
  236. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
  237. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
  238. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
  239. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
  240. М.К. Фомина, Д.Ф. Августинович, Т.Г. Толстикова
    Исследование эффектов комплекса буспирона с глицирризиновой кислотой на поведение мышей, находящихся в условиях формирования тревожно-депрессивного состояния
    Российский физиологический журнал им. И.М. Сеченова. 2014. Т. 100. № 7. С. 808-819. (Effects of buspirone complex with glycyrrhizic acid on behavior of mice with anxious-depressive state/ М.К. Fomina, В.А. Avgustinovich, T.G. Tolstikova// )
  241. Н.Л. Бажина, Е.Э. Ондар, Ю.М. Дерябина
    Специфика поглощения света в видимой и ультрафиолетовой области спектра гуминовыми кислотами почв западной части территории Тувы
    Вестник Оренбургского государственного университета. 2014. № 6 (167). С. 189-194. (Specificity light absorption in visible and ultraviolet regions of humic acids of soils western part of the territory Tuva/ Bazhina N.L., Ondar E.E., Deryabina Y.M.// )
  242. Н.Л. Бажина, Е.Э. Ондар, Ю.М. Дерябина
    Специфика поглощения света в видимой и ультрафиолетовой области спектра гуминовыми кислотами почв западной части территории Тувы
    Вестник Оренбургского государственного университета. 2014. № 6 (167). С. 189-194. (Specificity light absorption in visible and ultraviolet regions of humic acids of soils western part of the territory Tuva/ Bazhina N.L., Ondar E.E., Deryabina Y.M.// )
  243. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  244. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  245. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  246. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  247. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  248. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  249. S.V. Larionov, T.E. Kokina, V.F. Plyusnin, L.A. Glinskaya, A.V. Tkachev, Yu.A. Bryleva, N.V. Kuratieva, M.I. Rakhmanova, E.S. Vasilyev
    Synthesis, structure and photoluminescence of Zn(II) and Cd(II) complexes with pyridophenazine derivative
    Polyhedron, 2014, V. 77, Pp 75-80. doi:10.1016/j.poly.2014.04.011, IF=2.46
  250. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064), IF=0.351
  251. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064), IF=0.351
  252. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064), IF=0.351
  253. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064), IF=0.351
  254. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064), IF=0.351
  255. А.Л. Бычков, А.И. Денькин, В.Д. Тихова, О.И. Ломовский
    Расчет теплоты сгорания лигноцеллюлозы на основании данных элементного анализа
    Химия растительного сырья, 2014, N 3, C. 99-104
  256. А.Л. Бычков, А.И. Денькин, В.Д. Тихова, О.И. Ломовский
    Расчет теплоты сгорания лигноцеллюлозы на основании данных элементного анализа
    Химия растительного сырья, 2014, N 3, C. 99-104
  257. А.Л. Бычков, А.И. Денькин, В.Д. Тихова, О.И. Ломовский
    Расчет теплоты сгорания лигноцеллюлозы на основании данных элементного анализа
    Химия растительного сырья, 2014, N 3, C. 99-104
  258. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  259. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  260. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  261. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  262. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  263. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  264. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  265. Е.В. Третьяков, С.В. Фокин, Е.М. Зуева, А.О. Ткачева, Г.В. Романенко, А.С. Богомяков, С.В. Ларионов, С.А. Попов, В.И. Овчаренко
    Комплексы лантаноидов со спин-меченым пиразолилхинолином
    Известия Академии наук. Серия химическая. 2014. № 7. С. 1459-1464. (Complexes of lanthanides with spin-labeled pyrazolylquinoline/ E. V. Tretyakov, S. V. Fokin, E. M. Zueva, A. O. Tkacheva, G. V. Romanenko, A. S. Bogomyakov, S. V. Larionov, S. A. Popov, V. I. Ovcharenko// Russian Chemical Bulletin, 2014, V. 63, N 7, pp 1459-1464 doi:10.1007/s11172-014-0621-8), IF=0.509
  266. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  267. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  268. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  269. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  270. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  271. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Исследование превращений перекисных продуктов озонолиза олефинов в тетрагидрофуране при взаимодействи с гидрохлоридами гидроксиламина и семикарбазида
    Журнал органической химии. 2014. Т. 50. № 7. С. 948-953. (Transformations of peroxide products of olefin ozonolysis in tetrahydrofuran in reactions with hydroxylamine and semicarbazide hydrochlorides/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 7, pp 928-933. doi:10.1134/S1070428014070021), IF=0.675
  272. С.В. Аньков, Т.Г. Толстикова, М.В. Хвостов, А.А. Онищук, А.М. Бакланов, В.В. Болдырев
    Влияние наноаэрозольной формы лекарственных препаратов на их базовую активность
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 223-227. (Effect of the Nanoaerosol Form of Medical Products on Their Basic Activity/ S.V. Ankov, T.G. Tolstikova, M.V. Khvostov, A.A. Onischuk, A.M. Baklanov, V.V. Boldyrev// Chemistry for Sustainable Development. 2014. Т. 22. N 3. С. 223-227. (in russian))
  273. С.В. Аньков, Т.Г. Толстикова, М.В. Хвостов, А.А. Онищук, А.М. Бакланов, В.В. Болдырев
    Влияние наноаэрозольной формы лекарственных препаратов на их базовую активность
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 223-227. (Effect of the Nanoaerosol Form of Medical Products on Their Basic Activity/ S.V. Ankov, T.G. Tolstikova, M.V. Khvostov, A.A. Onischuk, A.M. Baklanov, V.V. Boldyrev// Chemistry for Sustainable Development. 2014. Т. 22. N 3. С. 223-227. (in russian))
  274. С.В. Аньков, Т.Г. Толстикова, М.В. Хвостов, А.А. Онищук, А.М. Бакланов, В.В. Болдырев
    Влияние наноаэрозольной формы лекарственных препаратов на их базовую активность
    Химия в интересах устойчивого развития. 2014. Т. 22. № 3. С. 223-227. (Effect of the Nanoaerosol Form of Medical Products on Their Basic Activity/ S.V. Ankov, T.G. Tolstikova, M.V. Khvostov, A.A. Onischuk, A.M. Baklanov, V.V. Boldyrev// Chemistry for Sustainable Development. 2014. Т. 22. N 3. С. 223-227. (in russian))
  275. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  276. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  277. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  278. Yu.S. Demidova, O.V. Ardashov, O.A. Simakova, I.L. Simakova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Isomerization of bicyclic terpene epoxides into allylic alcohols without changing of the initial structure
    Journal of Molecular Catalysis A: Chemical, 2014, V. 388–389, Pp 162–166. Special Issue on Biomass Catalysis. doi:10.1016/j.molcata.2013.09.016, IF=3.678
  279. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, V. N. Parmon
    The influence of the nature of phosphine ligand on palladium catalysts for cross-coupling of weakly nucleophilic potassium pentafluorophenyltrifluoroborate with ArHal and PhCH2Hal (Hal=Br, Cl)
    Tetrahedron, 2014, V.70, N, 23, P. 3720-3725. doi:10.1016/j.tet.2014.04.019, IF=2.816
  280. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, V. N. Parmon
    The influence of the nature of phosphine ligand on palladium catalysts for cross-coupling of weakly nucleophilic potassium pentafluorophenyltrifluoroborate with ArHal and PhCH2Hal (Hal=Br, Cl)
    Tetrahedron, 2014, V.70, N, 23, P. 3720-3725. doi:10.1016/j.tet.2014.04.019, IF=2.816
  281. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, V. N. Parmon
    The influence of the nature of phosphine ligand on palladium catalysts for cross-coupling of weakly nucleophilic potassium pentafluorophenyltrifluoroborate with ArHal and PhCH2Hal (Hal=Br, Cl)
    Tetrahedron, 2014, V.70, N, 23, P. 3720-3725. doi:10.1016/j.tet.2014.04.019, IF=2.816
  282. Е.Г. Ковалева, Л.С. Молочников, Е.В. Паршина, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Сu2+-содержащие композиционные материалы на основе диоксида циркония и порошковой целлюлозы: влияние заряда поверхности на их комплексообразующие и каталитические свойства
    Химическая физика. 2014. Т. 33. № 6. С. 27-36. (Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X), IF=0.335
  283. Е.Г. Ковалева, Л.С. Молочников, Е.В. Паршина, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Сu2+-содержащие композиционные материалы на основе диоксида циркония и порошковой целлюлозы: влияние заряда поверхности на их комплексообразующие и каталитические свойства
    Химическая физика. 2014. Т. 33. № 6. С. 27-36. (Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X), IF=0.335
  284. Е.Г. Ковалева, Л.С. Молочников, Е.В. Паршина, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Сu2+-содержащие композиционные материалы на основе диоксида циркония и порошковой целлюлозы: влияние заряда поверхности на их комплексообразующие и каталитические свойства
    Химическая физика. 2014. Т. 33. № 6. С. 27-36. (Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X), IF=0.335
  285. Е.Г. Ковалева, Л.С. Молочников, Е.В. Паршина, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Сu2+-содержащие композиционные материалы на основе диоксида циркония и порошковой целлюлозы: влияние заряда поверхности на их комплексообразующие и каталитические свойства
    Химическая физика. 2014. Т. 33. № 6. С. 27-36. (Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X), IF=0.335
  286. Е.Г. Ковалева, Л.С. Молочников, Е.В. Паршина, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Сu2+-содержащие композиционные материалы на основе диоксида циркония и порошковой целлюлозы: влияние заряда поверхности на их комплексообразующие и каталитические свойства
    Химическая физика. 2014. Т. 33. № 6. С. 27-36. (Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X), IF=0.335
  287. A. V. Lipeeva, E. E. Shults, M. M. Shakirov, M. A. Pokrovsky, A. G. Pokrovsky
    Synthesis and Cytotoxic Activity of a New Group of Heterocyclic Analogues of the Combretastatins
    Molecules 2014, 19(6), 7881-7900. doi:10.3390/molecules19067881, IF=2.95
  288. A. V. Lipeeva, E. E. Shults, M. M. Shakirov, M. A. Pokrovsky, A. G. Pokrovsky
    Synthesis and Cytotoxic Activity of a New Group of Heterocyclic Analogues of the Combretastatins
    Molecules 2014, 19(6), 7881-7900. doi:10.3390/molecules19067881, IF=2.95
  289. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  290. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  291. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  292. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  293. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  294. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  295. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  296. A. B. Burdukov, M. A. Vershinin, N. V. Pervukhina, E. G. Boguslvaskii, I. V. Eltsov, L. A. Shundrin, S. L. Selector, A. V. Shokurov, Ya. Z. Voloshin
    Towards the clathrochelate-based electrochromic materials: The case study of the first iron(II) cage complex with an annelated quinoxaline fragment
    Inorganic Chemistry Communications, 2014, V. 44, Pp 183-187. doi:10.1016/j.inoche.2014.03.032, IF=2.62
  297. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез фотолюминесцирующих соединений Eu(III), Sm(III) и Dy(III), содержащих анионы тетрафтортерефталевой кислоты
    Журнал общей химии. 2014. Т. 84. № 6. С. 1014-1019. (Preparation of photoluminescent compounds of Eu(III), Sm(III), and Dy(III) containing anions of tetrafluoroterephthalic acid/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, I. V. Korol’kov, O. V. Antonova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2014, V. 84, N 6, pp 1193-1197. doi:10.1134/S107036321406022X), IF=0.418
  298. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез фотолюминесцирующих соединений Eu(III), Sm(III) и Dy(III), содержащих анионы тетрафтортерефталевой кислоты
    Журнал общей химии. 2014. Т. 84. № 6. С. 1014-1019. (Preparation of photoluminescent compounds of Eu(III), Sm(III), and Dy(III) containing anions of tetrafluoroterephthalic acid/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, I. V. Korol’kov, O. V. Antonova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2014, V. 84, N 6, pp 1193-1197. doi:10.1134/S107036321406022X), IF=0.418
  299. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез фотолюминесцирующих соединений Eu(III), Sm(III) и Dy(III), содержащих анионы тетрафтортерефталевой кислоты
    Журнал общей химии. 2014. Т. 84. № 6. С. 1014-1019. (Preparation of photoluminescent compounds of Eu(III), Sm(III), and Dy(III) containing anions of tetrafluoroterephthalic acid/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, I. V. Korol’kov, O. V. Antonova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2014, V. 84, N 6, pp 1193-1197. doi:10.1134/S107036321406022X), IF=0.418
  300. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез фотолюминесцирующих соединений Eu(III), Sm(III) и Dy(III), содержащих анионы тетрафтортерефталевой кислоты
    Журнал общей химии. 2014. Т. 84. № 6. С. 1014-1019. (Preparation of photoluminescent compounds of Eu(III), Sm(III), and Dy(III) containing anions of tetrafluoroterephthalic acid/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, I. V. Korol’kov, O. V. Antonova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2014, V. 84, N 6, pp 1193-1197. doi:10.1134/S107036321406022X), IF=0.418
  301. С.В. Ларионов, Л.И. Мячина, Л.А. Шелудякова, И.В. Корольков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез фотолюминесцирующих соединений Eu(III), Sm(III) и Dy(III), содержащих анионы тетрафтортерефталевой кислоты
    Журнал общей химии. 2014. Т. 84. № 6. С. 1014-1019. (Preparation of photoluminescent compounds of Eu(III), Sm(III), and Dy(III) containing anions of tetrafluoroterephthalic acid/ S. V. Larionov, L. I. Myachina, L. A. Sheludyakova, I. V. Korol’kov, O. V. Antonova, V. M. Karpov, V. E. Platonov, V. P. Fadeeva// Russian Journal of General Chemistry, 2014, V. 84, N 6, pp 1193-1197. doi:10.1134/S107036321406022X), IF=0.418
  302. D. A. Parkhomenko, M. V. Edeleva, V. G. Kiselev, E. G. Bagryanskaya
    pH-Sensitive C-ON Bond Homolysis of Alkoxyamines of Imidazoline Series: A Theoretical Study
    J. Phys. Chem. B, 2014, 118 (20), pp 5542-5550. doi:10.1021/jp5024372, IF=3.377
  303. D. A. Parkhomenko, M. V. Edeleva, V. G. Kiselev, E. G. Bagryanskaya
    pH-Sensitive C-ON Bond Homolysis of Alkoxyamines of Imidazoline Series: A Theoretical Study
    J. Phys. Chem. B, 2014, 118 (20), pp 5542-5550. doi:10.1021/jp5024372, IF=3.377
  304. D. A. Parkhomenko, M. V. Edeleva, V. G. Kiselev, E. G. Bagryanskaya
    pH-Sensitive C-ON Bond Homolysis of Alkoxyamines of Imidazoline Series: A Theoretical Study
    J. Phys. Chem. B, 2014, 118 (20), pp 5542-5550. doi:10.1021/jp5024372, IF=3.377
  305. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  306. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  307. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  308. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  309. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  310. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  311. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  312. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  313. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
    Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
  314. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
    Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
  315. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
    Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
  316. A.S. Sokolova, О.I. Yarovaya, D.V. Korchagina, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, N.F. Salakhutdinov
    Camphor-based symmetric diimines as inhibitors of influenza virus reproduction
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 7, Pp 2141-2148. doi:10.1016/j.bmc.2014.02.038, IF=2.95
  317. S.F. Vasilevsky, D.S. Baranov, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, G.A. Tolstikov, I.V. Alabugin
    Click chemistry on diterpenes: anti-inflammatory activity of the acetylenic derivatives of levopimaric acid and products of their transformations
    ARKIVOС, 2014, V. 2014, Part (v), pp. 145 - 147. doi:10.3998/ark.5550190.p008.471, IF=1.75
  318. S.F. Vasilevsky, D.S. Baranov, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, G.A. Tolstikov, I.V. Alabugin
    Click chemistry on diterpenes: anti-inflammatory activity of the acetylenic derivatives of levopimaric acid and products of their transformations
    ARKIVOС, 2014, V. 2014, Part (v), pp. 145 - 147. doi:10.3998/ark.5550190.p008.471, IF=1.75
  319. S.F. Vasilevsky, D.S. Baranov, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, G.A. Tolstikov, I.V. Alabugin
    Click chemistry on diterpenes: anti-inflammatory activity of the acetylenic derivatives of levopimaric acid and products of their transformations
    ARKIVOС, 2014, V. 2014, Part (v), pp. 145 - 147. doi:10.3998/ark.5550190.p008.471, IF=1.75
  320. S.F. Vasilevsky, D.S. Baranov, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, G.A. Tolstikov, I.V. Alabugin
    Click chemistry on diterpenes: anti-inflammatory activity of the acetylenic derivatives of levopimaric acid and products of their transformations
    ARKIVOС, 2014, V. 2014, Part (v), pp. 145 - 147. doi:10.3998/ark.5550190.p008.471, IF=1.75
  321. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, Е.В. Стукань, В.М. Берестовицкая
    3,3,3-трибром-1-нитропропен: синтез и строение
    Журнал общей химии. 2014. Т. 84. № 5. С. 741-745. (3,3,3-Tribromo-1-nitropropene: Synthesis and structure/ N. A. Anisimova, E. K. Slobodchikova, A. A. Kuzhaeva, T. V. Rybalova, E. V. Stukan’, V. M. Berestovitskaya// Russian Journal of General Chemistry, 2014, V. 84, N 5, pp 834-838. doi:10.1134/S1070363214050089), IF=0.418
  322. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, Е.В. Стукань, В.М. Берестовицкая
    3,3,3-трибром-1-нитропропен: синтез и строение
    Журнал общей химии. 2014. Т. 84. № 5. С. 741-745. (3,3,3-Tribromo-1-nitropropene: Synthesis and structure/ N. A. Anisimova, E. K. Slobodchikova, A. A. Kuzhaeva, T. V. Rybalova, E. V. Stukan’, V. M. Berestovitskaya// Russian Journal of General Chemistry, 2014, V. 84, N 5, pp 834-838. doi:10.1134/S1070363214050089), IF=0.418
  323. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, Е.В. Стукань, В.М. Берестовицкая
    3,3,3-трибром-1-нитропропен: синтез и строение
    Журнал общей химии. 2014. Т. 84. № 5. С. 741-745. (3,3,3-Tribromo-1-nitropropene: Synthesis and structure/ N. A. Anisimova, E. K. Slobodchikova, A. A. Kuzhaeva, T. V. Rybalova, E. V. Stukan’, V. M. Berestovitskaya// Russian Journal of General Chemistry, 2014, V. 84, N 5, pp 834-838. doi:10.1134/S1070363214050089), IF=0.418
  324. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, Е.В. Стукань, В.М. Берестовицкая
    3,3,3-трибром-1-нитропропен: синтез и строение
    Журнал общей химии. 2014. Т. 84. № 5. С. 741-745. (3,3,3-Tribromo-1-nitropropene: Synthesis and structure/ N. A. Anisimova, E. K. Slobodchikova, A. A. Kuzhaeva, T. V. Rybalova, E. V. Stukan’, V. M. Berestovitskaya// Russian Journal of General Chemistry, 2014, V. 84, N 5, pp 834-838. doi:10.1134/S1070363214050089), IF=0.418
  325. Н.А. Анисимова, Е.К. Слободчикова, А.А. Кужаева, Т.В. Рыбалова, Е.В. Стукань, В.М. Берестовицкая
    3,3,3-трибром-1-нитропропен: синтез и строение
    Журнал общей химии. 2014. Т. 84. № 5. С. 741-745. (3,3,3-Tribromo-1-nitropropene: Synthesis and structure/ N. A. Anisimova, E. K. Slobodchikova, A. A. Kuzhaeva, T. V. Rybalova, E. V. Stukan’, V. M. Berestovitskaya// Russian Journal of General Chemistry, 2014, V. 84, N 5, pp 834-838. doi:10.1134/S1070363214050089), IF=0.418
  326. Д.Ф. Августинович, М.К. Фомина, И.В. Сорокина, Т.Г. Толстикова
    Комплексное исследование эффектов амида ламбертиановой кислоты у самок мышей, находящихся в условиях социального дискомфорта
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 5. С. 599-603. (Complex Investigation of the Effects of Lambertianic Acid Amide in Female Mice under Conditions of Social Discomfort/ D. F. Avgustinovich, M. K. Fomina, I. V. Sorokina, T. G. Tolstikova// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 5, pp 583-587. doi:10.1007/s10517-014-2621-y), IF=0.365
  327. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  328. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  329. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  330. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  331. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  332. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  333. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  334. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  335. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  336. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
    Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
    Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
  337. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  338. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  339. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  340. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  341. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  342. M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.I. Rakhmanova, A.Ya. Tikhonov, S.V. Larionov
    Zinc(II) complexes with an imidazolylpyridine ligand: luminescence and hydrogen bonding
    Journal of Coordination Chemistry, 2014, V. 67, N 4, 2014, pp 611-622. doi:10.1080/00958972.2014.892589, IF=2.223
  343. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  344. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  345. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  346. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  347. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  348. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  349. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  350. Ю.С. Чистяченко, М.В. Хвостов, А.И. Белоусов, Н.А. Жукова, М.Ю. Пахарукова, А.В. Катохин, С.С. Халиков, Т.Г. Толстикова, А.В. Душкин, В.А. Мордвинов, Н.З. Ляхов
    Физико-химические свойства и противоописторхозное действие механохимически синтезированных супрамолекулярных комплексов албендазола и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix gmelinii
    Доклады АН, Общая биология, 2014, Т.456, №6, p.741-744. doi:10.7868/S0869565214180273
  351. M.V. Edeleva, D.A. Parkhomenko, D.A. Morozov, S.A. Dobrynin, D.G. Trofimov, B. Kanagatov, I.A. Kirilyuk, E.G. Bagryanskaya
    Controlled/living polymerization of methyl methacrylate using new sterically hindered imidazoline nitroxides prepared via intramolecular 1,3-dipolar cycloaddition reaction
    Journal of Polymer Science Part A: Polymer Chemistry, 2014, V. 52, N 7, pp 929-943. doi:10.1002/pola.27071, IF=3.244
  352. M.V. Edeleva, D.A. Parkhomenko, D.A. Morozov, S.A. Dobrynin, D.G. Trofimov, B. Kanagatov, I.A. Kirilyuk, E.G. Bagryanskaya
    Controlled/living polymerization of methyl methacrylate using new sterically hindered imidazoline nitroxides prepared via intramolecular 1,3-dipolar cycloaddition reaction
    Journal of Polymer Science Part A: Polymer Chemistry, 2014, V. 52, N 7, pp 929-943. doi:10.1002/pola.27071, IF=3.244
  353. M.V. Edeleva, D.A. Parkhomenko, D.A. Morozov, S.A. Dobrynin, D.G. Trofimov, B. Kanagatov, I.A. Kirilyuk, E.G. Bagryanskaya
    Controlled/living polymerization of methyl methacrylate using new sterically hindered imidazoline nitroxides prepared via intramolecular 1,3-dipolar cycloaddition reaction
    Journal of Polymer Science Part A: Polymer Chemistry, 2014, V. 52, N 7, pp 929-943. doi:10.1002/pola.27071, IF=3.244
  354. М.В. Шашков, В.Н. Сидельников, П.А. Заикин
    Селективность неподвижных фаз на основе пиридиниевых ионных жидкостей для капиллярной газовой хроматографии
    Журнал физической химии. 2014. Т. 88. № 4. С. 714-719. (Selectivity of stationary phases based on pyridinium ionic liquids for capillary gas chromatography/ M. V. Shashkov, V. N. Sidelnikov, P. A. Zaikin// Russian Journal of Physical Chemistry A, 2014, V. 88, N 4, pp 717-721. doi:10.1134/S0036024414040268), IF=0.488
  355. М.В. Шашков, В.Н. Сидельников, П.А. Заикин
    Селективность неподвижных фаз на основе пиридиниевых ионных жидкостей для капиллярной газовой хроматографии
    Журнал физической химии. 2014. Т. 88. № 4. С. 714-719. (Selectivity of stationary phases based on pyridinium ionic liquids for capillary gas chromatography/ M. V. Shashkov, V. N. Sidelnikov, P. A. Zaikin// Russian Journal of Physical Chemistry A, 2014, V. 88, N 4, pp 717-721. doi:10.1134/S0036024414040268), IF=0.488
  356. Л.А. Богданова, Т.С. Морозкова, С.А. Амитина, Д.Г. Мажукин, В.П. Николин, Н.А. Попова, В.И. Каледин
    Двойственное влияние ингибиторов индоламин-2,3-диоксигеназы на терапевтическое действие циклофосфана и циклоплатама в отношении асцитной опухоли эрлиха у мышей
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 4. С. 507-510. (Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice/ L. A. Bogdanova, T. S. Morozkova, S. A. Amitina, D. G. Mazhukin, V. P. Nikolin, N. A. Popova, V. I. Kaledin// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 4, pp 506-509. doi:10.1007/s10517-014-2602-1), IF=0.365
  357. Л.А. Богданова, Т.С. Морозкова, С.А. Амитина, Д.Г. Мажукин, В.П. Николин, Н.А. Попова, В.И. Каледин
    Двойственное влияние ингибиторов индоламин-2,3-диоксигеназы на терапевтическое действие циклофосфана и циклоплатама в отношении асцитной опухоли эрлиха у мышей
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 4. С. 507-510. (Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice/ L. A. Bogdanova, T. S. Morozkova, S. A. Amitina, D. G. Mazhukin, V. P. Nikolin, N. A. Popova, V. I. Kaledin// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 4, pp 506-509. doi:10.1007/s10517-014-2602-1), IF=0.365
  358. Л.А. Богданова, Т.С. Морозкова, С.А. Амитина, Д.Г. Мажукин, В.П. Николин, Н.А. Попова, В.И. Каледин
    Двойственное влияние ингибиторов индоламин-2,3-диоксигеназы на терапевтическое действие циклофосфана и циклоплатама в отношении асцитной опухоли эрлиха у мышей
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 4. С. 507-510. (Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice/ L. A. Bogdanova, T. S. Morozkova, S. A. Amitina, D. G. Mazhukin, V. P. Nikolin, N. A. Popova, V. I. Kaledin// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 4, pp 506-509. doi:10.1007/s10517-014-2602-1), IF=0.365
  359. Л.А. Богданова, Т.С. Морозкова, С.А. Амитина, Д.Г. Мажукин, В.П. Николин, Н.А. Попова, В.И. Каледин
    Двойственное влияние ингибиторов индоламин-2,3-диоксигеназы на терапевтическое действие циклофосфана и циклоплатама в отношении асцитной опухоли эрлиха у мышей
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 4. С. 507-510. (Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice/ L. A. Bogdanova, T. S. Morozkova, S. A. Amitina, D. G. Mazhukin, V. P. Nikolin, N. A. Popova, V. I. Kaledin// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 4, pp 506-509. doi:10.1007/s10517-014-2602-1), IF=0.365
  360. Л.А. Богданова, Т.С. Морозкова, С.А. Амитина, Д.Г. Мажукин, В.П. Николин, Н.А. Попова, В.И. Каледин
    Двойственное влияние ингибиторов индоламин-2,3-диоксигеназы на терапевтическое действие циклофосфана и циклоплатама в отношении асцитной опухоли эрлиха у мышей
    Бюллетень экспериментальной биологии и медицины. 2014. Т. 157. № 4. С. 507-510. (Dual Effects of Indoleamine 2,3-Dioxygenase Inhibitors on the Therapeutic Effects of Cyclophosphamide and Cycloplatam on Ehrlich Ascites Tumor in Mice/ L. A. Bogdanova, T. S. Morozkova, S. A. Amitina, D. G. Mazhukin, V. P. Nikolin, N. A. Popova, V. I. Kaledin// Bulletin of Experimental Biology and Medicine, 2014, V. 157, N 4, pp 506-509. doi:10.1007/s10517-014-2602-1), IF=0.365
  361. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  362. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  363. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  364. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  365. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  366. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  367. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  368. Ю.В. Нестерова, Т.Н. Поветьева, Н.И. Суслов, Г.Н. Зюзьков, С.В. Пушкарский, С.Г. Аксиненко, Э.Э. Шульц, С.С. Кравцова, А.В. Крапивин
    Анальгетическая активность дитерпеновых алкалоидов аконита байкальского.
    Бюллетень экспериментальной биологии и медицины, 2014. Т. 157. № 4. С. 488-491 (Analgesic Activity of Diterpene Alkaloids from Aconitum Baikalensis/ Yu. V. Nesterova, T. N. Povet’yeva, N. I. Suslov, G. N. Zyuz’kov, S. V. Pushkarskii, S. G. Aksinenko, E. E. Schultz, S. S. Kravtsova, A. V. Krapivin// Bulletin of Experimental Biology and Medicine, August 2014, Volume 157, Issue 4, pp 488-491 doi:10.1007/s10517-014-2598-6), IF=0.365
  369. С.Ф. Василевский, Т.Ф. Михайловская, А.А. Степанов, В.И. Маматюк, Д.С. Фадеев
    Особенности основно-индуцируемой гетероциклизации вицинальных (R-этинил)фенилгидроксамовых кислот
    Журнал органической химии. 2014. Т. 50. № 4. С. 518-521. (Base-catalyzed heterocyclization of 2-(R-ethynyl)benzohydroxamic acids/ S. F. Vasilevskii, T. F. Mikhailovskaya, A. A. Stepanov, V. I. Mamatyuk, D. S. Fadeev// Russian Journal of Organic Chemistry, 2014, V. 50, N 4, pp 506-509. doi:10.1134/S1070428014040101), IF=0.675
  370. С.Ф. Василевский, Т.Ф. Михайловская, А.А. Степанов, В.И. Маматюк, Д.С. Фадеев
    Особенности основно-индуцируемой гетероциклизации вицинальных (R-этинил)фенилгидроксамовых кислот
    Журнал органической химии. 2014. Т. 50. № 4. С. 518-521. (Base-catalyzed heterocyclization of 2-(R-ethynyl)benzohydroxamic acids/ S. F. Vasilevskii, T. F. Mikhailovskaya, A. A. Stepanov, V. I. Mamatyuk, D. S. Fadeev// Russian Journal of Organic Chemistry, 2014, V. 50, N 4, pp 506-509. doi:10.1134/S1070428014040101), IF=0.675
  371. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Selective stepwise reduction of polynitroarenes using supercritical isopropanol as a source of hydrogen in a flow-type reactor in the presence of alumina
    Journal of Flow Chemistry, 2014, Vol. 4, N 3, 113-117. doi:10.1556/JFC-D-14-00004, IF=2.405
  372. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  373. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  374. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  375. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  376. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  377. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  378. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
  379. В.С. Глухачева, С.Г. Ильясов, Н.В. Плешкова
    Синтез и спектроскопическое исследование 5-нитросемикарбазона фурфурола
    Ползуновский вестник № 3, 2014, 120-123
  380. В.С. Глухачева, С.Г. Ильясов, Н.В. Плешкова
    Синтез и спектроскопическое исследование 5-нитросемикарбазона фурфурола
    Ползуновский вестник № 3, 2014, 120-123
  381. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  382. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  383. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  384. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  385. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  386. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  387. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  388. A.Yu. Makarov, E.A. Chulanova, N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, E. Lork, N.P. Gritsan, S.N. Konchenko, V.I. Ovcharenko, A.V. Zibarev
    A novel sulfur-nitrogen Pi-heterocyclic radical anion, (6H-1,2,3-benzodithiazo16-ylidene)malononitrilidyl, and its homo- and heterospin salts
    Polyhedron, 2014, V. 72, Pp 43-49. doi:10.1016/j.poly.2014.01.027, IF=2.46
  389. Е.Ю. Яковлева, И.К. Шундрина, Е.Ю. Герасимов, Т.А. Ваганова
    Формирование разделительных слоев в условиях термотренировки адсорбентов, модифицированных фторированным полиимидом
    Журнал физической химии. 2014. Т. 88. № 3. С. 508-516. (Formation of separating layers under conditions of the thermal aging of sorbents modified by fluorinated polyimide/ E. Yu. Yakovleva, I. K. Shundrina, E. Yu. Gerasimov, T. A. Vaganova// Russian Journal of Physical Chemistry A, 2014, V. 88, N 3, pp 521-529. doi:10.1134/S0036024414030297), IF=0.488
  390. Е.Ю. Яковлева, И.К. Шундрина, Е.Ю. Герасимов, Т.А. Ваганова
    Формирование разделительных слоев в условиях термотренировки адсорбентов, модифицированных фторированным полиимидом
    Журнал физической химии. 2014. Т. 88. № 3. С. 508-516. (Formation of separating layers under conditions of the thermal aging of sorbents modified by fluorinated polyimide/ E. Yu. Yakovleva, I. K. Shundrina, E. Yu. Gerasimov, T. A. Vaganova// Russian Journal of Physical Chemistry A, 2014, V. 88, N 3, pp 521-529. doi:10.1134/S0036024414030297), IF=0.488
  391. К.С. Талецкий, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычная трансформация первичных катион-радикалов в облученном жидком тетрагидрофуране.
    Доклады академии наук (Физическая химия), 2014, том 455, № 2, с. 171-174 (Unusual transformation of primary radical cations in irradiated liquid tetrahydrofuran/ K. S. Taletskiy, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, 2014, V. 455, N 1, pp 41-44 doi:10.1134/S0012501614030026), IF=0.474
  392. К.С. Талецкий, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычная трансформация первичных катион-радикалов в облученном жидком тетрагидрофуране.
    Доклады академии наук (Физическая химия), 2014, том 455, № 2, с. 171-174 (Unusual transformation of primary radical cations in irradiated liquid tetrahydrofuran/ K. S. Taletskiy, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, 2014, V. 455, N 1, pp 41-44 doi:10.1134/S0012501614030026), IF=0.474
  393. К.С. Талецкий, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычная трансформация первичных катион-радикалов в облученном жидком тетрагидрофуране.
    Доклады академии наук (Физическая химия), 2014, том 455, № 2, с. 171-174 (Unusual transformation of primary radical cations in irradiated liquid tetrahydrofuran/ K. S. Taletskiy, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, 2014, V. 455, N 1, pp 41-44 doi:10.1134/S0012501614030026), IF=0.474
  394. К.С. Талецкий, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычная трансформация первичных катион-радикалов в облученном жидком тетрагидрофуране.
    Доклады академии наук (Физическая химия), 2014, том 455, № 2, с. 171-174 (Unusual transformation of primary radical cations in irradiated liquid tetrahydrofuran/ K. S. Taletskiy, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Doklady Physical Chemistry, 2014, V. 455, N 1, pp 41-44 doi:10.1134/S0012501614030026), IF=0.474
  395. В.В. Шелковников, И.Ю. Каргаполова, С.В. Коротаев, Н.А. Орлова, И.П. Чуйков, В.А. Надолинный
    Люминесцентное детектирование анилинов с применением пирилоцианиновых красителей в растворах и адсорбированном состоянии
    Известия Академии наук, 2014, №3, С. 635-641. (Detection of anilines by luminescence spectroscopy using dissolved and adsorbed pyrylocyanine dyes/ V. V. Shelkovnikov, I. Yu. Kargapolova, S. V. Korotaev, N. A. Orlova, I. P. Chuikov, V. A. Nadolinnyi// Russian Chemical Bulletin, March 2014, Volume 63, Issue 3, pp 635-641. doi:10.1007/s11172-014-0485-y), IF=0.509
  396. И.В. Шилова, Т.П. Кукина, Н.И. Суслов, О.И. Сальникова, Р.Н. Мустафин
    Изучение липофильных компонентов густого экстракта травы Альфредии Поникшей и его ноотропных свойств
    Химико-фармацевтический журнал. 2014. Т. 48. № 3. С. 26-30. (Studies of the Lipophilic Components of a Dense Extract of the Herb Alfredia Cernua and its Nootropic Properties/ I. V. Shilova, T. P. Kukina, N. I. Suslov, O. I. Sal’nikova, R. N. Mustafin// Pharmaceutical Chemistry Journal, 2014, V. 48, N 3, pp 181-185. doi:10.1007/s11094-014-1074-y), IF=0.3
  397. И.В. Шилова, Т.П. Кукина, Н.И. Суслов, О.И. Сальникова, Р.Н. Мустафин
    Изучение липофильных компонентов густого экстракта травы Альфредии Поникшей и его ноотропных свойств
    Химико-фармацевтический журнал. 2014. Т. 48. № 3. С. 26-30. (Studies of the Lipophilic Components of a Dense Extract of the Herb Alfredia Cernua and its Nootropic Properties/ I. V. Shilova, T. P. Kukina, N. I. Suslov, O. I. Sal’nikova, R. N. Mustafin// Pharmaceutical Chemistry Journal, 2014, V. 48, N 3, pp 181-185. doi:10.1007/s11094-014-1074-y), IF=0.3
  398. И.В. Шилова, Т.П. Кукина, Н.И. Суслов, О.И. Сальникова, Р.Н. Мустафин
    Изучение липофильных компонентов густого экстракта травы Альфредии Поникшей и его ноотропных свойств
    Химико-фармацевтический журнал. 2014. Т. 48. № 3. С. 26-30. (Studies of the Lipophilic Components of a Dense Extract of the Herb Alfredia Cernua and its Nootropic Properties/ I. V. Shilova, T. P. Kukina, N. I. Suslov, O. I. Sal’nikova, R. N. Mustafin// Pharmaceutical Chemistry Journal, 2014, V. 48, N 3, pp 181-185. doi:10.1007/s11094-014-1074-y), IF=0.3
  399. E.M. Glebov, V.P. Chernetsov, V.P. Grivin, V.F. Plyusnin, A.B. Venediktov
    Photochemistry of Pt(SСN)2-6> complex in aqueous solutions
    Mendeleev Communications, 2014, V. 24, Iss. 2, Pp. 111-113. doi:10.1016/j.mencom.2014.03.016, IF=1.154
  400. E.M. Glebov, V.P. Chernetsov, V.P. Grivin, V.F. Plyusnin, A.B. Venediktov
    Photochemistry of Pt(SСN)2-6> complex in aqueous solutions
    Mendeleev Communications, 2014, V. 24, Iss. 2, Pp. 111-113. doi:10.1016/j.mencom.2014.03.016, IF=1.154
  401. E.M. Glebov, V.P. Chernetsov, V.P. Grivin, V.F. Plyusnin, A.B. Venediktov
    Photochemistry of Pt(SСN)2-6> complex in aqueous solutions
    Mendeleev Communications, 2014, V. 24, Iss. 2, Pp. 111-113. doi:10.1016/j.mencom.2014.03.016, IF=1.154
  402. E.M. Glebov, V.P. Chernetsov, V.P. Grivin, V.F. Plyusnin, A.B. Venediktov
    Photochemistry of Pt(SСN)2-6> complex in aqueous solutions
    Mendeleev Communications, 2014, V. 24, Iss. 2, Pp. 111-113. doi:10.1016/j.mencom.2014.03.016, IF=1.154
  403. E.G. Bagryanskaya, S.R. A. Marque
    Scavenging of Organic C-Centered Radicals by Nitroxides
    Chem. Rev., 2014, 114 (9), pp 5011-5056. doi:10.1021/cr4000946, IF=45.66
  404. О.В. Рыбачук, Ю.М. Дерябина, М.П. Сартаков, И.Д. Комиссаров
    Сравнительная характеристика элементного состава гуминовых и гиматомелановых кислот торфов Среднего Приобья.
    Аграрная наука Евро-Северо-Востока, 2014, №1(38), С.36-40.
  405. О.В. Рыбачук, Ю.М. Дерябина, М.П. Сартаков, И.Д. Комиссаров
    Сравнительная характеристика элементного состава гуминовых и гиматомелановых кислот торфов Среднего Приобья.
    Аграрная наука Евро-Северо-Востока, 2014, №1(38), С.36-40.
  406. О.В. Рыбачук, Ю.М. Дерябина, М.П. Сартаков, И.Д. Комиссаров
    Сравнительная характеристика элементного состава гуминовых и гиматомелановых кислот торфов Среднего Приобья.
    Аграрная наука Евро-Северо-Востока, 2014, №1(38), С.36-40.
  407. V.P. Sivcev, D.V. Korchagina, E.V. Suslov, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Efficient reduction of nitroarenes using supercritical alcohols as a source of hydrogen in flow-type reactor in the presence of alumina
    The Journal of Supercritical Fluids, 2014, V. 86, Pp 137-144. doi:10.1016/j.supflu.2013.12.012, IF=2.571
  408. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  409. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  410. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  411. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  412. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  413. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  414. K.V. Belyaeva, L.V. Andriyankova, L.P. Nikitina, A.G. Mal'kina, A.V. Afonin, I.A. Ushakov, I.Yu. Bagryanskaya, B.A. Trofimov
    Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones
    Tetrahedron, 2014, V.70, N 5, P. 1091-1098. doi:10.1016/j.tet.2013.10.094, IF=2.816
  415. Н.А. Анисимова, Е.К. Слободчикова, В.М. Берестовицкая, А.А. Кужаева, М.Е. Иванова, Т.В. Рыбалова
    Синтез и строение оксанорборненов, функционализированных нитро- и трихлорметильной группами
    Журнал общей химии. 2014. Т. 84. № 2. С. 249-261. (Synthesis and structure of oxanorbornenes functionalized by nitro- and trichloromethyl groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, A. A. Kuzhaeva, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2014, V. 84, N 2, pp 242-254. doi:10.1134/S1070363214020145), IF=0.418
  416. Н.А. Анисимова, Е.К. Слободчикова, В.М. Берестовицкая, А.А. Кужаева, М.Е. Иванова, Т.В. Рыбалова
    Синтез и строение оксанорборненов, функционализированных нитро- и трихлорметильной группами
    Журнал общей химии. 2014. Т. 84. № 2. С. 249-261. (Synthesis and structure of oxanorbornenes functionalized by nitro- and trichloromethyl groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, A. A. Kuzhaeva, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2014, V. 84, N 2, pp 242-254. doi:10.1134/S1070363214020145), IF=0.418
  417. Н.А. Анисимова, Е.К. Слободчикова, В.М. Берестовицкая, А.А. Кужаева, М.Е. Иванова, Т.В. Рыбалова
    Синтез и строение оксанорборненов, функционализированных нитро- и трихлорметильной группами
    Журнал общей химии. 2014. Т. 84. № 2. С. 249-261. (Synthesis and structure of oxanorbornenes functionalized by nitro- and trichloromethyl groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, A. A. Kuzhaeva, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2014, V. 84, N 2, pp 242-254. doi:10.1134/S1070363214020145), IF=0.418
  418. Н.А. Анисимова, Е.К. Слободчикова, В.М. Берестовицкая, А.А. Кужаева, М.Е. Иванова, Т.В. Рыбалова
    Синтез и строение оксанорборненов, функционализированных нитро- и трихлорметильной группами
    Журнал общей химии. 2014. Т. 84. № 2. С. 249-261. (Synthesis and structure of oxanorbornenes functionalized by nitro- and trichloromethyl groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, A. A. Kuzhaeva, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2014, V. 84, N 2, pp 242-254. doi:10.1134/S1070363214020145), IF=0.418
  419. Н.А. Анисимова, Е.К. Слободчикова, В.М. Берестовицкая, А.А. Кужаева, М.Е. Иванова, Т.В. Рыбалова
    Синтез и строение оксанорборненов, функционализированных нитро- и трихлорметильной группами
    Журнал общей химии. 2014. Т. 84. № 2. С. 249-261. (Synthesis and structure of oxanorbornenes functionalized by nitro- and trichloromethyl groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, A. A. Kuzhaeva, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2014, V. 84, N 2, pp 242-254. doi:10.1134/S1070363214020145), IF=0.418
  420. Л.С. Константинова, Е.А. Князева, И.Ю. Багрянская, Н.В. Обручникова, О.А. Ракитин
    Синтез новой гетероциклической системы - 4,8-дигидро-7H[1,2]дитиоло[3,4-b][1,2,5]оксадиазоло[3,4-e]пиразин-7-тиона
    Известия Академии наук. Серия химическая. 2014, N 2, с. 552-553. (Synthesis of 4,8-dihydro-7H-[1,2]dithiolo[3,4-b][1,2,5]oxadiazolo-[3,4-e]pyrazine-7-thione as a new heterocyclic system/ L. S. Konstantinova, E. A. Knyazeva, I. Yu. Bagryanskaya, N. V. Obruchnikova, O. A. Rakitin// Russian Chemical Bulletin, February 2014, Volume 63, Issue 2, pp 552-553 doi:10.1007/s11172-014-0469-y), IF=0.509
  421. Л.С. Константинова, Е.А. Князева, И.Ю. Багрянская, Н.В. Обручникова, О.А. Ракитин
    Синтез новой гетероциклической системы - 4,8-дигидро-7H[1,2]дитиоло[3,4-b][1,2,5]оксадиазоло[3,4-e]пиразин-7-тиона
    Известия Академии наук. Серия химическая. 2014, N 2, с. 552-553. (Synthesis of 4,8-dihydro-7H-[1,2]dithiolo[3,4-b][1,2,5]oxadiazolo-[3,4-e]pyrazine-7-thione as a new heterocyclic system/ L. S. Konstantinova, E. A. Knyazeva, I. Yu. Bagryanskaya, N. V. Obruchnikova, O. A. Rakitin// Russian Chemical Bulletin, February 2014, Volume 63, Issue 2, pp 552-553 doi:10.1007/s11172-014-0469-y), IF=0.509
  422. Л.С. Константинова, Е.А. Князева, И.Ю. Багрянская, Н.В. Обручникова, О.А. Ракитин
    Синтез новой гетероциклической системы - 4,8-дигидро-7H[1,2]дитиоло[3,4-b][1,2,5]оксадиазоло[3,4-e]пиразин-7-тиона
    Известия Академии наук. Серия химическая. 2014, N 2, с. 552-553. (Synthesis of 4,8-dihydro-7H-[1,2]dithiolo[3,4-b][1,2,5]oxadiazolo-[3,4-e]pyrazine-7-thione as a new heterocyclic system/ L. S. Konstantinova, E. A. Knyazeva, I. Yu. Bagryanskaya, N. V. Obruchnikova, O. A. Rakitin// Russian Chemical Bulletin, February 2014, Volume 63, Issue 2, pp 552-553 doi:10.1007/s11172-014-0469-y), IF=0.509
  423. Л.С. Константинова, Е.А. Князева, И.Ю. Багрянская, Н.В. Обручникова, О.А. Ракитин
    Синтез новой гетероциклической системы - 4,8-дигидро-7H[1,2]дитиоло[3,4-b][1,2,5]оксадиазоло[3,4-e]пиразин-7-тиона
    Известия Академии наук. Серия химическая. 2014, N 2, с. 552-553. (Synthesis of 4,8-dihydro-7H-[1,2]dithiolo[3,4-b][1,2,5]oxadiazolo-[3,4-e]pyrazine-7-thione as a new heterocyclic system/ L. S. Konstantinova, E. A. Knyazeva, I. Yu. Bagryanskaya, N. V. Obruchnikova, O. A. Rakitin// Russian Chemical Bulletin, February 2014, Volume 63, Issue 2, pp 552-553 doi:10.1007/s11172-014-0469-y), IF=0.509
  424. Л.М. Горностаев, И.С. Крюковская, Т.И. Лаврикова, М.В. Вигант, Ю.В. Гатилов
    Синтез 2-амино(алкиламино)-3-нитро-1,4-нафтохинонов
    Журнал органической химии. 2014. Т. 50. № 2. С. 214-218. (Synthesis of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones/ L. M. Gornostaev, I. S. Kryukovskaya, T. I. Lavrikova, M. V. Vigant, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2014, V. 50, N 2, pp 205-210. doi:10.1134/S1070428014020110), IF=0.675
  425. Л.М. Горностаев, И.С. Крюковская, Т.И. Лаврикова, М.В. Вигант, Ю.В. Гатилов
    Синтез 2-амино(алкиламино)-3-нитро-1,4-нафтохинонов
    Журнал органической химии. 2014. Т. 50. № 2. С. 214-218. (Synthesis of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones/ L. M. Gornostaev, I. S. Kryukovskaya, T. I. Lavrikova, M. V. Vigant, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2014, V. 50, N 2, pp 205-210. doi:10.1134/S1070428014020110), IF=0.675
  426. Л.М. Горностаев, И.С. Крюковская, Т.И. Лаврикова, М.В. Вигант, Ю.В. Гатилов
    Синтез 2-амино(алкиламино)-3-нитро-1,4-нафтохинонов
    Журнал органической химии. 2014. Т. 50. № 2. С. 214-218. (Synthesis of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones/ L. M. Gornostaev, I. S. Kryukovskaya, T. I. Lavrikova, M. V. Vigant, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2014, V. 50, N 2, pp 205-210. doi:10.1134/S1070428014020110), IF=0.675
  427. Л.М. Горностаев, И.С. Крюковская, Т.И. Лаврикова, М.В. Вигант, Ю.В. Гатилов
    Синтез 2-амино(алкиламино)-3-нитро-1,4-нафтохинонов
    Журнал органической химии. 2014. Т. 50. № 2. С. 214-218. (Synthesis of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones/ L. M. Gornostaev, I. S. Kryukovskaya, T. I. Lavrikova, M. V. Vigant, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2014, V. 50, N 2, pp 205-210. doi:10.1134/S1070428014020110), IF=0.675
  428. И.И. Олейник, И.В. Олейник, Д.Е. Зайцев, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. XVI. синтез (N-арил)салицилальдиминов, содержащих пент-4-енилоксигруппу, и комплексов дихлорида титана(IV) на их основе
    Журнал органической химии. 2014. Т. 50. № 2. С. 201-208. (Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XVI. Synthesis of (N-aryl)salicylaldimines containing pent-4-enyloxy group and their complexes with titanium(IV) dichloride/ I. I. Oleinik, I. V. Oleinik, D. E. Zaitsev, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 2, pp 191-199. doi:10.1134/S1070428014020092), IF=0.675
  429. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    Antidepressant Activity of 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin- 6-amine hydrochloride (TC-2153): Comparison with Classical Antidepressants
    Letters in Drug Design & Discovery, 2014, V. 11, N 2, pp.169-173. doi:10.2174/15701808113106660079, IF=0.961
  430. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    Antidepressant Activity of 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin- 6-amine hydrochloride (TC-2153): Comparison with Classical Antidepressants
    Letters in Drug Design & Discovery, 2014, V. 11, N 2, pp.169-173. doi:10.2174/15701808113106660079, IF=0.961
  431. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    Antidepressant Activity of 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin- 6-amine hydrochloride (TC-2153): Comparison with Classical Antidepressants
    Letters in Drug Design & Discovery, 2014, V. 11, N 2, pp.169-173. doi:10.2174/15701808113106660079, IF=0.961
  432. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    Antidepressant Activity of 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin- 6-amine hydrochloride (TC-2153): Comparison with Classical Antidepressants
    Letters in Drug Design & Discovery, 2014, V. 11, N 2, pp.169-173. doi:10.2174/15701808113106660079, IF=0.961
  433. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  434. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  435. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  436. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  437. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  438. A.V. Volod'ko, V.N. Davydova, E. Chusovitin, I.V. Sorokina, M.P. Dolgikh, T.G. Tolstikova, S.A. Balagan, N.G. Galkin, I.M. Yermak
    Soluble chitosan–carrageenan polyelectrolyte complexes and their gastroprotective activity
    Carbohydrate Polymers, 2014, V. 101, Pp 1087-1093. doi:10.1016/j.carbpol.2013.10.049, IF=3.915
  439. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  440. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  441. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  442. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  443. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  444. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  445. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  446. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  447. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
  448. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  449. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  450. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  451. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  452. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  453. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  454. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  455. M.N. Timofeeva, V.N. Panchenko, Z. Hasan, N.A. Khan, M.S. Mel'gunov, A.A. Abel, M.M. Matrosova, K.P. Volcho, S.H. Jhung
    Effect of iron content on selectivity in isomerization of alpha-pinene oxide to campholenic aldehyde over Fe-MMM-2 and Fe-VSB-5
    Applied Catalysis A: General, 2014, V. 469, Pp 427-433. doi:10.1016/j.apcata.2013.10.016, IF=3.674
  456. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  457. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  458. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  459. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  460. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  461. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  462. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
  463. Э.Э. Шульц, А.С. Кишкентаева, C.C. Патрушев, Г.А. Атажанова, С.М. Адекенов
    Модификации cесквитерпеновых лактонов c помощью реакции Хека. Некоторые результаты и перспективы.
    Фармацевтический бюллетень. 2014, №1-3, с. 20-28.
  464. Э.Э. Шульц, А.С. Кишкентаева, C.C. Патрушев, Г.А. Атажанова, С.М. Адекенов
    Модификации cесквитерпеновых лактонов c помощью реакции Хека. Некоторые результаты и перспективы.
    Фармацевтический бюллетень. 2014, №1-3, с. 20-28.
  465. Э.Э. Шульц, А.С. Кишкентаева, C.C. Патрушев, Г.А. Атажанова, С.М. Адекенов
    Модификации cесквитерпеновых лактонов c помощью реакции Хека. Некоторые результаты и перспективы.
    Фармацевтический бюллетень. 2014, №1-3, с. 20-28.
  466. A. Tkachev, D. Makarova, D. Domrachev, E. Romanenko, A. Nefedov, E. Karpova
    Monitoring of key secondary metabolites of isoprenoid nature in Siberian plants
    Chem. Listy – 2014. – Vol. 108 – s119., IF=0.195
  467. M.B. Bushuev, V.A. Daletsky, D.P. Pishchur, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Unprecedented bistability domain and interplay between spin crossover and polymorphism in a mononuclear iron(II) complex
    Dalton Trans., 2014,43(10), 3906-3910. doi:10.1039/C3DT53440E, IF=4.97
  468. M.B. Bushuev, V.A. Daletsky, D.P. Pishchur, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Unprecedented bistability domain and interplay between spin crossover and polymorphism in a mononuclear iron(II) complex
    Dalton Trans., 2014,43(10), 3906-3910. doi:10.1039/C3DT53440E, IF=4.97
  469. M.B. Bushuev, V.A. Daletsky, D.P. Pishchur, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Unprecedented bistability domain and interplay between spin crossover and polymorphism in a mononuclear iron(II) complex
    Dalton Trans., 2014,43(10), 3906-3910. doi:10.1039/C3DT53440E, IF=4.97
  470. M.B. Bushuev, V.A. Daletsky, D.P. Pishchur, Yu.V. Gatilov, I.V. Korolkov, E.B. Nikolaenkova, V.P. Krivopalov
    Unprecedented bistability domain and interplay between spin crossover and polymorphism in a mononuclear iron(II) complex
    Dalton Trans., 2014,43(10), 3906-3910. doi:10.1039/C3DT53440E, IF=4.97
  471. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  472. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  473. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  474. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  475. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  476. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  477. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  478. K.A. Vinogradova, V.F. Plyusnin, A.S. Kupryakov, M.I. Rakhmanova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, E.B. Nikolaenkova, V.P. Krivopalov, M.B. Bushuev
    Halide impact on emission of mononuclear copper(I) complexes with pyrazolylpyrimidine and triphenylphosphine
    Dalton Trans., 2014,43(7), 2953-2960. doi:10.1039/c3dt53040j, IF=4.97
  479. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
  480. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
  481. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
  482. O.V. Salomatina, A.V. Markov, E.B. Logashenko, D.V. Korchagina, M.A. Zenkova, N.F. Salakhutdinov, V.V. Vlassov, G.A. Tolstikov
    Synthesis of novel 2-cyano substituted glycyrrhetinic acid derivatives as inhibitors of cancer cells growth and NO production in LPS-activated J-774 cells
    Bioorganic & Medicinal Chemistry, 2014, V. 22, N 1, Pp 585-593. doi:10.1016/j.bmc.2013.10.049, IF=2.95
  483. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Содержание флавоноидов и гидроксикоричных кислот в листьях и плодах LONICERA CAERULEA (CAPRIFOLIACEAE) в популяциях горного алтая
    Растительные ресурсы. 2014. Т. 50. № 1. С. 105-121.
  484. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Содержание флавоноидов и гидроксикоричных кислот в листьях и плодах LONICERA CAERULEA (CAPRIFOLIACEAE) в популяциях горного алтая
    Растительные ресурсы. 2014. Т. 50. № 1. С. 105-121.
  485. Т.С. Фролова, О.И. Сальникова, Т.А. Дударева, Т.П. Кукина, О.И. Синицина
    Выделение помоловой кислоты из chamaenerion angustifolium и оценка ее потенциальной генотоксичности в бактериальных тест-системах
    Биоорганическая химия. 2014. Т. 40. № 1. С. 92-98. (Isolation of pomolic acid from Chamaenerion angustifolium and the evaluation of its potential genotoxicity in bacterial test systems/ T. S. Frolova, O. I. Sal’nikova, T. A. Dudareva, T. P. Kukina, O. I. Sinitsyna// Russian Journal of Bioorganic Chemistry, 2014, V. 40, N 1, pp 82-88. doi:10.1134/S1068162013060046), IF=0.623
  486. Т.С. Фролова, О.И. Сальникова, Т.А. Дударева, Т.П. Кукина, О.И. Синицина
    Выделение помоловой кислоты из chamaenerion angustifolium и оценка ее потенциальной генотоксичности в бактериальных тест-системах
    Биоорганическая химия. 2014. Т. 40. № 1. С. 92-98. (Isolation of pomolic acid from Chamaenerion angustifolium and the evaluation of its potential genotoxicity in bacterial test systems/ T. S. Frolova, O. I. Sal’nikova, T. A. Dudareva, T. P. Kukina, O. I. Sinitsyna// Russian Journal of Bioorganic Chemistry, 2014, V. 40, N 1, pp 82-88. doi:10.1134/S1068162013060046), IF=0.623
  487. М.А. Мяделец, Д.В. Домрачев, А.Н. Крикливая, Г.И. Высочина
    Зависимость состава эфирного масла monarda didyma l. ( lamiaceae) от возраста растений и характера сырья
    Химия растительного сырья. 2014. № 1. С. 215-219.
  488. М.А. Мяделец, Д.В. Домрачев, А.Н. Крикливая, Г.И. Высочина
    Зависимость состава эфирного масла monarda didyma l. ( lamiaceae) от возраста растений и характера сырья
    Химия растительного сырья. 2014. № 1. С. 215-219.
  489. М.А. Мяделец, Д.В. Домрачев, А.Н. Крикливая, Г.И. Высочина
    Зависимость состава эфирного масла monarda didyma l. ( lamiaceae) от возраста растений и характера сырья
    Химия растительного сырья. 2014. № 1. С. 215-219.
  490. И.В. Нечепуренко, Н.И. Комарова, О.Н. Потёмкин, Н.Ф. Салахутдинов
    Сезонная и возрастная динамика содержания берберина в интродуцированном berberis sibirica pall
    Химия растительного сырья. 2014. № 1. С. 195-202.
  491. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  492. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  493. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  494. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  495. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  496. Г.Ю. Ишмуратов, В.С. Тухватшин, Р.Р. Муслухов, А.С. Ерастов, А.В. Аллагулова, А.В. Баннова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза (1R,3R)-n-мент-4-ен-3-ола в присутствии пиридина
    Журнал органической химии. 2014. Т. 50. № 1. С. 141-143. (Transformations of peroxide ozonolysis products of (1R,3R)-p-menth-4-en-3-ol in the presence of pyridine/ G. Yu. Ishmuratov, V. S. Tukhvatshin, R. R. Muslukhov, A. S. Erastov, A. V. Allagulova, A. V. Bannova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 133-136. doi:10.1134/S1070428014010242), IF=0.675
  497. Е.В. Зайцева, Ю.В. Гатилов, С.А. Амитина, Р. Тамура, И.А. Григорьев, Д.Г. Мажукин
    Спироциклические нитроксильные радикалы 3-имидазолина с мезогенным заместителем при атоме C 4гетероцикла. синтез и кристаллическая структура
    Журнал органической химии. 2014. Т. 50. № 1. С. 78-83. (Spirocyclic 2,5-dihydro-1H-imidazole 1-oxyl radicals with a mesogenic substituent on C4. Synthesis and crystal structure/ E. V. Zaytseva, Yu. V. Gatilov, S. A. Amitina, R. Tamura, I. A. Grigor’ev, D. G. Mazhukin// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 72-77. doi:10.1134/S107042801401014X), IF=0.675
  498. V.V. Bardin, I.K. Shundrina, H.-J. Frohn
    Thermoanalytical and preparative investigations of the decomposition of potassium perfluoroorganyl(fluoro)borate salts, K[RFBF3] (RF = perfluoroalkyl, -alkenyl, -alkynyl, and -aryl groups) and K[(RF)2BF2] (RF = C6F5 and C6F13)
    Journal of Fluorine Chemistry, 2014, V. 157, Pp 73-78. doi:10.1016/j.jfluchem.2013.11.006, IF=1.952
  499. V. M. Tormyshev, O.Yu. Rogozhnikova, M. K. Bowman, D. V. Trukhin, T. I. Troitskaya, V. G. Vasiliev, L. A. Shundrin, H. J. Halpern
    Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
    European Journal of Organic Chemistry, 2014, V. 2014, N 2, pp 371-380. doi:10.1002/ejoc.201301161, IF=3.154
  500. V. M. Tormyshev, O.Yu. Rogozhnikova, M. K. Bowman, D. V. Trukhin, T. I. Troitskaya, V. G. Vasiliev, L. A. Shundrin, H. J. Halpern
    Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
    European Journal of Organic Chemistry, 2014, V. 2014, N 2, pp 371-380. doi:10.1002/ejoc.201301161, IF=3.154
  501. A.V. Artem’ev, N.K. Gusarova, A.O. Korocheva, S.F. Malysheva, Yu.V. Gatilov, B.A. Trofimov
    A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene
    Mendeleev Communications, 2014, V. 24, N 1, Pp 29-31. doi:10.1016/j.mencom.2013.12.009, IF=1.154
  502. A.V. Artem’ev, N.K. Gusarova, A.O. Korocheva, S.F. Malysheva, Yu.V. Gatilov, B.A. Trofimov
    A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene
    Mendeleev Communications, 2014, V. 24, N 1, Pp 29-31. doi:10.1016/j.mencom.2013.12.009, IF=1.154
  503. A.V. Artem’ev, N.K. Gusarova, A.O. Korocheva, S.F. Malysheva, Yu.V. Gatilov, B.A. Trofimov
    A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene
    Mendeleev Communications, 2014, V. 24, N 1, Pp 29-31. doi:10.1016/j.mencom.2013.12.009, IF=1.154
  504. A.V. Artem’ev, N.K. Gusarova, A.O. Korocheva, S.F. Malysheva, Yu.V. Gatilov, B.A. Trofimov
    A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene
    Mendeleev Communications, 2014, V. 24, N 1, Pp 29-31. doi:10.1016/j.mencom.2013.12.009, IF=1.154
  505. A.V. Artem’ev, N.K. Gusarova, A.O. Korocheva, S.F. Malysheva, Yu.V. Gatilov, B.A. Trofimov
    A shortcut to tris[2-(4-hydroxyphenyl)ethyl]phosphine oxide and 2-(4-hydroxyphenyl)ethylphosphinic acid via reaction of elemental phosphorus with 4-tert-butoxystyrene
    Mendeleev Communications, 2014, V. 24, N 1, Pp 29-31. doi:10.1016/j.mencom.2013.12.009, IF=1.154

2013

Reviews, articles

  1. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  2. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  3. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  4. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  5. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  6. M. Stekrova, N. Kumar, P. Maki-Arvela, A. Aho, J. Linden, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Opening of monoterpene epoxide to a potent anti-Parkinson compound of para-menthane structure over heterogeneous catalysts
    Reaction Kinetics, Mechanisms and Catalysis. 2013, V. 110, N 2, pp 449-458. doi:10.1007/s11144-013-0615-9, IF=1.103
  7. M. V. Khvostov, A. A. Chernonosov, T.G. Tolstikova, M. F. Kasakin, O. S. Fedorova, A. V. Dushkin
    Effect of Complexation with Arabinogalactan on Pharmacokinetics of “Guest” Drugs in Rats: For Example, Warfarin
    BioMed Research International, Volume 2013 (2013), Article ID 156381, 4 pages. doi:10.1155/2013/156381, IF=2.88
  8. M. V. Khvostov, A. A. Chernonosov, T.G. Tolstikova, M. F. Kasakin, O. S. Fedorova, A. V. Dushkin
    Effect of Complexation with Arabinogalactan on Pharmacokinetics of “Guest” Drugs in Rats: For Example, Warfarin
    BioMed Research International, Volume 2013 (2013), Article ID 156381, 4 pages. doi:10.1155/2013/156381, IF=2.88
  9. M. V. Khvostov, A. A. Chernonosov, T.G. Tolstikova, M. F. Kasakin, O. S. Fedorova, A. V. Dushkin
    Effect of Complexation with Arabinogalactan on Pharmacokinetics of “Guest” Drugs in Rats: For Example, Warfarin
    BioMed Research International, Volume 2013 (2013), Article ID 156381, 4 pages. doi:10.1155/2013/156381, IF=2.88
  10. M. V. Khvostov, A. A. Chernonosov, T.G. Tolstikova, M. F. Kasakin, O. S. Fedorova, A. V. Dushkin
    Effect of Complexation with Arabinogalactan on Pharmacokinetics of “Guest” Drugs in Rats: For Example, Warfarin
    BioMed Research International, Volume 2013 (2013), Article ID 156381, 4 pages. doi:10.1155/2013/156381, IF=2.88
  11. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Influence of triphenyl phosphate on degradation kinetics of ultrahigh-molecular-weight polyethylene in inert and oxidative media
    Procedia Engineering 62 ( 2013 ) 359-365. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.076
  12. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Influence of triphenyl phosphate on degradation kinetics of ultrahigh-molecular-weight polyethylene in inert and oxidative media
    Procedia Engineering 62 ( 2013 ) 359-365. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.076
  13. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Influence of triphenyl phosphate on degradation kinetics of ultrahigh-molecular-weight polyethylene in inert and oxidative media
    Procedia Engineering 62 ( 2013 ) 359-365. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.076
  14. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Influence of triphenyl phosphate on degradation kinetics of ultrahigh-molecular-weight polyethylene in inert and oxidative media
    Procedia Engineering 62 ( 2013 ) 359-365. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.076
  15. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Influence of triphenyl phosphate on degradation kinetics of ultrahigh-molecular-weight polyethylene in inert and oxidative media
    Procedia Engineering 62 ( 2013 ) 359-365. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.076
  16. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Combustion chemistry and decomposition kinetics of forest fuels
    Procedia Engineering 62 ( 2013 ) 182-193. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.054
  17. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Combustion chemistry and decomposition kinetics of forest fuels
    Procedia Engineering 62 ( 2013 ) 182-193. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.054
  18. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Combustion chemistry and decomposition kinetics of forest fuels
    Procedia Engineering 62 ( 2013 ) 182-193. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.054
  19. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Combustion chemistry and decomposition kinetics of forest fuels
    Procedia Engineering 62 ( 2013 ) 182-193. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.054
  20. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, I.K. Shundrina, H. Chend, N. Liu
    Combustion chemistry and decomposition kinetics of forest fuels
    Procedia Engineering 62 ( 2013 ) 182-193. 9th Asia-Oceania Symposium on Fire Science and Technology. doi:10.1016/j.proeng.2013.08.054
  21. O.P. Korobeinichev, A.A. Paletsky, L.V. Kuibida, M.B. Gonchikzhapov, I.K. Shundrina
    Reduction of flammability of ultrahigh-molecular-weight polyethylene by using triphenyl phosphate additives
    Proceedings of the Combustion Institute, 2013, V.. 34, 2, 2699–2706. doi:10.1016/j.proci.2012.06.045, IF=2.374
  22. O.P. Korobeinichev, A.A. Paletsky, L.V. Kuibida, M.B. Gonchikzhapov, I.K. Shundrina
    Reduction of flammability of ultrahigh-molecular-weight polyethylene by using triphenyl phosphate additives
    Proceedings of the Combustion Institute, 2013, V.. 34, 2, 2699–2706. doi:10.1016/j.proci.2012.06.045, IF=2.374
  23. O.P. Korobeinichev, A.A. Paletsky, L.V. Kuibida, M.B. Gonchikzhapov, I.K. Shundrina
    Reduction of flammability of ultrahigh-molecular-weight polyethylene by using triphenyl phosphate additives
    Proceedings of the Combustion Institute, 2013, V.. 34, 2, 2699–2706. doi:10.1016/j.proci.2012.06.045, IF=2.374
  24. O.P. Korobeinichev, A.A. Paletsky, L.V. Kuibida, M.B. Gonchikzhapov, I.K. Shundrina
    Reduction of flammability of ultrahigh-molecular-weight polyethylene by using triphenyl phosphate additives
    Proceedings of the Combustion Institute, 2013, V.. 34, 2, 2699–2706. doi:10.1016/j.proci.2012.06.045, IF=2.374
  25. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.A. Khokhrina, E.N. Shmidt, B.H. Um
    Low-Volatile Lipophilic Compounds in Needles, Defoliated Twigs, and Outer Bark of Pinus thunbergii
    Natural Product Communications, 2013, V. 8, N 12, P. 1759-1762., IF=0.955
  26. Е.Ю. Яковлева, И.К. Шундрина, Т.А. Ваганова
    Особенности разделения соединений неорганической и органической природы на модифицированном фторированным полиимидом оксиде алюминия
    Журнал аналитической химии. -2013. -Т.68. № 12. -С.1171–1178.. (Specific features of the separation of inorganic and organic compounds on alumina modified with fluorinated polyimide/ E. Yu. Yakovleva, I. K. Shundrina, T. A. Vaganova// Journal of Analytical Chemistry, 2013, V. 68, N 12, pp 1044-1051 doi:10.1134/S1061934813100110), IF=0.615
  27. D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov
    Phenolic compounds of Sophora flavescens Soland. of Russian origin
    Russian Journal of Bioorganic Chemistry, 2013, V., N 7, pp 755-760 .(Original Russian Text © D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 4, pp. 101–108.) doi:10.1134/S106816201307011X, IF=0.523
  28. D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov
    Phenolic compounds of Sophora flavescens Soland. of Russian origin
    Russian Journal of Bioorganic Chemistry, 2013, V., N 7, pp 755-760 .(Original Russian Text © D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 4, pp. 101–108.) doi:10.1134/S106816201307011X, IF=0.523
  29. D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov
    Phenolic compounds of Sophora flavescens Soland. of Russian origin
    Russian Journal of Bioorganic Chemistry, 2013, V., N 7, pp 755-760 .(Original Russian Text © D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 4, pp. 101–108.) doi:10.1134/S106816201307011X, IF=0.523
  30. M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina
    A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region
    Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 7, pp 733-738.(Original Russian Text © M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 1, pp. 111–117.) doi:10.1134/S1068162013070091, IF=0.523
  31. M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina
    A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region
    Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 7, pp 733-738.(Original Russian Text © M.A. Myadelets, D.V. Domrachev, V.A. Cheremushkina, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 1, pp. 111–117.) doi:10.1134/S1068162013070091, IF=0.523
  32. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  33. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  34. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  35. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  36. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  37. Т.Е. Кокина, Л.А. Глинская, А.М. Агафонцев, Е.В. Артимонова, Л.А. Шелудякова, И.В. Корольков, А.В. Ткачев, С.В. Ларионов
    Синтез и кристаллические структуры комплексов PdCl2 с хиральными оксимами α-(о-анизидино)каранона и α-(о-анизидино)пинанона
    Известия АН. Серия химическая, 2013, N 12, С. 2595-2602. (Complexes of PdCl2 with chiral oximes of α-(o-anisidino)caranone and α-(o-anisidino)pinanone: synthesis and crystal structures/ T. E. Kokina, L. A. Glinskaya, A. M. Agafontsev, E. V. Artimonova, L. A. Sheludyakova, I. V. Korol’kov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2013, V. 62, N 12, pp 2595-2602. doi:10.1007/s11172-013-0378-5), IF=0.423
  38. V.V. Bardin, H.-J. Frohn
    Thermal decomposition of 4-fluorobenzenediazonium perfluoroorganyl(fluoro)borates, [4-FC6H4N2]Y (Y = RFBF3, (RF = C6F5, C6F13, trans-C4F9CF=CF, cis-C6F13CF=CF, CF3C=C) and (C6F13)2BF2)
    Journal of Fluorine Chemistry, 2013, V. 156, P. 333-338 doi:10.1016/j.jfluchem.2013.08.001, IF=1.939
  39. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  40. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  41. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  42. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  43. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  44. A. Yu. Shabalin, N. Yu. Adonin, V. V. Bardin, S. A. Prikhod'ko, O.P. Taran, A.B. Ayushev, V. N. Parmon
    Synthesis of potassium 4-(1-azol-1-yl)tetrafluorophenyltrifluoroborates from K[C6F5BF3] and alkali metal azol-1-ides. The dramatic distinction in nucleophilicity of alkali metal azol-1-ides and dialkylamides
    Journal of Fluorine Chemistry, 2013, V. 156, P. 290-297. doi:10.1016/j.jfluchem.2013.07.011, IF=1.939
  45. M.V. Trushin, I.A. Arkharova, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    Genotoxicological safety assessment of a new antiparkinsonian substance ((1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)
    World Journal of Medical Sciences, 2013, Т. 8, N 4, С. 355-358. doi:10.5829/idosi.wjms.2013.8.4.1123
  46. M.V. Trushin, I.A. Arkharova, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov
    Genotoxicological safety assessment of a new antiparkinsonian substance ((1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol)
    World Journal of Medical Sciences, 2013, Т. 8, N 4, С. 355-358. doi:10.5829/idosi.wjms.2013.8.4.1123
  47. В.С. Глухачева, С.Г. Ильясов, А.О. Брызгалов, Т.Г. Толстикова
    Синтез и антиаритмическая активность калиевой соли нитросемикарбазон камфанона
    Ползуновский вестник, 2013, N 3, С. 140-143.
  48. В.С. Глухачева, С.Г. Ильясов, А.О. Брызгалов, Т.Г. Толстикова
    Синтез и антиаритмическая активность калиевой соли нитросемикарбазон камфанона
    Ползуновский вестник, 2013, N 3, С. 140-143.
  49. Н.В. Чухарева, В.Д. Тихова, О.Н. Зарубина, Л.В. Шишмина
    Изменение элементного состава и оптических свойств торфа под действием термической модификации
    Вестник Красноярского ГАУ, 2013, N 11, С.85-94.
  50. Н.В. Чухарева, В.Д. Тихова, О.Н. Зарубина, Л.В. Шишмина
    Изменение элементного состава и оптических свойств торфа под действием термической модификации
    Вестник Красноярского ГАУ, 2013, N 11, С.85-94.
  51. Н.В. Чухарева, В.Д. Тихова, О.Н. Зарубина, Л.В. Шишмина
    Изменение элементного состава и оптических свойств торфа под действием термической модификации
    Вестник Красноярского ГАУ, 2013, N 11, С.85-94.
  52. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  53. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  54. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  55. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  56. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  57. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  58. A.S. Sokolova, О. I. Yarovaya, А.V. Shernyukov, М.A. Pokrovsky, А.G. Pokrovsky, V.A. Lavrinenko, V.V. Zarubaev, T.S. Tretiak, P.M. Anfimov, O.I. Kiselev, A.B. Beklemishev, N.F. Salakhutdinov
    New quaternary ammonium camphor derivatives and their antiviral activity, genotoxic effects and cytotoxicity
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 21, P: 6690-6698. doi:10.1016/j.bmc.2013.08.014, IF=2.903
  59. В.И. Аникеев, В.П. Сивцев, К.П. Волчо, Н.Ф. Салахутдинов
    Превращения α и β -иононов в присутствии Al2O3 в сверхкритическом растворителе в реакторе проточного типа
    Журнал физической химии, 2013, Т. 87, N 11, С.1975–1977. (Transformations of alpha- and beta-ionones in the presence of Al2O3 in a supercritical solvent in a flow reactor/ V. I. Anikeev, V. P. Sivcev, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A A , 2013, V. 87, N 11, pp 1940-1942. doi:10.7868/S0044453713110046), IF=0.386
  60. В.Г. Меркулов, Д.В. Кабанов, В.Н. Митькин, И.А. Сукачева, В.П. Фадеева
    Исследование металлоносности фракций углеродистого вещества, выделенных флотацией из руд и технологических материалов Зун-Холбинского черносланцевого золоторудного месторождения, с применением ИНАА и других методов анализа. 1. Поведение матричных сидерофильных и халькофильных элементов при флотации
    Известия ВУЗов. Физика, 2013, Т. 56, N 11-3, С.238-242., IF=0.407
  61. В.Г. Меркулов, Д.В. Кабанов, В.Н. Митькин, И.А. Сукачева, В.П. Фадеева
    Исследование металлоносности фракций углеродистого вещества, выделенных флотацией из руд и технологических материалов Зун-Холбинского черносланцевого золоторудного месторождения, с применением ИНАА и других методов анализа. 1. Поведение матричных сидерофильных и халькофильных элементов при флотации
    Известия ВУЗов. Физика, 2013, Т. 56, N 11-3, С.238-242., IF=0.407
  62. В.Г. Меркулов, Д.В. Кабанов, В.Н. Митькин, И.А. Сукачева, В.П. Фадеева
    Исследование металлоносности фракций углеродистого вещества, выделенных флотацией из руд и технологических материалов Зун-Холбинского черносланцевого золоторудного месторождения, с применением ИНАА и других методов анализа. 1. Поведение матричных сидерофильных и халькофильных элементов при флотации
    Известия ВУЗов. Физика, 2013, Т. 56, N 11-3, С.238-242., IF=0.407
  63. В.Г. Меркулов, Д.В. Кабанов, В.Н. Митькин, И.А. Сукачева, В.П. Фадеева
    Исследование металлоносности фракций углеродистого вещества, выделенных флотацией из руд и технологических материалов Зун-Холбинского черносланцевого золоторудного месторождения, с применением ИНАА и других методов анализа. 1. Поведение матричных сидерофильных и халькофильных элементов при флотации
    Известия ВУЗов. Физика, 2013, Т. 56, N 11-3, С.238-242., IF=0.407
  64. A. E. Esenbaeva, E. E. Shul’ts, Yu. V. Gatilov, M. M. Shakirov, S. S. Patrushev, G. A. Atazhanova, A. B. Kenesheva, S. M. Adekenov
    Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity
    Chemistry of Natural Compounds, 2013, V. 49, N 5, P. 875-881. doi:10.1007/s10600-013-0768-9, IF=0.598
  65. A. E. Esenbaeva, E. E. Shul’ts, Yu. V. Gatilov, M. M. Shakirov, S. S. Patrushev, G. A. Atazhanova, A. B. Kenesheva, S. M. Adekenov
    Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity
    Chemistry of Natural Compounds, 2013, V. 49, N 5, P. 875-881. doi:10.1007/s10600-013-0768-9, IF=0.598
  66. A. E. Esenbaeva, E. E. Shul’ts, Yu. V. Gatilov, M. M. Shakirov, S. S. Patrushev, G. A. Atazhanova, A. B. Kenesheva, S. M. Adekenov
    Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity
    Chemistry of Natural Compounds, 2013, V. 49, N 5, P. 875-881. doi:10.1007/s10600-013-0768-9, IF=0.598
  67. A. E. Esenbaeva, E. E. Shul’ts, Yu. V. Gatilov, M. M. Shakirov, S. S. Patrushev, G. A. Atazhanova, A. B. Kenesheva, S. M. Adekenov
    Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity
    Chemistry of Natural Compounds, 2013, V. 49, N 5, P. 875-881. doi:10.1007/s10600-013-0768-9, IF=0.598
  68. С.В. Блинкова, М.М. Вьюшкова, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Изучение структурных особенностей анион-радикала 1,3,5-трифторбензола методами оптически детектируемого ЭПР и квантовой химии
    Известия АН. Серия химическая, 2013, N 11, С. 2311-2316. (Structural features of 1,3,5-trifluorobenzene radical anion, as studied by optically detected ESR spectroscopy and quantum chemistry/ S. V. Blinkova, M. M. Vyushkova, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Russian Chemical Bulletin, 2013, V. 62, N 11, pp 2311-2316. doi:10.1007/s11172-013-0335-3), IF=0.423
  69. С.В. Блинкова, М.М. Вьюшкова, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
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    Известия АН. Серия химическая, 2013, N 11, С. 2311-2316. (Structural features of 1,3,5-trifluorobenzene radical anion, as studied by optically detected ESR spectroscopy and quantum chemistry/ S. V. Blinkova, M. M. Vyushkova, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Russian Chemical Bulletin, 2013, V. 62, N 11, pp 2311-2316. doi:10.1007/s11172-013-0335-3), IF=0.423
  70. С.В. Блинкова, М.М. Вьюшкова, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Изучение структурных особенностей анион-радикала 1,3,5-трифторбензола методами оптически детектируемого ЭПР и квантовой химии
    Известия АН. Серия химическая, 2013, N 11, С. 2311-2316. (Structural features of 1,3,5-trifluorobenzene radical anion, as studied by optically detected ESR spectroscopy and quantum chemistry/ S. V. Blinkova, M. M. Vyushkova, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryansky, Yu. N. Molin// Russian Chemical Bulletin, 2013, V. 62, N 11, pp 2311-2316. doi:10.1007/s11172-013-0335-3), IF=0.423
  71. С.В. Блинкова, М.М. Вьюшкова, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
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  72. О.Н. Никуличева, А.П. Крысин, В.П. Фадеева, Е.А. Краснов, Е.Е. Назмутдинова
    Термоаналитический метод анализа биологически активных веществ на примере производных изоборнилфенолов
    Химико-фармацевтический журнал, 2013, Т. 47, 11, С. 46-49. (A Thermoanalytic Method for the Analysis of Biologically Active Substances using Isobornylphenol Derivatives as an Example/ O. N. Nikulicheva, A. P. Krysin, V. P. Fadeeva, E. A. Krasnov, E. E. Nazmutdinova// Pharmaceutical Chemistry Journal, 2014, V. 47, N 11, pp 616-619. doi:10.1007/s11094-014-1021-y), IF=0.319
  73. О.Н. Никуличева, А.П. Крысин, В.П. Фадеева, Е.А. Краснов, Е.Е. Назмутдинова
    Термоаналитический метод анализа биологически активных веществ на примере производных изоборнилфенолов
    Химико-фармацевтический журнал, 2013, Т. 47, 11, С. 46-49. (A Thermoanalytic Method for the Analysis of Biologically Active Substances using Isobornylphenol Derivatives as an Example/ O. N. Nikulicheva, A. P. Krysin, V. P. Fadeeva, E. A. Krasnov, E. E. Nazmutdinova// Pharmaceutical Chemistry Journal, 2014, V. 47, N 11, pp 616-619. doi:10.1007/s11094-014-1021-y), IF=0.319
  74. I.Sh. Steinberg, E.V. Vasilyev, A.Yu. Belikov
    Multilayer two-photon recording of microholograms in cationic ring-opening polymerization material
    Journal of Optics. - 2013. V. 15. N 10. - Article Number: 105403. doi:10.1088/2040-8978/15/10/105403, IF=1.99
  75. I.Sh. Steinberg, E.V. Vasilyev, A.Yu. Belikov
    Multilayer two-photon recording of microholograms in cationic ring-opening polymerization material
    Journal of Optics. - 2013. V. 15. N 10. - Article Number: 105403. doi:10.1088/2040-8978/15/10/105403, IF=1.99
  76. I.Yu. Drozdyuk, K.Yu. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya, M.V. Fedin
    Topology of exchange interactions in copper-nitroxide based molecular magnets studied by EPR
    Molecular Physics, 2013, V. 111, 18-19, SI, P. 2903-2907. doi:10.1080/00268976.2013.793848, IF=1.669
  77. I.Yu. Drozdyuk, K.Yu. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya, M.V. Fedin
    Topology of exchange interactions in copper-nitroxide based molecular magnets studied by EPR
    Molecular Physics, 2013, V. 111, 18-19, SI, P. 2903-2907. doi:10.1080/00268976.2013.793848, IF=1.669
  78. I.Yu. Drozdyuk, K.Yu. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya, M.V. Fedin
    Topology of exchange interactions in copper-nitroxide based molecular magnets studied by EPR
    Molecular Physics, 2013, V. 111, 18-19, SI, P. 2903-2907. doi:10.1080/00268976.2013.793848, IF=1.669
  79. I.Yu. Drozdyuk, K.Yu. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya, M.V. Fedin
    Topology of exchange interactions in copper-nitroxide based molecular magnets studied by EPR
    Molecular Physics, 2013, V. 111, 18-19, SI, P. 2903-2907. doi:10.1080/00268976.2013.793848, IF=1.669
  80. I.Yu. Drozdyuk, K.Yu. Maryunina, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya, M.V. Fedin
    Topology of exchange interactions in copper-nitroxide based molecular magnets studied by EPR
    Molecular Physics, 2013, V. 111, 18-19, SI, P. 2903-2907. doi:10.1080/00268976.2013.793848, IF=1.669
  81. И.А. Оськина, А.Я. Тихонов, И.Ю. Багрянская, Ю.В. Гатилов, О.С. Федорова
    Взаимодействие 4-гидроксикумарина с 2-ацетилоксиранами
    Журнал органической химии, 2013, Т. 49, N 10, С. 1517-1521. (Reaction of 4-hydroxycoumarin with 2-acetyloxiranes/ I. A. Os'kina, A. Ya. Tikhonov, I. Yu. Bagryanskaya, Yu. V. Gatilov, O. S. Fedorova// Russian Journal of Organic Chemistry, 2013, V. 49,N 10, pp 1497-1501 doi:10.1134/S1070428013100163), IF=0.469
  82. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов в системе метанол-вода
    Журнал органической химии, 2013, Т. 49, N 10, С.1439-1442. (Transformations of peroxide olefin ozonolysis products in methanol in the presence of water/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1415-1419 doi:10.1134/S1070428013100023), IF=0.513
  83. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов в системе метанол-вода
    Журнал органической химии, 2013, Т. 49, N 10, С.1439-1442. (Transformations of peroxide olefin ozonolysis products in methanol in the presence of water/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1415-1419 doi:10.1134/S1070428013100023), IF=0.513
  84. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов в системе метанол-вода
    Журнал органической химии, 2013, Т. 49, N 10, С.1439-1442. (Transformations of peroxide olefin ozonolysis products in methanol in the presence of water/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1415-1419 doi:10.1134/S1070428013100023), IF=0.513
  85. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов в системе метанол-вода
    Журнал органической химии, 2013, Т. 49, N 10, С.1439-1442. (Transformations of peroxide olefin ozonolysis products in methanol in the presence of water/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1415-1419 doi:10.1134/S1070428013100023), IF=0.513
  86. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов в системе метанол-вода
    Журнал органической химии, 2013, Т. 49, N 10, С.1439-1442. (Transformations of peroxide olefin ozonolysis products in methanol in the presence of water/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1415-1419 doi:10.1134/S1070428013100023), IF=0.513
  87. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  88. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  89. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  90. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  91. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  92. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  93. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.Р. Гарифуллина, Л.П. Боцман, З.И. Идрисова, Р.Р. Муслухов, Н.М. Ишмуратова, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
    Журнал органической химии, 2013, Т. 49, N 10, С.1433-1438. (Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. R. Garifullina, L. P. Botsman, Z. I. Idrisova, R. R. Muslukhov, N. M. Ishmuratova, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V. 49, N 10, pp 1409-1414 doi:10.1134/S1070428013100011), IF=0.513
  94. M.A. Gilinsky, A.D. Rogachev, N.I. Komarova, N.F. Salakhutdinov, G.A. Tolstikov, S.E. Naumenko, T.V. Latysheva
    Cardioprotective Effect of Resveratrol and Resveratroloside
    Cardiovascular & Hematological Agents in Medicinal Chemistry., 2013, V. 11 N 3, P. 207 - 210. doi:10.2174/187152571103140120103302
  95. M.A. Gilinsky, A.D. Rogachev, N.I. Komarova, N.F. Salakhutdinov, G.A. Tolstikov, S.E. Naumenko, T.V. Latysheva
    Cardioprotective Effect of Resveratrol and Resveratroloside
    Cardiovascular & Hematological Agents in Medicinal Chemistry., 2013, V. 11 N 3, P. 207 - 210. doi:10.2174/187152571103140120103302
  96. M.A. Gilinsky, A.D. Rogachev, N.I. Komarova, N.F. Salakhutdinov, G.A. Tolstikov, S.E. Naumenko, T.V. Latysheva
    Cardioprotective Effect of Resveratrol and Resveratroloside
    Cardiovascular & Hematological Agents in Medicinal Chemistry., 2013, V. 11 N 3, P. 207 - 210. doi:10.2174/187152571103140120103302
  97. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
    Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
    Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
  98. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
    Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
    Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
  99. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
    Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
    Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
  100. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
    Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
    Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
  101. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  102. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  103. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  104. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  105. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  106. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  107. A.N. Antimonova, N.I. Petrenko, M.M. Shakirov, T.V. Rybalova, T.S. Frolova, E.E. Shul’ts, T.P. Kukina, O.I. Sinitsyna, G.A. Tolstikov
    Synthesis and study of mutagenic properties of lupane triterpenoids containing 1,2,3-triazole fragments in the C-30 position
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 657-664. doi:10.1007/s10600-013-0702-1, IF=0.598
  108. Ю.В. Харитонов, Э.Э. Шульц, М.М. Шакиров, М.A. Покровский, А.Г. Покровский, Г.А. Толстиков
    Синтетические трансформации высших терпеноидов. Cообщение 31. Синтез 1,2,3-триазолилсодержащих фуранолабданоидов и изучение их цитотоксической активности
    Известия АН. Серия химическая, 2013, N 9, С. 2046-2055. (Synthetic transformation of higher terpenoids 31. Synthesis of 1,2,3-triazolyl-containing furan labdanoids and studies of their cytotoxic activity/ Yu. V. Kharitonov, E. E. Shul’ts, M. M. Shakirov, M. A. Pokrovskii, A. G. Pokrovskii, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 9, pp 2046-2055. doi:10.1007/s11172-013-0297-5), IF=0.423
  109. Л.М. Горностаев, Ю.Г. Халявина, Н.П. Грицан, Ю.В. Гатилов
    Об ацилировании 2-ариламино-5,8-дигидрокси-3-хлор-1,4-нафтохинонов
    Журнал органической химии, 2013, Т. 49, N 9, С. 1323-1327. (Acylation of 2-arylamino-3-chloro-5,8-dihydroxy-1,4-naphthoquinones/ L. M. Gornostaev, Yu. G. Khalyavina, N. P. Gritsan, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2013, V.49, N 9, pp 1307-1312. doi:10.1134/S107042801309011X), IF=0.469
  110. Л.М. Горностаев, Ю.Г. Халявина, Н.П. Грицан, Ю.В. Гатилов
    Об ацилировании 2-ариламино-5,8-дигидрокси-3-хлор-1,4-нафтохинонов
    Журнал органической химии, 2013, Т. 49, N 9, С. 1323-1327. (Acylation of 2-arylamino-3-chloro-5,8-dihydroxy-1,4-naphthoquinones/ L. M. Gornostaev, Yu. G. Khalyavina, N. P. Gritsan, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2013, V.49, N 9, pp 1307-1312. doi:10.1134/S107042801309011X), IF=0.469
  111. Л.М. Горностаев, Ю.Г. Халявина, Н.П. Грицан, Ю.В. Гатилов
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    Журнал органической химии, 2013, Т. 49, N 9, С. 1323-1327. (Acylation of 2-arylamino-3-chloro-5,8-dihydroxy-1,4-naphthoquinones/ L. M. Gornostaev, Yu. G. Khalyavina, N. P. Gritsan, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2013, V.49, N 9, pp 1307-1312. doi:10.1134/S107042801309011X), IF=0.469
  112. A.I. Govdi, S.F. Vasilevsky, N.V. Sokolova, I.V. Sorokina, T.G. Tolstikova, V.G. Nenajdenko
    Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity
    Mendeleev Communications, 2013, V. 23, N 5, P.260-261. doi:10.1016/j.mencom.2013.09.007, IF=1.52
  113. A.I. Govdi, S.F. Vasilevsky, N.V. Sokolova, I.V. Sorokina, T.G. Tolstikova, V.G. Nenajdenko
    Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity
    Mendeleev Communications, 2013, V. 23, N 5, P.260-261. doi:10.1016/j.mencom.2013.09.007, IF=1.52
  114. A.I. Govdi, S.F. Vasilevsky, N.V. Sokolova, I.V. Sorokina, T.G. Tolstikova, V.G. Nenajdenko
    Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity
    Mendeleev Communications, 2013, V. 23, N 5, P.260-261. doi:10.1016/j.mencom.2013.09.007, IF=1.52
  115. A.I. Govdi, S.F. Vasilevsky, N.V. Sokolova, I.V. Sorokina, T.G. Tolstikova, V.G. Nenajdenko
    Betulonic acid–peptide conjugates: synthesis and evaluation of anti-inflammatory activity
    Mendeleev Communications, 2013, V. 23, N 5, P.260-261. doi:10.1016/j.mencom.2013.09.007, IF=1.52
  116. A.V. Lonchakov, O.A. Rakitin, N.P. Gritsan, A.V. Zibarev
    Breathing Some New Life into an Old Topic: Chalcogen-Nitrogen π-Heterocycles as Electron Acceptors
    Molecules 2013, 18(8), 9850-9900. doi:10.3390/molecules18089850, IF=2.427
  117. A.V. Lonchakov, O.A. Rakitin, N.P. Gritsan, A.V. Zibarev
    Breathing Some New Life into an Old Topic: Chalcogen-Nitrogen π-Heterocycles as Electron Acceptors
    Molecules 2013, 18(8), 9850-9900. doi:10.3390/molecules18089850, IF=2.427
  118. A.V. Lonchakov, O.A. Rakitin, N.P. Gritsan, A.V. Zibarev
    Breathing Some New Life into an Old Topic: Chalcogen-Nitrogen π-Heterocycles as Electron Acceptors
    Molecules 2013, 18(8), 9850-9900. doi:10.3390/molecules18089850, IF=2.427
  119. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  120. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  121. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  122. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  123. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  124. Yu.S. Demidova, I.L. Simakova, M. Estrada, S. Beloshapkin, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A.V. Simakov, D.Y. Murzin
    One-pot myrtenol amination over Au nanoparticles supported on different metal oxides
    Applied Catalysis A: General, 2013, V. 456, P. 348-356 doi:10.1016/j.apcata.2013.06.013, IF=3.41
  125. А.А. Палецкий, М.Б. Гончикжапов, И.К. Шундрина, О.П. Коробейничев
    Механизм снижения горючести полиэтилена различного молекулярного веса добавками фосфорсодержащих соединений
    Известия Южного федерального университета. Технические науки, 2013, N 8, С. 57-67.
  126. А.А. Палецкий, М.Б. Гончикжапов, И.К. Шундрина, О.П. Коробейничев
    Механизм снижения горючести полиэтилена различного молекулярного веса добавками фосфорсодержащих соединений
    Известия Южного федерального университета. Технические науки, 2013, N 8, С. 57-67.
  127. А.А. Палецкий, М.Б. Гончикжапов, И.К. Шундрина, О.П. Коробейничев
    Механизм снижения горючести полиэтилена различного молекулярного веса добавками фосфорсодержащих соединений
    Известия Южного федерального университета. Технические науки, 2013, N 8, С. 57-67.
  128. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Transformations of monoterpenoid ketones in supercritical isopropanol/CO2 in a continuous flow reactor in the presence of alumina. Competitive reduction of olefinic double bond and carbonyl group
    Journal of Supercritical Fluids, 2013, V. 80, P. 9-14. doi:10.1016/j.supflu.2013.03.028, IF=2.732
  129. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
  130. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
  131. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
  132. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
  133. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
  134. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  135. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  136. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  137. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  138. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  139. S.N. Trukhan, V.F. Yudanov, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, M.K. Bowman, M.D. Krzyaniak, H. Chen, O.N. Martyanov
    Hyperfine interactions of narrow-line trityl radical with solvent molecules
    Journal of Magnetic Resonance, 2013, V. 233, P. 29-36. doi:10.1016/j.jmr.2013.04.017, IF=2.299
  140. М.Н. Соколов, М.А. Михайлов, А.В. Вировец, К.А. Брылев, Р.А. Бредихин, А.М. Максимов, В.Е. Платонов, В.П. Федин
    Синтез, строение и люминесцентные свойства октаэдрического кластерного комплекса молибдена [Mo6I8(SC6F4H)6]2–
    Известия АН. Серия химическая, 2013, N 8, С. 1764-1767. (Synthesis, structure, and luminescence of the octahedral molybdenum cluster [Mo6I8(SC6F4H)6]2–/ M. N. Sokolov, M. A. Mikhailov, A. V. Virovets, K. A. Brylev, R. A. Bredikhin, A. M. Maksimov, V. E. Platonov, V. P. Fedin// Russian Chemical Bulletin, 2013, V. 62, N 8, pp 1764-1767. doi:10.1007/s11172-013-0253-4), IF=0.423
  141. М.Н. Соколов, М.А. Михайлов, А.В. Вировец, К.А. Брылев, Р.А. Бредихин, А.М. Максимов, В.Е. Платонов, В.П. Федин
    Синтез, строение и люминесцентные свойства октаэдрического кластерного комплекса молибдена [Mo6I8(SC6F4H)6]2–
    Известия АН. Серия химическая, 2013, N 8, С. 1764-1767. (Synthesis, structure, and luminescence of the octahedral molybdenum cluster [Mo6I8(SC6F4H)6]2–/ M. N. Sokolov, M. A. Mikhailov, A. V. Virovets, K. A. Brylev, R. A. Bredikhin, A. M. Maksimov, V. E. Platonov, V. P. Fedin// Russian Chemical Bulletin, 2013, V. 62, N 8, pp 1764-1767. doi:10.1007/s11172-013-0253-4), IF=0.423
  142. М.Н. Соколов, М.А. Михайлов, А.В. Вировец, К.А. Брылев, Р.А. Бредихин, А.М. Максимов, В.Е. Платонов, В.П. Федин
    Синтез, строение и люминесцентные свойства октаэдрического кластерного комплекса молибдена [Mo6I8(SC6F4H)6]2–
    Известия АН. Серия химическая, 2013, N 8, С. 1764-1767. (Synthesis, structure, and luminescence of the octahedral molybdenum cluster [Mo6I8(SC6F4H)6]2–/ M. N. Sokolov, M. A. Mikhailov, A. V. Virovets, K. A. Brylev, R. A. Bredikhin, A. M. Maksimov, V. E. Platonov, V. P. Fedin// Russian Chemical Bulletin, 2013, V. 62, N 8, pp 1764-1767. doi:10.1007/s11172-013-0253-4), IF=0.423
  143. М.Н. Соколов, М.А. Михайлов, А.В. Вировец, К.А. Брылев, Р.А. Бредихин, А.М. Максимов, В.Е. Платонов, В.П. Федин
    Синтез, строение и люминесцентные свойства октаэдрического кластерного комплекса молибдена [Mo6I8(SC6F4H)6]2–
    Известия АН. Серия химическая, 2013, N 8, С. 1764-1767. (Synthesis, structure, and luminescence of the octahedral molybdenum cluster [Mo6I8(SC6F4H)6]2–/ M. N. Sokolov, M. A. Mikhailov, A. V. Virovets, K. A. Brylev, R. A. Bredikhin, A. M. Maksimov, V. E. Platonov, V. P. Fedin// Russian Chemical Bulletin, 2013, V. 62, N 8, pp 1764-1767. doi:10.1007/s11172-013-0253-4), IF=0.423
  144. М.Н. Соколов, М.А. Михайлов, А.В. Вировец, К.А. Брылев, Р.А. Бредихин, А.М. Максимов, В.Е. Платонов, В.П. Федин
    Синтез, строение и люминесцентные свойства октаэдрического кластерного комплекса молибдена [Mo6I8(SC6F4H)6]2–
    Известия АН. Серия химическая, 2013, N 8, С. 1764-1767. (Synthesis, structure, and luminescence of the octahedral molybdenum cluster [Mo6I8(SC6F4H)6]2–/ M. N. Sokolov, M. A. Mikhailov, A. V. Virovets, K. A. Brylev, R. A. Bredikhin, A. M. Maksimov, V. E. Platonov, V. P. Fedin// Russian Chemical Bulletin, 2013, V. 62, N 8, pp 1764-1767. doi:10.1007/s11172-013-0253-4), IF=0.423
  145. И.И. Олейник, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов XV. синтез (N-арил)салицилальдиминных лигандов, содержащих бут-3-енилоксигруппу, и комплексов дихлорида титана(IV) на их основе
    Журнал органической химии, 2013, Т. 49, N 8, С. 1168-1173. (Design of postmetallocene catalytic systems of arylimine type for olefi n polymerization: XV. Synthesis of (N-Aryl)salicylaldimine ligands containing a but-3-enyloxy group and their complexes with titanium(IV) dichloride/ I. I. Oleinik, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 8, pp 1150-1156 doi:10.1134/S1070428013080095), IF=0.513
  146. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  147. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  148. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  149. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  150. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  151. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  152. I.Yu. Drozdyuk, S.E. Tolstikov, E.V. Tretyakov, S.L. Veber, V.I. Ovcharenko, R.Z. Sagdeev, E.G. Bagryanskaya, M.V. Fedin
    Light-Induced Magnetostructural Anomalies in a Polymer Chain Complex of Cu(hfac)(2) with tert-Butylpyrazolylnitroxides
    Journal of Physical Chemistry A, 2013, V. 117, N 30, P. 6483-6488. doi:10.1021/jp403977n, IF=2.77
  153. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  154. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  155. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  156. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  157. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  158. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, N.A. Kolyvanov, I.Yu. Bagryanskaya, E.P. Doronina, N.K. Gusarova
    Three-component reaction between secondary phosphine sulfides, elemental selenium and vinyl ethers: the first examples of Markovnikov addition of thioselenophosphinic acids to double bond
    Tetrahedron, 2013, V. 69. N 30, P. 6185-6195. doi:10.1016/j.tet.2013.05.038, IF=2.802
  159. O.A. Krumkacheva, M.V. Fedin, D.N. Polovyanenko, L. Jicsinszky, S.R. Marque, E.G. Bagryanskaya
    Structural Equilibrium in New Nitroxide-Capped Cyclodextrins: CW and Pulse EPR Study
    Journal of Physical Chemistry B, 2013, V. 117, N 27, P. 8223-8231. doi:10.1021/jp404173j, IF=3.607
  160. O.A. Krumkacheva, M.V. Fedin, D.N. Polovyanenko, L. Jicsinszky, S.R. Marque, E.G. Bagryanskaya
    Structural Equilibrium in New Nitroxide-Capped Cyclodextrins: CW and Pulse EPR Study
    Journal of Physical Chemistry B, 2013, V. 117, N 27, P. 8223-8231. doi:10.1021/jp404173j, IF=3.607
  161. O.A. Krumkacheva, M.V. Fedin, D.N. Polovyanenko, L. Jicsinszky, S.R. Marque, E.G. Bagryanskaya
    Structural Equilibrium in New Nitroxide-Capped Cyclodextrins: CW and Pulse EPR Study
    Journal of Physical Chemistry B, 2013, V. 117, N 27, P. 8223-8231. doi:10.1021/jp404173j, IF=3.607
  162. O.A. Krumkacheva, M.V. Fedin, D.N. Polovyanenko, L. Jicsinszky, S.R. Marque, E.G. Bagryanskaya
    Structural Equilibrium in New Nitroxide-Capped Cyclodextrins: CW and Pulse EPR Study
    Journal of Physical Chemistry B, 2013, V. 117, N 27, P. 8223-8231. doi:10.1021/jp404173j, IF=3.607
  163. N.K. Gusarova, P.A. Volkov, N.I. Ivanova, Yu.V. Gatilov, B.A. Trofimov
    Oxidative cross-coupling between secondary phosphine selenides and thiols or dithiols: a facile regio-selective synthesis of thioselenophosphinic S-esters and S-diesters
    Tetrahedron Letters., 2013, V. 54, N 27, P. 3543-3545. doi:10.1016/j.tetlet.2013.04.117, IF=2.397
  164. N.K. Gusarova, P.A. Volkov, N.I. Ivanova, Yu.V. Gatilov, B.A. Trofimov
    Oxidative cross-coupling between secondary phosphine selenides and thiols or dithiols: a facile regio-selective synthesis of thioselenophosphinic S-esters and S-diesters
    Tetrahedron Letters., 2013, V. 54, N 27, P. 3543-3545. doi:10.1016/j.tetlet.2013.04.117, IF=2.397
  165. N.K. Gusarova, P.A. Volkov, N.I. Ivanova, Yu.V. Gatilov, B.A. Trofimov
    Oxidative cross-coupling between secondary phosphine selenides and thiols or dithiols: a facile regio-selective synthesis of thioselenophosphinic S-esters and S-diesters
    Tetrahedron Letters., 2013, V. 54, N 27, P. 3543-3545. doi:10.1016/j.tetlet.2013.04.117, IF=2.397
  166. N.K. Gusarova, P.A. Volkov, N.I. Ivanova, Yu.V. Gatilov, B.A. Trofimov
    Oxidative cross-coupling between secondary phosphine selenides and thiols or dithiols: a facile regio-selective synthesis of thioselenophosphinic S-esters and S-diesters
    Tetrahedron Letters., 2013, V. 54, N 27, P. 3543-3545. doi:10.1016/j.tetlet.2013.04.117, IF=2.397
  167. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  168. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  169. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  170. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  171. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  172. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  173. K.A. Vinogradova, V. P. Krivopalov., E.B. Nikolaenkova, N. V. Pervukhina., D. Yu. Naumov., M. I. Rakhmanova., E. G. Boguslavskya, L. A. Sheludyakova, M. B. Bushuev
    Synthesis and structures of copper(II), copper(I,II) and copper(I) complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine. Luminescence of copper(I) complexes
    Polyhedron, 2013, V. 57, P. 1-13. doi:10.1016/j.poly.2013.04.009, IF=1.812
  174. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  175. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  176. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  177. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  178. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  179. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  180. A.A. Bogush, G.A. Leonova, S.K. Krivonogov, V.A. Bobrov, V.D. Tikhova, L.M. Kondratyeva, A.E. Kuzmina, A.E. Maltsev
    Diagenetic transformation of sapropel from Lake Dukhovoe (East Baikal region, Russia)
    Procedia Earth and Planetary Science, 7(2013), P.81–84. doi:10.1016/j.proeps.2013.03.161
  181. G. Maksimova, N.A. Zhukova, E.V. Kashina, M.N. Lvova, T.G. Tolstikova, A.V. Katokhin, V.A. Mordvinov
    Role of Opisthorchis felineus in the induction of bile duct cancer in experimental opisthorchiasis
    FEBS Journal, 2013, V. 280, Special Issue: SI Supplement: 1, P. 395-395. doi:10.1111/febs.12340, IF=4.25
  182. G. Maksimova, N.A. Zhukova, E.V. Kashina, M.N. Lvova, T.G. Tolstikova, A.V. Katokhin, V.A. Mordvinov
    Role of Opisthorchis felineus in the induction of bile duct cancer in experimental opisthorchiasis
    FEBS Journal, 2013, V. 280, Special Issue: SI Supplement: 1, P. 395-395. doi:10.1111/febs.12340, IF=4.25
  183. G. Maksimova, N.A. Zhukova, E.V. Kashina, M.N. Lvova, T.G. Tolstikova, A.V. Katokhin, V.A. Mordvinov
    Role of Opisthorchis felineus in the induction of bile duct cancer in experimental opisthorchiasis
    FEBS Journal, 2013, V. 280, Special Issue: SI Supplement: 1, P. 395-395. doi:10.1111/febs.12340, IF=4.25
  184. G. Maksimova, N.A. Zhukova, E.V. Kashina, M.N. Lvova, T.G. Tolstikova, A.V. Katokhin, V.A. Mordvinov
    Role of Opisthorchis felineus in the induction of bile duct cancer in experimental opisthorchiasis
    FEBS Journal, 2013, V. 280, Special Issue: SI Supplement: 1, P. 395-395. doi:10.1111/febs.12340, IF=4.25
  185. G. Maksimova, N.A. Zhukova, E.V. Kashina, M.N. Lvova, T.G. Tolstikova, A.V. Katokhin, V.A. Mordvinov
    Role of Opisthorchis felineus in the induction of bile duct cancer in experimental opisthorchiasis
    FEBS Journal, 2013, V. 280, Special Issue: SI Supplement: 1, P. 395-395. doi:10.1111/febs.12340, IF=4.25
  186. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, В.И. Маматюк
    Физико-химические свойства стебля у ржи (Secale cereale L.) со стекловидной соломиной
    Вавиловский журнал генетики и селекции, 2013. Т. 17, N 2, С. 303-313. (Physicochemical Properties of Culms in Rye (Secale cereale L.) with a Brittle Stem/ A. A. Konovalov, I. K. Shundrina, E. V. Karpova, and V. I. Mamatyuk// Russian Journal of Genetics: Applied Research, 2013, V. 3, N. 6, pp. 455–463.)
  187. Г.С. Ширапова, С.В. Морозов, В.Б. Батоев, М.И. Богачев
    Мониторинг стойких органических загрязнителей в экосистеме дельты реки
    Известия СПбГЭТУ "ЛЭТИ", 2013, Т. 7, С. 92-98.
  188. Г.С. Ширапова, С.В. Морозов, В.Б. Батоев, М.И. Богачев
    Мониторинг стойких органических загрязнителей в экосистеме дельты реки
    Известия СПбГЭТУ "ЛЭТИ", 2013, Т. 7, С. 92-98.
  189. Г.С. Ширапова, С.В. Морозов, В.Б. Батоев, М.И. Богачев
    Мониторинг стойких органических загрязнителей в экосистеме дельты реки
    Известия СПбГЭТУ "ЛЭТИ", 2013, Т. 7, С. 92-98.
  190. Н.И. Ткачева, С.В. Морозов, И.А. Григорьев, Д.М. Могнонов, Н.А. Колчанов
    Модификация целлюлозы - перспективное направление в создании новых материалов
    Высокомолекулярные соединения, Сер. Б. -2013. -Т. 55. № 8. -С. 1086-1107. (Modification of Cellulose as a Promising Direction in the Design of New Materials/ N. I. Tkacheva, S. V. Morozov, I. A. Grigor’ev, D. M. Mognonov, N. A. Kolchanov// Polymer Science Series B, 2013, V. 55, N 7-8, pp 409-429. doi:10.1134/S1560090413070063), IF=0.439
  191. Н.И. Ткачева, С.В. Морозов, И.А. Григорьев, Д.М. Могнонов, Н.А. Колчанов
    Модификация целлюлозы - перспективное направление в создании новых материалов
    Высокомолекулярные соединения, Сер. Б. -2013. -Т. 55. № 8. -С. 1086-1107. (Modification of Cellulose as a Promising Direction in the Design of New Materials/ N. I. Tkacheva, S. V. Morozov, I. A. Grigor’ev, D. M. Mognonov, N. A. Kolchanov// Polymer Science Series B, 2013, V. 55, N 7-8, pp 409-429. doi:10.1134/S1560090413070063), IF=0.439
  192. А.В. Душкин, Ю.С. Чистяченко, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов, Г.А. Толстиков
    Фармакологические и физико-химические свойства механохимически синтезированных супрамолекулярных комплексов ацетилсалициловой кислоты и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix Gmelini
    Доклады Академии наукб 2013, Т. 451, N 1, C. 107--109. (Pharmacological and physicochemical properties of mechanochemically synthesized supramolecular complexes of acetylsalicylic acid and polysaccharide arabinogalactan from lrches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, T. G. Tolstikova, M. V. Khvostov, N. E. Polyakov, N. Z. Lyakhov, G. A. Tolstikov// Doklady Biochemistry and Biophysics, 2013, V. 451, N 1, pp 180-182 doi:10.1134/S1607672913040030), IF=0.321
  193. А.В. Душкин, Ю.С. Чистяченко, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов, Г.А. Толстиков
    Фармакологические и физико-химические свойства механохимически синтезированных супрамолекулярных комплексов ацетилсалициловой кислоты и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix Gmelini
    Доклады Академии наукб 2013, Т. 451, N 1, C. 107--109. (Pharmacological and physicochemical properties of mechanochemically synthesized supramolecular complexes of acetylsalicylic acid and polysaccharide arabinogalactan from lrches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, T. G. Tolstikova, M. V. Khvostov, N. E. Polyakov, N. Z. Lyakhov, G. A. Tolstikov// Doklady Biochemistry and Biophysics, 2013, V. 451, N 1, pp 180-182 doi:10.1134/S1607672913040030), IF=0.321
  194. А.В. Душкин, Ю.С. Чистяченко, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов, Г.А. Толстиков
    Фармакологические и физико-химические свойства механохимически синтезированных супрамолекулярных комплексов ацетилсалициловой кислоты и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix Gmelini
    Доклады Академии наукб 2013, Т. 451, N 1, C. 107--109. (Pharmacological and physicochemical properties of mechanochemically synthesized supramolecular complexes of acetylsalicylic acid and polysaccharide arabinogalactan from lrches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, T. G. Tolstikova, M. V. Khvostov, N. E. Polyakov, N. Z. Lyakhov, G. A. Tolstikov// Doklady Biochemistry and Biophysics, 2013, V. 451, N 1, pp 180-182 doi:10.1134/S1607672913040030), IF=0.321
  195. А.В. Душкин, Ю.С. Чистяченко, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов, Г.А. Толстиков
    Фармакологические и физико-химические свойства механохимически синтезированных супрамолекулярных комплексов ацетилсалициловой кислоты и полисахарида арабиногалактана из лиственниц Larix Sibirica и Larix Gmelini
    Доклады Академии наукб 2013, Т. 451, N 1, C. 107--109. (Pharmacological and physicochemical properties of mechanochemically synthesized supramolecular complexes of acetylsalicylic acid and polysaccharide arabinogalactan from lrches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, T. G. Tolstikova, M. V. Khvostov, N. E. Polyakov, N. Z. Lyakhov, G. A. Tolstikov// Doklady Biochemistry and Biophysics, 2013, V. 451, N 1, pp 180-182 doi:10.1134/S1607672913040030), IF=0.321
  196. E.A. Khokhrina, A.V. Shpatov, S.A. Popov, O.I. Sal'nikova, E.N. Shmidt, B.H. Um
    Non-Volatile Compounds of Needles, Trimmed Saplings, and Outer Bark of Pinus densiflora
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 561-565. doi:10.1007/s10600-013-0673-2, IF=0.598
  197. A.П. Крысин, О.И. Яковлев
    Создание защитного покрытия микроэлектроники от внешних воздействий на основе эпоксидных смол.
    Журнал прикладной химии, 2013, Т. 86, N.7, С.1064-1068. (Fabrication of coatings based on epoxy resins for environmental protection of microelectronics/ A. P. Krysin, O. I. Yakovlev// Russian Journal of Applied Chemistry, 2013, V. 86, N 7, pp 997-1000. doi:10.1134/S1070427213070094), IF=0.234
  198. Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, В.А. Самсонов, А.Я. Тихонов, В.А. Рябинин, А.Н. Синяков
    Синтез 4-(4-метоксифенил)-2,6-динитробензальдегида
    Журнал органической химии, 2013, Т. 49, N 7, С.1103-1105. (Synthesis of 4-(4-methoxyphenyl)-2,6-dinitrobenzaldehyde/ E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, V. A. Samsonov, A. Ya. Tikhonov, V. A. Ryabinin, A. N. Sinyakov// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1089-1091 doi:10.1134/S1070428013070245), IF=0.513
  199. Е.Б. Николаенкова, И.А. Оськина, В.А. Савельев, В.А. Самсонов, А.Я. Тихонов, В.А. Рябинин, А.Н. Синяков
    Синтез 4-(4-метоксифенил)-2,6-динитробензальдегида
    Журнал органической химии, 2013, Т. 49, N 7, С.1103-1105. (Synthesis of 4-(4-methoxyphenyl)-2,6-dinitrobenzaldehyde/ E. B. Nikolaenkova, I. A. Os’kina, V. A. Savel’ev, V. A. Samsonov, A. Ya. Tikhonov, V. A. Ryabinin, A. N. Sinyakov// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1089-1091 doi:10.1134/S1070428013070245), IF=0.513
  200. Н.М. Сторожок, Н.П. Медяник, А.П. Крысин, С.А. Креков, В.Е. Борисенко
    Синтез, структура и активность антиоксидантов «гибридного» строения на основе n-замещенных амидов салициловой кислоты
    Журнал органической химии, 2013, Т. 49, N 7, С. 1046-1049. (Synthesis, structure, and antioxidant activity of hybrid N-substituted salicylic acid amides/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, S. A. Krekov, V. E. Borisenko// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1031-1034 doi:10.1134/S1070428013070129), IF=0.513
  201. Н.М. Сторожок, Н.П. Медяник, А.П. Крысин, С.А. Креков, В.Е. Борисенко
    Синтез, структура и активность антиоксидантов «гибридного» строения на основе n-замещенных амидов салициловой кислоты
    Журнал органической химии, 2013, Т. 49, N 7, С. 1046-1049. (Synthesis, structure, and antioxidant activity of hybrid N-substituted salicylic acid amides/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, S. A. Krekov, V. E. Borisenko// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1031-1034 doi:10.1134/S1070428013070129), IF=0.513
  202. Н.М. Сторожок, Н.П. Медяник, А.П. Крысин, С.А. Креков, В.Е. Борисенко
    Синтез, структура и активность антиоксидантов «гибридного» строения на основе n-замещенных амидов салициловой кислоты
    Журнал органической химии, 2013, Т. 49, N 7, С. 1046-1049. (Synthesis, structure, and antioxidant activity of hybrid N-substituted salicylic acid amides/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, S. A. Krekov, V. E. Borisenko// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1031-1034 doi:10.1134/S1070428013070129), IF=0.513
  203. Н.М. Сторожок, Н.П. Медяник, А.П. Крысин, С.А. Креков, В.Е. Борисенко
    Синтез, структура и активность антиоксидантов «гибридного» строения на основе n-замещенных амидов салициловой кислоты
    Журнал органической химии, 2013, Т. 49, N 7, С. 1046-1049. (Synthesis, structure, and antioxidant activity of hybrid N-substituted salicylic acid amides/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, S. A. Krekov, V. E. Borisenko// Russian Journal of Organic Chemistry, 2013, V.49, N 7, pp 1031-1034 doi:10.1134/S1070428013070129), IF=0.513
  204. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  205. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  206. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  207. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  208. G.V. Teplov, E.V. Suslov, V.V. Zarubaev, A.A. Shtro, L.A. Karpinskaya, A.D. Rogachev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Synthesis of New Compounds Combining Adamantanamine and Monoterpene Fragments and their Antiviral Activity Against Influenza Virus A(H1N1)pdm09
    Letters in Drug Design & Discovery, 2013, V. 10, N 6, P. 477-485. doi:10.2174/1570180811310060002, IF=0.845
  209. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, Yu.V. Gatilov, A.V. Zibarev, O.A. Rakitin
    Reactions of vicinal nitroamines with sulfur monochloride-a short and convenient route to fused 1,2,5-thiadiazoles and their N-oxides
    Tetrahedron Letters., 2013, V. 54, N 24, P. 3075-3078. doi:10.1016/j.tetlet.2013.03.134, IF=2.397
  210. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, Yu.V. Gatilov, A.V. Zibarev, O.A. Rakitin
    Reactions of vicinal nitroamines with sulfur monochloride-a short and convenient route to fused 1,2,5-thiadiazoles and their N-oxides
    Tetrahedron Letters., 2013, V. 54, N 24, P. 3075-3078. doi:10.1016/j.tetlet.2013.03.134, IF=2.397
  211. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, Yu.V. Gatilov, A.V. Zibarev, O.A. Rakitin
    Reactions of vicinal nitroamines with sulfur monochloride-a short and convenient route to fused 1,2,5-thiadiazoles and their N-oxides
    Tetrahedron Letters., 2013, V. 54, N 24, P. 3075-3078. doi:10.1016/j.tetlet.2013.03.134, IF=2.397
  212. L.S. Konstantinova, E.A. Knyazeva, N.V. Obruchnikova, Yu.V. Gatilov, A.V. Zibarev, O.A. Rakitin
    Reactions of vicinal nitroamines with sulfur monochloride-a short and convenient route to fused 1,2,5-thiadiazoles and their N-oxides
    Tetrahedron Letters., 2013, V. 54, N 24, P. 3075-3078. doi:10.1016/j.tetlet.2013.03.134, IF=2.397
  213. O. Mikhalchenko, I. Il’ina, A. Pavlova, E. Morozova, D. Korchagina, T. Tolstikova, E. Pokushalov, K. Volcho, N.Salakhutdinov
    Synthesis and analgesic activity of new heterocyclic compounds derived from monoterpenoids
    Medicinal Chemistry Research, 2013, V. 22, N 6, P. 3026-3034. doi:10.1007/s00044-012-0310-9, IF=1.611
  214. В.П. Фадеева, С.В. Ларионов, Т.Г. Леонова, Е.М. Усков, М.И. Рахманова, В.Е. Платонов, В.М. Карпов
    Синтез и фотолюминесценция комплексных соединений Eu(III), Tb(III), содержащих анионы кислот 4-CF3C6F4COOH, 4-(CF3)2CFC6F4COOH
    Журнал общей химии. -2013. -Т. 83. № 6. -С. 986-991. (Synthesis and photoluminescence of Eu(III) and Tb(III) complex compounds containing anions of 4-CF3C6F4COOH and 4-(CF3)(2)CFC6F4COOH acids/ S. V. Larionov, T. G. Leonova, E. M. Uskov, M. I. Rakhmanova, V. E. Platonov, V. M. Karpov, V. P. Fadeeva// Russian Journal of General Chemistry, 2013, V. 83 N 6, Pp 1117-1122. doi:10.1134/S1070363213060194), IF=0.432
  215. В.П. Фадеева, С.В. Ларионов, Т.Г. Леонова, Е.М. Усков, М.И. Рахманова, В.Е. Платонов, В.М. Карпов
    Синтез и фотолюминесценция комплексных соединений Eu(III), Tb(III), содержащих анионы кислот 4-CF3C6F4COOH, 4-(CF3)2CFC6F4COOH
    Журнал общей химии. -2013. -Т. 83. № 6. -С. 986-991. (Synthesis and photoluminescence of Eu(III) and Tb(III) complex compounds containing anions of 4-CF3C6F4COOH and 4-(CF3)(2)CFC6F4COOH acids/ S. V. Larionov, T. G. Leonova, E. M. Uskov, M. I. Rakhmanova, V. E. Platonov, V. M. Karpov, V. P. Fadeeva// Russian Journal of General Chemistry, 2013, V. 83 N 6, Pp 1117-1122. doi:10.1134/S1070363213060194), IF=0.432
  216. В.П. Фадеева, С.В. Ларионов, Т.Г. Леонова, Е.М. Усков, М.И. Рахманова, В.Е. Платонов, В.М. Карпов
    Синтез и фотолюминесценция комплексных соединений Eu(III), Tb(III), содержащих анионы кислот 4-CF3C6F4COOH, 4-(CF3)2CFC6F4COOH
    Журнал общей химии. -2013. -Т. 83. № 6. -С. 986-991. (Synthesis and photoluminescence of Eu(III) and Tb(III) complex compounds containing anions of 4-CF3C6F4COOH and 4-(CF3)(2)CFC6F4COOH acids/ S. V. Larionov, T. G. Leonova, E. M. Uskov, M. I. Rakhmanova, V. E. Platonov, V. M. Karpov, V. P. Fadeeva// Russian Journal of General Chemistry, 2013, V. 83 N 6, Pp 1117-1122. doi:10.1134/S1070363213060194), IF=0.432
  217. В.П. Фадеева, С.В. Ларионов, Т.Г. Леонова, Е.М. Усков, М.И. Рахманова, В.Е. Платонов, В.М. Карпов
    Синтез и фотолюминесценция комплексных соединений Eu(III), Tb(III), содержащих анионы кислот 4-CF3C6F4COOH, 4-(CF3)2CFC6F4COOH
    Журнал общей химии. -2013. -Т. 83. № 6. -С. 986-991. (Synthesis and photoluminescence of Eu(III) and Tb(III) complex compounds containing anions of 4-CF3C6F4COOH and 4-(CF3)(2)CFC6F4COOH acids/ S. V. Larionov, T. G. Leonova, E. M. Uskov, M. I. Rakhmanova, V. E. Platonov, V. M. Karpov, V. P. Fadeeva// Russian Journal of General Chemistry, 2013, V. 83 N 6, Pp 1117-1122. doi:10.1134/S1070363213060194), IF=0.432
  218. Т.Е. Кокина, Н.Б. Горшков, Л.А. Глинская, Н.В. Куратьева, Л.А. Шелудякова, А.В. Ткачев, С.В. Ларионов
    Тиосемикарбазонами (+)-камфоры (L) и (–)-карвона (L1). кристаллическая структура L и [Zn(L)2Cl2]
    Координационная химия, 2013, Т. 39, N . 6, С. 340–348. (Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035), IF=0.465
  219. Т.Е. Кокина, Н.Б. Горшков, Л.А. Глинская, Н.В. Куратьева, Л.А. Шелудякова, А.В. Ткачев, С.В. Ларионов
    Тиосемикарбазонами (+)-камфоры (L) и (–)-карвона (L1). кристаллическая структура L и [Zn(L)2Cl2]
    Координационная химия, 2013, Т. 39, N . 6, С. 340–348. (Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035), IF=0.465
  220. Т.Е. Кокина, Н.Б. Горшков, Л.А. Глинская, Н.В. Куратьева, Л.А. Шелудякова, А.В. Ткачев, С.В. Ларионов
    Тиосемикарбазонами (+)-камфоры (L) и (–)-карвона (L1). кристаллическая структура L и [Zn(L)2Cl2]
    Координационная химия, 2013, Т. 39, N . 6, С. 340–348. (Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035), IF=0.465
  221. Т.Е. Кокина, Н.Б. Горшков, Л.А. Глинская, Н.В. Куратьева, Л.А. Шелудякова, А.В. Ткачев, С.В. Ларионов
    Тиосемикарбазонами (+)-камфоры (L) и (–)-карвона (L1). кристаллическая структура L и [Zn(L)2Cl2]
    Координационная химия, 2013, Т. 39, N . 6, С. 340–348. (Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035), IF=0.465
  222. Т.Е. Кокина, Н.Б. Горшков, Л.А. Глинская, Н.В. Куратьева, Л.А. Шелудякова, А.В. Ткачев, С.В. Ларионов
    Тиосемикарбазонами (+)-камфоры (L) и (–)-карвона (L1). кристаллическая структура L и [Zn(L)2Cl2]
    Координационная химия, 2013, Т. 39, N . 6, С. 340–348. (Synthesis of optically active Zn(II) complexes with thiosemicarbazones of (+)-camphor (L) and (-)-carvone (L1). The crystal structures of L and [Zn(L)2Cl2]/ T. E. Kokina, N. B. Gorshkov, L. A. Glinskaya, N. V. Kurat’eva, L. A. Sheludyakova, A. V. Tkachev, S. V. Larionov// Russian Journal of Coordination Chemistry, 2013, V. 39, N 6, Pp 442-449. doi:10.1134/S1070328413050035), IF=0.465
  223. O.Yu. Rogozhnikova, V.G. Vasiliev, T.I. Troitskaya, D.V. Trukhin, T.V. Mikhalina, H.J. Halpern, V.M. Tormyshev
    Generation of Trityl Radicals by Nucleophilic Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations and Practical and Convenient Large-Scale Synthesis of Persistent Tris(4-carboxy-2,3,5,6-tetrathiaaryl)methyl Radical
    European Journal of Organic Chemistry, 2013, V. 2013, N 16, P. 3347-3355. doi:10.1002/ejoc.201300176, IF=3.344
  224. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  225. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  226. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  227. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  228. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  229. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  230. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  231. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  232. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  233. N.A. Semenov, N.A. Pushkarevsky, E.A. Suturina, E.A. Chulanova, N.V. Kuratieva, A.S. Bogomyakov, I.G. Irtegova, N.V. Vasilieva, L.S. Konstantinova, N.P. Gritsan, O.A. Rakitin, V.I. Ovcharenko, S.N. Konchenko, A.V. Zibarev
    Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b]pyrazinidyl: New Heterospin (S1 = S2=1/2) Radical-Ion Salts
    Inorganic Chemistry, 2013, V. 52, N 11, P. 6654-6663. doi:10.1021/ic400659q, IF=4.592
  234. T.N. Drebushchak, N.A. Pankrushina, A.N. Mikheev, M.K. A. Thumm
    Crystalline products of tolbutamide decomposition in water after microwave treatment
    CrystEngComm, 2013, V. 15, N 18, P. 3582-3586. doi:10.1039/c3ce40145f, IF=3.878
  235. T.N. Drebushchak, N.A. Pankrushina, A.N. Mikheev, M.K. A. Thumm
    Crystalline products of tolbutamide decomposition in water after microwave treatment
    CrystEngComm, 2013, V. 15, N 18, P. 3582-3586. doi:10.1039/c3ce40145f, IF=3.878
  236. T.N. Drebushchak, N.A. Pankrushina, A.N. Mikheev, M.K. A. Thumm
    Crystalline products of tolbutamide decomposition in water after microwave treatment
    CrystEngComm, 2013, V. 15, N 18, P. 3582-3586. doi:10.1039/c3ce40145f, IF=3.878
  237. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  238. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  239. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  240. M. Stekroval, N. Kumarl, P. Maki-Arvelal, O.V. Ardashov, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin
    Selective Preparation of trans-Carveol over Ceria Supported Mesoporous Materials MCM-41 and SBA-15
    Materials, 2013, V.6, N 5, P. 2103-2118. doi:10.3390/ma6052103, IF=2.246
  241. А.А. Коновалов, И.К. Шундрина, В.И. Маматюк, Н.П. Гончаров
    Изучение прочности соломы у ржи secale cereale l. методом динамического механического анализа
    Доклады Российской академии сельскохозяйственных наук. -2013. -№ 5. -С. 3-6.
  242. А.А. Коновалов, И.К. Шундрина, В.И. Маматюк, Н.П. Гончаров
    Изучение прочности соломы у ржи secale cereale l. методом динамического механического анализа
    Доклады Российской академии сельскохозяйственных наук. -2013. -№ 5. -С. 3-6.
  243. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, Yu.V. Gatilov, I.A. Grigor'ev
    First spin-labeled cytisine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 311-315. doi:10.1007/s10600-013-0588-y, IF=0.598
  244. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, Yu.V. Gatilov, I.A. Grigor'ev
    First spin-labeled cytisine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 311-315. doi:10.1007/s10600-013-0588-y, IF=0.598
  245. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, Yu.V. Gatilov, I.A. Grigor'ev
    First spin-labeled cytisine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 311-315. doi:10.1007/s10600-013-0588-y, IF=0.598
  246. N.M. Slyn’ko, L.E. Tatarova, M.M. Shakirov, E.E. Shul’ts
    Synthesis of N-aryloxyalkylanabasine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 294-301. doi:10.1007/s10600-013-0585-1, IF=0.598
  247. N.M. Slyn’ko, L.E. Tatarova, M.M. Shakirov, E.E. Shul’ts
    Synthesis of N-aryloxyalkylanabasine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 294-301. doi:10.1007/s10600-013-0585-1, IF=0.598
  248. Г.В. Гиниятуллина, О.Б. Казакова, Н.И. Медведева, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Г.А. Толстиков
    Синтез аминопропиламинопроизводных бетулиновой и олеаноловой кислот
    Биоорганическая химия, 2013, Т. 39, N 3, С. 369. (Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids/ G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 3, pp 329-337 doi:10.1134/S1068162013020064), IF=0.523
  249. Г.В. Гиниятуллина, О.Б. Казакова, Н.И. Медведева, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Г.А. Толстиков
    Синтез аминопропиламинопроизводных бетулиновой и олеаноловой кислот
    Биоорганическая химия, 2013, Т. 39, N 3, С. 369. (Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids/ G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 3, pp 329-337 doi:10.1134/S1068162013020064), IF=0.523
  250. Г.В. Гиниятуллина, О.Б. Казакова, Н.И. Медведева, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Г.А. Толстиков
    Синтез аминопропиламинопроизводных бетулиновой и олеаноловой кислот
    Биоорганическая химия, 2013, Т. 39, N 3, С. 369. (Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids/ G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 3, pp 329-337 doi:10.1134/S1068162013020064), IF=0.523
  251. Г.А. Толстиков, В.А. Трофимов, Н.Ф. Салахутдинов
    Развитие медицинской химии в Сибирском отделении РАН
    Вестник Российской академии наук, 2013, Т. 83, N 5, С. 407. (The development of medical chemistry in the Siberian Branch of the Russian academy of sciences/ G. A. Tolstikov, B. A. Trofimov, N. F. Salakhutdinov// Herald of the Russian Academy of Sciences, 2013, V. 83, N 3, Pp 268-274 doi:10.1134/S1019331613020093), IF=0.214
  252. Л.М. Горностаев, А.Е. Девяшина, Ю.В. Гатилов
    О циклизации 2-хлор-3-(1,4-оксоциклогекса-2,5-диенилиденамино)1,4-дигидронафталин-1,4-дионов в 6-хлор-10,12а-дигидрокси-7 H,12а H-бензо[с]феноксазин-5-оны
    Журнал органической химии, 2013, Т. 49, N 5, С. 763-766. (Cyclization of 2-chloro-3-(1,4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-diones into 6-chloro-10,12a-dihydroxy-7H,12aH-benzo[c]phenoxazin-5-ones/ L.M. Gornostaev, A.E. Devyashina, Yu.V. Gatilov// Russian Journal of Organic Chemistry, 2013, V.49, N 5, pp 746-749 doi:10.1134/S1070428013050012), IF=0.513
  253. Л.М. Горностаев, А.Е. Девяшина, Ю.В. Гатилов
    О циклизации 2-хлор-3-(1,4-оксоциклогекса-2,5-диенилиденамино)1,4-дигидронафталин-1,4-дионов в 6-хлор-10,12а-дигидрокси-7 H,12а H-бензо[с]феноксазин-5-оны
    Журнал органической химии, 2013, Т. 49, N 5, С. 763-766. (Cyclization of 2-chloro-3-(1,4-oxocyclohexa-2,5-dienylideneamino)-1,4-dihydronaphthalene-1,4-diones into 6-chloro-10,12a-dihydroxy-7H,12aH-benzo[c]phenoxazin-5-ones/ L.M. Gornostaev, A.E. Devyashina, Yu.V. Gatilov// Russian Journal of Organic Chemistry, 2013, V.49, N 5, pp 746-749 doi:10.1134/S1070428013050012), IF=0.513
  254. A.Yu. Shabalin, N.Yu. Adonin, V.V. Bardin, S.A. Prikhod'ko, M.N. Timofeeva, M.V. Bykova, V.N. Parmon
    Synthesis of K[4-ROC6F4BF3] from potassium pentafluorophenyltrifluoroborate and O-nucleophiles
    Journal of Fluorine Chemistry, 2013, V. 156, P. 82-87. doi:10.1016/j.jfluchem.2013.01.020, IF=1.939
  255. A.Yu. Shabalin, N.Yu. Adonin, V.V. Bardin, S.A. Prikhod'ko, M.N. Timofeeva, M.V. Bykova, V.N. Parmon
    Synthesis of K[4-ROC6F4BF3] from potassium pentafluorophenyltrifluoroborate and O-nucleophiles
    Journal of Fluorine Chemistry, 2013, V. 156, P. 82-87. doi:10.1016/j.jfluchem.2013.01.020, IF=1.939
  256. A.Yu. Shabalin, N.Yu. Adonin, V.V. Bardin, S.A. Prikhod'ko, M.N. Timofeeva, M.V. Bykova, V.N. Parmon
    Synthesis of K[4-ROC6F4BF3] from potassium pentafluorophenyltrifluoroborate and O-nucleophiles
    Journal of Fluorine Chemistry, 2013, V. 156, P. 82-87. doi:10.1016/j.jfluchem.2013.01.020, IF=1.939
  257. A.Yu. Shabalin, N.Yu. Adonin, V.V. Bardin, S.A. Prikhod'ko, M.N. Timofeeva, M.V. Bykova, V.N. Parmon
    Synthesis of K[4-ROC6F4BF3] from potassium pentafluorophenyltrifluoroborate and O-nucleophiles
    Journal of Fluorine Chemistry, 2013, V. 156, P. 82-87. doi:10.1016/j.jfluchem.2013.01.020, IF=1.939
  258. A.Yu. Shabalin, N.Yu. Adonin, V.V. Bardin, S.A. Prikhod'ko, M.N. Timofeeva, M.V. Bykova, V.N. Parmon
    Synthesis of K[4-ROC6F4BF3] from potassium pentafluorophenyltrifluoroborate and O-nucleophiles
    Journal of Fluorine Chemistry, 2013, V. 156, P. 82-87. doi:10.1016/j.jfluchem.2013.01.020, IF=1.939
  259. A.M. Chibiryaev, I.V. Kozhevnikov, O.N. Martyanov
    High-temperature reaction of SiO2 with methanol: Nucleophilic assistance of some N-unsubstituted benzazoles
    Applied Catalysis A: General, 2013, V. 456, P. 159-167. doi:10.1016/j.apcata.2013.03.001, IF=3.41
  260. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  261. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  262. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  263. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  264. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  265. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  266. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  267. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  268. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  269. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  270. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  271. А.С. Кабанов, А.А. Сергеев, Л.Н. Шишкина, Л.Е. Булычев, М.О. Скарнович, А.А. Сергеев, Н.И. Бормотов, О.В. Пьянков, О.А. Серова, С.А. Боднев, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Сравнительное изучение противовирусной активности химических соединений в отношении ортопоксвирусов в экспериментах in vivo
    Вопросы вирусологии. 2013. Т. 58. № 4. С. 39-43.
  272. Н.Г. Власенко, М.Т. Егорычева, М.П. Половинка, Н.Ф. Салахутдинов
    Перспективные биологически активные вещества на яровой пшенице
    Защита и карантин растений, 2013, N 4, С. 36-37.
  273. Н.Г. Власенко, М.Т. Егорычева, М.П. Половинка, Н.Ф. Салахутдинов
    Перспективные биологически активные вещества на яровой пшенице
    Защита и карантин растений, 2013, N 4, С. 36-37.
  274. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
  275. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
  276. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
  277. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
  278. A.Yu. Makarov, F. Blockhuys, I.Yu. Bagryanskaya, Yu.V. Gatilov, M.M. Shakirov, A.V. Zibarev
    Experimental and Computational Study on the Structure and Properties of Herz Cations and Radicals: 1,2,3-Benzodithiazolium, 1,2,3-Benzodithiazolyl, and Their Se Congeners
    Inorganic Chemistry, 2013, V. 52, N 7, P. 3699-3710. doi:10.1021/ic302203t, IF=4.592
  279. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  280. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  281. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  282. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  283. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  284. A.V. Artem'ev, L.A. Oparina, N.K. Gusarova, N.A. Kolyvanov, O.V. Vysotskaya, I.Yu. Bagryanskaya, B.A. Trofimov
    Chemoselective synthesis of first representatives of bis(diorganothiophosphinyl) selenides, (R2P = S)(2)Se, from secondary phosphine sulfides and elemental selenium
    Inorganic Chemistry Communications, 2013, V. 30, P. 124-127. doi:10.1016/j.inoche.2013.01.019, IF=4.592
  285. М.А. Мяделец, Т.А. Воробьева, Д.В. Домрачев
    Состав эфирных масел некоторых видов рода agastache clayton ex gronov (lamiaceae), культивируемых в условиях среднего Урала
    Химия в интересах устойчивого развития, 2013, Т. 21, N 4., С. 419-423. (Composition of Essential Oils of Some Species of the Agastache Clayton ex Gronov Genus (Lamiaceae) Cultivated Under the Conditions of the Middle Urals/ M. A. Myadelets, T. A. Vorobyeva, D. V. Domrachev// Chemistry for Sustainable Development, 2013, Т. 21,. № 4, pp. 419-423. (in russian).)
  286. М.А. Мяделец, Т.А. Воробьева, Д.В. Домрачев
    Состав эфирных масел некоторых видов рода agastache clayton ex gronov (lamiaceae), культивируемых в условиях среднего Урала
    Химия в интересах устойчивого развития, 2013, Т. 21, N 4., С. 419-423. (Composition of Essential Oils of Some Species of the Agastache Clayton ex Gronov Genus (Lamiaceae) Cultivated Under the Conditions of the Middle Urals/ M. A. Myadelets, T. A. Vorobyeva, D. V. Domrachev// Chemistry for Sustainable Development, 2013, Т. 21,. № 4, pp. 419-423. (in russian).)
  287. M. Edeleva, S.R. Marque, K. Kabytaev, Y. Guillaneuf, D. Gigmes, E. Bagryanskaya
    H-transfer reaction during decomposition of N-(2-methylpropyl)- N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (SG1)-based alkoxyamines
    Journal of Polymer Science Part A: Polymer Chemistry, 2013, V. 51, N 6, P. 1323-1336. doi:10.1002/pola.26500, IF=3.542
  288. M. Edeleva, S.R. Marque, K. Kabytaev, Y. Guillaneuf, D. Gigmes, E. Bagryanskaya
    H-transfer reaction during decomposition of N-(2-methylpropyl)- N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (SG1)-based alkoxyamines
    Journal of Polymer Science Part A: Polymer Chemistry, 2013, V. 51, N 6, P. 1323-1336. doi:10.1002/pola.26500, IF=3.542
  289. M. Edeleva, S.R. Marque, K. Kabytaev, Y. Guillaneuf, D. Gigmes, E. Bagryanskaya
    H-transfer reaction during decomposition of N-(2-methylpropyl)- N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (SG1)-based alkoxyamines
    Journal of Polymer Science Part A: Polymer Chemistry, 2013, V. 51, N 6, P. 1323-1336. doi:10.1002/pola.26500, IF=3.542
  290. M. Edeleva, S.R. Marque, K. Kabytaev, Y. Guillaneuf, D. Gigmes, E. Bagryanskaya
    H-transfer reaction during decomposition of N-(2-methylpropyl)- N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (SG1)-based alkoxyamines
    Journal of Polymer Science Part A: Polymer Chemistry, 2013, V. 51, N 6, P. 1323-1336. doi:10.1002/pola.26500, IF=3.542
  291. M. Edeleva, S.R. Marque, K. Kabytaev, Y. Guillaneuf, D. Gigmes, E. Bagryanskaya
    H-transfer reaction during decomposition of N-(2-methylpropyl)- N-(1-diethylphosphono-2,2-dimethylpropyl)-N-oxyl (SG1)-based alkoxyamines
    Journal of Polymer Science Part A: Polymer Chemistry, 2013, V. 51, N 6, P. 1323-1336. doi:10.1002/pola.26500, IF=3.542
  292. Т.М. Уткина, Л.П. Потехина, О.Л. Карташова, А.В. Ткачев
    Регуляция персистентных свойств микроорганизмов растительными экстрактами хвойных растений
    Бюллетень Оренбургского научного центра УрО РАН, 2013, № 3, С. 13. (Regulation of persistent properties of microorganisms by plant extracts of coniferous plants/ T.M. Utkina, L.P. Potehina, O.L. Kartashova, А.V.Tkachev// )
  293. Т.М. Уткина, Л.П. Потехина, О.Л. Карташова, А.В. Ткачев
    Регуляция персистентных свойств микроорганизмов растительными экстрактами хвойных растений
    Бюллетень Оренбургского научного центра УрО РАН, 2013, № 3, С. 13. (Regulation of persistent properties of microorganisms by plant extracts of coniferous plants/ T.M. Utkina, L.P. Potehina, O.L. Kartashova, А.V.Tkachev// )
  294. Т.М. Уткина, Л.П. Потехина, О.Л. Карташова, А.В. Ткачев
    Регуляция персистентных свойств микроорганизмов растительными экстрактами хвойных растений
    Бюллетень Оренбургского научного центра УрО РАН, 2013, № 3, С. 13. (Regulation of persistent properties of microorganisms by plant extracts of coniferous plants/ T.M. Utkina, L.P. Potehina, O.L. Kartashova, А.V.Tkachev// )
  295. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  296. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  297. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  298. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  299. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  300. O.B. Kazakova, E.V. Tretyakova, I.E. Smirnova, T.I. Nazyrov, O.S. Kukovinets, G.A. Tolstikov, K.Y. Suponitskii
    An Efficient Oxyfunctionalization of Quinopimaric Acid Derivatives with Ozone
    Natural Product Communications, 2013, V. 8, N 3, P. 293-296., IF=0.955
  301. В.И. Аникеев, В.П. Сивцев, И.В. Ильина, Д.В. Корчагина, О.Б. Стаценко, К.П. Волчо, Н.Ф. Салахутдинов
    Превращения некоторых монотерпеноидов в присутствии альдегидов в сверхкритических растворителях
    Журнал физической химии, 2013, Т. 87, N 3., С. 403. (Transformations of several monoterpenoids in the presence of aldehydes in supercritical solvents/ V. I. Anikeev, V. P. Sivcev, I. V. Il’ina, D. V. Korchagina, O. B. Statsenko, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A , 2013, V. 87, N 3, Pp 382-387. doi:10.1134/S0036024413030023), IF=0.386
  302. В.И. Аникеев, В.П. Сивцев, И.В. Ильина, Д.В. Корчагина, О.Б. Стаценко, К.П. Волчо, Н.Ф. Салахутдинов
    Превращения некоторых монотерпеноидов в присутствии альдегидов в сверхкритических растворителях
    Журнал физической химии, 2013, Т. 87, N 3., С. 403. (Transformations of several monoterpenoids in the presence of aldehydes in supercritical solvents/ V. I. Anikeev, V. P. Sivcev, I. V. Il’ina, D. V. Korchagina, O. B. Statsenko, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A , 2013, V. 87, N 3, Pp 382-387. doi:10.1134/S0036024413030023), IF=0.386
  303. В.И. Аникеев, В.П. Сивцев, И.В. Ильина, Д.В. Корчагина, О.Б. Стаценко, К.П. Волчо, Н.Ф. Салахутдинов
    Превращения некоторых монотерпеноидов в присутствии альдегидов в сверхкритических растворителях
    Журнал физической химии, 2013, Т. 87, N 3., С. 403. (Transformations of several monoterpenoids in the presence of aldehydes in supercritical solvents/ V. I. Anikeev, V. P. Sivcev, I. V. Il’ina, D. V. Korchagina, O. B. Statsenko, K. P. Volcho, N. F. Salakhutdinov// Russian Journal of Physical Chemistry A , 2013, V. 87, N 3, Pp 382-387. doi:10.1134/S0036024413030023), IF=0.386
  304. Zh. Ganbaatar, E.E. Shul’ts, T.N. Petrova, M.M. Shakirov, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Furocoumarins from Peucedanum baicalense of mongolia flora and their cytotoxic activity
    Chemistry of Natural Compounds, 2013, V. 49, N, P. 99-102. doi:10.1007/s10600-013-0518-z, IF=0.598
  305. Zh. Ganbaatar, E.E. Shul’ts, T.N. Petrova, M.M. Shakirov, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Furocoumarins from Peucedanum baicalense of mongolia flora and their cytotoxic activity
    Chemistry of Natural Compounds, 2013, V. 49, N, P. 99-102. doi:10.1007/s10600-013-0518-z, IF=0.598
  306. Zh. Ganbaatar, E.E. Shul’ts, T.N. Petrova, M.M. Shakirov, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Furocoumarins from Peucedanum baicalense of mongolia flora and their cytotoxic activity
    Chemistry of Natural Compounds, 2013, V. 49, N, P. 99-102. doi:10.1007/s10600-013-0518-z, IF=0.598
  307. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  308. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  309. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  310. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  311. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  312. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  313. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  314. D.T. T. Huong, T.T. T. Thuy, T.T. Hien, N.T. Tra, N.Q. Tien, I.E. Smirnova, O.B. Kazakova, E.M. Minnibaeva, G.A. Tolstikov
    Synthesis and Cytotoxicity of Derivatives of Dipterocarpol, a Metabolite of Dipterocarpus alatus
    Chemistry of Natural Compounds, 2013, V. 49, N 1, P. 58-65. doi:10.1007/s10600-013-0505-4, IF=0.598
  315. И.В. Сорокина, И.Я. Майнагашев, Н.А. Жукова, Д.В. Корчагина, Т.Г. Толстикова, В.П. Николин, Н.А. Попова, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Противоопухолевая активность амидов дигидробетулоновой кислоты in vitro и in vivo
    Биоорганическая химия, 2013, Т. 39, N 2, С. 221-229. (Antitumor activity of amides of dihydrobetulonic acid in vitro and in vivo/ I. V. Sorokina, I. Ya. Mainagashev, N. A. Zhukova, D. V. Korchagina, T. G. Tolstikova, V. P. Nikolin, N. A. Popova, M. A. Pokrovskii, A. G. Pokrovskii, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 194-201 doi:10.1134/S106816201302012X), IF=0.523
  316. И.В. Сорокина, И.Я. Майнагашев, Н.А. Жукова, Д.В. Корчагина, Т.Г. Толстикова, В.П. Николин, Н.А. Попова, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Противоопухолевая активность амидов дигидробетулоновой кислоты in vitro и in vivo
    Биоорганическая химия, 2013, Т. 39, N 2, С. 221-229. (Antitumor activity of amides of dihydrobetulonic acid in vitro and in vivo/ I. V. Sorokina, I. Ya. Mainagashev, N. A. Zhukova, D. V. Korchagina, T. G. Tolstikova, V. P. Nikolin, N. A. Popova, M. A. Pokrovskii, A. G. Pokrovskii, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 194-201 doi:10.1134/S106816201302012X), IF=0.523
  317. И.В. Сорокина, И.Я. Майнагашев, Н.А. Жукова, Д.В. Корчагина, Т.Г. Толстикова, В.П. Николин, Н.А. Попова, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Противоопухолевая активность амидов дигидробетулоновой кислоты in vitro и in vivo
    Биоорганическая химия, 2013, Т. 39, N 2, С. 221-229. (Antitumor activity of amides of dihydrobetulonic acid in vitro and in vivo/ I. V. Sorokina, I. Ya. Mainagashev, N. A. Zhukova, D. V. Korchagina, T. G. Tolstikova, V. P. Nikolin, N. A. Popova, M. A. Pokrovskii, A. G. Pokrovskii, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 194-201 doi:10.1134/S106816201302012X), IF=0.523
  318. И.В. Сорокина, И.Я. Майнагашев, Н.А. Жукова, Д.В. Корчагина, Т.Г. Толстикова, В.П. Николин, Н.А. Попова, М.А. Покровский, А.Г. Покровский, Н.Ф. Салахутдинов
    Противоопухолевая активность амидов дигидробетулоновой кислоты in vitro и in vivo
    Биоорганическая химия, 2013, Т. 39, N 2, С. 221-229. (Antitumor activity of amides of dihydrobetulonic acid in vitro and in vivo/ I. V. Sorokina, I. Ya. Mainagashev, N. A. Zhukova, D. V. Korchagina, T. G. Tolstikova, V. P. Nikolin, N. A. Popova, M. A. Pokrovskii, A. G. Pokrovskii, N. F. Salakhutdinov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 194-201 doi:10.1134/S106816201302012X), IF=0.523
  319. А.Н. Антимонова, Н.И. Петренко, Э.Э. Шульц, Ю.Ф. Полиенко, M.М. Шакиров, И.Г. Иртегова, М.А. Покровский, К.М. Шерман, И.А. Григорьев, А.Г. Покровский, Г.А. Толстиков
    Синтетические трансформации высших терпеноидов. xxx*. синтез и цитотоксическая активность амидов бетулоновой кислоты, содержащих фрагменты нитроксильных радикалов
    Биоорганическая химия, 2013, Т. 39, N 2, С. 206-211. (Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals/ A. N. Antimonova, N. I. Petrenko, E. E. Shults, Yu. F. Polienko, M. M. Shakirov, I. G. Irtegova, M. A. Pokrovskii, K. M. Sherman, I. A. Grigor’ev, A. G. Pokrovskii, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 181-185 doi:10.1134/S1068162013020027), IF=0.523
  320. А.Н. Антимонова, Н.И. Петренко, Э.Э. Шульц, Ю.Ф. Полиенко, M.М. Шакиров, И.Г. Иртегова, М.А. Покровский, К.М. Шерман, И.А. Григорьев, А.Г. Покровский, Г.А. Толстиков
    Синтетические трансформации высших терпеноидов. xxx*. синтез и цитотоксическая активность амидов бетулоновой кислоты, содержащих фрагменты нитроксильных радикалов
    Биоорганическая химия, 2013, Т. 39, N 2, С. 206-211. (Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals/ A. N. Antimonova, N. I. Petrenko, E. E. Shults, Yu. F. Polienko, M. M. Shakirov, I. G. Irtegova, M. A. Pokrovskii, K. M. Sherman, I. A. Grigor’ev, A. G. Pokrovskii, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 181-185 doi:10.1134/S1068162013020027), IF=0.523
  321. A.G. Potapov, L.V. Politanskaya
    The study of the adsorption of 1,3-diethers on the MgCl2 surface
    Journal of Molecular Catalysia A-Chemical, 2013, V. 368, P. 159-162. doi:10.1016/j.molcata.2012.12.004, IF=3.187
  322. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  323. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  324. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  325. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  326. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  327. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  328. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  329. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  330. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  331. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  332. S.L. Veber, M.V. Fedin, K.Yu. Maryunina, K.N. Boldyrev, M.A. Sheglov, V.V. Kubarev, O.A. Shevchenko, N.A. Vinokurov, G.N. Kulipanov, R.Z. Sagdeev, V.I. Ovcharenko, E.G. Bagryanskaya
    Influence of Intense THz Radiation on Spin State of Photoswitchable Compound Cu(hfac)2LPr
    Journal of Physical Chemistry A, 2013, V. 117, N 7, P. 1483-1491. doi:10.1021/jp311404t, IF=2.77
  333. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.N. Shmidt, S.W. Kang, S.M. Kim, B.H. Um
    Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
    Chemistry & Biodiversity, 2013, V. 10, N 2, P. 198-208. doi:10.1002/cbdv.201200009, IF=1.807
  334. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.N. Shmidt, S.W. Kang, S.M. Kim, B.H. Um
    Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
    Chemistry & Biodiversity, 2013, V. 10, N 2, P. 198-208. doi:10.1002/cbdv.201200009, IF=1.807
  335. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.N. Shmidt, S.W. Kang, S.M. Kim, B.H. Um
    Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
    Chemistry & Biodiversity, 2013, V. 10, N 2, P. 198-208. doi:10.1002/cbdv.201200009, IF=1.807
  336. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
  337. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
  338. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
  339. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
  340. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
  341. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  342. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  343. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  344. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  345. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  346. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  347. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  348. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  349. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  350. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  351. А.С. Кабанов, А.А. Сергеев, Л.Е. Булычев, Н.И. Бормотов, Л.Н. Шишкина, А.А. Сергеев, С.А. Боднев, М.О. Скарнович, А.Р. Шевцов, Б.А. Селиванов, А.Я. Тихонов, А.П. Агафонов, А.Н. Сергеев
    Изучение противовирусной активности химически синтезированных соединений в отношении ортопоксвирусов в экспериментах in vitro
    Проблемы особо опасных инфекций, 2013, N 2, С. 54-59.
  352. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  353. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  354. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  355. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  356. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  357. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  358. Т.Е. Кокина, А.В. Ткачев, Л.И. Мячина, С.Н. Бизяев, Л.А. Шелудякова, Л.А. Глинская, И.В. Корольков, Е.Г. Богуславский, С.В. Ларионов
    Синтез и строение комплексов Pd(II) и Cu(II) c хиральными бис-α-аминооксимами, содержащими фрагменты терпеновых молекул (+)-3-карена или (+)-лимонена и 4,4'-метилендианилиновую линкерную группу. кристаллическая структура соединения [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]
    Журнал общей химии. -2013. -Т. 83. № 2. -С. 282-293. (Synthesis and structure of palladium(II) and copper(II) complexes with chiral bis-alpha-aminooximes containing (+)-3-carene or (+)-limonene fragments and 4,4 '-methylenedianiline linker. Crystal structure of the complex [Cu( I-PrOH)Cl 2(μ-H2L 3)CuCl2•H2O]/ T. E. Kokina, A. V. Tkachev, L. I. Myachina, S. N. Bizyaev, L. A. Sheludyakova, L. A. Glinskaya, I. V. Korol’kov, E. G. Boguslavskii, S. V. Larionov// Russian Journal of General Chemistry, 2013, V. 83, N 2, pp 336-347 doi:10.1134/S1070363213020175), IF=0.432
  359. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  360. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  361. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  362. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  363. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  364. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  365. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  366. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  367. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  368. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  369. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  370. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  371. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  372. О. Б. Казакова, И. Е. Смирнова, Х. Д. Т. Тху, Т. Т.Нгуен, Г. Н. Апрышко, О. С. Жукова, Н. И. Медведева, Т. И. Назыров, Е. В. Третьякова, И. В. Чудов, А. Ф. Исмагилова, К. Ю. Супоницкий, Д. В. Казаков, Ф. Э. Сафаров, Г. А. Толстиков
    Синтез, структура и фармакологическая активность (7R,8S)-эпокси-(13R,17R)-триоксоланабиетиновой кислоты
    Биоорганическая химия, 2013, Т. 39, N 2, С. 230-239. (Synthesis, structure, and pharmacological activity of (7R,8S)-epoxy-(13R,17R)-trioxolane abietic acid/ O. B. Kazakova, I. E. Smirnova, H. Do Tkhi Tkhu, Tkhankh Tra Nguen, G. N. Apryshko, O. S. Zhukova, N. I. Medvedeva, T. I. Nazyrov, E. V. Tret’yakova, I. V. Chudov, A. F. Ismagilova, K. Yu. Suponitsky, D. V. Kazakov, F. E. Safarov, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 202-210 doi:10.1134/S1068162013020088), IF=0.523
  373. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  374. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  375. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  376. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  377. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  378. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  379. Е.В. Третьяков, В.Г. Васильев, А.С. Богомяков, Г.В. Романенко, М.В. Федин, И.С. Антипин, С.Е. Соловьева, А.И. Коновалов, Р.З. Сагдеев, В.И. Овчаренко
    Синтез, структура и свойства нитронилнитроксильного тетрарадикала c каликс[4]ареновым остовом
    Известия АН. Серия химическая, 2013, N 2, C. 541-545 . (Synthesis, structure, and properties of nitronyl nitroxyl tetraradical with calix[4]arene framework/ E. V. Tret’yakov, V. G. Vasil’ev, A. S. Bogomyakov, G. V. Romanenko, M. V. Fedin, I. S. Antipin, S. E. Solov’eva, A. I. Konovalov, R. Z. Sagdeev, V. I. Ovcharenko// Russian Chemical Bulletin, 2013, V. 62, N 2, pp 543-547. doi:10.1007/s11172-013-0075-4), IF=0.423
  380. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение хлорорганическими пестицидами и полихлорированными бифенилами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 197-205. (Pollution of the Basin of Lake Baikal by Chlorinated Organic Pesticides: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 197-205. (in russian).)
  381. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение хлорорганическими пестицидами и полихлорированными бифенилами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 197-205. (Pollution of the Basin of Lake Baikal by Chlorinated Organic Pesticides: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 197-205. (in russian).)
  382. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение хлорорганическими пестицидами и полихлорированными бифенилами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 197-205. (Pollution of the Basin of Lake Baikal by Chlorinated Organic Pesticides: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 197-205. (in russian).)
  383. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение полиароматическими углеводородами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 189-195. (Pollution of the Basin of Lake Baikal by Polyaromatic Hydrocarbons: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 189-195. (in russian).)
  384. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение полиароматическими углеводородами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 189-195. (Pollution of the Basin of Lake Baikal by Polyaromatic Hydrocarbons: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 189-195. (in russian).)
  385. Г.С. Ширапова, Н.С. Утюжникова, О.А. Рабина, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Загрязнение полиароматическими углеводородами бассейна озера Байкал: озеро Гусиное
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 189-195. (Pollution of the Basin of Lake Baikal by Polyaromatic Hydrocarbons: Lake Gusinoye/ G.S. Shirapova, N.S. Utyuzhnikova, O.A. Rabina, A.I. Vyalkov, S.V. Morozov, V.B. Batoev// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 189-195. (in russian).)
  386. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  387. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  388. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  389. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  390. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  391. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  392. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  393. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  394. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  395. М.В. Харькова, А.В. Черепанова, Е.С. Морозкин, И.А. Запорожченко, П.П. Лактионов, А.А. Струнов, Е.В. Киселева, Т.Г. Толстикова, Н.В. Шикина, З.Р. Исмагилов, В.В. Власов
    Цитотоксические и иммуномодулирующие свойства наночастиц золота
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 179-188. (Cytotoxic and Immunomodulating Properties of Gold Nanoparticles/ M.V. Kharkova, A.V. Cherepanova, E.S. Morozkin, I.A. Zaporozhchenko, P.P. Laktionov, A.A. Strunov, E.V. Kiseleva, T.G. Tolstikova, N.V. Shikina, Z.R. Ismagilov, V.V. Vlasov// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 179-188. (in russian).)
  396. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  397. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  398. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  399. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  400. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  401. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  402. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  403. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  404. Е.С. Морозкин, И.А. Запорожченко, М.В. Харькова, А.В. Черепанова, П.П. Лактионов, В.В. Власов, Б.Г. Сухов, Г.Ф. Прозорова, Б.А. Трофимов, М.В. Хвостов, Т.Г. Толстикова
    Цитотоксические и иммуномодулирующие свойства нанокомпозитов серебра и платины
    Химия в интересах устойчивого развития, 2013, Т. 21, N 2, С. 155-163. (Cytotoxic and Immunomodulating Properties of Silver and Platinum Nanocomposites/ E.S. Morozkin, I.A. Zaporozhchenko, M.V. Kharkova, A.V. Cherepanova, P.P. Laktionov, V.V. Vlasov, B.G. Sukhov, G.F. Prozorova, B.A. Tofimov, M.V. Khvostov, T.G. Tolstikova// Chemistry for Sustainable Development, 2013, Т. 21,. № 2, pp. 155-163. (in russian).)
  405. V.V. Bardin, H.J. Frohn
    Preparation of first examples of RFC CIF4 molecules. A study of the fluorination of selected 1-iodoalk-1-ynes with xenon difluoride/boron trifluoride
    Journal of Fluorine Chemistry, 2013, V. 156, P. 98-104. doi:10.1016/j.jfluchem.2013.01.006, IF=1.939
  406. M.B. Bushuev, Yu.V. Gatilov, E.B. Nikolaenkova, V.G. Vasiliev, V.P. Krivopalov
    Mono-, di-, tetra- and heptanuclear copper(II) complexes with 4-(3,5-di-R-1H-pyrazol-1-yl)-6-methyl-2-(pyridin-2-yl)pyrimidines (R = H, Me): Syntheses, crystal structures and electrospray ionization mass spectrometry
    Inorganic Chemica Acta, 2013, V. 395, P. 95-103. doi:10.1016/j.ica.2012.10.018, IF=1.687
  407. O.V. Zalomaeva, N.V. Maksimchuk, A.M. Chibiryaev, K.A. Kovalenko, V.P. Fedin, B.S. Balzhinimaev
    Synthesis of cyclic carbonates from epoxides or olefins and CO2 catalyzed by metal-organic frameworks and quaternary ammonium salts
    Journal of Energy Chemistry, 2013, V. 22, N 1, P. 130-135. doi:10.1016/S2095-4956(13)60017-0
  408. O.V. Zalomaeva, N.V. Maksimchuk, A.M. Chibiryaev, K.A. Kovalenko, V.P. Fedin, B.S. Balzhinimaev
    Synthesis of cyclic carbonates from epoxides or olefins and CO2 catalyzed by metal-organic frameworks and quaternary ammonium salts
    Journal of Energy Chemistry, 2013, V. 22, N 1, P. 130-135. doi:10.1016/S2095-4956(13)60017-0
  409. O.V. Zalomaeva, N.V. Maksimchuk, A.M. Chibiryaev, K.A. Kovalenko, V.P. Fedin, B.S. Balzhinimaev
    Synthesis of cyclic carbonates from epoxides or olefins and CO2 catalyzed by metal-organic frameworks and quaternary ammonium salts
    Journal of Energy Chemistry, 2013, V. 22, N 1, P. 130-135. doi:10.1016/S2095-4956(13)60017-0
  410. O.V. Zalomaeva, N.V. Maksimchuk, A.M. Chibiryaev, K.A. Kovalenko, V.P. Fedin, B.S. Balzhinimaev
    Synthesis of cyclic carbonates from epoxides or olefins and CO2 catalyzed by metal-organic frameworks and quaternary ammonium salts
    Journal of Energy Chemistry, 2013, V. 22, N 1, P. 130-135. doi:10.1016/S2095-4956(13)60017-0
  411. O.V. Zalomaeva, N.V. Maksimchuk, A.M. Chibiryaev, K.A. Kovalenko, V.P. Fedin, B.S. Balzhinimaev
    Synthesis of cyclic carbonates from epoxides or olefins and CO2 catalyzed by metal-organic frameworks and quaternary ammonium salts
    Journal of Energy Chemistry, 2013, V. 22, N 1, P. 130-135. doi:10.1016/S2095-4956(13)60017-0
  412. M.l Elyashberg, K. Blinov, S. Molodtsov, A. J. Williams
    Structure Revision of Asperjinone Using Computer-Assisted Structure Elucidation Methods
    Journal of Natural Products, 2013, 76 (1), pp 113–116. doi:10.1021/np300218g, IF=3.285
  413. M.l Elyashberg, K. Blinov, S. Molodtsov, A. J. Williams
    Structure Revision of Asperjinone Using Computer-Assisted Structure Elucidation Methods
    Journal of Natural Products, 2013, 76 (1), pp 113–116. doi:10.1021/np300218g, IF=3.285
  414. M.l Elyashberg, K. Blinov, S. Molodtsov, A. J. Williams
    Structure Revision of Asperjinone Using Computer-Assisted Structure Elucidation Methods
    Journal of Natural Products, 2013, 76 (1), pp 113–116. doi:10.1021/np300218g, IF=3.285
  415. D. Parkhomenko, E.G. Bagryanskaya, S.R. Marque, D. Siri
    Intramolecular proton transfer (IPT) in alkoxyamine: a theoretical investigation
    Phys Chem Chem Phys , 2913, V. 15, N 33, P. 13862-13871. Physical Chemistry Chemical Physics, V.15, N 33, P: 13862-13871. doi:10.1039/c3cp50821h, IF=3.828
  416. D. Parkhomenko, E.G. Bagryanskaya, S.R. Marque, D. Siri
    Intramolecular proton transfer (IPT) in alkoxyamine: a theoretical investigation
    Phys Chem Chem Phys , 2913, V. 15, N 33, P. 13862-13871. Physical Chemistry Chemical Physics, V.15, N 33, P: 13862-13871. doi:10.1039/c3cp50821h, IF=3.828
  417. D. Parkhomenko, E.G. Bagryanskaya, S.R. Marque, D. Siri
    Intramolecular proton transfer (IPT) in alkoxyamine: a theoretical investigation
    Phys Chem Chem Phys , 2913, V. 15, N 33, P. 13862-13871. Physical Chemistry Chemical Physics, V.15, N 33, P: 13862-13871. doi:10.1039/c3cp50821h, IF=3.828
  418. М.А. Мяделец, О.Ю. Васильева, Д.В. Домрачев
    Исследование химического состава эфирных масел ORIGANUM VULGARE L. с различной окраской цветков
    Химия растительного сырья, 2013, N 1, С. 129-136.
  419. М.А. Мяделец, О.Ю. Васильева, Д.В. Домрачев
    Исследование химического состава эфирных масел ORIGANUM VULGARE L. с различной окраской цветков
    Химия растительного сырья, 2013, N 1, С. 129-136.
  420. Н.З. Ляхов, А.В. Душкин, Т.Г. Толстикова
    Эффективные и безопасные лекарства — разработки сибирских ученых
    Известия АН. Серия химическая, 2013, N 1, С. 233-239. (Efficient and safe medicines developed by Siberian scientists/ N. Z. Lyakhov, A. V. Dushkin, T. G. Tolstikova// Russian Chemical Bulletin, 2013, V. 62, N 1, pp: 235-241. doi:10.1007/s11172-013-0036-y), IF=0.423
  421. Н.З. Ляхов, А.В. Душкин, Т.Г. Толстикова
    Эффективные и безопасные лекарства — разработки сибирских ученых
    Известия АН. Серия химическая, 2013, N 1, С. 233-239. (Efficient and safe medicines developed by Siberian scientists/ N. Z. Lyakhov, A. V. Dushkin, T. G. Tolstikova// Russian Chemical Bulletin, 2013, V. 62, N 1, pp: 235-241. doi:10.1007/s11172-013-0036-y), IF=0.423
  422. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М.С. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Синтез биологически активных циклопентаноидов из гексахлорциклопентадиена
    Известия АН. Серия химическая, 2013, N 1, С. 225-232. (Science-intensive utilization of environmentally harmful polychlorocarbons. Synthesis of biologically active cyclopentanoids from hexachlorocyclopentadiene/ G. A. Tolstikov, S. A. Ismailov, F. A. Gimalova, N. A. Ivanova, M. S. Miftakhov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 226-234 doi:10.1007/s11172-013-0035-z), IF=0.423
  423. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М.С. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Синтез биологически активных циклопентаноидов из гексахлорциклопентадиена
    Известия АН. Серия химическая, 2013, N 1, С. 225-232. (Science-intensive utilization of environmentally harmful polychlorocarbons. Synthesis of biologically active cyclopentanoids from hexachlorocyclopentadiene/ G. A. Tolstikov, S. A. Ismailov, F. A. Gimalova, N. A. Ivanova, M. S. Miftakhov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 226-234 doi:10.1007/s11172-013-0035-z), IF=0.423
  424. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М.С. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Синтез биологически активных циклопентаноидов из гексахлорциклопентадиена
    Известия АН. Серия химическая, 2013, N 1, С. 225-232. (Science-intensive utilization of environmentally harmful polychlorocarbons. Synthesis of biologically active cyclopentanoids from hexachlorocyclopentadiene/ G. A. Tolstikov, S. A. Ismailov, F. A. Gimalova, N. A. Ivanova, M. S. Miftakhov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 226-234 doi:10.1007/s11172-013-0035-z), IF=0.423
  425. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М.С. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Синтез биологически активных циклопентаноидов из гексахлорциклопентадиена
    Известия АН. Серия химическая, 2013, N 1, С. 225-232. (Science-intensive utilization of environmentally harmful polychlorocarbons. Synthesis of biologically active cyclopentanoids from hexachlorocyclopentadiene/ G. A. Tolstikov, S. A. Ismailov, F. A. Gimalova, N. A. Ivanova, M. S. Miftakhov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 226-234 doi:10.1007/s11172-013-0035-z), IF=0.423
  426. Д.Н. Соколов, М.Е. Рахманова, О.А. Лузина, А.В. Шернюков, Н.Ф. Салахутдинов
    Синтез новых производных (+)-усниновой кислоты с флавоновым остовом
    Известия АН. Серия химическая, 2013, N 1, С. 211–215. (Synthesis of new (+)-usnic acid derivatives with the flavone structure/ D. N. Sokolov, M. E. Rakhmanova, O. A. Luzina, A. V. Shernyukov, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 212-216 doi:10.1007/s11172-013-0031-3), IF=0.423
  427. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  428. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  429. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  430. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  431. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  432. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  433. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  434. П.А. Волков, Н.И. Иванова, Н.К. Гусарова, Л.А. Опарина, Л.И. Ларина, О.В. Высоцкая, Н.А. Колыванов, И.Ю. Багрянская, Б.А. Трофимов
    Синтез оксазолидиновых фосфинхалькогенидов из виниловых эфиров аминоспиртов
    Известия АН. Серия химическая, 2013, N 1, С. 107-110. (Synthesis of oxazolidinylphosphine chalcogenides from aminoethyl vinyl ethers/ P. A. Volkov, N. I. Ivanova, N. K. Gusarova, L. A. Oparina, L. I. Larina, O. V. Vysotskaya, N. A. Kolyvanov, I. Yu. Bagryanskaya, B. A. Trofimov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 107-110 doi:10.1007/s11172-013-0015-3), IF=0.423
  435. И.Б. Абдрахманов, И.М. Борисов, Р.Р. Исмагилов, Н.Г. Нигматуллин, Р.Н. Хуснитдинов, Г.А. Толстиков
    Особенности механизма аминоперегруппировки Кляйзена
    Известия АН. Серия химическая, 2013, N 1, C. 83-87. (Regularities of the amino-Claisen rearrangement mechanism/ I. B. Abdrakhmanov, I. M. Borisov, R. R. Ismagilov, N. G. Nigmatullin, R. N. Khusnitdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 83-87. doi:10.1007/s11172-013-0010-8), IF=0.423
  436. И.Б. Абдрахманов, И.М. Борисов, Р.Р. Исмагилов, Н.Г. Нигматуллин, Р.Н. Хуснитдинов, Г.А. Толстиков
    Особенности механизма аминоперегруппировки Кляйзена
    Известия АН. Серия химическая, 2013, N 1, C. 83-87. (Regularities of the amino-Claisen rearrangement mechanism/ I. B. Abdrakhmanov, I. M. Borisov, R. R. Ismagilov, N. G. Nigmatullin, R. N. Khusnitdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 83-87. doi:10.1007/s11172-013-0010-8), IF=0.423
  437. И.Б. Абдрахманов, И.М. Борисов, Р.Р. Исмагилов, Н.Г. Нигматуллин, Р.Н. Хуснитдинов, Г.А. Толстиков
    Особенности механизма аминоперегруппировки Кляйзена
    Известия АН. Серия химическая, 2013, N 1, C. 83-87. (Regularities of the amino-Claisen rearrangement mechanism/ I. B. Abdrakhmanov, I. M. Borisov, R. R. Ismagilov, N. G. Nigmatullin, R. N. Khusnitdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 83-87. doi:10.1007/s11172-013-0010-8), IF=0.423
  438. И.Б. Абдрахманов, И.М. Борисов, Р.Р. Исмагилов, Н.Г. Нигматуллин, Р.Н. Хуснитдинов, Г.А. Толстиков
    Особенности механизма аминоперегруппировки Кляйзена
    Известия АН. Серия химическая, 2013, N 1, C. 83-87. (Regularities of the amino-Claisen rearrangement mechanism/ I. B. Abdrakhmanov, I. M. Borisov, R. R. Ismagilov, N. G. Nigmatullin, R. N. Khusnitdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 83-87. doi:10.1007/s11172-013-0010-8), IF=0.423
  439. И.Б. Абдрахманов, И.М. Борисов, Р.Р. Исмагилов, Н.Г. Нигматуллин, Р.Н. Хуснитдинов, Г.А. Толстиков
    Особенности механизма аминоперегруппировки Кляйзена
    Известия АН. Серия химическая, 2013, N 1, C. 83-87. (Regularities of the amino-Claisen rearrangement mechanism/ I. B. Abdrakhmanov, I. M. Borisov, R. R. Ismagilov, N. G. Nigmatullin, R. N. Khusnitdinov, G. A. Tolstikov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 83-87. doi:10.1007/s11172-013-0010-8), IF=0.423
  440. Е.В. Пантелеева, А.С. Кондратьев, Л.И. Горюнов, В.В. Коваль, Е.А. Лукьянец, В.Д. Штейнгарц
    Синтез фталонитрилов с ω-алкенильными, ω-(алкилсульфанил)алкильными и ω-(алкилсульфонил)алкильными заместителями и производных фталоцианина на их основе
    Журнал органической химии, 2013, Т. 49, N 1, С. 142-148. (Synthesis of phthalonitriles containing omega-alkenyl, omega-(alkylsulfanyl)alkyl, and omega-(alkylsulfonyl)alkyl substituents and phthalocyanine derivatives based thereon/ E. V. Panteleeva, A. S. Kondrat’ev, L. I. Goryunov, V. V. Koval’, E. A. Luk’yanets, V. D. Shteingarts// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 138-144 doi:10.1134/S1070428013010235), IF=0.513
  441. Е.В. Пантелеева, А.С. Кондратьев, Л.И. Горюнов, В.В. Коваль, Е.А. Лукьянец, В.Д. Штейнгарц
    Синтез фталонитрилов с ω-алкенильными, ω-(алкилсульфанил)алкильными и ω-(алкилсульфонил)алкильными заместителями и производных фталоцианина на их основе
    Журнал органической химии, 2013, Т. 49, N 1, С. 142-148. (Synthesis of phthalonitriles containing omega-alkenyl, omega-(alkylsulfanyl)alkyl, and omega-(alkylsulfonyl)alkyl substituents and phthalocyanine derivatives based thereon/ E. V. Panteleeva, A. S. Kondrat’ev, L. I. Goryunov, V. V. Koval’, E. A. Luk’yanets, V. D. Shteingarts// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 138-144 doi:10.1134/S1070428013010235), IF=0.513
  442. О.И. Каргина, Л.М. Горностаев, А.А. Нефёдов
    Гетероциклизаций 1-S,S-диалкил-N-(9,10-антрахинон-1-ил)сульфоксимидов в нафто[1,2,3-cd]индол-6(2 H)-оны
    Журнал органической химии, 2013, Т. 49, N 1, С. 79-85. (Synthesis of S,S-dialkyl-N-(9,10-dioxo-9,10-dihydroanthracen-1-yl)sulfoximides and specificities of their base-catalyzed intramolecular heterocyclizations into naphtho[1,2,3-cd]-indol-6(2H)-ones/ O. I. Kargina, L.M. Gornostaev, A.A. Nefedov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 70-77 doi:10.1134/S1070428013010132), IF=0.513
  443. О.И. Каргина, Л.М. Горностаев, А.А. Нефёдов
    Гетероциклизаций 1-S,S-диалкил-N-(9,10-антрахинон-1-ил)сульфоксимидов в нафто[1,2,3-cd]индол-6(2 H)-оны
    Журнал органической химии, 2013, Т. 49, N 1, С. 79-85. (Synthesis of S,S-dialkyl-N-(9,10-dioxo-9,10-dihydroanthracen-1-yl)sulfoximides and specificities of their base-catalyzed intramolecular heterocyclizations into naphtho[1,2,3-cd]-indol-6(2H)-ones/ O. I. Kargina, L.M. Gornostaev, A.A. Nefedov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 70-77 doi:10.1134/S1070428013010132), IF=0.513
  444. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  445. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  446. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  447. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  448. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  449. G.Yu. Ishmuratov, A.V. Bannova, E.R. Latypova, V.S. Tukhvatshin, O.S. Kukovinets, R.R. Muslukhov, G.A. Tolstikov
    Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds
    Журнал органической химии, 2013, Т. 49, N 1, С.52-55. (Transformations of peroxide ozonolysis products of (R)-Menth-4-en-3-one in the presence of nitrogen-containing organic compounds/ G. Yu. Ishmuratov, A. V. Bannova, E. R. Latypova, V. S. Tukhvatshin, O. S. Kukovinets, R. R. Muslukhov, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 42-45. doi:10.1134/S1070428013010089), IF=0.513
  450. A.V. Pozdeeva, N.I. Komarova, V.G. Vasiliev, A.D. Rogachev, N.F. Salakhutdinov, G.A. Tolstikov
    Aryloxyacetamides derived from resveratroloside and pinostilbenoside
    Mendeleev Communications, 2013, V. 23, N 1, P. 37-38. doi:10.1016/j.mencom.2013.01.013, IF=1.52
  451. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49
  452. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49
  453. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49
  454. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49
  455. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49
  456. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, E.P. Doronina, S.I. Verkhoturova, V.F. Sidorkin, B.A. Trofimov
    Alkali Metal Thioselenophosphinates, M[SeSPR2]: One-Pot Multicomponent Synthesis, DFT Study, and Synthetic Application
    Eur. J. Inorg. Chem, 2013, V. 2013, N 3, p. 415–426, doi:10.1002/ejic.201200947, IF=3.49

2012

Reviews, articles

  1. V.M. Tormyshev, A.M. Genaev, G.E. Sal'nikov, O.Yu. Rogozhnikova, T.I. Troitskaya, D.V. Trukhin, V.I. Mamatyuk, D.S. Fadeev, H.J. Halpern
    Triarylmethanols with Bulky Aryl Groups and the NOESY/EXSY Experimental Observation of a Two-Ring-Flip Mechanism for the Helicity Reversal of Molecular Propellers
    Eur.J. Org. Chem., 2012, N 3, 623-629. doi:10.1002/ejoc.201101243, IF=3.206
  2. S.M. Adekenov, E.E. Shul'ts, Yu.V. Gatilov, A.A. Lomzov, G.A. Atazhanova, A.N. Kupriyanov
    15,16-Epoxy-3,13(16),14-Neoclerodatrien-17,12:18,19-diolide, a new compound from Galatella punctata
    Chem. Nat. Compd., 2012, V. 48, N 6, pp. 946-949. doi:10.1007/s10600-013-0435-1, IF=1.29
  3. S.M. Adekenov, E.E. Shul'ts, Yu.V. Gatilov, A.A. Lomzov, G.A. Atazhanova, A.N. Kupriyanov
    15,16-Epoxy-3,13(16),14-Neoclerodatrien-17,12:18,19-diolide, a new compound from Galatella punctata
    Chem. Nat. Compd., 2012, V. 48, N 6, pp. 946-949. doi:10.1007/s10600-013-0435-1, IF=1.29
  4. S.M. Adekenov, E.E. Shul'ts, Yu.V. Gatilov, A.A. Lomzov, G.A. Atazhanova, A.N. Kupriyanov
    15,16-Epoxy-3,13(16),14-Neoclerodatrien-17,12:18,19-diolide, a new compound from Galatella punctata
    Chem. Nat. Compd., 2012, V. 48, N 6, pp. 946-949. doi:10.1007/s10600-013-0435-1, IF=1.29
  5. S.M. Adekenov, E.E. Shul'ts, Yu.V. Gatilov, A.A. Lomzov, G.A. Atazhanova, A.N. Kupriyanov
    15,16-Epoxy-3,13(16),14-Neoclerodatrien-17,12:18,19-diolide, a new compound from Galatella punctata
    Chem. Nat. Compd., 2012, V. 48, N 6, pp. 946-949. doi:10.1007/s10600-013-0435-1, IF=1.29
  6. Н.А. Жукова, Д.Е. Семенов, Е.П. Бессергенева, И.В. Сорокина, Т.Г. Толстикова
    Коррекция лекарственно-индуцированной гепатотоксичности новыми тритерпеновыми производными при перевиваемой лимфоме RLS
    Бюлл. Эксп. Биол. Мед., 2012, Т. 154, № 9, С. 356-360. (Correction of Drug-Induced Hepatotoxicity with New Triterpene Derivatives in Transplanted RLS Lymphoma/ N. A. Zhukova, D. E. Semenov, E. P. Bessergeneva, I. V. Sorokina, T. G. Tolstikova// B EXP BIOL MED+, 2012, V. 154, N 3, pp 370-374. doi:10.1007/s10517-013-1953-3)
  7. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, А.В. Павлова, М.В. Хвостов
    Гель-хроматографическое и токсикологическое исследование механохимических превращений водорастворимых полисахаридов
    Хим.-фарм. журн., 2012, Т. 46, № 10, 53-56. (Gel chromatographic and toxicological studies of the mechanochemical transformations of water-soluble polysaccharides/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, A. V. Pavlova, M. V. Khvostov// PHARM CHEM J+, 2012, V. 46, N 10, pp. 630-633. doi:10.1007/s11094-013-0859-8), IF=0.372
  8. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, А.В. Павлова, М.В. Хвостов
    Гель-хроматографическое и токсикологическое исследование механохимических превращений водорастворимых полисахаридов
    Хим.-фарм. журн., 2012, Т. 46, № 10, 53-56. (Gel chromatographic and toxicological studies of the mechanochemical transformations of water-soluble polysaccharides/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, A. V. Pavlova, M. V. Khvostov// PHARM CHEM J+, 2012, V. 46, N 10, pp. 630-633. doi:10.1007/s11094-013-0859-8), IF=0.372
  9. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  10. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  11. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  12. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  13. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  14. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  15. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  16. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  17. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  18. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  19. N.A. Pushkarevsky, A.V. Lonchakov, N.A. Semenov, E. Lork, L.I. Buravov, L.S. Konstantinova, T.G. Silber, N. Robertson, N.P. Gritsan, O.A. Rakitin, J.D. Woollins, E.B. Yagubskii, A.V. Zibarev
    First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: design, synthesis, crystal structures, electronic and electrical properties
    Synthetic Met., 2012, V. 162, 2267-2276. doi:10.1016/j.synthmet.2012.10.026, IF=1.828
  20. D.A. Morozov, I.A. Kirilyuk, D.A. Komarov, A. Goti, I.Yu. Bagryanskaya, N.V. Kuratieva, I.A. Grigor’ev
    Synthesis of a Chiral C2-Symmetric Sterically Hindered Pyrrolidine Nitroxide Radical via Combined Iterative Nucleophilic Additions and Intramolecular 1,3-Dipolar Cycloadditions to Cyclic Nitrones
    J. Org. Chem., 2012, V. 77, N 23, 10688-10698. doi:10.1021/jo3019158, IF=4.449
  21. D.A. Morozov, I.A. Kirilyuk, D.A. Komarov, A. Goti, I.Yu. Bagryanskaya, N.V. Kuratieva, I.A. Grigor’ev
    Synthesis of a Chiral C2-Symmetric Sterically Hindered Pyrrolidine Nitroxide Radical via Combined Iterative Nucleophilic Additions and Intramolecular 1,3-Dipolar Cycloadditions to Cyclic Nitrones
    J. Org. Chem., 2012, V. 77, N 23, 10688-10698. doi:10.1021/jo3019158, IF=4.449
  22. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  23. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  24. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  25. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  26. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  27. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  28. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  29. V.V. Martemyanov, I.M. Dubovskiy, I.A. Belousova, S.V. Pavlushin, D.V. Domrachev, M.J. Rantala, J.-P. Salminen, S.A. Bakhvalov, V.V. Glupov
    Rapid induced resistance of silver birch affects both innate immunity and performance of gypsy moths: the role of plant chemical defenses
    Arthropod-Plant Interactions, 2012, V. 6, N 4, pp 507-518. doi:10.1007/s11829-012-9202-7
  30. М.И. Дергачева, О.А. Некрасова, Д.И. Васильева, В.П. Фадеева
    Элементный состав гуминовых кислот целинных черноземов разных условий формирования
    Вестник Оренбургского государственного университета, 2012, № 12(146), 90-96.
  31. М.И. Дергачева, О.А. Некрасова, Д.И. Васильева, В.П. Фадеева
    Элементный состав гуминовых кислот целинных черноземов разных условий формирования
    Вестник Оренбургского государственного университета, 2012, № 12(146), 90-96.
  32. М.И. Дергачева, О.А. Некрасова, Д.И. Васильева, В.П. Фадеева
    Элементный состав гуминовых кислот целинных черноземов разных условий формирования
    Вестник Оренбургского государственного университета, 2012, № 12(146), 90-96.
  33. В.И. Аникеев, И.В. Ильина, К.П. Волчо, Н.Ф. Салахутдинов
    Циклизация цитронеллаля в сверхкритическом растворителе в реакторе проточного типа в присутствии Al2O3
    Журн. физ. химии, 2012, Т. 86, № 12, 2054-2057. (Cyclization of citronellal in a supercritical solvent in a flow reactor in the presence of Al2O3/ V.I. Anikeev, I.V. Il'ina, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2012, V. 86, N 12, pp.1917-1919. doi:10.1134/S0036024412120035), IF=0.458
  34. D.V. Domrachev, E.V. Karpova, S.N. Goroshkevich, A.V. Tkachev
    __Comparative analysis of volatiles from needles of five-needle pines of northern and eastern Eurasia
    Russ. J. Bioorg. Chem., 2012, V. 38, N 7, 780-789. (published in Khimija Rastitel’nogo Syr’ja, 2011, No. 4, pp. 89–98.) (Comparative analysis of volatiles from needles of five-needle pines of northern and eastern Eurasia/ D.V. Domrachev, E.V. Karpova, S.N. Goroshkevich, A.V. Tkachev// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp. 780-789. doi:10.1134/S1068162012070059), IF=0.635
  35. G. Yu. Ishmuratov, M.P. Yakovleva, E.F. Valeeva, V.A. Vydrina, G.A. Tolstikov
    Monoterpene ketones in the synthesis of optically active insect pheromones
    Russ. J. Bioorg. Chem., 2012, V. 38, N 7, 667-688. doi:10.1134/S1068162012070084, IF=0.635
  36. G. Yu. Ishmuratov, M.P. Yakovleva, E.F. Valeeva, V.A. Vydrina, G.A. Tolstikov
    Monoterpene ketones in the synthesis of optically active insect pheromones
    Russ. J. Bioorg. Chem., 2012, V. 38, N 7, 667-688. doi:10.1134/S1068162012070084, IF=0.635
  37. G. Yu. Ishmuratov, M.P. Yakovleva, E.F. Valeeva, V.A. Vydrina, G.A. Tolstikov
    Monoterpene ketones in the synthesis of optically active insect pheromones
    Russ. J. Bioorg. Chem., 2012, V. 38, N 7, 667-688. doi:10.1134/S1068162012070084, IF=0.635
  38. G. Yu. Ishmuratov, M.P. Yakovleva, E.F. Valeeva, V.A. Vydrina, G.A. Tolstikov
    Monoterpene ketones in the synthesis of optically active insect pheromones
    Russ. J. Bioorg. Chem., 2012, V. 38, N 7, 667-688. doi:10.1134/S1068162012070084, IF=0.635
  39. Д.Ф. Августинович, Т.Г. Толстикова
    Комбированное введение фенибута и буспирона: экспериментальное исследование
    Вопросы биологической медицинской и фармацевтической химии, 2012, №12, C. 59-63. (Joint effect of phenibut AND buspirone: experimental study/ D.F. Avgustinovich, T.G. Tolstikova// Вопросы биологической медицинской и фармацевтической химии. - 2012. - №12. - C. 59-63.), IF=0.305
  40. Т.П. Мартьянов, Е.Н. Ушаков, В.А. Савельев, Л.С. Клименко
    Краунсодержащие нафто- и антрахиноны: синтез и комплексообразование с катионами щелочных и щелочноземельных металлов
    Изв. АН, Cер. хим., 2012, Т. 61, № 12, 2261–2273. (Crown-containing naphtho- and anthraquinones: synthesis and complexation with alkali and alkaline-earth metal cations/ T. P. Martyanov, E. N. Ushakov, V. A. Savelyev, L. S. Klimenko// RUSS CHEM B+, 2012, V. 61, N 12, pp. 2282-2294. doi:10.1007/s11172-012-0323-z)
  41. Т.П. Мартьянов, Е.Н. Ушаков, В.А. Савельев, Л.С. Клименко
    Краунсодержащие нафто- и антрахиноны: синтез и комплексообразование с катионами щелочных и щелочноземельных металлов
    Изв. АН, Cер. хим., 2012, Т. 61, № 12, 2261–2273. (Crown-containing naphtho- and anthraquinones: synthesis and complexation with alkali and alkaline-earth metal cations/ T. P. Martyanov, E. N. Ushakov, V. A. Savelyev, L. S. Klimenko// RUSS CHEM B+, 2012, V. 61, N 12, pp. 2282-2294. doi:10.1007/s11172-012-0323-z)
  42. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  43. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  44. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  45. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  46. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  47. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, И.В. Корольков, Е.М. Усков, О.В. Антонова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез, строение п-HOOCC6F4COOH ˙ H2O (H2L ˙H2O) и люминесцирующих координационных полимеров
    Координац. химия, 2012, Т. 38, № 12, 827-823. (Syntheses and structures of p-HOOCC6F4COOH˙H2O (H2L ˙H2O) and luminescent coordination polymers [Tb2(H2O)4(L)3˙2H2O] n and Tb2(Phen)2(L)3˙2H2O/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, I.V. Korol'kov, E.M. Uskov, O.V. Antonova, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2012, V. 38, N 12, pp. 717-723. doi:10.1134/S1070328412110036), IF=0.546
  48. P.A. Potashov, V.I. Borovkov, N.P. Gritsan, V.A. Bagryansky, Y.N. Molin, L.N. Shchegoleva
    Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies
    J. Physi. Chem. A, 2012, V. 116, N 12, 3110-3117. doi:10.1021/jp2113208, IF=2.946
  49. P.A. Potashov, V.I. Borovkov, N.P. Gritsan, V.A. Bagryansky, Y.N. Molin, L.N. Shchegoleva
    Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies
    J. Physi. Chem. A, 2012, V. 116, N 12, 3110-3117. doi:10.1021/jp2113208, IF=2.946
  50. P.A. Potashov, V.I. Borovkov, N.P. Gritsan, V.A. Bagryansky, Y.N. Molin, L.N. Shchegoleva
    Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies
    J. Physi. Chem. A, 2012, V. 116, N 12, 3110-3117. doi:10.1021/jp2113208, IF=2.946
  51. P.A. Potashov, V.I. Borovkov, N.P. Gritsan, V.A. Bagryansky, Y.N. Molin, L.N. Shchegoleva
    Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies
    J. Physi. Chem. A, 2012, V. 116, N 12, 3110-3117. doi:10.1021/jp2113208, IF=2.946
  52. P.A. Potashov, V.I. Borovkov, N.P. Gritsan, V.A. Bagryansky, Y.N. Molin, L.N. Shchegoleva
    Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies
    J. Physi. Chem. A, 2012, V. 116, N 12, 3110-3117. doi:10.1021/jp2113208, IF=2.946
  53. D.N. Sokolov, V.V. Zarubaev, A.A. Shtro, O.A. Luzina, N.I. Komarova, N.F. Salakhutdinov, O.I. Kiselev
    Anti-viral activity of (-)- and (+)-usnic acids and their derivatives against influenza virus A(H1N1)2009
    Bioorg. Med. Chem. Lett., V. 22, N. 23, 7060-7064. doi:10.1016/j.bmcl.2012.09.084, IF=2.553
  54. D.N. Sokolov, V.V. Zarubaev, A.A. Shtro, O.A. Luzina, N.I. Komarova, N.F. Salakhutdinov, O.I. Kiselev
    Anti-viral activity of (-)- and (+)-usnic acids and their derivatives against influenza virus A(H1N1)2009
    Bioorg. Med. Chem. Lett., V. 22, N. 23, 7060-7064. doi:10.1016/j.bmcl.2012.09.084, IF=2.553
  55. D.N. Sokolov, V.V. Zarubaev, A.A. Shtro, O.A. Luzina, N.I. Komarova, N.F. Salakhutdinov, O.I. Kiselev
    Anti-viral activity of (-)- and (+)-usnic acids and their derivatives against influenza virus A(H1N1)2009
    Bioorg. Med. Chem. Lett., V. 22, N. 23, 7060-7064. doi:10.1016/j.bmcl.2012.09.084, IF=2.553
  56. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, I.Yu. Bagryanskaya
    One-Pot Halogen-Free Synthesis of 2,3-Dihydro-1H-inden-2-yl-phosphinic Acid from 1H-indene and Elemental Phosphorus via the Trofimov-Gusarova Reaction
    Heteroatom Chem., 2012, V. 23, N 6, 568-573. doi:10.1002/hc.21051, IF=1.243
  57. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, I.Yu. Bagryanskaya
    One-Pot Halogen-Free Synthesis of 2,3-Dihydro-1H-inden-2-yl-phosphinic Acid from 1H-indene and Elemental Phosphorus via the Trofimov-Gusarova Reaction
    Heteroatom Chem., 2012, V. 23, N 6, 568-573. doi:10.1002/hc.21051, IF=1.243
  58. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, I.Yu. Bagryanskaya
    One-Pot Halogen-Free Synthesis of 2,3-Dihydro-1H-inden-2-yl-phosphinic Acid from 1H-indene and Elemental Phosphorus via the Trofimov-Gusarova Reaction
    Heteroatom Chem., 2012, V. 23, N 6, 568-573. doi:10.1002/hc.21051, IF=1.243
  59. Г.С. Ширапова, В.Б. Батоев, А.И. Вялков, С.В. Морозов
    Геоэкологическая оценка загрязнения озера Гусиного стойкими органическими загрязнителями
    Вестник Бурятского государственного университета, 2012. № SB, 280-283.
  60. Г.С. Ширапова, В.Б. Батоев, А.И. Вялков, С.В. Морозов
    Геоэкологическая оценка загрязнения озера Гусиного стойкими органическими загрязнителями
    Вестник Бурятского государственного университета, 2012. № SB, 280-283.
  61. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Transformations of acetophenone and its derivatives in supercritical fluid isopropanol/CO2 in a continuous flow reactor in the presence of alumina
    J. Supercri.l Fluid., 2012, V. 70, 35–39. doi:10.1016/j.supflu.2012.05.012, IF=2.859
  62. V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Transformations of acetophenone and its derivatives in supercritical fluid isopropanol/CO2 in a continuous flow reactor in the presence of alumina
    J. Supercri.l Fluid., 2012, V. 70, 35–39. doi:10.1016/j.supflu.2012.05.012, IF=2.859
  63. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  64. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  65. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  66. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  67. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  68. М.Б. Бушуев, Б.А. Селиванов, Н.В. Первухина, Д.Ю. Наумов, М.И. Рахманова, Л.А. Шелудякова, А.Я. Тихонов, С.В. Ларионов
    Люминесцирующие комплексы цинка(II) и кадмия(II) на основе 2-(4,5-диметил-1Н-имидазол-2-ил)пиридина и 2-(1-гидрокси-4,5-диметил-1Н-имидазол-2-ил)пиридина
    Журн. общ. химии, 2012, T. 82, № 11, 1870-1877. (Luminescent zinc(II) and cadmium(II) complexes based on 2-(4,5-dimethyl-1H-imidazol-2-yl)pyridine and 2-(1-hydroxy-4,5-dimethyl-1H-imidazol-2-yl)pyridine/ M.B. Bushuev, B.A. Selivanov, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, L.A. Sheludyakova, A.Ya. Tikhonov, S.V. Larionov// RUSS J GEN CHEM+, 2012, V.82, N 11, pp. 1859-1868. doi:10.1134/S1070363212110230), IF=0.467
  69. I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, A.N. Lobov, K.Yu. Suponitskii
    Ozonolysis of cyclomusalenone and its derivatives
    Chem. Nat. Compd., 2012, V. 48, N 5, 816-820. doi:10.1007/s10600-012-0391-1, IF=1.29
  70. I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, A.N. Lobov, K.Yu. Suponitskii
    Ozonolysis of cyclomusalenone and its derivatives
    Chem. Nat. Compd., 2012, V. 48, N 5, 816-820. doi:10.1007/s10600-012-0391-1, IF=1.29
  71. I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, A.N. Lobov, K.Yu. Suponitskii
    Ozonolysis of cyclomusalenone and its derivatives
    Chem. Nat. Compd., 2012, V. 48, N 5, 816-820. doi:10.1007/s10600-012-0391-1, IF=1.29
  72. I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, A.N. Lobov, K.Yu. Suponitskii
    Ozonolysis of cyclomusalenone and its derivatives
    Chem. Nat. Compd., 2012, V. 48, N 5, 816-820. doi:10.1007/s10600-012-0391-1, IF=1.29
  73. I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, A.N. Lobov, K.Yu. Suponitskii
    Ozonolysis of cyclomusalenone and its derivatives
    Chem. Nat. Compd., 2012, V. 48, N 5, 816-820. doi:10.1007/s10600-012-0391-1, IF=1.29
  74. С.Ф. Василевский, А.А. Степанов, Д.С. Фадеев
    Двойственная реакционная способность диазониевых солей, образуемых 1-амино-2-ацетилинил-9,10-антрахинонами
    Изв. АН, Cер. хим., 2012, Т. 61, № 11, 2071-2078. (Dual reactivity of diazonium salts derived from 1-amino-2-ethynyl-9,10-anthraquinones/ S. F. Vasilevsky, A. A. Stepanov, D. S. Fadeev// RUSS CHEM B+, 2012, V. 61, N 11, pp. 2088-2095. doi:10.1007/s11172-012-0292-2), IF=0.379
  75. С.Ф. Василевский, А.А. Степанов, Д.С. Фадеев
    Двойственная реакционная способность диазониевых солей, образуемых 1-амино-2-ацетилинил-9,10-антрахинонами
    Изв. АН, Cер. хим., 2012, Т. 61, № 11, 2071-2078. (Dual reactivity of diazonium salts derived from 1-amino-2-ethynyl-9,10-anthraquinones/ S. F. Vasilevsky, A. A. Stepanov, D. S. Fadeev// RUSS CHEM B+, 2012, V. 61, N 11, pp. 2088-2095. doi:10.1007/s11172-012-0292-2), IF=0.379
  76. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  77. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  78. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  79. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  80. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  81. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  82. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  83. С.В. Сысолятин, В.Н. Сурмачев, В.В. Малыхин, А.И. Калашников, И.А. Сурмачева, Е.Г. Сонина, А.С. Дубков, Г.А. Толстиков, Э.Э. Шульц, Н.Ф. Cалахутдинов, У.М. Джемилев
    Получение производных бетулина. Na{N-[3-Оксо-20(29)-лупен-28-оил]-9-аминононаноил}-3-амино-3-фенилпропионовая кислота
    Хим.-фарм. журн., 2012, Т. 46, № 8, 15-18. (Synthesis of Betulin Derivatives: N '{N-[3-OXO-20(29)-Lupen-28-OYL]-9-Aminononanoyl}3-Amino-3-Phenylpropionic Acid/ S.V. Sysolyatin, V.N. Surmachev, V.V. Malykhin, A.I. Kalashnikov, I.A. Surmacheva, E.G. Sonina, A.S. Dubkov, G.A. Tolstikov, E.E. Shul'ts, N.F. Salakhutdinov, U.M. Dzhemilev// PHARM CHEM J+, 2012, V. 46, N 8, pp. 473-477. doi:10.1007/s11094-012-0828-7), IF=0.372
  84. Л.А. Глинская, З.А. Савельева, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Кристаллическая и молекулярная структура соединения [Zn(HL)Cl] • EtOH, (H2L= хиральный бис(ментановый) пропилендиаминодиоксим)
    Журн. cтруктур. химии, 2012, Т. 53, № 6, 1136-1141. (Crystal and molecular structure of the [Zn(HL)Cl]center dot EtOH compound, (H2L = chiral bis(menthane)propylenediaminodioxime)/ L.A. Glinskaya, Z.A. Savel’eva, S.N. Bizyaev, A.V. Tkachev, S.V. Larionov// J STRUCT CHEM+, 2012, V. 53, N 6, pp. 1111-1117. doi:10.1134/S0022476612060145), IF=0.586
  85. Л.А. Глинская, З.А. Савельева, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Кристаллическая и молекулярная структура соединения [Zn(HL)Cl] • EtOH, (H2L= хиральный бис(ментановый) пропилендиаминодиоксим)
    Журн. cтруктур. химии, 2012, Т. 53, № 6, 1136-1141. (Crystal and molecular structure of the [Zn(HL)Cl]center dot EtOH compound, (H2L = chiral bis(menthane)propylenediaminodioxime)/ L.A. Glinskaya, Z.A. Savel’eva, S.N. Bizyaev, A.V. Tkachev, S.V. Larionov// J STRUCT CHEM+, 2012, V. 53, N 6, pp. 1111-1117. doi:10.1134/S0022476612060145), IF=0.586
  86. Л.А. Глинская, З.А. Савельева, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Кристаллическая и молекулярная структура соединения [Zn(HL)Cl] • EtOH, (H2L= хиральный бис(ментановый) пропилендиаминодиоксим)
    Журн. cтруктур. химии, 2012, Т. 53, № 6, 1136-1141. (Crystal and molecular structure of the [Zn(HL)Cl]center dot EtOH compound, (H2L = chiral bis(menthane)propylenediaminodioxime)/ L.A. Glinskaya, Z.A. Savel’eva, S.N. Bizyaev, A.V. Tkachev, S.V. Larionov// J STRUCT CHEM+, 2012, V. 53, N 6, pp. 1111-1117. doi:10.1134/S0022476612060145), IF=0.586
  87. E.G. Bagryanskaya, S.R. A. Marque, Yu.P. Tsentalovitch
    Alkoxyamine re-formation reaction. Effects of the nitroxide fragment: a multiparameter analysis
    J. Org. Chem., 2012, V. 77, N 11, 4996-5005. doi:10.1021/jo300459z, IF=4.449
  88. E.G. Bagryanskaya, S.R. A. Marque, Yu.P. Tsentalovitch
    Alkoxyamine re-formation reaction. Effects of the nitroxide fragment: a multiparameter analysis
    J. Org. Chem., 2012, V. 77, N 11, 4996-5005. doi:10.1021/jo300459z, IF=4.449
  89. M.V. Khvostov, T.G. Tolstikova, A.A. Chernonosov, O.S. Fedorova, G.I. Lifshits
    Pharmacokinetic Alterations of Warfarin in its clathrate With Arabinogalactan
    Asian J. Pharm. Clin. Res., 2012, V. 5, Suppl. 4, 251-252.
  90. M.V. Khvostov, T.G. Tolstikova, A.A. Chernonosov, O.S. Fedorova, G.I. Lifshits
    Pharmacokinetic Alterations of Warfarin in its clathrate With Arabinogalactan
    Asian J. Pharm. Clin. Res., 2012, V. 5, Suppl. 4, 251-252.
  91. M.V. Khvostov, T.G. Tolstikova, A.A. Chernonosov, O.S. Fedorova, G.I. Lifshits
    Pharmacokinetic Alterations of Warfarin in its clathrate With Arabinogalactan
    Asian J. Pharm. Clin. Res., 2012, V. 5, Suppl. 4, 251-252.
  92. Д.Е. Семёнов, Н.А. Жукова, Е.П. Бессергенева, И.В. Сорокина, Д.С. Баев, Б.М. Глухов, Г.И. Непомнящих, Т.Г. Толстикова
    Влияние тритерпеновых производных на общую численность гепатоцитов в печени крыс с токсическим гепатитом
    Бюлл. Эксп. Биол. Мед., 2012, Т. 153, № 6, 837-840. (Effect of Triterpene Derivatives on the Total Hepatocyte Count in the Liver of Rats with Toxic Hepatitis/ D. E. Semenov, N. A. Zhukova, E. P. Bessergeneva, I. V. Sorokina, D. S. Baev, B. M. Glukhov, G. I. Nepomnyaschikh, T. G. Tolstikova// B EXP BIOL MED+, 2012, V.153, N 6, pp 859-862. doi:10.1007/s10517-012-1844-z), IF=0.305
  93. Д.Е. Семёнов, Н.А. Жукова, Е.П. Бессергенева, И.В. Сорокина, Д.С. Баев, Б.М. Глухов, Г.И. Непомнящих, Т.Г. Толстикова
    Влияние тритерпеновых производных на общую численность гепатоцитов в печени крыс с токсическим гепатитом
    Бюлл. Эксп. Биол. Мед., 2012, Т. 153, № 6, 837-840. (Effect of Triterpene Derivatives on the Total Hepatocyte Count in the Liver of Rats with Toxic Hepatitis/ D. E. Semenov, N. A. Zhukova, E. P. Bessergeneva, I. V. Sorokina, D. S. Baev, B. M. Glukhov, G. I. Nepomnyaschikh, T. G. Tolstikova// B EXP BIOL MED+, 2012, V.153, N 6, pp 859-862. doi:10.1007/s10517-012-1844-z), IF=0.305
  94. Д.Е. Семёнов, Н.А. Жукова, Е.П. Бессергенева, И.В. Сорокина, Д.С. Баев, Б.М. Глухов, Г.И. Непомнящих, Т.Г. Толстикова
    Влияние тритерпеновых производных на общую численность гепатоцитов в печени крыс с токсическим гепатитом
    Бюлл. Эксп. Биол. Мед., 2012, Т. 153, № 6, 837-840. (Effect of Triterpene Derivatives on the Total Hepatocyte Count in the Liver of Rats with Toxic Hepatitis/ D. E. Semenov, N. A. Zhukova, E. P. Bessergeneva, I. V. Sorokina, D. S. Baev, B. M. Glukhov, G. I. Nepomnyaschikh, T. G. Tolstikova// B EXP BIOL MED+, 2012, V.153, N 6, pp 859-862. doi:10.1007/s10517-012-1844-z), IF=0.305
  95. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  96. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  97. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  98. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  99. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  100. И.Е., Смирнова, До Тхи Тху Х., О.Б. Казакова, Г.А.Толстиков, О.С. Куковинец , А.Н. Лобов, К.Ю. Супоницкий
    Озонолиз диптерокарпола и его производных
    Журн. Орган. Химии, 2012, Т.48, №10, 1374-1379. (Ozonolysis of dipterocarpol and its derivatives/ I.E. Smirnova, H. Do Thi Thu, O.B. Kazakova, G.A. Tolstikov, O.S. Kukovinets, A.N. Lobov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1370-1376. doi:10.1134/S1070428012100193), IF=0.648
  101. О.Б.Казакова, Г.В.Гиниятуллина, Н.И. Медведева, Г.А. Толстиков
    Синтез тритерпенового конъюгата со спермидином
    Журн. Орган. Химии, 2012, V. 48, №10, 1370-1373 (Synthesis of a triterpene-spermidine conjugate/ O.B. Kazakova, G.V. Giniyatullina, N.I. Medvedeva, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100181), IF=0.556
  102. О.Б.Казакова, Г.В.Гиниятуллина, Н.И. Медведева, Г.А. Толстиков
    Синтез тритерпенового конъюгата со спермидином
    Журн. Орган. Химии, 2012, V. 48, №10, 1370-1373 (Synthesis of a triterpene-spermidine conjugate/ O.B. Kazakova, G.V. Giniyatullina, N.I. Medvedeva, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100181), IF=0.556
  103. О.Б.Казакова, Г.В.Гиниятуллина, Н.И. Медведева, Г.А. Толстиков
    Синтез тритерпенового конъюгата со спермидином
    Журн. Орган. Химии, 2012, V. 48, №10, 1370-1373 (Synthesis of a triterpene-spermidine conjugate/ O.B. Kazakova, G.V. Giniyatullina, N.I. Medvedeva, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100181), IF=0.556
  104. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  105. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  106. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  107. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  108. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  109. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Л.Р. Гарифуллина, Р.Р. Муслухов, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов при действии семикарбазида в метаноле
    Журн. Орган. Химии, 2012, Т. 48, № 10, 1278-1282. (Transformations of peroxide products of olefin ozonolysis under the action of semicarbazide in methanol/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman , G.V. Nasibullina , L.R. Garifullina, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 10, pp. 1366-1369. doi:10.1134/S1070428012100028), IF=0.648
  110. I.A. Kirilyuk, Yu.F. Polienko, O.A. Krumkacheva, R.K. Strizhakov, Yu.V. Gatilov, I.A. Grigor’ev, E.G. Bagryanskaya
    Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides of Pyrroline and Pyrrolidine Series, Including Thiol-Specific Spin Label: An Analogue of MTSSL with Long Relaxation Time
    J. Org. Chem., 2012, V. 77, N 18, 8016–8027. doi:10.1021/jo301235j, IF=4.449
  111. I.A. Kirilyuk, Yu.F. Polienko, O.A. Krumkacheva, R.K. Strizhakov, Yu.V. Gatilov, I.A. Grigor’ev, E.G. Bagryanskaya
    Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides of Pyrroline and Pyrrolidine Series, Including Thiol-Specific Spin Label: An Analogue of MTSSL with Long Relaxation Time
    J. Org. Chem., 2012, V. 77, N 18, 8016–8027. doi:10.1021/jo301235j, IF=4.449
  112. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  113. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  114. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  115. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  116. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  117. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  118. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  119. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
  120. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  121. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  122. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  123. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  124. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  125. И.Г. Боярских, А.И. Сысо, С.А. Худяев, А.И. Бакиянов, С.П. Колотухин, В.Г. Васильев, О.В. Чанкина
    Особенности элементного и биохимического состава Lonicera caeruleaL. в локальной геологически активной зоне Катунского хребта (Горный Алтай)
    Геофизические процессы и биосфера, 2012, Т.11, № 3, 40-59.
  126. М.Б. Гончикжапов, А.А. Палецкий, Л.В. Куйбида, И.К. Шундрина, О.П. Коробейничев
    Снижение горючести сверхвысокомолекулярного полиэтилена добавками трифенилфосфата
    Физика горения и взрыва, 2012, Т.48, № 5, 97-109. (Reducing the flammability of ultra-high-molecular-weight polyethylene by triphenyl phosphate additives/ M. B. Gonchikzhapov, A. A. Paletsky, L. V. Kuibida, I. K. Shundrina, O. P. Korobeinichev// COMBUST EXPLO SHOCK+, 2012, V. 48, N 5, pp 579-589. doi:10.1134/S0010508212050097), IF=0.538
  127. М.Б. Гончикжапов, А.А. Палецкий, Л.В. Куйбида, И.К. Шундрина, О.П. Коробейничев
    Снижение горючести сверхвысокомолекулярного полиэтилена добавками трифенилфосфата
    Физика горения и взрыва, 2012, Т.48, № 5, 97-109. (Reducing the flammability of ultra-high-molecular-weight polyethylene by triphenyl phosphate additives/ M. B. Gonchikzhapov, A. A. Paletsky, L. V. Kuibida, I. K. Shundrina, O. P. Korobeinichev// COMBUST EXPLO SHOCK+, 2012, V. 48, N 5, pp 579-589. doi:10.1134/S0010508212050097), IF=0.538
  128. М.Б. Гончикжапов, А.А. Палецкий, Л.В. Куйбида, И.К. Шундрина, О.П. Коробейничев
    Снижение горючести сверхвысокомолекулярного полиэтилена добавками трифенилфосфата
    Физика горения и взрыва, 2012, Т.48, № 5, 97-109. (Reducing the flammability of ultra-high-molecular-weight polyethylene by triphenyl phosphate additives/ M. B. Gonchikzhapov, A. A. Paletsky, L. V. Kuibida, I. K. Shundrina, O. P. Korobeinichev// COMBUST EXPLO SHOCK+, 2012, V. 48, N 5, pp 579-589. doi:10.1134/S0010508212050097), IF=0.538
  129. М.Б. Гончикжапов, А.А. Палецкий, Л.В. Куйбида, И.К. Шундрина, О.П. Коробейничев
    Снижение горючести сверхвысокомолекулярного полиэтилена добавками трифенилфосфата
    Физика горения и взрыва, 2012, Т.48, № 5, 97-109. (Reducing the flammability of ultra-high-molecular-weight polyethylene by triphenyl phosphate additives/ M. B. Gonchikzhapov, A. A. Paletsky, L. V. Kuibida, I. K. Shundrina, O. P. Korobeinichev// COMBUST EXPLO SHOCK+, 2012, V. 48, N 5, pp 579-589. doi:10.1134/S0010508212050097), IF=0.538
  130. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  131. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  132. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  133. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  134. A. Zakharenko, D. Sokolov, O. Luzina, M. Sukhanova, S. Khodyreva, O. Zakharova, N. Salakhutdinov, O. Lavrik
    Influence of Usnic Acid and its Derivatives on the Activity of Mammalian Poly(ADP-ribose)polymerase 1 and DNA Polymerase β
    Med. Chem., 2012, V. 8, № 5, 883-893. doi:10.2174/1573406411309050013, IF=1.496
  135. I.V. Kozhevnikov, A.L. Nuzhdin, G.A. Bukhtiyarova, O.N. Martyanov, A.M. Chibiryaev
    Tetramethyl orthosilicate as a sharp-selective catalyst of C-methylation of indole by supercritical methanol
    The Journal of Supercritical Fluids, 2012, V. 69, 82-90. doi:10.1016/j.supflu.2012.05.013, IF=2.859
  136. I.V. Kozhevnikov, A.L. Nuzhdin, G.A. Bukhtiyarova, O.N. Martyanov, A.M. Chibiryaev
    Tetramethyl orthosilicate as a sharp-selective catalyst of C-methylation of indole by supercritical methanol
    The Journal of Supercritical Fluids, 2012, V. 69, 82-90. doi:10.1016/j.supflu.2012.05.013, IF=2.859
  137. I.V. Kozhevnikov, A.L. Nuzhdin, G.A. Bukhtiyarova, O.N. Martyanov, A.M. Chibiryaev
    Tetramethyl orthosilicate as a sharp-selective catalyst of C-methylation of indole by supercritical methanol
    The Journal of Supercritical Fluids, 2012, V. 69, 82-90. doi:10.1016/j.supflu.2012.05.013, IF=2.859
  138. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, P.A. Potashov, V.A. Bagryansky, Yu.N. Molin
    Radical ions with nearly degenerate ground state: Correlation between the rate of spin-lattice relaxation and the structure of adiabatic potential energy surface
    J. Chem. Phys., 2012, V. 137, N 10, 104305-104318. doi:10.1063/1.4749247, IF=3.332
  139. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, P.A. Potashov, V.A. Bagryansky, Yu.N. Molin
    Radical ions with nearly degenerate ground state: Correlation between the rate of spin-lattice relaxation and the structure of adiabatic potential energy surface
    J. Chem. Phys., 2012, V. 137, N 10, 104305-104318. doi:10.1063/1.4749247, IF=3.332
  140. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, P.A. Potashov, V.A. Bagryansky, Yu.N. Molin
    Radical ions with nearly degenerate ground state: Correlation between the rate of spin-lattice relaxation and the structure of adiabatic potential energy surface
    J. Chem. Phys., 2012, V. 137, N 10, 104305-104318. doi:10.1063/1.4749247, IF=3.332
  141. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, P.A. Potashov, V.A. Bagryansky, Yu.N. Molin
    Radical ions with nearly degenerate ground state: Correlation between the rate of spin-lattice relaxation and the structure of adiabatic potential energy surface
    J. Chem. Phys., 2012, V. 137, N 10, 104305-104318. doi:10.1063/1.4749247, IF=3.332
  142. В.А. Самсонов, Ю.В. Гатилов, Л.Б. Володарский
    Синтез 1,6-дигидро-1,6-дигидроксибензо[1,2-d:3,4-d']бистриазола, 4- и 5-нитро-1,6-дигидро-1,6-дигидроксибензо[1,2-d:3,4-d'']бистриазола и 4,7-дигидро-1,4,7-тригидрокси-1Н-бензо[1,2-d:3,4-d':5,6-d'']трис[1,2,3]триазола
    Изв. АН, Cер. хим., 2012, Т. 61, № 9, 1760-1766. (Synthesis of 1,6-dihydro-1,6-dihydroxybenzo[1,2-d:3,4-d']bistriazole, 4- and 5-nitro-1,6-dihydro-1,6-dihydroxybenzo[1,2-d:3,4-d']bistriazole and 4,7-dihydro-1,4,7-trihydroxy-1H-benzo-[1,2-d:3,4-d':5,6-d'']tris[1,2,3]triazole/ V. A. Samsonov, Yu. V. Gatilov, L. B. Volodarskii// RUSS CHEM B+, 2012, V. 61, N 9, pp. 1776-1782. doi:10.1007/s11172-012-0244-x), IF=0.379
  143. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  144. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  145. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  146. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  147. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  148. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  149. Н.И. Иванчева, С.Я. Хайкин, Е.В. Свиридова, С.П. Федоров, Д.В. Саниева, О.В. Молев, И.В. Олейник, С.С. Иванчев
    Моноцентровые самоиммобилизующиеся катализаторы полимеризации этилена на основе функционализированных феноксииминных титангалоидных комплексов, для получения сверхвысокомолекулярного полиэтилена
    Журн. прикл. химии, 2012, Т. 85, В. 9, 1493-1501. (Multicentered self-immobilized ethylene polymerization catalysts based on functionalized titanium halide salicylaldiminate complexes for the synthesis of ultra-high-molecular-weight polyethylene/ N. I. Ivancheva, S. Ya. Khaikin, E. V. Sviridova, S. P. Fedorov, D. V. Sanieva, O. V. Molev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2012, V. 85, N 9, pp 1404-1412. doi:10.1134/S1070427212090170), IF=0.282
  150. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, V.A. Daletsky, G.A. Berezovskii, L.A. Sheludyakova, V.A. Varnek
    Spin crossover complex [FeL12](ClO4)2.H2O (L1 = 4-methyl-2,6-bis(1H-pyrazol-1-yl)pyrimidine): Synthesis and properties
    Polyhedron, 2012, V. 43, N 1, 81-88. doi:10.1016/j.poly.2012.05.039, IF=2.56
  151. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, V.A. Daletsky, G.A. Berezovskii, L.A. Sheludyakova, V.A. Varnek
    Spin crossover complex [FeL12](ClO4)2.H2O (L1 = 4-methyl-2,6-bis(1H-pyrazol-1-yl)pyrimidine): Synthesis and properties
    Polyhedron, 2012, V. 43, N 1, 81-88. doi:10.1016/j.poly.2012.05.039, IF=2.56
  152. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, V.A. Daletsky, G.A. Berezovskii, L.A. Sheludyakova, V.A. Varnek
    Spin crossover complex [FeL12](ClO4)2.H2O (L1 = 4-methyl-2,6-bis(1H-pyrazol-1-yl)pyrimidine): Synthesis and properties
    Polyhedron, 2012, V. 43, N 1, 81-88. doi:10.1016/j.poly.2012.05.039, IF=2.56
  153. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, V.A. Daletsky, G.A. Berezovskii, L.A. Sheludyakova, V.A. Varnek
    Spin crossover complex [FeL12](ClO4)2.H2O (L1 = 4-methyl-2,6-bis(1H-pyrazol-1-yl)pyrimidine): Synthesis and properties
    Polyhedron, 2012, V. 43, N 1, 81-88. doi:10.1016/j.poly.2012.05.039, IF=2.56
  154. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, V.A. Daletsky, G.A. Berezovskii, L.A. Sheludyakova, V.A. Varnek
    Spin crossover complex [FeL12](ClO4)2.H2O (L1 = 4-methyl-2,6-bis(1H-pyrazol-1-yl)pyrimidine): Synthesis and properties
    Polyhedron, 2012, V. 43, N 1, 81-88. doi:10.1016/j.poly.2012.05.039, IF=2.56
  155. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Комплексный подход к лечению асептического некроза головки бедренной кости
    Фундаментальные исследования, 2012, № 8, 193-196.
  156. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Комплексный подход к лечению асептического некроза головки бедренной кости
    Фундаментальные исследования, 2012, № 8, 193-196.
  157. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Комплексный подход к лечению асептического некроза головки бедренной кости
    Фундаментальные исследования, 2012, № 8, 193-196.
  158. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Комплексный подход к лечению асептического некроза головки бедренной кости
    Фундаментальные исследования, 2012, № 8, 193-196.
  159. D.A. Komarov, I. Dhimitruka, I.A. Kirilyuk, D.G. Trofimiov, I.A. Grigor’ev, J.L. Zweier, V.V. Khramtsov
    Electron Paramagnetic Resonance Monitoring of Ischemia-Induced Myocardial Oxygen Depletion and Acidosis in Isolated Rat Hearts Using Soluble Paramagnetic Probes
    Magn. Reson. Med., 2012, V. 68, N 2, 649–655. doi:10.1002/mrm.23251, IF=2.963
  160. D.A. Komarov, I. Dhimitruka, I.A. Kirilyuk, D.G. Trofimiov, I.A. Grigor’ev, J.L. Zweier, V.V. Khramtsov
    Electron Paramagnetic Resonance Monitoring of Ischemia-Induced Myocardial Oxygen Depletion and Acidosis in Isolated Rat Hearts Using Soluble Paramagnetic Probes
    Magn. Reson. Med., 2012, V. 68, N 2, 649–655. doi:10.1002/mrm.23251, IF=2.963
  161. D.A. Komarov, I. Dhimitruka, I.A. Kirilyuk, D.G. Trofimiov, I.A. Grigor’ev, J.L. Zweier, V.V. Khramtsov
    Electron Paramagnetic Resonance Monitoring of Ischemia-Induced Myocardial Oxygen Depletion and Acidosis in Isolated Rat Hearts Using Soluble Paramagnetic Probes
    Magn. Reson. Med., 2012, V. 68, N 2, 649–655. doi:10.1002/mrm.23251, IF=2.963
  162. Д.С. Баранов, В.И. Маматюк, Ю.В. Гатилов, С.Ф. Василевский
    Реакция 2-метил-4-арилбут-3-ин-2-олов с тиомочевиной — новый способ синтеза 5,5-диметил-4-арилметилиден-4,5-дигидротиазол-2-аминов
    Изв. АН, Cер. хим., 2012, Т. 61, № 8, 1554-1558. (Reaction of 4-aryl-2-methylbut-3-yn-2-ols with thiourea as a new approach to the synthesis of 4-arylmethylidene-5,5-dimethyl-4,5-dihydrothiazole-2-amines/ D. S. Baranov, V. I. Mamatyuk, Yu. V. Gatilov, S. F. Vasilevsky// RUSS CHEM B+, 2012, V. 61, N 8, pp. 1570-1574. doi:10.1007/s11172-012-0208-1), IF=0.379
  163. Д.С. Баранов, В.И. Маматюк, Ю.В. Гатилов, С.Ф. Василевский
    Реакция 2-метил-4-арилбут-3-ин-2-олов с тиомочевиной — новый способ синтеза 5,5-диметил-4-арилметилиден-4,5-дигидротиазол-2-аминов
    Изв. АН, Cер. хим., 2012, Т. 61, № 8, 1554-1558. (Reaction of 4-aryl-2-methylbut-3-yn-2-ols with thiourea as a new approach to the synthesis of 4-arylmethylidene-5,5-dimethyl-4,5-dihydrothiazole-2-amines/ D. S. Baranov, V. I. Mamatyuk, Yu. V. Gatilov, S. F. Vasilevsky// RUSS CHEM B+, 2012, V. 61, N 8, pp. 1570-1574. doi:10.1007/s11172-012-0208-1), IF=0.379
  164. И.Г. Капица, Е.В. Суслов, Г.В. Теплов, Д.В. Корчагина, Н.И. Комарова, К.П. Волчо, Т.А. Воронина, А.И. Шевела, Н.Ф. Салахутдинов
    Синтез и анксиолитическая активность производных 2-аминоадамантана, содержащих монотерпеновые фрагменты
    Хим.-фарм. журн., 2012, Т. 46, № 5, 3-5. (Synthesis and Anxiolytic Activity of 2-Aminoadamantane Derivatives Containing Monoterpene Fragments/ I.G. Kapitsa, E.V. Suslov, G.V. Teplov, D.V. Korchagina, N.I. Komarova, K.P. Volcho, T.A. Voronina, A.I. Shevela, N.F. Salakhutdinov// PHARM CHEM J+, 2012, V. 46, N 5, pp. 263-265. doi:10.1007/s11094-012-0775-3), IF=0.372
  165. И.Г. Капица, Е.В. Суслов, Г.В. Теплов, Д.В. Корчагина, Н.И. Комарова, К.П. Волчо, Т.А. Воронина, А.И. Шевела, Н.Ф. Салахутдинов
    Синтез и анксиолитическая активность производных 2-аминоадамантана, содержащих монотерпеновые фрагменты
    Хим.-фарм. журн., 2012, Т. 46, № 5, 3-5. (Synthesis and Anxiolytic Activity of 2-Aminoadamantane Derivatives Containing Monoterpene Fragments/ I.G. Kapitsa, E.V. Suslov, G.V. Teplov, D.V. Korchagina, N.I. Komarova, K.P. Volcho, T.A. Voronina, A.I. Shevela, N.F. Salakhutdinov// PHARM CHEM J+, 2012, V. 46, N 5, pp. 263-265. doi:10.1007/s11094-012-0775-3), IF=0.372
  166. И.Г. Капица, Е.В. Суслов, Г.В. Теплов, Д.В. Корчагина, Н.И. Комарова, К.П. Волчо, Т.А. Воронина, А.И. Шевела, Н.Ф. Салахутдинов
    Синтез и анксиолитическая активность производных 2-аминоадамантана, содержащих монотерпеновые фрагменты
    Хим.-фарм. журн., 2012, Т. 46, № 5, 3-5. (Synthesis and Anxiolytic Activity of 2-Aminoadamantane Derivatives Containing Monoterpene Fragments/ I.G. Kapitsa, E.V. Suslov, G.V. Teplov, D.V. Korchagina, N.I. Komarova, K.P. Volcho, T.A. Voronina, A.I. Shevela, N.F. Salakhutdinov// PHARM CHEM J+, 2012, V. 46, N 5, pp. 263-265. doi:10.1007/s11094-012-0775-3), IF=0.372
  167. И.И. Олейник, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов XIV. Синтез (N-аллилоксиарил)салицилальдиминных лигандов и комплексов дихлорида титана(iv) на их основе
    Журн. Орган. Химии, 2012, Т. 48, № 8, 1075-1084. (Design of postmetallocene catalytic systems of arylimine type for olefin polymerization: XIV. Synthesis of (N-Allyloxyaryl)salicylaldimine ligands and their complexes with titanium(IV) dichloride/ I. I. Oleinik, I. V. Oleinik, S. S.Ivanchev, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 8, pp. 1071-1080. doi:10.1134/S1070428012080076), IF=0.648
  168. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  169. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  170. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  171. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  172. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  173. N.A. Semenov, N.A. Pushkarevsky, J. Beckmann, P. Finke, E. Lork, R. Mews, I.Yu. Bagryanskaya, Yu.V. Gatilov, S.N. Konchenko, V.G. Vasiliev, A.V. Zibarev
    Tellurium-nitrogen π-heterocyclic chemistry: synthesis, structure and reactivity toward halides and pyridine of 3,4-dicyano-1,2,5-telluradiazole
    Eur. J. Inorg. Chem., 2012, N 23, 3693-3703. doi:10.1002/ejic.201200376, IF=3.49
  174. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, D.Yu. Naumov, S.N. Konchenko, N.A. Semenov, A.V. Zibarev
    Iridium complexes with 2,1,3-benzothiadiazole and related ligands
    Polyhedron, 2012, V. 42, N 1, 168-174. doi:10.1016/j.poly.2012.05.015, IF=2.56
  175. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, D.Yu. Naumov, S.N. Konchenko, N.A. Semenov, A.V. Zibarev
    Iridium complexes with 2,1,3-benzothiadiazole and related ligands
    Polyhedron, 2012, V. 42, N 1, 168-174. doi:10.1016/j.poly.2012.05.015, IF=2.56
  176. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, D.Yu. Naumov, S.N. Konchenko, N.A. Semenov, A.V. Zibarev
    Iridium complexes with 2,1,3-benzothiadiazole and related ligands
    Polyhedron, 2012, V. 42, N 1, 168-174. doi:10.1016/j.poly.2012.05.015, IF=2.56
  177. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, D.Yu. Naumov, S.N. Konchenko, N.A. Semenov, A.V. Zibarev
    Iridium complexes with 2,1,3-benzothiadiazole and related ligands
    Polyhedron, 2012, V. 42, N 1, 168-174. doi:10.1016/j.poly.2012.05.015, IF=2.56
  178. D.A. Bashirov, T.S. Sukhikh, N.V. Kuratieva, D.Yu. Naumov, S.N. Konchenko, N.A. Semenov, A.V. Zibarev
    Iridium complexes with 2,1,3-benzothiadiazole and related ligands
    Polyhedron, 2012, V. 42, N 1, 168-174. doi:10.1016/j.poly.2012.05.015, IF=2.56
  179. M.P. Polovinka, N.I. Komarova, D.V. Korchagina, D.N. Sokolov, O.A. Luzina, N.G. Vlasenko, A.A. Malyuga, E.V. Romanova, N.F. Salakhutdinov
    Secondary metabolites of the lichen Cladonia stellaris
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 392-395. doi:10.1007/s10600-012-0259-4, IF=1.29
  180. M.P. Polovinka, N.I. Komarova, D.V. Korchagina, D.N. Sokolov, O.A. Luzina, N.G. Vlasenko, A.A. Malyuga, E.V. Romanova, N.F. Salakhutdinov
    Secondary metabolites of the lichen Cladonia stellaris
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 392-395. doi:10.1007/s10600-012-0259-4, IF=1.29
  181. M.P. Polovinka, N.I. Komarova, D.V. Korchagina, D.N. Sokolov, O.A. Luzina, N.G. Vlasenko, A.A. Malyuga, E.V. Romanova, N.F. Salakhutdinov
    Secondary metabolites of the lichen Cladonia stellaris
    Chem. Nat. Compd., 2012, V. 48, N 3, pp. 392-395. doi:10.1007/s10600-012-0259-4, IF=1.29
  182. Е.А. Ефремова, В.А. Марченко, Е.И. Черняк, С.В. Морозов
    Фармакокинетические характеристики аверсектина С – действующего вещества противопаразитарных кормовых гранул и определение его остаточных количеств в органах и тканях овец
    Хим.-фарм. журн., 2012, Т. 46, № 4, 54-56. (Pharmacokinetic characteristics of aversectin C, the parent substance of antiparasitic fodder granules, and its residual content in organs and tissues of sheep/ E.A. Efremova, V.A. Marchenko, E.I . Chernyak, S.V. Morozov// PHARM CHEM J+, 2012, V. 46, N 4, pp. 253-255. doi:10.1007/s11094-012-0773-5), IF=0.372
  183. Е.А. Ефремова, В.А. Марченко, Е.И. Черняк, С.В. Морозов
    Фармакокинетические характеристики аверсектина С – действующего вещества противопаразитарных кормовых гранул и определение его остаточных количеств в органах и тканях овец
    Хим.-фарм. журн., 2012, Т. 46, № 4, 54-56. (Pharmacokinetic characteristics of aversectin C, the parent substance of antiparasitic fodder granules, and its residual content in organs and tissues of sheep/ E.A. Efremova, V.A. Marchenko, E.I . Chernyak, S.V. Morozov// PHARM CHEM J+, 2012, V. 46, N 4, pp. 253-255. doi:10.1007/s11094-012-0773-5), IF=0.372
  184. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  185. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  186. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  187. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  188. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  189. Yu. Chen, Y.C. Hung, M.Y. Hong, A.A. Onischuk, J.C. Chiou, I.V. Sorokina, T. Tolstikova, G.S. Huang
    Control of In Vivo Transport and Toxicity of Nanoparticles by Tea Melanin
    Journal of Nanomaterials, 2012, V. 2012, Article ID 746960, 11 pages. doi:10.1155/2012/746960
  190. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
  191. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
  192. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
  193. A.V. Kulikov, M.A. Tikhonova, E.A. Kulikova, K.P. Volcho, T.M. Khomenko, N.F. Salakhutdinov, N.K. Popova
    A new synthetic varacin analogue, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride (TC-2153), decreased hereditary catalepsy and increased the BDNF gene expression in the hippocampus in mice
    Psychopharmacology, 2012, V. 221, N 3, 469–478. doi:10.1007/s00213-011-2594-8, IF=4.77
  194. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  195. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  196. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  197. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  198. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  199. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  200. А.Э. Сазонов, В.А. Мордвинов, Г.А. Максимова, Н.А. Жукова, Е.В. Кашина, М.Н. Львова, А.В. Катохин, Т.Г. Толстикова, И.П. Каминский
    Экспериментальная модель описторхоза на хомяках (Mesocricetus auratus)
    Бюлл. Сибирской медицины, 2012, № 6, C.59-65
  201. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  202. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  203. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  204. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  205. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  206. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  207. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  208. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  209. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  210. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов
    Новые комплексные препараты на основе экстрактов лиственницы и лишайника – эффективное средство повышения урожайности яровой пшеницы
    Химия в интересах устойчивого развития, 2012, № 6, 713-720.
  211. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов
    Новые комплексные препараты на основе экстрактов лиственницы и лишайника – эффективное средство повышения урожайности яровой пшеницы
    Химия в интересах устойчивого развития, 2012, № 6, 713-720.
  212. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов
    Новые комплексные препараты на основе экстрактов лиственницы и лишайника – эффективное средство повышения урожайности яровой пшеницы
    Химия в интересах устойчивого развития, 2012, № 6, 713-720.
  213. V.V. Bardin, H.-J. Frohn
    Perfluoroorganylxenonium(II) salts from reactions of XeF2 or [FXe][SbF6] with selected perfluorinated alk-1-yn-1-yl- and alk-1-en-1-yltrifluoroborates in aHF
    J. Fluorine Chem., 2012, V. 138, 28-33. doi:10.1016/j.jfluchem.2012.03.014, IF=2.32
  214. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  215. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  216. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  217. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  218. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  219. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  220. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  221. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  222. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  223. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  224. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  225. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  226. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  227. E.A. Khatuntseva, V.M. Men’shov, A.S. Shashkov, Y.E. Tsvetkov, R.N. Stepanenko, R.Ya. Vlasenko, E.E. Shults, G.A. Tolstikov, T.G. Tolstikova, D.S. Baev, V.A. Kaledin, N.A. Popova, V.P. Nikolin, P.P. Laktionov, A.V. Cherepanova, T.V. Kulakovskaya, E.V. Kulakovskaya, N.E. Nifantiev
    Triterpenoid saponins from the roots of Acanthophyllum gypsophiloides Regel
    Beilstein J. Org. Chem., 2012, V. 8, 763-775. doi:10.3762/bjoc.8.87, IF=2.516
  228. K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.B. Bushuev
    Copper(II) and copper(I) tetra fluoroborate complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)- 6-(piperidin-1-yl)pyrimidine (L): Synthesis, structures and luminescence
    Inorg. Chim. Acta, 2012, V. 386, 116-121. doi:10.1016/j.ica.2012.02.004, IF=1.845
  229. K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.B. Bushuev
    Copper(II) and copper(I) tetra fluoroborate complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)- 6-(piperidin-1-yl)pyrimidine (L): Synthesis, structures and luminescence
    Inorg. Chim. Acta, 2012, V. 386, 116-121. doi:10.1016/j.ica.2012.02.004, IF=1.845
  230. K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.B. Bushuev
    Copper(II) and copper(I) tetra fluoroborate complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)- 6-(piperidin-1-yl)pyrimidine (L): Synthesis, structures and luminescence
    Inorg. Chim. Acta, 2012, V. 386, 116-121. doi:10.1016/j.ica.2012.02.004, IF=1.845
  231. K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.B. Bushuev
    Copper(II) and copper(I) tetra fluoroborate complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)- 6-(piperidin-1-yl)pyrimidine (L): Synthesis, structures and luminescence
    Inorg. Chim. Acta, 2012, V. 386, 116-121. doi:10.1016/j.ica.2012.02.004, IF=1.845
  232. K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, L.A. Sheludyakova, M.B. Bushuev
    Copper(II) and copper(I) tetra fluoroborate complexes with 4-(3,5-diphenyl-1H-pyrazol-1-yl)- 6-(piperidin-1-yl)pyrimidine (L): Synthesis, structures and luminescence
    Inorg. Chim. Acta, 2012, V. 386, 116-121. doi:10.1016/j.ica.2012.02.004, IF=1.845
  233. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  234. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  235. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  236. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  237. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  238. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
    Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
    Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
  239. Т.Г. Толстикова, Н.А. Жукова, Д.Е. Семёнов, Е.П. Бессергенева, И.В. Сорокина, Д.С. Баев, Б.М. Глухов
    Биохимические показатели крови и количество гепатоцитов в печени крыс с токсическим гепатитом при действии аланинамида бетулоновой кислоты
    Фундаментальные исследования, 2012, № 5, 120-123.
  240. Т.Г. Толстикова, Н.А. Жукова, Д.Е. Семёнов, Е.П. Бессергенева, И.В. Сорокина, Д.С. Баев, Б.М. Глухов
    Биохимические показатели крови и количество гепатоцитов в печени крыс с токсическим гепатитом при действии аланинамида бетулоновой кислоты
    Фундаментальные исследования, 2012, № 5, 120-123.
  241. M.N. Simonov, P.A. Zaikin, I.L. Simakova
    Highly selective catalytic propylene glycol synthesis from alkyl lactate over copper on silica: Performance and mechanism
    Appl. Cat. B, 2012, V.119–120, 340-347. doi:10.1016/j.apcatb.2012.03.003, IF=5.625
  242. M.N. Simonov, P.A. Zaikin, I.L. Simakova
    Highly selective catalytic propylene glycol synthesis from alkyl lactate over copper on silica: Performance and mechanism
    Appl. Cat. B, 2012, V.119–120, 340-347. doi:10.1016/j.apcatb.2012.03.003, IF=5.625
  243. S. E. Kiyamova, N. K. Khidyrova, T. P. Kukina, Kh. M. Shakhidoyatov
    Neutral constituents from leaves of plants of the family Malvacea. I. Abutilon theophrasti
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 297-298. doi:10.1007/s10600-012-0225-1, IF=1.29
  244. S. E. Kiyamova, N. K. Khidyrova, T. P. Kukina, Kh. M. Shakhidoyatov
    Neutral constituents from leaves of plants of the family Malvacea. I. Abutilon theophrasti
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 297-298. doi:10.1007/s10600-012-0225-1, IF=1.29
  245. S. E. Kiyamova, N. K. Khidyrova, T. P. Kukina, Kh. M. Shakhidoyatov
    Neutral constituents from leaves of plants of the family Malvacea. I. Abutilon theophrasti
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 297-298. doi:10.1007/s10600-012-0225-1, IF=1.29
  246. E.E. Shul'ts, S.S. Patrushev, A.V. Belovodskii, M.M. Shakirov, T.V. Rybalova, A.G. Pokrovskii, M.A. Pokrovskii, G.A. Tolstikov, S.M. Adekenov
    Synthetic transformations of sesquiterpene lactones. V.* Synthesis and cytotoxicity of 13-aryl-substituted tourneforin derivatives
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 245-249. doi:10.1007/s10600-012-0214-4, IF=1.29
  247. E.E. Shul'ts, S.S. Patrushev, A.V. Belovodskii, M.M. Shakirov, T.V. Rybalova, A.G. Pokrovskii, M.A. Pokrovskii, G.A. Tolstikov, S.M. Adekenov
    Synthetic transformations of sesquiterpene lactones. V.* Synthesis and cytotoxicity of 13-aryl-substituted tourneforin derivatives
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 245-249. doi:10.1007/s10600-012-0214-4, IF=1.29
  248. E.E. Shul'ts, A.V. Belovodskii, M.M. Shakirov, Yu.V. Gatilov, A.G. Pokrovskii, M.A. Pokrovskii, G.A. Tolstikov
    Synthetic transformations of sesquiterpene lactones. IV.* Synthesis and transformations of gem-dichlorocyclopropyl-substituted isoalantolactone derivatives
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 238-244. doi:10.1007/s10600-012-0213-5, IF=1.29
  249. E.E. Shul'ts, Zh. Ganbaatar, T.N. Petrova, M.M. Shakirov, I.Yu. Bagryanskaya, V.V. Taraskin, L.D. Radnaeva, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Plant coumarins. IX.* Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 211-217. doi:10.1007/s10600-012-0207-3, IF=1.29
  250. E.E. Shul'ts, Zh. Ganbaatar, T.N. Petrova, M.M. Shakirov, I.Yu. Bagryanskaya, V.V. Taraskin, L.D. Radnaeva, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Plant coumarins. IX.* Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 211-217. doi:10.1007/s10600-012-0207-3, IF=1.29
  251. E.E. Shul'ts, Zh. Ganbaatar, T.N. Petrova, M.M. Shakirov, I.Yu. Bagryanskaya, V.V. Taraskin, L.D. Radnaeva, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Plant coumarins. IX.* Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 211-217. doi:10.1007/s10600-012-0207-3, IF=1.29
  252. E.E. Shul'ts, Zh. Ganbaatar, T.N. Petrova, M.M. Shakirov, I.Yu. Bagryanskaya, V.V. Taraskin, L.D. Radnaeva, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Plant coumarins. IX.* Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 211-217. doi:10.1007/s10600-012-0207-3, IF=1.29
  253. E.E. Shul'ts, Zh. Ganbaatar, T.N. Petrova, M.M. Shakirov, I.Yu. Bagryanskaya, V.V. Taraskin, L.D. Radnaeva, D. Otgonsuren, A.G. Pokrovskii, G.A. Tolstikov
    Plant coumarins. IX.* Phenolic compounds of Ferulopsis hystrix growing in Mongolia. Cytotoxic activity of 8,9-dihydrofurocoumarins
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 211-217. doi:10.1007/s10600-012-0207-3, IF=1.29
  254. N. K. Khidyrova, M. Zh. Rakhmatova, T. P. Kukina, R. Kh. Shakhidoyatov, Kh. M. Shakhidoyatov
    Polyprenols and triterpenoids from leaves of Alcea nudiflora
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 180-184. doi:10.1007/s10600-012-0199-z, IF=1.29
  255. N. K. Khidyrova, M. Zh. Rakhmatova, T. P. Kukina, R. Kh. Shakhidoyatov, Kh. M. Shakhidoyatov
    Polyprenols and triterpenoids from leaves of Alcea nudiflora
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 180-184. doi:10.1007/s10600-012-0199-z, IF=1.29
  256. N. K. Khidyrova, M. Zh. Rakhmatova, T. P. Kukina, R. Kh. Shakhidoyatov, Kh. M. Shakhidoyatov
    Polyprenols and triterpenoids from leaves of Alcea nudiflora
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 180-184. doi:10.1007/s10600-012-0199-z, IF=1.29
  257. N. K. Khidyrova, M. Zh. Rakhmatova, T. P. Kukina, R. Kh. Shakhidoyatov, Kh. M. Shakhidoyatov
    Polyprenols and triterpenoids from leaves of Alcea nudiflora
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 180-184. doi:10.1007/s10600-012-0199-z, IF=1.29
  258. Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov
    Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives
    Биоорган. Химия, 2012, Т. 38, № 3, 374-381 (Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives/ Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov// RUSS J BIOORG CHEM+, 2012, V. 38, N 3, pp. 328-334. doi:10.1134/S1068162012030028), IF=0.635
  259. Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov
    Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives
    Биоорган. Химия, 2012, Т. 38, № 3, 374-381 (Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives/ Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov// RUSS J BIOORG CHEM+, 2012, V. 38, N 3, pp. 328-334. doi:10.1134/S1068162012030028), IF=0.635
  260. Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov
    Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives
    Биоорган. Химия, 2012, Т. 38, № 3, 374-381 (Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives/ Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov// RUSS J BIOORG CHEM+, 2012, V. 38, N 3, pp. 328-334. doi:10.1134/S1068162012030028), IF=0.635
  261. Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov
    Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives
    Биоорган. Химия, 2012, Т. 38, № 3, 374-381 (Study of Skin Anti-Ageing and Anti-Inflammatory Effects of Dihydroquercetin, Natural Triterpenoids, and Their Synthetic Derivatives/ Ch.W. Lee, N.H. Park, J.W. Kim, B.H. Um, A.V. Shpatov, E.E. Shults, I.V. Sorokina, S.A. Popov// RUSS J BIOORG CHEM+, 2012, V. 38, N 3, pp. 328-334. doi:10.1134/S1068162012030028), IF=0.635
  262. Н.A. Туманов, Н.A. Панкрушина, A.A. Нефедов, Е.В. Болдырева
    Нанопористый сольват N,N-фталоил-глицина
    Журн. cтруктур. химии, 2012, Т. 53, № 3, 611-614. (Nanoporous solvate of N,N-phthaloyl-glycine/ N. A. Tumanov, N. A. Pankrushina, A. A. Nefedov, E. V. Boldyreva// J STRUCT CHEM+, 2012, V. 53, N 3, pp. 606-609. doi:10.1134/S0022476612030298), IF=0.586
  263. Н.A. Туманов, Н.A. Панкрушина, A.A. Нефедов, Е.В. Болдырева
    Нанопористый сольват N,N-фталоил-глицина
    Журн. cтруктур. химии, 2012, Т. 53, № 3, 611-614. (Nanoporous solvate of N,N-phthaloyl-glycine/ N. A. Tumanov, N. A. Pankrushina, A. A. Nefedov, E. V. Boldyreva// J STRUCT CHEM+, 2012, V. 53, N 3, pp. 606-609. doi:10.1134/S0022476612030298), IF=0.586
  264. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
    Heat capacity of methacetin in a temperature range of 6 to 300 K
    J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
  265. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
    Heat capacity of methacetin in a temperature range of 6 to 300 K
    J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
  266. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
    Heat capacity of methacetin in a temperature range of 6 to 300 K
    J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
  267. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
    Heat capacity of methacetin in a temperature range of 6 to 300 K
    J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
  268. А.Г. Шушарин, М.П. Половинка, В.В. Морозов
    Новый способ лечения синовита и кисты Бейкера у пациентов с ревматоидным артритом
    Международный журнал прикладных и фундаментальных исследований, 2012. № 4, 61-62. full text
  269. А.Г. Шушарин, М.П. Половинка, В.В. Морозов
    Новый способ лечения синовита и кисты Бейкера у пациентов с ревматоидным артритом
    Международный журнал прикладных и фундаментальных исследований, 2012. № 4, 61-62. full text
  270. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Лечение асептического некроза головки бедренной кости инъекциями перфторана в сочетании с лазеротерапией
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 51-52.
  271. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Лечение асептического некроза головки бедренной кости инъекциями перфторана в сочетании с лазеротерапией
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 51-52.
  272. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Лечение асептического некроза головки бедренной кости инъекциями перфторана в сочетании с лазеротерапией
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 51-52.
  273. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Опыт лечения асептического некроза головки бедренной кости, стартовавшего после операции эндопротезирования
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 44-46.
  274. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Опыт лечения асептического некроза головки бедренной кости, стартовавшего после операции эндопротезирования
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 44-46.
  275. А.Г. Шушарин, М.П. Половинка, В.П. Прохоренко, В.В. Морозов
    Опыт лечения асептического некроза головки бедренной кости, стартовавшего после операции эндопротезирования
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 44-46.
  276. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, В. Морозов
    Случаи асептического некроза головки бедренной кости у пациентов с рецидивирующим генитальным герпесом: клинический пример, опыт лечения
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 28-29.
  277. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, В. Морозов
    Случаи асептического некроза головки бедренной кости у пациентов с рецидивирующим генитальным герпесом: клинический пример, опыт лечения
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 28-29.
  278. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, В. Морозов
    Случаи асептического некроза головки бедренной кости у пациентов с рецидивирующим генитальным герпесом: клинический пример, опыт лечения
    Международный журнал прикладных и фундаментальных исследований, 2012, № 4, 28-29.
  279. Г.Ю. Ишмуратов, Н.М. Ишмуратова, М.П. Яковлева, К.А. Тамбовцев, Г.А. Толстиков
    Неизвестные функции «маточного вещества» в гнезде пчел
    Известия Уфимского научного центра РАН, 2012, № 4, 108-112.
  280. Г.Ю. Ишмуратов, Н.М. Ишмуратова, М.П. Яковлева, К.А. Тамбовцев, Г.А. Толстиков
    Неизвестные функции «маточного вещества» в гнезде пчел
    Известия Уфимского научного центра РАН, 2012, № 4, 108-112.
  281. Г.Ю. Ишмуратов, Н.М. Ишмуратова, М.П. Яковлева, К.А. Тамбовцев, Г.А. Толстиков
    Неизвестные функции «маточного вещества» в гнезде пчел
    Известия Уфимского научного центра РАН, 2012, № 4, 108-112.
  282. Г.Ю. Ишмуратов, Н.М. Ишмуратова, М.П. Яковлева, К.А. Тамбовцев, Г.А. Толстиков
    Неизвестные функции «маточного вещества» в гнезде пчел
    Известия Уфимского научного центра РАН, 2012, № 4, 108-112.
  283. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Из гексахлорциклопентадиена в биоактивные циклопентаноиды
    Известия Уфимского научного центра РАН, 2012, № 4, 28-39.
  284. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Из гексахлорциклопентадиена в биоактивные циклопентаноиды
    Известия Уфимского научного центра РАН, 2012, № 4, 28-39.
  285. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Из гексахлорциклопентадиена в биоактивные циклопентаноиды
    Известия Уфимского научного центра РАН, 2012, № 4, 28-39.
  286. Г.А. Толстиков, С.А. Исмаилов, Ф.А. Гималова, Н.А. Иванова, М. Мифтахов
    Наукоемкая утилизация экологически опасных «полихлоркарбогенов». Из гексахлорциклопентадиена в биоактивные циклопентаноиды
    Известия Уфимского научного центра РАН, 2012, № 4, 28-39.
  287. Н.А. Попова, В.П. Николин, В.И. Каледин, И.А. Кирилюк, И.А. Григорьев
    Защитное действие темпола при облысении, вызываемом циклофосфамидом у мышей
    Сибирский онкологический журнал, 2012, № 4, 57-59. (Defensive effect of tempol in alopecia caused by cyclophosphamide in mice/ N.A. Popova, V.P. Nikolin, V.I. Kaledin, I.A. Kirilyuk, I.A. Grigoryev// )
  288. Н.А. Попова, В.П. Николин, В.И. Каледин, И.А. Кирилюк, И.А. Григорьев
    Защитное действие темпола при облысении, вызываемом циклофосфамидом у мышей
    Сибирский онкологический журнал, 2012, № 4, 57-59. (Defensive effect of tempol in alopecia caused by cyclophosphamide in mice/ N.A. Popova, V.P. Nikolin, V.I. Kaledin, I.A. Kirilyuk, I.A. Grigoryev// )
  289. Н.А. Попова, В.П. Николин, В.И. Каледин, И.А. Кирилюк, И.А. Григорьев
    Защитное действие темпола при облысении, вызываемом циклофосфамидом у мышей
    Сибирский онкологический журнал, 2012, № 4, 57-59. (Defensive effect of tempol in alopecia caused by cyclophosphamide in mice/ N.A. Popova, V.P. Nikolin, V.I. Kaledin, I.A. Kirilyuk, I.A. Grigoryev// )
  290. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Лечение асептического некроза ТБС с применением локальной инъекционной терапии под УЗ-контролем
    Современные проблемы науки и образования, 2012, № 4, URL: http://www.science-education.ru/104-6807
  291. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Лечение асептического некроза ТБС с применением локальной инъекционной терапии под УЗ-контролем
    Современные проблемы науки и образования, 2012, № 4, URL: http://www.science-education.ru/104-6807
  292. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Лечение асептического некроза ТБС с применением локальной инъекционной терапии под УЗ-контролем
    Современные проблемы науки и образования, 2012, № 4, URL: http://www.science-education.ru/104-6807
  293. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Лечение асептического некроза ТБС с применением локальной инъекционной терапии под УЗ-контролем
    Современные проблемы науки и образования, 2012, № 4, URL: http://www.science-education.ru/104-6807
  294. А.В. Душкин, Т.Г. Толстикова
    Новое "лицо" закомых лекарств
    Наука из первых рук, 2012, № 4 (46), 18-25.
  295. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Эффективный подход к лечению больных с асептическим некрозом головки бедренной кости
    Вестник НГУ. Сер.: Биология, клиническая медицина, 2012, Т. 10, № 4, 161-165.
  296. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Эффективный подход к лечению больных с асептическим некрозом головки бедренной кости
    Вестник НГУ. Сер.: Биология, клиническая медицина, 2012, Т. 10, № 4, 161-165.
  297. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Эффективный подход к лечению больных с асептическим некрозом головки бедренной кости
    Вестник НГУ. Сер.: Биология, клиническая медицина, 2012, Т. 10, № 4, 161-165.
  298. А.Г. Шушарин, М.П. Половинка, В.М. Прохоренко, А.И. Шевела, В.В. Власов
    Эффективный подход к лечению больных с асептическим некрозом головки бедренной кости
    Вестник НГУ. Сер.: Биология, клиническая медицина, 2012, Т. 10, № 4, 161-165.
  299. М.А. Мяделец, Д.В. Домрачев, С.В. Водолазова
    Исследование химического состава эфирных масел NEPETA SIBIRICA L., THYMUS PETRAEUS L. И SCHIZONEPETA MULTIFIDA L., произрастающих на территории республики хакасия
    Химия растительного сырья, 2012, № 4, 119-124.
  300. М.А. Мяделец, Д.В. Домрачев, С.В. Водолазова
    Исследование химического состава эфирных масел NEPETA SIBIRICA L., THYMUS PETRAEUS L. И SCHIZONEPETA MULTIFIDA L., произрастающих на территории республики хакасия
    Химия растительного сырья, 2012, № 4, 119-124.
  301. Д.Н. Оленников, Л.М. Танхаева, Н.А. Панкрушина, Д.В. Санданов
    __Фенольные соединения sophora SOPHORA FLAVESCENS SOLAND, произрастающей в России
    Химия растительного сырья, 2012, № 4, 101-108. (Phenolic compounds of Sophora flavescens Soland. of Russian origin/ D. N. Olennikov, L. M. Tankhaeva, N. A. Pankrushina, D. V. Sandanov// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 755-760. doi:10.1134/S106816201307011X)
  302. Д.Н. Оленников, Л.М. Танхаева, Н.А. Панкрушина, Д.В. Санданов
    __Фенольные соединения sophora SOPHORA FLAVESCENS SOLAND, произрастающей в России
    Химия растительного сырья, 2012, № 4, 101-108. (Phenolic compounds of Sophora flavescens Soland. of Russian origin/ D. N. Olennikov, L. M. Tankhaeva, N. A. Pankrushina, D. V. Sandanov// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 755-760. doi:10.1134/S106816201307011X)
  303. Д.Н. Оленников, Л.М. Танхаева, Н.А. Панкрушина, Д.В. Санданов
    __Фенольные соединения sophora SOPHORA FLAVESCENS SOLAND, произрастающей в России
    Химия растительного сырья, 2012, № 4, 101-108. (Phenolic compounds of Sophora flavescens Soland. of Russian origin/ D. N. Olennikov, L. M. Tankhaeva, N. A. Pankrushina, D. V. Sandanov// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 755-760. doi:10.1134/S106816201307011X)
  304. Н.И. Иванчева, Д.В. Саниева, С.П. Федоров, И.В. Олейник, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Самоиммобилизующиеся катализаторы полимеризации этилена на основе различных феноксииминных галоидных комплексов титана
    Изв. АН, Cер. хим., 2012, Т. 61, № 4, 833-839. (Self-immobilized catalysts for ethylene polymerization based on various phenoxyimine titanium halide complexes/ N.I. Ivancheva, D.V. Sanieva, S.P. Fedorov, I.V. Oleinik, I.I. Oleinik, G.A. Tolstikov, S.S.Ivanchev// RUSS CHEM B+ , 2012, V. 61, N 4, pp.836-842. doi:10.1007/s11172-012-0116-4), IF=0.379
  305. Н.И. Иванчева, Д.В. Саниева, С.П. Федоров, И.В. Олейник, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Самоиммобилизующиеся катализаторы полимеризации этилена на основе различных феноксииминных галоидных комплексов титана
    Изв. АН, Cер. хим., 2012, Т. 61, № 4, 833-839. (Self-immobilized catalysts for ethylene polymerization based on various phenoxyimine titanium halide complexes/ N.I. Ivancheva, D.V. Sanieva, S.P. Fedorov, I.V. Oleinik, I.I. Oleinik, G.A. Tolstikov, S.S.Ivanchev// RUSS CHEM B+ , 2012, V. 61, N 4, pp.836-842. doi:10.1007/s11172-012-0116-4), IF=0.379
  306. Н.И. Иванчева, Д.В. Саниева, С.П. Федоров, И.В. Олейник, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Самоиммобилизующиеся катализаторы полимеризации этилена на основе различных феноксииминных галоидных комплексов титана
    Изв. АН, Cер. хим., 2012, Т. 61, № 4, 833-839. (Self-immobilized catalysts for ethylene polymerization based on various phenoxyimine titanium halide complexes/ N.I. Ivancheva, D.V. Sanieva, S.P. Fedorov, I.V. Oleinik, I.I. Oleinik, G.A. Tolstikov, S.S.Ivanchev// RUSS CHEM B+ , 2012, V. 61, N 4, pp.836-842. doi:10.1007/s11172-012-0116-4), IF=0.379
  307. Н.И. Иванчева, Д.В. Саниева, С.П. Федоров, И.В. Олейник, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Самоиммобилизующиеся катализаторы полимеризации этилена на основе различных феноксииминных галоидных комплексов титана
    Изв. АН, Cер. хим., 2012, Т. 61, № 4, 833-839. (Self-immobilized catalysts for ethylene polymerization based on various phenoxyimine titanium halide complexes/ N.I. Ivancheva, D.V. Sanieva, S.P. Fedorov, I.V. Oleinik, I.I. Oleinik, G.A. Tolstikov, S.S.Ivanchev// RUSS CHEM B+ , 2012, V. 61, N 4, pp.836-842. doi:10.1007/s11172-012-0116-4), IF=0.379
  308. V.I. Borovkov, I.S. Ivanishko, V.A. Reznikov, I.V. Beregovaya
    Turning on the triplet state channel in the excess electron scavenging by nitroxyl radicals in liquid alkanes
    Chem. Phys. Lett., 2012, V. 531, 86-89. doi:10.1016/j.cplett.2012.02.011, IF=2.336
  309. V.I. Borovkov, I.S. Ivanishko, V.A. Reznikov, I.V. Beregovaya
    Turning on the triplet state channel in the excess electron scavenging by nitroxyl radicals in liquid alkanes
    Chem. Phys. Lett., 2012, V. 531, 86-89. doi:10.1016/j.cplett.2012.02.011, IF=2.336
  310. A.V. Artem'Ev, N.K. Gusarova, S.F. Malysheva, Y.V. Gatilov, V.I. Mamatyuk
    Efficient synthesis of lupininium, anabasinium and quininium thioselenophosphinates via a multi-component reaction between secondary phosphines, sulfur, selenium and alkaloids
    Org. Prep. Proced. Int., 2012, V. 44, N 3, 262-270. doi:10.1080/00304948.2012.676523, IF=1.14
  311. A.V. Artem'Ev, N.K. Gusarova, S.F. Malysheva, Y.V. Gatilov, V.I. Mamatyuk
    Efficient synthesis of lupininium, anabasinium and quininium thioselenophosphinates via a multi-component reaction between secondary phosphines, sulfur, selenium and alkaloids
    Org. Prep. Proced. Int., 2012, V. 44, N 3, 262-270. doi:10.1080/00304948.2012.676523, IF=1.14
  312. A.V. Artem'Ev, N.K. Gusarova, S.F. Malysheva, Y.V. Gatilov, V.I. Mamatyuk
    Efficient synthesis of lupininium, anabasinium and quininium thioselenophosphinates via a multi-component reaction between secondary phosphines, sulfur, selenium and alkaloids
    Org. Prep. Proced. Int., 2012, V. 44, N 3, 262-270. doi:10.1080/00304948.2012.676523, IF=1.14
  313. M.B. Bushuev, Y.V. Gatilov, V.P. Krivopalov, E.B. Nikolaenkova
    Copper(II) complex with 6-(3,5-dimethyl-1H-pyrazol-1-yl)-2-(pyridin-2-yl)pyrimidin-4-amine: synthesis, crystal structure, and electronic spectroscopy
    J. Coord. Chem., 2012, V. 65, N 3, 550-558. doi:10.1080/00958972.2012.657187, IF=1.547
  314. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  315. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  316. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  317. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  318. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  319. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  320. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  321. Y.Z. Voloshin, I.G. Belaya, A.S. Belov, A.M. Maksimov, V.E. Platonov, A.V. Vologzhanina, Z.A. Starikova, A.V. Dolganov, V.V. Novikov, Y.N. Bubnov
    Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis- clathrochelate iron(II) and cobalt(II,III) dioximates with ribbet perfluoroarylsulfide substituents
    J. Chem. Soc., Dalton Trans, 2012, V.41, N. 3,. 737-746. doi: 10.1039/c1dt10500k, IF=3.838
  322. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  323. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  324. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  325. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  326. M.M. Kutuzov, A.L. Zakharenko, M.V. Sukhanova, S.N. Khodyreva, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Polysulfide compounds as inhibitors of the key base excision repair enzymes
    Biopolym. Cell, 2012, V. 28, N 3, 239–241. doi:10.7124/bc.28.3
  327. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  328. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  329. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  330. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  331. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  332. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  333. A.L. Zakharenko, O.V. Salomatina, M.V. Sukhanova, M.M. Kutuzov, E.S. Ilina, S.N. Khodyreva, V. Schreiber, N.F. Salakhutdinov, O.I. Lavrik
    Glycyrrhetinic acid and its derivatives as inhibitors of poly(ADP-ribose)polymerases 1 and 2, apurinic/apyrimidinic endonuclease 1 and DNA polymerase β
    Biopolym. Cell, 2012, V. 28, N 3, 223–228. doi:10.7124/bc.28.3
  334. A.D. Rogachev, N.I. Komarova, D.V. Korchagina, V.G. Vasil'Ev, N.F. Salakhutdinov, G.A. Tolstikov, A.V. Pozdeeva
    REACTION OF SEVERAL RESVERATROL GLYCOSIDE DERIVATIVES WITH HYPOCHLORITES IN VARIOUS MEDIA
    Chem. Nat. Compd., 2012, V. 48, N 1, pp. 1-7. doi:10.1007/s10600-012-0146-z, IF=1.29
  335. Г.Ю. Ишмуратов, В.А. Выдрина, Г.В. Насибуллина, А.Г. Толстиков, Г.А. Толстиков
    Природные алифатические непредельные кислоты, содержащие кислородные функции. синтез и биологическая активность
    Химия растительного сырья, 2012, № 3, 5-36.
  336. Г.Ю. Ишмуратов, В.А. Выдрина, Г.В. Насибуллина, А.Г. Толстиков, Г.А. Толстиков
    Природные алифатические непредельные кислоты, содержащие кислородные функции. синтез и биологическая активность
    Химия растительного сырья, 2012, № 3, 5-36.
  337. Г.Ю. Ишмуратов, В.А. Выдрина, Г.В. Насибуллина, А.Г. Толстиков, Г.А. Толстиков
    Природные алифатические непредельные кислоты, содержащие кислородные функции. синтез и биологическая активность
    Химия растительного сырья, 2012, № 3, 5-36.
  338. Г.Ю. Ишмуратов, В.А. Выдрина, Г.В. Насибуллина, А.Г. Толстиков, Г.А. Толстиков
    Природные алифатические непредельные кислоты, содержащие кислородные функции. синтез и биологическая активность
    Химия растительного сырья, 2012, № 3, 5-36.
  339. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез и молекулярная структура 1α,10α,:9β,1β:19β,28--триэпокси-А-нео-5β-метил-25-нор-18α-олеана
    Журн. Орган. Химии, 2012, Т. 48, № 3, 459–461. (Synthesis and Molecular Structure of 1α,10α,:9β,1β:19β,28-Triepoxy-A-neo-5β-methyl-25-nor-18α,-oleane/ O.B. Kazakova, E.F. Khusnutdinova, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 3, pp. 460-462. doi:10.1134/S1070428012030220), IF=0.556
  340. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез и молекулярная структура 1α,10α,:9β,1β:19β,28--триэпокси-А-нео-5β-метил-25-нор-18α-олеана
    Журн. Орган. Химии, 2012, Т. 48, № 3, 459–461. (Synthesis and Molecular Structure of 1α,10α,:9β,1β:19β,28-Triepoxy-A-neo-5β-methyl-25-nor-18α,-oleane/ O.B. Kazakova, E.F. Khusnutdinova, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 3, pp. 460-462. doi:10.1134/S1070428012030220), IF=0.556
  341. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез и молекулярная структура 1α,10α,:9β,1β:19β,28--триэпокси-А-нео-5β-метил-25-нор-18α-олеана
    Журн. Орган. Химии, 2012, Т. 48, № 3, 459–461. (Synthesis and Molecular Structure of 1α,10α,:9β,1β:19β,28-Triepoxy-A-neo-5β-methyl-25-nor-18α,-oleane/ O.B. Kazakova, E.F. Khusnutdinova, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2012, V.48, N 3, pp. 460-462. doi:10.1134/S1070428012030220), IF=0.556
  342. V.V. Bardin, N.Yu. Adonin, H.-J. Frohn
    Reactions of perfluorinated alkenyltrifluoroborates, alkynyltrifluoroborates, and selected hydrocarbon analogues with the halogenating agents Hal2 (Hal = F, Cl, Br), “BrF” (BrF3-Br2 1:1), and Icl
    Z. Anorg. Allg. Chem., 2012, V. 638, N 3/4, 565-579. doi:10.1002/zaac.201100276, IF=1.248
  343. V.V. Bardin, N.Yu. Adonin, H.-J. Frohn
    Reactions of fluoroalk-1-en-1-yltrifluoroborate and perfluoroalk-1-yn-1-yltrifluoroborate salts and selected hydrocarbon analogues with hydrogen fluoride and with halogenating agents in aHF and in basic solvents
    J. Fluorine Chem., 2012, V. 135, 114-128. doi:10.1016/j.jfluchem.2011.09.011, IF=2.32
  344. L.V. Politanskaya, I.P. Chuikov, Е.А. Kolodina, M.S. Shvartsberg, V.D. Shteingarts
    Synthesis of polyfluorinated orthoalkynylanilines
    J. Fluorine Chem., 2012, V. 135, 97-107. doi:0.1016/j.jfluchem.2011.09.008, IF=2.32
  345. L.V. Politanskaya, I.P. Chuikov, Е.А. Kolodina, M.S. Shvartsberg, V.D. Shteingarts
    Synthesis of polyfluorinated orthoalkynylanilines
    J. Fluorine Chem., 2012, V. 135, 97-107. doi:0.1016/j.jfluchem.2011.09.008, IF=2.32
  346. D.S. Baranov, A.A. Ryabichev, S.F. Vasilevsky, V.I. Mamatyuk, Y.V. Gatilov, V.G. Kartsev
    Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-oles and guanidine
    Mendeleev Commun., 2012, V. 22, N 2, 114-116. doi:10.1016/j.mencom.2012.03.022, IF=0.901
  347. D.S. Baranov, A.A. Ryabichev, S.F. Vasilevsky, V.I. Mamatyuk, Y.V. Gatilov, V.G. Kartsev
    Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-oles and guanidine
    Mendeleev Commun., 2012, V. 22, N 2, 114-116. doi:10.1016/j.mencom.2012.03.022, IF=0.901
  348. D.S. Baranov, A.A. Ryabichev, S.F. Vasilevsky, V.I. Mamatyuk, Y.V. Gatilov, V.G. Kartsev
    Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-oles and guanidine
    Mendeleev Commun., 2012, V. 22, N 2, 114-116. doi:10.1016/j.mencom.2012.03.022, IF=0.901
  349. D.S. Baranov, A.A. Ryabichev, S.F. Vasilevsky, V.I. Mamatyuk, Y.V. Gatilov, V.G. Kartsev
    Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-oles and guanidine
    Mendeleev Commun., 2012, V. 22, N 2, 114-116. doi:10.1016/j.mencom.2012.03.022, IF=0.901
  350. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  351. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  352. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  353. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  354. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  355. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  356. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  357. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  358. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  359. D.V. Kazakov, A.R. Timerbaev, F.E. Safarov, T.I. Nazirov, O.B. Kazakova, G.Y. Ishmuratov, A.O. Terent'ev, D.A. Borisov, A.G. Tolstikov, G.A. Tolstikov, W. Adam
    Chemiluminescence from the biomimetic reaction of 1,2,4-trioxolanes and 1,2,4,5-tetroxanes with ferrous ions
    RSC Adv., 2012, V. 2, N 1, 107-110. doi:10.1039/C1RA00784J
  360. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  361. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  362. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  363. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  364. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  365. В.Ю. Крюков, О.А. Лузина, М.П. Половинка, О.Н. Ярославцева, Н.Ф. Салахутдинов, В.В. Глупов
    Скрининг модификантов усниновой кислоты – потенциальных синергистов энтомопатогенного гриба Beauveria Bassiana для регуляции численности колорадского жука
    Агрохимия, 2012, № 2, 59-66. (Screening of Usnic Acid Derivatives as Potential Synergists of the Entomopathogenic Fungus Beauveria bassiana for the Control of Colorado Potato Beetle/ Kryukov V.Yu.1, Luzina O.A.2, Yaroslavtseva O.N.1, Polovinka M.P.2, Salakhutdinov N.F.2, Glupov V.V.// Agricultural Chemistry)
  366. В.Ю. Крюков, О.А. Лузина, М.П. Половинка, О.Н. Ярославцева, Н.Ф. Салахутдинов, В.В. Глупов
    Скрининг модификантов усниновой кислоты – потенциальных синергистов энтомопатогенного гриба Beauveria Bassiana для регуляции численности колорадского жука
    Агрохимия, 2012, № 2, 59-66. (Screening of Usnic Acid Derivatives as Potential Synergists of the Entomopathogenic Fungus Beauveria bassiana for the Control of Colorado Potato Beetle/ Kryukov V.Yu.1, Luzina O.A.2, Yaroslavtseva O.N.1, Polovinka M.P.2, Salakhutdinov N.F.2, Glupov V.V.// Agricultural Chemistry)
  367. В.Ю. Крюков, О.А. Лузина, М.П. Половинка, О.Н. Ярославцева, Н.Ф. Салахутдинов, В.В. Глупов
    Скрининг модификантов усниновой кислоты – потенциальных синергистов энтомопатогенного гриба Beauveria Bassiana для регуляции численности колорадского жука
    Агрохимия, 2012, № 2, 59-66. (Screening of Usnic Acid Derivatives as Potential Synergists of the Entomopathogenic Fungus Beauveria bassiana for the Control of Colorado Potato Beetle/ Kryukov V.Yu.1, Luzina O.A.2, Yaroslavtseva O.N.1, Polovinka M.P.2, Salakhutdinov N.F.2, Glupov V.V.// Agricultural Chemistry)
  368. В.И. Аникеев, И.В. Ильина, С.Ю. Курбакова, А.А. Нефедов, К.П. Волчо, Н.Ф. Салахутдинов
    Окисление α-пинена кислородом воздуха в сверхкритическом растворителе в присутствии комплексов Co(II)
    Журн. физ. химии, 2012, Т. 86, № 2, 244-250. (Oxidation of alpha-pinene by atmospheric oxygen in the supercritical CO2-ethyl acetate system in the presence of Co(II) complexes/ V.I. Anikeev, I.V. Il'ina, S.Yu. Kurbakova, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2012, V. 86, N 2, pp.190-195. doi:10.1134/S0036024412010049), IF=0.458
  369. И.В. Шилова, Т.П. Кукина, О.И. Сальникова, Н.И. Суслов
    Хромато-масс-спектрометрическое исследование этанольного экстракта из надземной части FILIPENDULA ULMARIA (ROSACEAE)
    Растительные ресурсы, 2012, № 2, 244-253.
  370. И.В. Шилова, Т.П. Кукина, О.И. Сальникова, Н.И. Суслов
    Хромато-масс-спектрометрическое исследование этанольного экстракта из надземной части FILIPENDULA ULMARIA (ROSACEAE)
    Растительные ресурсы, 2012, № 2, 244-253.
  371. H.-J. Frohn, V.V. Bardin
    Reaction of Organylxenonium(II) Salts, [RXe][Y], with Organyl Iodides, R'I, in Anhydrous HF: Scope and Limitation of a New Synthetic Approach to Iodonium Salts, [RR'I][Y]
    Inorg. Chem., 2012, V. 51, N 4, 2616-2620. doi:10.1021/ic202576v, IF=4.6
  372. Н.М. Сторожок, Н.П. Медяник, A.П. Крысин, И.П. Поздняков, С.А. Креков
    Взаимосвязь химической структуры и антиоксидантных свойств N-замещенных амидов салициловой кислоты
    Кинетика и катализ, 2012, Т. 53, № 2, 170-180. (Interrelation between the chemical structure and antioxidant properties of N-substituted amides of salicylic acid/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, I. P. Pozdnyakov, S. A. Krekov// Kinetics and Catalysis, 2012, V. 53, N 2, pp 162-171. doi:10.1134/S0023158412020115), IF=0.638
  373. Н.М. Сторожок, Н.П. Медяник, A.П. Крысин, И.П. Поздняков, С.А. Креков
    Взаимосвязь химической структуры и антиоксидантных свойств N-замещенных амидов салициловой кислоты
    Кинетика и катализ, 2012, Т. 53, № 2, 170-180. (Interrelation between the chemical structure and antioxidant properties of N-substituted amides of salicylic acid/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, I. P. Pozdnyakov, S. A. Krekov// Kinetics and Catalysis, 2012, V. 53, N 2, pp 162-171. doi:10.1134/S0023158412020115), IF=0.638
  374. Н.М. Сторожок, Н.П. Медяник, A.П. Крысин, И.П. Поздняков, С.А. Креков
    Взаимосвязь химической структуры и антиоксидантных свойств N-замещенных амидов салициловой кислоты
    Кинетика и катализ, 2012, Т. 53, № 2, 170-180. (Interrelation between the chemical structure and antioxidant properties of N-substituted amides of salicylic acid/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, I. P. Pozdnyakov, S. A. Krekov// Kinetics and Catalysis, 2012, V. 53, N 2, pp 162-171. doi:10.1134/S0023158412020115), IF=0.638
  375. Н.М. Сторожок, Н.П. Медяник, A.П. Крысин, И.П. Поздняков, С.А. Креков
    Взаимосвязь химической структуры и антиоксидантных свойств N-замещенных амидов салициловой кислоты
    Кинетика и катализ, 2012, Т. 53, № 2, 170-180. (Interrelation between the chemical structure and antioxidant properties of N-substituted amides of salicylic acid/ N. M. Storozhok, N. P. Medyanik, A. P. Krysin, I. P. Pozdnyakov, S. A. Krekov// Kinetics and Catalysis, 2012, V. 53, N 2, pp 162-171. doi:10.1134/S0023158412020115), IF=0.638
  376. А.Е. Девяшина, Л.М. Горностаев, Ю.В. Гатилов
    О взаимодействии 2-(4-гидроксианилино)-1,4-нафтохинонов с церий аммонийнитратом и хлорохроматом пиридиния
    Журн. Орган. Химии, 2012, Т. 48, № 2, 245-251. (Reactions of 2-(4-hydroxyanilino)-1,4-naphthoquinones with cerium ammonium nitrate and pyridinium chlorochromate/ A.E. Devyashina, L.M. Gornostaev, YuV. Gatilov// RUSS J ORG CHEM+, 2012, V.48, N 2, pp. 234-240. doi:10.1134/S1070428012020121), IF=0.648
  377. А.Е. Девяшина, Л.М. Горностаев, Ю.В. Гатилов
    О взаимодействии 2-(4-гидроксианилино)-1,4-нафтохинонов с церий аммонийнитратом и хлорохроматом пиридиния
    Журн. Орган. Химии, 2012, Т. 48, № 2, 245-251. (Reactions of 2-(4-hydroxyanilino)-1,4-naphthoquinones with cerium ammonium nitrate and pyridinium chlorochromate/ A.E. Devyashina, L.M. Gornostaev, YuV. Gatilov// RUSS J ORG CHEM+, 2012, V.48, N 2, pp. 234-240. doi:10.1134/S1070428012020121), IF=0.648
  378. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
    Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
    Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901
  379. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
    Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
    Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901
  380. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
    Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
    Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901
  381. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
    Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
    Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901
  382. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
    Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
    Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901
  383. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  384. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  385. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  386. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  387. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  388. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  389. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  390. M.B. Bushuev, V.P. Krivopalov, E.V. Lider, N.V. Semikolenova, N.V. Pervukhina, D.Yu. Naumov, L.G. Lavrenova, V.A. Zakharov, S.V. Larionov
    Synthesis, crystal structure and catalytic activity in ethylene polymerization
    Polyhedron, 2012, V. 31, N 1, 235-240. doi:10.1016/j.poly.2011.09.024, IF=2.56
  391. S.S. Ivanchev, A.V. Yakimansky, N.I. Ivancheva, I.I. Oleinik, G.A. Tolstikov
    Ethylene polymerization using catalysts based on binuclear phenoxiimine titanium halide complex
    Eur. Polym. J., 2012, V. 45, N 1, 191-199. doi:10.1016/j.eurpolymj.2011.10.020, IF=2.739
  392. S.S. Ivanchev, A.V. Yakimansky, N.I. Ivancheva, I.I. Oleinik, G.A. Tolstikov
    Ethylene polymerization using catalysts based on binuclear phenoxiimine titanium halide complex
    Eur. Polym. J., 2012, V. 45, N 1, 191-199. doi:10.1016/j.eurpolymj.2011.10.020, IF=2.739
  393. S.S. Ivanchev, A.V. Yakimansky, N.I. Ivancheva, I.I. Oleinik, G.A. Tolstikov
    Ethylene polymerization using catalysts based on binuclear phenoxiimine titanium halide complex
    Eur. Polym. J., 2012, V. 45, N 1, 191-199. doi:10.1016/j.eurpolymj.2011.10.020, IF=2.739
  394. Е.Д. Васильева, В.И. Каледин, В.П. Николин, Н.А. Попова, И.А. Кирилюк, И.А. Григорьев
    Ускоренное отторжение иммуногенной опухоли у мышей при ингибировании активности индоламин-2,3-диоксигеназы этилпируватом
    Сибирский онкологический журнал, 2012, № 1, 41-44. (Enhanced immunogenic tumor rejection in mice when inhibiting activity of indoleamine 2,3-dioxygenase with ethyl pyruvate/ E.D. Vasilyeva, V.I. Kaledin, V.P. Nikolin, N.А. Popova, I.А. Kirilyuk, I.А. Grigoryev// Сибирский онкологический журнал, 2012, № 1, 41-44. (in russian).)
  395. Е.Д. Васильева, В.И. Каледин, В.П. Николин, Н.А. Попова, И.А. Кирилюк, И.А. Григорьев
    Ускоренное отторжение иммуногенной опухоли у мышей при ингибировании активности индоламин-2,3-диоксигеназы этилпируватом
    Сибирский онкологический журнал, 2012, № 1, 41-44. (Enhanced immunogenic tumor rejection in mice when inhibiting activity of indoleamine 2,3-dioxygenase with ethyl pyruvate/ E.D. Vasilyeva, V.I. Kaledin, V.P. Nikolin, N.А. Popova, I.А. Kirilyuk, I.А. Grigoryev// Сибирский онкологический журнал, 2012, № 1, 41-44. (in russian).)
  396. Е.Д. Васильева, В.И. Каледин, В.П. Николин, Н.А. Попова, И.А. Кирилюк, И.А. Григорьев
    Ускоренное отторжение иммуногенной опухоли у мышей при ингибировании активности индоламин-2,3-диоксигеназы этилпируватом
    Сибирский онкологический журнал, 2012, № 1, 41-44. (Enhanced immunogenic tumor rejection in mice when inhibiting activity of indoleamine 2,3-dioxygenase with ethyl pyruvate/ E.D. Vasilyeva, V.I. Kaledin, V.P. Nikolin, N.А. Popova, I.А. Kirilyuk, I.А. Grigoryev// Сибирский онкологический журнал, 2012, № 1, 41-44. (in russian).)
  397. Е.Д. Васильева, В.И. Каледин, В.П. Николин, Н.А. Попова, И.А. Кирилюк, И.А. Григорьев
    Ускоренное отторжение иммуногенной опухоли у мышей при ингибировании активности индоламин-2,3-диоксигеназы этилпируватом
    Сибирский онкологический журнал, 2012, № 1, 41-44. (Enhanced immunogenic tumor rejection in mice when inhibiting activity of indoleamine 2,3-dioxygenase with ethyl pyruvate/ E.D. Vasilyeva, V.I. Kaledin, V.P. Nikolin, N.А. Popova, I.А. Kirilyuk, I.А. Grigoryev// Сибирский онкологический журнал, 2012, № 1, 41-44. (in russian).)
  398. I.V. Il'ina, V.P. Sivcev, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    The Meerwein-Ponndorf-Verley type reaction in a mixture of supercritical isopropanol/CO2 in a continuous flow reactor in the presence of alumina
    J. Supercri.l Fluid., 2012, V. 61, 115–118. doi:10.1016/j.supflu.2011.10.004, IF=2.859
  399. M. Elyashberg, K. Blinov, S. Molodtsov, A. Williams
    Elucidating ‘undecipherable’ chemical structures using computer-assisted structure elucidation approaches
    Magn. Res. Chem., 2012, V. 50, N 1, 22–27. doi:10.1002/mrc.2849, IF=1.437
  400. M. Elyashberg, K. Blinov, S. Molodtsov, A. Williams
    Elucidating ‘undecipherable’ chemical structures using computer-assisted structure elucidation approaches
    Magn. Res. Chem., 2012, V. 50, N 1, 22–27. doi:10.1002/mrc.2849, IF=1.437
  401. M. Elyashberg, K. Blinov, S. Molodtsov, A. Williams
    Elucidating ‘undecipherable’ chemical structures using computer-assisted structure elucidation approaches
    Magn. Res. Chem., 2012, V. 50, N 1, 22–27. doi:10.1002/mrc.2849, IF=1.437
  402. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  403. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  404. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  405. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  406. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  407. E.A. Mostovich, Y. Borozdina, V. Enkelmann, K. Removic-Langer, B. Wolf, M. Lang, M. Baumgarten
    _Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets
    Cryst. Growth Des., 2012, V. 12. № 1, 54-59. doi:10.1021/cg201224g, IF=4.388
  408. G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, Yu.A. Galkina, R.R. Muslukhov, G.A. Tolstikov
    Low-temperature hydride reduction of (3 r)-carvomentholactone
    Chem. Nat. Compd., 2012, V. 47, N 6, 896-898. doi:10.1007/s10600-012-0098-3, IF=1.29
  409. G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, Yu.A. Galkina, R.R. Muslukhov, G.A. Tolstikov
    Low-temperature hydride reduction of (3 r)-carvomentholactone
    Chem. Nat. Compd., 2012, V. 47, N 6, 896-898. doi:10.1007/s10600-012-0098-3, IF=1.29
  410. G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, Yu.A. Galkina, R.R. Muslukhov, G.A. Tolstikov
    Low-temperature hydride reduction of (3 r)-carvomentholactone
    Chem. Nat. Compd., 2012, V. 47, N 6, 896-898. doi:10.1007/s10600-012-0098-3, IF=1.29
  411. G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, Yu.A. Galkina, R.R. Muslukhov, G.A. Tolstikov
    Low-temperature hydride reduction of (3 r)-carvomentholactone
    Chem. Nat. Compd., 2012, V. 47, N 6, 896-898. doi:10.1007/s10600-012-0098-3, IF=1.29
  412. G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, Yu.A. Galkina, R.R. Muslukhov, G.A. Tolstikov
    Low-temperature hydride reduction of (3 r)-carvomentholactone
    Chem. Nat. Compd., 2012, V. 47, N 6, 896-898. doi:10.1007/s10600-012-0098-3, IF=1.29
  413. Ю.В. Харитонов, Э.Э. Шульц, M.М. Шакиров, М.А. Покровский, А.Г. Покровский, Г.А. Толстиков
    Синтетические трансформации высших терпеноидов. XXVI. 16-Aцетиламинометиллабда-ноиды и их цитотоксическая активность
    Биоорган. Химия, 2012, Т. 38, № 1, 127-136. (Synthetic Transformations of Higher Terpenoids. XXVI. 16-Acetylaminomethyllabdanoids and Their Cytotoxicity/ Yu.V. Kharitonov, E.E. Shul'ts, M.M. Shakirov, M.A. Pokrovsky, A.G. Pokrovsky, G.A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 1, pp. 107-115. doi:10.1134/S1068162011060082), IF=0.635
  414. Ю.В. Харитонов, Э.Э. Шульц, M.М. Шакиров, М.А. Покровский, А.Г. Покровский, Г.А. Толстиков
    Синтетические трансформации высших терпеноидов. XXVI. 16-Aцетиламинометиллабда-ноиды и их цитотоксическая активность
    Биоорган. Химия, 2012, Т. 38, № 1, 127-136. (Synthetic Transformations of Higher Terpenoids. XXVI. 16-Acetylaminomethyllabdanoids and Their Cytotoxicity/ Yu.V. Kharitonov, E.E. Shul'ts, M.M. Shakirov, M.A. Pokrovsky, A.G. Pokrovsky, G.A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 1, pp. 107-115. doi:10.1134/S1068162011060082), IF=0.635
  415. М.А. Мяделец, Д.В. Домрачев, В.А. Черемушкина
    __Исследование химического состава эфирных масел некоторых видов семейства Lamiaceae L., культивируемых в условиях Западной Сибири
    Химия растительного сырья, 2012, № 1, 111-117. (A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region/ M. A. Myadelets, D. V. Domrachev, V. A. Cheremushkina// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 733-738. doi:10.1134/S1068162013070091)
  416. М.А. Мяделец, Д.В. Домрачев, В.А. Черемушкина
    __Исследование химического состава эфирных масел некоторых видов семейства Lamiaceae L., культивируемых в условиях Западной Сибири
    Химия растительного сырья, 2012, № 1, 111-117. (A study of the chemical composition of essential oils of some species from the Lamiaceae L. family cultivated in the Western Siberian Region/ M. A. Myadelets, D. V. Domrachev, V. A. Cheremushkina// RUSS J BIOORG CHEM+, 2013, V.39, N 7, pp 733-738. doi:10.1134/S1068162013070091)
  417. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723
  418. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723
  419. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723
  420. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723
  421. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723
  422. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.В. Насибуллина, Р.Р. Муслухов, Д.В. Казаков, Г.А. Толстиков
    Исследование озонолитических превращений (S)-(-)-лимонена.
    Журн. Орган. Химии, 2012, Т. 48, № 1, 26-32. (Ozonolytic transformations of (S)-(-)-limonene/ G.Yu. Ishmuratov, Yu.V. Legostaeva, L.P. Botsman, G.V. Nasibullina, R.R. Muslukhov, D.V. Kazakov, G.A. Tolstikov// RUSS J ORG CHEM+, 2012, V.48, N 1, pp. 18-24. doi:10.1134/S1070428012010034), IF=0.723

2011

Reviews, articles

  1. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, И.П. Байкова, Л. Запрутко, Г.Н. Апрышко
    Синтез и противоопухолевая активность аминопропоксипроизводных бетулина, эритродиола и уваола
    Биоорганическая химия, 2011, Т. 37, № 3, 414-424. (Synthesis and Antitumor Activity of Aminopropoxy Derivatives of Betulin, Erythrodiol, and Uvaol/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov, I.P. Baikova, L. Zaprutko, G.N. Apryshko// RUSS J BIOORG CHEM+, 2011, V. 37, N 3, 369-379. doi:10.1134/S1068162011030101), IF=0.546
  2. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, И.П. Байкова, Л. Запрутко, Г.Н. Апрышко
    Синтез и противоопухолевая активность аминопропоксипроизводных бетулина, эритродиола и уваола
    Биоорганическая химия, 2011, Т. 37, № 3, 414-424. (Synthesis and Antitumor Activity of Aminopropoxy Derivatives of Betulin, Erythrodiol, and Uvaol/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov, I.P. Baikova, L. Zaprutko, G.N. Apryshko// RUSS J BIOORG CHEM+, 2011, V. 37, N 3, 369-379. doi:10.1134/S1068162011030101), IF=0.546
  3. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, И.П. Байкова, Л. Запрутко, Г.Н. Апрышко
    Синтез и противоопухолевая активность аминопропоксипроизводных бетулина, эритродиола и уваола
    Биоорганическая химия, 2011, Т. 37, № 3, 414-424. (Synthesis and Antitumor Activity of Aminopropoxy Derivatives of Betulin, Erythrodiol, and Uvaol/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov, I.P. Baikova, L. Zaprutko, G.N. Apryshko// RUSS J BIOORG CHEM+, 2011, V. 37, N 3, 369-379. doi:10.1134/S1068162011030101), IF=0.546
  4. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, И.П. Байкова, Л. Запрутко, Г.Н. Апрышко
    Синтез и противоопухолевая активность аминопропоксипроизводных бетулина, эритродиола и уваола
    Биоорганическая химия, 2011, Т. 37, № 3, 414-424. (Synthesis and Antitumor Activity of Aminopropoxy Derivatives of Betulin, Erythrodiol, and Uvaol/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov, I.P. Baikova, L. Zaprutko, G.N. Apryshko// RUSS J BIOORG CHEM+, 2011, V. 37, N 3, 369-379. doi:10.1134/S1068162011030101), IF=0.546
  5. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, И.П. Байкова, Л. Запрутко, Г.Н. Апрышко
    Синтез и противоопухолевая активность аминопропоксипроизводных бетулина, эритродиола и уваола
    Биоорганическая химия, 2011, Т. 37, № 3, 414-424. (Synthesis and Antitumor Activity of Aminopropoxy Derivatives of Betulin, Erythrodiol, and Uvaol/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov, I.P. Baikova, L. Zaprutko, G.N. Apryshko// RUSS J BIOORG CHEM+, 2011, V. 37, N 3, 369-379. doi:10.1134/S1068162011030101), IF=0.546
  6. Н.М. Сторожок, Н.В. Гуреева, Р.А. Халитов, А.С. Сторожок, A.П. Крысин
    Антиоксидантное действие синтетических аналогов и индивидуальных веществ радиолы розовой и кетона малины
    Химико-фармацевтический журнал, 2011 , Т. 45, № 12, 23-26. (Antioxidant activity of synthetic analogs and pure active principles of rhodiola rosea and raspberry ketone/ N. M. Storozhok, N. V. Gureeva, R. A. Khalitov, A. S. Storozhok, A. P. Krysin// PHARM CHEM J+, 2012, V. 45, N 12, pp 732-735. doi:10.1007/s11094-012-0713-4), IF=0.372
  7. Н.М. Сторожок, Н.В. Гуреева, Р.А. Халитов, А.С. Сторожок, A.П. Крысин
    Антиоксидантное действие синтетических аналогов и индивидуальных веществ радиолы розовой и кетона малины
    Химико-фармацевтический журнал, 2011 , Т. 45, № 12, 23-26. (Antioxidant activity of synthetic analogs and pure active principles of rhodiola rosea and raspberry ketone/ N. M. Storozhok, N. V. Gureeva, R. A. Khalitov, A. S. Storozhok, A. P. Krysin// PHARM CHEM J+, 2012, V. 45, N 12, pp 732-735. doi:10.1007/s11094-012-0713-4), IF=0.372
  8. Н.М. Сторожок, Н.В. Гуреева, Р.А. Халитов, А.С. Сторожок, A.П. Крысин
    Антиоксидантное действие синтетических аналогов и индивидуальных веществ радиолы розовой и кетона малины
    Химико-фармацевтический журнал, 2011 , Т. 45, № 12, 23-26. (Antioxidant activity of synthetic analogs and pure active principles of rhodiola rosea and raspberry ketone/ N. M. Storozhok, N. V. Gureeva, R. A. Khalitov, A. S. Storozhok, A. P. Krysin// PHARM CHEM J+, 2012, V. 45, N 12, pp 732-735. doi:10.1007/s11094-012-0713-4), IF=0.372
  9. Н.М. Сторожок, Н.В. Гуреева, Р.А. Халитов, А.С. Сторожок, A.П. Крысин
    Антиоксидантное действие синтетических аналогов и индивидуальных веществ радиолы розовой и кетона малины
    Химико-фармацевтический журнал, 2011 , Т. 45, № 12, 23-26. (Antioxidant activity of synthetic analogs and pure active principles of rhodiola rosea and raspberry ketone/ N. M. Storozhok, N. V. Gureeva, R. A. Khalitov, A. S. Storozhok, A. P. Krysin// PHARM CHEM J+, 2012, V. 45, N 12, pp 732-735. doi:10.1007/s11094-012-0713-4), IF=0.372
  10. E.V. Burdel'naya, M.A. Zhunusova, A.Zh. Turmukhambetov, R.B. Seidakhmetova, E.E. Shul'ts, Yu.V. Gatilov, S.M. Adekenov
    ALKALOIDS FROM ROOTS OF Aconitum monticola
    Chem. Nat. Compd., 2011, V. 47, N 6, pp 1032-1034. doi:10.1007/s10600-012-0140-5, IF=0.693
  11. E.V. Burdel'naya, M.A. Zhunusova, A.Zh. Turmukhambetov, R.B. Seidakhmetova, E.E. Shul'ts, Yu.V. Gatilov, S.M. Adekenov
    ALKALOIDS FROM ROOTS OF Aconitum monticola
    Chem. Nat. Compd., 2011, V. 47, N 6, pp 1032-1034. doi:10.1007/s10600-012-0140-5, IF=0.693
  12. E.V. Burdel'naya, M.A. Zhunusova, A.Zh. Turmukhambetov, R.B. Seidakhmetova, E.E. Shul'ts, Yu.V. Gatilov, S.M. Adekenov
    ALKALOIDS FROM ROOTS OF Aconitum monticola
    Chem. Nat. Compd., 2011, V. 47, N 6, pp 1032-1034. doi:10.1007/s10600-012-0140-5, IF=0.693
  13. E.V. Burdel'naya, M.A. Zhunusova, A.Zh. Turmukhambetov, R.B. Seidakhmetova, E.E. Shul'ts, Yu.V. Gatilov, S.M. Adekenov
    ALKALOIDS FROM ROOTS OF Aconitum monticola
    Chem. Nat. Compd., 2011, V. 47, N 6, pp 1032-1034. doi:10.1007/s10600-012-0140-5, IF=0.693
  14. E.V. Burdel'naya, M.A. Zhunusova, A.Zh. Turmukhambetov, R.B. Seidakhmetova, E.E. Shul'ts, Yu.V. Gatilov, S.M. Adekenov
    ALKALOIDS FROM ROOTS OF Aconitum monticola
    Chem. Nat. Compd., 2011, V. 47, N 6, pp 1032-1034. doi:10.1007/s10600-012-0140-5, IF=0.693
  15. Г.Ю. Ишмуратов, М.П. Яковлева, Э.Ф. Валеева, В.А. Выдрина, Г.А. Толстиков
    Монотерпеновые кетоны в синтезе оптически активных феромонов насекомых
    Химия растительного сырья, 2011, № 2, 5-26. (Monoterpene ketones in the synthesis of optically active insect pheromones/ G. Yu. Ishmuratov, M. P. Yakovleva, E. F. Valeeva, V. A. Vydrina, G. A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 667-688 doi:10.1134/S1068162012070084)
  16. Г.Ю. Ишмуратов, М.П. Яковлева, Э.Ф. Валеева, В.А. Выдрина, Г.А. Толстиков
    Монотерпеновые кетоны в синтезе оптически активных феромонов насекомых
    Химия растительного сырья, 2011, № 2, 5-26. (Monoterpene ketones in the synthesis of optically active insect pheromones/ G. Yu. Ishmuratov, M. P. Yakovleva, E. F. Valeeva, V. A. Vydrina, G. A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 667-688 doi:10.1134/S1068162012070084)
  17. Г.Ю. Ишмуратов, М.П. Яковлева, Э.Ф. Валеева, В.А. Выдрина, Г.А. Толстиков
    Монотерпеновые кетоны в синтезе оптически активных феромонов насекомых
    Химия растительного сырья, 2011, № 2, 5-26. (Monoterpene ketones in the synthesis of optically active insect pheromones/ G. Yu. Ishmuratov, M. P. Yakovleva, E. F. Valeeva, V. A. Vydrina, G. A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 667-688 doi:10.1134/S1068162012070084)
  18. Г.Ю. Ишмуратов, М.П. Яковлева, Э.Ф. Валеева, В.А. Выдрина, Г.А. Толстиков
    Монотерпеновые кетоны в синтезе оптически активных феромонов насекомых
    Химия растительного сырья, 2011, № 2, 5-26. (Monoterpene ketones in the synthesis of optically active insect pheromones/ G. Yu. Ishmuratov, M. P. Yakovleva, E. F. Valeeva, V. A. Vydrina, G. A. Tolstikov// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 667-688 doi:10.1134/S1068162012070084)
  19. J. Ganbaatar, E.E. Shults, D. Otgonsuren, L.D. Radnaeva, V.V. Taraskin, D. Badamkhand
    Coumarins from Peucedanum hystrix growing in Mongolia
    Mongolian J. Chem., 2011, V 12, N 38, 42-49.
  20. J. Ganbaatar, E.E. Shults, D. Otgonsuren, L.D. Radnaeva, V.V. Taraskin, D. Badamkhand
    Coumarins from Peucedanum hystrix growing in Mongolia
    Mongolian J. Chem., 2011, V 12, N 38, 42-49.
  21. J. Ganbaatar, E.E. Shults, D. Otgonsuren, L.D. Radnaeva, V.V. Taraskin, D. Badamkhand
    Coumarins from Peucedanum hystrix growing in Mongolia
    Mongolian J. Chem., 2011, V 12, N 38, 42-49.
  22. J. Ganbaatar, E.E. Shults, D. Otgonsuren, L.D. Radnaeva, V.V. Taraskin, D. Badamkhand
    Coumarins from Peucedanum hystrix growing in Mongolia
    Mongolian J. Chem., 2011, V 12, N 38, 42-49.
  23. J. Ganbaatar, E.E. Shults, D. Otgonsuren, L.D. Radnaeva, V.V. Taraskin, D. Badamkhand
    Coumarins from Peucedanum hystrix growing in Mongolia
    Mongolian J. Chem., 2011, V 12, N 38, 42-49.
  24. К.Н. Сорокина, А.А. Тулупов, Т.Г. Толстикова, В.Ю. Усов
    Современные подходы к созданию контрастных препаратов для магнитно-резонансной томографической диагностики
    Бюллетень сибирской медицины, 2011, № 6, 79-85.
  25. К.Н. Сорокина, А.А. Тулупов, Т.Г. Толстикова, В.Ю. Усов
    Современные подходы к созданию контрастных препаратов для магнитно-резонансной томографической диагностики
    Бюллетень сибирской медицины, 2011, № 6, 79-85.
  26. В.В. Коковкин, В.Ф. Рапута, А.Н. Романов, С.В. Морозов
    Исследование процессов регионального загрязнения снегового покрова городами юга Западной Сибири
    Ползуновский вестник, 2011, № 4-2, 89-93.
  27. В.В. Коковкин, В.Ф. Рапута, А.Н. Романов, С.В. Морозов
    Исследование процессов регионального загрязнения снегового покрова городами юга Западной Сибири
    Ползуновский вестник, 2011, № 4-2, 89-93.
  28. В.В. Коковкин, В.Ф. Рапута, А.Н. Романов, С.В. Морозов
    Исследование процессов регионального загрязнения снегового покрова городами юга Западной Сибири
    Ползуновский вестник, 2011, № 4-2, 89-93.
  29. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  30. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  31. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  32. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  33. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  34. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  35. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  36. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  37. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  38. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  39. А.Н. Романов, В.Ф. Рапута, С.В. Морозов, Н.Н. Безуглова, Г.С. Зинченко, А.О. Ковригин, В.В. Коковкин, А.О. Люцигер, В.Е. Павлов, Д.Н. Трошкин, И.А. Хвостов, К.О. Шутова
    Полиароматические углеводороды в снежном покрове г. Барнаула
    Ползуновский вестник, 2011, № 4-2, 78-80.
  40. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  41. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  42. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  43. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  44. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  45. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  46. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  47. Б.А. Селиванов, Е.Ф. Беланов, Н.И. Бормотов, С.М. Балахнин, О.А. Серова, В.А. Святченко, Н.Н. Киселев, Е.И. Казачинская, В.Б. Локтев, А.Я. Тихонов
    Производные трицикло[3.2.2.02,4]нон-8-ен-6,7-дикарбоновой кислоты высокоэффективно ингибируют репликацию различных видов ортопоксвирусов
    Доклады Академии наук, 2011, Т. 441, № 3, 414–418. (Tricyclo[3.2.2.02,4]non-8-en-6,7-dicarbonic acid derivatives efficiently inhibits the replication of different orthopoxvirus species/ B. A. Selivanov, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, V. A. Svyatchenko, N. N. Kiselev, E. I. Kazachinskaya, V. B. Loktev, A. Ya. Tikhonov// Doklady Biological Sciences, 2011, V.441, N 1, pp 424-428 doi:10.1134/S0012496611060135)
  48. I.A. Boldov, A.S. Kuchyanov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov
    Fiber-optic sensor for butylamine
    J. Phys.: Conf. Ser., 2011, V. 291, 012041. doi:10.1088/1742-6596/291/1/012041
  49. I.A. Boldov, A.S. Kuchyanov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov
    Fiber-optic sensor for butylamine
    J. Phys.: Conf. Ser., 2011, V. 291, 012041. doi:10.1088/1742-6596/291/1/012041
  50. I.A. Boldov, A.S. Kuchyanov, A.I. Plekhanov, N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov
    Fiber-optic sensor for butylamine
    J. Phys.: Conf. Ser., 2011, V. 291, 012041. doi:10.1088/1742-6596/291/1/012041
  51. N.P. Gritsan, A.Yu. Makarov, A.V. Zibarev
    A new approach to chalcogen-nitrogen π-heterocyclic radicals
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 449-466. doi:10.1007/s00723-011-0240-6, IF=1.126
  52. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  53. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  54. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  55. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  56. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  57. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  58. S.V. Blinkova, L.N. Shchegoleva, I.V. Beregovaya, M.M. Vyushkova, V.A. Bagryansky, Yu.N. Molin
    Intramolecular Dynamics of the 1,2,4-Trifluorobenzene Radical Anion: An Optically Detected EPR and Quantum Chemistry Study
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 229-238. doi:10.1007/s00723-011-0265-x, IF=1.126
  59. S.V. Blinkova, L.N. Shchegoleva, I.V. Beregovaya, M.M. Vyushkova, V.A. Bagryansky, Yu.N. Molin
    Intramolecular Dynamics of the 1,2,4-Trifluorobenzene Radical Anion: An Optically Detected EPR and Quantum Chemistry Study
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 229-238. doi:10.1007/s00723-011-0265-x, IF=1.126
  60. S.V. Blinkova, L.N. Shchegoleva, I.V. Beregovaya, M.M. Vyushkova, V.A. Bagryansky, Yu.N. Molin
    Intramolecular Dynamics of the 1,2,4-Trifluorobenzene Radical Anion: An Optically Detected EPR and Quantum Chemistry Study
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 229-238. doi:10.1007/s00723-011-0265-x, IF=1.126
  61. S.V. Blinkova, L.N. Shchegoleva, I.V. Beregovaya, M.M. Vyushkova, V.A. Bagryansky, Yu.N. Molin
    Intramolecular Dynamics of the 1,2,4-Trifluorobenzene Radical Anion: An Optically Detected EPR and Quantum Chemistry Study
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 229-238. doi:10.1007/s00723-011-0265-x, IF=1.126
  62. L.I. Goryunov, S.I. Zhivetyeva, G.A. Nevinsky, V.D. Shteingarts
    Synthesis of diphenyl(X)phosphonium betaines (X = CH3, C6H5, 2,5-F2C6H3) from hexafluoro-1,4-naphthoquinone
    ARKIVOC, 2011, (viii), 185-191.full text doi:10.3998/ark.5550190.0012.814, IF=1.95
  63. К.P. Volcho, I.V. Il'ina, N.F. Salakhutdinov, V.I. Anikeev
    Reactivity of verbenol and verbenone epoxides in supercritical solvents
    ARKIVOC, 2011, (viii), 134-140. doi:10.3998/ark.5550190.0012.809, IF=1.95
  64. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  65. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  66. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  67. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  68. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  69. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  70. С.В. Ларионов, Т.Е. Кокина, А.М. Агафонцев, К.С. Маренин, Л.А. Глинская, И.В. Корольков, М.И. Рахманова, Е.М. Усков, П.Е. Плюснин, А.В. Ткачев
    Синтез и свойства комплексов ZnII и CdII с хиральными N-производными аминоуксусной кислоты на основе природных монотерпенов (+)-3-карена и (-)-α-пинена. Кристаллическая структура координационного полимера [Zn(HL)Cl •2H2O]n
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 12, 2506-2513. (Synthesis and properties of ZnII and CdII complexes with chiral N-derivatives of aminoacetic acid based on natural monoterpenes (+)-3-carene and (-)-α-pinene. Crystal structure of coordination polymer [Zn(HL)Cl •2H2O]n/ S.V. Larionov, T.E. Kokina, A.M. Agafontsev, K.S. Marenin, L.A. Glinskaya, I.V. Korol'kov, M.I. Rakhmanova, E.M. Uskov, P.E. Plyusnin, A.V. Tkachev// RUSS CHEM B+, 2011, V. 60, N 12, pp 2555-2563 doi:10.1007/s11172-011-0393-3), IF=0.629
  71. A.G. Makarov, T.D. Grayfer, A.Yu. Makarov, I.Yu. Bagryanskaya, V.G. Vasiliev, A.V. Zibarev
    Reactivity of extended chalcogen-nitrogen π-systems: compounds Ar-Se-N=S=N-Se-Ar
    Mendeleev Commun., 2011, V. 21, N 6, 320-322. doi:10.1016/j.mencom.2011.11.009, IF=0.814
  72. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  73. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  74. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  75. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  76. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  77. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
    Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
    J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
  78. I.V. Il'ina, S.Yu. Kurbakova, K.P. Volcho, N.F. Salakhutdinov, V.I. Anikeev
    Meerwein-Ponndorf-Verley reduction of aldehydes formed in situ from α- and β-pinene epoxides in a supercritical fluid in the presence of alumina
    J. Saudi Chem. Soc., 2011, V. 15, N 4, 313-317. doi:10.1016/j.jscs.2011.07.010
  79. G.Yu. Ishmuratov, V.A. Vydrina, G.V. Nasibullina, M.P. Yakovleva, R.R. Muslukhov, G.A. Tolstikov
    New approach to the synthesis of 9-oxo-2E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 789-791. doi:10.1007/s10600-011-0060-9, IF=0.693
  80. G.Yu. Ishmuratov, V.A. Vydrina, G.V. Nasibullina, M.P. Yakovleva, R.R. Muslukhov, G.A. Tolstikov
    New approach to the synthesis of 9-oxo-2E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 789-791. doi:10.1007/s10600-011-0060-9, IF=0.693
  81. G.Yu. Ishmuratov, V.A. Vydrina, G.V. Nasibullina, M.P. Yakovleva, R.R. Muslukhov, G.A. Tolstikov
    New approach to the synthesis of 9-oxo-2E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 789-791. doi:10.1007/s10600-011-0060-9, IF=0.693
  82. G.Yu. Ishmuratov, V.A. Vydrina, G.V. Nasibullina, M.P. Yakovleva, R.R. Muslukhov, G.A. Tolstikov
    New approach to the synthesis of 9-oxo-2E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 789-791. doi:10.1007/s10600-011-0060-9, IF=0.693
  83. G.Yu. Ishmuratov, V.A. Vydrina, G.V. Nasibullina, M.P. Yakovleva, R.R. Muslukhov, G.A. Tolstikov
    New approach to the synthesis of 9-oxo-2E-decenoic acid, a multifunctional pheromone of queen honeybee, from the telomer of butadiene and water
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 789-791. doi:10.1007/s10600-011-0060-9, IF=0.693
  84. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  85. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  86. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  87. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  88. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  89. O.B. Kazakova, N.I. Medvedeva, I.A. Samoilova, I.P. Baikova, G.A. Tolstikov, V.E. Kataev, V.F. Mironov
    Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes
    Chem. Nat. Compd., 2011, V. 47, N 5, pp 752-758. doi:10.1007/s10600-011-0050-y, IF=0.693
  90. А.И. Говди, С.Ф. Василевский, В.Г. Ненайденко, Н.В. Соколова, Г.А. Толстиков
    Синтез 1,2,3-триазольных конъюгатов бетулоновой кислоты с пептидами на основе 1,3-циклоприсоединения
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 11, 2354-2359. (1,3-Cycloaddition synthesis of 1,2,3-triazole conjugates of betulonic acid with peptides/ A. I. Govdi, S. F. Vasilevsky, V. G. Nenajdenko, N. V. Sokolova, G. A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2401-2405. doi:10.1007/s11172-011-0369-3), IF=0.629
  91. А.И. Говди, С.Ф. Василевский, В.Г. Ненайденко, Н.В. Соколова, Г.А. Толстиков
    Синтез 1,2,3-триазольных конъюгатов бетулоновой кислоты с пептидами на основе 1,3-циклоприсоединения
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 11, 2354-2359. (1,3-Cycloaddition synthesis of 1,2,3-triazole conjugates of betulonic acid with peptides/ A. I. Govdi, S. F. Vasilevsky, V. G. Nenajdenko, N. V. Sokolova, G. A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2401-2405. doi:10.1007/s11172-011-0369-3), IF=0.629
  92. А.И. Говди, С.Ф. Василевский, В.Г. Ненайденко, Н.В. Соколова, Г.А. Толстиков
    Синтез 1,2,3-триазольных конъюгатов бетулоновой кислоты с пептидами на основе 1,3-циклоприсоединения
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 11, 2354-2359. (1,3-Cycloaddition synthesis of 1,2,3-triazole conjugates of betulonic acid with peptides/ A. I. Govdi, S. F. Vasilevsky, V. G. Nenajdenko, N. V. Sokolova, G. A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2401-2405. doi:10.1007/s11172-011-0369-3), IF=0.629
  93. А.И. Говди, С.Ф. Василевский, В.Г. Ненайденко, Н.В. Соколова, Г.А. Толстиков
    Синтез 1,2,3-триазольных конъюгатов бетулоновой кислоты с пептидами на основе 1,3-циклоприсоединения
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, N 11, 2354-2359. (1,3-Cycloaddition synthesis of 1,2,3-triazole conjugates of betulonic acid with peptides/ A. I. Govdi, S. F. Vasilevsky, V. G. Nenajdenko, N. V. Sokolova, G. A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 11, pp 2401-2405. doi:10.1007/s11172-011-0369-3), IF=0.629
  94. Н.П. Грицан, А.В. Зибарев
    Синтез и свойства халькоген-азотных π-гетероциклических анион-радикальных солей
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 11, 2091-2100. (Chalcogen-nitrogen π-heterocyclic radical anion salts: the synthesis and properties/ N.P. Gritsan, A.V. Zibarev// RUSS CHEM B+, 2011, V. 60, N 11, pp 2131-2140. doi:10.1007/s11172-011-0331-4), IF=0.629
  95. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, Г.А. Толстиков, Л.В. Спирихин
    Cинтез гетероциклических производных дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, Т. 47, N 10, 1547-1550.. (Synthesis of heterocyclic derivatives of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, G.A. Tolstikov, L.V. Spirikhin// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp. 1547–1550. doi:10.1134/S1070428011100228), IF=0.634
  96. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, Г.А. Толстиков, Л.В. Спирихин
    Cинтез гетероциклических производных дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, Т. 47, N 10, 1547-1550.. (Synthesis of heterocyclic derivatives of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, G.A. Tolstikov, L.V. Spirikhin// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp. 1547–1550. doi:10.1134/S1070428011100228), IF=0.634
  97. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, Г.А. Толстиков, Л.В. Спирихин
    Cинтез гетероциклических производных дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, Т. 47, N 10, 1547-1550.. (Synthesis of heterocyclic derivatives of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, G.A. Tolstikov, L.V. Spirikhin// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp. 1547–1550. doi:10.1134/S1070428011100228), IF=0.634
  98. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, Г.А. Толстиков, Л.В. Спирихин
    Cинтез гетероциклических производных дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, Т. 47, N 10, 1547-1550.. (Synthesis of heterocyclic derivatives of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, G.A. Tolstikov, L.V. Spirikhin// RUSS J ORG CHEM+, 2011, V. 47, N 10, pp. 1547–1550. doi:10.1134/S1070428011100228), IF=0.634
  99. С.В. Ларионов, З.А. Савельева, Г.В. Романенко, Е.М. Усков, М.И. Рахманова, С.А. Попов, А.В. Ткачев
    Синтез, структура и синяя фотолюминесценция координационного цепочечного полимера [Cd2(L)Cl4]n (L = 2-(3,5 диметилпиразол-1-ил)-4-метилхинолин)
    Координационная химия, 2011, Т. 37, № 10, 723-727. (Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058), IF=0.591
  100. С.В. Ларионов, З.А. Савельева, Г.В. Романенко, Е.М. Усков, М.И. Рахманова, С.А. Попов, А.В. Ткачев
    Синтез, структура и синяя фотолюминесценция координационного цепочечного полимера [Cd2(L)Cl4]n (L = 2-(3,5 диметилпиразол-1-ил)-4-метилхинолин)
    Координационная химия, 2011, Т. 37, № 10, 723-727. (Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058), IF=0.591
  101. С.В. Ларионов, З.А. Савельева, Г.В. Романенко, Е.М. Усков, М.И. Рахманова, С.А. Попов, А.В. Ткачев
    Синтез, структура и синяя фотолюминесценция координационного цепочечного полимера [Cd2(L)Cl4]n (L = 2-(3,5 диметилпиразол-1-ил)-4-метилхинолин)
    Координационная химия, 2011, Т. 37, № 10, 723-727. (Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058), IF=0.591
  102. С.В. Ларионов, З.А. Савельева, Г.В. Романенко, Е.М. Усков, М.И. Рахманова, С.А. Попов, А.В. Ткачев
    Синтез, структура и синяя фотолюминесценция координационного цепочечного полимера [Cd2(L)Cl4]n (L = 2-(3,5 диметилпиразол-1-ил)-4-метилхинолин)
    Координационная химия, 2011, Т. 37, № 10, 723-727. (Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058), IF=0.591
  103. С.В. Ларионов, З.А. Савельева, Г.В. Романенко, Е.М. Усков, М.И. Рахманова, С.А. Попов, А.В. Ткачев
    Синтез, структура и синяя фотолюминесценция координационного цепочечного полимера [Cd2(L)Cl4]n (L = 2-(3,5 диметилпиразол-1-ил)-4-метилхинолин)
    Координационная химия, 2011, Т. 37, № 10, 723-727. (Synthesis, structure, and blue photoluminescence of the coordination chain polymer [Cd2(L)Cl4]n (L = 2-(3,5- dimethylpyrazol-1-yl)-4-methylquinoline)/ S.V. Larionov, Z.A. Savel'Eva, E.M. Uskov, M.I. Rakhmanova, G.V. Romanenko, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 10, pp 719-724. doi:10.1134/S1070328411100058), IF=0.591
  104. Е.Н. Степанова, О.А. Рабина, С.В. Морозов
    Динамика показателей качества и безопасности новых видов растительных масложировых продуктов при хранении
    Техника и технология пищевых производств, 2011, № 3 (22), 37-41.
  105. А.М. Чибиряев, А. Ермакова, И.В. Кожевников
    Параметры активации термической изомеризации β-пинена в сверхкритических и газофазных условиях.
    Журнал физической химии, 2011, Т. 85, № 9, 1621-1632. (Activation parameters of supercritical and gas-phase β-pinene thermal isomerization/ A. M. Chibiryaev, A. Yermakova, I. V. Kozhevnikov// RUSS J PHYS CHEM A+, 2011, V. 85, N 9, pp 1505-1515. doi:10.1134/S0036024411090068), IF=0.503
  106. В.И. Боровков, А.Г. Матвеева, И.С. Иванишко, И.В. Береговая, В.А. Резников
    Проявление статистического спинового фактора при захвате избыточных электронов стабильными нитроксильными радикалами
    Доклады Академии наук, 2011, Т. 440, № 3, 361-364. (Spin statistical factor in the reactions of excess electron scavenging by stable nitroxyl radicals/ V.I. Borovkov, A.G. Matveeva, I.S. Ivanishko, I.V. Beregovaya, V.A. Reznikov// DOKL PHYS CHEM, 2011, V.440, , N 1, pp. 174-177. doi:10.1134/S0012501611090065 Part: 1), IF=0.23
  107. В.И. Боровков, А.Г. Матвеева, И.С. Иванишко, И.В. Береговая, В.А. Резников
    Проявление статистического спинового фактора при захвате избыточных электронов стабильными нитроксильными радикалами
    Доклады Академии наук, 2011, Т. 440, № 3, 361-364. (Spin statistical factor in the reactions of excess electron scavenging by stable nitroxyl radicals/ V.I. Borovkov, A.G. Matveeva, I.S. Ivanishko, I.V. Beregovaya, V.A. Reznikov// DOKL PHYS CHEM, 2011, V.440, , N 1, pp. 174-177. doi:10.1134/S0012501611090065 Part: 1), IF=0.23
  108. В.И. Боровков, А.Г. Матвеева, И.С. Иванишко, И.В. Береговая, В.А. Резников
    Проявление статистического спинового фактора при захвате избыточных электронов стабильными нитроксильными радикалами
    Доклады Академии наук, 2011, Т. 440, № 3, 361-364. (Spin statistical factor in the reactions of excess electron scavenging by stable nitroxyl radicals/ V.I. Borovkov, A.G. Matveeva, I.S. Ivanishko, I.V. Beregovaya, V.A. Reznikov// DOKL PHYS CHEM, 2011, V.440, , N 1, pp. 174-177. doi:10.1134/S0012501611090065 Part: 1), IF=0.23
  109. D. V. Sandanov, N. A. Pankrushina
    Alkaloid content in various parts of Sophora flavescens
    Chem. Nat. Compd., 2011, V. 47, N 4, pp 669-670. doi:10.1007/s10600-011-0029-8, IF=0.693
  110. Т.Г. Толстикова, М.В. Хвостов, А.О. Брызгалов, И.Ф. Беленичев, С.В. Павлов
    Глицидипин — перспективный гипотензивный и кардиопротективный агент
    Бюлл. Эксп. Биол. Мед., 2011 , V. 151, # 5, 532-535. (Glycidipine, a Promising Hypotensive and Cardioprotective Agent/ T.G. Tolstikova, M.V. Khvostov, A.O. Bryzgalov, I.F. Belenichev, S.V. Pavlov// B EXP BIOL MED+, 2011, V.151, N 5, pp 597-600. doi:10.1007/s10517-011-1391-z), IF=0.305
  111. Т.Г. Толстикова, М.В. Хвостов, А.О. Брызгалов, И.Ф. Беленичев, С.В. Павлов
    Глицидипин — перспективный гипотензивный и кардиопротективный агент
    Бюлл. Эксп. Биол. Мед., 2011 , V. 151, # 5, 532-535. (Glycidipine, a Promising Hypotensive and Cardioprotective Agent/ T.G. Tolstikova, M.V. Khvostov, A.O. Bryzgalov, I.F. Belenichev, S.V. Pavlov// B EXP BIOL MED+, 2011, V.151, N 5, pp 597-600. doi:10.1007/s10517-011-1391-z), IF=0.305
  112. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  113. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  114. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  115. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  116. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  117. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  118. E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung
    Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе
    Биоорганическая химия, 2011, Т. 37, № 5, 637-644. (Inhibitory Effect of Ursolic Acid Derivatives on Recombinant Human Aldose Reductasе/ E.H. Lee, S.A. Popov, J.Yo. Lee, A.V. Shpatov, T.P. Kukina, S.W. Kang, C.-H. Pan, B.H. Um, S.H. Jung// RUSS J BIOORG CHEM+, 2011, V.37, N 5, pp 569-577. doi:10.1134/S1068162011050050), IF=0.546
  119. О. Б. Казакова, Г. В. Гиниятуллина, Г. А. Толстиков
    Синтез А-секометиленамино- и замещенных амидоксимотритерпеноидов
    Биоорганическая химия, 2011, Т. 37, N 5, 690-696. (Synthesis of A-secomethylenamino- and substituted amidoximotriterpenoids/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov// RUSS J BIOORG CHEM+, 2011, V. 37, N 5, 619-625. doi:10.1134/S1068162011050086), IF=0.546
  120. О. Б. Казакова, Г. В. Гиниятуллина, Г. А. Толстиков
    Синтез А-секометиленамино- и замещенных амидоксимотритерпеноидов
    Биоорганическая химия, 2011, Т. 37, N 5, 690-696. (Synthesis of A-secomethylenamino- and substituted amidoximotriterpenoids/ O.B. Kazakova, G.V. Giniyatullina, G.A. Tolstikov// RUSS J BIOORG CHEM+, 2011, V. 37, N 5, 619-625. doi:10.1134/S1068162011050086), IF=0.546
  121. С.А. Осадчий, В.Г. Шубин, Л.П. Козлова, В.С. Варламенко, М.Л. Филипенко, У.А. Боярских
    Усовершенствование способов получения этидия бромистого и синтез этидия этилсульфата – нового флуоресцентного красителя для обнаружения нуклеиновых кислот
    Журнал прикладной химии, 2011, Т. 84, В. 9, 1491-1498. (Improvement of Ways to Obtain Ethidium Bromide and Synthesis of Ethidium Ethyl Sulfate, a New Fluorescent Dye for Detection of Nucleic Acids/ S.A. Osadchii, V.G. Shubin, L.P. Kozlova, V.S. Varlamenko, M.L. Filipenko, U.A. Boyarskikh// RUSS J APPL CHEM+, 2011, V. 84, N 9, pp. 1541-1548. doi:10.1134/S107042721109014X), IF=0.261
  122. С.А. Осадчий, В.Г. Шубин, Л.П. Козлова, В.С. Варламенко, М.Л. Филипенко, У.А. Боярских
    Усовершенствование способов получения этидия бромистого и синтез этидия этилсульфата – нового флуоресцентного красителя для обнаружения нуклеиновых кислот
    Журнал прикладной химии, 2011, Т. 84, В. 9, 1491-1498. (Improvement of Ways to Obtain Ethidium Bromide and Synthesis of Ethidium Ethyl Sulfate, a New Fluorescent Dye for Detection of Nucleic Acids/ S.A. Osadchii, V.G. Shubin, L.P. Kozlova, V.S. Varlamenko, M.L. Filipenko, U.A. Boyarskikh// RUSS J APPL CHEM+, 2011, V. 84, N 9, pp. 1541-1548. doi:10.1134/S107042721109014X), IF=0.261
  123. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  124. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  125. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  126. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  127. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  128. И.Е. Смирнова, О.Б. Казакова, Е.В. Третьякова, А.Н. Лобов, Л.В. Спирихин, Г.А. Толстиков, К.Ю. Супоницкий
    Селективное бромирование дигидрохинопимаровой кислоты
    Журнал органической химии, 2011, V. 47, N 9, 1362-1366. (Selective bromination of dihydroquinopimaric acid/ I.E. Smirnova, O.B. Kazakova, E.V. Tret'yakova, A.N. Lobov, L.V. Spirikhin, G.A. Tolstikov, K.Yu. Suponitskii// RUSS J ORG CHEM+, 2011, V. 47, N 9, pp. 1385-1389. doi:10.1134/S1070428011090223), IF=0.634
  129. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  130. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  131. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  132. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  133. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  134. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  135. С.В. Ларионов, Л.И. Мячина, Р.Ф. Клевцова, Л.А. Глинская, Н.В. Куратьева, Е.М. Усков, М.И. Рахманова, В.М. Карпов, В.Е. Платонов, В.П. Фадеева
    Синтез и фотолюминесценция комплексов цинка(II) с тетрафтортерефталевой кислотой (H2L). Кристаллическая cтруктура координационного полимера [Zn(H2O)4L•4H2О]n
    Координационная химия, 2011, Т. 37, № 9, 651-657. (Synthesis and photoluminescence of Zinc(II) complexes with tetrafluoroterephthalic acid (H2L). Crystal structure of coordination polymer [Zn(H2O)4L•4H2О]n/ S.V. Larionov, L.I. Myachina, R.F. Klevtsova, L.A. Glinskaya, N.V. Kurat'Eva, E.M. Uskov, M.I. Rakhmanov, V.M. Karpov, V.E. Platonov, V.P. Fadeeva// RUSS J COORD CHEM+, 2011, V. 37, N 9, pp 650-656. doi:10.1134/S1070328411090041), IF=0.591
  136. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  137. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  138. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  139. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  140. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  141. S. Roy, M.P. Davydova, R. Pal, K. Gilmore, G.A. Tolstikov, S.F. Vasilevsky, I.V. Alabugin
    Dissecting Alkynes: Full Cleavage of Polarized C C Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
    J. Org. Chem., 2011, 76 (18), pp 7482-7490. doi:10.1021/jo201259j, IF=4.1
  142. I.S. Ivanishko, I.V. Beregovaya, S. Hartmann, W. Koehler, V.I. Borovkov
    Intrinsic Reaction Parameters for Electron Transfer from Aromatic Radical Anions to Vicinal Dibromoalkanes in Alkane Solutions
    J. Phys. Chem. A., 2011, V. 115, 9861-9875. doi:10.1021/jp2040828, IF=2.732
  143. I.S. Ivanishko, I.V. Beregovaya, S. Hartmann, W. Koehler, V.I. Borovkov
    Intrinsic Reaction Parameters for Electron Transfer from Aromatic Radical Anions to Vicinal Dibromoalkanes in Alkane Solutions
    J. Phys. Chem. A., 2011, V. 115, 9861-9875. doi:10.1021/jp2040828, IF=2.732
  144. I.S. Ivanishko, I.V. Beregovaya, S. Hartmann, W. Koehler, V.I. Borovkov
    Intrinsic Reaction Parameters for Electron Transfer from Aromatic Radical Anions to Vicinal Dibromoalkanes in Alkane Solutions
    J. Phys. Chem. A., 2011, V. 115, 9861-9875. doi:10.1021/jp2040828, IF=2.732
  145. I.S. Ivanishko, I.V. Beregovaya, S. Hartmann, W. Koehler, V.I. Borovkov
    Intrinsic Reaction Parameters for Electron Transfer from Aromatic Radical Anions to Vicinal Dibromoalkanes in Alkane Solutions
    J. Phys. Chem. A., 2011, V. 115, 9861-9875. doi:10.1021/jp2040828, IF=2.732
  146. А.М. Чибиряев, А. Ермакова, И.В. Кожевников
    Кинетическая модель обратимых реакций при термической изомеризации α-пинена
    Журнал физической химии, 2011, Т. 85, № 8, 1460–1471. (Reaction reversibility in α-pinene thermal isomerization: improving the kinetic model/ A. M. Chibiryaev, A. Ermakova, I. V. Kozhevnikov// RUSS J PHYS CHEM A+, 2011, V. 85, N 8, pp 1347-1357. doi:10.1134/S0036024411090068), IF=0.503
  147. Т.Е. Кокина, Л.А. Шелудякова, А.В.Ткачев, Е.Г. Богуславский, А.М. Агафонцев, Н.Б. Горшков, С.В.Ларионов
    Синтез и свойства комплексов Cu(II) и Pd(II) с хиральными бис-α-сульфанил-оксимами - производными природного моно терпена α-пинена
    Журнал общей химии, 2011, Т. 81. № 8, С. 1306-1312. (Synthesis and properties of Cu(II) and Pd(ii) complexes with chiral bis-α-sulfanyl oxymes, the derivatives of natural monoterpene, α-pinene/ T.E. Kokina, L.A. Sheludyakova, A.V. Tkachev, E.G. Boguslavskii, A.M. Agafontsev, N.B. Gorshkov, S.V. Larionov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 651-1657. doi:10.1134/S1070363211080123), IF=0.393
  148. Т.Е. Кокина, Л.А. Шелудякова, А.В.Ткачев, Е.Г. Богуславский, А.М. Агафонцев, Н.Б. Горшков, С.В.Ларионов
    Синтез и свойства комплексов Cu(II) и Pd(II) с хиральными бис-α-сульфанил-оксимами - производными природного моно терпена α-пинена
    Журнал общей химии, 2011, Т. 81. № 8, С. 1306-1312. (Synthesis and properties of Cu(II) and Pd(ii) complexes with chiral bis-α-sulfanyl oxymes, the derivatives of natural monoterpene, α-pinene/ T.E. Kokina, L.A. Sheludyakova, A.V. Tkachev, E.G. Boguslavskii, A.M. Agafontsev, N.B. Gorshkov, S.V. Larionov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 651-1657. doi:10.1134/S1070363211080123), IF=0.393
  149. Т.Е. Кокина, Л.А. Шелудякова, А.В.Ткачев, Е.Г. Богуславский, А.М. Агафонцев, Н.Б. Горшков, С.В.Ларионов
    Синтез и свойства комплексов Cu(II) и Pd(II) с хиральными бис-α-сульфанил-оксимами - производными природного моно терпена α-пинена
    Журнал общей химии, 2011, Т. 81. № 8, С. 1306-1312. (Synthesis and properties of Cu(II) and Pd(ii) complexes with chiral bis-α-sulfanyl oxymes, the derivatives of natural monoterpene, α-pinene/ T.E. Kokina, L.A. Sheludyakova, A.V. Tkachev, E.G. Boguslavskii, A.M. Agafontsev, N.B. Gorshkov, S.V. Larionov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 651-1657. doi:10.1134/S1070363211080123), IF=0.393
  150. Т.Е. Кокина, Л.А. Шелудякова, А.В.Ткачев, Е.Г. Богуславский, А.М. Агафонцев, Н.Б. Горшков, С.В.Ларионов
    Синтез и свойства комплексов Cu(II) и Pd(II) с хиральными бис-α-сульфанил-оксимами - производными природного моно терпена α-пинена
    Журнал общей химии, 2011, Т. 81. № 8, С. 1306-1312. (Synthesis and properties of Cu(II) and Pd(ii) complexes with chiral bis-α-sulfanyl oxymes, the derivatives of natural monoterpene, α-pinene/ T.E. Kokina, L.A. Sheludyakova, A.V. Tkachev, E.G. Boguslavskii, A.M. Agafontsev, N.B. Gorshkov, S.V. Larionov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 651-1657. doi:10.1134/S1070363211080123), IF=0.393
  151. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  152. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  153. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  154. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  155. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  156. О.Б. Казакова, Э.Ф. Хуснутдинова, А.Н. Лобов, Т.И. Зверева, Ю.В. Легостаева, Г.А. Толстиков, В.Н. Хрусталев
    Необычное протекание озонолиза 2,3-индоло-28-оксоаллобетулина
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 8, 1753-1754. (Unusual ozonolysis pattern for 28-oxo-2,3-indoloallobetulin/ O. B. Kazakova, E. F. Khusnutdinova, A. N. Lobov, T. I. Zvereva, Yu. V. Legostaeva, G. A. Tolstikov, V. N. Khrustalev// RUSS CHEM B+, 2011, V. 60, N 8, pp. 1781-1783. doi:10.1007/s11172-011-0267-8), IF=0.469
  157. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Необычное поведение метилидентрифенилфосфорана в реакциях с семичленными лактолами
    Журнал органической химии, 2011, V. 47, N 8, 1127-1129. (Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1142-1145. doi:10.1134/S1070428011080045), IF=0.556
  158. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Необычное поведение метилидентрифенилфосфорана в реакциях с семичленными лактолами
    Журнал органической химии, 2011, V. 47, N 8, 1127-1129. (Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1142-1145. doi:10.1134/S1070428011080045), IF=0.556
  159. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Необычное поведение метилидентрифенилфосфорана в реакциях с семичленными лактолами
    Журнал органической химии, 2011, V. 47, N 8, 1127-1129. (Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1142-1145. doi:10.1134/S1070428011080045), IF=0.556
  160. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Необычное поведение метилидентрифенилфосфорана в реакциях с семичленными лактолами
    Журнал органической химии, 2011, V. 47, N 8, 1127-1129. (Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1142-1145. doi:10.1134/S1070428011080045), IF=0.556
  161. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Необычное поведение метилидентрифенилфосфорана в реакциях с семичленными лактолами
    Журнал органической химии, 2011, V. 47, N 8, 1127-1129. (Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1142-1145. doi:10.1134/S1070428011080045), IF=0.556
  162. Г.А. Селиванова, Е.В. Амосов, Л.И. Горюнов, С.В. Балина, В.Г. Васильев, Г.Е. Сальников, Е.А. Лукьянец, В.Д. Штейнгарц
    Синтез производных 2,3’,4’-трициандифенила и тетрафенилфталоцианинов на их основе
    Журнал органической химии, 2011, Т. 47, N 8, 1222-1227. (Synthesis of 2,3',4'-tricyanobiphenyl derivatives and tetraphenylphthalocyanines based thereon/ G.A. Selivanova, E.V. Amosov, L.I. Goryunov, S.V. Balina, V.G. Vasil'ev, G.E. Sal'nikov, E.A. Luk'yanets, V.D. Shteingarts// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1240-1246. doi:10.1134/S1070428011080215), IF=0.634
  163. M.V. Edeleva, I.A. Kirilyuk, I.F. Zhurko, D.A. Parkhomenko, Y.P. Tsentalovich, E.G. Bagryanskaya
    pH-Sensitive C_ON Bond Homolysis of Alkoxyamines of Imidazoline Series with Multiple Ionizable Groups As an Approach for Control of Nitroxide Mediated Polymerization
    J. Org. Chem., 2011, 76 (14), pp 5558–5573. doi:10.1021/jo200341m, IF=4.1
  164. M.V. Edeleva, I.A. Kirilyuk, I.F. Zhurko, D.A. Parkhomenko, Y.P. Tsentalovich, E.G. Bagryanskaya
    pH-Sensitive C_ON Bond Homolysis of Alkoxyamines of Imidazoline Series with Multiple Ionizable Groups As an Approach for Control of Nitroxide Mediated Polymerization
    J. Org. Chem., 2011, 76 (14), pp 5558–5573. doi:10.1021/jo200341m, IF=4.1
  165. M.V. Edeleva, I.A. Kirilyuk, I.F. Zhurko, D.A. Parkhomenko, Y.P. Tsentalovich, E.G. Bagryanskaya
    pH-Sensitive C_ON Bond Homolysis of Alkoxyamines of Imidazoline Series with Multiple Ionizable Groups As an Approach for Control of Nitroxide Mediated Polymerization
    J. Org. Chem., 2011, 76 (14), pp 5558–5573. doi:10.1021/jo200341m, IF=4.1
  166. С.А. Кондратьев, В.И. Ростовцев, О.И. Яровая, Н.Ф. Салахутдинов
    Флотореагенты на основе скипидара и их использование при флотации медно-никелевой руды
    Физ.-техн. Пробл. Разр. Полезн. Ископ. (J. Min. Sci), 2011, № 4, 117-124. (Turpentine-based flotation agents in copper-nickel ore flotation/ S.A. Kondrat'ev, V.I. Rostovtsev, O.I. Yarovaya, N.F. Salakhutdinov// J MIN SCI+, -2011, V. 47, N 4, pp 514-521. doi:10.1134/S1062739147040149), IF=0.389
  167. С.А. Кондратьев, В.И. Ростовцев, О.И. Яровая, Н.Ф. Салахутдинов
    Флотореагенты на основе скипидара и их использование при флотации медно-никелевой руды
    Физ.-техн. Пробл. Разр. Полезн. Ископ. (J. Min. Sci), 2011, № 4, 117-124. (Turpentine-based flotation agents in copper-nickel ore flotation/ S.A. Kondrat'ev, V.I. Rostovtsev, O.I. Yarovaya, N.F. Salakhutdinov// J MIN SCI+, -2011, V. 47, N 4, pp 514-521. doi:10.1134/S1062739147040149), IF=0.389
  168. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  169. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  170. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  171. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  172. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  173. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, М.Г. Первова, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Строение и характеристики кобальт-содержащих гибридных систем хитозана – катализаторов окисления олефинов
    Журнал физической химии, 2011, Т. 85, № 7, 1261–1267. (Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211), IF=0.503
  174. И.В. Нечепуренко, У.А. Боярских, Н.И. Комарова, М.П. Половинка, М.Л. Филипенко, Г.И. Лифшиц, Н.Ф. Салахутдинов, Г.А. Толстиков
    Влияние берберина и его бром- и иод-производных на уровень экспрессии гена рецептора ЛПНП в клетках HepG2
    Доклады Академии наук, 2011, Т. 439, № 3, 346-350. (LDLR Up-Regulatory Activity of Berberine and Its Bromo and Iodo Derivatives in Human Liver HepG2 Cells/ I.V. Nechepurenko, U.A. Boyarskikh, N.I. Komarova, M.P. Polovinka, M.L. Filipenko, G.I. Lifshits, N.F. Salakhutdinov, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 1, pp. 204-208. doi:10.1134/S0012500811070093 Part: 1), IF=0.256
  175. И.В. Нечепуренко, У.А. Боярских, Н.И. Комарова, М.П. Половинка, М.Л. Филипенко, Г.И. Лифшиц, Н.Ф. Салахутдинов, Г.А. Толстиков
    Влияние берберина и его бром- и иод-производных на уровень экспрессии гена рецептора ЛПНП в клетках HepG2
    Доклады Академии наук, 2011, Т. 439, № 3, 346-350. (LDLR Up-Regulatory Activity of Berberine and Its Bromo and Iodo Derivatives in Human Liver HepG2 Cells/ I.V. Nechepurenko, U.A. Boyarskikh, N.I. Komarova, M.P. Polovinka, M.L. Filipenko, G.I. Lifshits, N.F. Salakhutdinov, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 1, pp. 204-208. doi:10.1134/S0012500811070093 Part: 1), IF=0.256
  176. И.В. Нечепуренко, У.А. Боярских, Н.И. Комарова, М.П. Половинка, М.Л. Филипенко, Г.И. Лифшиц, Н.Ф. Салахутдинов, Г.А. Толстиков
    Влияние берберина и его бром- и иод-производных на уровень экспрессии гена рецептора ЛПНП в клетках HepG2
    Доклады Академии наук, 2011, Т. 439, № 3, 346-350. (LDLR Up-Regulatory Activity of Berberine and Its Bromo and Iodo Derivatives in Human Liver HepG2 Cells/ I.V. Nechepurenko, U.A. Boyarskikh, N.I. Komarova, M.P. Polovinka, M.L. Filipenko, G.I. Lifshits, N.F. Salakhutdinov, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 1, pp. 204-208. doi:10.1134/S0012500811070093 Part: 1), IF=0.256
  177. A.S. Chubarov, M.M. Shakirov, I.V. Koptyug, R.Z. Sagdeev, D.G. Knorre, T.S. Godovikova
    Synthesis and characterization of fluorinated homocysteine derivatives as potential molecular probes for 19 F magnetic resonance spectroscopy and imaging
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 13, 4050-4053. doi:10.1016/j.bmcl.2011.04.119, IF=2.661
  178. A.S. Chubarov, M.M. Shakirov, I.V. Koptyug, R.Z. Sagdeev, D.G. Knorre, T.S. Godovikova
    Synthesis and characterization of fluorinated homocysteine derivatives as potential molecular probes for 19 F magnetic resonance spectroscopy and imaging
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 13, 4050-4053. doi:10.1016/j.bmcl.2011.04.119, IF=2.661
  179. A.S. Chubarov, M.M. Shakirov, I.V. Koptyug, R.Z. Sagdeev, D.G. Knorre, T.S. Godovikova
    Synthesis and characterization of fluorinated homocysteine derivatives as potential molecular probes for 19 F magnetic resonance spectroscopy and imaging
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 13, 4050-4053. doi:10.1016/j.bmcl.2011.04.119, IF=2.661
  180. A.S. Chubarov, M.M. Shakirov, I.V. Koptyug, R.Z. Sagdeev, D.G. Knorre, T.S. Godovikova
    Synthesis and characterization of fluorinated homocysteine derivatives as potential molecular probes for 19 F magnetic resonance spectroscopy and imaging
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 13, 4050-4053. doi:10.1016/j.bmcl.2011.04.119, IF=2.661
  181. A.S. Chubarov, M.M. Shakirov, I.V. Koptyug, R.Z. Sagdeev, D.G. Knorre, T.S. Godovikova
    Synthesis and characterization of fluorinated homocysteine derivatives as potential molecular probes for 19 F magnetic resonance spectroscopy and imaging
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 13, 4050-4053. doi:10.1016/j.bmcl.2011.04.119, IF=2.661
  182. И.А. Болдов, А.С. Кучьянов, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Оптоволоконный химический сенсор на соединения аминного типа
    Физика твердого тела, 2011, Т. 53, № 6, 1088-1090. (Fiber-optic chemical sensor of amine-type compounds/ I. A. Boldov, A. S. Kuch’yanov, A. I. Plekhanov, N. A. Orlova, I. Yu. Kargapolova, V. V. Shelkovnikov// PHYS SOLID STATE+, 2011, V. 53, N 6, pp 1152-1154. doi:10.1134/S1063783411060072), IF=0.726
  183. И.А. Болдов, А.С. Кучьянов, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Оптоволоконный химический сенсор на соединения аминного типа
    Физика твердого тела, 2011, Т. 53, № 6, 1088-1090. (Fiber-optic chemical sensor of amine-type compounds/ I. A. Boldov, A. S. Kuch’yanov, A. I. Plekhanov, N. A. Orlova, I. Yu. Kargapolova, V. V. Shelkovnikov// PHYS SOLID STATE+, 2011, V. 53, N 6, pp 1152-1154. doi:10.1134/S1063783411060072), IF=0.726
  184. И.А. Болдов, А.С. Кучьянов, А.И. Плеханов, Н.А. Орлова, И.Ю. Каргаполова, В.В. Шелковников
    Оптоволоконный химический сенсор на соединения аминного типа
    Физика твердого тела, 2011, Т. 53, № 6, 1088-1090. (Fiber-optic chemical sensor of amine-type compounds/ I. A. Boldov, A. S. Kuch’yanov, A. I. Plekhanov, N. A. Orlova, I. Yu. Kargapolova, V. V. Shelkovnikov// PHYS SOLID STATE+, 2011, V. 53, N 6, pp 1152-1154. doi:10.1134/S1063783411060072), IF=0.726
  185. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Исследование строения гибридных систем хитозана с помощью рН-чувствительного нитроксильного радикала
    Журнал физической химии, 2011, Т. 85, № 6, 1086–1091. (Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239), IF=0.503
  186. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Исследование строения гибридных систем хитозана с помощью рН-чувствительного нитроксильного радикала
    Журнал физической химии, 2011, Т. 85, № 6, 1086–1091. (Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239), IF=0.503
  187. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Исследование строения гибридных систем хитозана с помощью рН-чувствительного нитроксильного радикала
    Журнал физической химии, 2011, Т. 85, № 6, 1086–1091. (Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239), IF=0.503
  188. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
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    Журнал физической химии, 2011, Т. 85, № 6, 1086–1091. (Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239), IF=0.503
  189. А.В. Мехаев, А.В. Пестов, Л.С. Молочников, Е.Г. Ковалева, Ю.Г. Ятлук, И.А. Григорьев, И.А. Кирилюк
    Исследование строения гибридных систем хитозана с помощью рН-чувствительного нитроксильного радикала
    Журнал физической химии, 2011, Т. 85, № 6, 1086–1091. (Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239), IF=0.503
  190. А.П. Крысин, Т.Б. Хлебникова
    Бис-[3-(3,5-диалкил-4-гидроксифенил)пропил]моно-и дисульфиды в качестве стабилизаторов сэвилена.
    Журнал общей химии, 2011, Т. 81, N. 6, 966-969. (Bis[3-(3,5-dialkyl-4-hydroxyphenyl)propyl]mono- and disulfides as the Sevilen stabilizers/ A. P. Krysin, T. B. Khlebnikova// RUSS J ORG CHEM+, 2011, V. 47, N 6, pp. 1159-1162. doi:10.1134/S1070363211060144), IF=0.393
  191. С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Т.Е. Кокина, А.В. Шпатов
    Кристаллическая и молекулярная структура 3,5-диметил-1H-пиразолида 3-О-ацетилурсоловой кислоты
    Журнал структурной химии, 2011, Т. 52, № 3, 599-604. (Crystal and molecular structure of 3,5-dimethyl-1H-pyrazolide of 3-O-acetyl ursolic acid/ S. A. Popov, L. A. Glinskaya, T. E. Kokina, R. F. Klevtsova, A. V. Shpatov// J STRUCT CHEM+, 201, V. 52, N 3, pp 582-588. doi:10.1134/S0022476611030206), IF=0.546
  192. С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Т.Е. Кокина, А.В. Шпатов
    Кристаллическая и молекулярная структура 3,5-диметил-1H-пиразолида 3-О-ацетилурсоловой кислоты
    Журнал структурной химии, 2011, Т. 52, № 3, 599-604. (Crystal and molecular structure of 3,5-dimethyl-1H-pyrazolide of 3-O-acetyl ursolic acid/ S. A. Popov, L. A. Glinskaya, T. E. Kokina, R. F. Klevtsova, A. V. Shpatov// J STRUCT CHEM+, 201, V. 52, N 3, pp 582-588. doi:10.1134/S0022476611030206), IF=0.546
  193. С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Т.Е. Кокина, А.В. Шпатов
    Кристаллическая и молекулярная структура 3,5-диметил-1H-пиразолида 3-О-ацетилурсоловой кислоты
    Журнал структурной химии, 2011, Т. 52, № 3, 599-604. (Crystal and molecular structure of 3,5-dimethyl-1H-pyrazolide of 3-O-acetyl ursolic acid/ S. A. Popov, L. A. Glinskaya, T. E. Kokina, R. F. Klevtsova, A. V. Shpatov// J STRUCT CHEM+, 201, V. 52, N 3, pp 582-588. doi:10.1134/S0022476611030206), IF=0.546
  194. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  195. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  196. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  197. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  198. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  199. С. В. Ларионов, З. А. Савельева, Р. Ф. Клевцова, Л. А. Глинская, Е. М. Усков, М.И. Рахманова, С. А. Попов, А. В. Ткачев
    Кристаллическая структура сольвата [Cd2L2Cl4]•CH2Cl2 (L = пиразолилхинолин - производное монотерпеноида (+)-3-карена) и фотолюминесценция хирального комплекса CdLCl2
    Журнал структурной химии, 2011, V. 52, N 3, 547–553. (Crystal structure of solvate [Cd2L2Cl4]•CH2Cl2 (L = pyrazolylquinoline, the derivative of monoterpenoid (+)-3-carene) and photoluminescence of chiral complex CdLCl2/ S.V. Larionov, Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, M.I. Rakhmanova, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 201, V. 52, N 3, pp 531-537. doi:10.1134/S0022476611030127), IF=0.546
  200. А.Н. Михеев, В.Г. Макотченко, Н.А. Панкрушина, М.О. Коротких, А.В. Аржанников, M.K. A. Thumm
    _Особенности химических реакций в отсутствие растворителей при микроволновом воздействии
    Химия в интересах устойчивого развития, 2011, Т. 19, № 6, 669-677. (Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.)
  201. А.Н. Михеев, В.Г. Макотченко, Н.А. Панкрушина, М.О. Коротких, А.В. Аржанников, M.K. A. Thumm
    _Особенности химических реакций в отсутствие растворителей при микроволновом воздействии
    Химия в интересах устойчивого развития, 2011, Т. 19, № 6, 669-677. (Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.)
  202. А.Н. Михеев, В.Г. Макотченко, Н.А. Панкрушина, М.О. Коротких, А.В. Аржанников, M.K. A. Thumm
    _Особенности химических реакций в отсутствие растворителей при микроволновом воздействии
    Химия в интересах устойчивого развития, 2011, Т. 19, № 6, 669-677. (Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.)
  203. А.Н. Михеев, В.Г. Макотченко, Н.А. Панкрушина, М.О. Коротких, А.В. Аржанников, M.K. A. Thumm
    _Особенности химических реакций в отсутствие растворителей при микроволновом воздействии
    Химия в интересах устойчивого развития, 2011, Т. 19, № 6, 669-677. (Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.)
  204. А.Н. Михеев, В.Г. Макотченко, Н.А. Панкрушина, М.О. Коротких, А.В. Аржанников, M.K. A. Thumm
    _Особенности химических реакций в отсутствие растворителей при микроволновом воздействии
    Химия в интересах устойчивого развития, 2011, Т. 19, № 6, 669-677. (Features of Chemical Reactions in the Absence of Solvents under Microwave Action/ A. N. Mikheev, V. G. Makotchenko, N. A. Pankrushina, M. O. Korotkikh, A.V. Arzhannikov, М. К. А. Thumm// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 669-677.)
  205. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  206. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  207. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  208. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  209. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  210. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  211. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  212. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  213. M.B. Bushuev, K.A. Vinogradova, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova, E.M. Uskov, L.A. Sheludyakova, A.V. Alekseev, S.V. Larionov
    Zinc(II) and cadmium(II) complexes based on 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine (L): Synthesis, structure, luminescence. Double lone pair–p interactions in the structure of ZnL2Cl2
    Inorg. Chim. Acta, 2011, V. 371, N 1, 88-94. doi:10.1016/j.ica.2011.03.007, IF=1.899
  214. E.A. Suturina, N.A. Semenov, A.V. Lonchakov, I.Yu. Bagryanskaya, Yu.V. Gatilov, I.G. Irtegova, N.V. Vasilieva, E. Lork, R. Mews, N.P. Gritsan, A.V. Zibarev
    Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
    J. Phys. Chem. A., 2011, V. 115, 4851–4860. doi:10.1021/jp2019523, IF=2.732
  215. E.A. Suturina, N.A. Semenov, A.V. Lonchakov, I.Yu. Bagryanskaya, Yu.V. Gatilov, I.G. Irtegova, N.V. Vasilieva, E. Lork, R. Mews, N.P. Gritsan, A.V. Zibarev
    Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
    J. Phys. Chem. A., 2011, V. 115, 4851–4860. doi:10.1021/jp2019523, IF=2.732
  216. E.A. Suturina, N.A. Semenov, A.V. Lonchakov, I.Yu. Bagryanskaya, Yu.V. Gatilov, I.G. Irtegova, N.V. Vasilieva, E. Lork, R. Mews, N.P. Gritsan, A.V. Zibarev
    Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
    J. Phys. Chem. A., 2011, V. 115, 4851–4860. doi:10.1021/jp2019523, IF=2.732
  217. E.A. Suturina, N.A. Semenov, A.V. Lonchakov, I.Yu. Bagryanskaya, Yu.V. Gatilov, I.G. Irtegova, N.V. Vasilieva, E. Lork, R. Mews, N.P. Gritsan, A.V. Zibarev
    Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
    J. Phys. Chem. A., 2011, V. 115, 4851–4860. doi:10.1021/jp2019523, IF=2.732
  218. E.A. Suturina, N.A. Semenov, A.V. Lonchakov, I.Yu. Bagryanskaya, Yu.V. Gatilov, I.G. Irtegova, N.V. Vasilieva, E. Lork, R. Mews, N.P. Gritsan, A.V. Zibarev
    Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
    J. Phys. Chem. A., 2011, V. 115, 4851–4860. doi:10.1021/jp2019523, IF=2.732
  219. М.Ю. Круглова, М.А. Ханина, Д.Л. Макарова, Д.В. Домрачев
    Исследование эфирного масла из надземной части Filipendula ulmaria (L.) Maxim
    Медицина и образование в Сибири, 2011 , № 5, статья 13
  220. М.Ю. Круглова, М.А. Ханина, Д.Л. Макарова, Д.В. Домрачев
    Исследование эфирного масла из надземной части Filipendula ulmaria (L.) Maxim
    Медицина и образование в Сибири, 2011 , № 5, статья 13
  221. М.Ю. Круглова, М.А. Ханина, Д.Л. Макарова, Д.В. Домрачев
    Исследование эфирного масла из надземной части Filipendula ulmaria (L.) Maxim
    Медицина и образование в Сибири, 2011 , № 5, статья 13
  222. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova
    Zinc(II) and cadmium(II) complexes based on 2-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(4-methoxyphenyl)pyrimidine-4-carboxylic acid: synthesis, structure, luminescence
    Inorg. Chem. Commun., 2011, V. 14, N 5, 749-752. doi:10.1016/j.inoche.2011.02.027, IF=1.973
  223. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova
    Zinc(II) and cadmium(II) complexes based on 2-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(4-methoxyphenyl)pyrimidine-4-carboxylic acid: synthesis, structure, luminescence
    Inorg. Chem. Commun., 2011, V. 14, N 5, 749-752. doi:10.1016/j.inoche.2011.02.027, IF=1.973
  224. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova
    Zinc(II) and cadmium(II) complexes based on 2-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(4-methoxyphenyl)pyrimidine-4-carboxylic acid: synthesis, structure, luminescence
    Inorg. Chem. Commun., 2011, V. 14, N 5, 749-752. doi:10.1016/j.inoche.2011.02.027, IF=1.973
  225. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, N.V. Pervukhina, D.Yu. Naumov, M.I. Rakhmanova
    Zinc(II) and cadmium(II) complexes based on 2-(3,5-dimethyl-1H-pyrazol-1-yl)-6-(4-methoxyphenyl)pyrimidine-4-carboxylic acid: synthesis, structure, luminescence
    Inorg. Chem. Commun., 2011, V. 14, N 5, 749-752. doi:10.1016/j.inoche.2011.02.027, IF=1.973
  226. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  227. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  228. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  229. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  230. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  231. A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov
    Luminescent properties of new naphthylnitroxyl radicals
    High Energ. Chem. (Химия высоких энергий), 2011 , V. 45, N 5, 416-432. (Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134), IF=0.814
  232. E.A. Krasnov, I.P. Kaminskii, T.V. Kadyrova, E.E. Shul'ts
    Isolation of repin from the aerial part of Gentaurea scabiosa
    Chem. Nat. Compd., 2011, V. 47, N 2, pp 311-312. doi:10.1007/s10600-011-9917-1, IF=0.693
  233. E.A. Krasnov, I.P. Kaminskii, T.V. Kadyrova, E.E. Shul'ts
    Isolation of repin from the aerial part of Gentaurea scabiosa
    Chem. Nat. Compd., 2011, V. 47, N 2, pp 311-312. doi:10.1007/s10600-011-9917-1, IF=0.693
  234. E.A. Krasnov, I.P. Kaminskii, T.V. Kadyrova, E.E. Shul'ts
    Isolation of repin from the aerial part of Gentaurea scabiosa
    Chem. Nat. Compd., 2011, V. 47, N 2, pp 311-312. doi:10.1007/s10600-011-9917-1, IF=0.693
  235. Л.И. Горюнов, J. Grobe, В.Д. Штейнгарц, R. Mews
    Синтез (2-Х,3-Y-фенил)диметилфосфанов (X, Y = Me2P, H; Me2P, F; Br, F) и их комплесов с PdCl2
    Журнал органической химии, 2011, Т. 47, N 5, 773–775. (Synthesis of (2-X,3-Y-Phenyl)dimethylphosphanes (X, Y = Me2P, H; Me2P, F; Br, F) and their complexes with PdCl2/ L.I. Goryunov, V.D. Shteingarts, J. Grobe, R. Mews// RUSS J ORG CHEM+, 2011, V. 47, N 5, pp. 780-782. doi:10.1134/S1070428011050204), IF=0.634
  236. Л.И. Горюнов, J. Grobe, В.Д. Штейнгарц, R. Mews
    Синтез (2-Х,3-Y-фенил)диметилфосфанов (X, Y = Me2P, H; Me2P, F; Br, F) и их комплесов с PdCl2
    Журнал органической химии, 2011, Т. 47, N 5, 773–775. (Synthesis of (2-X,3-Y-Phenyl)dimethylphosphanes (X, Y = Me2P, H; Me2P, F; Br, F) and their complexes with PdCl2/ L.I. Goryunov, V.D. Shteingarts, J. Grobe, R. Mews// RUSS J ORG CHEM+, 2011, V. 47, N 5, pp. 780-782. doi:10.1134/S1070428011050204), IF=0.634
  237. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов, Г.А. Толстиков
    "Биус" - эффективное средство повышения урожайности яровой пшеницы и картофеля
    Химия в интересах устойчивого развития, 2011, Т. 19, № 5, 547-553. ("Bius" - an Efficient Tool to Increase the Crop Capacity of Spring Wheat and Potatoes/ M. P. Polovinka, N. G. Vlasenko, A. A. Malyuga, M. T. Egorycheva, N. F. Salakhutdinov, G.A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 637-642.)
  238. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов, Г.А. Толстиков
    "Биус" - эффективное средство повышения урожайности яровой пшеницы и картофеля
    Химия в интересах устойчивого развития, 2011, Т. 19, № 5, 547-553. ("Bius" - an Efficient Tool to Increase the Crop Capacity of Spring Wheat and Potatoes/ M. P. Polovinka, N. G. Vlasenko, A. A. Malyuga, M. T. Egorycheva, N. F. Salakhutdinov, G.A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 637-642.)
  239. М.П. Половинка, Н.Г. Власенко, А.А. Малюга, М.Т. Егорычева, Н.Ф. Салахутдинов, Г.А. Толстиков
    "Биус" - эффективное средство повышения урожайности яровой пшеницы и картофеля
    Химия в интересах устойчивого развития, 2011, Т. 19, № 5, 547-553. ("Bius" - an Efficient Tool to Increase the Crop Capacity of Spring Wheat and Potatoes/ M. P. Polovinka, N. G. Vlasenko, A. A. Malyuga, M. T. Egorycheva, N. F. Salakhutdinov, G.A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 6, 637-642.)
  240. O.V. Ardashov, V.V. Zarubaev, A.A. Shtro, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Antiviral activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its derivatives against influenza A(H1N1)2009 virus
    Lett. Drug Des. Discov., 2011, V. 8, N 4, 375-380. doi:10.2174/157018011794839411, IF=0.667
  241. O.V. Ardashov, V.V. Zarubaev, A.A. Shtro, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Antiviral activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its derivatives against influenza A(H1N1)2009 virus
    Lett. Drug Des. Discov., 2011, V. 8, N 4, 375-380. doi:10.2174/157018011794839411, IF=0.667
  242. O.V. Ardashov, V.V. Zarubaev, A.A. Shtro, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Kiselev
    Antiviral activity of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol and its derivatives against influenza A(H1N1)2009 virus
    Lett. Drug Des. Discov., 2011, V. 8, N 4, 375-380. doi:10.2174/157018011794839411, IF=0.667
  243. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  244. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  245. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  246. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  247. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  248. M. Kozuleva, I. Klenina, I. Proskuryakov, I. Kirilyuk, B. Ivanov
    Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity
    FEBS Lett., 2011, V. 585, N 7, 1067-1071. doi:10.1016/j.febslet.2011.03.004, IF=3.601
  249. M. Kozuleva, I. Klenina, I. Proskuryakov, I. Kirilyuk, B. Ivanov
    Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity
    FEBS Lett., 2011, V. 585, N 7, 1067-1071. doi:10.1016/j.febslet.2011.03.004, IF=3.601
  250. M. Kozuleva, I. Klenina, I. Proskuryakov, I. Kirilyuk, B. Ivanov
    Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity
    FEBS Lett., 2011, V. 585, N 7, 1067-1071. doi:10.1016/j.febslet.2011.03.004, IF=3.601
  251. M. Kozuleva, I. Klenina, I. Proskuryakov, I. Kirilyuk, B. Ivanov
    Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity
    FEBS Lett., 2011, V. 585, N 7, 1067-1071. doi:10.1016/j.febslet.2011.03.004, IF=3.601
  252. А.Г. Шушарин, В.В. Морозов, М.П. Половинка
    Медицинское тепловидение – современные возможности метода
    Современные проблемы науки и образования, 2011 , № 4, URL: www.science-education.ru/98-4726
  253. А.Г. Шушарин, В.В. Морозов, М.П. Половинка
    Медицинское тепловидение – современные возможности метода
    Современные проблемы науки и образования, 2011 , № 4, URL: www.science-education.ru/98-4726
  254. А.П. Гардымова, А.Я. Тихонов, В.Я. Зырянов
    Оптическая мультистабильность в композиционном материале на основе полимера, жидкого кристалла и ионного сурфактанта при воздействии электрического поля
    Перспективные материалы, 2011, № 4, 32–35.
  255. А.П. Гардымова, А.Я. Тихонов, В.Я. Зырянов
    Оптическая мультистабильность в композиционном материале на основе полимера, жидкого кристалла и ионного сурфактанта при воздействии электрического поля
    Перспективные материалы, 2011, № 4, 32–35.
  256. А.В. Куликов, М.А. Тихонова, Е.А. Куликова, Т.М. Хоменко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, Н.К. Попова
    Влияние нового потенциального психотропного препарата гидрохлорида 8-(трифторметил)-1,2,3,4,5-бензопентатиепин-6-амина на экспрессию генов, вовлеченных в метаболизм и рецепцию медиатора серотонина, в головном мозге мышей
    Молекулярная биология, 2011, Т. 45, № 2, 282–288. (Effect of a new potential psychotropic drug, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride, on the expression of serotonin-related genes in the mouse brain/ A.V. Kulikov, M.A. Tikhonova, N.K. Popova, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, E.A. Kulikova// MOL BIOL+, -2011, V. 45, N 2, pp 251-257. doi:10.1134/S0026893310061044), IF=0.653
  257. А.В. Куликов, М.А. Тихонова, Е.А. Куликова, Т.М. Хоменко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, Н.К. Попова
    Влияние нового потенциального психотропного препарата гидрохлорида 8-(трифторметил)-1,2,3,4,5-бензопентатиепин-6-амина на экспрессию генов, вовлеченных в метаболизм и рецепцию медиатора серотонина, в головном мозге мышей
    Молекулярная биология, 2011, Т. 45, № 2, 282–288. (Effect of a new potential psychotropic drug, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride, on the expression of serotonin-related genes in the mouse brain/ A.V. Kulikov, M.A. Tikhonova, N.K. Popova, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, E.A. Kulikova// MOL BIOL+, -2011, V. 45, N 2, pp 251-257. doi:10.1134/S0026893310061044), IF=0.653
  258. А.В. Куликов, М.А. Тихонова, Е.А. Куликова, Т.М. Хоменко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, Н.К. Попова
    Влияние нового потенциального психотропного препарата гидрохлорида 8-(трифторметил)-1,2,3,4,5-бензопентатиепин-6-амина на экспрессию генов, вовлеченных в метаболизм и рецепцию медиатора серотонина, в головном мозге мышей
    Молекулярная биология, 2011, Т. 45, № 2, 282–288. (Effect of a new potential psychotropic drug, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride, on the expression of serotonin-related genes in the mouse brain/ A.V. Kulikov, M.A. Tikhonova, N.K. Popova, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, E.A. Kulikova// MOL BIOL+, -2011, V. 45, N 2, pp 251-257. doi:10.1134/S0026893310061044), IF=0.653
  259. А.В. Куликов, М.А. Тихонова, Е.А. Куликова, Т.М. Хоменко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, Н.К. Попова
    Влияние нового потенциального психотропного препарата гидрохлорида 8-(трифторметил)-1,2,3,4,5-бензопентатиепин-6-амина на экспрессию генов, вовлеченных в метаболизм и рецепцию медиатора серотонина, в головном мозге мышей
    Молекулярная биология, 2011, Т. 45, № 2, 282–288. (Effect of a new potential psychotropic drug, 8-(trifluoromethyl)-1,2,3,4,5-benzopentathiepin-6-amine hydrochloride, on the expression of serotonin-related genes in the mouse brain/ A.V. Kulikov, M.A. Tikhonova, N.K. Popova, T.M. Khomenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, E.A. Kulikova// MOL BIOL+, -2011, V. 45, N 2, pp 251-257. doi:10.1134/S0026893310061044), IF=0.653
  260. A.V. Pivtsov, L.V. Kulik, A.Yu. Makarov, F. Blockhuys
    Pulse EPR and ENDOR study of 1,2,3-benzodithiazolyl, 2,1,3-benzothiaselenazolyl and 1,2,3-benzodiselenazolyl radicals
    Phys. Chem. Chem. Phys., 2011, V. 13, N 9, 3873-3880. doi:10.1039/c0cp02051f, IF=3.453
  261. A.V. Pivtsov, L.V. Kulik, A.Yu. Makarov, F. Blockhuys
    Pulse EPR and ENDOR study of 1,2,3-benzodithiazolyl, 2,1,3-benzothiaselenazolyl and 1,2,3-benzodiselenazolyl radicals
    Phys. Chem. Chem. Phys., 2011, V. 13, N 9, 3873-3880. doi:10.1039/c0cp02051f, IF=3.453
  262. A.V. Pivtsov, L.V. Kulik, A.Yu. Makarov, F. Blockhuys
    Pulse EPR and ENDOR study of 1,2,3-benzodithiazolyl, 2,1,3-benzothiaselenazolyl and 1,2,3-benzodiselenazolyl radicals
    Phys. Chem. Chem. Phys., 2011, V. 13, N 9, 3873-3880. doi:10.1039/c0cp02051f, IF=3.453
  263. A.Yu. Makarov, V.V. Zhivonitko, A.G. Makarov, S.B. Zikirin, I.Yu. Bagryanskaya, V.A. Bagryansky, Yu.V. Gatilov, I.G. Irtegova, M.M. Shakirov, A.V. Zibarev
    Interaction of 1,3,2,4-Benzodithiadiazines and Their 1-Se Congeners with Ph3P and Some Properties of the Iminophosphorane Products
    Inorg. Chem., 2011, V. 50, 3017–3027. doi:10.1021/ic102565x, IF=4.324
  264. A.Yu. Makarov, V.V. Zhivonitko, A.G. Makarov, S.B. Zikirin, I.Yu. Bagryanskaya, V.A. Bagryansky, Yu.V. Gatilov, I.G. Irtegova, M.M. Shakirov, A.V. Zibarev
    Interaction of 1,3,2,4-Benzodithiadiazines and Their 1-Se Congeners with Ph3P and Some Properties of the Iminophosphorane Products
    Inorg. Chem., 2011, V. 50, 3017–3027. doi:10.1021/ic102565x, IF=4.324
  265. Т.Н. Дребущак, Н.А. Панкрушина, Е.В. Болдырева
    Полиморфные превращения нового типа в толбутамиде: необычное низкотемпературное конформационное упорядочение.
    Доклады Академии наук, 2011, Т. 437, № 4, 507-510. (A new type of polymorphic transformation in tolbutamide: Unusual low-temperature conformation ordering/ T. N. Drebushchak, N. A. Pankrushina, E. V. Boldyreva// DOKL PHYS CHEM, 2011, V. 437, N 2, pp. 61-64. doi:10.1134/S0012501611040014), IF=0.256
  266. Т.Н. Дребущак, Н.А. Панкрушина, Е.В. Болдырева
    Полиморфные превращения нового типа в толбутамиде: необычное низкотемпературное конформационное упорядочение.
    Доклады Академии наук, 2011, Т. 437, № 4, 507-510. (A new type of polymorphic transformation in tolbutamide: Unusual low-temperature conformation ordering/ T. N. Drebushchak, N. A. Pankrushina, E. V. Boldyreva// DOKL PHYS CHEM, 2011, V. 437, N 2, pp. 61-64. doi:10.1134/S0012501611040014), IF=0.256
  267. Д.В. Домрачев, Е.В. Карпова, С.Н. Горошкевич, А.В. Ткачев
    __Сравнительный анализ летучих веществ хвои пятихвойных сосен северной и восточной Евразии
    Химия растительного сырья, 2011, № 4, 89-98. (Comparative analysis of volatiles from needles of five-needle pines of northern and eastern Eurasia/ D. V. Domrachev, E. V. Karpova, S. N. Goroshkevich, A. V. Tkachev// RUSS J BIOORG CHEM+, 2012, V. 38, N 7, pp 780-789. doi:10.1134/S1068162012070059)
  268. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  269. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  270. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  271. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  272. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  273. О.Б. Казакова, Н.И. Медведева, Э.Ю. Ямансаров, Л.В. Спирихин, Э.Ф. Хуснутдинова, О.С. Куковинец, Г.А. Толстиков
    Синтез хлорвиниловых производных на основе бетулина
    Химия в интересах устойчивого развития, 2011, Т. 19, № 4, 373-376. (Synthesis of Chlorovinyl Derivatives Based on Betulin/ O. B. Kazakova, N. I. Medvedeva, E.Y. Yamansarov, L. V. Spirikhin, E. F. Khusnutdinova, O. S. Kukovinets, G. A. Tolstikov// Chemistry for Sustainable Development, 2011, Т. 19, № 4, 373-376.)
  274. S.I. Dikalov, I.A. Kirilyuk, M.A. Voinov, I.A. Grigor’ev
    EPR detection of cellular and mitochondrial superoxide using cyclic hydroxylamines
    Free Rad. Res., 2011, V. 45, N 4, 417–430. doi:10.3109/10715762.2010.540242, IF=2.805
  275. A.L. Buchachenko, D.A. Kuznetsov, N.N. Breslavskaya, L.N. Shchegoleva, S.E. Arkhangelsky
    Calcium induced ATP synthesis: Isotope effect, magnetic parameters and mechanism
    Chemical Physics Letters, 2011,.V. 505, N 4–6, pp 130–134. doi:10.1016/j.cplett.2011.02.036, IF=2.279
  276. A.L. Buchachenko, D.A. Kuznetsov, N.N. Breslavskaya, L.N. Shchegoleva, S.E. Arkhangelsky
    Calcium induced ATP synthesis: Isotope effect, magnetic parameters and mechanism
    Chemical Physics Letters, 2011,.V. 505, N 4–6, pp 130–134. doi:10.1016/j.cplett.2011.02.036, IF=2.279
  277. A.L. Buchachenko, D.A. Kuznetsov, N.N. Breslavskaya, L.N. Shchegoleva, S.E. Arkhangelsky
    Calcium induced ATP synthesis: Isotope effect, magnetic parameters and mechanism
    Chemical Physics Letters, 2011,.V. 505, N 4–6, pp 130–134. doi:10.1016/j.cplett.2011.02.036, IF=2.279
  278. A.L. Buchachenko, D.A. Kuznetsov, N.N. Breslavskaya, L.N. Shchegoleva, S.E. Arkhangelsky
    Calcium induced ATP synthesis: Isotope effect, magnetic parameters and mechanism
    Chemical Physics Letters, 2011,.V. 505, N 4–6, pp 130–134. doi:10.1016/j.cplett.2011.02.036, IF=2.279
  279. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
    Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
    ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
  280. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
    Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
    ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
  281. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
    Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
    ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
  282. E.B. Logashenko, O.V. Salomatina, A.V. Markov, D.V. Korchagina, N.F. Salakhutdinov, G.A. Tolstikov, V.V. Vlasov, M.A. Zenkova
    Synthesis of Pro-Apoptopic Activity of Novel Glycyrrhetinic Acid Derivatives
    ChemBioChem, 2011, V. 12, N 5, 784-794. doi:10.1002/cbic.201000618, IF=3.944
  283. И.Г. Боярских, Ю.В. Юшкова, Е.И. Черняк, С.В. Морозов
    Содержание биологически активных фенольных соединений в плодах Lonicera caerulea L. различного происхождения в условиях лесостепи Приобья
    Вестник Алтайского государственного аграрного университета, 2011, Т. 77, № 3, 39-45.
  284. И.Г. Боярских, Ю.В. Юшкова, Е.И. Черняк, С.В. Морозов
    Содержание биологически активных фенольных соединений в плодах Lonicera caerulea L. различного происхождения в условиях лесостепи Приобья
    Вестник Алтайского государственного аграрного университета, 2011, Т. 77, № 3, 39-45.
  285. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, Yu.V. Gatilov, V.I. Mamatyuk, N.K. Gusarova
    Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium and amines
    J. Sulfur Chem., 2011, V. 32, N 3, 599-610. doi:10.1080/17415993.2011.628993, IF=0.75
  286. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, Yu.V. Gatilov, V.I. Mamatyuk, N.K. Gusarova
    Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium and amines
    J. Sulfur Chem., 2011, V. 32, N 3, 599-610. doi:10.1080/17415993.2011.628993, IF=0.75
  287. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, Yu.V. Gatilov, V.I. Mamatyuk, N.K. Gusarova
    Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium and amines
    J. Sulfur Chem., 2011, V. 32, N 3, 599-610. doi:10.1080/17415993.2011.628993, IF=0.75
  288. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, Yu.V. Gatilov, V.I. Mamatyuk, N.K. Gusarova
    Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium and amines
    J. Sulfur Chem., 2011, V. 32, N 3, 599-610. doi:10.1080/17415993.2011.628993, IF=0.75
  289. Е.В. Паршина, Л.С. Молочников, Е.Г. Ковалева, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Кислотность среды и каталитические свойства композиционных материалов на основе диоксидов кремния и титана и порошковой целлюлозы в присутствии ионов Cu2+
    Журнал физической химии, 2011, Т. 85, № 3, 520–525. (Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X), IF=0.503
  290. Е.В. Паршина, Л.С. Молочников, Е.Г. Ковалева, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Кислотность среды и каталитические свойства композиционных материалов на основе диоксидов кремния и титана и порошковой целлюлозы в присутствии ионов Cu2+
    Журнал физической химии, 2011, Т. 85, № 3, 520–525. (Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X), IF=0.503
  291. Е.В. Паршина, Л.С. Молочников, Е.Г. Ковалева, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Кислотность среды и каталитические свойства композиционных материалов на основе диоксидов кремния и титана и порошковой целлюлозы в присутствии ионов Cu2+
    Журнал физической химии, 2011, Т. 85, № 3, 520–525. (Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X), IF=0.503
  292. Е.В. Паршина, Л.С. Молочников, Е.Г. Ковалева, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Кислотность среды и каталитические свойства композиционных материалов на основе диоксидов кремния и титана и порошковой целлюлозы в присутствии ионов Cu2+
    Журнал физической химии, 2011, Т. 85, № 3, 520–525. (Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X), IF=0.503
  293. Е.В. Паршина, Л.С. Молочников, Е.Г. Ковалева, А.Б. Шишмаков, Ю.В. Микушина, И.А. Кирилюк, И.А. Григорьев
    Кислотность среды и каталитические свойства композиционных материалов на основе диоксидов кремния и титана и порошковой целлюлозы в присутствии ионов Cu2+
    Журнал физической химии, 2011, Т. 85, № 3, 520–525. (Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X), IF=0.503
  294. Н.Ю. Адонин, В.В. Бардин, У. Флёрке, Х.-И. Фрон
    Новый синтетический подход к аддуктам трис(перфторалкил)диалкиламиноборана с диалкиламинами
    Журнал общей химии, 2011, Т. 81, N. 3, 413-420. (New approach to the synthesis of tris(perfluoroalkyl)borane adducts with dialkylamines/ N. Yu. Adonin, V. V. Bardin, U. Florke, H. -J. Fron// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 509-516. doi:10.1134/S107036321103011X), IF=0.393
  295. Н.Ю. Адонин, В.В. Бардин, У. Флёрке, Х.-И. Фрон
    Новый синтетический подход к аддуктам трис(перфторалкил)диалкиламиноборана с диалкиламинами
    Журнал общей химии, 2011, Т. 81, N. 3, 413-420. (New approach to the synthesis of tris(perfluoroalkyl)borane adducts with dialkylamines/ N. Yu. Adonin, V. V. Bardin, U. Florke, H. -J. Fron// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 509-516. doi:10.1134/S107036321103011X), IF=0.393
  296. G.V. Giniyatullina, O.B. Kazakova, E.V. Salimova, G.A. Tolstikov
    Synthesis of new betulonic and oleanonic acid amides
    Chem. Nat. Compd., 2011, V. 47, N 1, pp 68-72. doi:10.1007/s10600-011-9832-5, IF=0.693
  297. G.V. Giniyatullina, O.B. Kazakova, E.V. Salimova, G.A. Tolstikov
    Synthesis of new betulonic and oleanonic acid amides
    Chem. Nat. Compd., 2011, V. 47, N 1, pp 68-72. doi:10.1007/s10600-011-9832-5, IF=0.693
  298. G.V. Giniyatullina, O.B. Kazakova, E.V. Salimova, G.A. Tolstikov
    Synthesis of new betulonic and oleanonic acid amides
    Chem. Nat. Compd., 2011, V. 47, N 1, pp 68-72. doi:10.1007/s10600-011-9832-5, IF=0.693
  299. В.В. Шелковников, В.А. Лоскутов, Е.В. Васильев, Н.В. Васильева, В.А. Рябинин, А.Н. Синяков
    Новые фотогенераторы кислоты на основе сульфониевых производных тиоксантен-9-она для детритилирования в процессе синтеза олигонуклеотидов
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 3, 548-556. (New acid photogenerators based on thioxanthen-9-one sulfonium derivatives for detritylation in the oligonucleotide synthesis/ V. V. Shelkovnikov, V. A. Loskutov, E. V. Vasil’ev, N. V. Shekleina, V. A. Ryabinin, A. N. Sinyakov// RUSS CHEM B+, 2011, V. 60, N 3, pp. 561-569. doi:10.1007/s11172-011-0087-x), IF=0.629
  300. В.В. Шелковников, В.А. Лоскутов, Е.В. Васильев, Н.В. Васильева, В.А. Рябинин, А.Н. Синяков
    Новые фотогенераторы кислоты на основе сульфониевых производных тиоксантен-9-она для детритилирования в процессе синтеза олигонуклеотидов
    Известия Академии Наук. Сер. Хим., 2011, Т. 60, № 3, 548-556. (New acid photogenerators based on thioxanthen-9-one sulfonium derivatives for detritylation in the oligonucleotide synthesis/ V. V. Shelkovnikov, V. A. Loskutov, E. V. Vasil’ev, N. V. Shekleina, V. A. Ryabinin, A. N. Sinyakov// RUSS CHEM B+, 2011, V. 60, N 3, pp. 561-569. doi:10.1007/s11172-011-0087-x), IF=0.629
  301. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Новая реакция в химии алюминийорганических соединений
    Журнал органической химии, 2011, V. 47, N 3, 471-472. (Novel Reaction in the Chemistry of Organoaluminum Compounds/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 472-473. doi:10.1134/S1070428011030304), IF=0.634
  302. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Новая реакция в химии алюминийорганических соединений
    Журнал органической химии, 2011, V. 47, N 3, 471-472. (Novel Reaction in the Chemistry of Organoaluminum Compounds/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 472-473. doi:10.1134/S1070428011030304), IF=0.634
  303. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Новая реакция в химии алюминийорганических соединений
    Журнал органической химии, 2011, V. 47, N 3, 471-472. (Novel Reaction in the Chemistry of Organoaluminum Compounds/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 472-473. doi:10.1134/S1070428011030304), IF=0.634
  304. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Новая реакция в химии алюминийорганических соединений
    Журнал органической химии, 2011, V. 47, N 3, 471-472. (Novel Reaction in the Chemistry of Organoaluminum Compounds/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 472-473. doi:10.1134/S1070428011030304), IF=0.634
  305. Г.Ю. Ишмуратов, В.А. Выдрина, М.П. Яковлева, Э.Ф. Валеева, Р.Р. Муслухов, Г.А. Толстиков
    Новая реакция в химии алюминийорганических соединений
    Журнал органической химии, 2011, V. 47, N 3, 471-472. (Novel Reaction in the Chemistry of Organoaluminum Compounds/ G.Yu. Ishmuratov, V.A. Vydrina, M.P. Yakovleva, E.F. Valeeva, R.R. Muslukhov, G.A. Tolstikov// RUSS J ORG CHEM+, 2011, V. 47, N 3, pp. 472-473. doi:10.1134/S1070428011030304), IF=0.634
  306. В.Е. Павлов, С.В. Морозов, В.Ф. Рапута, В.В. Коковкин, И.В. Хвостов
    Закономерности аэрозольных выпадений полиароматических углеводородов в сфере влияния г. Барнаула
    Химия в интересах устойчивого развития, 2011, Т. 19, № 3, 287-294. (Investigation of Aerosol Precipitation of Polyaromatic Hydrocarbons in the Sphere of Influence of Barnaul/ V. E. Pavlov, S. V.Morozov, V. F. Raputa, V. V. Kokovkin, I. V Khvostov// Chemistry for Sustainable Development, 2011, Т. 19, № 3, 287-294.)
  307. В.Е. Павлов, С.В. Морозов, В.Ф. Рапута, В.В. Коковкин, И.В. Хвостов
    Закономерности аэрозольных выпадений полиароматических углеводородов в сфере влияния г. Барнаула
    Химия в интересах устойчивого развития, 2011, Т. 19, № 3, 287-294. (Investigation of Aerosol Precipitation of Polyaromatic Hydrocarbons in the Sphere of Influence of Barnaul/ V. E. Pavlov, S. V.Morozov, V. F. Raputa, V. V. Kokovkin, I. V Khvostov// Chemistry for Sustainable Development, 2011, Т. 19, № 3, 287-294.)
  308. В.Е. Павлов, С.В. Морозов, В.Ф. Рапута, В.В. Коковкин, И.В. Хвостов
    Закономерности аэрозольных выпадений полиароматических углеводородов в сфере влияния г. Барнаула
    Химия в интересах устойчивого развития, 2011, Т. 19, № 3, 287-294. (Investigation of Aerosol Precipitation of Polyaromatic Hydrocarbons in the Sphere of Influence of Barnaul/ V. E. Pavlov, S. V.Morozov, V. F. Raputa, V. V. Kokovkin, I. V Khvostov// Chemistry for Sustainable Development, 2011, Т. 19, № 3, 287-294.)
  309. В.Е. Павлов, С.В. Морозов, В.Ф. Рапута, В.В. Коковкин, И.В. Хвостов
    Закономерности аэрозольных выпадений полиароматических углеводородов в сфере влияния г. Барнаула
    Химия в интересах устойчивого развития, 2011, Т. 19, № 3, 287-294. (Investigation of Aerosol Precipitation of Polyaromatic Hydrocarbons in the Sphere of Influence of Barnaul/ V. E. Pavlov, S. V.Morozov, V. F. Raputa, V. V. Kokovkin, I. V Khvostov// Chemistry for Sustainable Development, 2011, Т. 19, № 3, 287-294.)
  310. T.G. Tolstikova, M.V. Khvostov, G.I. Lifshits, A.V. Dushkin, E.S. Meteleva
    Alteration of Warfarin’s Pharmacologic Properties in Clathrates with Glycyrrhizic Acid and Arabinogalactan
    Lett. Drug Des. Discov., 2011, V. 8, N 3, 201-204. doi:10.2174/157018011794578222, IF=0.667
  311. T.G. Tolstikova, M.V. Khvostov, G.I. Lifshits, A.V. Dushkin, E.S. Meteleva
    Alteration of Warfarin’s Pharmacologic Properties in Clathrates with Glycyrrhizic Acid and Arabinogalactan
    Lett. Drug Des. Discov., 2011, V. 8, N 3, 201-204. doi:10.2174/157018011794578222, IF=0.667
  312. T.G. Tolstikova, M.V. Khvostov, G.I. Lifshits, A.V. Dushkin, E.S. Meteleva
    Alteration of Warfarin’s Pharmacologic Properties in Clathrates with Glycyrrhizic Acid and Arabinogalactan
    Lett. Drug Des. Discov., 2011, V. 8, N 3, 201-204. doi:10.2174/157018011794578222, IF=0.667
  313. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  314. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  315. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  316. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  317. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  318. O.B. Kazakova, D.V. Kazakov, E.Yu. Yamansarov, N.I. Medvedeva, G.A. Tolstikov, K.Yu. Suponitsky, D.E. Arkhipov
    Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
    Tetrahedron Lett., 2011, V. 52, N 9, 976-979. doi:10.1016/j.tetlet.2010.12.047, IF=2.618
  319. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  320. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  321. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  322. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  323. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  324. Н.С. Фурса, П.Ю. Шкроботько, Д.Л. Макарова, Д.В. Домрачев, С.В. Панченко, И.В. Чикина, О.А. Колосова
    Изучение компонентного состава валерианового эфирного масла полученного паровой дистилляцией
    Вестник Воронежского государственного университета. Сер.: Химия, биология, фармация, 2011 , № 2, 233-239.
  325. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Изменение метаболизма Lonicera caerulea L. в тектонически активной зоне Горного Алтая (Северо-Чуйский хр.)
    Растительный мир Азиатской России, 2011, № 2, 114-119.
  326. И.Г. Боярских, В.Г. Васильев, Т.А. Кукушкина
    Изменение метаболизма Lonicera caerulea L. в тектонически активной зоне Горного Алтая (Северо-Чуйский хр.)
    Растительный мир Азиатской России, 2011, № 2, 114-119.
  327. П.В. Никульшин, А.М. Максимов, В.Е. Платонов, А.И. Лотков, Л.Л. Мейснер
    Получение 1,4-дибромтетра­фторбензола из 4-бромтетра­фторбензолтиола и брома. Превращения 1,4-дибромтетра­фторбензола с KSH
    Fluorine notes, 2011, Is. 2 (75). http://notes.fluorine1.ru/public/2011/2_2011/letters/letter2.html
  328. П.В. Никульшин, А.М. Максимов, В.Е. Платонов, А.И. Лотков, Л.Л. Мейснер
    Получение 1,4-дибромтетра­фторбензола из 4-бромтетра­фторбензолтиола и брома. Превращения 1,4-дибромтетра­фторбензола с KSH
    Fluorine notes, 2011, Is. 2 (75). http://notes.fluorine1.ru/public/2011/2_2011/letters/letter2.html
  329. Y.P. Tsentalovich, V.V. Yanshole, Y.F. Polienko, S.V. Morozov, I.A. Grigor’ev
    Deactivation of Excited States of Kynurenine Covalently Linked to Nitroxides
    Photochem. Photobiol., 2011, V. 81, N 1, 22-31. doi:10.1111/j.1751-1097.2010.00841.x, IF=2.678
  330. Y.P. Tsentalovich, V.V. Yanshole, Y.F. Polienko, S.V. Morozov, I.A. Grigor’ev
    Deactivation of Excited States of Kynurenine Covalently Linked to Nitroxides
    Photochem. Photobiol., 2011, V. 81, N 1, 22-31. doi:10.1111/j.1751-1097.2010.00841.x, IF=2.678
  331. Д.В. Казаков, О.Б. Казакова, Г.Ю. Ишмуратов, А.О. Терентьев, Г.И. Никишин, Г.А. Толстиков
    Хемилюминесценция – основа нового подхода к исследованию фармакологически перспективных агентов пероксидной природы
    Доклады Академии наук, 2011, Т. 436, № 6, 774-779. (Chemiluminescence as a Base for a New Approach to the Study of Pharmacologically Promising Peroxide Agents/ D.V. Kazakov, O.B. Kazakova, G.Yu. Ishmuratov, A.O. Terent'ev, G.I. Nikishin, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 2, pp. 34-38. doi:10.1134/S0012500811010022), IF=0.256
  332. Д.В. Казаков, О.Б. Казакова, Г.Ю. Ишмуратов, А.О. Терентьев, Г.И. Никишин, Г.А. Толстиков
    Хемилюминесценция – основа нового подхода к исследованию фармакологически перспективных агентов пероксидной природы
    Доклады Академии наук, 2011, Т. 436, № 6, 774-779. (Chemiluminescence as a Base for a New Approach to the Study of Pharmacologically Promising Peroxide Agents/ D.V. Kazakov, O.B. Kazakova, G.Yu. Ishmuratov, A.O. Terent'ev, G.I. Nikishin, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 2, pp. 34-38. doi:10.1134/S0012500811010022), IF=0.256
  333. Д.В. Казаков, О.Б. Казакова, Г.Ю. Ишмуратов, А.О. Терентьев, Г.И. Никишин, Г.А. Толстиков
    Хемилюминесценция – основа нового подхода к исследованию фармакологически перспективных агентов пероксидной природы
    Доклады Академии наук, 2011, Т. 436, № 6, 774-779. (Chemiluminescence as a Base for a New Approach to the Study of Pharmacologically Promising Peroxide Agents/ D.V. Kazakov, O.B. Kazakova, G.Yu. Ishmuratov, A.O. Terent'ev, G.I. Nikishin, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 2, pp. 34-38. doi:10.1134/S0012500811010022), IF=0.256
  334. Д.В. Казаков, О.Б. Казакова, Г.Ю. Ишмуратов, А.О. Терентьев, Г.И. Никишин, Г.А. Толстиков
    Хемилюминесценция – основа нового подхода к исследованию фармакологически перспективных агентов пероксидной природы
    Доклады Академии наук, 2011, Т. 436, № 6, 774-779. (Chemiluminescence as a Base for a New Approach to the Study of Pharmacologically Promising Peroxide Agents/ D.V. Kazakov, O.B. Kazakova, G.Yu. Ishmuratov, A.O. Terent'ev, G.I. Nikishin, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 2, pp. 34-38. doi:10.1134/S0012500811010022), IF=0.256
  335. Д.В. Казаков, О.Б. Казакова, Г.Ю. Ишмуратов, А.О. Терентьев, Г.И. Никишин, Г.А. Толстиков
    Хемилюминесценция – основа нового подхода к исследованию фармакологически перспективных агентов пероксидной природы
    Доклады Академии наук, 2011, Т. 436, № 6, 774-779. (Chemiluminescence as a Base for a New Approach to the Study of Pharmacologically Promising Peroxide Agents/ D.V. Kazakov, O.B. Kazakova, G.Yu. Ishmuratov, A.O. Terent'ev, G.I. Nikishin, G.A. Tolstikov// DOKL CHEM, 2011, V. 439, N 2, pp. 34-38. doi:10.1134/S0012500811010022), IF=0.256
  336. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  337. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  338. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  339. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  340. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  341. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  342. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  343. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  344. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899
  345. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, B.A. Trofimov
    Reaction of primary phosphines with elemental sulfur and alkali metal hydroxides (MOH, M = Na, K, Cs): a novel and facile three-component synthesis of trithiophosphonates
    Tetrahedron Lett., 2011, V. 52, N 3, 398-400. doi:10.1016/j.tetlet.2010.11.075, IF=2.618
  346. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, B.A. Trofimov
    Reaction of primary phosphines with elemental sulfur and alkali metal hydroxides (MOH, M = Na, K, Cs): a novel and facile three-component synthesis of trithiophosphonates
    Tetrahedron Lett., 2011, V. 52, N 3, 398-400. doi:10.1016/j.tetlet.2010.11.075, IF=2.618
  347. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, B.A. Trofimov
    Reaction of primary phosphines with elemental sulfur and alkali metal hydroxides (MOH, M = Na, K, Cs): a novel and facile three-component synthesis of trithiophosphonates
    Tetrahedron Lett., 2011, V. 52, N 3, 398-400. doi:10.1016/j.tetlet.2010.11.075, IF=2.618
  348. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, B.A. Trofimov
    Reaction of primary phosphines with elemental sulfur and alkali metal hydroxides (MOH, M = Na, K, Cs): a novel and facile three-component synthesis of trithiophosphonates
    Tetrahedron Lett., 2011, V. 52, N 3, 398-400. doi:10.1016/j.tetlet.2010.11.075, IF=2.618
  349. M.B. Bushuev, E.V. Peresypkina, V.P. Krivopalov, A.V. Virovets, L.G. Lavrenova, O.P. Shkurko
    Synthesis of copper(II) complexes with 3,5-bis(4,6-dimethylpyrimidin-2-yl)-4H-1,2,4-triazol-4-amine (L). Molecular and crystal structures of L and [Cu2L2C4]*2MeCN
    Inorg. Chim. Acta, 2011, V. 365, N 1, 384-390. doi:10.1016/j.ica.2010.09.046, IF=1.899
  350. M.B. Bushuev, E.V. Peresypkina, V.P. Krivopalov, A.V. Virovets, L.G. Lavrenova, O.P. Shkurko
    Synthesis of copper(II) complexes with 3,5-bis(4,6-dimethylpyrimidin-2-yl)-4H-1,2,4-triazol-4-amine (L). Molecular and crystal structures of L and [Cu2L2C4]*2MeCN
    Inorg. Chim. Acta, 2011, V. 365, N 1, 384-390. doi:10.1016/j.ica.2010.09.046, IF=1.899
  351. M.B. Bushuev, E.V. Peresypkina, V.P. Krivopalov, A.V. Virovets, L.G. Lavrenova, O.P. Shkurko
    Synthesis of copper(II) complexes with 3,5-bis(4,6-dimethylpyrimidin-2-yl)-4H-1,2,4-triazol-4-amine (L). Molecular and crystal structures of L and [Cu2L2C4]*2MeCN
    Inorg. Chim. Acta, 2011, V. 365, N 1, 384-390. doi:10.1016/j.ica.2010.09.046, IF=1.899
  352. M.B. Bushuev, E.V. Peresypkina, V.P. Krivopalov, A.V. Virovets, L.G. Lavrenova, O.P. Shkurko
    Synthesis of copper(II) complexes with 3,5-bis(4,6-dimethylpyrimidin-2-yl)-4H-1,2,4-triazol-4-amine (L). Molecular and crystal structures of L and [Cu2L2C4]*2MeCN
    Inorg. Chim. Acta, 2011, V. 365, N 1, 384-390. doi:10.1016/j.ica.2010.09.046, IF=1.899
  353. Л.Н. Прибыткова, А.В. Ткачев, С.С. Зоркальцев, С.И. Писарева, С.В. Тузова
    Изучение химического состава и антиоксидантной активности полифенолов Artemisia santolinifolia
    Сибирский медицинский журнал (г. Томск), 2011 , Т. 26, № 1, В. 2, 65-67.
  354. Л.Н. Прибыткова, А.В. Ткачев, С.С. Зоркальцев, С.И. Писарева, С.В. Тузова
    Изучение химического состава и антиоксидантной активности полифенолов Artemisia santolinifolia
    Сибирский медицинский журнал (г. Томск), 2011 , Т. 26, № 1, В. 2, 65-67.
  355. Л.Н. Прибыткова, А.В. Ткачев, С.С. Зоркальцев, С.И. Писарева, С.В. Тузова
    Изучение химического состава и антиоксидантной активности полифенолов Artemisia santolinifolia
    Сибирский медицинский журнал (г. Томск), 2011 , Т. 26, № 1, В. 2, 65-67.
  356. Л.Н. Прибыткова, А.В. Ткачев, С.С. Зоркальцев, С.И. Писарева, С.В. Тузова
    Изучение химического состава и антиоксидантной активности полифенолов Artemisia santolinifolia
    Сибирский медицинский журнал (г. Томск), 2011 , Т. 26, № 1, В. 2, 65-67.
  357. Н.С. Устюжникова, Г.С. Ширапова, Е.И. Черняк, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Двустворчатый моллюск (Colletopterum ponderosum sedakovi) – универсальный биоиндикатор загрязнения бассейна озера Байкал стойкими органическим загрязнителями
    Инженерная экология, 2011, № 1, 55-63.
  358. Н.С. Устюжникова, Г.С. Ширапова, Е.И. Черняк, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Двустворчатый моллюск (Colletopterum ponderosum sedakovi) – универсальный биоиндикатор загрязнения бассейна озера Байкал стойкими органическим загрязнителями
    Инженерная экология, 2011, № 1, 55-63.
  359. Н.С. Устюжникова, Г.С. Ширапова, Е.И. Черняк, А.И. Вялков, С.В. Морозов, В.Б. Батоев
    Двустворчатый моллюск (Colletopterum ponderosum sedakovi) – универсальный биоиндикатор загрязнения бассейна озера Байкал стойкими органическим загрязнителями
    Инженерная экология, 2011, № 1, 55-63.
  360. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new polyfluorinated 1,4-naphthoquinones with divers substituents in the quinine moiety
    Bioorg. Med. Chem. 2011, V. 19, 256-260. doi: 10.1016/j.bmc.2010.11.027, IF=2.977
  361. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new polyfluorinated 1,4-naphthoquinones with divers substituents in the quinine moiety
    Bioorg. Med. Chem. 2011, V. 19, 256-260. doi: 10.1016/j.bmc.2010.11.027, IF=2.977
  362. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new polyfluorinated 1,4-naphthoquinones with divers substituents in the quinine moiety
    Bioorg. Med. Chem. 2011, V. 19, 256-260. doi: 10.1016/j.bmc.2010.11.027, IF=2.977
  363. А.А. Слепухина, В.О. Пустыльняк, А.Н. Антимонова, Н.И. Петренко, Э.Э. Шульц, А.Г. Покровский
    Особенности антинеопластического действия производных бетулиновой кислоты in vitro
    Вестн. НГУ Сер. Биол. Клин. Мед., 2011, Т. 9, № 1, 21-29. (FEATURES OF ANTINEOPLASTIC ACTION OF BETULINIC ACID DERIVATIVES IN VITRO/ Slepukhina A. A., Pustylnyak V. O., Antimonova A. N., Petrenko N. I., Schultz E. E., Pokrovsky A. G.// )
  364. А.А. Слепухина, В.О. Пустыльняк, А.Н. Антимонова, Н.И. Петренко, Э.Э. Шульц, А.Г. Покровский
    Особенности антинеопластического действия производных бетулиновой кислоты in vitro
    Вестн. НГУ Сер. Биол. Клин. Мед., 2011, Т. 9, № 1, 21-29. (FEATURES OF ANTINEOPLASTIC ACTION OF BETULINIC ACID DERIVATIVES IN VITRO/ Slepukhina A. A., Pustylnyak V. O., Antimonova A. N., Petrenko N. I., Schultz E. E., Pokrovsky A. G.// )
  365. В.А. Агеев, Д.Л. Макарова, Д.В. Домрачев, А.П. Родин, М.А. Ханина
    Изучение химического состава эфирного масла Aegopodium podagraria L. флоры Сибири
    Химия растительного сырья, 2011, № 1, 129-132.
  366. В.А. Агеев, Д.Л. Макарова, Д.В. Домрачев, А.П. Родин, М.А. Ханина
    Изучение химического состава эфирного масла Aegopodium podagraria L. флоры Сибири
    Химия растительного сырья, 2011, № 1, 129-132.
  367. В.А. Агеев, Д.Л. Макарова, Д.В. Домрачев, А.П. Родин, М.А. Ханина
    Изучение химического состава эфирного масла Aegopodium podagraria L. флоры Сибири
    Химия растительного сырья, 2011, № 1, 129-132.
  368. В.А. Агеев, Д.Л. Макарова, Д.В. Домрачев, А.П. Родин, М.А. Ханина
    Изучение химического состава эфирного масла Aegopodium podagraria L. флоры Сибири
    Химия растительного сырья, 2011, № 1, 129-132.
  369. М. П. Давыдова, С. Ф. Василевский, Г. А. Толстиков
    Новое превращение α-ацетиленовых кетонов под действием этилендиамина
    Известия Академии Наук. Сер. Хим., 2011, V. 60, N 1, 180-181. (New transformation of α-acetylenic ketones under the action of 1,2-diaminoethane/ M.P. Davydova, S.F. Vasilevskii, G.A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 1, pp. 188-190. doi:10.1007/s11172-011-0030-1), IF=0.629
  370. М. П. Давыдова, С. Ф. Василевский, Г. А. Толстиков
    Новое превращение α-ацетиленовых кетонов под действием этилендиамина
    Известия Академии Наук. Сер. Хим., 2011, V. 60, N 1, 180-181. (New transformation of α-acetylenic ketones under the action of 1,2-diaminoethane/ M.P. Davydova, S.F. Vasilevskii, G.A. Tolstikov// RUSS CHEM B+, 2011, V. 60, N 1, pp. 188-190. doi:10.1007/s11172-011-0030-1), IF=0.629
  371. Н.И. Иванчева, В.К. Бадаев, Е.В. Свиридова, Д.А. Николаев, И.В. Олейник, С.С. Иванчёв
    Особенности полимеризации этилена на самоиммобилизирующихся каталитических системах на основе бис(фенокси иминных) комплексов титана
    Журнал прикладной химии, 2011, Т. 84, В. 1, 118-123. (Specific features of ethylene polymerization on self-immobilizing catalytic systems based on titanium bis(phenoxy imine) complexes/ N. I. Ivancheva, V. K. Badaev, E. V. Sviridova, D. A. Nikolaev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2011, V. 84, N 1, pp. 118-123. doi:10.1134/S1070427211010204), IF=0.261
  372. Н.И. Иванчева, В.К. Бадаев, Е.В. Свиридова, Д.А. Николаев, И.В. Олейник, С.С. Иванчёв
    Особенности полимеризации этилена на самоиммобилизирующихся каталитических системах на основе бис(фенокси иминных) комплексов титана
    Журнал прикладной химии, 2011, Т. 84, В. 1, 118-123. (Specific features of ethylene polymerization on self-immobilizing catalytic systems based on titanium bis(phenoxy imine) complexes/ N. I. Ivancheva, V. K. Badaev, E. V. Sviridova, D. A. Nikolaev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2011, V. 84, N 1, pp. 118-123. doi:10.1134/S1070427211010204), IF=0.261
  373. Н.И. Иванчева, В.К. Бадаев, Е.В. Свиридова, Д.А. Николаев, И.В. Олейник, С.С. Иванчёв
    Особенности полимеризации этилена на самоиммобилизирующихся каталитических системах на основе бис(фенокси иминных) комплексов титана
    Журнал прикладной химии, 2011, Т. 84, В. 1, 118-123. (Specific features of ethylene polymerization on self-immobilizing catalytic systems based on titanium bis(phenoxy imine) complexes/ N. I. Ivancheva, V. K. Badaev, E. V. Sviridova, D. A. Nikolaev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2011, V. 84, N 1, pp. 118-123. doi:10.1134/S1070427211010204), IF=0.261
  374. Н.И. Иванчева, В.К. Бадаев, Е.В. Свиридова, Д.А. Николаев, И.В. Олейник, С.С. Иванчёв
    Особенности полимеризации этилена на самоиммобилизирующихся каталитических системах на основе бис(фенокси иминных) комплексов титана
    Журнал прикладной химии, 2011, Т. 84, В. 1, 118-123. (Specific features of ethylene polymerization on self-immobilizing catalytic systems based on titanium bis(phenoxy imine) complexes/ N. I. Ivancheva, V. K. Badaev, E. V. Sviridova, D. A. Nikolaev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2011, V. 84, N 1, pp. 118-123. doi:10.1134/S1070427211010204), IF=0.261
  375. Н.И. Иванчева, В.К. Бадаев, Е.В. Свиридова, Д.А. Николаев, И.В. Олейник, С.С. Иванчёв
    Особенности полимеризации этилена на самоиммобилизирующихся каталитических системах на основе бис(фенокси иминных) комплексов титана
    Журнал прикладной химии, 2011, Т. 84, В. 1, 118-123. (Specific features of ethylene polymerization on self-immobilizing catalytic systems based on titanium bis(phenoxy imine) complexes/ N. I. Ivancheva, V. K. Badaev, E. V. Sviridova, D. A. Nikolaev, I. V. Oleinik, S. S. Ivanchev// RUSS J APPL CHEM+, 2011, V. 84, N 1, pp. 118-123. doi:10.1134/S1070427211010204), IF=0.261
  376. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Е.М. Усков, Л.А. Глинская, С.А. Попов, А.В. Ткачев
    Синтез и фотолюминесценция хиральных соединений [ZnLCl2] • EtOH и ZnLCl2, где L – производное (+)-3-карена, содержащее фрагнменты пиразолина и хинолина. Кристаллическая структура [ZnLCl2] •EtOH
    Координационная химия, 2011, Т. 37, № 1, 3–9. (Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036), IF=0.591
  377. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Е.М. Усков, Л.А. Глинская, С.А. Попов, А.В. Ткачев
    Синтез и фотолюминесценция хиральных соединений [ZnLCl2] • EtOH и ZnLCl2, где L – производное (+)-3-карена, содержащее фрагнменты пиразолина и хинолина. Кристаллическая структура [ZnLCl2] •EtOH
    Координационная химия, 2011, Т. 37, № 1, 3–9. (Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036), IF=0.591
  378. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Е.М. Усков, Л.А. Глинская, С.А. Попов, А.В. Ткачев
    Синтез и фотолюминесценция хиральных соединений [ZnLCl2] • EtOH и ZnLCl2, где L – производное (+)-3-карена, содержащее фрагнменты пиразолина и хинолина. Кристаллическая структура [ZnLCl2] •EtOH
    Координационная химия, 2011, Т. 37, № 1, 3–9. (Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036), IF=0.591
  379. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Е.М. Усков, Л.А. Глинская, С.А. Попов, А.В. Ткачев
    Синтез и фотолюминесценция хиральных соединений [ZnLCl2] • EtOH и ZnLCl2, где L – производное (+)-3-карена, содержащее фрагнменты пиразолина и хинолина. Кристаллическая структура [ZnLCl2] •EtOH
    Координационная химия, 2011, Т. 37, № 1, 3–9. (Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036), IF=0.591
  380. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Е.М. Усков, Л.А. Глинская, С.А. Попов, А.В. Ткачев
    Синтез и фотолюминесценция хиральных соединений [ZnLCl2] • EtOH и ZnLCl2, где L – производное (+)-3-карена, содержащее фрагнменты пиразолина и хинолина. Кристаллическая структура [ZnLCl2] •EtOH
    Координационная химия, 2011, Т. 37, № 1, 3–9. (Synthesis and photoluminescence of the chiral compounds [ZnLCl2] • EtOH и ZnLCl2, where L is the (+)-3-Carene derivative containing pyrazoline and quinoline fragments: Crystal structure of [ZnLCl2] •EtOH/ S.V. Larionov, Z.A. Savel'Eva, R.F. Klevtsova, E.M. Uskov, L.A. Glinskaya, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2011, V. 37, N 1, pp 1-7. doi:10.1134/S1070328410121036), IF=0.591
  381. S. F.Vasilevsky, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, V.I. Mamatuyk, I.V. Alabugin
    Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 1, 62-65. doi:10.1016/j.bmcl.2010.11.072, IF=2.661
  382. S. F.Vasilevsky, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, V.I. Mamatuyk, I.V. Alabugin
    Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 1, 62-65. doi:10.1016/j.bmcl.2010.11.072, IF=2.661
  383. S. F.Vasilevsky, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, V.I. Mamatuyk, I.V. Alabugin
    Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry
    Bioorg. Med. Chem. Lett., 2011, V. 21, N 1, 62-65. doi:10.1016/j.bmcl.2010.11.072, IF=2.661
  384. Д.Ф. Августинович, М.К. Фомина, И.В. Сорокина, Т.Г. Толстикова
    Эффекты хронического введения комплекса буспирона с глицирризиновой кислотой на биохимические показатели крови тревожно-депрессивных мышей
    Вопр. Биол. Мед. Фарм. Хим., 2011, № 1, 28-30.

2010

Reviews, articles

  1. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  2. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  3. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  4. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  5. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  6. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  7. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  8. Е.К. Емельянова, А.Ю. Алексеев, А.В. Мокеева, М.В. Тарасова, М.А. Шестопалов, Е.В. Карпова, В.А. Забелин, А.М. Шестопалов, Т.Н. Ильичева
    Биорекультивация загрязненных нефтью объектов
    Вестн. НГУ Сер. Биол. Клин. Мед., 2010 , Т. 8, № 4, С. 155-161.
  9. С.Г. Ильясов, М.В. Чикина, Т.Г. Толстикова
    Синтез 4,5-дизамещенных производных имидазолин-2-онов взаимодействием глиоксаля с моноалкилмочевинами
    Ползуновский вестник, 2010, № 4-1, C. 9-12.
  10. С.Г. Ильясов, М.В. Чикина, Т.Г. Толстикова
    Синтез 4,5-дизамещенных производных имидазолин-2-онов взаимодействием глиоксаля с моноалкилмочевинами
    Ползуновский вестник, 2010, № 4-1, C. 9-12.
  11. A.V. Belovodskii, E.E. Shul'ts, M.M. Shakirov, V.E. Romanov, B.Z. Elmuradov, K.M. Shakhidoyatov, G.A. Tolstikov
    Synthesis of hybrid molecules containing fragments of sesquiterpene lactones and plant alkaloids
    Chemistry of Natural Compounds, 2010, V. 46, N 6, pp 880-885. doi:10.1007/s10600-011-9774-y, IF=0.572
  12. A.V. Belovodskii, E.E. Shul'ts, M.M. Shakirov, V.E. Romanov, B.Z. Elmuradov, K.M. Shakhidoyatov, G.A. Tolstikov
    Synthesis of hybrid molecules containing fragments of sesquiterpene lactones and plant alkaloids
    Chemistry of Natural Compounds, 2010, V. 46, N 6, pp 880-885. doi:10.1007/s10600-011-9774-y, IF=0.572
  13. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после ее дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (_Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104)
  14. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после ее дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (_Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104)
  15. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после ее дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (_Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104)
  16. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после ее дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (_Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104)
  17. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после ее дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (_Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V.V. Martemyanov, D.V. Domrachev, S.V. Pavlushin, I.A. Belousova, S.A. Bakhvalov, A.V. Tkachev, V.V. Glupov// Doklady Biological Sciences, 2010, V. 435, N 1, pp 407-410 doi:10.1134/S0012496610060104)
  18. A.A. Bobko, I.A. Kirilyuk, N.P. Gritsan, D.N. Polovyanenko, I.A. Grigor’ev, V.V. Khramtsov, E.G. Bagryanskaya
    EPR and Quantum Chemical Studies of the pH-sensitive Imidazoline and Imidazolidine Nitroxides with Bulky Substituents
    Appl. Magn. Reson., 2010, V. 39, 437–451. doi:10.1007/s00723-010-0179-z, IF=0.819
  19. A.A. Bobko, I.A. Kirilyuk, N.P. Gritsan, D.N. Polovyanenko, I.A. Grigor’ev, V.V. Khramtsov, E.G. Bagryanskaya
    EPR and Quantum Chemical Studies of the pH-sensitive Imidazoline and Imidazolidine Nitroxides with Bulky Substituents
    Appl. Magn. Reson., 2010, V. 39, 437–451. doi:10.1007/s00723-010-0179-z, IF=0.819
  20. A.A. Bobko, I.A. Kirilyuk, N.P. Gritsan, D.N. Polovyanenko, I.A. Grigor’ev, V.V. Khramtsov, E.G. Bagryanskaya
    EPR and Quantum Chemical Studies of the pH-sensitive Imidazoline and Imidazolidine Nitroxides with Bulky Substituents
    Appl. Magn. Reson., 2010, V. 39, 437–451. doi:10.1007/s00723-010-0179-z, IF=0.819
  21. A.A. Bobko, I.A. Kirilyuk, N.P. Gritsan, D.N. Polovyanenko, I.A. Grigor’ev, V.V. Khramtsov, E.G. Bagryanskaya
    EPR and Quantum Chemical Studies of the pH-sensitive Imidazoline and Imidazolidine Nitroxides with Bulky Substituents
    Appl. Magn. Reson., 2010, V. 39, 437–451. doi:10.1007/s00723-010-0179-z, IF=0.819
  22. Н.А. Жукова, И.В. Сорокина, Т.Г. Толстикова, Е.Л. Лушникова, Л.М. Непомнящих, Д.Е. Семенов
    Структура печени мышей с перевитой карциномой легких Льюис при полихимиотерапии и коррекции бетулоновой кислотой и её производными
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 108-112. (Structure of the Liver in Mice with Transplanted Lewis Carcinoma during Polychemotherapy and Correction with Betulonic Acid and Its Derivatives/ N. A. Zhukova, I. V. Sorokina, T. G. Tolstikova, E. L. Lushnikova, L. M. Nepomnyashih, D. E. Semenov// B EXP BIOL MED+, 2010, V. 150, N 1, pp 96-99. doi:10.1007/s10517-010-1079-9), IF=0.264
  23. Н.А. Жукова, И.В. Сорокина, Т.Г. Толстикова, Е.Л. Лушникова, Л.М. Непомнящих, Д.Е. Семенов
    Структура печени мышей с перевитой карциномой легких Льюис при полихимиотерапии и коррекции бетулоновой кислотой и её производными
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 108-112. (Structure of the Liver in Mice with Transplanted Lewis Carcinoma during Polychemotherapy and Correction with Betulonic Acid and Its Derivatives/ N. A. Zhukova, I. V. Sorokina, T. G. Tolstikova, E. L. Lushnikova, L. M. Nepomnyashih, D. E. Semenov// B EXP BIOL MED+, 2010, V. 150, N 1, pp 96-99. doi:10.1007/s10517-010-1079-9), IF=0.264
  24. Н.А. Жукова, И.В. Сорокина, Т.Г. Толстикова, Е.Л. Лушникова, Л.М. Непомнящих, Д.Е. Семенов
    Структура печени мышей с перевитой карциномой легких Льюис при полихимиотерапии и коррекции бетулоновой кислотой и её производными
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 108-112. (Structure of the Liver in Mice with Transplanted Lewis Carcinoma during Polychemotherapy and Correction with Betulonic Acid and Its Derivatives/ N. A. Zhukova, I. V. Sorokina, T. G. Tolstikova, E. L. Lushnikova, L. M. Nepomnyashih, D. E. Semenov// B EXP BIOL MED+, 2010, V. 150, N 1, pp 96-99. doi:10.1007/s10517-010-1079-9), IF=0.264
  25. И.А. Кирилюк, В.И. Каледин, Н.А. Попова, В.П. Николин, Е.Д. Васильева, И.А. Григорьев, Л.М. Непомнящих
    Нитроксильный антиоксидант ТРРА-ТЕМРО повышает эффективность противоопухолевой терапии на модели перевиваемой лимфосаркомы мышей
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 85-89. (Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2), IF=0.264
  26. И.А. Кирилюк, В.И. Каледин, Н.А. Попова, В.П. Николин, Е.Д. Васильева, И.А. Григорьев, Л.М. Непомнящих
    Нитроксильный антиоксидант ТРРА-ТЕМРО повышает эффективность противоопухолевой терапии на модели перевиваемой лимфосаркомы мышей
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 85-89. (Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2), IF=0.264
  27. И.А. Кирилюк, В.И. Каледин, Н.А. Попова, В.П. Николин, Е.Д. Васильева, И.А. Григорьев, Л.М. Непомнящих
    Нитроксильный антиоксидант ТРРА-ТЕМРО повышает эффективность противоопухолевой терапии на модели перевиваемой лимфосаркомы мышей
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 85-89. (Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2), IF=0.264
  28. И.А. Кирилюк, В.И. Каледин, Н.А. Попова, В.П. Николин, Е.Д. Васильева, И.А. Григорьев, Л.М. Непомнящих
    Нитроксильный антиоксидант ТРРА-ТЕМРО повышает эффективность противоопухолевой терапии на модели перевиваемой лимфосаркомы мышей
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 85-89. (Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2), IF=0.264
  29. И.А. Кирилюк, В.И. Каледин, Н.А. Попова, В.П. Николин, Е.Д. Васильева, И.А. Григорьев, Л.М. Непомнящих
    Нитроксильный антиоксидант ТРРА-ТЕМРО повышает эффективность противоопухолевой терапии на модели перевиваемой лимфосаркомы мышей
    Бюлл. Эксп. Биол. Мед., 2010, Т. 150, № 7, С. 85-89. (Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2), IF=0.264
  30. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  31. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  32. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  33. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  34. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  35. E.N. Medvedeva, N.A. Neverova, T.E. Fedorova, V.A. Babkin, E.S. Meteleva, A.V. Dushkin, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh
    _Structural transformation of arabinogalactan from the Siberian Larch during mechanochemical processing and the biological properties of the products
    Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101, IF=0.472
  36. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  37. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  38. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  39. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  40. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  41. О.Б. Казакова, Н.И. Медведева, И.П. Байкова, Г.А. Толстиков, Т.В. Лопатина, М.С. Юнусов, Л. Запрутко
    Синтез ацилатов тритерпеноидов – эффективных ингибиторов вирусов гриппа А (H1N1) и папилломы
    Биоорганическая химия, 2010, V. 36, N 6, С. 841-848. (Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses/ O. B. Kazakova, N. I. Medvedeva, I. P. Baikova, G. A. Tolstikov, T. V. Lopatina, M. S. Yunusov, L. Zaprutko// RUSS J BIOORG CHEM+, 2010, V.36, N 6, pp 771-778. doi:10.1134/S1068162010060142), IF=0.711
  42. В.В. Шелковников, Е.Ф. Пен, Е.В. Васильев, И.Ш. Штейнберг, П.Е. Твердохлеб, Ю. А. Щепеткин
    Методы исследования голографических фотополимерных материалов
    Журнал структурной химии, 2010, Т. 51, № 7 (дополн.), S96-S103. (Methods for investigation of holographic photopolymer materials/ V. V. Shelkovnikov, E. F. Pen, E. V. Vasilyev, I. Sh. Steinberg, P. E. Tverdokhleb, Yu. A. Shepetkin// J STRUCT CHEM+, 2010, V. 51, N 1 Supplement, pp 91-99. doi:10.1007/s10947-010-0195-8), IF=0.453
  43. В.В. Шелковников, Е.Ф. Пен, Е.В. Васильев, И.Ш. Штейнберг, П.Е. Твердохлеб, Ю. А. Щепеткин
    Методы исследования голографических фотополимерных материалов
    Журнал структурной химии, 2010, Т. 51, № 7 (дополн.), S96-S103. (Methods for investigation of holographic photopolymer materials/ V. V. Shelkovnikov, E. F. Pen, E. V. Vasilyev, I. Sh. Steinberg, P. E. Tverdokhleb, Yu. A. Shepetkin// J STRUCT CHEM+, 2010, V. 51, N 1 Supplement, pp 91-99. doi:10.1007/s10947-010-0195-8), IF=0.453
  44. В.В. Шелковников, Е.Ф. Пен, Е.В. Васильев, И.Ш. Штейнберг, П.Е. Твердохлеб, Ю. А. Щепеткин
    Методы исследования голографических фотополимерных материалов
    Журнал структурной химии, 2010, Т. 51, № 7 (дополн.), S96-S103. (Methods for investigation of holographic photopolymer materials/ V. V. Shelkovnikov, E. F. Pen, E. V. Vasilyev, I. Sh. Steinberg, P. E. Tverdokhleb, Yu. A. Shepetkin// J STRUCT CHEM+, 2010, V. 51, N 1 Supplement, pp 91-99. doi:10.1007/s10947-010-0195-8), IF=0.453
  45. В.В. Шелковников, Е.Ф. Пен, Е.В. Васильев, И.Ш. Штейнберг, П.Е. Твердохлеб, Ю. А. Щепеткин
    Методы исследования голографических фотополимерных материалов
    Журнал структурной химии, 2010, Т. 51, № 7 (дополн.), S96-S103. (Methods for investigation of holographic photopolymer materials/ V. V. Shelkovnikov, E. F. Pen, E. V. Vasilyev, I. Sh. Steinberg, P. E. Tverdokhleb, Yu. A. Shepetkin// J STRUCT CHEM+, 2010, V. 51, N 1 Supplement, pp 91-99. doi:10.1007/s10947-010-0195-8), IF=0.453
  46. И.И. Олейник, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Удобный способ синтеза 3,5-дизамещенных N-салицилиден-4-аллилоксианилинов
    Журнал органической химии, 2010, Т. 46, N 12, C. 1873-1875. (Convenient synthesis of 3,5-disubstituted N-Salicylidene-4-allyloxyanilines/ I. I. Oleinik, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 12, pp 1888-1890. doi:10.1134/S1070428010120195), IF=0.524
  47. V. A. Samsonov, G. E. Sal'nikov, L. B. Volodarskii
    Semmler-Wolff aromatization of 4-hydroxyimino-4,5,6,7-tetrahydro-[2,1,3]benzoxadiazole and 4-hydroxyimino-4,5,6,7-tetrahydro[2,1,3]benzoxadiazole 1-oxide and some properties of the obtained amines
    Chemistry of Heterocyclic Compounds, 2010, V. 46, N 7, pp 868-878. doi:10.1007/s10593-010-0596-9, IF=0.699
  48. A.П. Крысин, Н.У. Халикова, T.B. Хлебникова, Н.И. Ногина, В.И. Маматюк
    γ-Гидроксипропилирование 2,6-диалкил(арил)фенолов аллиловым спиртом и его производными
    Журнал общей химии, 2010, Т. 80, N 11, C. 1826-1833. (γ-hydroxypropylation of 2,6-dialkyl(aryl)phenols with allyl alcohol and its derivatives/ A. P. Krysin, N. U. Khalikova, T. B. Khlebnikova, N. I. Nogina, V. I. Mamatyuk// RUSS J GEN CHEM+, 2010, V. 80, N 11, pp 2290-2297 doi:10.1134/S1070363210110101), IF=0.393
  49. A.П. Крысин, Н.У. Халикова, T.B. Хлебникова, Н.И. Ногина, В.И. Маматюк
    γ-Гидроксипропилирование 2,6-диалкил(арил)фенолов аллиловым спиртом и его производными
    Журнал общей химии, 2010, Т. 80, N 11, C. 1826-1833. (γ-hydroxypropylation of 2,6-dialkyl(aryl)phenols with allyl alcohol and its derivatives/ A. P. Krysin, N. U. Khalikova, T. B. Khlebnikova, N. I. Nogina, V. I. Mamatyuk// RUSS J GEN CHEM+, 2010, V. 80, N 11, pp 2290-2297 doi:10.1134/S1070363210110101), IF=0.393
  50. A.П. Крысин, Н.У. Халикова, T.B. Хлебникова, Н.И. Ногина, В.И. Маматюк
    γ-Гидроксипропилирование 2,6-диалкил(арил)фенолов аллиловым спиртом и его производными
    Журнал общей химии, 2010, Т. 80, N 11, C. 1826-1833. (γ-hydroxypropylation of 2,6-dialkyl(aryl)phenols with allyl alcohol and its derivatives/ A. P. Krysin, N. U. Khalikova, T. B. Khlebnikova, N. I. Nogina, V. I. Mamatyuk// RUSS J GEN CHEM+, 2010, V. 80, N 11, pp 2290-2297 doi:10.1134/S1070363210110101), IF=0.393
  51. G. V. Giniyatullina, O. B. Kazakova, G. A. Tolstikov
    Synthesis of 3-deoxy-3β-(3-aminopropoxyamino) derivatives of oleanolic and ursolic acids
    .Chemistry of Natural Compounds, 2010, V. 46, N 5, pp 760-762. doi:10.1007/s10600-010-9734-y, IF=0.572
  52. G. V. Giniyatullina, O. B. Kazakova, G. A. Tolstikov
    Synthesis of 3-deoxy-3β-(3-aminopropoxyamino) derivatives of oleanolic and ursolic acids
    .Chemistry of Natural Compounds, 2010, V. 46, N 5, pp 760-762. doi:10.1007/s10600-010-9734-y, IF=0.572
  53. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов
    Журнал органической химии, 2010, Т. 46, N 11, C. 1591-1617. (Transformations of peroxide products of olefins ozonolysis/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, G. A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 11, pp 1593-1621. doi:10.1134/S1070428010110011), IF=0.524
  54. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов
    Журнал органической химии, 2010, Т. 46, N 11, C. 1591-1617. (Transformations of peroxide products of olefins ozonolysis/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, G. A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 11, pp 1593-1621. doi:10.1134/S1070428010110011), IF=0.524
  55. Г.Ю. Ишмуратов, Ю.В. Легостаева, Л.П. Боцман, Г.А. Толстиков
    Превращения перекисных продуктов озонолиза олефинов
    Журнал органической химии, 2010, Т. 46, N 11, C. 1591-1617. (Transformations of peroxide products of olefins ozonolysis/ G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, G. A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 11, pp 1593-1621. doi:10.1134/S1070428010110011), IF=0.524
  56. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
    One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
    Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
  57. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
    One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
    Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
  58. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
    One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
    Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
  59. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
    One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
    Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
  60. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
    One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
    Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
  61. А.П. Крысин, И.И. Пустовских, В.А. Коптюг
    О синтезе 4-(ω-гидроксиалкил)-2,6-ди-трет-бутилфенолов и свойствах сульфидов, полученных на их основе
    Журнал общей химии, 2010, Т. 80, N. 10, C. 1691-1696. (Synthesis of 4-(ω-hydroxyalkyl)-2,6-di-tert-butylphenols and the properties of related sulfides/ A. P. Krysin, I. I. Pustovskikh, V. A. Koptyug// RUSS J GEN CHEM+, 2010, V. 80, N 10, pp 2001-2006. doi:10.1134/S1070363210100208), IF=0.393
  62. В.А. Васин, П.С. Петров, А.М. Генаев, В.А. Гиндин, В.В. Разин
    О пространственном строении метил 6,7-эндо,син-дибром-7-анти-(фенилсульфонил)бицикло[3.1.1]гептан-6-экзо-карбоксилата
    Журнал структурной химии, 2010, Т. 51, № 5, C. 982-988. (On the spatial structure of methyl 6,7-endo, sin-dibrom-7-anti-(phenylsulfonyl) bicyclo[3.1.1]heptane-6-exo-carboxylate/ V. A. Vasin, P. S. Petrov, M. Genaev, V. A. Gindin, V. V. Razin// J STRUCT CHEM+, 2010, V. 51, N 5, pp 949-955. doi:10.1007/s10947-010-0144-6), IF=0.453
  63. В.А. Васин, П.С. Петров, А.М. Генаев, В.А. Гиндин, В.В. Разин
    О пространственном строении метил 6,7-эндо,син-дибром-7-анти-(фенилсульфонил)бицикло[3.1.1]гептан-6-экзо-карбоксилата
    Журнал структурной химии, 2010, Т. 51, № 5, C. 982-988. (On the spatial structure of methyl 6,7-endo, sin-dibrom-7-anti-(phenylsulfonyl) bicyclo[3.1.1]heptane-6-exo-carboxylate/ V. A. Vasin, P. S. Petrov, M. Genaev, V. A. Gindin, V. V. Razin// J STRUCT CHEM+, 2010, V. 51, N 5, pp 949-955. doi:10.1007/s10947-010-0144-6), IF=0.453
  64. В.А. Васин, П.С. Петров, А.М. Генаев, В.А. Гиндин, В.В. Разин
    О пространственном строении метил 6,7-эндо,син-дибром-7-анти-(фенилсульфонил)бицикло[3.1.1]гептан-6-экзо-карбоксилата
    Журнал структурной химии, 2010, Т. 51, № 5, C. 982-988. (On the spatial structure of methyl 6,7-endo, sin-dibrom-7-anti-(phenylsulfonyl) bicyclo[3.1.1]heptane-6-exo-carboxylate/ V. A. Vasin, P. S. Petrov, M. Genaev, V. A. Gindin, V. V. Razin// J STRUCT CHEM+, 2010, V. 51, N 5, pp 949-955. doi:10.1007/s10947-010-0144-6), IF=0.453
  65. В.А. Васин, П.С. Петров, А.М. Генаев, В.А. Гиндин, В.В. Разин
    О пространственном строении метил 6,7-эндо,син-дибром-7-анти-(фенилсульфонил)бицикло[3.1.1]гептан-6-экзо-карбоксилата
    Журнал структурной химии, 2010, Т. 51, № 5, C. 982-988. (On the spatial structure of methyl 6,7-endo, sin-dibrom-7-anti-(phenylsulfonyl) bicyclo[3.1.1]heptane-6-exo-carboxylate/ V. A. Vasin, P. S. Petrov, M. Genaev, V. A. Gindin, V. V. Razin// J STRUCT CHEM+, 2010, V. 51, N 5, pp 949-955. doi:10.1007/s10947-010-0144-6), IF=0.453
  66. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453
  67. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453
  68. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453
  69. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453
  70. А.Б. Бурдуков, К.С. Беккер, Г.А. Степанов, А.Л. Богатырев, Н.В. Первухина, А.С. Богомяков, В.А. Резников
    Структура и магнитные свойства новых хелатных комплексов меди (II) и никеля(II) с нитроксильным радикалом этил-2-(1-оксил-2,2,5,5-тетраметилимидазолидин-4-илиден)-3-оксопропаноатом
    Журнал структурной химии, 2010, Т. 51, № 5, C. 951-956. (Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3), IF=0.453
  71. H.J. Frohn, V.V. Bardin
    Explored routes to unknown polyfluoroorganyliodine hexafluorides, RFIF6
    J. Fluorine Chem., 2010, V. 131, N 10, 1000-1006. doi:10.1016/j.jfluchem.2010.07.005, IF=1.73
  72. H.-J. Frohn, M. Giesen, V.V. Bardin
    New types of asymmetrical bromonium salts [RF(RF')Br]Y where RF and/or RF' represent perfluorinated aryl, alkenyl, and alkynyl groups
    J. Fluorine Chem., 2010, V. 131, N 10, 969-974. doi:10.1016/j.jfluchem.2010.06.022, IF=1.73
  73. H.-J. Frohn, M. Giesen, V.V. Bardin
    New types of asymmetrical bromonium salts [RF(RF')Br]Y where RF and/or RF' represent perfluorinated aryl, alkenyl, and alkynyl groups
    J. Fluorine Chem., 2010, V. 131, N 10, 969-974. doi:10.1016/j.jfluchem.2010.06.022, IF=1.73
  74. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, N.V. Kuratieva, A.Yu. Makarov, M.M. Shakirov, A.V. Alexeyev, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The first observation of the E,Z configuration of Ar-X-N=S=N-X-Ar (X = S, Se) chains in the crystalline state
    Eur. J. Inorg. Chem., 2010, 30, 4801-4810. doi:10.1002/ejic.201000607, IF=2.94
  75. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, N.V. Kuratieva, A.Yu. Makarov, M.M. Shakirov, A.V. Alexeyev, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The first observation of the E,Z configuration of Ar-X-N=S=N-X-Ar (X = S, Se) chains in the crystalline state
    Eur. J. Inorg. Chem., 2010, 30, 4801-4810. doi:10.1002/ejic.201000607, IF=2.94
  76. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, N.V. Kuratieva, A.Yu. Makarov, M.M. Shakirov, A.V. Alexeyev, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The first observation of the E,Z configuration of Ar-X-N=S=N-X-Ar (X = S, Se) chains in the crystalline state
    Eur. J. Inorg. Chem., 2010, 30, 4801-4810. doi:10.1002/ejic.201000607, IF=2.94
  77. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, N.V. Kuratieva, A.Yu. Makarov, M.M. Shakirov, A.V. Alexeyev, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The first observation of the E,Z configuration of Ar-X-N=S=N-X-Ar (X = S, Se) chains in the crystalline state
    Eur. J. Inorg. Chem., 2010, 30, 4801-4810. doi:10.1002/ejic.201000607, IF=2.94
  78. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, N.V. Kuratieva, A.Yu. Makarov, M.M. Shakirov, A.V. Alexeyev, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The first observation of the E,Z configuration of Ar-X-N=S=N-X-Ar (X = S, Se) chains in the crystalline state
    Eur. J. Inorg. Chem., 2010, 30, 4801-4810. doi:10.1002/ejic.201000607, IF=2.94
  79. Н.В. Чуканов, С.А. Попов, Т.Н. Дребущак, В.А. Резников
    Механизм миграции заместителя в производных 1,2,3,7a-тетрагидроимидазо[1,2-b]изоксазола
    Известия Академии наук. Сер.хим., 2010, № 9, C. 1769-1777. (Mechanism of the migration of the substituent in 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives/ N.V. Chukanov, S.A. Popov, T.N. Drebushchak, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 9, pp 1817-1826. doi:10.1007/s11172-010-0318-6), IF=0.416
  80. Н.В. Чуканов, С.А. Попов, Т.Н. Дребущак, В.А. Резников
    Механизм миграции заместителя в производных 1,2,3,7a-тетрагидроимидазо[1,2-b]изоксазола
    Известия Академии наук. Сер.хим., 2010, № 9, C. 1769-1777. (Mechanism of the migration of the substituent in 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives/ N.V. Chukanov, S.A. Popov, T.N. Drebushchak, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 9, pp 1817-1826. doi:10.1007/s11172-010-0318-6), IF=0.416
  81. В.П. Кривопалов, М.Б. Бушуев, Ю.В. Гатилов, О.П. Шкурко
    Синтез симметричных ди(пиримидин-2-ил)-1,2,4-триазолов и ди(пиримидин-2-ил)-1,2,4,5-тетразинов
    Известия Академии наук. Сер.хим., 2010, № 9, C. 1760-1768. (Synthesis of symmetrical di(pyrimidin-2-yl)-1,2,4-triazoles and di(pyrimidin-2-yl)-1,2,4,5-tetrazines/ V.P. Krivopalov, M.B. Bushuev, Yu.V. Gatilov, Yu.V. Gatilov// RUSS CHEM B+, 2010, V. 59, N 9, pp 1808-1816. doi:10.1007/s11172-010-0317-7), IF=0.416
  82. З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, С.А. Попов, А.В. Ткачев, С.В. Ларионов
    Синтез и структура хиральных комплексов PdCl2 с пиразолинолхинолином и пиразолинхинолином, построенным на основе монотерпеноида (+)-3-карена
    Координационная химия, 2010, Т. 36, № 9, C. 691–698. (Chiral complexes of PdCl2 with hydroxypyrazolylquinoline and pyrazolylquinoline based on the monoterpenoid (+)-3-carene: Synthesis and structures/ Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, S.V. Larionov, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 9, pp 685-692. doi:10.1134/S1070328410090083), IF=0.605
  83. З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, С.А. Попов, А.В. Ткачев, С.В. Ларионов
    Синтез и структура хиральных комплексов PdCl2 с пиразолинолхинолином и пиразолинхинолином, построенным на основе монотерпеноида (+)-3-карена
    Координационная химия, 2010, Т. 36, № 9, C. 691–698. (Chiral complexes of PdCl2 with hydroxypyrazolylquinoline and pyrazolylquinoline based on the monoterpenoid (+)-3-carene: Synthesis and structures/ Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, S.V. Larionov, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 9, pp 685-692. doi:10.1134/S1070328410090083), IF=0.605
  84. З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, С.А. Попов, А.В. Ткачев, С.В. Ларионов
    Синтез и структура хиральных комплексов PdCl2 с пиразолинолхинолином и пиразолинхинолином, построенным на основе монотерпеноида (+)-3-карена
    Координационная химия, 2010, Т. 36, № 9, C. 691–698. (Chiral complexes of PdCl2 with hydroxypyrazolylquinoline and pyrazolylquinoline based on the monoterpenoid (+)-3-carene: Synthesis and structures/ Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, S.V. Larionov, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 9, pp 685-692. doi:10.1134/S1070328410090083), IF=0.605
  85. З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, С.А. Попов, А.В. Ткачев, С.В. Ларионов
    Синтез и структура хиральных комплексов PdCl2 с пиразолинолхинолином и пиразолинхинолином, построенным на основе монотерпеноида (+)-3-карена
    Координационная химия, 2010, Т. 36, № 9, C. 691–698. (Chiral complexes of PdCl2 with hydroxypyrazolylquinoline and pyrazolylquinoline based on the monoterpenoid (+)-3-carene: Synthesis and structures/ Z.A. Savel'eva, R.F. Klevtsova, L.A. Glinskaya, S.V. Larionov, S.A. Popov, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 9, pp 685-692. doi:10.1134/S1070328410090083), IF=0.605
  86. H.-J. Frohn, M. Giesen, D. Welting, V.V. Bardin
    Bis(perfluoroorganyl)bromonium salts [(RF)2Br]Y (RF = aryl, alkenyl, and alkynyl
    J. Fluorine Chem., 2010, V. 131, N 9, 922-932. doi:10.1016/j.jfluchem.2010.06.006, IF=1.73
  87. H.-J. Frohn, M. Giesen, D. Welting, V.V. Bardin
    Bis(perfluoroorganyl)bromonium salts [(RF)2Br]Y (RF = aryl, alkenyl, and alkynyl
    J. Fluorine Chem., 2010, V. 131, N 9, 922-932. doi:10.1016/j.jfluchem.2010.06.006, IF=1.73
  88. H.-J. Frohn, M. Giesen, D. Welting, V.V. Bardin
    Bis(perfluoroorganyl)bromonium salts [(RF)2Br]Y (RF = aryl, alkenyl, and alkynyl
    J. Fluorine Chem., 2010, V. 131, N 9, 922-932. doi:10.1016/j.jfluchem.2010.06.006, IF=1.73
  89. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  90. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  91. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  92. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  93. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  94. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  95. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  96. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  97. N.A. Semenov, N.A. Pushkarevsky, A.V. Lonchakov, A.S. Bogomyakov, E.A. Pritchina, E.A. Suturina, N.P. Gritsan, S.N. Konchenko, R. Mews, V.I. Ovcharenko, A.V. Zibarev
    Heterospin π-heterocyclic radical-anion salt: synthesis, structure and magnetic properties of decamethylchromocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
    Inorg. Chem., 2010, V. 49, N 16, 7558-7564. doi:10.1021/ic101064c, IF=4.657
  98. R. Halevy, V. Tormyshev, A. Blank
    Microimaging of Oxygen Concentration near Live Photosynthetic Cells by Electron Spin Resonance
    Biophys. J., 2010, V. 99, N 3, 971–978. doi:10.1016/j.bpj.2010.05.002, IF=4.389
  99. R. Halevy, V. Tormyshev, A. Blank
    Microimaging of Oxygen Concentration near Live Photosynthetic Cells by Electron Spin Resonance
    Biophys. J., 2010, V. 99, N 3, 971–978. doi:10.1016/j.bpj.2010.05.002, IF=4.389
  100. Т.Г. Толстикова, М.В. Хвостов, А.О. Брызгалов, А.В. Душкин, Г.А. Толстиков
    Арабиногалактан - растительный полисахарид как новое средство для клатрирования фармаконов
    Доклады Академии наук, 2010, T. 433, № 5, C. 713-714. (Arabinogalactan, a plant polysaccharide, as a new tool for pharmacon clathration/ T. G. Tolstikova, M. V. Khvostov, A. O. Bryzgalov, A. V. Dushkin, G. A. Tolstikov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 247-248. doi:10.1134/S0012496610040034)
  101. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  102. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  103. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  104. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  105. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  106. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  107. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  108. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
    Photoinduced tautomeric transformations of xanthurenic acid
    Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
  109. М.Ю. Васильева, С.П. Федоров, Д.А. Николаев, И.И. Олейник, С.С. Иванчёв
    Полимеризация этилена в присутствии бис(феноксииминных) комплексов титана, содержащих различные заместители в феноксигруппе
    Высокомол. Соед. Сер. Б, 2010 , Т. 52, N 8, С. 1483-1490. (Polymerization of ethylene in the presence of bis(phenoxyimine) complexes of titanium chloride that contain various substituents in a phenoxy group/ M. Yu. Vasil’eva, S. P. Fedorov, D. A. Nikolaev, I. I. Oleinik, S. S. Ivanchev// Polymer Science Series B, 2010, V. 52, IN 7-8, pp 443-449 doi:10.1134/S1560090410070080), IF=0.421
  110. М.Ю. Васильева, С.П. Федоров, Д.А. Николаев, И.И. Олейник, С.С. Иванчёв
    Полимеризация этилена в присутствии бис(феноксииминных) комплексов титана, содержащих различные заместители в феноксигруппе
    Высокомол. Соед. Сер. Б, 2010 , Т. 52, N 8, С. 1483-1490. (Polymerization of ethylene in the presence of bis(phenoxyimine) complexes of titanium chloride that contain various substituents in a phenoxy group/ M. Yu. Vasil’eva, S. P. Fedorov, D. A. Nikolaev, I. I. Oleinik, S. S. Ivanchev// Polymer Science Series B, 2010, V. 52, IN 7-8, pp 443-449 doi:10.1134/S1560090410070080), IF=0.421
  111. М.Ю. Васильева, С.П. Федоров, Д.А. Николаев, И.И. Олейник, С.С. Иванчёв
    Полимеризация этилена в присутствии бис(феноксииминных) комплексов титана, содержащих различные заместители в феноксигруппе
    Высокомол. Соед. Сер. Б, 2010 , Т. 52, N 8, С. 1483-1490. (Polymerization of ethylene in the presence of bis(phenoxyimine) complexes of titanium chloride that contain various substituents in a phenoxy group/ M. Yu. Vasil’eva, S. P. Fedorov, D. A. Nikolaev, I. I. Oleinik, S. S. Ivanchev// Polymer Science Series B, 2010, V. 52, IN 7-8, pp 443-449 doi:10.1134/S1560090410070080), IF=0.421
  112. М.Ю. Васильева, С.П. Федоров, Д.А. Николаев, И.И. Олейник, С.С. Иванчёв
    Полимеризация этилена в присутствии бис(феноксииминных) комплексов титана, содержащих различные заместители в феноксигруппе
    Высокомол. Соед. Сер. Б, 2010 , Т. 52, N 8, С. 1483-1490. (Polymerization of ethylene in the presence of bis(phenoxyimine) complexes of titanium chloride that contain various substituents in a phenoxy group/ M. Yu. Vasil’eva, S. P. Fedorov, D. A. Nikolaev, I. I. Oleinik, S. S. Ivanchev// Polymer Science Series B, 2010, V. 52, IN 7-8, pp 443-449 doi:10.1134/S1560090410070080), IF=0.421
  113. S.F. Cheatham, M. Kline, R.R. Sasaki, K.A. Blinov, M.E. Elyashberg, S.G. Molodtsov
    Enhanced automated structure elucidation by inclusion of two-bond specific data
    Magn. Reson. Chem., 2010, V. 48, N 8, 571-574. doi:10.1002/mrc.2622, IF=1.611
  114. S.F. Cheatham, M. Kline, R.R. Sasaki, K.A. Blinov, M.E. Elyashberg, S.G. Molodtsov
    Enhanced automated structure elucidation by inclusion of two-bond specific data
    Magn. Reson. Chem., 2010, V. 48, N 8, 571-574. doi:10.1002/mrc.2622, IF=1.611
  115. S.F. Cheatham, M. Kline, R.R. Sasaki, K.A. Blinov, M.E. Elyashberg, S.G. Molodtsov
    Enhanced automated structure elucidation by inclusion of two-bond specific data
    Magn. Reson. Chem., 2010, V. 48, N 8, 571-574. doi:10.1002/mrc.2622, IF=1.611
  116. S.F. Cheatham, M. Kline, R.R. Sasaki, K.A. Blinov, M.E. Elyashberg, S.G. Molodtsov
    Enhanced automated structure elucidation by inclusion of two-bond specific data
    Magn. Reson. Chem., 2010, V. 48, N 8, 571-574. doi:10.1002/mrc.2622, IF=1.611
  117. S.F. Cheatham, M. Kline, R.R. Sasaki, K.A. Blinov, M.E. Elyashberg, S.G. Molodtsov
    Enhanced automated structure elucidation by inclusion of two-bond specific data
    Magn. Reson. Chem., 2010, V. 48, N 8, 571-574. doi:10.1002/mrc.2622, IF=1.611
  118. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.Yu. Makarov, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The molecular structure of N,N’-disulfinyl-3,4,5,6-tetrafluro-1,2-diaminobenzene: a computational and X-ray diffraction study
    J. Mol. Struct., 2010, V. 978, N 1-3, 158-162. doi:10.1016/j.molstruc.2010.01.070, IF=1.55
  119. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.Yu. Makarov, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The molecular structure of N,N’-disulfinyl-3,4,5,6-tetrafluro-1,2-diaminobenzene: a computational and X-ray diffraction study
    J. Mol. Struct., 2010, V. 978, N 1-3, 158-162. doi:10.1016/j.molstruc.2010.01.070, IF=1.55
  120. A.G. Makarov, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.Yu. Makarov, K. Tersago, C. Van Alsenoy, F. Blockhuys, A.V. Zibarev
    The molecular structure of N,N’-disulfinyl-3,4,5,6-tetrafluro-1,2-diaminobenzene: a computational and X-ray diffraction study
    J. Mol. Struct., 2010, V. 978, N 1-3, 158-162. doi:10.1016/j.molstruc.2010.01.070, IF=1.55
  121. М.Б. Бушуев, В.П. Кривопалов, В.А. Далецкий, В.А. Варнек, Л.А. Шелудякова, И.В. Юшина, О.П. Шкуркo
    Высокоспиновый комплек FeL2(NCS)2•MeOH (L = 3,5-ди(пиримидин-2-ил)-4Н-1,2,4-триазол-4-амин). Синтез и свойства
    Журнал общей химии, 2010, Т. 80, N 8, C. 1391-1397. (High-spin complex [FeL2(NCS)(2)]center dot H2O [L=3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine]: Synthesis and properties/ M.B. Bushuev, V.P. Krivopalov, V.A. Daletskii, V.A. Varnek, L.A. Sheludyakova, I.V. Yushina, O.P. Shkurko// RUSS J GEN CHEM+, 2010, V. 80, N 8, pp 1703-1709. doi:10.1134/S1070363210080220), IF=0.393
  122. М.Б. Бушуев, В.П. Кривопалов, В.А. Далецкий, В.А. Варнек, Л.А. Шелудякова, И.В. Юшина, О.П. Шкуркo
    Высокоспиновый комплек FeL2(NCS)2•MeOH (L = 3,5-ди(пиримидин-2-ил)-4Н-1,2,4-триазол-4-амин). Синтез и свойства
    Журнал общей химии, 2010, Т. 80, N 8, C. 1391-1397. (High-spin complex [FeL2(NCS)(2)]center dot H2O [L=3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine]: Synthesis and properties/ M.B. Bushuev, V.P. Krivopalov, V.A. Daletskii, V.A. Varnek, L.A. Sheludyakova, I.V. Yushina, O.P. Shkurko// RUSS J GEN CHEM+, 2010, V. 80, N 8, pp 1703-1709. doi:10.1134/S1070363210080220), IF=0.393
  123. М.Б. Бушуев, В.П. Кривопалов, В.А. Далецкий, В.А. Варнек, Л.А. Шелудякова, И.В. Юшина, О.П. Шкуркo
    Высокоспиновый комплек FeL2(NCS)2•MeOH (L = 3,5-ди(пиримидин-2-ил)-4Н-1,2,4-триазол-4-амин). Синтез и свойства
    Журнал общей химии, 2010, Т. 80, N 8, C. 1391-1397. (High-spin complex [FeL2(NCS)(2)]center dot H2O [L=3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine]: Synthesis and properties/ M.B. Bushuev, V.P. Krivopalov, V.A. Daletskii, V.A. Varnek, L.A. Sheludyakova, I.V. Yushina, O.P. Shkurko// RUSS J GEN CHEM+, 2010, V. 80, N 8, pp 1703-1709. doi:10.1134/S1070363210080220), IF=0.393
  124. М.Б. Бушуев, В.П. Кривопалов, В.А. Далецкий, В.А. Варнек, Л.А. Шелудякова, И.В. Юшина, О.П. Шкуркo
    Высокоспиновый комплек FeL2(NCS)2•MeOH (L = 3,5-ди(пиримидин-2-ил)-4Н-1,2,4-триазол-4-амин). Синтез и свойства
    Журнал общей химии, 2010, Т. 80, N 8, C. 1391-1397. (High-spin complex [FeL2(NCS)(2)]center dot H2O [L=3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine]: Synthesis and properties/ M.B. Bushuev, V.P. Krivopalov, V.A. Daletskii, V.A. Varnek, L.A. Sheludyakova, I.V. Yushina, O.P. Shkurko// RUSS J GEN CHEM+, 2010, V. 80, N 8, pp 1703-1709. doi:10.1134/S1070363210080220), IF=0.393
  125. М.Б. Бушуев, В.П. Кривопалов, В.А. Далецкий, В.А. Варнек, Л.А. Шелудякова, И.В. Юшина, О.П. Шкуркo
    Высокоспиновый комплек FeL2(NCS)2•MeOH (L = 3,5-ди(пиримидин-2-ил)-4Н-1,2,4-триазол-4-амин). Синтез и свойства
    Журнал общей химии, 2010, Т. 80, N 8, C. 1391-1397. (High-spin complex [FeL2(NCS)(2)]center dot H2O [L=3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amine]: Synthesis and properties/ M.B. Bushuev, V.P. Krivopalov, V.A. Daletskii, V.A. Varnek, L.A. Sheludyakova, I.V. Yushina, O.P. Shkurko// RUSS J GEN CHEM+, 2010, V. 80, N 8, pp 1703-1709. doi:10.1134/S1070363210080220), IF=0.393
  126. Е.В. Колякина, М.А. Лазарев, М.В. Павловская, И.А. Кирилюк, И.Ф. Журко, И.А. Григорьев, Д.Ф. Гришин
    Нитроксильные радикалы имидазолинового ряда как агенты псевдоживой полимеризации стирола
    Известия Академии наук. Сер.хим., 2010 , № 8, C. 1519-1527. (Nitroxyl radicals of the imidazoline series as agents of pseudoliving polymerization of styrene/ E.V. Kolyakina, M.A. Lazarev, M.V. Pavlovskaya, I.A. Kirilyuk, I.F. Zhurko, I.A. Grigor'ev, D.F. Grishin// RUSS CHEM B+, 2010, V. 59, N 8, pp 1556-1564 doi:10.1007/s11172-010-0278-x), IF=0.416
  127. Е.В. Колякина, М.А. Лазарев, М.В. Павловская, И.А. Кирилюк, И.Ф. Журко, И.А. Григорьев, Д.Ф. Гришин
    Нитроксильные радикалы имидазолинового ряда как агенты псевдоживой полимеризации стирола
    Известия Академии наук. Сер.хим., 2010 , № 8, C. 1519-1527. (Nitroxyl radicals of the imidazoline series as agents of pseudoliving polymerization of styrene/ E.V. Kolyakina, M.A. Lazarev, M.V. Pavlovskaya, I.A. Kirilyuk, I.F. Zhurko, I.A. Grigor'ev, D.F. Grishin// RUSS CHEM B+, 2010, V. 59, N 8, pp 1556-1564 doi:10.1007/s11172-010-0278-x), IF=0.416
  128. Е.В. Колякина, М.А. Лазарев, М.В. Павловская, И.А. Кирилюк, И.Ф. Журко, И.А. Григорьев, Д.Ф. Гришин
    Нитроксильные радикалы имидазолинового ряда как агенты псевдоживой полимеризации стирола
    Известия Академии наук. Сер.хим., 2010 , № 8, C. 1519-1527. (Nitroxyl radicals of the imidazoline series as agents of pseudoliving polymerization of styrene/ E.V. Kolyakina, M.A. Lazarev, M.V. Pavlovskaya, I.A. Kirilyuk, I.F. Zhurko, I.A. Grigor'ev, D.F. Grishin// RUSS CHEM B+, 2010, V. 59, N 8, pp 1556-1564 doi:10.1007/s11172-010-0278-x), IF=0.416
  129. Е.В. Колякина, М.А. Лазарев, М.В. Павловская, И.А. Кирилюк, И.Ф. Журко, И.А. Григорьев, Д.Ф. Гришин
    Нитроксильные радикалы имидазолинового ряда как агенты псевдоживой полимеризации стирола
    Известия Академии наук. Сер.хим., 2010 , № 8, C. 1519-1527. (Nitroxyl radicals of the imidazoline series as agents of pseudoliving polymerization of styrene/ E.V. Kolyakina, M.A. Lazarev, M.V. Pavlovskaya, I.A. Kirilyuk, I.F. Zhurko, I.A. Grigor'ev, D.F. Grishin// RUSS CHEM B+, 2010, V. 59, N 8, pp 1556-1564 doi:10.1007/s11172-010-0278-x), IF=0.416
  130. В.М. Тапилин, Н.Н. Булгаков, А.П. Чупахин, А.А. Политов, А.Г. Друганов
    К механизму механохимической димеризации антрацена. Различные возможные пути реакции
    Журнал структурной химии., 2010, Т. 51, № 4, C. 664-670. (On Mechanochemical Dimerization of Anthracene. Different Possible Reaction Pathways/ V. M. Tapilin, N. N. Bulgakov, A. P. Chupakhin, A. A. Politov, A. G. Druganov// J STRUCT CHEM+, 2010, V. 51, N 4, pp 635-641. doi:10.1007/s10947-010-0093-0), IF=0.453
  131. В.М. Тапилин, Н.Н. Булгаков, А.П. Чупахин, А.А. Политов, А.Г. Друганов
    К механизму механохимической димеризации антрацена. Различные возможные пути реакции
    Журнал структурной химии., 2010, Т. 51, № 4, C. 664-670. (On Mechanochemical Dimerization of Anthracene. Different Possible Reaction Pathways/ V. M. Tapilin, N. N. Bulgakov, A. P. Chupakhin, A. A. Politov, A. G. Druganov// J STRUCT CHEM+, 2010, V. 51, N 4, pp 635-641. doi:10.1007/s10947-010-0093-0), IF=0.453
  132. В.М. Тапилин, Н.Н. Булгаков, А.П. Чупахин, А.А. Политов, А.Г. Друганов
    К механизму механохимической димеризации антрацена. Различные возможные пути реакции
    Журнал структурной химии., 2010, Т. 51, № 4, C. 664-670. (On Mechanochemical Dimerization of Anthracene. Different Possible Reaction Pathways/ V. M. Tapilin, N. N. Bulgakov, A. P. Chupakhin, A. A. Politov, A. G. Druganov// J STRUCT CHEM+, 2010, V. 51, N 4, pp 635-641. doi:10.1007/s10947-010-0093-0), IF=0.453
  133. В.М. Тапилин, Н.Н. Булгаков, А.П. Чупахин, А.А. Политов, А.Г. Друганов
    К механизму механохимической димеризации антрацена. Различные возможные пути реакции
    Журнал структурной химии., 2010, Т. 51, № 4, C. 664-670. (On Mechanochemical Dimerization of Anthracene. Different Possible Reaction Pathways/ V. M. Tapilin, N. N. Bulgakov, A. P. Chupakhin, A. A. Politov, A. G. Druganov// J STRUCT CHEM+, 2010, V. 51, N 4, pp 635-641. doi:10.1007/s10947-010-0093-0), IF=0.453
  134. Е.А. Конева, Д.В. Корчагина, Ю.В. Гатилов, А.М. Генаев, А.П. Крысин, К.П. Волчо, А.Г. Толстиков, Н.Ф. Салахутдинов
    Новые хиральные лиганды из (+)-α-пинена
    Журнал органической химии, 2010, Т. 46, N 8, C. 1111-1117. (New Chiral Ligands Based on (+)-α-Pinene/ E.A. Koneva, D.V. Korchagina, Yu.V. Gatilov, A.M. Genaev, A.P. Krysin, K.P. Volcho, A.G. Tolstikov, N.F. Salakhutdinov// RUSS J ORG CHEM+, 2010, V. 46, N 8, pp 1109-1115. doi:10.1134/S1070428010080014), IF=0.524
  135. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, А.М. Агафонцев, А.В. Ткачев
    Ситез сольватов комплекса меди(II) с хиральным морфолинооксимом кариофилланового типа (HL). Структура соединения Cu(HL)Cl2 • CHCl3
    Координационная химия, 2010, Т. 36, № 8, C. 583–588. (Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X), IF=0.605
  136. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, А.М. Агафонцев, А.В. Ткачев
    Ситез сольватов комплекса меди(II) с хиральным морфолинооксимом кариофилланового типа (HL). Структура соединения Cu(HL)Cl2 • CHCl3
    Координационная химия, 2010, Т. 36, № 8, C. 583–588. (Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X), IF=0.605
  137. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, А.М. Агафонцев, А.В. Ткачев
    Ситез сольватов комплекса меди(II) с хиральным морфолинооксимом кариофилланового типа (HL). Структура соединения Cu(HL)Cl2 • CHCl3
    Координационная химия, 2010, Т. 36, № 8, C. 583–588. (Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X), IF=0.605
  138. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, А.М. Агафонцев, А.В. Ткачев
    Ситез сольватов комплекса меди(II) с хиральным морфолинооксимом кариофилланового типа (HL). Структура соединения Cu(HL)Cl2 • CHCl3
    Координационная химия, 2010, Т. 36, № 8, C. 583–588. (Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X), IF=0.605
  139. С.В. Ларионов, Л.И. Мячина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, А.М. Агафонцев, А.В. Ткачев
    Ситез сольватов комплекса меди(II) с хиральным морфолинооксимом кариофилланового типа (HL). Структура соединения Cu(HL)Cl2 • CHCl3
    Координационная химия, 2010, Т. 36, № 8, C. 583–588. (Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 • CHCl3/ S.V. Larionov, L.I. Myachina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, A.M. Agafontsev, A.V. Tkachev// RUSS J COORD CHEM+, 2010, V. 36, № 8, pp 579-584. doi:10.1134/S107032841008004X), IF=0.605
  140. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  141. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  142. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  143. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  144. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  145. O.B. Kazakova, N.I. Medvedeva, G.A. Tolstikov, O.S. Kukovinets, E.Y. Yamansarov, L.V. Spirikhin, A.T. Gubaidullin
    Synthesis of terminal acetylenes using POCl3 in pyridine as applied to natural triterpenoids
    Mendeleev Commun., 2010, V. 20, N 4, P. 234-236. doi:10.1016/j.mencom.2010.06.018, IF=0.768
  146. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  147. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  148. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  149. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  150. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  151. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  152. T.V. Popova, J. Reinbolt, B. Eresmann, M.M. Shakirov, M.V. Serebriakova, Y.v. Gerassimova, D.G. Knorre, T.S. Godovikova
    Why do p-nitro-substituted aryl azyds provide unintended dark reactions with protein ?
    J. Photochem. Photobiol. B., 2010, V. 100, N. 1, 19-29. doi:10.1016/j.jphotobiol.2010.04.004, IF=1.871
  153. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  154. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  155. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  156. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  157. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  158. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  159. O. B. Kazakova, N. I. Medvedeva, O. S. Kukovinets, G. A. Tolstikov, E. F. Khusnutdinova, L. Zaprutko, B. Bednarczyk-Cwynar, Z. Paryzek
    Хемоселективное окисление производных олеаноловой кислоты озоном
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 397-399. doi:10.1007/s10600-010-9627-0, IF=0.572
  160. O. B. Kazakova, E. F. Khusnutdinova, O. S. Kukovinets, T. I. Zvereva, G. A. Tolstikov
    Effective synthesis of 2,3-seco-2,3-dicarboxyplatanic acid
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 393-396. doi:10.1007/s10600-010-9626-1, IF=0.572
  161. O. B. Kazakova, E. F. Khusnutdinova, O. S. Kukovinets, T. I. Zvereva, G. A. Tolstikov
    Effective synthesis of 2,3-seco-2,3-dicarboxyplatanic acid
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 393-396. doi:10.1007/s10600-010-9626-1, IF=0.572
  162. O. B. Kazakova, E. F. Khusnutdinova, O. S. Kukovinets, T. I. Zvereva, G. A. Tolstikov
    Effective synthesis of 2,3-seco-2,3-dicarboxyplatanic acid
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 393-396. doi:10.1007/s10600-010-9626-1, IF=0.572
  163. O. B. Kazakova, E. F. Khusnutdinova, O. S. Kukovinets, T. I. Zvereva, G. A. Tolstikov
    Effective synthesis of 2,3-seco-2,3-dicarboxyplatanic acid
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 393-396. doi:10.1007/s10600-010-9626-1, IF=0.572
  164. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  165. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  166. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  167. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  168. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  169. O. B. Kazakova, E. V. Tret’yakova, A. R. Abdrakhmanova, N. N. Kabal’nova, O. S. Kukovinets, G. A. Tolstikov, T. I. Nazyrov
    Oxidation of quinopimaric acid derivatives by dimethyldioxirane
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 388-389. doi:10.1007/s10600-010-9624-3, IF=0.572
  170. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  171. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  172. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  173. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  174. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  175. I. E. Smirnova, E. V. Tret’yakova, O. B. Kazakova, L. V. Spirikhin, G. A. Tolstikov, V. E. Kataev, R. Z. Musin
    Synthesis and modification of diterpenoids with two dihydroquinopimaric acid skeletons
    Chemistry of Natural Compounds, 2010, V. 46, N 3, pp 383-387. doi:10.1007/s10600-010-9623-4, IF=0.467
  176. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез новых производных олеан-18(19)-ена из аллобетулина
    Биоорганическая химия, 2010, V. 36, N 4, С. 552-555. (Synthesis of new olean-18(19)-ene derivatives from allobetulin/ O. B. Kazakova, E. F. Khusnutdinova, G. A. Tolstikov, K. Yu. Suponitsky// RUSS J BIOORG CHEM+, 2010, V.36, N 4, pp 512-515. doi:10.1134/S1068162010040102), IF=0.472
  177. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез новых производных олеан-18(19)-ена из аллобетулина
    Биоорганическая химия, 2010, V. 36, N 4, С. 552-555. (Synthesis of new olean-18(19)-ene derivatives from allobetulin/ O. B. Kazakova, E. F. Khusnutdinova, G. A. Tolstikov, K. Yu. Suponitsky// RUSS J BIOORG CHEM+, 2010, V.36, N 4, pp 512-515. doi:10.1134/S1068162010040102), IF=0.472
  178. О.Б. Казакова, Э.Ф. Хуснутдинова, Г.А. Толстиков, К.Ю. Супоницкий
    Синтез новых производных олеан-18(19)-ена из аллобетулина
    Биоорганическая химия, 2010, V. 36, N 4, С. 552-555. (Synthesis of new olean-18(19)-ene derivatives from allobetulin/ O. B. Kazakova, E. F. Khusnutdinova, G. A. Tolstikov, K. Yu. Suponitsky// RUSS J BIOORG CHEM+, 2010, V.36, N 4, pp 512-515. doi:10.1134/S1068162010040102), IF=0.472
  179. O.B. Kazakova, G.V. Giniyatullina, E.Yu. Yamansarov, G.A. Tolstikov
    Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus
    Bioorg. Med. Chem. Lett., 2010, V. 20, N 14, 4088-4090. doi:10.1016/j.bmcl.2010.05.083, IF=2.65
  180. O.B. Kazakova, G.V. Giniyatullina, E.Yu. Yamansarov, G.A. Tolstikov
    Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus
    Bioorg. Med. Chem. Lett., 2010, V. 20, N 14, 4088-4090. doi:10.1016/j.bmcl.2010.05.083, IF=2.65
  181. O.B. Kazakova, G.V. Giniyatullina, E.Yu. Yamansarov, G.A. Tolstikov
    Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus
    Bioorg. Med. Chem. Lett., 2010, V. 20, N 14, 4088-4090. doi:10.1016/j.bmcl.2010.05.083, IF=2.65
  182. Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
    Molecular diffusion in porous media by PGSE ESR
    Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
  183. Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
    Molecular diffusion in porous media by PGSE ESR
    Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
  184. Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
    Molecular diffusion in porous media by PGSE ESR
    Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
  185. Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
    Molecular diffusion in porous media by PGSE ESR
    Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
  186. Т.А. Асташова, Н.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Методы коррекции окислительного стресса и эндотоксикоза в период завершения и угасания репродуктивного цикла (экспериментальное исследование)
    Физиотерапия, бальнеология и реабилитация, 2010, № 6, 35-39.
  187. Т.А. Асташова, Н.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Методы коррекции окислительного стресса и эндотоксикоза в период завершения и угасания репродуктивного цикла (экспериментальное исследование)
    Физиотерапия, бальнеология и реабилитация, 2010, № 6, 35-39.
  188. Т.А. Асташова, Н.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Методы коррекции окислительного стресса и эндотоксикоза в период завершения и угасания репродуктивного цикла (экспериментальное исследование)
    Физиотерапия, бальнеология и реабилитация, 2010, № 6, 35-39.
  189. Т.А. Асташова, Н.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Методы коррекции окислительного стресса и эндотоксикоза в период завершения и угасания репродуктивного цикла (экспериментальное исследование)
    Физиотерапия, бальнеология и реабилитация, 2010, № 6, 35-39.
  190. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова
    Изучение антиатерогенных эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Атеросклероз, 2010, Т. 6, № 1, С. 5-11. (STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian))
  191. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова
    Изучение антиатерогенных эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Атеросклероз, 2010, Т. 6, № 1, С. 5-11. (STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian))
  192. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова
    Изучение антиатерогенных эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Атеросклероз, 2010, Т. 6, № 1, С. 5-11. (STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian))
  193. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова
    Изучение антиатерогенных эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Атеросклероз, 2010, Т. 6, № 1, С. 5-11. (STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian))
  194. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова
    Изучение антиатерогенных эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Атеросклероз, 2010, Т. 6, № 1, С. 5-11. (STUDY OF ANTIATHEROGENIC EFFECTS OF SIMVAGLYZIN ON RABBIT'S HYPERCHOLESTEROLEMIA MODEL/ Yu.I. Ragino, V.А. Vavilin, N.F. Salakhutdinov, S.I. Makarova, Е.М. Stakhneva, О.G. Safronova// Атеросклероз, 2010, Т. 6, № 1, 5-11.(in russian))
  195. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new alkylamino- and phenylamino-containing polyfluorinated derivatives of 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 2321–2326. doi:10.1016/j.ejmech.2010.02.009, IF=3.269
  196. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new alkylamino- and phenylamino-containing polyfluorinated derivatives of 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 2321–2326. doi:10.1016/j.ejmech.2010.02.009, IF=3.269
  197. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new alkylamino- and phenylamino-containing polyfluorinated derivatives of 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 2321–2326. doi:10.1016/j.ejmech.2010.02.009, IF=3.269
  198. O.A. Zakharova, L.I. Goryunov, N.M. Troshkova, L.P. Ovchinnikova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new n-butylamino and sulfur-containing derivatives of polyfluorinated 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 270-274. doi:10.1016/j.ejmech.2009.10.00, IF=3.269
  199. O.A. Zakharova, L.I. Goryunov, N.M. Troshkova, L.P. Ovchinnikova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new n-butylamino and sulfur-containing derivatives of polyfluorinated 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 270-274. doi:10.1016/j.ejmech.2009.10.00, IF=3.269
  200. O.A. Zakharova, L.I. Goryunov, N.M. Troshkova, L.P. Ovchinnikova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new n-butylamino and sulfur-containing derivatives of polyfluorinated 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 270-274. doi:10.1016/j.ejmech.2009.10.00, IF=3.269
  201. Д.П. Зубенко, И.А. Кирилюк, S. Marque, И.П. Чуйков, Е.Г. Багрянская
    Роль алкильного фрагмента инициирующего алкоксиамина в псевдоживой полимеризации стирола
    Высокомол. Соед. Сер. Б, 2010, Т. 52, N 6, С. 1030-1042. (Role of the alkyl fragment of initiating alkoxyamine in nitroxide mediated polymerization of styrene/ D. P. Zubenko, I. A. Kirilyuk, S. Marque, I. P. Chuikov, E. G. Bagryanskaya// Polymer Science Series B, 2010, V. 52, N 5-6, pp 327-338. doi:10.1134/S156009041005009X), IF=0.289
  202. Д.П. Зубенко, И.А. Кирилюк, S. Marque, И.П. Чуйков, Е.Г. Багрянская
    Роль алкильного фрагмента инициирующего алкоксиамина в псевдоживой полимеризации стирола
    Высокомол. Соед. Сер. Б, 2010, Т. 52, N 6, С. 1030-1042. (Role of the alkyl fragment of initiating alkoxyamine in nitroxide mediated polymerization of styrene/ D. P. Zubenko, I. A. Kirilyuk, S. Marque, I. P. Chuikov, E. G. Bagryanskaya// Polymer Science Series B, 2010, V. 52, N 5-6, pp 327-338. doi:10.1134/S156009041005009X), IF=0.289
  203. Д.П. Зубенко, И.А. Кирилюк, S. Marque, И.П. Чуйков, Е.Г. Багрянская
    Роль алкильного фрагмента инициирующего алкоксиамина в псевдоживой полимеризации стирола
    Высокомол. Соед. Сер. Б, 2010, Т. 52, N 6, С. 1030-1042. (Role of the alkyl fragment of initiating alkoxyamine in nitroxide mediated polymerization of styrene/ D. P. Zubenko, I. A. Kirilyuk, S. Marque, I. P. Chuikov, E. G. Bagryanskaya// Polymer Science Series B, 2010, V. 52, N 5-6, pp 327-338. doi:10.1134/S156009041005009X), IF=0.289
  204. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  205. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  206. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  207. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  208. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  209. M.A. Tikhonova, E.L. Alperina, T.G. Tolstikova, V.Yu. Bazovkina, G.V. Idova, A.V. Kulikov, N.K. Popova
    _Effects of Chronic Fluoxetine Treatment on Catalepsy and the Immune Response in Mice with a Genetic Predisposition to Freezing Reactions: The Roles of Types 1A and 2A Serotonin Receptors and the tph2 and SERT Genes
    Neuroscience and Behavioral Physiology, 2010,V . 40, N 5, P. 521-527 doi:10.1007/s11055-010-9291-7
  210. Е.Ф. Пен, И.Г. Шаталов, В.В. Шелковников
    Экспериментальные исследования и моделирование голографических фотонных кристаллов с дефектами пространственной и зонной структур
    Автометрия, 2010, Т. 46, № 3, С. 64-73. (Experimental Study and Modeling of Holographic Photonic Crystals with Defects of the Spatial and Band-Gap Structures/ E. F. Pen, I. G. Shatalov, V. V. Shelkovnikov// )
  211. Е.Ф. Пен, И.Г. Шаталов, В.В. Шелковников
    Экспериментальные исследования и моделирование голографических фотонных кристаллов с дефектами пространственной и зонной структур
    Автометрия, 2010, Т. 46, № 3, С. 64-73. (Experimental Study and Modeling of Holographic Photonic Crystals with Defects of the Spatial and Band-Gap Structures/ E. F. Pen, I. G. Shatalov, V. V. Shelkovnikov// )
  212. Н.А. Семенов, И.Ю. Багрянская, А.В. Алексеев, Ю.В. Гатилов, Э. Лорк, Р. Мевс, Г.-Ф. Рошенталер, А.В. Зибарев
    Новые молекулярные комплексы тримера перфтор-орто-фениленртути с гетероциклическими соединениями
    Журнал структурной химии, 2010, Т. 51, № 3, C. 569-574. (New molecular complexes of trimeric perfluoro-ortho-phenylene mercury with heterocyclic compounds/ N.A. Semenov, I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, A.V. Alekseev, E. Lork, R. Mews, G.-V. Roeschentaler// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 552-557. doi:10.1007/s10947-010-0080-5), IF=0.453
  213. Н.А. Семенов, И.Ю. Багрянская, А.В. Алексеев, Ю.В. Гатилов, Э. Лорк, Р. Мевс, Г.-Ф. Рошенталер, А.В. Зибарев
    Новые молекулярные комплексы тримера перфтор-орто-фениленртути с гетероциклическими соединениями
    Журнал структурной химии, 2010, Т. 51, № 3, C. 569-574. (New molecular complexes of trimeric perfluoro-ortho-phenylene mercury with heterocyclic compounds/ N.A. Semenov, I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, A.V. Alekseev, E. Lork, R. Mews, G.-V. Roeschentaler// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 552-557. doi:10.1007/s10947-010-0080-5), IF=0.453
  214. Н.А. Семенов, И.Ю. Багрянская, А.В. Алексеев, Ю.В. Гатилов, Э. Лорк, Р. Мевс, Г.-Ф. Рошенталер, А.В. Зибарев
    Новые молекулярные комплексы тримера перфтор-орто-фениленртути с гетероциклическими соединениями
    Журнал структурной химии, 2010, Т. 51, № 3, C. 569-574. (New molecular complexes of trimeric perfluoro-ortho-phenylene mercury with heterocyclic compounds/ N.A. Semenov, I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, A.V. Alekseev, E. Lork, R. Mews, G.-V. Roeschentaler// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 552-557. doi:10.1007/s10947-010-0080-5), IF=0.453
  215. Н.А. Семенов, И.Ю. Багрянская, А.В. Алексеев, Ю.В. Гатилов, Э. Лорк, Р. Мевс, Г.-Ф. Рошенталер, А.В. Зибарев
    Новые молекулярные комплексы тримера перфтор-орто-фениленртути с гетероциклическими соединениями
    Журнал структурной химии, 2010, Т. 51, № 3, C. 569-574. (New molecular complexes of trimeric perfluoro-ortho-phenylene mercury with heterocyclic compounds/ N.A. Semenov, I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, A.V. Alekseev, E. Lork, R. Mews, G.-V. Roeschentaler// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 552-557. doi:10.1007/s10947-010-0080-5), IF=0.453
  216. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, С.А. Попов, А.В. Ткачев
    Кристаллическая структура и фотолюминесценция оптически активного комплекса [ZnL1Cl2], где L1 = пиразолинхинолин-производное монотерпеноида (+)-3-карена
    Журнал структурной химии, 2010, Т. 51, № 3, C. 537-543. (Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2), IF=0.453
  217. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, С.А. Попов, А.В. Ткачев
    Кристаллическая структура и фотолюминесценция оптически активного комплекса [ZnL1Cl2], где L1 = пиразолинхинолин-производное монотерпеноида (+)-3-карена
    Журнал структурной химии, 2010, Т. 51, № 3, C. 537-543. (Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2), IF=0.453
  218. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, С.А. Попов, А.В. Ткачев
    Кристаллическая структура и фотолюминесценция оптически активного комплекса [ZnL1Cl2], где L1 = пиразолинхинолин-производное монотерпеноида (+)-3-карена
    Журнал структурной химии, 2010, Т. 51, № 3, C. 537-543. (Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2), IF=0.453
  219. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, С.А. Попов, А.В. Ткачев
    Кристаллическая структура и фотолюминесценция оптически активного комплекса [ZnL1Cl2], где L1 = пиразолинхинолин-производное монотерпеноида (+)-3-карена
    Журнал структурной химии, 2010, Т. 51, № 3, C. 537-543. (Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2), IF=0.453
  220. С.В. Ларионов, З.А. Савельева, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, С.А. Попов, А.В. Ткачев
    Кристаллическая структура и фотолюминесценция оптически активного комплекса [ZnL1Cl2], где L1 = пиразолинхинолин-производное монотерпеноида (+)-3-карена
    Журнал структурной химии, 2010, Т. 51, № 3, C. 537-543. (Crystal structure and photoluminescence of the optically active complex [ZnL1Cl2], where L1 = pyrazolylquinoline - a derivative of monoterpenoid (+)-3-carene/ S.V. Larionov, Z.A. Savels'eva, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, S.A. Popov, A.V. Tkachev// J STRUCT CHEM+, 2010, V. 51, N 3, pp. 519-525. doi:10.1007/s10947-010-0075-2), IF=0.453
  221. Я.А. Чиркова, В.Я. Денисов, Ю.В. Гатилов, И.Ю. Багрянская, Т.В. Рыбалова
    Синтез и структура 2-фенилантра[9,1-bc]пиррол-6-она
    Журнал органической химии, 2010, Т. 46, N 6, C. 871-877. (Synthesis and structure of 2-phenylanthra[9,1-bc]pyrrol-6-one/ Ya. A. Chirkova, V. Ya. Denisov, Yu. V. Gatilov, I. Yu. Bagryanskaya, T. V. Rybalova// RUSS J ORG CHEM+, 2010, V. 46, N 6, pp 866-870. doi:10.1134/S107042801006014X), IF=0.524
  222. Я.А. Чиркова, В.Я. Денисов, Ю.В. Гатилов, И.Ю. Багрянская, Т.В. Рыбалова
    Синтез и структура 2-фенилантра[9,1-bc]пиррол-6-она
    Журнал органической химии, 2010, Т. 46, N 6, C. 871-877. (Synthesis and structure of 2-phenylanthra[9,1-bc]pyrrol-6-one/ Ya. A. Chirkova, V. Ya. Denisov, Yu. V. Gatilov, I. Yu. Bagryanskaya, T. V. Rybalova// RUSS J ORG CHEM+, 2010, V. 46, N 6, pp 866-870. doi:10.1134/S107042801006014X), IF=0.524
  223. М.Т. Егорычева, Н.Г. Власенко, М.П. Половинка, Н.Ф. Салахутдинов
    «Биоклад» - эффективный протравитель семян пшеницы
    Химия в интересах устойчивого развития, 2010, Т. 18, № 6, C. 729-733. ("Bioklad" as Efficient Protectant of the Seeds of Spring Wheat/ M. T. Egorycheva, N. G. Vlasenko, M. P. Polovinka, N. F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 6, pp.729-733. (in russian))
  224. М.Т. Егорычева, Н.Г. Власенко, М.П. Половинка, Н.Ф. Салахутдинов
    «Биоклад» - эффективный протравитель семян пшеницы
    Химия в интересах устойчивого развития, 2010, Т. 18, № 6, C. 729-733. ("Bioklad" as Efficient Protectant of the Seeds of Spring Wheat/ M. T. Egorycheva, N. G. Vlasenko, M. P. Polovinka, N. F. Salakhutdinov// Chemistry for Sustainable Development, 2010, V.18., № 6, pp.729-733. (in russian))
  225. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Г.А. Толстиков
    Механохимическое получение и свойства водорастворимых межмолекулярных комплексов полисахаридов и бета-циклодекстрина с лекарственными веществами
    Химия в интересах устойчивого развития, 2010, Т. 18, № 6, C. 719-728. (Mechanochemical Preparation and Properties of Water-Soluble Intermolecular Complexes of Polysaccharides and $beta;-Cyclodextrin with Pharmaceutical Substances/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, M. V. Khvostov, G. A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 46, pp. 719-728. (in russian))
  226. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Г.А. Толстиков
    Механохимическое получение и свойства водорастворимых межмолекулярных комплексов полисахаридов и бета-циклодекстрина с лекарственными веществами
    Химия в интересах устойчивого развития, 2010, Т. 18, № 6, C. 719-728. (Mechanochemical Preparation and Properties of Water-Soluble Intermolecular Complexes of Polysaccharides and $beta;-Cyclodextrin with Pharmaceutical Substances/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, M. V. Khvostov, G. A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 46, pp. 719-728. (in russian))
  227. N.V. Vasilieva, I.G. Irtegova, N.P. Gritsan, A.V. Lonchakov, A.Yu. Makarov, L.A. Shundrin, A.V. Zibarev
    Redox properties and radical anions of fluorinated 2,1,3-benzothia(selena)diazoles and related compounds
    J. Phys. Org. Chem., 2010, V. 23, N 6, 536-543. doi:10.1002/poc.1637, IF=1.601
  228. N.V. Vasilieva, I.G. Irtegova, N.P. Gritsan, A.V. Lonchakov, A.Yu. Makarov, L.A. Shundrin, A.V. Zibarev
    Redox properties and radical anions of fluorinated 2,1,3-benzothia(selena)diazoles and related compounds
    J. Phys. Org. Chem., 2010, V. 23, N 6, 536-543. doi:10.1002/poc.1637, IF=1.601
  229. Т.Г. Толстикова, Н.В. Бухтиярова, М.В. Хвостов
    Некоторые аспекты метаболитотропного механизма кардиопротективного действия тиотриазолина при артериальной гипертензии
    Запорожский медицинский журнал, 2010, Т. 12, № 5, 74-79. http://www.nbuv.gov.ua/portal/chem_biol/zmzh/index.html
  230. N.P. Isaev, L.V. Kulik, I.A. Kirilyuk, V.A. Reznikov, I.A. Grigor’ev, S.A. Dzuba
    Fast stochastic librations and slow small-angle rotations of molecules in glasses observed on nitroxide spin probes by stimulated electron spin echo spectroscopy
    J. Non-Cryst. Solids 2010, 356, 1037-1042. doi:10.1016/j.jnoncrysol.2010.01.018, IF=1.251
  231. N.P. Isaev, L.V. Kulik, I.A. Kirilyuk, V.A. Reznikov, I.A. Grigor’ev, S.A. Dzuba
    Fast stochastic librations and slow small-angle rotations of molecules in glasses observed on nitroxide spin probes by stimulated electron spin echo spectroscopy
    J. Non-Cryst. Solids 2010, 356, 1037-1042. doi:10.1016/j.jnoncrysol.2010.01.018, IF=1.251
  232. N.P. Isaev, L.V. Kulik, I.A. Kirilyuk, V.A. Reznikov, I.A. Grigor’ev, S.A. Dzuba
    Fast stochastic librations and slow small-angle rotations of molecules in glasses observed on nitroxide spin probes by stimulated electron spin echo spectroscopy
    J. Non-Cryst. Solids 2010, 356, 1037-1042. doi:10.1016/j.jnoncrysol.2010.01.018, IF=1.251
  233. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  234. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  235. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  236. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  237. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  238. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  239. I.A. Tikhonova, K.I. Tugashov, F.M. Dolgushin, A.A. Yakovenko, P.V. Petrovskii, G.G. Furin, A.P. Zaraisky, V.B. Shur
    Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds
    J. Organomet. Chem., 2007, V. 692, N 5, 953-962. doi:10.1016/j.jorganchem.2006.10.048, IF=2.346
  240. R. I. Dzhalmakhanbetova, Yu V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Synthesis and molecular structure of halohydrins of the guaianolide ludartin
    Chemistry of Natural Compounds, 2010, V. 46, N 2, pp 222-226. doi:10.1007/s10600-010-9574-9, IF=0.572
  241. R. I. Dzhalmakhanbetova, Yu V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Synthesis and molecular structure of halohydrins of the guaianolide ludartin
    Chemistry of Natural Compounds, 2010, V. 46, N 2, pp 222-226. doi:10.1007/s10600-010-9574-9, IF=0.572
  242. R. I. Dzhalmakhanbetova, Yu V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Synthesis and molecular structure of halohydrins of the guaianolide ludartin
    Chemistry of Natural Compounds, 2010, V. 46, N 2, pp 222-226. doi:10.1007/s10600-010-9574-9, IF=0.572
  243. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, Н.И. Медведева, Т.М. Уткина, О.Л. Карташова
    Синтез, модификация и антимикробная активность N-метилпиперазиниламидов тритерпеновых кислот
    Биоорганическая химия, 2010, V. 36, N 3, С. 416-422. (Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, N. I. Medvedeva, T. M. Utkina, O. L. Kartashova// RUSS J BIOORG CHEM+, 2010, V.36, N 3, pp 383-389. doi:10.1134/S1068162010030155), IF=0.711
  244. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, Н.И. Медведева, Т.М. Уткина, О.Л. Карташова
    Синтез, модификация и антимикробная активность N-метилпиперазиниламидов тритерпеновых кислот
    Биоорганическая химия, 2010, V. 36, N 3, С. 416-422. (Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, N. I. Medvedeva, T. M. Utkina, O. L. Kartashova// RUSS J BIOORG CHEM+, 2010, V.36, N 3, pp 383-389. doi:10.1134/S1068162010030155), IF=0.711
  245. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, Н.И. Медведева, Т.М. Уткина, О.Л. Карташова
    Синтез, модификация и антимикробная активность N-метилпиперазиниламидов тритерпеновых кислот
    Биоорганическая химия, 2010, V. 36, N 3, С. 416-422. (Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, N. I. Medvedeva, T. M. Utkina, O. L. Kartashova// RUSS J BIOORG CHEM+, 2010, V.36, N 3, pp 383-389. doi:10.1134/S1068162010030155), IF=0.711
  246. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, Н.И. Медведева, Т.М. Уткина, О.Л. Карташова
    Синтез, модификация и антимикробная активность N-метилпиперазиниламидов тритерпеновых кислот
    Биоорганическая химия, 2010, V. 36, N 3, С. 416-422. (Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, N. I. Medvedeva, T. M. Utkina, O. L. Kartashova// RUSS J BIOORG CHEM+, 2010, V.36, N 3, pp 383-389. doi:10.1134/S1068162010030155), IF=0.711
  247. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, Н.И. Медведева, Т.М. Уткина, О.Л. Карташова
    Синтез, модификация и антимикробная активность N-метилпиперазиниламидов тритерпеновых кислот
    Биоорганическая химия, 2010, V. 36, N 3, С. 416-422. (Synthesis, modification, and antimicrobial activity of the N-methylpiperazinyl amides of triterpenic acids/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, N. I. Medvedeva, T. M. Utkina, O. L. Kartashova// RUSS J BIOORG CHEM+, 2010, V.36, N 3, pp 383-389. doi:10.1134/S1068162010030155), IF=0.711
  248. И.И. Олейник, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. XIII. Синтез тетрадентатных бис(2-гидрокси-1-нафтальдиминных) лигандов и их комплексов с дихлоридом титана(IV)
    Журнал органической химии, 2010, Т. 46, N 5, C. 751-757. (Design of postmetallocene catalytic systems of aryliminetype for olefins polymerization: XIII. Synthesis of tetradentate bis(2-hydroxy-1-naphthaldimine) ligands and their complexes with titanium(IV) dichloride/ I. I. Oleinik, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// RUSS J ORG CHEM+, 2010, V. 46, N 5, pp 746-752. doi:10.1134/S1070428010050246), IF=0.524
  249. Л.М. Горностаев, Е.А. Бочарова, Л.В. Долгушина, И.Ю. Багрянская, Ю.В. Гатилов
    Синтез 4(6)-амино-6(4)-галоген-2,1,3-бензоксадиазолов
    Журнал органической химии, 2010, Т. 46, N 5, C. 702-706. (Synthesis of 4(6)-amino-6(4)-halo-2,1,3-benzoxadiazoles/ L. M. Gornostaev, E. A. Bocharova, L. V. Dolgushina, I. Yu. Bagryanskaya, Yu. V. Gatilov// RUSS J ORG CHEM+, 2010, V. 46, N 5, pp 693-698. doi:10.1134/S1070428010050179), IF=0.524
  250. Л.М. Горностаев, Е.А. Бочарова, Л.В. Долгушина, И.Ю. Багрянская, Ю.В. Гатилов
    Синтез 4(6)-амино-6(4)-галоген-2,1,3-бензоксадиазолов
    Журнал органической химии, 2010, Т. 46, N 5, C. 702-706. (Synthesis of 4(6)-amino-6(4)-halo-2,1,3-benzoxadiazoles/ L. M. Gornostaev, E. A. Bocharova, L. V. Dolgushina, I. Yu. Bagryanskaya, Yu. V. Gatilov// RUSS J ORG CHEM+, 2010, V. 46, N 5, pp 693-698. doi:10.1134/S1070428010050179), IF=0.524
  251. Л.М. Горностаев, Е.А. Бочарова, Л.В. Долгушина, И.Ю. Багрянская, Ю.В. Гатилов
    Синтез 4(6)-амино-6(4)-галоген-2,1,3-бензоксадиазолов
    Журнал органической химии, 2010, Т. 46, N 5, C. 702-706. (Synthesis of 4(6)-amino-6(4)-halo-2,1,3-benzoxadiazoles/ L. M. Gornostaev, E. A. Bocharova, L. V. Dolgushina, I. Yu. Bagryanskaya, Yu. V. Gatilov// RUSS J ORG CHEM+, 2010, V. 46, N 5, pp 693-698. doi:10.1134/S1070428010050179), IF=0.524
  252. А.П. Крысин, В.С. Кобрин, И.В. Сорокина
    n-Тирозол. Синтез и свойства.
    Химия в интересах устойчивого развития, 2010. Т. 18. № 5. С. 543-550. (p-Thyrozole: Synthesis and Properties/ A. P. Krysin, V. S. Kobrin, I. V. Sorokina// Chemistry for Sustainable Development, 2010, V.18., № 5, pp. 543-550. (in russian))
  253. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  254. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  255. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  256. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  257. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  258. M.B. Bushuev, V.P. Krivopalov, N.V. Pervukhina, D.Yu. Naumov, G.G. Moskalenko, K.A. Vinogradova, L.A. Sheludyakova, S.V. Larionov
    Copper(II) complexes based on a new chelating 4-(3,5-diphenyl-1H-pyrazol-1-yl)-6-(piperidin-1-yl)pyrimidine ligand: Synthesis and crystal structures. Lone pair–π, C-H–π, π–π and C-H–A (A = N, Cl) non-covalent interactions
    Inorg. Chim. Acta, 2010, v. 363, N 7, 1547-1555. doi:10.1016/j.ica.2010.01.013, IF=2.322
  259. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  260. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  261. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  262. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  263. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  264. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
    CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
    J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
  265. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  266. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  267. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  268. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  269. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  270. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  271. O.B. Kazakova, E.V. Tretyakova, O.S. Kukovinets, A.R. Abdrakhmanova, N.N. Kabalnova, D.V. Kazakov, G.A. Tolstikov, A.T. Gubaidullin
    Synthesis of nontrivial quinopimaric acid derivatives by oxidation with dimethyldioxirane
    Tetrahedron Letters, 2010, V. 51, N 14, Pp 1832–1835. doi:10.1016/j.tetlet.2010.01.117, IF=2.66
  272. E.A. Efremova, V.A. Marchenko, D. Erdenelzhargal, S.V. Morozov, E.I. Chernyak
    Pharmacokinetic characteristics of aversectine C – substance antiphrastic fodder granules active substances and determination of it’s remains in organs and tissues of cattle
    Оношлох эрдэм дэвшилт арга, (Монголия), 2010, N 4, 130-133.
  273. E.A. Efremova, V.A. Marchenko, D. Erdenelzhargal, S.V. Morozov, E.I. Chernyak
    Pharmacokinetic characteristics of aversectine C – substance antiphrastic fodder granules active substances and determination of it’s remains in organs and tissues of cattle
    Оношлох эрдэм дэвшилт арга, (Монголия), 2010, N 4, 130-133.
  274. E.A. Efremova, V.A. Marchenko, D. Erdenelzhargal, S.V. Morozov, E.I. Chernyak
    Pharmacokinetic characteristics of aversectine C – substance antiphrastic fodder granules active substances and determination of it’s remains in organs and tissues of cattle
    Оношлох эрдэм дэвшилт арга, (Монголия), 2010, N 4, 130-133.
  275. Т.А. Асташова, И.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Свободные жирные кислоты для оценки и развития эндотоксикоза, окислительного стресса и меотдов их коррекции в период завершения и угасания репродуктивного цикла
    Вестн. Восстановит. Мед., 2010, № 4, С. 35-38.
  276. Т.А. Асташова, И.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Свободные жирные кислоты для оценки и развития эндотоксикоза, окислительного стресса и меотдов их коррекции в период завершения и угасания репродуктивного цикла
    Вестн. Восстановит. Мед., 2010, № 4, С. 35-38.
  277. Т.А. Асташова, И.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Свободные жирные кислоты для оценки и развития эндотоксикоза, окислительного стресса и меотдов их коррекции в период завершения и угасания репродуктивного цикла
    Вестн. Восстановит. Мед., 2010, № 4, С. 35-38.
  278. Т.А. Асташова, И.Н. Бурчак, Е.В. Старкова, В.В. Асташов, С.В. Морозов
    Свободные жирные кислоты для оценки и развития эндотоксикоза, окислительного стресса и меотдов их коррекции в период завершения и угасания репродуктивного цикла
    Вестн. Восстановит. Мед., 2010, № 4, С. 35-38.
  279. Т.Г. Толстикова, М.В. Хвостов, А.О. Брызгалов, А.В. Душкин
    Улучшение фармакологических свойств нифедипина путем механохимического комплексирования с глицирризиновой кислотой
    Биомедицинская химия, 2010, Т. 56, N 2, С. 187-194. (IMPROVEMENT OF PHARMACOLOGICAL VALUES OF THE NIFEDIPINE BY MEANS OF MECHANOCHEMICAL COMPLEXATION WITH GLYCYRRHIZIC ACID/ // )
  280. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  281. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  282. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  283. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  284. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  285. А.Г. Матвеева, Д.В. Стась, Е.М. Глебов, В.П. Гривин, В.В. Королев, В.Ф. Плюснин, В.А. Резников
    Межмолекулярное и внутримолекулярное тушение фотолюминесценции карбазола имидазолиновыми радикалами
    Известия Академии наук. Сер.хим., 2010, № 4, C. 755-762. (Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x), IF=0.416
  286. Т.Е. Кокина, Р.Ф. Клевцова, Л.А. Глинская, Е.Г. Богуславский, Е.А. Конева, К.П. Волчо, С.В. Ларионов
    Синтез и свойства комплекса CuII с хиральным основанием Шиффа (H2L) на основе природного монотерпена (+)-6h-пинена, и его сольвата с ацетонитрилом. Кристаллическая структура [Cu(HL)Cl]•H2O
    Известия Академии наук. Сер.хим., 2010, № 4, C. 698-702. (Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y), IF=0.416
  287. Т.Е. Кокина, Р.Ф. Клевцова, Л.А. Глинская, Е.Г. Богуславский, Е.А. Конева, К.П. Волчо, С.В. Ларионов
    Синтез и свойства комплекса CuII с хиральным основанием Шиффа (H2L) на основе природного монотерпена (+)-6h-пинена, и его сольвата с ацетонитрилом. Кристаллическая структура [Cu(HL)Cl]•H2O
    Известия Академии наук. Сер.хим., 2010, № 4, C. 698-702. (Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y), IF=0.416
  288. Т.Е. Кокина, Р.Ф. Клевцова, Л.А. Глинская, Е.Г. Богуславский, Е.А. Конева, К.П. Волчо, С.В. Ларионов
    Синтез и свойства комплекса CuII с хиральным основанием Шиффа (H2L) на основе природного монотерпена (+)-6h-пинена, и его сольвата с ацетонитрилом. Кристаллическая структура [Cu(HL)Cl]•H2O
    Известия Академии наук. Сер.хим., 2010, № 4, C. 698-702. (Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y), IF=0.416
  289. Т.Е. Кокина, Р.Ф. Клевцова, Л.А. Глинская, Е.Г. Богуславский, Е.А. Конева, К.П. Волчо, С.В. Ларионов
    Синтез и свойства комплекса CuII с хиральным основанием Шиффа (H2L) на основе природного монотерпена (+)-6h-пинена, и его сольвата с ацетонитрилом. Кристаллическая структура [Cu(HL)Cl]•H2O
    Известия Академии наук. Сер.хим., 2010, № 4, C. 698-702. (Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y), IF=0.416
  290. Т.Е. Кокина, Р.Ф. Клевцова, Л.А. Глинская, Е.Г. Богуславский, Е.А. Конева, К.П. Волчо, С.В. Ларионов
    Синтез и свойства комплекса CuII с хиральным основанием Шиффа (H2L) на основе природного монотерпена (+)-6h-пинена, и его сольвата с ацетонитрилом. Кристаллическая структура [Cu(HL)Cl]•H2O
    Известия Академии наук. Сер.хим., 2010, № 4, C. 698-702. (Complex of CuII with a chiral Schiff base (H2L) derived from the natural monoterpene (+)-6h-pinene. Synthesis and the properties of the complex and its solvate with acetonitrile. Crystal structure of [Cu(HL)Cl]•H2O/ T.E. Kokina, R.F. Klevtsova, L.A. Glinskaya, E.G. Boguslavskii, E.A. Koneva, K.P. Volcho, S.V. Larionov// RUSS CHEM B+, 2010, V. 59, N 4, pp 712-716. doi:10.1007/s11172-010-0151-y), IF=0.416
  291. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  292. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  293. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  294. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  295. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  296. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  297. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  298. Т.Г. Толстикова, Е.А. Морозова, М.В. Хвостов, П.П. Лактионов, E.C. Морозкин, З.Р. Исмагилов, О.Ю. Подъячева, С.В. Сысолятин, А.Б. Ворожцов, Р.К. Тухтаев, Ч.Н. Барнаков
    Изучение биобезопасности нановеществ и наноматериалов
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 527-534. (Investigation of Biological Safety of Nanosubstances and Nanomaterials/ T.G. Tolstikova, E.A. Morozova, M.V. Khvostov, P.P. Laktionov, E.S. Morozkin, Z.R. Ismagilov, O.Yu. Podyacheva, S.V. Sysolyatin, A.B. Vorozhtsov, R.K. Tukhtaev, Ch.N. Barnakov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 527-534. (in russian))
  299. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих, Г.А. Толстиков
    Комплексирование фармаконов с глицирризиновой кислотой - путь создания лекарственных препаратов повышенной эффективности
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 517-525. (Complexation of Pharmacons with Glycyrrhizic Acid as a Route to the Development of the Preparations with Enhanced Efficiency/ A.V. Dushkin, E.S. Meteleva, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 517-525. (in russian))
  300. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих, Г.А. Толстиков
    Комплексирование фармаконов с глицирризиновой кислотой - путь создания лекарственных препаратов повышенной эффективности
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 517-525. (Complexation of Pharmacons with Glycyrrhizic Acid as a Route to the Development of the Preparations with Enhanced Efficiency/ A.V. Dushkin, E.S. Meteleva, T.G. Tolstikova, M.V. Khvostov, M.P. Dolgikh, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 517-525. (in russian))
  301. Т.Г. Толстикова, Е.А. Морозова, С.В. Сысолятин, А.И. Калашников, Ю.И. Жукова, В.Н. Сурмачев
    Синтез и биологическая активность производных 2,4,6,8,10,12-гексаазатетрацикло[5.5.0.03,11.05,9]додекана
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 511-516. (Synthesis and Biological Activity of 2,4,6,8,10,12-Hexaazatetracyclo[5.5.0.03,11.05,9]dodecane/ T.G. Tolstikova, E.A. Morozova, S.V. Sysolyatin, A.I. Kalashnikov, Yu.I. Zhukova, V.N. Surmachev// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.511-516. (in russian))
  302. Т.Г. Толстикова, Е.А. Морозова, С.В. Сысолятин, А.И. Калашников, Ю.И. Жукова, В.Н. Сурмачев
    Синтез и биологическая активность производных 2,4,6,8,10,12-гексаазатетрацикло[5.5.0.03,11.05,9]додекана
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 511-516. (Synthesis and Biological Activity of 2,4,6,8,10,12-Hexaazatetracyclo[5.5.0.03,11.05,9]dodecane/ T.G. Tolstikova, E.A. Morozova, S.V. Sysolyatin, A.I. Kalashnikov, Yu.I. Zhukova, V.N. Surmachev// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.511-516. (in russian))
  303. Т.Г. Толстикова, Е.А. Морозова, С.В. Сысолятин, А.И. Калашников, Ю.И. Жукова, В.Н. Сурмачев
    Синтез и биологическая активность производных 2,4,6,8,10,12-гексаазатетрацикло[5.5.0.03,11.05,9]додекана
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 511-516. (Synthesis and Biological Activity of 2,4,6,8,10,12-Hexaazatetracyclo[5.5.0.03,11.05,9]dodecane/ T.G. Tolstikova, E.A. Morozova, S.V. Sysolyatin, A.I. Kalashnikov, Yu.I. Zhukova, V.N. Surmachev// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.511-516. (in russian))
  304. Т.Г. Толстикова, Е.А. Морозова, С.В. Сысолятин, А.И. Калашников, Ю.И. Жукова, В.Н. Сурмачев
    Синтез и биологическая активность производных 2,4,6,8,10,12-гексаазатетрацикло[5.5.0.03,11.05,9]додекана
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 511-516. (Synthesis and Biological Activity of 2,4,6,8,10,12-Hexaazatetracyclo[5.5.0.03,11.05,9]dodecane/ T.G. Tolstikova, E.A. Morozova, S.V. Sysolyatin, A.I. Kalashnikov, Yu.I. Zhukova, V.N. Surmachev// Chemistry for Sustainable Development, 2010, V.18., № 4, pp.511-516. (in russian))
  305. А.А. Степанов, С.Ф. Василевский, Г.А. Толстиков
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    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 505-510. (Ethynilation of Lappaconitine as a Route to Modification of Alkaloids/ A.A. Stepanov, S.F. Vasilevsky, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 505-510. (in russian))
  306. А.А. Степанов, С.Ф. Василевский, Г.А. Толстиков
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    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 505-510. (Ethynilation of Lappaconitine as a Route to Modification of Alkaloids/ A.A. Stepanov, S.F. Vasilevsky, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 505-510. (in russian))
  307. Н.А. Жукова, И.В. Сорокина, Т.Г. Толстикова, М.П. Долгих, Д.Е. Семенов
    Влияние бетулоновой кислоты и ее производных на морфологию почек животных с перевитой карциномой легких Льюис на фоне полихимиотерапии и без ее воздействия
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 483-488. (Effect of Betulonic Acid and Its Derivatives on the Morphology of Kidneys in the Animals with Transplanted Pulmonary Lewis Carcinoma at the Background of Polychemotherapy and without It/ N.A. Zhukova, I.V. Sorokina, T.G. Tolstikova, M.P. Dolgikh, D.E. Semenov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 483-488. (in russian))
  308. А.И. Говди, И.В. Сорокина, Т.Г. Толстикова, С.Ф. Василевский, Г.А. Толстиков
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    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 477-482. (Synthesis and Biological Activity of the New Acetylenic Derivatives of Betulonic Acid Amide/ A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, S.F. Vasilevsky, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 477-482. (in russian))
  309. А.И. Говди, И.В. Сорокина, Т.Г. Толстикова, С.Ф. Василевский, Г.А. Толстиков
    Синтез и биологическая активность новых ацетиленовых производных бетулоновой кислоты
    Химия в интересах устойчивого развития, 2010, Т. 18, № 4, C. 477-482. (Synthesis and Biological Activity of the New Acetylenic Derivatives of Betulonic Acid Amide/ A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, S.F. Vasilevsky, G.A. Tolstikov// Chemistry for Sustainable Development, 2010, V.18., № 4, pp. 477-482. (in russian))
  310. Zh.S. Nurmaganbetov, E.E. Shultz, S.V. Chernov, A.Zh. Turmukhambetov, R.B. Seydakhmetova, M.M. Shakirov, G.A. Tolstikov, S.M. Adekenov
    Synthesis of substituted indolizino[8,7-b]indoles from harmine and their biological activity
    Chemistry of Heterocyclic Compounds, 2010, V. 46, N 12, 1494-1499. doi:10.1007/s10593-011-0698-z, IF=0.699
  311. Zh.S. Nurmaganbetov, E.E. Shultz, S.V. Chernov, A.Zh. Turmukhambetov, R.B. Seydakhmetova, M.M. Shakirov, G.A. Tolstikov, S.M. Adekenov
    Synthesis of substituted indolizino[8,7-b]indoles from harmine and their biological activity
    Chemistry of Heterocyclic Compounds, 2010, V. 46, N 12, 1494-1499. doi:10.1007/s10593-011-0698-z, IF=0.699
  312. Zh.S. Nurmaganbetov, E.E. Shultz, S.V. Chernov, A.Zh. Turmukhambetov, R.B. Seydakhmetova, M.M. Shakirov, G.A. Tolstikov, S.M. Adekenov
    Synthesis of substituted indolizino[8,7-b]indoles from harmine and their biological activity
    Chemistry of Heterocyclic Compounds, 2010, V. 46, N 12, 1494-1499. doi:10.1007/s10593-011-0698-z, IF=0.699
  313. Zh.S. Nurmaganbetov, E.E. Shultz, S.V. Chernov, A.Zh. Turmukhambetov, R.B. Seydakhmetova, M.M. Shakirov, G.A. Tolstikov, S.M. Adekenov
    Synthesis of substituted indolizino[8,7-b]indoles from harmine and their biological activity
    Chemistry of Heterocyclic Compounds, 2010, V. 46, N 12, 1494-1499. doi:10.1007/s10593-011-0698-z, IF=0.699
  314. E.M. Suleimenov, A.V. Tkachev, S.M. Adekenov
    Essential oil from Kazakhstan Artemisia species
    Chemistry of Natural Compounds, 2010, V. 46, N 1, pp 135-139. doi:10.1007/s10600-010-9548-y, IF=0.572
  315. E.M. Suleimenov, A.V. Tkachev, S.M. Adekenov
    Essential oil from Kazakhstan Artemisia species
    Chemistry of Natural Compounds, 2010, V. 46, N 1, pp 135-139. doi:10.1007/s10600-010-9548-y, IF=0.572
  316. G.T. Zharylgasina, L.A. Musina, B.I. Tuleuov, S.M. Adekenov, I.Yu. Bagryanskaya, M.M. Shakirov, E.E. Shul'Ts
    Алкалоиды Eminium Lehmanni Bunge O. KuntzeAlkaloids of Eminium lehmannii
    Chemistry of Natural Compounds, 2010, V. 46, N 1, pp 154-157. doi:10.1007/s10600-010-9554-0, IF=0.572
  317. G.T. Zharylgasina, L.A. Musina, B.I. Tuleuov, S.M. Adekenov, I.Yu. Bagryanskaya, M.M. Shakirov, E.E. Shul'Ts
    Алкалоиды Eminium Lehmanni Bunge O. KuntzeAlkaloids of Eminium lehmannii
    Chemistry of Natural Compounds, 2010, V. 46, N 1, pp 154-157. doi:10.1007/s10600-010-9554-0, IF=0.572
  318. G.T. Zharylgasina, L.A. Musina, B.I. Tuleuov, S.M. Adekenov, I.Yu. Bagryanskaya, M.M. Shakirov, E.E. Shul'Ts
    Алкалоиды Eminium Lehmanni Bunge O. KuntzeAlkaloids of Eminium lehmannii
    Chemistry of Natural Compounds, 2010, V. 46, N 1, pp 154-157. doi:10.1007/s10600-010-9554-0, IF=0.572
  319. В.И. Аникеев, A. Ермакова, A.M. Чибиряев, И.В. Кожевников
    Кинетика термических превращений монотерпеновых соединений в сверхкритических низших спиртах
    Кинетика и катализ, 2010, Т. 51. № 2, C. 176-209. (Kinetics of thermal conversions of monoterpenic compounds in supercritical lower alcohols/ V. I. Anikeev, A. Ermakova, A. M. Chibiryaev, I. V. Kozhevnikov// Kinetics and Catalysis, 2010, V. 51, Т 2, pp 162-193. doi:10.1134/S0023158410020035), IF=0.69
  320. В.И. Аникеев, A. Ермакова, A.M. Чибиряев, И.В. Кожевников
    Кинетика термических превращений монотерпеновых соединений в сверхкритических низших спиртах
    Кинетика и катализ, 2010, Т. 51. № 2, C. 176-209. (Kinetics of thermal conversions of monoterpenic compounds in supercritical lower alcohols/ V. I. Anikeev, A. Ermakova, A. M. Chibiryaev, I. V. Kozhevnikov// Kinetics and Catalysis, 2010, V. 51, Т 2, pp 162-193. doi:10.1134/S0023158410020035), IF=0.69
  321. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  322. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  323. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  324. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  325. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  326. О.Б. Казакова, Е.В. Третьякова, О.С. Куковинец, Г.А. Толстиков, Т.И. Назыров, И.В. Чудов, А.Ф. Исмагилова
    Синтез и фармакологическая активность амидов и продукта озонолиза малеопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 6, С. 832-840. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262 doi:10.1134/S1068162010020160), IF=0.711
  327. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  328. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  329. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  330. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  331. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  332. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  333. О.Б. Казакова, Е.В. Третьякова, И.Е. Смирнова, Л.В. Спирихин, Г.А. Толстиков, Е.В. Чудов, Г.В. Базекин, А.Ф. Исмагилова
    Синтез и противовоспалительная активность производных хинопимаровой кислоты
    Биоорганическая химия, 2010, V. 36, N 2, С. 277-282. (The synthesis and anti-inflammatory activity of quinopimaric acid derivatives/ O. B. Kazakova, E. V. Tret’yakova, I. E. Smirnova, L. V. Spirikhin, G. A. Tolstikov, I. V. Chudov, G. V. Bazekin, A. F. Ismagilova// RUSS J BIOORG CHEM+, 2010, V.36, N 2, pp 257-262. doi:10.1134/S1068162010020160), IF=0.472
  334. I. Kirilyuk, D. Polovyanenko, S. Semenov, I. Grigor’ev, O. Gerasko, V. Fedin, E. Bagryanskaya
    Inclusion Complexes of Nitroxides of Pyrrolidine and Imidazoline Series with Cucurbit[7]uril
    J. Phys. Chem. B, 2010, V. 114, N 4, 1719-1728. doi:10.1021/jp9103678, IF=3.47
  335. I. Kirilyuk, D. Polovyanenko, S. Semenov, I. Grigor’ev, O. Gerasko, V. Fedin, E. Bagryanskaya
    Inclusion Complexes of Nitroxides of Pyrrolidine and Imidazoline Series with Cucurbit[7]uril
    J. Phys. Chem. B, 2010, V. 114, N 4, 1719-1728. doi:10.1021/jp9103678, IF=3.47
  336. I. Kirilyuk, D. Polovyanenko, S. Semenov, I. Grigor’ev, O. Gerasko, V. Fedin, E. Bagryanskaya
    Inclusion Complexes of Nitroxides of Pyrrolidine and Imidazoline Series with Cucurbit[7]uril
    J. Phys. Chem. B, 2010, V. 114, N 4, 1719-1728. doi:10.1021/jp9103678, IF=3.47
  337. I. Kirilyuk, D. Polovyanenko, S. Semenov, I. Grigor’ev, O. Gerasko, V. Fedin, E. Bagryanskaya
    Inclusion Complexes of Nitroxides of Pyrrolidine and Imidazoline Series with Cucurbit[7]uril
    J. Phys. Chem. B, 2010, V. 114, N 4, 1719-1728. doi:10.1021/jp9103678, IF=3.47
  338. П.Ю. Шкроботько, А.В. Ткачёв, М.С. Юсубов, М.В. Белоусов, Н.С. Фурса
    Валериана лекарственная: компонентный состав летучих веществ листьев в окрестностях г. Ярославля и в окрестностях г. Запорожья
    Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , N. 2, 141-150. (VALERIANA OFFICINALIS: COMPONENT COMPOSITION OF VOLATILE COMPOUNDS IN THE LEAVES FROM THE OUT SKIRTS OF YAROSLAVL AND ZAPOROJIE/ P. Ju. Shkrobotko, A. V. Tkachev, M.S. Jusubov, M. V. Belousov, N. S. Fursa// Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , В. 2, 141-150.)
  339. П.Ю. Шкроботько, А.В. Ткачёв, М.С. Юсубов, М.В. Белоусов, Н.С. Фурса
    Валериана лекарственная: компонентный состав летучих веществ листьев в окрестностях г. Ярославля и в окрестностях г. Запорожья
    Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , N. 2, 141-150. (VALERIANA OFFICINALIS: COMPONENT COMPOSITION OF VOLATILE COMPOUNDS IN THE LEAVES FROM THE OUT SKIRTS OF YAROSLAVL AND ZAPOROJIE/ P. Ju. Shkrobotko, A. V. Tkachev, M.S. Jusubov, M. V. Belousov, N. S. Fursa// Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , В. 2, 141-150.)
  340. П.Ю. Шкроботько, А.В. Ткачёв, М.С. Юсубов, М.В. Белоусов, Н.С. Фурса
    Валериана лекарственная: компонентный состав летучих веществ листьев в окрестностях г. Ярославля и в окрестностях г. Запорожья
    Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , N. 2, 141-150. (VALERIANA OFFICINALIS: COMPONENT COMPOSITION OF VOLATILE COMPOUNDS IN THE LEAVES FROM THE OUT SKIRTS OF YAROSLAVL AND ZAPOROJIE/ P. Ju. Shkrobotko, A. V. Tkachev, M.S. Jusubov, M. V. Belousov, N. S. Fursa// Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , В. 2, 141-150.)
  341. П.Ю. Шкроботько, А.В. Ткачёв, М.С. Юсубов, М.В. Белоусов, Н.С. Фурса
    Валериана лекарственная: компонентный состав летучих веществ листьев в окрестностях г. Ярославля и в окрестностях г. Запорожья
    Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , N. 2, 141-150. (VALERIANA OFFICINALIS: COMPONENT COMPOSITION OF VOLATILE COMPOUNDS IN THE LEAVES FROM THE OUT SKIRTS OF YAROSLAVL AND ZAPOROJIE/ P. Ju. Shkrobotko, A. V. Tkachev, M.S. Jusubov, M. V. Belousov, N. S. Fursa// Российский медико-биологический вестник им. акад. И.П. Павлова, 2010 , В. 2, 141-150.)
  342. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после её дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104)
  343. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после её дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104)
  344. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после её дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104)
  345. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после её дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104)
  346. В.В. Мартемьянов, Д.В. Домрачев, С.В. Павлушин, И.А. Белоусова, С.А. Бахвалов, А.В. Ткачёв, В.В. Глупов
    Индукция синтеза терпеноидов в листьях березы повислой после её дефолиации гусеницами непарного шелкопряда
    Доклады Академии наук, 2010. Т. 435. № 2. С. 278-281. (Induction of terpenoid synthesis in leaves of silver birch after defoliation caused by gypsy moth caterpillars/ V. V. Martemyanov, D. V. Domrachev, S. V. Pavlushin, I. A. Belousova, S. A. Bakhvalov, A. V. Tkachev, V. V. Glupov// Doklady Biological Sciences, 2010, V. 433, N 1, pp 407-410. doi:10.1134/S0012496610060104)
  347. Е.А. Ефремова, В.А. Марченко, Е.И. Черняк, С.В. Морозов
    Фармакокинентика аверсектина С и его остаточные количества в органах и тканях маралов
    Росс. Паразитол. Ж., 2010, № 2, 107-111.
  348. Е.А. Ефремова, В.А. Марченко, Е.И. Черняк, С.В. Морозов
    Фармакокинентика аверсектина С и его остаточные количества в органах и тканях маралов
    Росс. Паразитол. Ж., 2010, № 2, 107-111.
  349. V.I. Anikeev, I.V. Il'ina, K.P. Volcho, A. Yermakova, N.F. Salakhutdinov
    Reactivity of α-pinene epoxide in supercritical solvents
    J. Supercrit. Fluid., 2010, V. 52, N 1, 71–75. doi:10.1016/j.supflu.2009.11.003, IF=2.638
  350. V.I. Anikeev, I.V. Il'ina, K.P. Volcho, A. Yermakova, N.F. Salakhutdinov
    Reactivity of α-pinene epoxide in supercritical solvents
    J. Supercrit. Fluid., 2010, V. 52, N 1, 71–75. doi:10.1016/j.supflu.2009.11.003, IF=2.638
  351. О.В. Саломатина, Е.Б. Логашенко, Д.В. Корчагина, Н.Ф. Салахутдинов, М.А. Зенкова, В.В. Власов, Г.А. Толстиков
    Новые производные глицерретовой кислоты: синтез и биологическая активность
    Доклады Академии наук, 2010, Т. 430, N 4, C. 498–501. (Synthesis and biological activity of novel glycyrrhetic acid derivatives/ O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova, V.V. Vlasov, G.A. Tolstikov// Doklady Chemistry, 2010, V. 430, N 2, pp 35-38. doi:10.1134/S0012500810020011 Part: 2), IF=0.204
  352. О.В. Саломатина, Е.Б. Логашенко, Д.В. Корчагина, Н.Ф. Салахутдинов, М.А. Зенкова, В.В. Власов, Г.А. Толстиков
    Новые производные глицерретовой кислоты: синтез и биологическая активность
    Доклады Академии наук, 2010, Т. 430, N 4, C. 498–501. (Synthesis and biological activity of novel glycyrrhetic acid derivatives/ O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova, V.V. Vlasov, G.A. Tolstikov// Doklady Chemistry, 2010, V. 430, N 2, pp 35-38. doi:10.1134/S0012500810020011 Part: 2), IF=0.204
  353. О.В. Саломатина, Е.Б. Логашенко, Д.В. Корчагина, Н.Ф. Салахутдинов, М.А. Зенкова, В.В. Власов, Г.А. Толстиков
    Новые производные глицерретовой кислоты: синтез и биологическая активность
    Доклады Академии наук, 2010, Т. 430, N 4, C. 498–501. (Synthesis and biological activity of novel glycyrrhetic acid derivatives/ O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova, V.V. Vlasov, G.A. Tolstikov// Doklady Chemistry, 2010, V. 430, N 2, pp 35-38. doi:10.1134/S0012500810020011 Part: 2), IF=0.204
  354. Н.А. Анисимова, В.М. Берестовицкая, И.Ю. Багрянская, М.Е. Иванова, Г.А. Беркова, А.А. Кужаева
    Акрилаты и их 3-нитро производные в реакциях с антраценом
    Журнал общей химии, 2010, Т. 80, N 2, C. 283-290. (Acrylate and its 3-nitro derivatives in reactions with anthracene/ N. A. Anisimova, V. M. Berestovitskaya, I. S. Bagryanskaya, M. E. Ivanova, G. A. Berkova, A. A. Kuzhaeva// RUSS J GEN CHEM+, 2010, V. 80, N 2, pp 308-315. doi:10.1134/S1070363210020209), IF=0.393
  355. Н.А. Анисимова, В.М. Берестовицкая, И.Ю. Багрянская, М.Е. Иванова, Г.А. Беркова, А.А. Кужаева
    Акрилаты и их 3-нитро производные в реакциях с антраценом
    Журнал общей химии, 2010, Т. 80, N 2, C. 283-290. (Acrylate and its 3-nitro derivatives in reactions with anthracene/ N. A. Anisimova, V. M. Berestovitskaya, I. S. Bagryanskaya, M. E. Ivanova, G. A. Berkova, A. A. Kuzhaeva// RUSS J GEN CHEM+, 2010, V. 80, N 2, pp 308-315. doi:10.1134/S1070363210020209), IF=0.393
  356. Н.А. Анисимова, В.М. Берестовицкая, И.Ю. Багрянская, М.Е. Иванова, Г.А. Беркова, А.А. Кужаева
    Акрилаты и их 3-нитро производные в реакциях с антраценом
    Журнал общей химии, 2010, Т. 80, N 2, C. 283-290. (Acrylate and its 3-nitro derivatives in reactions with anthracene/ N. A. Anisimova, V. M. Berestovitskaya, I. S. Bagryanskaya, M. E. Ivanova, G. A. Berkova, A. A. Kuzhaeva// RUSS J GEN CHEM+, 2010, V. 80, N 2, pp 308-315. doi:10.1134/S1070363210020209), IF=0.393
  357. Н.А. Анисимова, В.М. Берестовицкая, И.Ю. Багрянская, М.Е. Иванова, Г.А. Беркова, А.А. Кужаева
    Акрилаты и их 3-нитро производные в реакциях с антраценом
    Журнал общей химии, 2010, Т. 80, N 2, C. 283-290. (Acrylate and its 3-nitro derivatives in reactions with anthracene/ N. A. Anisimova, V. M. Berestovitskaya, I. S. Bagryanskaya, M. E. Ivanova, G. A. Berkova, A. A. Kuzhaeva// RUSS J GEN CHEM+, 2010, V. 80, N 2, pp 308-315. doi:10.1134/S1070363210020209), IF=0.393
  358. Н.А. Анисимова, В.М. Берестовицкая, И.Ю. Багрянская, М.Е. Иванова, Г.А. Беркова, А.А. Кужаева
    Акрилаты и их 3-нитро производные в реакциях с антраценом
    Журнал общей химии, 2010, Т. 80, N 2, C. 283-290. (Acrylate and its 3-nitro derivatives in reactions with anthracene/ N. A. Anisimova, V. M. Berestovitskaya, I. S. Bagryanskaya, M. E. Ivanova, G. A. Berkova, A. A. Kuzhaeva// RUSS J GEN CHEM+, 2010, V. 80, N 2, pp 308-315. doi:10.1134/S1070363210020209), IF=0.393
  359. А.Н. Синяков, А.А. Рябинин, Г.А. Максакова, В.В. Шелковников, В.А. Лоскутов, Е.В. Васильев, Н.В. Шеклеина
    Сульфониевые производных тиоксантенона – новый класс соединений для фотодетритилирования в микрочиповом олигонуклеотидном синтезе
    Биоорганическая химия, 2010, V. 36, N 1, С. 139-141. (Sulfonium derivatives of thioxanthenone, a new class of photodetritylating agents for microarray oligonucleotide synthesis/ A. N. Sinyakov, A. A. Ryabinin, G. A. Maksakova, V. V. Shelkovnikov, V. A. Loskutov, E. V. Vasil’ev, N. V. Shekleina// RUSS J BIOORG CHEM+, 2010, V.36, N 1, pp 130-132. doi:10.1134/S1068162010010152), IF=0.472
  360. А.Н. Синяков, А.А. Рябинин, Г.А. Максакова, В.В. Шелковников, В.А. Лоскутов, Е.В. Васильев, Н.В. Шеклеина
    Сульфониевые производных тиоксантенона – новый класс соединений для фотодетритилирования в микрочиповом олигонуклеотидном синтезе
    Биоорганическая химия, 2010, V. 36, N 1, С. 139-141. (Sulfonium derivatives of thioxanthenone, a new class of photodetritylating agents for microarray oligonucleotide synthesis/ A. N. Sinyakov, A. A. Ryabinin, G. A. Maksakova, V. V. Shelkovnikov, V. A. Loskutov, E. V. Vasil’ev, N. V. Shekleina// RUSS J BIOORG CHEM+, 2010, V.36, N 1, pp 130-132. doi:10.1134/S1068162010010152), IF=0.472
  361. А.Н. Синяков, А.А. Рябинин, Г.А. Максакова, В.В. Шелковников, В.А. Лоскутов, Е.В. Васильев, Н.В. Шеклеина
    Сульфониевые производных тиоксантенона – новый класс соединений для фотодетритилирования в микрочиповом олигонуклеотидном синтезе
    Биоорганическая химия, 2010, V. 36, N 1, С. 139-141. (Sulfonium derivatives of thioxanthenone, a new class of photodetritylating agents for microarray oligonucleotide synthesis/ A. N. Sinyakov, A. A. Ryabinin, G. A. Maksakova, V. V. Shelkovnikov, V. A. Loskutov, E. V. Vasil’ev, N. V. Shekleina// RUSS J BIOORG CHEM+, 2010, V.36, N 1, pp 130-132. doi:10.1134/S1068162010010152), IF=0.472
  362. С.З. Кусов, Ю.В. Гатилов, И.Ю. Багрянская, Г.В. Романенко, Т.А. Ваганова, И.К. Шундрина, Е.В. Малыхин
    Супрамолекулярные 1D-ансамбли полифторированных арилендиаминов и 18-краун-6
    Известия Академии наук. Сер.хим., 2010, № 2, C. 375-382. (Supramolecular 1D assemblies of polyfluorinated arylenediamines and 18-crown-6/ S. Z. Kusov, Yu. V. Gatilov, I. Yu. Bagryanskaya, G. V. Romanenko, T. A. Vaganova, I. K. Shundrina, E. V. Malykhin// RUSS CHEM B+, 2010, V. 59, N 2, pp 382-390. doi:10.1007/s11172-010-0090-7), IF=0.416
  363. И.В. Зибарева, А.В. Зибарев, В.М. Бузник
    Российская нанонаука: библиометрический анализ на основе баз данных STN International
    Химия в интересах устойчивого развития, 2010, Т. 18, № 2, C. 215-227. (Russian Nanoscience: Bibliometric Analysis Relying on the STN International Database/ I.V. Zibareva, A.V. Zibarev, V.M. Bouznik// Chemistry for Sustainable Development, 2010, V. 18. № 2. pp. 201-219. (in russian))
  364. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  365. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  366. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  367. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  368. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  369. В.М. Бузник, И.В. Зибарева, А.В. Зибарев
    Библиометрические индикаторы российских химических исследований начала 21-ого века на основе баз данных сети STN International
    Вестник РФФИ, 2010 , N 1, С. 11-18
  370. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  371. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  372. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  373. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  374. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  375. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  376. Г.Г. Полякова, Т.П. Кукина, Н.В. Пашенова, О.И. Сальникова, В.В. Стасова
    Применение мицелиальных экстрактов для изучения механизмов устойчивости хвойных к офиостомовым грибам
    Иммунопатология, аллергология, инфектология, 2010, № 1, C. 124-127.
  377. Г.Г. Полякова, Т.П. Кукина, Н.В. Пашенова, О.И. Сальникова, В.В. Стасова
    Применение мицелиальных экстрактов для изучения механизмов устойчивости хвойных к офиостомовым грибам
    Иммунопатология, аллергология, инфектология, 2010, № 1, C. 124-127.
  378. Г.Г. Полякова, Т.П. Кукина, Н.В. Пашенова, О.И. Сальникова, В.В. Стасова
    Применение мицелиальных экстрактов для изучения механизмов устойчивости хвойных к офиостомовым грибам
    Иммунопатология, аллергология, инфектология, 2010, № 1, C. 124-127.
  379. A.M. Chibiryaev, A. Yermakova, I.V. Kozhevnikov
    Chemical and phase equilibria calculation of α-pinene hydration in CO2-expanded liquid
    J. Supercrit. Fluid., 2010, V. 51, N 3, 295-305. doi:10.1016/j.supflu.2009.11.001, IF=2.638
  380. В.И. Аникеев, И.В. Ильина, К.П. Волчо, А. Ермакова, Н.Ф. Салахутдинов
    Реакции термолиза эпоксидов α-пинена и вербенона в сверхкритических растворителях
    Журнал физической химии (А), 2010, Т. 84, N 7, C. 1233–1239. (The thermolysis of &alpha-pinene and verbenone epoxides in supercritical solvents/ V.I. Anikeev, A. Ermakova, I.V. Il'Ina, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2010, V. 84, № 7, pp 1112-1117. doi:10.1134/S0036024410070058), IF=0.437
  381. В.И. Аникеев, И.В. Ильина, К.П. Волчо, А. Ермакова, Н.Ф. Салахутдинов
    Реакции термолиза эпоксидов α-пинена и вербенона в сверхкритических растворителях
    Журнал физической химии (А), 2010, Т. 84, N 7, C. 1233–1239. (The thermolysis of &alpha-pinene and verbenone epoxides in supercritical solvents/ V.I. Anikeev, A. Ermakova, I.V. Il'Ina, K.P. Volcho, N.F. Salakhutdinov// RUSS J PHYS CHEM A+, 2010, V. 84, № 7, pp 1112-1117. doi:10.1134/S0036024410070058), IF=0.437
  382. D.A. Morozov, I.A. Kirilyuk, Yu.V. Gatilov, I.Yu. Bagryanskaya, Ju.Yu. Bozhko, D.A. Komarov, I.A. Grigor'ev
    Intramolecular 1,3-dipolar cycloaddition of alkenylnitrones of the 4H-imidazole series: synthesis of a new nitroxide pH-sensitive spin probe
    Synthesis, 2010, N 2, 343-348. doi:10.1055/s-0029-1217109, IF=2.572
  383. D.A. Morozov, I.A. Kirilyuk, Yu.V. Gatilov, I.Yu. Bagryanskaya, Ju.Yu. Bozhko, D.A. Komarov, I.A. Grigor'ev
    Intramolecular 1,3-dipolar cycloaddition of alkenylnitrones of the 4H-imidazole series: synthesis of a new nitroxide pH-sensitive spin probe
    Synthesis, 2010, N 2, 343-348. doi:10.1055/s-0029-1217109, IF=2.572
  384. С.В. Ларионов, Л.И. Мячина, Е.Г. Богуславский, Р.В. Андреев, Г.И. Бородкин, В.Г. Шубин
    Комплексы Cu(II) и Pd (II) c 2-R-1,3,11,11c-тетраазациклопента[c]фенантренами
    Журнал общей химии, 2010, Т. 80, N 1, C. 139-143. (Complexes of Cu(II) and Pd(II) with 2-R-1,3,11,11c-tetraazacyclopenta[c]phenanthrenes/ S.B. Larionov, L.I. Myachina, E.G. Boguslavskii, R.V. Andreev, G.I. Borodkin, // RUSS J GEN CHEM+, 2010, V. 80, N 1, pp 133-136. doi:10.1134/S1070363210010184), IF=0.393
  385. С.В. Ларионов, Л.И. Мячина, Е.Г. Богуславский, Р.В. Андреев, Г.И. Бородкин, В.Г. Шубин
    Комплексы Cu(II) и Pd (II) c 2-R-1,3,11,11c-тетраазациклопента[c]фенантренами
    Журнал общей химии, 2010, Т. 80, N 1, C. 139-143. (Complexes of Cu(II) and Pd(II) with 2-R-1,3,11,11c-tetraazacyclopenta[c]phenanthrenes/ S.B. Larionov, L.I. Myachina, E.G. Boguslavskii, R.V. Andreev, G.I. Borodkin, // RUSS J GEN CHEM+, 2010, V. 80, N 1, pp 133-136. doi:10.1134/S1070363210010184), IF=0.393
  386. С.В. Ларионов, Л.И. Мячина, Е.Г. Богуславский, Р.В. Андреев, Г.И. Бородкин, В.Г. Шубин
    Комплексы Cu(II) и Pd (II) c 2-R-1,3,11,11c-тетраазациклопента[c]фенантренами
    Журнал общей химии, 2010, Т. 80, N 1, C. 139-143. (Complexes of Cu(II) and Pd(II) with 2-R-1,3,11,11c-tetraazacyclopenta[c]phenanthrenes/ S.B. Larionov, L.I. Myachina, E.G. Boguslavskii, R.V. Andreev, G.I. Borodkin, // RUSS J GEN CHEM+, 2010, V. 80, N 1, pp 133-136. doi:10.1134/S1070363210010184), IF=0.393
  387. А.Г. Покровский, В.О. Пустыльняк, В.А. Шаманин, А.В. Соколова, Э.Э. Шульц, Г.А. Толстиков
    Эффект производных бетулоновой кислоты на экспрессию генов апоптоза в опухолевых лимфоидных клетках человека
    Вестн. НГУ, Сер. Биол. Клин. Мед., 2010, Т. 8, № 1, С. 14-22.
  388. А.Г. Покровский, В.О. Пустыльняк, В.А. Шаманин, А.В. Соколова, Э.Э. Шульц, Г.А. Толстиков
    Эффект производных бетулоновой кислоты на экспрессию генов апоптоза в опухолевых лимфоидных клетках человека
    Вестн. НГУ, Сер. Биол. Клин. Мед., 2010, Т. 8, № 1, С. 14-22.
  389. А.Г. Покровский, В.О. Пустыльняк, В.А. Шаманин, А.В. Соколова, Э.Э. Шульц, Г.А. Толстиков
    Эффект производных бетулоновой кислоты на экспрессию генов апоптоза в опухолевых лимфоидных клетках человека
    Вестн. НГУ, Сер. Биол. Клин. Мед., 2010, Т. 8, № 1, С. 14-22.
  390. О.Б. Казакова, Г.А. Толстиков, К.Ю. Супоницкий
    Одностадийный путь к тритерпеноидам ряда германикана из аллобетулина
    Биоорганическая химия, 2010, V. 36, N 1, С. 142-144. (A one-step approach to the synthesis of germanicane triterpenoids from allobetulin/ O. B. Kazakova, G. A. Tolstikov, K. Yu. Suponitskii// RUSS J BIOORG CHEM+, 2010, V.36, N 1, pp 133-135. doi:10.1134/S1068162010010164), IF=0.472
  391. О.Б. Казакова, Г.А. Толстиков, К.Ю. Супоницкий
    Одностадийный путь к тритерпеноидам ряда германикана из аллобетулина
    Биоорганическая химия, 2010, V. 36, N 1, С. 142-144. (A one-step approach to the synthesis of germanicane triterpenoids from allobetulin/ O. B. Kazakova, G. A. Tolstikov, K. Yu. Suponitskii// RUSS J BIOORG CHEM+, 2010, V.36, N 1, pp 133-135. doi:10.1134/S1068162010010164), IF=0.472
  392. Г.Ю. Ишмуратов, Ю.В. Легостаева, А.Х. Шаяхметова, Л.П. Боцман, Г.А. Толстиков
    Эффективный синтез метил (R)-3-гидроксинонаноата - производного микрокомпонента плазмы крови человека - из касторового масла
    Химия растительного сырья, 2010, N 1, 193-194.
  393. Г.Ю. Ишмуратов, Ю.В. Легостаева, А.Х. Шаяхметова, Л.П. Боцман, Г.А. Толстиков
    Эффективный синтез метил (R)-3-гидроксинонаноата - производного микрокомпонента плазмы крови человека - из касторового масла
    Химия растительного сырья, 2010, N 1, 193-194.
  394. Г.Ю. Ишмуратов, Ю.В. Легостаева, А.Х. Шаяхметова, Л.П. Боцман, Г.А. Толстиков
    Эффективный синтез метил (R)-3-гидроксинонаноата - производного микрокомпонента плазмы крови человека - из касторового масла
    Химия растительного сырья, 2010, N 1, 193-194.
  395. Г.Ю. Ишмуратов, Ю.В. Легостаева, А.Х. Шаяхметова, Л.П. Боцман, Г.А. Толстиков
    Эффективный синтез метил (R)-3-гидроксинонаноата - производного микрокомпонента плазмы крови человека - из касторового масла
    Химия растительного сырья, 2010, N 1, 193-194.
  396. А.В. Стародубов, Д.В. Домрачев, А.В. Ткачёв
    Состав эфирного масла кедрового стланика (Pinus pumila) из Хабаровского края
    Химия растительного сырья, 2010, № 1, 81-86.
  397. В.В. Яньшоле, И.А. Кирилюк, И.А. Григорьев, С.В. Морозов, Ю.П. Центалович
    Изучение антиоксидантных свойств нитроксильных радикалов и гидроксиламинов при взаимодействии с триплетным и дезаминированным кинуренином
    Известия Академии наук. Сер.хим., 2010, № 1, C. 67-75. (Antioxidative properties of nitroxyl radicals and hydroxyamines in reactions with triplet and deaminated kynurenine/ V.V. Yan'shole, I.A. Kirilyuk, I.A. Grigor'ev, S.V. Morozov, Yu.P. Tsentalovicha// RUSS CHEM B+, 2010, V. 59, N 1, pp 66-74. doi:10.1007/s11172-010-0046-y), IF=0.416
  398. В.В. Яньшоле, И.А. Кирилюк, И.А. Григорьев, С.В. Морозов, Ю.П. Центалович
    Изучение антиоксидантных свойств нитроксильных радикалов и гидроксиламинов при взаимодействии с триплетным и дезаминированным кинуренином
    Известия Академии наук. Сер.хим., 2010, № 1, C. 67-75. (Antioxidative properties of nitroxyl radicals and hydroxyamines in reactions with triplet and deaminated kynurenine/ V.V. Yan'shole, I.A. Kirilyuk, I.A. Grigor'ev, S.V. Morozov, Yu.P. Tsentalovicha// RUSS CHEM B+, 2010, V. 59, N 1, pp 66-74. doi:10.1007/s11172-010-0046-y), IF=0.416
  399. В.Ф. Рапута, В.В. Коковкин, С.В. Морозов
    Экспериментальные исследования и численный анализ процессов загрязнения снегового покрова в окрестностях крупной автомагистрали г. Новосибирска
    Химия в интересах устойчивого развития, 2010, Т. 18, № 1, C. 63-70. (Experimental Investigation and Numerical Analysis of the Processes of Propagation of Snow Cover Pollution near a Major Highway/ V. F. Raputa, V. V. Kokovkin, S. V. Morozov// Chemistry for Sustainable Development, 2010, V.18., № 1, pp. 63-70. (in russian))
  400. В.Ф. Рапута, В.В. Коковкин, С.В. Морозов
    Экспериментальные исследования и численный анализ процессов загрязнения снегового покрова в окрестностях крупной автомагистрали г. Новосибирска
    Химия в интересах устойчивого развития, 2010, Т. 18, № 1, C. 63-70. (Experimental Investigation and Numerical Analysis of the Processes of Propagation of Snow Cover Pollution near a Major Highway/ V. F. Raputa, V. V. Kokovkin, S. V. Morozov// Chemistry for Sustainable Development, 2010, V.18., № 1, pp. 63-70. (in russian))
  401. N.M. Troshkova, L.I. Goryunov, Yu.V. Gatilov, G.A. Nevinsky, V.D. Shteingarts
    Aminodefluorination of 2-X-pentafluoro-1,4-naphthoquinones (X = NHnBu, NEt2, and OMe)
    J. Fluorine Chem., 2010, V. 131, N 1, 70-77. doi:10.1016/j.jfluchem.2009.10.007, IF=1.73

2009

Reviews, articles

  1. Г.А. Коваленко , Л.В. Перминова , Е.И. Черняк., Л.И. Сапунова
    ИССЛЕДОВАНИЕ МАКРОКИНЕТИКИ ГЕТЕРОГЕННОГО ПРОЦЕССА ИЗОМЕРИЗАЦИИ МОНОСАХАРИДОВ С УЧАСТИЕМ НЕ РАСТУЩИХ КЛЕТОК ПРОДУЦЕНТА ГЛЮКОЗОИЗОМЕРАЗЫ ARTHROBACTER NICOTIANAE, ИММОБИЛИЗОВАННЫХ В SIO 2 - КСЕРОГЕЛЕ
    Биотехнология, 2009, № 5, 63-73. (Investigation on Macrokinetics of Heterogeneous Process of Monosaccharide Isomerization using NonGrowing Cells of a Glucose isomerase Producer Arthrobacter nicotianae Immobilized in SiO2-Xerogel/ G.A. Kovalenko, L.V. Perminova, E.I. Chernyak, L.I. Sapunova// Applied Biochemistry and Microbiology December 2010, V. 46, N 7, pp 697-705 doi:10.1134/S0003683810070045), IF=0.67
  2. Г.А. Коваленко , Л.В. Перминова , Е.И. Черняк., Л.И. Сапунова
    ИССЛЕДОВАНИЕ МАКРОКИНЕТИКИ ГЕТЕРОГЕННОГО ПРОЦЕССА ИЗОМЕРИЗАЦИИ МОНОСАХАРИДОВ С УЧАСТИЕМ НЕ РАСТУЩИХ КЛЕТОК ПРОДУЦЕНТА ГЛЮКОЗОИЗОМЕРАЗЫ ARTHROBACTER NICOTIANAE, ИММОБИЛИЗОВАННЫХ В SIO 2 - КСЕРОГЕЛЕ
    Биотехнология, 2009, № 5, 63-73. (Investigation on Macrokinetics of Heterogeneous Process of Monosaccharide Isomerization using NonGrowing Cells of a Glucose isomerase Producer Arthrobacter nicotianae Immobilized in SiO2-Xerogel/ G.A. Kovalenko, L.V. Perminova, E.I. Chernyak, L.I. Sapunova// Applied Biochemistry and Microbiology December 2010, V. 46, N 7, pp 697-705 doi:10.1134/S0003683810070045), IF=0.67
  3. Г.А. Коваленко , Л.В. Перминова , Е.И. Черняк., Л.И. Сапунова
    ИССЛЕДОВАНИЕ МАКРОКИНЕТИКИ ГЕТЕРОГЕННОГО ПРОЦЕССА ИЗОМЕРИЗАЦИИ МОНОСАХАРИДОВ С УЧАСТИЕМ НЕ РАСТУЩИХ КЛЕТОК ПРОДУЦЕНТА ГЛЮКОЗОИЗОМЕРАЗЫ ARTHROBACTER NICOTIANAE, ИММОБИЛИЗОВАННЫХ В SIO 2 - КСЕРОГЕЛЕ
    Биотехнология, 2009, № 5, 63-73. (Investigation on Macrokinetics of Heterogeneous Process of Monosaccharide Isomerization using NonGrowing Cells of a Glucose isomerase Producer Arthrobacter nicotianae Immobilized in SiO2-Xerogel/ G.A. Kovalenko, L.V. Perminova, E.I. Chernyak, L.I. Sapunova// Applied Biochemistry and Microbiology December 2010, V. 46, N 7, pp 697-705 doi:10.1134/S0003683810070045), IF=0.67
  4. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  5. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  6. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  7. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  8. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  9. Е.Н. Медведева, Н.А. Неверова, Т.Е. Федорова, В.А. Бабкин, Е.С. Метелева, А.В. Душкин, Т.Г. Толстикова, М.В. Хвостов, М.П. Долгих
    _Структурные превращения арабиногалактана из лиственницы сибирской при механохимической обработке и биологические свойства продуктов
    Химия растительного сырья, 2009, № 3, 49-56. (Structural transformations of arabinogalactan from the Siberian larch during mechanochemical processing and the biological properties of the products/ E. N. Medvedeva, N. A. Neverova, T. E. Fedorova, V. A. Babkin, E. S. Meteleva, A. V. Dushkin, T. G. Tolstikova, M. V. Khvostov, M. P. Dolgikh// Russian Journal of Bioorganic Chemistry, 2010, V. 36, N 7, pp 853-859 doi:10.1134/S1068162010070101)
  10. O. A. Snytnikova, L. V. Kopylova, E. I. Chernyak, S. V. Morozov, N.G. Kolosova, Y.P. Tsentalovich
    Tryptophan and kynurenine levels in lenses of Wistar and accelerated-senescence OXYS rats/
    Mol. Vis., 2009, V.15, 2780-2788., IF=2.463
  11. O. A. Snytnikova, L. V. Kopylova, E. I. Chernyak, S. V. Morozov, N.G. Kolosova, Y.P. Tsentalovich
    Tryptophan and kynurenine levels in lenses of Wistar and accelerated-senescence OXYS rats/
    Mol. Vis., 2009, V.15, 2780-2788., IF=2.463
  12. O. A. Snytnikova, L. V. Kopylova, E. I. Chernyak, S. V. Morozov, N.G. Kolosova, Y.P. Tsentalovich
    Tryptophan and kynurenine levels in lenses of Wistar and accelerated-senescence OXYS rats/
    Mol. Vis., 2009, V.15, 2780-2788., IF=2.463
  13. O. A. Snytnikova, L. V. Kopylova, E. I. Chernyak, S. V. Morozov, N.G. Kolosova, Y.P. Tsentalovich
    Tryptophan and kynurenine levels in lenses of Wistar and accelerated-senescence OXYS rats/
    Mol. Vis., 2009, V.15, 2780-2788., IF=2.463
  14. В.В. Коковкин, В.Ф. Рапута, С.В. Морозов
    Модели и методы контроля аэрозольных выпадений примеси в окрестности автомагистрали
    Горный информационно-аналитический бюллетень, 2009 , № 17, N 12, C.97-102.
  15. В.В. Коковкин, В.Ф. Рапута, С.В. Морозов
    Модели и методы контроля аэрозольных выпадений примеси в окрестности автомагистрали
    Горный информационно-аналитический бюллетень, 2009 , № 17, N 12, C.97-102.
  16. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  17. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  18. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  19. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  20. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  21. В.В. Мартемьянов, С.А. Бахвалов, Дж. Рантала, И.М. Дубовский, Э.Э. Шульц, А.Г. Стрельников, В.В. Глупов
    Реакция гусениц непарного шелкопряда Lymantria dispar L., инфицированных вирусом ядерного полиэдроза, на индуцированную резистентность березы Betula pendula Roth.
    Экология. 2009, Т. 40, N 6, С. 434-439. (The response of gypsy moth (Lymantria dispar L.) larvae infected with nuclear polyhedrosis virus to induced resistance in birch (Betula pendula Roth.)/ V.V. Martemyanov, S.A. Bakhvalov, I.M. Dubovskiy, I.A. Belousova, A.G. Strel'nikov, V.V. Glupov, M.J. Rantala, E.E. Shul'ts// Russian Journal of Ecology, 2009, V. 40, N 6, pp 434-439. doi:10.1134/S1067413609060095), IF=0.296
  22. K. Suzuki, D.G. Mazhukin, H. Takahashi, Y. Uchida, R. Tamura, I.A. Grigor’ev
    Synthesis and stereochemistry of novel rigid nitroxide biradicals based on paramagnetic pyrrolidine core
    Heterocycles, 2009, V. 78, 3091-3099. doi:10.3987/COM-09-11821, IF=0.98
  23. K. Suzuki, D.G. Mazhukin, H. Takahashi, Y. Uchida, R. Tamura, I.A. Grigor’ev
    Synthesis and stereochemistry of novel rigid nitroxide biradicals based on paramagnetic pyrrolidine core
    Heterocycles, 2009, V. 78, 3091-3099. doi:10.3987/COM-09-11821, IF=0.98
  24. K. Suzuki, D.G. Mazhukin, H. Takahashi, Y. Uchida, R. Tamura, I.A. Grigor’ev
    Synthesis and stereochemistry of novel rigid nitroxide biradicals based on paramagnetic pyrrolidine core
    Heterocycles, 2009, V. 78, 3091-3099. doi:10.3987/COM-09-11821, IF=0.98
  25. K. Suzuki, D.G. Mazhukin, H. Takahashi, Y. Uchida, R. Tamura, I.A. Grigor’ev
    Synthesis and stereochemistry of novel rigid nitroxide biradicals based on paramagnetic pyrrolidine core
    Heterocycles, 2009, V. 78, 3091-3099. doi:10.3987/COM-09-11821, IF=0.98
  26. A. I. Plekhanov, A. I. Gorkovenko, N. A. Orlova, A. E. Simanchuk, and V. V. Shelkovnikov
    Comparative Study of the Nonlinear Optical Properties of Molecular J and H Aggregates in Thin Films
    High Energy Chemistry, 2009, V.. 43, No. 7, pp. 607–610. doi:10.1134/S0018143909070194, IF=0.577
  27. A. I. Plekhanov, A. I. Gorkovenko, N. A. Orlova, A. E. Simanchuk, and V. V. Shelkovnikov
    Comparative Study of the Nonlinear Optical Properties of Molecular J and H Aggregates in Thin Films
    High Energy Chemistry, 2009, V.. 43, No. 7, pp. 607–610. doi:10.1134/S0018143909070194, IF=0.577
  28. A. I. Plekhanov, A. I. Gorkovenko, N. A. Orlova, A. E. Simanchuk, and V. V. Shelkovnikov
    Comparative Study of the Nonlinear Optical Properties of Molecular J and H Aggregates in Thin Films
    High Energy Chemistry, 2009, V.. 43, No. 7, pp. 607–610. doi:10.1134/S0018143909070194, IF=0.577
  29. N.A. Orlova, I.Yu. Kargapolova, V.V. Shelkovnikov, A.I. Plekhanov
    Luminescent Silica Nanoparticles Modified with a Functional Pyrylocyanine Dye
    High Energy Chemistry, 2009, V.. 43, №. 7, pp. 602-606. doi:10.1134/S0018143909070182, IF=0.577
  30. С.П. Ващенко, В.П. Лукашов, С.В. Морозов, Х.С. Пак
    Исследование плазмохимической переработки масла, содержащего полихлорированные бифенилы/
    Теплофизика и аэромеханика, 2009, Т.16, N 4, с.661-670. (Study on the plasma treatment of waste oil containing PCB/ H.S. Park, V.P. Lukashov, S.P. Vashchenko, S.V. Morozov// Thermophysics and Aeromechanics, 2009, V. 16, N 4, pp 611-620. doi:10.1134/S0869864309040106)
  31. С.П. Ващенко, В.П. Лукашов, С.В. Морозов, Х.С. Пак
    Исследование плазмохимической переработки масла, содержащего полихлорированные бифенилы/
    Теплофизика и аэромеханика, 2009, Т.16, N 4, с.661-670. (Study on the plasma treatment of waste oil containing PCB/ H.S. Park, V.P. Lukashov, S.P. Vashchenko, S.V. Morozov// Thermophysics and Aeromechanics, 2009, V. 16, N 4, pp 611-620. doi:10.1134/S0869864309040106)
  32. С.П. Ващенко, В.П. Лукашов, С.В. Морозов, Х.С. Пак
    Исследование плазмохимической переработки масла, содержащего полихлорированные бифенилы/
    Теплофизика и аэромеханика, 2009, Т.16, N 4, с.661-670. (Study on the plasma treatment of waste oil containing PCB/ H.S. Park, V.P. Lukashov, S.P. Vashchenko, S.V. Morozov// Thermophysics and Aeromechanics, 2009, V. 16, N 4, pp 611-620. doi:10.1134/S0869864309040106)
  33. М.П.Сартаков, В.Д.Тихова
    Графостатистический анализ и спектроскопия ЯМР 13С молекул гуминовых кислот торфов среднего Приобья.
    Вестник КрасГАУ, N 6, 2009, с.76-80.
  34. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  35. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  36. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  37. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  38. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  39. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  40. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  41. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  42. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  43. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  44. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  45. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  46. В.И. Каледин, Н.А. Жукова, В.П. Николин, Н.А. Попова, М.Д. Беляев, Н.В. Багинская, Е.А. Литвинова, Т.Г. Толстикова, Е.Л. Лушникова, Д.Е. Семёнов
    Гепатокарцинома-29-метастазирующая перевиваемая опухоль мышей, вызывающая кахексию
    Бюллетень экспериментальноой биологии и медицины, 2009 , Т. 148, № 12, C. 664-667. (Hepatocarcinoma-29, a Metastasizing Transplantable Mouse Tumor Inducing Cachexia/ V. I. Kaledin, N. A. Zhukova, V. P. Nikolin, N. A. Popova, M. D. Beliaev, N. V. Baginskaya, E. A. Litvinova, T. G. Tolstikova, E. L. Lushnikova, D. E. Semenov// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 6, pp 903-907 doi:10.1007/s10517-010-0848-9), IF=0.257
  47. Л.А. Шундрин, П.В. Мельников, Е.А. Поленов
    Внутреннее заторможенное вращение CF3-группы в анион-радикале 2-трифторметилнитробензола в смесях ДМФА:H2O
    Журнал структурной химии, 2009, Т.50, N 6. С.1121-1131. (Hindered internal rotation of the CF3 group in the 2-trifluoromethylnitrobenzene radical anion in DMF:H2O mixtures/ L. A. Shundrin, P. V. Melnikov, E. A. Polenov// Journal of Structural Chemistry, 2009, V. 50, N 6, pp 1071-1081 doi:10.1007/s10947-009-0158-0), IF=0.578
  48. Л.А. Шундрин, П.В. Мельников, Е.А. Поленов
    Внутреннее заторможенное вращение CF3-группы в анион-радикале 2-трифторметилнитробензола в смесях ДМФА:H2O
    Журнал структурной химии, 2009, Т.50, N 6. С.1121-1131. (Hindered internal rotation of the CF3 group in the 2-trifluoromethylnitrobenzene radical anion in DMF:H2O mixtures/ L. A. Shundrin, P. V. Melnikov, E. A. Polenov// Journal of Structural Chemistry, 2009, V. 50, N 6, pp 1071-1081 doi:10.1007/s10947-009-0158-0), IF=0.578
  49. С.Г. Ильясов, А.А. Лобанова, И.Ю. Багрянская, Т.В. Рыбалова, Ю.В. Гатилов
    Исследование структуры N,N'-динитро-мочевины и её солей физико-химическими методами
    Журнал структурной химии, 2009, Т. 50, N 6, С. 1115-1120. (Physicochemical studies of the structure of N,N'-dinitrourea and its salts/ S. G. Il’yasov, A. A. Lobanova, I. Yu. Bagryanskaya, T. V. Rybalova, Yu. V. Gatilov// Journal of Structural Chemistry, 2009, V. 50, N 6, pp 1066-1070 doi:10.1007/s10947-009-0157-1), IF=0.578
  50. С.Г. Ильясов, А.А. Лобанова, И.Ю. Багрянская, Т.В. Рыбалова, Ю.В. Гатилов
    Исследование структуры N,N'-динитро-мочевины и её солей физико-химическими методами
    Журнал структурной химии, 2009, Т. 50, N 6, С. 1115-1120. (Physicochemical studies of the structure of N,N'-dinitrourea and its salts/ S. G. Il’yasov, A. A. Lobanova, I. Yu. Bagryanskaya, T. V. Rybalova, Yu. V. Gatilov// Journal of Structural Chemistry, 2009, V. 50, N 6, pp 1066-1070 doi:10.1007/s10947-009-0157-1), IF=0.578
  51. Л.И. Горюнов, И. Гробе, В.Д. Штейнгарц, Е. Вюсвайн, Р. Мевс
    Диметилфосфинодегалогенирование пентафторхлорбензола, 2,3- и 2,6-дифторбромбензола действием Me2Pli
    Журнал органической химии, 2009, Т. 45, N 12, с. 1860-1862 (Reaction of chloropentafluorobenzene and 2,3-and 2,6-difluorobromobenzenes with lithium dimethylphosphide/ L.I. Goryunov, J. Grobe, V.D. Shteingarts, R. Mews, E.U. Wurthwein// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1859-1861 doi:10.1134/S1070428009120197), IF=0.556
  52. Л.И. Горюнов, И. Гробе, В.Д. Штейнгарц, Е. Вюсвайн, Р. Мевс
    Диметилфосфинодегалогенирование пентафторхлорбензола, 2,3- и 2,6-дифторбромбензола действием Me2Pli
    Журнал органической химии, 2009, Т. 45, N 12, с. 1860-1862 (Reaction of chloropentafluorobenzene and 2,3-and 2,6-difluorobromobenzenes with lithium dimethylphosphide/ L.I. Goryunov, J. Grobe, V.D. Shteingarts, R. Mews, E.U. Wurthwein// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1859-1861 doi:10.1134/S1070428009120197), IF=0.556
  53. Л.И. Горюнов, И. Гробе, В.Д. Штейнгарц, Е. Вюсвайн, Р. Мевс
    Диметилфосфинодегалогенирование пентафторхлорбензола, 2,3- и 2,6-дифторбромбензола действием Me2Pli
    Журнал органической химии, 2009, Т. 45, N 12, с. 1860-1862 (Reaction of chloropentafluorobenzene and 2,3-and 2,6-difluorobromobenzenes with lithium dimethylphosphide/ L.I. Goryunov, J. Grobe, V.D. Shteingarts, R. Mews, E.U. Wurthwein// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1859-1861 doi:10.1134/S1070428009120197), IF=0.556
  54. М.А. Ленский, Э.Э. Шульц, А.А. Андрощук, Г.А. Толстиков
    Взаимодействие трифенилового эфира борной кислоты с 1,3,5-триоксаном.
    Журнал органической химии, 2009, Т. 45, N 12. C. 1780-1783. (Reaction of triphenyl borate with 1,3,5-trioxane/ M.A. Lenskii, E.E. Shul'ts, A.A. Androshchuk, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1772-1775. doi:10.1134/S1070428009120045), IF=0.556
  55. М.А. Ленский, Э.Э. Шульц, А.А. Андрощук, Г.А. Толстиков
    Взаимодействие трифенилового эфира борной кислоты с 1,3,5-триоксаном.
    Журнал органической химии, 2009, Т. 45, N 12. C. 1780-1783. (Reaction of triphenyl borate with 1,3,5-trioxane/ M.A. Lenskii, E.E. Shul'ts, A.A. Androshchuk, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1772-1775. doi:10.1134/S1070428009120045), IF=0.556
  56. М.А. Ленский, Э.Э. Шульц, А.А. Андрощук, Г.А. Толстиков
    Реакция трифенилбората с 1,3,5-триоксаном
    Журнал органической химии, 2009, Т. 45, N 12, 1780–1783. (Reaction of triphenyl borate with 1,3,5-trioxane/ M.A. Lenskii, E.E. Shul'ts, A.A. Androshchuk, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1772-1775 doi:10.1134/S1070428009120045), IF=0.556
  57. М.А. Ленский, Э.Э. Шульц, А.А. Андрощук, Г.А. Толстиков
    Реакция трифенилбората с 1,3,5-триоксаном
    Журнал органической химии, 2009, Т. 45, N 12, 1780–1783. (Reaction of triphenyl borate with 1,3,5-trioxane/ M.A. Lenskii, E.E. Shul'ts, A.A. Androshchuk, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1772-1775 doi:10.1134/S1070428009120045), IF=0.556
  58. A.L. Buchachenko, L.N. Shchegoleva, N.N. Breslavskaya
    Paramagnetic Complexes of Magnesium as mediators in enzimatic ATP synthesis: DFT calcukations of magnetic parameters.
    Chem. Phys. Letters, 2009, V. 483, N 1-3, 77-80. doi:10.1016/j.cplett.2009.10.044, IF=2.168
  59. A.L. Buchachenko, L.N. Shchegoleva, N.N. Breslavskaya
    Paramagnetic Complexes of Magnesium as mediators in enzimatic ATP synthesis: DFT calcukations of magnetic parameters.
    Chem. Phys. Letters, 2009, V. 483, N 1-3, 77-80. doi:10.1016/j.cplett.2009.10.044, IF=2.168
  60. М.П.Сартаков, В.Д.Тихова
    Термическая характеристика гуминовых кислот торфов среднего Приобья.
    Вестник КрасГАУ, N 11, 2009, с.26-29.
  61. А.В. Шернюков, А.Я. Майганашев, Д.В. Корчагина, Ю.В. Гатилов, Н.Ф. Салахутдинов, Г.А. Толстиков
    Спироциклизация 2,3-секо-28-оксо-19b,28-эпокси-18a-олеан-2,3-ангидрида с бензиламинами
    Доклады Академии наук (Химия), 2009, т.429, №3, C.339-342. (Spirocyclization of 2,3-seco-19 beta,28-epoxy-28-oxo-18 alpha-olean-2,3-dicarboxylic anhydride with benzylamines/ A.V. Shernyukov, I.Ya. Mainagashev, D.V. Korchagina, Yu.V. Gatilov, N.F. Salakhutdinov, G.A. Tolstikov// Doklady Chemistry, 2009, V.429,N 1, pp 286-289 doi:10.1134/S0012500809110081), IF=0.231
  62. A.A. Tazetdinova, O.A. Luzina, M.P. Polovinka, N.F. Salakhutdinov, G.A. Tolstikov
    Amino-derivatives of usninic acid
    Chemistry of Natural Compounds, 2009, V. 45, N 6, pp 800-804. doi:10.1007/s10600-010-9502-z, IF=0.467
  63. В.В. Литвак, А.С. Кондратьев, В.Д. Штейнгарц
    Синтез β-функционализированных этил(полифторарил)сульфидов, -сульфоксидов и -сульфонов на основе пентафторбензойной кислоты
    Журнал органической химии, 2009, Т. 45, N 6, 1648-53. (Synthesis of beta-Functionalized Ethyl Polyfluoroaryl Sulfides, Sulfoxides, and Sulfones Underlain by Pentafluorobenzoic Acid/ V.V. Litvak, A.S. Kondrat'ev, V.D. Shteimgarts// Russian Journal of Organic Chemistry, 2009, V. 45, N 11, pp 1637-1643. doi:10.1134/S1070428009110104), IF=0.556
  64. С.В. Ларионов, Л.А. Глинская, Т.Г. Леонова, Р.Ф. Клевцова, Е.М. Усков, В.Е. Платонов, В.М. Карпов, В.П. Фадеева
    Люминесцентные свойства комплексов Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) и Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Структура комплекса Tb22(H2O)8(C6F5COO)6] и его изомера в супрамолекулярном соединении [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH
    Координационная химия, 2009, Т.35. N 11, С. 808-816. (Luminescence properties of complexes Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) and Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Structures of the Tb22(H2O)8(C6F5COO)6] complex and its isomer in the supramolecular compound [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH/ S.V. Larionov, L.A. Glinskaya, T.G. Leonova, R.F. Klevtsova, E.M. Uskov, V.E. Platonov, V.M. Karpov, V.P. Fadeeva// Russian Journal of Coordination Chemistry, 2009, V. 35, N 11, pp 798-806. doi:10.1134/S1070328409110025), IF=0.533
  65. С.В. Ларионов, Л.А. Глинская, Т.Г. Леонова, Р.Ф. Клевцова, Е.М. Усков, В.Е. Платонов, В.М. Карпов, В.П. Фадеева
    Люминесцентные свойства комплексов Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) и Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Структура комплекса Tb22(H2O)8(C6F5COO)6] и его изомера в супрамолекулярном соединении [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH
    Координационная химия, 2009, Т.35. N 11, С. 808-816. (Luminescence properties of complexes Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) and Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Structures of the Tb22(H2O)8(C6F5COO)6] complex and its isomer in the supramolecular compound [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH/ S.V. Larionov, L.A. Glinskaya, T.G. Leonova, R.F. Klevtsova, E.M. Uskov, V.E. Platonov, V.M. Karpov, V.P. Fadeeva// Russian Journal of Coordination Chemistry, 2009, V. 35, N 11, pp 798-806. doi:10.1134/S1070328409110025), IF=0.533
  66. С.В. Ларионов, Л.А. Глинская, Т.Г. Леонова, Р.Ф. Клевцова, Е.М. Усков, В.Е. Платонов, В.М. Карпов, В.П. Фадеева
    Люминесцентные свойства комплексов Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) и Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Структура комплекса Tb22(H2O)8(C6F5COO)6] и его изомера в супрамолекулярном соединении [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH
    Координационная химия, 2009, Т.35. N 11, С. 808-816. (Luminescence properties of complexes Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) and Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Structures of the Tb22(H2O)8(C6F5COO)6] complex and its isomer in the supramolecular compound [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH/ S.V. Larionov, L.A. Glinskaya, T.G. Leonova, R.F. Klevtsova, E.M. Uskov, V.E. Platonov, V.M. Karpov, V.P. Fadeeva// Russian Journal of Coordination Chemistry, 2009, V. 35, N 11, pp 798-806. doi:10.1134/S1070328409110025), IF=0.533
  67. С.В. Ларионов, Л.А. Глинская, Т.Г. Леонова, Р.Ф. Клевцова, Е.М. Усков, В.Е. Платонов, В.М. Карпов, В.П. Фадеева
    Люминесцентные свойства комплексов Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) и Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Структура комплекса Tb22(H2O)8(C6F5COO)6] и его изомера в супрамолекулярном соединении [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH
    Координационная химия, 2009, Т.35. N 11, С. 808-816. (Luminescence properties of complexes Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) and Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Structures of the Tb22(H2O)8(C6F5COO)6] complex and its isomer in the supramolecular compound [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH/ S.V. Larionov, L.A. Glinskaya, T.G. Leonova, R.F. Klevtsova, E.M. Uskov, V.E. Platonov, V.M. Karpov, V.P. Fadeeva// Russian Journal of Coordination Chemistry, 2009, V. 35, N 11, pp 798-806. doi:10.1134/S1070328409110025), IF=0.533
  68. С.В. Ларионов, Л.А. Глинская, Т.Г. Леонова, Р.Ф. Клевцова, Е.М. Усков, В.Е. Платонов, В.М. Карпов, В.П. Фадеева
    Люминесцентные свойства комплексов Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) и Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Структура комплекса Tb22(H2O)8(C6F5COO)6] и его изомера в супрамолекулярном соединении [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH
    Координационная химия, 2009, Т.35. N 11, С. 808-816. (Luminescence properties of complexes Ln(Phen)(C6F5COO)3 (Ln=Tb, Eu) and Ln(C6F5COO)5•nH2O (Ln=Tb, n=2; Ln=Eu, n=1). Structures of the Tb22(H2O)8(C6F5COO)6] complex and its isomer in the supramolecular compound [Tb2(H2O)8(C6F5COO)6]•2C6F5COOH/ S.V. Larionov, L.A. Glinskaya, T.G. Leonova, R.F. Klevtsova, E.M. Uskov, V.E. Platonov, V.M. Karpov, V.P. Fadeeva// Russian Journal of Coordination Chemistry, 2009, V. 35, N 11, pp 798-806. doi:10.1134/S1070328409110025), IF=0.533
  69. D.S. Baranov, S.F. Vasilevsky, V.I. Mamatyuk, Yu.V. Gatilov
    Multichannel reaction of 1-(3'-hydroxy-3'-methylbutynyl)-9,10-anthraquinone with guanidine
    Mendeleev Commun., 2009, V. 19, N 6, 326–328. doi:10.1016/j.mencom.2009.11.011, IF=0.609
  70. D.S. Baranov, S.F. Vasilevsky, V.I. Mamatyuk, Yu.V. Gatilov
    Multichannel reaction of 1-(3'-hydroxy-3'-methylbutynyl)-9,10-anthraquinone with guanidine
    Mendeleev Commun., 2009, V. 19, N 6, 326–328. doi:10.1016/j.mencom.2009.11.011, IF=0.609
  71. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
    Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
    J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
  72. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
    Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
    J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
  73. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
    Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
    J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
  74. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
    Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
    J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
  75. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
    Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
    J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
  76. L.Yu. Safina, G.A. Selivanova, K.Yu. Koltunov, V.D. Shteingarts
    Synthesis of polyfluorinated 4-phenyl-3,4-dihydroquinolin-2-ones and quinolin-2-ones via superacidic activation of N-(polyfluorophenyl)cinnamamide
    Tetrahedron Lett., 2009, V. 50, N 37, pp 5245–5247. doi:10.1016/j.tetlet.2009.07.013, IF=2.538
  77. M.J. Afonin, V.A. Maksakov, V.P. Kirin, L.A. Scheludyakova, A.V. Golovin, V.G. Vasil'ev
    Transformations of allylamine and N-allylacetamide on triosmium cluster complexes with hemilabile ligands
    Polyhedron, 2009 , V. 28, N 13, 2754-2758. doi:10.1016/j.poly.2009.05.070, IF=1.8
  78. M.J. Afonin, V.A. Maksakov, V.P. Kirin, L.A. Scheludyakova, A.V. Golovin, V.G. Vasil'ev
    Transformations of allylamine and N-allylacetamide on triosmium cluster complexes with hemilabile ligands
    Polyhedron, 2009 , V. 28, N 13, 2754-2758. doi:10.1016/j.poly.2009.05.070, IF=1.8
  79. M.J. Afonin, V.A. Maksakov, V.P. Kirin, L.A. Scheludyakova, A.V. Golovin, V.G. Vasil'ev
    Transformations of allylamine and N-allylacetamide on triosmium cluster complexes with hemilabile ligands
    Polyhedron, 2009 , V. 28, N 13, 2754-2758. doi:10.1016/j.poly.2009.05.070, IF=1.8
  80. M.J. Afonin, V.A. Maksakov, V.P. Kirin, L.A. Scheludyakova, A.V. Golovin, V.G. Vasil'ev
    Transformations of allylamine and N-allylacetamide on triosmium cluster complexes with hemilabile ligands
    Polyhedron, 2009 , V. 28, N 13, 2754-2758. doi:10.1016/j.poly.2009.05.070, IF=1.8
  81. M.J. Afonin, V.A. Maksakov, V.P. Kirin, L.A. Scheludyakova, A.V. Golovin, V.G. Vasil'ev
    Transformations of allylamine and N-allylacetamide on triosmium cluster complexes with hemilabile ligands
    Polyhedron, 2009 , V. 28, N 13, 2754-2758. doi:10.1016/j.poly.2009.05.070, IF=1.8
  82. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  83. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  84. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  85. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  86. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  87. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  88. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, O.V. Borovkova, G.G. Dultseva, V.V. Boldyrev, V.M. Fomin
    Analgesic effect of ibuprofen nanoparticles
    J. Aerosol Med. Pulm. D., 2009, V. 22, N 3, 245-253. doi:10.1089/jamp.2008.0721, IF=2.108
  89. Т.Г. Толстикова, Н.А. Жукова, И.В. Сорокина, М.П. Долгих, Т.В. Огородникова, М.В. Бородавкина, Ю.Л. Дугина, С.А. Сергеева
    Противоязвенная активность препаратов сверхмалых доз антител на модели хронической язвы у крыс
    Бюллетень экспериментальноой биологии и медицины, 2009, Т. 148, Приложение , C. 181-183 (Antiulcer Activity of Preparations Containing Ultralow Doses of Antibodies in Modeled Chronic Ulcer in Rats/ T. G. Tolstikova, N. A. Zhukova, I. V. Sorokina, M. P. Dolgikh, T. V. Ogorodnikova, M. V. Borodavkina, Yu. L. Dugina, S. A. Sergeeva// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 3, pp 540-542 doi:10.1007/s10517-010-0759-9), IF=0.257
  90. Т.Г. Толстикова, Н.А. Жукова, И.В. Сорокина, М.П. Долгих, Т.В. Огородникова, М.В. Бородавкина, Ю.Л. Дугина, С.А. Сергеева
    Противоязвенная активность препаратов сверхмалых доз антител на модели хронической язвы у крыс
    Бюллетень экспериментальноой биологии и медицины, 2009, Т. 148, Приложение , C. 181-183 (Antiulcer Activity of Preparations Containing Ultralow Doses of Antibodies in Modeled Chronic Ulcer in Rats/ T. G. Tolstikova, N. A. Zhukova, I. V. Sorokina, M. P. Dolgikh, T. V. Ogorodnikova, M. V. Borodavkina, Yu. L. Dugina, S. A. Sergeeva// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 3, pp 540-542 doi:10.1007/s10517-010-0759-9), IF=0.257
  91. Т.Г. Толстикова, Н.А. Жукова, И.В. Сорокина, М.П. Долгих, Т.В. Огородникова, М.В. Бородавкина, Ю.Л. Дугина, С.А. Сергеева
    Противоязвенная активность препаратов сверхмалых доз антител на модели хронической язвы у крыс
    Бюллетень экспериментальноой биологии и медицины, 2009, Т. 148, Приложение , C. 181-183 (Antiulcer Activity of Preparations Containing Ultralow Doses of Antibodies in Modeled Chronic Ulcer in Rats/ T. G. Tolstikova, N. A. Zhukova, I. V. Sorokina, M. P. Dolgikh, T. V. Ogorodnikova, M. V. Borodavkina, Yu. L. Dugina, S. A. Sergeeva// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 3, pp 540-542 doi:10.1007/s10517-010-0759-9), IF=0.257
  92. Т.Г. Толстикова, Н.А. Жукова, И.В. Сорокина, М.П. Долгих, Т.В. Огородникова, М.В. Бородавкина, Ю.Л. Дугина, С.А. Сергеева
    Противоязвенная активность препаратов сверхмалых доз антител на модели хронической язвы у крыс
    Бюллетень экспериментальноой биологии и медицины, 2009, Т. 148, Приложение , C. 181-183 (Antiulcer Activity of Preparations Containing Ultralow Doses of Antibodies in Modeled Chronic Ulcer in Rats/ T. G. Tolstikova, N. A. Zhukova, I. V. Sorokina, M. P. Dolgikh, T. V. Ogorodnikova, M. V. Borodavkina, Yu. L. Dugina, S. A. Sergeeva// Bulletin of Experimental Biology and Medicine, 2009, V. 148, N 3, pp 540-542 doi:10.1007/s10517-010-0759-9), IF=0.257
  93. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, В.Е. Катаев, Р.З. Мусин
    Синтез и модификация тритерпеноидов с двумя лупановыми каркасами
    Биоорганическая химия, 2009, Т. 35, N 5, C. 714-720. (Synthesis and modification of triterpenoids with two lupan backbones/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, V. E. Kataev, R. Z. Musin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 5, pp 645-650 doi:10.1134/S1068162009050173), IF=0.711
  94. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, В.Е. Катаев, Р.З. Мусин
    Синтез и модификация тритерпеноидов с двумя лупановыми каркасами
    Биоорганическая химия, 2009, Т. 35, N 5, C. 714-720. (Synthesis and modification of triterpenoids with two lupan backbones/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, V. E. Kataev, R. Z. Musin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 5, pp 645-650 doi:10.1134/S1068162009050173), IF=0.711
  95. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, В.Е. Катаев, Р.З. Мусин
    Синтез и модификация тритерпеноидов с двумя лупановыми каркасами
    Биоорганическая химия, 2009, Т. 35, N 5, C. 714-720. (Synthesis and modification of triterpenoids with two lupan backbones/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, V. E. Kataev, R. Z. Musin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 5, pp 645-650 doi:10.1134/S1068162009050173), IF=0.711
  96. О.Б. Казакова, Г.В. Гиниятуллина, Г.А. Толстиков, В.Е. Катаев, Р.З. Мусин
    Синтез и модификация тритерпеноидов с двумя лупановыми каркасами
    Биоорганическая химия, 2009, Т. 35, N 5, C. 714-720. (Synthesis and modification of triterpenoids with two lupan backbones/ O. B. Kazakova, G. V. Giniyatullina, G. A. Tolstikov, V. E. Kataev, R. Z. Musin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 5, pp 645-650 doi:10.1134/S1068162009050173), IF=0.711
  97. З.А. Савельева, С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, А.В. Ткачев, С.В. Ларионов
    Синтез, структура и люминесцентные свойства комплекса ZnLCl2, где L = 2-(3,5-диметилпиразол-1-ил)-4-метилхинолин
    Известия Академии наук, серия химическая. 2009, N 9, С. 1780-1783 (Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9), IF=0.469
  98. З.А. Савельева, С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, А.В. Ткачев, С.В. Ларионов
    Синтез, структура и люминесцентные свойства комплекса ZnLCl2, где L = 2-(3,5-диметилпиразол-1-ил)-4-метилхинолин
    Известия Академии наук, серия химическая. 2009, N 9, С. 1780-1783 (Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9), IF=0.469
  99. З.А. Савельева, С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, А.В. Ткачев, С.В. Ларионов
    Синтез, структура и люминесцентные свойства комплекса ZnLCl2, где L = 2-(3,5-диметилпиразол-1-ил)-4-метилхинолин
    Известия Академии наук, серия химическая. 2009, N 9, С. 1780-1783 (Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9), IF=0.469
  100. З.А. Савельева, С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, А.В. Ткачев, С.В. Ларионов
    Синтез, структура и люминесцентные свойства комплекса ZnLCl2, где L = 2-(3,5-диметилпиразол-1-ил)-4-метилхинолин
    Известия Академии наук, серия химическая. 2009, N 9, С. 1780-1783 (Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9), IF=0.469
  101. З.А. Савельева, С.А. Попов, Р.Ф. Клевцова, Л.А. Глинская, Е.М. Усков, А.В. Ткачев, С.В. Ларионов
    Синтез, структура и люминесцентные свойства комплекса ZnLCl2, где L = 2-(3,5-диметилпиразол-1-ил)-4-метилхинолин
    Известия Академии наук, серия химическая. 2009, N 9, С. 1780-1783 (Synthesis, structure, and luminescence properties of complex ZnLCl2 (L is 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline)/ Z.A. Savel'eva, S.A. Popov, R.F. Klevtsova, L.A. Glinskaya, E.M. Uskov, A.V. Tkachev, S.V. Larionova// Russian Chemical Bulletin, 2009, V. 58, N 9, pp 1837-1840 doi:10.1007/s11172-009-0250-9), IF=0.469
  102. Л.И. Горюнов, Н.М. Трошкова, Г.А. Невинский, В.Д. Штейнгарц
    Синтез производных 2-аминопентафтор-1,4-нафтохинона
    Журнал органической химии, 2009, Т. 45, N 6, 851–856. (Synthesis of 2-aminopentafluoro-1,4-naphthoquinone derivatives/ L.I. Goryunov, N.M. Troshkova, G.A. Nevinskii, V.D. Shteingarts// Russian Journal of Organic Chemistry, 2009, V. 45, N 6, pp 835-841 doi:10.1134/S1070428009060050), IF=0.556
  103. З.А. Савельева, Л.А. Глинская, С.А. Попов, Р.Ф. Клевцова, А.В. Ткачев, С.В. Ларионов
    Синтез комплексов Pd(II), содержащих протонированную форму или молекулу 2-(3,5-диметилпиразол-1-ил)-4-метилхинолина (L). Кристаллическая структура [Pd(HL)Cl3]
    Координационная химия, 2009, Т.35. N 9, С. 678-683 (Synthesis of Pd(II) complexes containing the protonated form or molecule of 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline (L) The crystal structure of [Pd(HL)Cl3]/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 9, pp 668-673. doi:10.1134/S1070328409090073), IF=0.533
  104. З.А. Савельева, Л.А. Глинская, С.А. Попов, Р.Ф. Клевцова, А.В. Ткачев, С.В. Ларионов
    Синтез комплексов Pd(II), содержащих протонированную форму или молекулу 2-(3,5-диметилпиразол-1-ил)-4-метилхинолина (L). Кристаллическая структура [Pd(HL)Cl3]
    Координационная химия, 2009, Т.35. N 9, С. 678-683 (Synthesis of Pd(II) complexes containing the protonated form or molecule of 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline (L) The crystal structure of [Pd(HL)Cl3]/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 9, pp 668-673. doi:10.1134/S1070328409090073), IF=0.533
  105. З.А. Савельева, Л.А. Глинская, С.А. Попов, Р.Ф. Клевцова, А.В. Ткачев, С.В. Ларионов
    Синтез комплексов Pd(II), содержащих протонированную форму или молекулу 2-(3,5-диметилпиразол-1-ил)-4-метилхинолина (L). Кристаллическая структура [Pd(HL)Cl3]
    Координационная химия, 2009, Т.35. N 9, С. 678-683 (Synthesis of Pd(II) complexes containing the protonated form or molecule of 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline (L) The crystal structure of [Pd(HL)Cl3]/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 9, pp 668-673. doi:10.1134/S1070328409090073), IF=0.533
  106. З.А. Савельева, Л.А. Глинская, С.А. Попов, Р.Ф. Клевцова, А.В. Ткачев, С.В. Ларионов
    Синтез комплексов Pd(II), содержащих протонированную форму или молекулу 2-(3,5-диметилпиразол-1-ил)-4-метилхинолина (L). Кристаллическая структура [Pd(HL)Cl3]
    Координационная химия, 2009, Т.35. N 9, С. 678-683 (Synthesis of Pd(II) complexes containing the protonated form or molecule of 2-(3,5-dimethylpyrazol-1-yl)-4-methylquinoline (L) The crystal structure of [Pd(HL)Cl3]/ Z.A. Savel'eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, S.A. Popov, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 9, pp 668-673. doi:10.1134/S1070328409090073), IF=0.533
  107. N.Yu. Adonin, S.A. Prikhod'ko, V.V. Bardin, V.N. Parmon
    The first example of the ortho-directing effect of the weakly coordinating substituent [-BF3]- in the catalytic hydrodefluorination of the pentafluorophenyltrifluoroborate anion
    Mendeleev Commun., 2009, V. 19, N 5, 260-262. doi:10.1016/j.mencom.2009.09.009, IF=0.609
  108. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov, I.V. Alabugin
    An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to Sampangine Derivatives and Polycyclic Aromatic Amides
    J. Org. Chem., 2009, V. 74, N 16, 6143–6150. doi:10.1021/jo9008904, IF=3.951
  109. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov, I.V. Alabugin
    An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to Sampangine Derivatives and Polycyclic Aromatic Amides
    J. Org. Chem., 2009, V. 74, N 16, 6143–6150. doi:10.1021/jo9008904, IF=3.951
  110. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov, I.V. Alabugin
    An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to Sampangine Derivatives and Polycyclic Aromatic Amides
    J. Org. Chem., 2009, V. 74, N 16, 6143–6150. doi:10.1021/jo9008904, IF=3.951
  111. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  112. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  113. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  114. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  115. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  116. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
    J.Chem.Phys., 2009, V. 131, N 6, Article number 064505. doi:10.1063/1.3206909, IF=3.148
  117. С.С. Иванчев, М.Ю. Васильева, Н.И. Иванчева, В.К. Бадаев, И.И. Олейник, Е.В. Свиридова, Г.А. Толстиков
    Особенности полимеризации этилена на самоиммобилизующихся бис(феноксииминных) каталитических системах.
    Высокомолекулярные соединения Серия А, 2009, Т. 51, № 8, C. 1538-1545. (Polymerization of ethylene with self-immobilizing bis(phenoxyimine) catalytic systems/ S. S. Ivanchev, M. Yu. Vasil’eva, N. I. Ivancheva, V. K. Badaev, I. I. Oleinik, E. V. Sviridova, G. A. Tolstikov// Polymer Science Series B, 2009, V. 51, N 7-8, pp 276-282 doi:10.1134/S1560090409070100), IF=0.542
  118. С.С. Иванчев, М.Ю. Васильева, Н.И. Иванчева, В.К. Бадаев, И.И. Олейник, Е.В. Свиридова, Г.А. Толстиков
    Особенности полимеризации этилена на самоиммобилизующихся бис(феноксииминных) каталитических системах.
    Высокомолекулярные соединения Серия А, 2009, Т. 51, № 8, C. 1538-1545. (Polymerization of ethylene with self-immobilizing bis(phenoxyimine) catalytic systems/ S. S. Ivanchev, M. Yu. Vasil’eva, N. I. Ivancheva, V. K. Badaev, I. I. Oleinik, E. V. Sviridova, G. A. Tolstikov// Polymer Science Series B, 2009, V. 51, N 7-8, pp 276-282 doi:10.1134/S1560090409070100), IF=0.542
  119. С.С. Иванчев, М.Ю. Васильева, Н.И. Иванчева, В.К. Бадаев, И.И. Олейник, Е.В. Свиридова, Г.А. Толстиков
    Особенности полимеризации этилена на самоиммобилизующихся бис(феноксииминных) каталитических системах.
    Высокомолекулярные соединения Серия А, 2009, Т. 51, № 8, C. 1538-1545. (Polymerization of ethylene with self-immobilizing bis(phenoxyimine) catalytic systems/ S. S. Ivanchev, M. Yu. Vasil’eva, N. I. Ivancheva, V. K. Badaev, I. I. Oleinik, E. V. Sviridova, G. A. Tolstikov// Polymer Science Series B, 2009, V. 51, N 7-8, pp 276-282 doi:10.1134/S1560090409070100), IF=0.542
  120. С.С. Иванчев, М.Ю. Васильева, Н.И. Иванчева, В.К. Бадаев, И.И. Олейник, Е.В. Свиридова, Г.А. Толстиков
    Особенности полимеризации этилена на самоиммобилизующихся бис(феноксииминных) каталитических системах.
    Высокомолекулярные соединения Серия А, 2009, Т. 51, № 8, C. 1538-1545. (Polymerization of ethylene with self-immobilizing bis(phenoxyimine) catalytic systems/ S. S. Ivanchev, M. Yu. Vasil’eva, N. I. Ivancheva, V. K. Badaev, I. I. Oleinik, E. V. Sviridova, G. A. Tolstikov// Polymer Science Series B, 2009, V. 51, N 7-8, pp 276-282 doi:10.1134/S1560090409070100), IF=0.542
  121. С.С. Иванчев, М.Ю. Васильева, Н.И. Иванчева, В.К. Бадаев, И.И. Олейник, Е.В. Свиридова, Г.А. Толстиков
    Особенности полимеризации этилена на самоиммобилизующихся бис(феноксииминных) каталитических системах.
    Высокомолекулярные соединения Серия А, 2009, Т. 51, № 8, C. 1538-1545. (Polymerization of ethylene with self-immobilizing bis(phenoxyimine) catalytic systems/ S. S. Ivanchev, M. Yu. Vasil’eva, N. I. Ivancheva, V. K. Badaev, I. I. Oleinik, E. V. Sviridova, G. A. Tolstikov// Polymer Science Series B, 2009, V. 51, N 7-8, pp 276-282 doi:10.1134/S1560090409070100), IF=0.542
  122. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  123. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  124. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  125. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  126. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  127. Г.М. Максимов, Р.И. Максимовская, О.А. Холдеева, М.А. Федотов, В.И. Зайковский, В.Г. Васильев, С.С. Арзуманов
    Структура и свойства гетерополикислоты H8(PW11TiO39)2O.
    Журнал структурной химии, 2009, Т. 50, N 4, С. 648-657. (Structure and properties of H8(PW11TiO39)2O heteropoly acid/ G. M. Maksimov, R. I. Maksimovskaya, O. A. Kholdeeva, M. A. Fedotov, V. I. Zaikovskii, V. G. Vasil’ev, S. S. Arzumanov// Journal of Structural Chemistry, 2009, V. 50, N 4, pp 618-627 doi:10.1007/s10947-009-0097-9), IF=0.578
  128. I. K. Shundrina, T. A. Vaganova, S. Z. Kusov, V. I. Rodionov, E. V. Karpova, V. V. Koval, Yu. V. Gerasimova, E. V. Malykhin
    Synthesis and characterization of polyamides based on novel isometric perfuorinated naphthylenediamine
    J. Fluor. Chem., 2009, V 130, N 8, 733–741. doi:10.1016/j.jfluchem.2009.05.019, IF=1.593
  129. I. K. Shundrina, T. A. Vaganova, S. Z. Kusov, V. I. Rodionov, E. V. Karpova, V. V. Koval, Yu. V. Gerasimova, E. V. Malykhin
    Synthesis and characterization of polyamides based on novel isometric perfuorinated naphthylenediamine
    J. Fluor. Chem., 2009, V 130, N 8, 733–741. doi:10.1016/j.jfluchem.2009.05.019, IF=1.593
  130. S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
    Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
  131. S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
    Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
  132. S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
    Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
  133. L.V. Kopylova, O.A. Snytnikova, E.I. Chernyak, S.V. Morozov, M.D. E. Forbes, Y.P. Tsentalovich
    Kinetics and mechanism of thermal decomposition of kynurenines and biomolecular conjugates: Ramifications for the modification of mammalian eye lens proteins /
    Org. Biomol. Chem., 2009, V. 7, N 14, 2958–2966. doi:0.1039/b903196k, IF=3.549
  134. L.V. Kopylova, O.A. Snytnikova, E.I. Chernyak, S.V. Morozov, M.D. E. Forbes, Y.P. Tsentalovich
    Kinetics and mechanism of thermal decomposition of kynurenines and biomolecular conjugates: Ramifications for the modification of mammalian eye lens proteins /
    Org. Biomol. Chem., 2009, V. 7, N 14, 2958–2966. doi:0.1039/b903196k, IF=3.549
  135. L.V. Kopylova, O.A. Snytnikova, E.I. Chernyak, S.V. Morozov, M.D. E. Forbes, Y.P. Tsentalovich
    Kinetics and mechanism of thermal decomposition of kynurenines and biomolecular conjugates: Ramifications for the modification of mammalian eye lens proteins /
    Org. Biomol. Chem., 2009, V. 7, N 14, 2958–2966. doi:0.1039/b903196k, IF=3.549
  136. L.V. Kopylova, O.A. Snytnikova, E.I. Chernyak, S.V. Morozov, M.D. E. Forbes, Y.P. Tsentalovich
    Kinetics and mechanism of thermal decomposition of kynurenines and biomolecular conjugates: Ramifications for the modification of mammalian eye lens proteins /
    Org. Biomol. Chem., 2009, V. 7, N 14, 2958–2966. doi:0.1039/b903196k, IF=3.549
  137. A.Zh. Turmukhambetov, M.T. Agedilova, Zh.S. Nurmaganbetov, A.V. Kazantsev, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya
    Synthesis of quaternary salts of Peganum harmala alkaloids
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 601-603. doi:10.1007/s10600-009-9381-3, IF=0.467
  138. A.Zh. Turmukhambetov, M.T. Agedilova, Zh.S. Nurmaganbetov, A.V. Kazantsev, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya
    Synthesis of quaternary salts of Peganum harmala alkaloids
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 601-603. doi:10.1007/s10600-009-9381-3, IF=0.467
  139. A.Zh. Turmukhambetov, M.T. Agedilova, Zh.S. Nurmaganbetov, A.V. Kazantsev, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya
    Synthesis of quaternary salts of Peganum harmala alkaloids
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 601-603. doi:10.1007/s10600-009-9381-3, IF=0.467
  140. A.Zh. Turmukhambetov, M.T. Agedilova, Zh.S. Nurmaganbetov, A.V. Kazantsev, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya
    Synthesis of quaternary salts of Peganum harmala alkaloids
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 601-603. doi:10.1007/s10600-009-9381-3, IF=0.467
  141. A.Zh. Turmukhambetov, M.T. Agedilova, Zh.S. Nurmaganbetov, A.V. Kazantsev, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya
    Synthesis of quaternary salts of Peganum harmala alkaloids
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 601-603. doi:10.1007/s10600-009-9381-3, IF=0.467
  142. R. I. Dzhalmakhanbetova, M. A. Rodichev, Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Epoxidation of sesquiterpene lactones tourneforin and ludartin
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 503-506. doi:10.1007/s10600-009-9399-6, IF=0.467
  143. R. I. Dzhalmakhanbetova, M. A. Rodichev, Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Epoxidation of sesquiterpene lactones tourneforin and ludartin
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 503-506. doi:10.1007/s10600-009-9399-6, IF=0.467
  144. R. I. Dzhalmakhanbetova, M. A. Rodichev, Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Epoxidation of sesquiterpene lactones tourneforin and ludartin
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 503-506. doi:10.1007/s10600-009-9399-6, IF=0.467
  145. R. I. Dzhalmakhanbetova, M. A. Rodichev, Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova, S. M. Adekenov
    Epoxidation of sesquiterpene lactones tourneforin and ludartin
    Chemistry of Natural Compounds, 2009, V. 45, N 4, pp 503-506. doi:10.1007/s10600-009-9399-6, IF=0.467
  146. R.M. Kondratenko, L.A. Baltina, L.A. Baltina Jr, O.A. Plyasunova, A.G. Pokrovskii, G.A. Tolstikov
    Synthesis of new hetero- and carbocyclic aromatic amides of glycyrrhizic acid as potential anti-HIV agents
    Pharm. Chem. J., 2009, V. 43, N 7, 383-388. doi:10.1007/s11094-009-0316-x
  147. R.M. Kondratenko, L.A. Baltina, L.A. Baltina Jr, O.A. Plyasunova, A.G. Pokrovskii, G.A. Tolstikov
    Synthesis of new hetero- and carbocyclic aromatic amides of glycyrrhizic acid as potential anti-HIV agents
    Pharm. Chem. J., 2009, V. 43, N 7, 383-388. doi:10.1007/s11094-009-0316-x
  148. R.M. Kondratenko, L.A. Baltina, L.A. Baltina Jr, O.A. Plyasunova, A.G. Pokrovskii, G.A. Tolstikov
    Synthesis of new hetero- and carbocyclic aromatic amides of glycyrrhizic acid as potential anti-HIV agents
    Pharm. Chem. J., 2009, V. 43, N 7, 383-388. doi:10.1007/s11094-009-0316-x
  149. R.M. Kondratenko, L.A. Baltina, L.A. Baltina Jr, O.A. Plyasunova, A.G. Pokrovskii, G.A. Tolstikov
    Synthesis of new hetero- and carbocyclic aromatic amides of glycyrrhizic acid as potential anti-HIV agents
    Pharm. Chem. J., 2009, V. 43, N 7, 383-388. doi:10.1007/s11094-009-0316-x
  150. R.M. Kondratenko, L.A. Baltina, L.A. Baltina Jr, O.A. Plyasunova, A.G. Pokrovskii, G.A. Tolstikov
    Synthesis of new hetero- and carbocyclic aromatic amides of glycyrrhizic acid as potential anti-HIV agents
    Pharm. Chem. J., 2009, V. 43, N 7, 383-388. doi:10.1007/s11094-009-0316-x
  151. У.М. Джемилев, Г.А. Толстиков, Р.И. Хуснутдинов
    Гидроаминироание сопряженных диенов, катализируемое комплексами переходных металлов
    Журнал органической химии, 2009, Т. 45, N N 7, 975-1001. (Hydroamination of conjugated dienes catalyzed by transition metal complexes/ U. M. Dzhemilev, G. A. Tolstikov, R. I. Khusnutdinov// Russian Journal of Organic Chemistry, 2009, V. 45, N 7, pp 957-987 doi:10.1134/S107042800907001X), IF=0.556
  152. У.М. Джемилев, Г.А. Толстиков, Р.И. Хуснутдинов
    Гидроаминироание сопряженных диенов, катализируемое комплексами переходных металлов
    Журнал органической химии, 2009, Т. 45, N N 7, 975-1001. (Hydroamination of conjugated dienes catalyzed by transition metal complexes/ U. M. Dzhemilev, G. A. Tolstikov, R. I. Khusnutdinov// Russian Journal of Organic Chemistry, 2009, V. 45, N 7, pp 957-987 doi:10.1134/S107042800907001X), IF=0.556
  153. V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasilieva, I.A. Kirilyuk, I.A. Grigor’ev
    TEMPOL reduces the therapeutic effect of cyclophosphamide on an experimantal tumour model
    Free Rad.Res., 2009, V. 43, N 7, pp 685-690. doi:10.1080/10715760902998198, IF=2.825
  154. V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasilieva, I.A. Kirilyuk, I.A. Grigor’ev
    TEMPOL reduces the therapeutic effect of cyclophosphamide on an experimantal tumour model
    Free Rad.Res., 2009, V. 43, N 7, pp 685-690. doi:10.1080/10715760902998198, IF=2.825
  155. V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasilieva, I.A. Kirilyuk, I.A. Grigor’ev
    TEMPOL reduces the therapeutic effect of cyclophosphamide on an experimantal tumour model
    Free Rad.Res., 2009, V. 43, N 7, pp 685-690. doi:10.1080/10715760902998198, IF=2.825
  156. V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasilieva, I.A. Kirilyuk, I.A. Grigor’ev
    TEMPOL reduces the therapeutic effect of cyclophosphamide on an experimantal tumour model
    Free Rad.Res., 2009, V. 43, N 7, pp 685-690. doi:10.1080/10715760902998198, IF=2.825
  157. О.А. Рабина, С.В. Морозов, Е.Н. Степанова
    Разработка ароматизированных функциональных масложировых продуктов
    Масложировая промышленность, 2009 , № 6, 20-21.
  158. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, В.А. Багрянский, Ю.Н. Молин
    Псевдовращение как возможная причина быстрой парамагнитной релаксации в ион-радикалах с вырожденным или квазивырожденным основным состоянием.
    Доклады Академии наук (Физ. Хим.) , T. 426, No 5, 2009, C. 639-643. (Pseudorotation as a possible origin of fast paramagnetic relaxation in radical ions with a degenerate or quasi-degenerate ground state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2009, V. 424, N 2, pp 108-112 doi:10.1134/S0012501609060025), IF=0.564
  159. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, В.А. Багрянский, Ю.Н. Молин
    Псевдовращение как возможная причина быстрой парамагнитной релаксации в ион-радикалах с вырожденным или квазивырожденным основным состоянием.
    Доклады Академии наук (Физ. Хим.) , T. 426, No 5, 2009, C. 639-643. (Pseudorotation as a possible origin of fast paramagnetic relaxation in radical ions with a degenerate or quasi-degenerate ground state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2009, V. 424, N 2, pp 108-112 doi:10.1134/S0012501609060025), IF=0.564
  160. В.И. Боровков, И.В. Береговая, Л.Н. Щеголева, В.А. Багрянский, Ю.Н. Молин
    Псевдовращение как возможная причина быстрой парамагнитной релаксации в ион-радикалах с вырожденным или квазивырожденным основным состоянием.
    Доклады Академии наук (Физ. Хим.) , T. 426, No 5, 2009, C. 639-643. (Pseudorotation as a possible origin of fast paramagnetic relaxation in radical ions with a degenerate or quasi-degenerate ground state/ V. I. Borovkov, I. V. Beregovaya, L. N. Shchegoleva, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2009, V. 424, N 2, pp 108-112 doi:10.1134/S0012501609060025), IF=0.564
  161. А.П. Крысин, Т.Б. Хлебникова, Б.М. Хлебников, В.Г. Васильев, Л.М. Покровский
    О селективных способах получения 6-трет-бутил-2-метилфенола и 6-трет-бутил-2,4-диметилфенола.
    Журнал общей химии. 2009. Т. 79. Вып. 6. C.984-990. (About selective methods of synthesis of 6-tert-butyl-2-methylphenol and 6-tert-butyl-2,4-dimethylphenol/ A. P. Krysin, T. B. Khlebnikova, B. M. Khlebnikov, L. M. Pokrovskii, V. G. Vasil’ev// Russian Journal of General Chemistry, 2009, V. 79, N 6, pp 1156-1162 doi:10.1134/S1070363209060218), IF=0.469
  162. А.П. Крысин, Т.Б. Хлебникова, Б.М. Хлебников, В.Г. Васильев, Л.М. Покровский
    О селективных способах получения 6-трет-бутил-2-метилфенола и 6-трет-бутил-2,4-диметилфенола.
    Журнал общей химии. 2009. Т. 79. Вып. 6. C.984-990. (About selective methods of synthesis of 6-tert-butyl-2-methylphenol and 6-tert-butyl-2,4-dimethylphenol/ A. P. Krysin, T. B. Khlebnikova, B. M. Khlebnikov, L. M. Pokrovskii, V. G. Vasil’ev// Russian Journal of General Chemistry, 2009, V. 79, N 6, pp 1156-1162 doi:10.1134/S1070363209060218), IF=0.469
  163. Е.А. Конева, К.П. Волчо, Д.В. Корчагина, Н.Ф. Салахутдинов, А.Г. Толстиков
    Синтез новых хиральных оснований Шиффа на основе (+)-3-карена и использование их в асимметрическом металлокомплексном окислении сульфидов
    Журнал органической химии, 2009, Т. 45, N 6. С. 832-841. (Synthesis of new chiral schiff bases from (+)-3-carene and their use in asymmetric oxidation of sulfides catalyzed by metal complexes/ E.A. Koneva, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov, A.G. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 6, pp 815-824 doi:10.1134/S1070428009060037), IF=0.556
  164. О.С. Куковинец, Т.И. Зверева, В.Г. Касрадзе, М.И. Абдуллин, Г.А. Толстиков
    Новый подход к синтезу феромонов и ювеноидов с малыми циклами в молекуле
    Химия в интересах устойчивого развития, 2008, Т. 16, N 6, C. 731-734.
  165. О.С. Куковинец, Т.И. Зверева, В.Г. Касрадзе, М.И. Абдуллин, Г.А. Толстиков
    Новый подход к синтезу феромонов и ювеноидов с малыми циклами в молекуле
    Химия в интересах устойчивого развития, 2008, Т. 16, N 6, C. 731-734.
  166. О.С. Куковинец, Т.И. Зверева, В.Г. Касрадзе, М.И. Абдуллин, Г.А. Толстиков
    Новый подход к синтезу феромонов и ювеноидов с малыми циклами в молекуле
    Химия в интересах устойчивого развития, 2008, Т. 16, N 6, C. 731-734.
  167. О.С. Куковинец, Т.И. Зверева, В.Г. Касрадзе, М.И. Абдуллин, Г.А. Толстиков
    Новый подход к синтезу феромонов и ювеноидов с малыми циклами в молекуле
    Химия в интересах устойчивого развития, 2008, Т. 16, N 6, C. 731-734.
  168. E. Lork, R. Mews, A.V. Zibarev
    Hydrolysis product of [Na(15-crown-5)] salt of [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl radical anion
    Mendeleev Commun., 2009, V. 19, N 3, 147-148. doi:10.1016/j.mencom.2009.05.011, IF=0.609
  169. E. Lork, R. Mews, A.V. Zibarev
    Hydrolysis product of [Na(15-crown-5)] salt of [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl radical anion
    Mendeleev Commun., 2009, V. 19, N 3, 147-148. doi:10.1016/j.mencom.2009.05.011, IF=0.609
  170. E.A. Pritchina, N.P. Gritsan, A.V. Zibarev, T. Bally
    Photochemical study on reactivity of tetrasulfur tetranitride, S4N4
    Inorg. Chem., 2009, V. 48, N 9, 4075-4082. doi:10.1021/ic802145x, IF=4.146
  171. E.A. Pritchina, N.P. Gritsan, A.V. Zibarev, T. Bally
    Photochemical study on reactivity of tetrasulfur tetranitride, S4N4
    Inorg. Chem., 2009, V. 48, N 9, 4075-4082. doi:10.1021/ic802145x, IF=4.146
  172. E.A. Pritchina, N.P. Gritsan, A.V. Zibarev, T. Bally
    Photochemical study on reactivity of tetrasulfur tetranitride, S4N4
    Inorg. Chem., 2009, V. 48, N 9, 4075-4082. doi:10.1021/ic802145x, IF=4.146
  173. A. Froelich, O.B. Kazakova, G.A. Tolstikov, A.K. Gzella
    (E)-17β,19-Epoxymethano-17,23,24-tridemethyl-4-nor-5β,18α-olean-3-one oxime
    Acta Crystallogr. E., 2009, E65, pat. 6, pp. O1262. doi:10.1107/S1600536809016675, IF=0.367
  174. A. Froelich, O.B. Kazakova, G.A. Tolstikov, A.K. Gzella
    (E)-17β,19-Epoxymethano-17,23,24-tridemethyl-4-nor-5β,18α-olean-3-one oxime
    Acta Crystallogr. E., 2009, E65, pat. 6, pp. O1262. doi:10.1107/S1600536809016675, IF=0.367
  175. A. Froelich, O.B. Kazakova, G.A. Tolstikov, A.K. Gzella
    (E)-17β,19-Epoxymethano-17,23,24-tridemethyl-4-nor-5β,18α-olean-3-one oxime
    Acta Crystallogr. E., 2009, E65, pat. 6, pp. O1262. doi:10.1107/S1600536809016675, IF=0.367
  176. Г.А. Коваленко, Л.В.Перминова, Е.И.Черняк, Л.И.Сапунова
    Исследование гетерогенного процесса изомеризации моносахаридов с участием иммобилизованных нерастущих клеток продуцента глюкозоизомеразы Arthrobacter nicotianae
    Биотехнология, 2009, №5, C. 63-73.
  177. Г.А. Коваленко, Л.В.Перминова, Е.И.Черняк, Л.И.Сапунова
    Исследование гетерогенного процесса изомеризации моносахаридов с участием иммобилизованных нерастущих клеток продуцента глюкозоизомеразы Arthrobacter nicotianae
    Биотехнология, 2009, №5, C. 63-73.
  178. Г.А. Коваленко, Л.В.Перминова, Е.И.Черняк, Л.И.Сапунова
    Исследование гетерогенного процесса изомеризации моносахаридов с участием иммобилизованных нерастущих клеток продуцента глюкозоизомеразы Arthrobacter nicotianae
    Биотехнология, 2009, №5, C. 63-73.
  179. Е.Ю. Яковлева, В.Ю. Белоцерковская, В.П. Фадеева, Г.С. Литвак, Е.А. Паукштис, Д.Э. Бабушкин
    Влияние химической модификации на газохроматографические свойства полимерных сорбентов полисорба-1 , хайсепа q и диатомитового носителя хромосорба р naw
    Журнал физической химии, 2009, Т. 83, N 5, С.972-977. (The effect of chemical modification on the chromatographic properties of polymeric adsorbents polysorb-1 and hisep Q and the diatomite carrier chromosorb P NAW/ E.Y. Yakovleva, V.Y. Belotserkovskaya, V.P. Fadeeva, G.S. Litvak, E.A. Paukshtis, D.E. Babushkin// Russian Journal of Physical Chemistry A, 2009, V . 83, N 5, pp. 849-853. doi:10.1134/S003602440905029X), IF=0.474
  180. Е.Ю. Яковлева, В.Ю. Белоцерковская, В.П. Фадеева, Г.С. Литвак, Е.А. Паукштис, Д.Э. Бабушкин
    Влияние химической модификации на газохроматографические свойства полимерных сорбентов полисорба-1 , хайсепа q и диатомитового носителя хромосорба р naw
    Журнал физической химии, 2009, Т. 83, N 5, С.972-977. (The effect of chemical modification on the chromatographic properties of polymeric adsorbents polysorb-1 and hisep Q and the diatomite carrier chromosorb P NAW/ E.Y. Yakovleva, V.Y. Belotserkovskaya, V.P. Fadeeva, G.S. Litvak, E.A. Paukshtis, D.E. Babushkin// Russian Journal of Physical Chemistry A, 2009, V . 83, N 5, pp. 849-853. doi:10.1134/S003602440905029X), IF=0.474
  181. Е.Ю. Яковлева, В.Ю. Белоцерковская, В.П. Фадеева, Г.С. Литвак, Е.А. Паукштис, Д.Э. Бабушкин
    Влияние химической модификации на газохроматографические свойства полимерных сорбентов полисорба-1 , хайсепа q и диатомитового носителя хромосорба р naw
    Журнал физической химии, 2009, Т. 83, N 5, С.972-977. (The effect of chemical modification on the chromatographic properties of polymeric adsorbents polysorb-1 and hisep Q and the diatomite carrier chromosorb P NAW/ E.Y. Yakovleva, V.Y. Belotserkovskaya, V.P. Fadeeva, G.S. Litvak, E.A. Paukshtis, D.E. Babushkin// Russian Journal of Physical Chemistry A, 2009, V . 83, N 5, pp. 849-853. doi:10.1134/S003602440905029X), IF=0.474
  182. Е.Ю. Яковлева, В.Ю. Белоцерковская, В.П. Фадеева, Г.С. Литвак, Е.А. Паукштис, Д.Э. Бабушкин
    Влияние химической модификации на газохроматографические свойства полимерных сорбентов полисорба-1 , хайсепа q и диатомитового носителя хромосорба р naw
    Журнал физической химии, 2009, Т. 83, N 5, С.972-977. (The effect of chemical modification on the chromatographic properties of polymeric adsorbents polysorb-1 and hisep Q and the diatomite carrier chromosorb P NAW/ E.Y. Yakovleva, V.Y. Belotserkovskaya, V.P. Fadeeva, G.S. Litvak, E.A. Paukshtis, D.E. Babushkin// Russian Journal of Physical Chemistry A, 2009, V . 83, N 5, pp. 849-853. doi:10.1134/S003602440905029X), IF=0.474
  183. Е.Ю. Яковлева, В.Ю. Белоцерковская, В.П. Фадеева, Г.С. Литвак, Е.А. Паукштис, Д.Э. Бабушкин
    Влияние химической модификации на газохроматографические свойства полимерных сорбентов полисорба-1 , хайсепа q и диатомитового носителя хромосорба р naw
    Журнал физической химии, 2009, Т. 83, N 5, С.972-977. (The effect of chemical modification on the chromatographic properties of polymeric adsorbents polysorb-1 and hisep Q and the diatomite carrier chromosorb P NAW/ E.Y. Yakovleva, V.Y. Belotserkovskaya, V.P. Fadeeva, G.S. Litvak, E.A. Paukshtis, D.E. Babushkin// Russian Journal of Physical Chemistry A, 2009, V . 83, N 5, pp. 849-853. doi:10.1134/S003602440905029X), IF=0.474
  184. I.V. Nechepurenko, N.I. Komarova, I.N. Kuzovkina, M.Yu. Vdovitchenko, M.P. Polovinka, N.F. Salakhutdinov
    Isolation and identification of 4',6-dimethoxy-7-hydroxyisoflavone from roots of Hedysarum theinum cultivated in vitro
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 420-421. doi:10.1007/s10600-009-9327-9, IF=0.467
  185. I.V. Nechepurenko, N.I. Komarova, I.N. Kuzovkina, M.Yu. Vdovitchenko, M.P. Polovinka, N.F. Salakhutdinov
    Isolation and identification of 4',6-dimethoxy-7-hydroxyisoflavone from roots of Hedysarum theinum cultivated in vitro
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 420-421. doi:10.1007/s10600-009-9327-9, IF=0.467
  186. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  187. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  188. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  189. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  190. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  191. G. Yu. Ishmuratov, Yu. V. Legostaeva, L. P. Botsman, M. P. Yakovleva, O. O. Shakhanova, R. R. Muslukhov, G. A. Tolstikov
    Transformations of peroxide ozonolysis products of natural olefins by N-containing organic compounds in methanol
    Chemistry of Natural Compounds, 2009, V. 45, N 3, pp 318-321. doi:10.1007/s10600-009-9354-6, IF=0.467
  192. О.Б. Флехтер, И.Е. Смирнова, Е.В. Третьякова, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко
    Синтез конъюгатов дигидрохинопимаровой кислоты с аминокислотами
    Биоорганическая химия, 2009, Т. 35, N 3, C. 424-430. (Synthesis of dihydroquinopimaric acid conjugates with amino acids/ O. B. Flekhter, I. E. Smirnova, E. V. Tret’yakova, G. A. Tolstikov, O. V. Savinova, E. I. Boreko// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 3, pp 385-390 doi:10.1134/S1068162009030157), IF=0.711
  193. О.Б. Флехтер, И.Е. Смирнова, Е.В. Третьякова, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко
    Синтез конъюгатов дигидрохинопимаровой кислоты с аминокислотами
    Биоорганическая химия, 2009, Т. 35, N 3, C. 424-430. (Synthesis of dihydroquinopimaric acid conjugates with amino acids/ O. B. Flekhter, I. E. Smirnova, E. V. Tret’yakova, G. A. Tolstikov, O. V. Savinova, E. I. Boreko// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 3, pp 385-390 doi:10.1134/S1068162009030157), IF=0.711
  194. О.Б. Флехтер, И.Е. Смирнова, Е.В. Третьякова, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко
    Синтез конъюгатов дигидрохинопимаровой кислоты с аминокислотами
    Биоорганическая химия, 2009, Т. 35, N 3, C. 424-430. (Synthesis of dihydroquinopimaric acid conjugates with amino acids/ O. B. Flekhter, I. E. Smirnova, E. V. Tret’yakova, G. A. Tolstikov, O. V. Savinova, E. I. Boreko// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 3, pp 385-390 doi:10.1134/S1068162009030157), IF=0.711
  195. О.Б. Флехтер, И.Е. Смирнова, Е.В. Третьякова, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко
    Синтез конъюгатов дигидрохинопимаровой кислоты с аминокислотами
    Биоорганическая химия, 2009, Т. 35, N 3, C. 424-430. (Synthesis of dihydroquinopimaric acid conjugates with amino acids/ O. B. Flekhter, I. E. Smirnova, E. V. Tret’yakova, G. A. Tolstikov, O. V. Savinova, E. I. Boreko// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 3, pp 385-390 doi:10.1134/S1068162009030157), IF=0.711
  196. О.Б. Флехтер, И.Е. Смирнова, Е.В. Третьякова, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко
    Синтез конъюгатов дигидрохинопимаровой кислоты с аминокислотами
    Биоорганическая химия, 2009, Т. 35, N 3, C. 424-430. (Synthesis of dihydroquinopimaric acid conjugates with amino acids/ O. B. Flekhter, I. E. Smirnova, E. V. Tret’yakova, G. A. Tolstikov, O. V. Savinova, E. I. Boreko// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 3, pp 385-390 doi:10.1134/S1068162009030157), IF=0.711
  197. Д.Ю. Сафина, Г.А. Селиванова, И.Ю. Багрянская, В.Д. Штейнгарц
    Взаимодействие фторированных по бензольному кольцу хинолинов с азотцентрированными нуклеофилами
    Известия академии наук, серия химическая, 2009, N 5, С. 1022-1033 (Reaction of quinolines fluorinated at the benzene ring with nitrogen-centered nucleophiles/ L.Yu. Safina, G.A. Selivanova, I.Yu. Bagryanskaya, V.D. Shteingarts// Russian Chemical Bulletin, 2009, V. 58, N 5, pp 1049-1061 doi:10.1007/s11172-009-0134-z), IF=0.469
  198. А.Ж. Турмухамбетов, Г.К. Мукушева, Р.Б. Сейдахметова, Э.Э. Шульц, М.М. Шакиров, И.Ю. Багрянская, Ю.В. Гатилов, С.М. Адекенов
    Синтез и антимикробная активность четвертичных солей алкалоида глауцина
    Химико-фармацевтический журнал, 2009, т. 43. №5. 24-27. (Synthesis and antimicrobial activity of quaternary salts of the alkaloid glaucine/ A.Zh. Turmukhambetov, G.K. Mukusheva, R.B. Seidakhmetova, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya, Yu.V. Gatilov// Pharmaceutical Chemistry Journal, 2009, V. 43, N 5, pp. 255-257. doi:10.1007/s11094-009-0283-2)
  199. А.Ж. Турмухамбетов, Г.К. Мукушева, Р.Б. Сейдахметова, Э.Э. Шульц, М.М. Шакиров, И.Ю. Багрянская, Ю.В. Гатилов, С.М. Адекенов
    Синтез и антимикробная активность четвертичных солей алкалоида глауцина
    Химико-фармацевтический журнал, 2009, т. 43. №5. 24-27. (Synthesis and antimicrobial activity of quaternary salts of the alkaloid glaucine/ A.Zh. Turmukhambetov, G.K. Mukusheva, R.B. Seidakhmetova, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya, Yu.V. Gatilov// Pharmaceutical Chemistry Journal, 2009, V. 43, N 5, pp. 255-257. doi:10.1007/s11094-009-0283-2)
  200. А.Ж. Турмухамбетов, Г.К. Мукушева, Р.Б. Сейдахметова, Э.Э. Шульц, М.М. Шакиров, И.Ю. Багрянская, Ю.В. Гатилов, С.М. Адекенов
    Синтез и антимикробная активность четвертичных солей алкалоида глауцина
    Химико-фармацевтический журнал, 2009, т. 43. №5. 24-27. (Synthesis and antimicrobial activity of quaternary salts of the alkaloid glaucine/ A.Zh. Turmukhambetov, G.K. Mukusheva, R.B. Seidakhmetova, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya, Yu.V. Gatilov// Pharmaceutical Chemistry Journal, 2009, V. 43, N 5, pp. 255-257. doi:10.1007/s11094-009-0283-2)
  201. А.Ж. Турмухамбетов, Г.К. Мукушева, Р.Б. Сейдахметова, Э.Э. Шульц, М.М. Шакиров, И.Ю. Багрянская, Ю.В. Гатилов, С.М. Адекенов
    Синтез и антимикробная активность четвертичных солей алкалоида глауцина
    Химико-фармацевтический журнал, 2009, т. 43. №5. 24-27. (Synthesis and antimicrobial activity of quaternary salts of the alkaloid glaucine/ A.Zh. Turmukhambetov, G.K. Mukusheva, R.B. Seidakhmetova, S.M. Adekenov, E.E. Shults, M.M. Shakirov, I.Yu. Bagryanskaya, Yu.V. Gatilov// Pharmaceutical Chemistry Journal, 2009, V. 43, N 5, pp. 255-257. doi:10.1007/s11094-009-0283-2)
  202. Ю.С. Косенкова, М.П. Половинка, Д.В. Корчагина, Н.И. Комарова, Н.Ю. Курочкина, В.А. Черемушкина, Н.Ф. Салахутдинов
    Сезонная динамика накопления риккардина С в Primula macrocalyx Bge.
    Химия в интересах устойчивого развития, 2009, Т.17, N 5, С. 507-511.
  203. Ю.С. Косенкова, М.П. Половинка, Д.В. Корчагина, Н.И. Комарова, Н.Ю. Курочкина, В.А. Черемушкина, Н.Ф. Салахутдинов
    Сезонная динамика накопления риккардина С в Primula macrocalyx Bge.
    Химия в интересах устойчивого развития, 2009, Т.17, N 5, С. 507-511.
  204. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  205. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  206. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  207. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  208. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  209. М.А. Тихонова, Е.Л. Альперина, Т.Г. Толстикова, Д.В. Базовкина, В.Ю. Ди, Г.В. Идова, Н.К. Попова
    _Влияние хронического введения флуоксетина на каталепсию иммунный ответ мышей с генетической предрасположенностью к реакции замирания: роль серотониновых рецепторов 1а и 2а типов и генов tph2 иsert
    Журнал высшей нервной деятельности, 2009, т. 59, №2, C.237-244. (Effects of Chronic Fluoxetine Treatment on Catalepsy and Immune Response in Mice Genetically Predisposed to Freezing Reaction: the Role of 5-HT1A and 5-HT2A Receptors and Tph2 and SERT Genes/ M.A.Tikhonova , E.L. Al'perina, T.G. Tolstikova, D.V. Bazovkina, Di VIu, G.V. Idova, A.V. Kulikov, N.K. Popova// ZHURNAL VYSSHEI NERVNOI DEYATELNOSTI IMENI I P PAVLOVA, 2010, V. 59, N 2, pp 237-244 Zh Vyssh Nerv Deiat Im I P Pavlova. 2009 Mar-Apr;59(2):237-44.), IF=0.296
  210. А.А. Онищук, Т.Г. Толстикова, И.В. Сорокина, А.М. Бакланов, В.В. Карасев, В.В. Болдырев, В.М. Фомин
    Эффект наночастиц индометацина при осаждении в легких. (Получение наноразмерных аэрозольных форм слаборастворимых в воде лекарственных препаратов)
    Доклады Академии наук (Биохимия и биофизика), 2009,Т.425, №5, C. 692-695 (Production of nanoaerosols of sparingly water-soluble drugs: The effect of indomethacin nanoparticles/ A. A. Onishchuk, T. G. Tolstikova, I. V. Sorokina, A. M. Baklanov, V. V. Karasev, V. V. Boldyrev, V. M. Fomin// Doklady Biochemistry and Biophysics, 2009, V. 425, N 1, pp 106-109 doi:10.1134/S1607672909020136)
  211. А.А. Онищук, Т.Г. Толстикова, И.В. Сорокина, А.М. Бакланов, В.В. Карасев, В.В. Болдырев, В.М. Фомин
    Эффект наночастиц индометацина при осаждении в легких. (Получение наноразмерных аэрозольных форм слаборастворимых в воде лекарственных препаратов)
    Доклады Академии наук (Биохимия и биофизика), 2009,Т.425, №5, C. 692-695 (Production of nanoaerosols of sparingly water-soluble drugs: The effect of indomethacin nanoparticles/ A. A. Onishchuk, T. G. Tolstikova, I. V. Sorokina, A. M. Baklanov, V. V. Karasev, V. V. Boldyrev, V. M. Fomin// Doklady Biochemistry and Biophysics, 2009, V. 425, N 1, pp 106-109 doi:10.1134/S1607672909020136)
  212. А.А. Онищук, Т.Г. Толстикова, И.В. Сорокина, А.М. Бакланов, В.В. Карасев, В.В. Болдырев, В.М. Фомин
    Эффект наночастиц индометацина при осаждении в легких. (Получение наноразмерных аэрозольных форм слаборастворимых в воде лекарственных препаратов)
    Доклады Академии наук (Биохимия и биофизика), 2009,Т.425, №5, C. 692-695 (Production of nanoaerosols of sparingly water-soluble drugs: The effect of indomethacin nanoparticles/ A. A. Onishchuk, T. G. Tolstikova, I. V. Sorokina, A. M. Baklanov, V. V. Karasev, V. V. Boldyrev, V. M. Fomin// Doklady Biochemistry and Biophysics, 2009, V. 425, N 1, pp 106-109 doi:10.1134/S1607672909020136)
  213. А.А. Онищук, Т.Г. Толстикова, И.В. Сорокина, А.М. Бакланов, В.В. Карасев, В.В. Болдырев, В.М. Фомин
    Эффект наночастиц индометацина при осаждении в легких. (Получение наноразмерных аэрозольных форм слаборастворимых в воде лекарственных препаратов)
    Доклады Академии наук (Биохимия и биофизика), 2009,Т.425, №5, C. 692-695 (Production of nanoaerosols of sparingly water-soluble drugs: The effect of indomethacin nanoparticles/ A. A. Onishchuk, T. G. Tolstikova, I. V. Sorokina, A. M. Baklanov, V. V. Karasev, V. V. Boldyrev, V. M. Fomin// Doklady Biochemistry and Biophysics, 2009, V. 425, N 1, pp 106-109 doi:10.1134/S1607672909020136)
  214. А.А. Онищук, Т.Г. Толстикова, И.В. Сорокина, А.М. Бакланов, В.В. Карасев, В.В. Болдырев, В.М. Фомин
    Эффект наночастиц индометацина при осаждении в легких. (Получение наноразмерных аэрозольных форм слаборастворимых в воде лекарственных препаратов)
    Доклады Академии наук (Биохимия и биофизика), 2009,Т.425, №5, C. 692-695 (Production of nanoaerosols of sparingly water-soluble drugs: The effect of indomethacin nanoparticles/ A. A. Onishchuk, T. G. Tolstikova, I. V. Sorokina, A. M. Baklanov, V. V. Karasev, V. V. Boldyrev, V. M. Fomin// Doklady Biochemistry and Biophysics, 2009, V. 425, N 1, pp 106-109 doi:10.1134/S1607672909020136)
  215. Л.А. Шундрин, Е.А. Поленов
    Термодинамические активационные параметры заторможенного вращения CF3- группы в анион-радикале 4-нитрофенилтрифторметилсульфона в ДМФА
    Журнал структурной химии, 2009, Т. 50,N 2. С. 267-274. (Thermodynamic activation parameters of hindered rotation of the CF3 group in the 4-nitrophenyltrifluoromethylsulfone radical anion in DMF/ L. A. Shundrin, E. A. Polenov// Journal of Structural Chemistry, 2009, V. 50, N 2, pp 251-259 doi:10.1007/s10947-009-0036-9), IF=0.578
  216. Г.А. Толстиков, И.И. Олейник, И.В. Олейник, С.С. Иванчёв
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. XII. Синтез тетрадентатных биссалицилальдиминных лигандов.
    Журнал органической химии, 2009, Т. 45, N 4, С. 543-550. (Design of postmetallocene Schiff base-like catalytic systems for polymerization of olefins: XII. Synthesis of tetradentate bis-salicylaldehyde imine ligands/ I. I. Oleinik, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 4, pp 528-535 doi:10.1134/S1070428009040101), IF=0.556
  217. С.В. Ларионов, А.В. Ткачев, Л.И. Мячина, З.А. Савельева, Л.А. Глинская, Р.Ф. Клевцова, А.М. Агафонцев, С.Н. Бизяев
    Синтез двухъядерных комплексов PdCl2 с хиральным мета-α,α'-диаминоксилолдиоксимами H2L1, H2L2, H2L3 - производными терпенов (+)-3-карена, (R)-(+)-лимонена и (S)-(-)-α-пинена. Кристаллическая структура [Pd2(H2L1)Cl4]
    Координационная химия, 2009, Т.35. N 4, С. 291-300 (Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095), IF=0.533
  218. С.В. Ларионов, А.В. Ткачев, Л.И. Мячина, З.А. Савельева, Л.А. Глинская, Р.Ф. Клевцова, А.М. Агафонцев, С.Н. Бизяев
    Синтез двухъядерных комплексов PdCl2 с хиральным мета-α,α'-диаминоксилолдиоксимами H2L1, H2L2, H2L3 - производными терпенов (+)-3-карена, (R)-(+)-лимонена и (S)-(-)-α-пинена. Кристаллическая структура [Pd2(H2L1)Cl4]
    Координационная химия, 2009, Т.35. N 4, С. 291-300 (Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095), IF=0.533
  219. С.В. Ларионов, А.В. Ткачев, Л.И. Мячина, З.А. Савельева, Л.А. Глинская, Р.Ф. Клевцова, А.М. Агафонцев, С.Н. Бизяев
    Синтез двухъядерных комплексов PdCl2 с хиральным мета-α,α'-диаминоксилолдиоксимами H2L1, H2L2, H2L3 - производными терпенов (+)-3-карена, (R)-(+)-лимонена и (S)-(-)-α-пинена. Кристаллическая структура [Pd2(H2L1)Cl4]
    Координационная химия, 2009, Т.35. N 4, С. 291-300 (Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095), IF=0.533
  220. С.В. Ларионов, А.В. Ткачев, Л.И. Мячина, З.А. Савельева, Л.А. Глинская, Р.Ф. Клевцова, А.М. Агафонцев, С.Н. Бизяев
    Синтез двухъядерных комплексов PdCl2 с хиральным мета-α,α'-диаминоксилолдиоксимами H2L1, H2L2, H2L3 - производными терпенов (+)-3-карена, (R)-(+)-лимонена и (S)-(-)-α-пинена. Кристаллическая структура [Pd2(H2L1)Cl4]
    Координационная химия, 2009, Т.35. N 4, С. 291-300 (Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095), IF=0.533
  221. С.В. Ларионов, А.В. Ткачев, Л.И. Мячина, З.А. Савельева, Л.А. Глинская, Р.Ф. Клевцова, А.М. Агафонцев, С.Н. Бизяев
    Синтез двухъядерных комплексов PdCl2 с хиральным мета-α,α'-диаминоксилолдиоксимами H2L1, H2L2, H2L3 - производными терпенов (+)-3-карена, (R)-(+)-лимонена и (S)-(-)-α-пинена. Кристаллическая структура [Pd2(H2L1)Cl4]
    Координационная химия, 2009, Т.35. N 4, С. 291-300 (Synthesis of binuclear complexes of PdCl2 with chiral α,α'-diamino-meta-xylene dioximes H2L1, H2L2, and H2L3, the derivatives of the terpenes (+)-3-carene, R-(+)-limonene, and (S)-(-)-α-pinene. Crystal structure of [Pd2(H2L1)Cl4]/ S.V. Larionov, L.I. Myachina, Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, A.V. Tkachev, A.M. Agafontsev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 4, pp 286-295. doi:10.1134/S1070328409040095), IF=0.533
  222. V.S. Minkov, N.A. Tumanov, B.A. Kolesov, E.V. Boldyreva, S.N. Bizyaev
    _Phase Transitions in the Crystals of L- and DL-Cysteine on Cooling: The Role of the Hydrogen-Bond Distortions and the Side-Chain Motions. 2. DL-Cysteine
    J. Phys. Chem. B, 2009 , V. 113, N 15, 5262-5272. doi:10.1021/jp810355a, IF=4.189
  223. V.S. Minkov, N.A. Tumanov, B.A. Kolesov, E.V. Boldyreva, S.N. Bizyaev
    _Phase Transitions in the Crystals of L- and DL-Cysteine on Cooling: The Role of the Hydrogen-Bond Distortions and the Side-Chain Motions. 2. DL-Cysteine
    J. Phys. Chem. B, 2009 , V. 113, N 15, 5262-5272. doi:10.1021/jp810355a, IF=4.189
  224. V.S. Minkov, N.A. Tumanov, B.A. Kolesov, E.V. Boldyreva, S.N. Bizyaev
    _Phase Transitions in the Crystals of L- and DL-Cysteine on Cooling: The Role of the Hydrogen-Bond Distortions and the Side-Chain Motions. 2. DL-Cysteine
    J. Phys. Chem. B, 2009 , V. 113, N 15, 5262-5272. doi:10.1021/jp810355a, IF=4.189
  225. V.S. Minkov, N.A. Tumanov, B.A. Kolesov, E.V. Boldyreva, S.N. Bizyaev
    _Phase Transitions in the Crystals of L- and DL-Cysteine on Cooling: The Role of the Hydrogen-Bond Distortions and the Side-Chain Motions. 2. DL-Cysteine
    J. Phys. Chem. B, 2009 , V. 113, N 15, 5262-5272. doi:10.1021/jp810355a, IF=4.189
  226. M. Voinov, I. Kirilyuk, A. Smirnov
    Spin-labeled pH-sensitive phospholipids for interfacial pKa determination: synthesis and characterization in aqueous and micellar solutions.
    J. Phys. Chem. B. 2009, V. 113, N 11, 3453–3460. doi:10.1021/jp810993s, IF=4.189
  227. M. Elyashberg, K. Blinov, S. Molodtsov, Y. Smurnyy, A.J. Williams, T. Churanova
    Computer-assisted methods for molecular structure elucidation: realizing a spectroscopist/'s dream
    Journal of Cheminformatics 2009, 1:3, http://www.jcheminf.com/content/1/1/3 doi:10.1186/1758-2946-1-3
  228. M. Elyashberg, K. Blinov, S. Molodtsov, Y. Smurnyy, A.J. Williams, T. Churanova
    Computer-assisted methods for molecular structure elucidation: realizing a spectroscopist/'s dream
    Journal of Cheminformatics 2009, 1:3, http://www.jcheminf.com/content/1/1/3 doi:10.1186/1758-2946-1-3
  229. M. Elyashberg, K. Blinov, S. Molodtsov, Y. Smurnyy, A.J. Williams, T. Churanova
    Computer-assisted methods for molecular structure elucidation: realizing a spectroscopist/'s dream
    Journal of Cheminformatics 2009, 1:3, http://www.jcheminf.com/content/1/1/3 doi:10.1186/1758-2946-1-3
  230. M. Elyashberg, K. Blinov, S. Molodtsov, Y. Smurnyy, A.J. Williams, T. Churanova
    Computer-assisted methods for molecular structure elucidation: realizing a spectroscopist/'s dream
    Journal of Cheminformatics 2009, 1:3, http://www.jcheminf.com/content/1/1/3 doi:10.1186/1758-2946-1-3
  231. M. Elyashberg, K. Blinov, S. Molodtsov, Y. Smurnyy, A.J. Williams, T. Churanova
    Computer-assisted methods for molecular structure elucidation: realizing a spectroscopist/'s dream
    Journal of Cheminformatics 2009, 1:3, http://www.jcheminf.com/content/1/1/3 doi:10.1186/1758-2946-1-3
  232. Ya.Y. Woldman, S.V. Semenov, A.A. Bobko, I.A. Kirilyuk, J.F. Polienko, M.A. Voinov, E.G. Bagryanskaya, V.V. Khramtsov
    Design of liposome-based pH sensitive nanoSPIN probes: nano-sized particles with incorporated nitroxides.
    The Analyst, 2009, V. 134, N 5, 904 – 910. doi:10.1039/b818184e, IF=3.76
  233. Ya.Y. Woldman, S.V. Semenov, A.A. Bobko, I.A. Kirilyuk, J.F. Polienko, M.A. Voinov, E.G. Bagryanskaya, V.V. Khramtsov
    Design of liposome-based pH sensitive nanoSPIN probes: nano-sized particles with incorporated nitroxides.
    The Analyst, 2009, V. 134, N 5, 904 – 910. doi:10.1039/b818184e, IF=3.76
  234. Ya.Y. Woldman, S.V. Semenov, A.A. Bobko, I.A. Kirilyuk, J.F. Polienko, M.A. Voinov, E.G. Bagryanskaya, V.V. Khramtsov
    Design of liposome-based pH sensitive nanoSPIN probes: nano-sized particles with incorporated nitroxides.
    The Analyst, 2009, V. 134, N 5, 904 – 910. doi:10.1039/b818184e, IF=3.76
  235. Ya.Y. Woldman, S.V. Semenov, A.A. Bobko, I.A. Kirilyuk, J.F. Polienko, M.A. Voinov, E.G. Bagryanskaya, V.V. Khramtsov
    Design of liposome-based pH sensitive nanoSPIN probes: nano-sized particles with incorporated nitroxides.
    The Analyst, 2009, V. 134, N 5, 904 – 910. doi:10.1039/b818184e, IF=3.76
  236. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    High-pressure thermolysis of sulfate turpentine.
    J. Supercrit. Fluid., 2009, V. 48, N 2, 139-145. doi:10.1016/j.supflu.2008.10.013, IF=2.427
  237. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    High-pressure thermolysis of sulfate turpentine.
    J. Supercrit. Fluid., 2009, V. 48, N 2, 139-145. doi:10.1016/j.supflu.2008.10.013, IF=2.427
  238. M. F. Kosterina, T. V. Rybalova, Yu. V. Gatilov, Yu. Yu. Morzherin
    Reaction of (π-alkoxyphenyl)-acetothioamides with acetylene-dicarboxylic esters
    Chemistry of Heterocyclic Compounds, 2009, V. 45, N 4, pp 422-425. doi:10.1007/s10593-009-0291-x, IF=0.462
  239. M. F. Kosterina, T. V. Rybalova, Yu. V. Gatilov, Yu. Yu. Morzherin
    Reaction of (π-alkoxyphenyl)-acetothioamides with acetylene-dicarboxylic esters
    Chemistry of Heterocyclic Compounds, 2009, V. 45, N 4, pp 422-425. doi:10.1007/s10593-009-0291-x, IF=0.462
  240. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  241. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  242. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  243. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  244. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  245. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  246. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  247. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  248. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  249. О.Б. Флехтер, Н.И. Медведева, Г.А. Толстиков, Ф.З. Галин, М.С. Юнусов, Х. Нгуен Тхи Май, Т. Лье Вьет, О.В. Савинова, Е.И. Бореко, Л.П. Титов, И.В. Глухов
    Синтез производных олеан-18(19)-ена из бетулина
    Биоорганическая химия, 2009, Т. 35, N 2, C. 253-259. (Synthesis of olean-18(19)-ene derivatives from betulin/ O. B. Flekhter, N. I. Medvedeva, G.A. Tolstikov, F. Z. Galin, M. S. Yunusov, Huong Nguen Thi Mai, Le Viet Tien, I. V. Savinova, E. I. Boreko, L. P. Titov, I. V. Glukhov// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 2, pp 233-239 doi:10.1134/S1068162009020125), IF=0.711
  250. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  251. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  252. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  253. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  254. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  255. Т.Е. Кокина, Л.А. Глинская, Р.Ф. Клевцова, Е.Г. Богуславский, Л.А. Шелудякова, С.Н. Бизяев, А.В. Ткачев, С.В. Ларионов
    Синтез и свойства комплексов Cu(II) с хиральным бис-{(E)-[(1S,4R)-Δ7,8-1-амино-2-пара-менталиден]аминогидрокси}метаном (L) - производным природного терпеноида (R)-(+)-лимонена. Кристаллическая структура сольвата [Cu(L)(μ-Cl)CuCl3] x изо-PrOH.
    Координационная химия, 2009, Т.35. N 3, С. 202-211 (Synthesis and properties of the Cu(II) complexes with chiral bis{(E)-[(1S,4R)-δ7,8-1-amino-2-para-menthalidene]aminohydroxy} methane (L - A derivative of natural terpenoid (R)-(+)-limonene). Crystal structure of the [Cu(L)(μ-Cl)CuCl3] • iso-PrOH solvate/ T.E. Kokina, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, L..A. Sheludyakova, S.V. Larionov, S.N. Bisyaev, A.V. Tkachev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 3, pp 200-209. doi:10.1134/S1070328409030075), IF=0.533
  256. H.-J. Frohn, F. Bailly, D. Welting, V.V. Bardin
    A widely varying range of products in reactions of C6F5BrF2, C6F5IF2, and C6F5IF4 with Lewis acids of different strength
    J. Fluor. Chem., 2009, V 130, N 3, 301-307. doi:10.1016/j.jfluchem.2008.11.004, IF=1.593
  257. H.-J. Frohn, F. Bailly, D. Welting, V.V. Bardin
    A widely varying range of products in reactions of C6F5BrF2, C6F5IF2, and C6F5IF4 with Lewis acids of different strength
    J. Fluor. Chem., 2009, V 130, N 3, 301-307. doi:10.1016/j.jfluchem.2008.11.004, IF=1.593
  258. H.-J. Frohn, F. Bailly, D. Welting, V.V. Bardin
    A widely varying range of products in reactions of C6F5BrF2, C6F5IF2, and C6F5IF4 with Lewis acids of different strength
    J. Fluor. Chem., 2009, V 130, N 3, 301-307. doi:10.1016/j.jfluchem.2008.11.004, IF=1.593
  259. T.G. Tolstikova, M.V. Khvostov, A.O. Bryzgalov, A.V. Dushkin, E.S. Meteleva
    Complex of nifedipine with Glycyrrhizic Acid as a novel water-soluble antihypertensive and antiarrhythmic agent
    Lett. Drug Des. Discov., 2009, V. 6, N 2, 155-158. doi:10.2174/157018009787582688, IF=0.786
  260. T.G. Tolstikova, M.V. Khvostov, A.O. Bryzgalov, A.V. Dushkin, E.S. Meteleva
    Complex of nifedipine with Glycyrrhizic Acid as a novel water-soluble antihypertensive and antiarrhythmic agent
    Lett. Drug Des. Discov., 2009, V. 6, N 2, 155-158. doi:10.2174/157018009787582688, IF=0.786
  261. H.-J. Frohn, F. Bailly, V.V. Bardin
    The first perfluoro alkyl(aryl)iodonium salt synthesised on two complementary routes
    Mendeleev Commun., 2009, V. 19, N 2, 67-68. doi:10.1016/j.mencom.2009.03.004, IF=0.609
  262. H.-J. Frohn, F. Bailly, V.V. Bardin
    The first perfluoro alkyl(aryl)iodonium salt synthesised on two complementary routes
    Mendeleev Commun., 2009, V. 19, N 2, 67-68. doi:10.1016/j.mencom.2009.03.004, IF=0.609
  263. I.V. Beregovaya, L.N. Shchegoleva, V.I. Borovkov
    Pseudorotation in Radical Cations of low-symmetric decalin molecules
    J. Phys. Chem. A., 2009, V.113, N 8, 1555-1558. doi:10.1021/jp807568g, IF=2.871
  264. Т.А. Асташова, Ю.Э. Бергман, О.В. Казаков, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркеры эндотоксикоза в условиях модели адентии и ее немедикаментозной коррекции
    Лазерная медицина 2009, 13, 2, С.39-44.
  265. Т.А. Асташова, Ю.Э. Бергман, О.В. Казаков, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркеры эндотоксикоза в условиях модели адентии и ее немедикаментозной коррекции
    Лазерная медицина 2009, 13, 2, С.39-44.
  266. Т.А. Асташова, Ю.Э. Бергман, О.В. Казаков, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркеры эндотоксикоза в условиях модели адентии и ее немедикаментозной коррекции
    Лазерная медицина 2009, 13, 2, С.39-44.
  267. Т.А. Асташова, Ю.Э. Бергман, О.В. Казаков, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркеры эндотоксикоза в условиях модели адентии и ее немедикаментозной коррекции
    Лазерная медицина 2009, 13, 2, С.39-44.
  268. Т.П. Кукина, И.А. Горбунова, И.И. Баяндина
    Биологическая активность ланостаноидов из грибов и растений.
    Иммунопатология, аллергология, инфектология. 2009; 2, C. 144.
  269. Т.П. Кукина, И.А. Горбунова, И.И. Баяндина
    Биологическая активность ланостаноидов из грибов и растений.
    Иммунопатология, аллергология, инфектология. 2009; 2, C. 144.
  270. C.Ф. Василевский, А.И. Говди, Э.Э. Шульц, М.М. Шакиров, И.В. Алабугин, Г.А. Толстиков
    Синтез первых представителей ацетиленовых производных бетулоновой кислоты
    Доклады Академии наук (Химия), 2009. Т. 24. № 5. С. 631-635. (Synthesis of the first acetylene derivatives of betulonic acid/ S.F. Vasilevskii, A.I. Govdi, E.E. Shul'ts, M.M. Shakirov, I.V. Alabugin, G.A. Tolstikov// Doklady Chemistry, 2009, V. 424, N 2, pp 39-42 doi:10.1134/S0012500809020050), IF=0.231
  271. C.Ф. Василевский, А.И. Говди, Э.Э. Шульц, М.М. Шакиров, И.В. Алабугин, Г.А. Толстиков
    Синтез первых представителей ацетиленовых производных бетулоновой кислоты
    Доклады Академии наук (Химия), 2009. Т. 24. № 5. С. 631-635. (Synthesis of the first acetylene derivatives of betulonic acid/ S.F. Vasilevskii, A.I. Govdi, E.E. Shul'ts, M.M. Shakirov, I.V. Alabugin, G.A. Tolstikov// Doklady Chemistry, 2009, V. 424, N 2, pp 39-42 doi:10.1134/S0012500809020050), IF=0.231
  272. C.Ф. Василевский, А.И. Говди, Э.Э. Шульц, М.М. Шакиров, И.В. Алабугин, Г.А. Толстиков
    Синтез первых представителей ацетиленовых производных бетулоновой кислоты
    Доклады Академии наук (Химия), 2009. Т. 24. № 5. С. 631-635. (Synthesis of the first acetylene derivatives of betulonic acid/ S.F. Vasilevskii, A.I. Govdi, E.E. Shul'ts, M.M. Shakirov, I.V. Alabugin, G.A. Tolstikov// Doklady Chemistry, 2009, V. 424, N 2, pp 39-42 doi:10.1134/S0012500809020050), IF=0.231
  273. Т.Г. Толстикова, А.О. Брызгалов, М.В. Хвостов, Г.И. Лифшиц, А.В. Душкин, Е.С. Метелева
    Исследование стевиозида как комплексообразующего растительного гликозида
    Вестник НГУ, Серия Биология, клиническая медицина, 2009, Т.7, N.2,C. 119- 123.
  274. Т.Г. Толстикова, А.О. Брызгалов, М.В. Хвостов, Г.И. Лифшиц, А.В. Душкин, Е.С. Метелева
    Исследование стевиозида как комплексообразующего растительного гликозида
    Вестник НГУ, Серия Биология, клиническая медицина, 2009, Т.7, N.2,C. 119- 123.
  275. Т.Г. Толстикова, А.О. Брызгалов, М.В. Хвостов, Г.И. Лифшиц, А.В. Душкин, Е.С. Метелева
    Исследование стевиозида как комплексообразующего растительного гликозида
    Вестник НГУ, Серия Биология, клиническая медицина, 2009, Т.7, N.2,C. 119- 123.
  276. И.Ю. Багрянская, Е.В. Барташевич, Д.К. Никулов, Ю.В. Гатилов, А.В. Зибарев
    Межмолекулярные взаимодействия и структурная дихотомия в кристаллах 1,3,2,4-бензодитиадиазинов
    Журнал структурной химии, 2009, Т. 50, N 1, С. 133-143. (Intermolecular interactions and structural dichotomy in 1,3,2,4-benzodithiadiazine crystals/ I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, E.V. Bartashevich, D.K. Nikulov// Journal of Structural Chemistry, 2009, V. 50, N 1, pp 127-136. doi:10.1007/s10947-009-0017-z), IF=0.578
  277. И.Ю. Багрянская, Е.В. Барташевич, Д.К. Никулов, Ю.В. Гатилов, А.В. Зибарев
    Межмолекулярные взаимодействия и структурная дихотомия в кристаллах 1,3,2,4-бензодитиадиазинов
    Журнал структурной химии, 2009, Т. 50, N 1, С. 133-143. (Intermolecular interactions and structural dichotomy in 1,3,2,4-benzodithiadiazine crystals/ I.Y. Bagryanskaya, Y.V. Gatilov, A.V. Zibarev, E.V. Bartashevich, D.K. Nikulov// Journal of Structural Chemistry, 2009, V. 50, N 1, pp 127-136. doi:10.1007/s10947-009-0017-z), IF=0.578
  278. М.В. Королевич, С.Г. Кириллова, В.Н. Пиоттух-Пелецкий, В.М. Андрианов
    Интерпретация ИК спектров эпоксисахаридов на основе теоретического расчёта частот и интенсивностей нормальных колебаний
    Журнал структурной химии, 2009, Т. 50, N 1, С. 47-57. (Interpretation of IR spectra of epoxysaccharides based on the theoretical calculation of frequencies and intensities of normal vibrations/ M. V. Korolevich, S. G. Kirillova, V. N. Piottukh-Peletskii, V. M. Andrianov// Journal of Structural Chemistry, 2009, V. 50, N 1, pp 41-51 doi:10.1007/s10947-009-0006-2), IF=0.578
  279. М.В. Королевич, С.Г. Кириллова, В.Н. Пиоттух-Пелецкий, В.М. Андрианов
    Интерпретация ИК спектров эпоксисахаридов на основе теоретического расчёта частот и интенсивностей нормальных колебаний
    Журнал структурной химии, 2009, Т. 50, N 1, С. 47-57. (Interpretation of IR spectra of epoxysaccharides based on the theoretical calculation of frequencies and intensities of normal vibrations/ M. V. Korolevich, S. G. Kirillova, V. N. Piottukh-Peletskii, V. M. Andrianov// Journal of Structural Chemistry, 2009, V. 50, N 1, pp 41-51 doi:10.1007/s10947-009-0006-2), IF=0.578
  280. М.В. Королевич, С.Г. Кириллова, В.Н. Пиоттух-Пелецкий, В.М. Андрианов
    Интерпретация ИК спектров эпоксисахаридов на основе теоретического расчёта частот и интенсивностей нормальных колебаний
    Журнал структурной химии, 2009, Т. 50, N 1, С. 47-57. (Interpretation of IR spectra of epoxysaccharides based on the theoretical calculation of frequencies and intensities of normal vibrations/ M. V. Korolevich, S. G. Kirillova, V. N. Piottukh-Peletskii, V. M. Andrianov// Journal of Structural Chemistry, 2009, V. 50, N 1, pp 41-51 doi:10.1007/s10947-009-0006-2), IF=0.578
  281. Т.Г. Толстикова, Е.А. Морозова, А.В. Болкунов, С.Е. Толстиков
    Тебаин как предшественник опиодных анальгетиков (Обзор
    Химия в интересах устойчивого развития, 2009, Т.17, N 2, C. 115-133.
  282. З.А. Савельева, А.В. Ткачев, Л.А. Глинская, С.Н. Бизяев, Р.Ф. Клевцова, С.В. Ларионов
    Синтез двухъядерных комплексов PdCl2 с хиральным этилендиаминодиоксимом (H2L1), пиперазинодиоксимом (H2L2) и пропилендиаминодиоксимом (H2L3), производными природного монотерпеноида (R )-(+)-лимонена. Кристаллические структуры [Pd2(H2L1)Cl4] и [Pd2(H2L2)Cl4].
    Координационная химия, 2009, Т.35. N 2, С. 130-137. (Synthesis of binuclear complexes of PdCl2 with chiral ethylenediamine dioxime (H2L1), piperazine dioxime (H2L2), and propylenediamine dioxime (H2L3), the derivatives of the natural monoterpenoid R-(+)-limonene. The crystal structures of [Pd2(H2L1)Cl4]] and [Pd2(H2L2)Cl4]/ Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 2, pp 128-135. doi:10.1134/S1070328409020079), IF=0.533
  283. З.А. Савельева, А.В. Ткачев, Л.А. Глинская, С.Н. Бизяев, Р.Ф. Клевцова, С.В. Ларионов
    Синтез двухъядерных комплексов PdCl2 с хиральным этилендиаминодиоксимом (H2L1), пиперазинодиоксимом (H2L2) и пропилендиаминодиоксимом (H2L3), производными природного монотерпеноида (R )-(+)-лимонена. Кристаллические структуры [Pd2(H2L1)Cl4] и [Pd2(H2L2)Cl4].
    Координационная химия, 2009, Т.35. N 2, С. 130-137. (Synthesis of binuclear complexes of PdCl2 with chiral ethylenediamine dioxime (H2L1), piperazine dioxime (H2L2), and propylenediamine dioxime (H2L3), the derivatives of the natural monoterpenoid R-(+)-limonene. The crystal structures of [Pd2(H2L1)Cl4]] and [Pd2(H2L2)Cl4]/ Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 2, pp 128-135. doi:10.1134/S1070328409020079), IF=0.533
  284. З.А. Савельева, А.В. Ткачев, Л.А. Глинская, С.Н. Бизяев, Р.Ф. Клевцова, С.В. Ларионов
    Синтез двухъядерных комплексов PdCl2 с хиральным этилендиаминодиоксимом (H2L1), пиперазинодиоксимом (H2L2) и пропилендиаминодиоксимом (H2L3), производными природного монотерпеноида (R )-(+)-лимонена. Кристаллические структуры [Pd2(H2L1)Cl4] и [Pd2(H2L2)Cl4].
    Координационная химия, 2009, Т.35. N 2, С. 130-137. (Synthesis of binuclear complexes of PdCl2 with chiral ethylenediamine dioxime (H2L1), piperazine dioxime (H2L2), and propylenediamine dioxime (H2L3), the derivatives of the natural monoterpenoid R-(+)-limonene. The crystal structures of [Pd2(H2L1)Cl4]] and [Pd2(H2L2)Cl4]/ Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 2, pp 128-135. doi:10.1134/S1070328409020079), IF=0.533
  285. З.А. Савельева, А.В. Ткачев, Л.А. Глинская, С.Н. Бизяев, Р.Ф. Клевцова, С.В. Ларионов
    Синтез двухъядерных комплексов PdCl2 с хиральным этилендиаминодиоксимом (H2L1), пиперазинодиоксимом (H2L2) и пропилендиаминодиоксимом (H2L3), производными природного монотерпеноида (R )-(+)-лимонена. Кристаллические структуры [Pd2(H2L1)Cl4] и [Pd2(H2L2)Cl4].
    Координационная химия, 2009, Т.35. N 2, С. 130-137. (Synthesis of binuclear complexes of PdCl2 with chiral ethylenediamine dioxime (H2L1), piperazine dioxime (H2L2), and propylenediamine dioxime (H2L3), the derivatives of the natural monoterpenoid R-(+)-limonene. The crystal structures of [Pd2(H2L1)Cl4]] and [Pd2(H2L2)Cl4]/ Z.A. Savel'Eva, L.A. Glinskaya, R.F. Klevtsova, S.V. Larionov, A.V. Tkachev, S.N. Bizyaev// Russian Journal of Coordination Chemistry, 2009, V. 35, N 2, pp 128-135. doi:10.1134/S1070328409020079), IF=0.533
  286. S.N. Konchenko, N.P. Gritsan, A.V. Lonchakov, U. Radius, A.V. Zibarev
    Isolation of the 2,1,3-benzothiadiazolidyl radical anion: X-ray structure and properties of a [K(THF)][C6H4N2S] salt
    Mendeleev Commun., 2009, V. 19, N 1, 7-9. doi:10.1016/j.mencom.2009.01.003, IF=0.609
  287. S.N. Konchenko, N.P. Gritsan, A.V. Lonchakov, U. Radius, A.V. Zibarev
    Isolation of the 2,1,3-benzothiadiazolidyl radical anion: X-ray structure and properties of a [K(THF)][C6H4N2S] salt
    Mendeleev Commun., 2009, V. 19, N 1, 7-9. doi:10.1016/j.mencom.2009.01.003, IF=0.609
  288. S.N. Konchenko, N.P. Gritsan, A.V. Lonchakov, U. Radius, A.V. Zibarev
    Isolation of the 2,1,3-benzothiadiazolidyl radical anion: X-ray structure and properties of a [K(THF)][C6H4N2S] salt
    Mendeleev Commun., 2009, V. 19, N 1, 7-9. doi:10.1016/j.mencom.2009.01.003, IF=0.609
  289. S.N. Konchenko, N.P. Gritsan, A.V. Lonchakov, U. Radius, A.V. Zibarev
    Isolation of the 2,1,3-benzothiadiazolidyl radical anion: X-ray structure and properties of a [K(THF)][C6H4N2S] salt
    Mendeleev Commun., 2009, V. 19, N 1, 7-9. doi:10.1016/j.mencom.2009.01.003, IF=0.609
  290. Н.М. Ишмуратова, Г.Ю. Ишмуратов, Г.А. Толстиков, М.Г. Гиниятуллин
    Феромонный стимулирующий препарат «Аписил» в пчеловодстве
    Вестник Российской академии сельскохозяйственных наук, 2009, № 1, C. 78-80.
  291. Н.М. Ишмуратова, Г.Ю. Ишмуратов, Г.А. Толстиков, М.Г. Гиниятуллин
    Феромонный стимулирующий препарат «Аписил» в пчеловодстве
    Вестник Российской академии сельскохозяйственных наук, 2009, № 1, C. 78-80.
  292. Н.М. Ишмуратова, Г.Ю. Ишмуратов, Г.А. Толстиков, М.Г. Гиниятуллин
    Феромонный стимулирующий препарат «Аписил» в пчеловодстве
    Вестник Российской академии сельскохозяйственных наук, 2009, № 1, C. 78-80.
  293. M.E. Elyashberg, K.A. Blinov, S.G. Molodtsov, T.S. Churanova, A.J. Williams
    Applications of Computer-Aided Methods of Structure Elucidation to the Revision of Chemical Structures. I. Structure Revision of γ-Lamellarin.
    The ChemSpider Journal of Chemistry 2009, http://www.chemmantis.com/Article.aspx?id=889
  294. M.E. Elyashberg, K.A. Blinov, S.G. Molodtsov, T.S. Churanova, A.J. Williams
    Applications of Computer-Aided Methods of Structure Elucidation to the Revision of Chemical Structures. I. Structure Revision of γ-Lamellarin.
    The ChemSpider Journal of Chemistry 2009, http://www.chemmantis.com/Article.aspx?id=889
  295. M.E. Elyashberg, K.A. Blinov, S.G. Molodtsov, T.S. Churanova, A.J. Williams
    Applications of Computer-Aided Methods of Structure Elucidation to the Revision of Chemical Structures. I. Structure Revision of γ-Lamellarin.
    The ChemSpider Journal of Chemistry 2009, http://www.chemmantis.com/Article.aspx?id=889
  296. M.E. Elyashberg, K.A. Blinov, S.G. Molodtsov, T.S. Churanova, A.J. Williams
    Applications of Computer-Aided Methods of Structure Elucidation to the Revision of Chemical Structures. I. Structure Revision of γ-Lamellarin.
    The ChemSpider Journal of Chemistry 2009, http://www.chemmantis.com/Article.aspx?id=889
  297. И.В. Мацейчик, Е.С. Добрыдина, И.Ф. Бейзель, О.И. Ломоввский, С.В. Морозов
    Биологически активные вещества пюреобразных продуктов переработки растительного сырья/
    Хранение и переработка сельхозсырья, 2009, Т.10, с.24-26.
  298. И.В. Мацейчик, Е.С. Добрыдина, И.Ф. Бейзель, О.И. Ломоввский, С.В. Морозов
    Биологически активные вещества пюреобразных продуктов переработки растительного сырья/
    Хранение и переработка сельхозсырья, 2009, Т.10, с.24-26.
  299. И.В. Мацейчик, Е.С. Добрыдина, И.Ф. Бейзель, О.И. Ломоввский, С.В. Морозов
    Биологически активные вещества пюреобразных продуктов переработки растительного сырья/
    Хранение и переработка сельхозсырья, 2009, Т.10, с.24-26.
  300. И.В. Мацейчик, Е.С. Добрыдина, И.Ф. Бейзель, О.И. Ломоввский, С.В. Морозов
    Биологически активные вещества пюреобразных продуктов переработки растительного сырья/
    Хранение и переработка сельхозсырья, 2009, Т.10, с.24-26.
  301. Е.Н.Демидова, В.М.Матюк, А.И.Драчев, А.Б.Гильман, А.М.Максимов, В.Е.Платонов
    Полимерные пленки, полученные из гексафторбензола в разряде постоянного тока
    Химия высоких энергий, 2009, Т.41, №1, 59-43. (Polymer films prepared from hexafluorobenzene in direct-current discharge/ E.N. Demidova, V.M. Matyuk, A.I. Drachev, A.B. Gil'man, A.M. Maksimov, V.E. Platonov// High Energy Chemistry, 2009, V. 43, N 1, pp 56-60. doi:10.1134/S0018143909010093), IF=0.577
  302. Е.Н.Демидова, В.М.Матюк, А.И.Драчев, А.Б.Гильман, А.М.Максимов, В.Е.Платонов
    Полимерные пленки, полученные из гексафторбензола в разряде постоянного тока
    Химия высоких энергий, 2009, Т.41, №1, 59-43. (Polymer films prepared from hexafluorobenzene in direct-current discharge/ E.N. Demidova, V.M. Matyuk, A.I. Drachev, A.B. Gil'man, A.M. Maksimov, V.E. Platonov// High Energy Chemistry, 2009, V. 43, N 1, pp 56-60. doi:10.1134/S0018143909010093), IF=0.577
  303. Е.Н.Демидова, В.М.Матюк, А.И.Драчев, А.Б.Гильман, А.М.Максимов, В.Е.Платонов
    Полимерные пленки, полученные из гексафторбензола в разряде постоянного тока
    Химия высоких энергий, 2009, Т.41, №1, 59-43. (Polymer films prepared from hexafluorobenzene in direct-current discharge/ E.N. Demidova, V.M. Matyuk, A.I. Drachev, A.B. Gil'man, A.M. Maksimov, V.E. Platonov// High Energy Chemistry, 2009, V. 43, N 1, pp 56-60. doi:10.1134/S0018143909010093), IF=0.577
  304. Е.Н.Демидова, В.М.Матюк, А.И.Драчев, А.Б.Гильман, А.М.Максимов, В.Е.Платонов
    Полимерные пленки, полученные из гексафторбензола в разряде постоянного тока
    Химия высоких энергий, 2009, Т.41, №1, 59-43. (Polymer films prepared from hexafluorobenzene in direct-current discharge/ E.N. Demidova, V.M. Matyuk, A.I. Drachev, A.B. Gil'man, A.M. Maksimov, V.E. Platonov// High Energy Chemistry, 2009, V. 43, N 1, pp 56-60. doi:10.1134/S0018143909010093), IF=0.577
  305. A. Ермакова, A.M. Чибиряев, И.В. Кожевников, В.И. Аникеев
    Термодинамика сложных реакционных смесей в докритическом и сверхкритическом состояниях.
    Сверхкритические флюиды: теория и практика, 2009, 4 (1), с. 18-48.
  306. A. Ермакова, A.M. Чибиряев, И.В. Кожевников, В.И. Аникеев
    Термодинамика сложных реакционных смесей в докритическом и сверхкритическом состояниях.
    Сверхкритические флюиды: теория и практика, 2009, 4 (1), с. 18-48.
  307. Л.В. Фролова, В.Н. Пиоттух-Пелецкий, Л.С. Филатова, Л.И. Макаров
    Классификация научных публикаций в области химии на основе метода таксономии рефератов статей
    Вестник НГУ, Серия: Информационные технологии, 2009, т. 7, N 1, C. 43-51.
  308. Т.А. Дуда, Л.Л. Свешникова, В.К. Хлесткин, К.А. Дембо, Л.Г. Янусова
    Пленки ленгмюра–блоджетт гидроксамовой кислоты ряда хиноксалинона
    Журнал физической химии, 2009, Т. 83, N 4, С. 758-764. (Langmuir-Blodgett Films of Hydroxamic Acid of the Quinoxalinone Series/ T.A. Duda, L.L. Sveshnikova, V.K. Khlestkin, K.A. Dembo, L.G. Yanusova// Russian Journal of Physical Chemistry A, 2009, V . 83, N 4, pp 654-659. doi:10.1134/S0036024409040232), IF=0.437
  309. Т.А. Дуда, Л.Л. Свешникова, В.К. Хлесткин, К.А. Дембо, Л.Г. Янусова
    Пленки ленгмюра–блоджетт гидроксамовой кислоты ряда хиноксалинона
    Журнал физической химии, 2009, Т. 83, N 4, С. 758-764. (Langmuir-Blodgett Films of Hydroxamic Acid of the Quinoxalinone Series/ T.A. Duda, L.L. Sveshnikova, V.K. Khlestkin, K.A. Dembo, L.G. Yanusova// Russian Journal of Physical Chemistry A, 2009, V . 83, N 4, pp 654-659. doi:10.1134/S0036024409040232), IF=0.437
  310. Т.А. Дуда, Л.Л. Свешникова, В.К. Хлесткин, К.А. Дембо, Л.Г. Янусова
    Пленки ленгмюра–блоджетт гидроксамовой кислоты ряда хиноксалинона
    Журнал физической химии, 2009, Т. 83, N 4, С. 758-764. (Langmuir-Blodgett Films of Hydroxamic Acid of the Quinoxalinone Series/ T.A. Duda, L.L. Sveshnikova, V.K. Khlestkin, K.A. Dembo, L.G. Yanusova// Russian Journal of Physical Chemistry A, 2009, V . 83, N 4, pp 654-659. doi:10.1134/S0036024409040232), IF=0.437
  311. Т.А. Дуда, Л.Л. Свешникова, В.К. Хлесткин, К.А. Дембо, Л.Г. Янусова
    Пленки ленгмюра–блоджетт гидроксамовой кислоты ряда хиноксалинона
    Журнал физической химии, 2009, Т. 83, N 4, С. 758-764. (Langmuir-Blodgett Films of Hydroxamic Acid of the Quinoxalinone Series/ T.A. Duda, L.L. Sveshnikova, V.K. Khlestkin, K.A. Dembo, L.G. Yanusova// Russian Journal of Physical Chemistry A, 2009, V . 83, N 4, pp 654-659. doi:10.1134/S0036024409040232), IF=0.437
  312. V. V. Shelkovnikov, Z. M. Ivanova, A. I. Plekhanov, E. V. Spesivtsev, S. V. Rykhlitsky
    Formation of pseudoisocyanine J-aggregates during thin-film formation
    Journal of Applied Spectroscopy, 2009, V. 76, N 1, pp 66-72. doi:10.1007/s10812-009-9148-4
  313. V. V. Shelkovnikov, Z. M. Ivanova, A. I. Plekhanov, E. V. Spesivtsev, S. V. Rykhlitsky
    Formation of pseudoisocyanine J-aggregates during thin-film formation
    Journal of Applied Spectroscopy, 2009, V. 76, N 1, pp 66-72. doi:10.1007/s10812-009-9148-4
  314. V. V. Shelkovnikov, Z. M. Ivanova, A. I. Plekhanov, E. V. Spesivtsev, S. V. Rykhlitsky
    Formation of pseudoisocyanine J-aggregates during thin-film formation
    Journal of Applied Spectroscopy, 2009, V. 76, N 1, pp 66-72. doi:10.1007/s10812-009-9148-4
  315. Н.И. Иванчева, А.Ю. Кострова, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Каталитическая активность новых биядерных бис(фенокси-иминных) комплексов хлорида ти¬тана для полимеризации этилена
    Доклады Академии наук (Физ. Хим.) , т. 424, № 3, C. 340-343. (Catalytic activity of new binuclear titanium chloride bis(phenoxyimine) complexes in ethylene polymerization/ N. I. Ivancheva, A. Yu. Kostrova, I. I. Oleinik, G. A. Tolstikov, S. S. Ivanchev// Doklady Physical Chemistry, 2009, V. 424, N 1, pp 17-20 doi:10.1134/S0012501609010059), IF=0.564
  316. Н.И. Иванчева, А.Ю. Кострова, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Каталитическая активность новых биядерных бис(фенокси-иминных) комплексов хлорида ти¬тана для полимеризации этилена
    Доклады Академии наук (Физ. Хим.) , т. 424, № 3, C. 340-343. (Catalytic activity of new binuclear titanium chloride bis(phenoxyimine) complexes in ethylene polymerization/ N. I. Ivancheva, A. Yu. Kostrova, I. I. Oleinik, G. A. Tolstikov, S. S. Ivanchev// Doklady Physical Chemistry, 2009, V. 424, N 1, pp 17-20 doi:10.1134/S0012501609010059), IF=0.564
  317. Н.И. Иванчева, А.Ю. Кострова, И.И. Олейник, Г.А. Толстиков, С.С. Иванчев
    Каталитическая активность новых биядерных бис(фенокси-иминных) комплексов хлорида ти¬тана для полимеризации этилена
    Доклады Академии наук (Физ. Хим.) , т. 424, № 3, C. 340-343. (Catalytic activity of new binuclear titanium chloride bis(phenoxyimine) complexes in ethylene polymerization/ N. I. Ivancheva, A. Yu. Kostrova, I. I. Oleinik, G. A. Tolstikov, S. S. Ivanchev// Doklady Physical Chemistry, 2009, V. 424, N 1, pp 17-20 doi:10.1134/S0012501609010059), IF=0.564
  318. I.V. Nechepurenko, N.I. Komarova, M.P. Polovinka, D.V. Korchagina, N.F. Salakhutdinov, Yu.V. Gerasimova, V.V. Koval
    Structure of oligomeric proanthocyanidines from Hedysarum thienum roots studied by thiolysis and MALDI-TOF MS
    Chemistry of Natural Compounds, 2009, V. 45, N 1, pp 32-39. doi:10.1007/s10600-009-9216-2, IF=0.467
  319. I.V. Nechepurenko, N.I. Komarova, M.P. Polovinka, D.V. Korchagina, N.F. Salakhutdinov, Yu.V. Gerasimova, V.V. Koval
    Structure of oligomeric proanthocyanidines from Hedysarum thienum roots studied by thiolysis and MALDI-TOF MS
    Chemistry of Natural Compounds, 2009, V. 45, N 1, pp 32-39. doi:10.1007/s10600-009-9216-2, IF=0.467
  320. О.Б. Флехтер, Н.И. Mедведева, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко, Ф.М. Долгушин
    Модифицированные по циклу А амиды бетулоновой кислоты с аминокислотами: синтез и ингибирование репродукции вируса гриппа А
    Биоорганическая химия, 2009, Т. 35, N 1, C. 129-133. (Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction/ O. B. Flekhter, N. I. Medvedeva, G. A. Tolstikov, O. V. Savinova, E. I. Boreko, F. M. Dolgushin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 1, pp 118-122 doi:10.1134/S1068162009010154), IF=0.711
  321. О.Б. Флехтер, Н.И. Mедведева, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко, Ф.М. Долгушин
    Модифицированные по циклу А амиды бетулоновой кислоты с аминокислотами: синтез и ингибирование репродукции вируса гриппа А
    Биоорганическая химия, 2009, Т. 35, N 1, C. 129-133. (Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction/ O. B. Flekhter, N. I. Medvedeva, G. A. Tolstikov, O. V. Savinova, E. I. Boreko, F. M. Dolgushin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 1, pp 118-122 doi:10.1134/S1068162009010154), IF=0.711
  322. О.Б. Флехтер, Н.И. Mедведева, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко, Ф.М. Долгушин
    Модифицированные по циклу А амиды бетулоновой кислоты с аминокислотами: синтез и ингибирование репродукции вируса гриппа А
    Биоорганическая химия, 2009, Т. 35, N 1, C. 129-133. (Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction/ O. B. Flekhter, N. I. Medvedeva, G. A. Tolstikov, O. V. Savinova, E. I. Boreko, F. M. Dolgushin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 1, pp 118-122 doi:10.1134/S1068162009010154), IF=0.711
  323. О.Б. Флехтер, Н.И. Mедведева, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко, Ф.М. Долгушин
    Модифицированные по циклу А амиды бетулоновой кислоты с аминокислотами: синтез и ингибирование репродукции вируса гриппа А
    Биоорганическая химия, 2009, Т. 35, N 1, C. 129-133. (Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction/ O. B. Flekhter, N. I. Medvedeva, G. A. Tolstikov, O. V. Savinova, E. I. Boreko, F. M. Dolgushin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 1, pp 118-122 doi:10.1134/S1068162009010154), IF=0.711
  324. О.Б. Флехтер, Н.И. Mедведева, Г.А. Толстиков, О.В. Савинова, Е.И. Бореко, Ф.М. Долгушин
    Модифицированные по циклу А амиды бетулоновой кислоты с аминокислотами: синтез и ингибирование репродукции вируса гриппа А
    Биоорганическая химия, 2009, Т. 35, N 1, C. 129-133. (Betulonic amides modified at cycle a by amino acids: Synthesis and inhibition of flu A virus reproduction/ O. B. Flekhter, N. I. Medvedeva, G. A. Tolstikov, O. V. Savinova, E. I. Boreko, F. M. Dolgushin// Russian Journal of Bioorganic Chemistry, 2009, V. 35, N 1, pp 118-122 doi:10.1134/S1068162009010154), IF=0.711
  325. И.И. Олейник, А.И. Кочнев, И.В. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. X. Синтез феноксииминных лигандов, содержащих объемные заместители.
    Журнал органической химии, 2009, Т. 45, N 1, с. 38-43. (Design of Schiff base-like postmetallocene catalytic systems for polymerization of olefins: X. Synthesis of phenoxy imino ligands with bulky substituents/ I. I. Oleinik, A. I. Kochnev, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 1, pp 30-36 doi:10.1134/S1070428009010059), IF=0.556
  326. Г.С. Жиловский, И.И. Олейник, С.С. Иванчёв, Г.А. Толстиков
    Дизайн постметаллоценовых каталитических систем арилиминного типа для полимеризации олефинов. XI. Синтез арилиминов 2-ацетил-6-бромпиридина, содержащих циклоалкильные заместители.
    Журнал органической химии, 2009, Т. 45, N 1, С. 51-54. (Design of postmetallocene Schiff base-like catalytic systems for polymerization of olefins: XI. Synthesis of Schiff bases containing cycloalkyl substituents from 2-acetyl-6-bromopyridine/ G. S. Zhilovskii, I. I. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2009, V. 45, N 1, pp 44-47 doi:10.1134/S1070428009010072), IF=0.556
  327. G.V. Giniyatullina, O.B. Flekhter, G.A. Tolstikov
    Synthesis of squalamine analogues on the basis of lupane triterpenoids
    Mendeleev Commun., 2009, V. 19, N 1, 32-33. doi:10.1016/j.mencom.2009.01.013, IF=0.609
  328. G.V. Giniyatullina, O.B. Flekhter, G.A. Tolstikov
    Synthesis of squalamine analogues on the basis of lupane triterpenoids
    Mendeleev Commun., 2009, V. 19, N 1, 32-33. doi:10.1016/j.mencom.2009.01.013, IF=0.609
  329. Т.П. Кукина, И.А. Горбунова, И.И. Баяндина, О.И. Сальникова
    Хемотаксономические особенности видов Armillaria.
    Хвойные бореальной зоны, 2009, 1, с. 72-75.
  330. Т.П. Кукина, И.А. Горбунова, И.И. Баяндина, О.И. Сальникова
    Хемотаксономические особенности видов Armillaria.
    Хвойные бореальной зоны, 2009, 1, с. 72-75.

2008

Reviews, articles

  1. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  2. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  3. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  4. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  5. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  6. A.G. Matveeva, F.B. Sviridenko, V.V. Korolev, L.V. Kuibida, D.V. Stass, L.A. Shundrin, V.A. Reznikov, G.G. Grampp
    Difficulties in Building Radiation-Generated Three-Spin Systems Using Spin-Labeled Luminophores
    J. Phys. Chem. A, 2008, V. 112, N 2,183-193. doi:10.1021/jp076835e, IF=2.917
  7. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    Calculation of phase diagrams of heterophase two- and three-component liquid mixtures «α-pinene–water» and «α-pinene-water-ethanol».
    Chem. Engin.Science, 2008, V.63, N 24, 5854-5859. doi:10.1016/j.ces.2008.08.020, IF=1.774
  8. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    Calculation of phase diagrams of heterophase two- and three-component liquid mixtures «α-pinene–water» and «α-pinene-water-ethanol».
    Chem. Engin.Science, 2008, V.63, N 24, 5854-5859. doi:10.1016/j.ces.2008.08.020, IF=1.774
  9. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  10. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  11. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  12. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  13. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  14. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  15. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  16. В.А. Вавилин, Н.Ф. Салахутдинов, Ю.И. Рагино, Н.Е. Поляков, М.Б. Тарабан, Е.В. Лешина, Е.М. Стахнева, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Гипохолестеринемические свойства комплексного соединения симвастатина с глицирризиновой кислотой (симваглизина) в экспериментальных моделях
    Биомед. Химия, 2008, Т. 54, № 3, 301-313. (The cholesterol lowering properties of the complex compound simvastatin with glycyrrhizic acid (simvaglyzin) in experimental models/ V. A. Vavilin, N. F. Salakhutdinov, Yu. I. Ragino, N. E. Polyakov, M. B. Taraban, T. V. Leshina, E. M. Stakhneva, V. V. Lyakhovich, Yu. P. Nikitin, G. A. Tolstikov// Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry, 2008, V/ 2, N 4, pp 373-380 doi:10.1134/S1990750808040070)
  17. N.Yu. Adonin, V.V. Bardin, H.J. Frohn
    Polyfluoroorganoboron-Oxygen Compounds. 7. Studies of conversion of [C6HnF5-nB(OMe)3]- into [(C6HnF5-n)2B(OMe)2]- (n = 0, 1)
    Coll. Czech. Chem. Commun., 2008, V. 73, N 12, 1681-1692. doi:10.1135/cccc20081681, IF=0.879
  18. L.I. Goryunov, J. Grobe, V.D. Shteingarts
    Compounds R1R2EMMe3 (E = P, As; M = Si,Sn) - Convenient and Versatile Reagents for the Synthesis of Tertiary Fluoroarylphosphanes and -Arsanes
    Coll. Czech. Chem. Commun., 2008, V. 73, N 12, 1612–1622. doi:10.1135/cccc20081612, IF=0.879
  19. М.В. Павловская, И.А. Кирилюк, А.А. Щепалов, И.А. Григорьев, Д.Ф. Гришин
    Полимеризация стирола и метилметакрилата а присутствии 2,2-диэтил-4,5,5-триметил-2,5-дигидроимидазол-1-оксила
    Высокомол. Соедин., Сер. Б, 2008, Т. 50, № 12, 2181-2187. (Polymerization of styrene and methyl methacrylate in the presence of 2,2-diethyl-4,5,5-trimethyl-2,5-dihydroimidazol-1-oxyl/ M.V. Pavlovskaya, I.A. Kirilyuk, A.A. Shchepalov, I.A. Grigoriev, D.F. Grishin// Polymer Science Series B, 2008, V. 50, N 11-12, pp 356-361 doi:10.1134/S1560090408110134), IF=0.34
  20. М.В. Павловская, И.А. Кирилюк, А.А. Щепалов, И.А. Григорьев, Д.Ф. Гришин
    Полимеризация стирола и метилметакрилата а присутствии 2,2-диэтил-4,5,5-триметил-2,5-дигидроимидазол-1-оксила
    Высокомол. Соедин., Сер. Б, 2008, Т. 50, № 12, 2181-2187. (Polymerization of styrene and methyl methacrylate in the presence of 2,2-diethyl-4,5,5-trimethyl-2,5-dihydroimidazol-1-oxyl/ M.V. Pavlovskaya, I.A. Kirilyuk, A.A. Shchepalov, I.A. Grigoriev, D.F. Grishin// Polymer Science Series B, 2008, V. 50, N 11-12, pp 356-361 doi:10.1134/S1560090408110134), IF=0.34
  21. М.В. Павловская, И.А. Кирилюк, А.А. Щепалов, И.А. Григорьев, Д.Ф. Гришин
    Полимеризация стирола и метилметакрилата а присутствии 2,2-диэтил-4,5,5-триметил-2,5-дигидроимидазол-1-оксила
    Высокомол. Соедин., Сер. Б, 2008, Т. 50, № 12, 2181-2187. (Polymerization of styrene and methyl methacrylate in the presence of 2,2-diethyl-4,5,5-trimethyl-2,5-dihydroimidazol-1-oxyl/ M.V. Pavlovskaya, I.A. Kirilyuk, A.A. Shchepalov, I.A. Grigoriev, D.F. Grishin// Polymer Science Series B, 2008, V. 50, N 11-12, pp 356-361 doi:10.1134/S1560090408110134), IF=0.34
  22. T.N. Drebushchak, N.V. Chukanov, E.V. Boldyreva
    Two polymorphs of chlorpropamide: the δ-form and the high-temperature ε-form
    Acta Crystallogr. C, 2008, V. 64, N 12, O623-O625. doi:10.1107/S0108270108034550, IF=0.718
  23. T.N. Drebushchak, N.V. Chukanov, E.V. Boldyreva
    Two polymorphs of chlorpropamide: the δ-form and the high-temperature ε-form
    Acta Crystallogr. C, 2008, V. 64, N 12, O623-O625. doi:10.1107/S0108270108034550, IF=0.718
  24. Yu.A. Chesalov, V.P. Baltakhinov, T.N. Drebushchak, E.V. Boldyreva, N.V. Chukanov, V.A. Drebushchak
    FT-IR and FT-Raman spectra of five polymorphs of chlorpropamide. Experimental study and ab initio calculations
    J. Mol. Struct., 2008, V. 891, N 1-3, 75-86. doi:10.1016/j.molstruc.2008.03.006, IF=1.485
  25. Yu.A. Chesalov, V.P. Baltakhinov, T.N. Drebushchak, E.V. Boldyreva, N.V. Chukanov, V.A. Drebushchak
    FT-IR and FT-Raman spectra of five polymorphs of chlorpropamide. Experimental study and ab initio calculations
    J. Mol. Struct., 2008, V. 891, N 1-3, 75-86. doi:10.1016/j.molstruc.2008.03.006, IF=1.485
  26. Yu.A. Chesalov, V.P. Baltakhinov, T.N. Drebushchak, E.V. Boldyreva, N.V. Chukanov, V.A. Drebushchak
    FT-IR and FT-Raman spectra of five polymorphs of chlorpropamide. Experimental study and ab initio calculations
    J. Mol. Struct., 2008, V. 891, N 1-3, 75-86. doi:10.1016/j.molstruc.2008.03.006, IF=1.485
  27. Yu.A. Chesalov, V.P. Baltakhinov, T.N. Drebushchak, E.V. Boldyreva, N.V. Chukanov, V.A. Drebushchak
    FT-IR and FT-Raman spectra of five polymorphs of chlorpropamide. Experimental study and ab initio calculations
    J. Mol. Struct., 2008, V. 891, N 1-3, 75-86. doi:10.1016/j.molstruc.2008.03.006, IF=1.485
  28. Yu.A. Chesalov, V.P. Baltakhinov, T.N. Drebushchak, E.V. Boldyreva, N.V. Chukanov, V.A. Drebushchak
    FT-IR and FT-Raman spectra of five polymorphs of chlorpropamide. Experimental study and ab initio calculations
    J. Mol. Struct., 2008, V. 891, N 1-3, 75-86. doi:10.1016/j.molstruc.2008.03.006, IF=1.485
  29. Е.Л. Головкина, Е.Г. Ковалёва, Л.С. Молочников, М. Хартман, Ч. Говиндасами, И.А. Григорьев, И.А. Кирилюк
    Метод спинового pH зонда в исследовании мезопористого молекулярного сита SBA-15
    Сорбционные и хроматографические процессы 2008, Т. 8, N 6, 971-985.
  30. Е.Л. Головкина, Е.Г. Ковалёва, Л.С. Молочников, М. Хартман, Ч. Говиндасами, И.А. Григорьев, И.А. Кирилюк
    Метод спинового pH зонда в исследовании мезопористого молекулярного сита SBA-15
    Сорбционные и хроматографические процессы 2008, Т. 8, N 6, 971-985.
  31. Е.Л. Головкина, Е.Г. Ковалёва, Л.С. Молочников, М. Хартман, Ч. Говиндасами, И.А. Григорьев, И.А. Кирилюк
    Метод спинового pH зонда в исследовании мезопористого молекулярного сита SBA-15
    Сорбционные и хроматографические процессы 2008, Т. 8, N 6, 971-985.
  32. Е.Л. Головкина, Е.Г. Ковалёва, Л.С. Молочников, М. Хартман, Ч. Говиндасами, И.А. Григорьев, И.А. Кирилюк
    Метод спинового pH зонда в исследовании мезопористого молекулярного сита SBA-15
    Сорбционные и хроматографические процессы 2008, Т. 8, N 6, 971-985.
  33. Е.Л. Головкина, Е.Г. Ковалёва, Л.С. Молочников, М. Хартман, Ч. Говиндасами, И.А. Григорьев, И.А. Кирилюк
    Метод спинового pH зонда в исследовании мезопористого молекулярного сита SBA-15
    Сорбционные и хроматографические процессы 2008, Т. 8, N 6, 971-985.
  34. N. Pankrushina, I. Nikitina, E. Chernjak, C. Myz, T. Shakhtshneider, V. Boldyrev
    Solvent-free mechanochemical modification of lappakonifine and piroxicam
    Mater. Manuf. Process., 2008, V.23, N 6, 561-565. doi:10.1080/10426910802157870, IF=0.611
  35. N. Pankrushina, I. Nikitina, E. Chernjak, C. Myz, T. Shakhtshneider, V. Boldyrev
    Solvent-free mechanochemical modification of lappakonifine and piroxicam
    Mater. Manuf. Process., 2008, V.23, N 6, 561-565. doi:10.1080/10426910802157870, IF=0.611
  36. N. Pankrushina, I. Nikitina, E. Chernjak, C. Myz, T. Shakhtshneider, V. Boldyrev
    Solvent-free mechanochemical modification of lappakonifine and piroxicam
    Mater. Manuf. Process., 2008, V.23, N 6, 561-565. doi:10.1080/10426910802157870, IF=0.611
  37. В.Д. Тихова, В.П. Фадеева, М.И. Дергачева, М.М. Шакиров
    Использование кислотного гидролиза для анализа состава гуминовых кислот разного генезиса
    Журнал прикладной химии, 2008, Т. 81, N 11, 1841-1846. (Analysis of humic acids from various soils using acid hydrolysis/ V. D. Tikhova, V. P. Fadeeva, M. I. Dergacheva, M. M. Shakirov// Russian Journal of Applied Chemistry November 2008, Volume 81, Issue 11, pp 1957-1962 doi:10.1134/S1070427208110177), IF=0.268
  38. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  39. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  40. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  41. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  42. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  43. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  44. И.Е. Смирнова, Е.В. Третьякова, О.Б. Флехтер, Л.В. Спирихин, Ф.З. Галин, Г.А. Толстиков, З.А. Старикова, А.А. Корлюков
    Синтез, строение и ацилирование гидроксипроизводных дигидрохинопимаровой кислоты
    Журнал органической химии, 2008, Т. 44, N 11. С. 1623-1629. (Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives/ I.E. Smirnova, E.V. Tretiyakova, O.B. Flekhter, L.V. Spirikhin, F.Z. Galin, G.A. Tolstikov, Z.A. Starikova, A.A. Korlyukov// Russian Journal of Organic Chemistry, 2008, V. 44, N 11, pp 1598-1605. doi:10.1134/S1070428008110055), IF=0.51
  45. А.Г. Мустафин, А.Р. Гимадиева, И.Б. Абдрахманов, Г.А. Толстиков
    Синтез и модификация β-D-ксилофуранозилнуклеозидов
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 735-738.
  46. А.Г. Мустафин, А.Р. Гимадиева, И.Б. Абдрахманов, Г.А. Толстиков
    Синтез и модификация β-D-ксилофуранозилнуклеозидов
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 735-738.
  47. А.Г. Мустафин, А.Р. Гимадиева, И.Б. Абдрахманов, Г.А. Толстиков
    Синтез и модификация β-D-ксилофуранозилнуклеозидов
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 735-738.
  48. О.Б. Казакова, Г.А. Толстиков
    Тритерпеноиды лупанового ряда. Медицинские перспективы
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 727-730.
  49. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, В.А. Выдрина, Р.Р. Муслухов, Г.А. Толстиков
    Экзо и эндо-гормоны насекомых: синтез и создание препаратов для регулирования их численности, поведения и жизнедеятельности
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 721-725.
  50. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, В.А. Выдрина, Р.Р. Муслухов, Г.А. Толстиков
    Экзо и эндо-гормоны насекомых: синтез и создание препаратов для регулирования их численности, поведения и жизнедеятельности
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 721-725.
  51. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, В.А. Выдрина, Р.Р. Муслухов, Г.А. Толстиков
    Экзо и эндо-гормоны насекомых: синтез и создание препаратов для регулирования их численности, поведения и жизнедеятельности
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 721-725.
  52. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, В.А. Выдрина, Р.Р. Муслухов, Г.А. Толстиков
    Экзо и эндо-гормоны насекомых: синтез и создание препаратов для регулирования их численности, поведения и жизнедеятельности
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 721-725.
  53. Г.Ю. Ишмуратов, М.П. Яковлева, Н.М. Ишмуратова, В.А. Выдрина, Р.Р. Муслухов, Г.А. Толстиков
    Экзо и эндо-гормоны насекомых: синтез и создание препаратов для регулирования их численности, поведения и жизнедеятельности
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 721-725.
  54. Ф.А. Валеев, О.Ю. Краснослободцева, Ш.М. Салихов, Г.А. Толстиков
    Левоглюкозан, левоглюкозенон, (+)-δ-кадинол и изоцемброл в синтезе низкомолекулярных биорегуляторов и цитостатиков
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 709-713.
  55. Ф.А. Валеев, О.Ю. Краснослободцева, Ш.М. Салихов, Г.А. Толстиков
    Левоглюкозан, левоглюкозенон, (+)-δ-кадинол и изоцемброл в синтезе низкомолекулярных биорегуляторов и цитостатиков
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 709-713.
  56. Ф.А. Валеев, О.Ю. Краснослободцева, Ш.М. Салихов, Г.А. Толстиков
    Левоглюкозан, левоглюкозенон, (+)-δ-кадинол и изоцемброл в синтезе низкомолекулярных биорегуляторов и цитостатиков
    Химия в инстересах устойчивого развития, 2008, Т. 16, N 6, 709-713.
  57. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
    Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
    Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
  58. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
    Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
    Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
  59. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
    Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
    Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
  60. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
    Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
    Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
  61. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
    Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
    Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
  62. C. Becker, G. Roshchupkina, T. Rybalova, Yu. Gatilov, G. Romanenko, V. Reznikov
    Unexpected formation of polycyclic oxygen-containing spiro-heterocycles in the reactions of 2,4-dihydro-3H-pyrrol-3-one 1 oxides with benzaldehyde
    Mendeleev Commun., 2008, V. 18, N 6, Pp 297-299. doi:10.1016/j.mencom.2008.11.002, IF=0.73
  63. M. Edeleva, S.R. A. Marque, D. Bertin, D. Gigmes, Y. Guillaneuf, S.V. Morozov, E.G. Bagryanskaya
    Hydrogen-Transfer Reaction in Nitroxide Mediated Polymerization of Methyl Methacrylate:2,2-Diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxylnitroxide vs. TEMPO
    J. Polym. Sci. Pol. Chem., 2008, V. 46, N 20, 6828-6842. doi:10.1002/pola.22991, IF=3.529
  64. M. Edeleva, S.R. A. Marque, D. Bertin, D. Gigmes, Y. Guillaneuf, S.V. Morozov, E.G. Bagryanskaya
    Hydrogen-Transfer Reaction in Nitroxide Mediated Polymerization of Methyl Methacrylate:2,2-Diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxylnitroxide vs. TEMPO
    J. Polym. Sci. Pol. Chem., 2008, V. 46, N 20, 6828-6842. doi:10.1002/pola.22991, IF=3.529
  65. M. Edeleva, S.R. A. Marque, D. Bertin, D. Gigmes, Y. Guillaneuf, S.V. Morozov, E.G. Bagryanskaya
    Hydrogen-Transfer Reaction in Nitroxide Mediated Polymerization of Methyl Methacrylate:2,2-Diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxylnitroxide vs. TEMPO
    J. Polym. Sci. Pol. Chem., 2008, V. 46, N 20, 6828-6842. doi:10.1002/pola.22991, IF=3.529
  66. M. Edeleva, S.R. A. Marque, D. Bertin, D. Gigmes, Y. Guillaneuf, S.V. Morozov, E.G. Bagryanskaya
    Hydrogen-Transfer Reaction in Nitroxide Mediated Polymerization of Methyl Methacrylate:2,2-Diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxylnitroxide vs. TEMPO
    J. Polym. Sci. Pol. Chem., 2008, V. 46, N 20, 6828-6842. doi:10.1002/pola.22991, IF=3.529
  67. M. Edeleva, S.R. A. Marque, D. Bertin, D. Gigmes, Y. Guillaneuf, S.V. Morozov, E.G. Bagryanskaya
    Hydrogen-Transfer Reaction in Nitroxide Mediated Polymerization of Methyl Methacrylate:2,2-Diphenyl-3-phenylimino-2,3-dihydroindol-1-yloxylnitroxide vs. TEMPO
    J. Polym. Sci. Pol. Chem., 2008, V. 46, N 20, 6828-6842. doi:10.1002/pola.22991, IF=3.529
  68. Y.V. Gerasimova, D.G. Knorre, M.M. Shakirov, T.S. Godovikova
    Human serum albumin as a catalyst of RNA cleavage: N-homocysteinylation and N-phosphorylation by oligonucleotide affinity reagent alter the reactivity of the protein
    Bioorg. Med. Chem. Lett., 2008, V. 18, N 20, 5396-5398. doi:10.1016/j.bmcl.2008.09.049, IF=2.604
  69. Y.V. Gerasimova, D.G. Knorre, M.M. Shakirov, T.S. Godovikova
    Human serum albumin as a catalyst of RNA cleavage: N-homocysteinylation and N-phosphorylation by oligonucleotide affinity reagent alter the reactivity of the protein
    Bioorg. Med. Chem. Lett., 2008, V. 18, N 20, 5396-5398. doi:10.1016/j.bmcl.2008.09.049, IF=2.604
  70. A.M. Чибиряев, A. Ермакова, И.В. Кожевников
    Сравнительная реакционная способность α-пинена в реакции термолиза для газофазных и сверхкритических условий
    Сверхкрит. Флюиды: Теор. Практ., 2008, Т. 3, № 4, 66-82.
  71. S. F. Vasilevsky, M. P. Davydova, G. A. Tolstikov
    Heterocyclic analogs of combretastatin A-4
    Chemistry of Heterocyclic Compounds, 2008, V. 44, N 10, pp 1257-1261. doi:10.1007/s10593-009-0171-4, IF=0.462
  72. S. F. Vasilevsky, M. P. Davydova, G. A. Tolstikov
    Heterocyclic analogs of combretastatin A-4
    Chemistry of Heterocyclic Compounds, 2008, V. 44, N 10, pp 1257-1261. doi:10.1007/s10593-009-0171-4, IF=0.462
  73. А.В. Вураско, Б.Н. Дрикер, Е.В. Карпова, Л.А. Алешина, Н.В. Мелех
    Свойства целлюлозных волокон, полученных при натронных варках с антрахиноном, обработанным в ультразвуковом поле
    Химия растительного сырья, 2008, № 4, 5-11.
  74. А.В. Вураско, Б.Н. Дрикер, Е.В. Карпова, Л.А. Алешина, Н.В. Мелех
    Свойства целлюлозных волокон, полученных при натронных варках с антрахиноном, обработанным в ультразвуковом поле
    Химия растительного сырья, 2008, № 4, 5-11.
  75. А.В. Вураско, Б.Н. Дрикер, Е.В. Карпова, Л.А. Алешина, Н.В. Мелех
    Свойства целлюлозных волокон, полученных при натронных варках с антрахиноном, обработанным в ультразвуковом поле
    Химия растительного сырья, 2008, № 4, 5-11.
  76. А.В. Вураско, Б.Н. Дрикер, Е.В. Карпова, Л.А. Алешина, Н.В. Мелех
    Свойства целлюлозных волокон, полученных при натронных варках с антрахиноном, обработанным в ультразвуковом поле
    Химия растительного сырья, 2008, № 4, 5-11.
  77. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  78. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  79. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  80. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  81. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  82. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  83. Савельева З.А., Глинская Л.А., Клевцова Р.Ф., Богуславский E.Г., Попов С.А., Семиколенова Н.В., Ткачев А.В., Захаров В.А., Ларионов С.В.
    СИНТЕЗ И СВОЙСТВА КОМПЛЕКСОВ МЕДИ(II) И КОБАЛЬТА(II) C ХИРАЛЬНЫМ ПРОИЗВОДНЫМ ПИРАЗОЛИН-5-ОЛА, ПОЛУЧЕННОГО НА ОСНОВЕ ТЕРПЕНА (+)-3-КАРЕНА
    Координационная химия, 2008, V. 34, N 10, 774-779 (Copper(II) and cobalt(II) complexes with a chiral 5-pyrazolone derivative obtained from the terpene (+)-3-carene: Synthesis and properties/ Z.A. Savel’eva, L.A. Glinskaya, R.F. Klevtsova, E.G. Boguslavskii, S.A. Popov, N.V. Semikolenova, A.V. Tkachev, V.A. Zakharov, S.V. Larionov// Russian Journal of Coordination Chemistry, 2008, V. 34, N 10, pp 766-771 doi:10.1134/S1070328408100102), IF=0.533
  84. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  85. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  86. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  87. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  88. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  89. A.A. Onischuk, T.G. Tolstikova, I.V. Sorokina, N.A. Zhukova, A.M. Baklanov, V.V. Karasev, G.G. Dulstseva, V.V. Boldyrev, V.M. Fomin
    Anti-inflammatory effect from indomethacin nanoparticles inhaled by male mice
    J. Aerosol Med., 2008, V. 21, N 3, 231-244. doi:10.1089/jamp.2007.0672
  90. В.В. Шелковников, А.И. Плеханов, Н.А. Орлова
    Нанометровые пленки полиметиновых красителей в оптической памяти и нелинейной оптике
    Российские нанотехнологии, 2008, Т. 3, № 9-10, 36-57.
  91. I.S. Steinberg, V.A. Loskutov, V.V. Shelkovnikov, Y.A. Shepetkin
    Two-photon recording of microholograms in photopolymer materials with new cationic thioxanthone photoinitiators
    Opt. Commun., 2008, V. 281, N 17, 4297-4301. doi:10.1016/j.optcom.2008.05.031, IF=1.314
  92. I.S. Steinberg, V.A. Loskutov, V.V. Shelkovnikov, Y.A. Shepetkin
    Two-photon recording of microholograms in photopolymer materials with new cationic thioxanthone photoinitiators
    Opt. Commun., 2008, V. 281, N 17, 4297-4301. doi:10.1016/j.optcom.2008.05.031, IF=1.314
  93. M.V. Korolevich, S.G. Kirillova, V.N. Piottukh-Peletsky, V.M. Andrianov
    Theoretical analysis of the IR spectrum of methyl-3,4-anhydro-α-D-talohexopyranoside
    J. Appl. Spectr., 2008, V. 75, N 5, 613-620. doi:10.1007/s10812-008-9112-8
  94. M.V. Korolevich, S.G. Kirillova, V.N. Piottukh-Peletsky, V.M. Andrianov
    Theoretical analysis of the IR spectrum of methyl-3,4-anhydro-α-D-talohexopyranoside
    J. Appl. Spectr., 2008, V. 75, N 5, 613-620. doi:10.1007/s10812-008-9112-8
  95. M.V. Korolevich, S.G. Kirillova, V.N. Piottukh-Peletsky, V.M. Andrianov
    Theoretical analysis of the IR spectrum of methyl-3,4-anhydro-α-D-talohexopyranoside
    J. Appl. Spectr., 2008, V. 75, N 5, 613-620. doi:10.1007/s10812-008-9112-8
  96. Yu. V. Shinkarenko, V. G. Vasil'ev
    Phenolcarboxylic acids from Myosotis krylovii and M. palustris
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 632-633. doi:10.1007/s10600-008-9130-z, IF=0.442
  97. G. V. Giniyatullina, O. B. Flekhter, I. P. Baikova, Z. A. Starikova, G. A. Tolstikov
    Effective synthesis of methyl 3β-amino-3-deoxybetulinate
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 603-605. doi:10.1007/s10600-008-9138-4, IF=0.442
  98. G. V. Giniyatullina, O. B. Flekhter, I. P. Baikova, Z. A. Starikova, G. A. Tolstikov
    Effective synthesis of methyl 3β-amino-3-deoxybetulinate
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 603-605. doi:10.1007/s10600-008-9138-4, IF=0.442
  99. G. V. Giniyatullina, O. B. Flekhter, I. P. Baikova, Z. A. Starikova, G. A. Tolstikov
    Effective synthesis of methyl 3β-amino-3-deoxybetulinate
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 603-605. doi:10.1007/s10600-008-9138-4, IF=0.442
  100. G. V. Giniyatullina, O. B. Flekhter, I. P. Baikova, Z. A. Starikova, G. A. Tolstikov
    Effective synthesis of methyl 3β-amino-3-deoxybetulinate
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 603-605. doi:10.1007/s10600-008-9138-4, IF=0.442
  101. Zh. Ganbaatar, B. Gantumur, S.A. Osadchii, E.E. Shul'ts, M.M. Shakirov, G.A. Tolstikov
    Plant Coumarins. 3. (+)-PTeryxin from Peucedanum terebinthaceum
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 578-581. doi:10.1007/s10600-008-9144-6, IF=0.442
  102. Zh. Ganbaatar, B. Gantumur, S.A. Osadchii, E.E. Shul'ts, M.M. Shakirov, G.A. Tolstikov
    Plant Coumarins. 3. (+)-PTeryxin from Peucedanum terebinthaceum
    Chemistry of Natural Compounds, 2008, V. 44, N 5, pp 578-581. doi:10.1007/s10600-008-9144-6, IF=0.442
  103. И.Ю. Багрянская, М.А. Гришина, Л.Ю. Cафина, Г.А. Селиванова, В.А. Потемкин, Ю.В. Гатилов
    Рентгеноструктурные и квантово-топологические исследования межмолекулярных взаимодействий в гомокристаллах частично фторированных хинолинов
    Журнал структурной химии, 2008, Т. 49, N 5, 933-941. (X-ray and quantum-topological studies of intermolecular interactions in partially fluorinated quinoline crystals/ I. Yu. Bagryanskaya, M. A. Grishina, L. Yu. Safina, G. A. Selivanova, V. A. Potemkin, Yu. V. Gatilov// Journal of Structural Chemistry, 2008, V. 49, N 5, pp 901-908 doi:10.1007/s10947-008-0155-8), IF=0.481
  104. И.Ю. Багрянская, М.А. Гришина, Л.Ю. Cафина, Г.А. Селиванова, В.А. Потемкин, Ю.В. Гатилов
    Рентгеноструктурные и квантово-топологические исследования межмолекулярных взаимодействий в гомокристаллах частично фторированных хинолинов
    Журнал структурной химии, 2008, Т. 49, N 5, 933-941. (X-ray and quantum-topological studies of intermolecular interactions in partially fluorinated quinoline crystals/ I. Yu. Bagryanskaya, M. A. Grishina, L. Yu. Safina, G. A. Selivanova, V. A. Potemkin, Yu. V. Gatilov// Journal of Structural Chemistry, 2008, V. 49, N 5, pp 901-908 doi:10.1007/s10947-008-0155-8), IF=0.481
  105. И.Ю. Багрянская, М.А. Гришина, Л.Ю. Cафина, Г.А. Селиванова, В.А. Потемкин, Ю.В. Гатилов
    Рентгеноструктурные и квантово-топологические исследования межмолекулярных взаимодействий в гомокристаллах частично фторированных хинолинов
    Журнал структурной химии, 2008, Т. 49, N 5, 933-941. (X-ray and quantum-topological studies of intermolecular interactions in partially fluorinated quinoline crystals/ I. Yu. Bagryanskaya, M. A. Grishina, L. Yu. Safina, G. A. Selivanova, V. A. Potemkin, Yu. V. Gatilov// Journal of Structural Chemistry, 2008, V. 49, N 5, pp 901-908 doi:10.1007/s10947-008-0155-8), IF=0.481
  106. О.В. Столярова, Л.Р. Михайлова, Л.А. Балтина-мл, Т.М. Габбасов, Л.А. Балтина, Г.А. Толстиков
    Оптимизация метода получения моноаммонийной соли глицирризиновой кислоты из корней солодки уральской (Glycyrrhiza uralensis Fisher) сибирских популяций
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 5, 571-576.
  107. О.В. Столярова, Л.Р. Михайлова, Л.А. Балтина-мл, Т.М. Габбасов, Л.А. Балтина, Г.А. Толстиков
    Оптимизация метода получения моноаммонийной соли глицирризиновой кислоты из корней солодки уральской (Glycyrrhiza uralensis Fisher) сибирских популяций
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 5, 571-576.
  108. О.В. Столярова, Л.Р. Михайлова, Л.А. Балтина-мл, Т.М. Габбасов, Л.А. Балтина, Г.А. Толстиков
    Оптимизация метода получения моноаммонийной соли глицирризиновой кислоты из корней солодки уральской (Glycyrrhiza uralensis Fisher) сибирских популяций
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 5, 571-576.
  109. О.В. Столярова, Л.Р. Михайлова, Л.А. Балтина-мл, Т.М. Габбасов, Л.А. Балтина, Г.А. Толстиков
    Оптимизация метода получения моноаммонийной соли глицирризиновой кислоты из корней солодки уральской (Glycyrrhiza uralensis Fisher) сибирских популяций
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 5, 571-576.
  110. О.В. Столярова, Л.Р. Михайлова, Л.А. Балтина-мл, Т.М. Габбасов, Л.А. Балтина, Г.А. Толстиков
    Оптимизация метода получения моноаммонийной соли глицирризиновой кислоты из корней солодки уральской (Glycyrrhiza uralensis Fisher) сибирских популяций
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 5, 571-576.
  111. V.A. Drebushchak, T.N. Drebushchak, N.V. Chukanov, E.V. Boldyreva
    Transitions among five polymorphs of chlorpropamide near the melting point
    J. Therm. Anal. Calorim., 2008, V. 93, N 2, 343-351. doi:0.1007/s10973-007-8822-0, IF=2.217
  112. V.A. Drebushchak, T.N. Drebushchak, N.V. Chukanov, E.V. Boldyreva
    Transitions among five polymorphs of chlorpropamide near the melting point
    J. Therm. Anal. Calorim., 2008, V. 93, N 2, 343-351. doi:0.1007/s10973-007-8822-0, IF=2.217
  113. V.A. Drebushchak, T.N. Drebushchak, N.V. Chukanov, E.V. Boldyreva
    Transitions among five polymorphs of chlorpropamide near the melting point
    J. Therm. Anal. Calorim., 2008, V. 93, N 2, 343-351. doi:0.1007/s10973-007-8822-0, IF=2.217
  114. В.П. Фадеева, В.И. Вершинин, Е.А. Кузьмина
    Определение серы в органических соединениях с применением барий-селективного электрода
    Журнал аналитической химии, 2008. Т. 63, № 8, 848-851. (Determination of sulfur in organic compounds using a barium-selective electrode/ V. P. Fadeeva, V. I. Vershinin, E. A. Kuzmina// Journal of Analytical Chemistry, 2008, Т. 63, № 8, С. 775-778. doi:10.1134/S106193480808011X), IF=0.602
  115. В.П. Фадеева, В.И. Вершинин, Е.А. Кузьмина
    Определение серы в органических соединениях с применением барий-селективного электрода
    Журнал аналитической химии, 2008. Т. 63, № 8, 848-851. (Determination of sulfur in organic compounds using a barium-selective electrode/ V. P. Fadeeva, V. I. Vershinin, E. A. Kuzmina// Journal of Analytical Chemistry, 2008, Т. 63, № 8, С. 775-778. doi:10.1134/S106193480808011X), IF=0.602
  116. N.V. Chukanov, S.A. Popov, G.V. Romanenko, V.A. Reznikov
    The unusual thermal transformations of the dimethyl 2,2,3,3-tetramethyl-7a-R-1,2,3,7a-tatrahydroimidazo[1,2-b]isoxazole-6,7-dicarboxylate derivatives
    Tetrahedron, 2008, V. 64, N 30-31, 7432-7436. doi:10.1016/j.tet.2008.05.038, IF=2.868
  117. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  118. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  119. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  120. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  121. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  122. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  123. Ю.И. Рагино, В.А. Вавилин, Н.Ф. Салахутдинов, С.И. Макарова, Е.М. Стахнева, О.Г. Сафронова, В.В. Ляхович, Ю.П. Никитин, Г.А. Толстиков
    Изучение антиоксидантного и нормализующего функцию эндотелия эффектов симваглизина на модели гиперхолестеринемии у кроликов
    Бюлл. Эксперимент. Биологии и Медицины, 2008, Т. 146, № 8, 171-175. (Antioxidant and endothelium-stabilizing effects of simvaglyzin on rabbits with experimental hypercholesterolemia/ Yu.I. Ragino, V.A. Vavilin, N.F. Salakhutdinov, S.I. Makarova, E.M. Stakhneva, O.G. Safronova, V.V. Lyakhovich, Yu.P. Nikitin, G.A. Tolstikov// Bulletin of Experimental Biology and Medicine, 2008, V. 146, N 2, pp 206-209 doi:10.1007/s10517-008-0252-x), IF=0.248
  124. В.Н. Ковтонюк, Л.С. Кобрина, Г. Хауфе
    Пентафторфенилирование ароматических соединений при действии 6-нитро-4,5,6,7,8-пентафтор-1-оксаспиро[2,5]окта-4,7-диена и AlCl3
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 8, 1654-1656. (Pentafluorophenylation of aromatic compounds with 4,5,6,7,8-pentafluoro-6-nitro-1-oxaspiro[2.5]octa-4,7-diene/ V. N. Kovtonyuk, L. S. Kobrina, G. Haufe// Russian Chemical Bulletin, 2008, V. 57, N 8, Pp 1686-1688 doi:10.1007/s11172-008-0222-5), IF=0.537
  125. Е.А. Конева, Т.М. Хоменко, С.Ю. Курбакова, Н.И. Комарова, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов, А.Г. Толстиков, Г.А. Толстиков
    Получение оптически активного омепразола с использованием каталитических комплексов ионов ванадия с хиральными основаниями Шиффа
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 8, 1648-1653. (Synthesis of optically active omeprazole by catalysis with vanadyl complexes with chiral Schiff bases/ E.A. Koneva, T.M. Khomenko, S.Yu. Kurbakova, N.I. Komarova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, G.A. Tolstikov, A.G. Tolstikov// Russian Chemical Bulletin, 2008, V. 57, N 8, Pp 1680-1685. doi:10.1007/s11172-008-0221-6), IF=0.537
  126. В.А. Стоник, Г.А. Толстиков
    Natural products: Designing Russian medications
    Вестник РАН, 2008, Т. 78, № 4, 338-345. (Natural products: Designing Russian medications/ V. A. Stonik, G. A. Tolstikov// Herald of the Russian Academy of Sciences, 2008, V. 78, N 4, pp 338-345. doi:10.1134/S1019331608040023), IF=0.317
  127. И.В. Машевская, З.Г. Алиев, Д.Г. Мажукин, С.А. Попов, А.Я. Тихонов, А.Н. Масливец
    Пятичленные 2,3-диоксогетероциклы. LXII. Взаимодействие 3-ароил-1Н-пирроло[2,1-c][1,4]бензоксазин-1,2,4-трионов с 1,2-бис(гидроксиамино)циклогексаном. Необычная перегруппировка в системе хиноксалино-спиро-пиррола
    Журнал органической химии, 2008, Т. 44, N 8, 1202-1206. (Five-membered 2,3-dioxo heterocycles: LXII. Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with N,N'-dihydroxycyclohexane-1,2-diamine. Unusual rearrangement in the spiro[quinoxaline-2,2'-pyrrole] system/ I.V. Mashevskaya, A.N. Maslivets, Z.G. Aliev, D.G. Mazhukin, S.A. Popov, A.Ya. Tikhonov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, P. 1189-1193. doi:10.1134/S1070428008080149), IF=0.51
  128. И.В. Машевская, З.Г. Алиев, Д.Г. Мажукин, С.А. Попов, А.Я. Тихонов, А.Н. Масливец
    Пятичленные 2,3-диоксогетероциклы. LXII. Взаимодействие 3-ароил-1Н-пирроло[2,1-c][1,4]бензоксазин-1,2,4-трионов с 1,2-бис(гидроксиамино)циклогексаном. Необычная перегруппировка в системе хиноксалино-спиро-пиррола
    Журнал органической химии, 2008, Т. 44, N 8, 1202-1206. (Five-membered 2,3-dioxo heterocycles: LXII. Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with N,N'-dihydroxycyclohexane-1,2-diamine. Unusual rearrangement in the spiro[quinoxaline-2,2'-pyrrole] system/ I.V. Mashevskaya, A.N. Maslivets, Z.G. Aliev, D.G. Mazhukin, S.A. Popov, A.Ya. Tikhonov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, P. 1189-1193. doi:10.1134/S1070428008080149), IF=0.51
  129. И.В. Машевская, З.Г. Алиев, Д.Г. Мажукин, С.А. Попов, А.Я. Тихонов, А.Н. Масливец
    Пятичленные 2,3-диоксогетероциклы. LXII. Взаимодействие 3-ароил-1Н-пирроло[2,1-c][1,4]бензоксазин-1,2,4-трионов с 1,2-бис(гидроксиамино)циклогексаном. Необычная перегруппировка в системе хиноксалино-спиро-пиррола
    Журнал органической химии, 2008, Т. 44, N 8, 1202-1206. (Five-membered 2,3-dioxo heterocycles: LXII. Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with N,N'-dihydroxycyclohexane-1,2-diamine. Unusual rearrangement in the spiro[quinoxaline-2,2'-pyrrole] system/ I.V. Mashevskaya, A.N. Maslivets, Z.G. Aliev, D.G. Mazhukin, S.A. Popov, A.Ya. Tikhonov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, P. 1189-1193. doi:10.1134/S1070428008080149), IF=0.51
  130. Муслухов P.P., Шаяхметова А., Яковлева М., Шитикова О.В., Ишмуратов Г.Ю., Толстиков Г.А.
    Исследование реакции гидроборирования-окисления производных рицинолевой кислоты
    Журнал органической химии, 2008, Т. 44, N 8. С. 1145-1148. (Hydroboration-oxidation of ricinoleic acid derivatives/ R.R. Muslukhov, A.K. Shayakhmetova, M.P. Yalkovleva, O.V. Shitikova, G.Y. Ishmuratov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, pp 1130-1133 doi:10.1134/S1070428008080046), IF=0.51
  131. Муслухов P.P., Шаяхметова А., Яковлева М., Шитикова О.В., Ишмуратов Г.Ю., Толстиков Г.А.
    Исследование реакции гидроборирования-окисления производных рицинолевой кислоты
    Журнал органической химии, 2008, Т. 44, N 8. С. 1145-1148. (Hydroboration-oxidation of ricinoleic acid derivatives/ R.R. Muslukhov, A.K. Shayakhmetova, M.P. Yalkovleva, O.V. Shitikova, G.Y. Ishmuratov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, pp 1130-1133 doi:10.1134/S1070428008080046), IF=0.51
  132. Муслухов P.P., Шаяхметова А., Яковлева М., Шитикова О.В., Ишмуратов Г.Ю., Толстиков Г.А.
    Исследование реакции гидроборирования-окисления производных рицинолевой кислоты
    Журнал органической химии, 2008, Т. 44, N 8. С. 1145-1148. (Hydroboration-oxidation of ricinoleic acid derivatives/ R.R. Muslukhov, A.K. Shayakhmetova, M.P. Yalkovleva, O.V. Shitikova, G.Y. Ishmuratov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, pp 1130-1133 doi:10.1134/S1070428008080046), IF=0.51
  133. Муслухов P.P., Шаяхметова А., Яковлева М., Шитикова О.В., Ишмуратов Г.Ю., Толстиков Г.А.
    Исследование реакции гидроборирования-окисления производных рицинолевой кислоты
    Журнал органической химии, 2008, Т. 44, N 8. С. 1145-1148. (Hydroboration-oxidation of ricinoleic acid derivatives/ R.R. Muslukhov, A.K. Shayakhmetova, M.P. Yalkovleva, O.V. Shitikova, G.Y. Ishmuratov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, pp 1130-1133 doi:10.1134/S1070428008080046), IF=0.51
  134. Муслухов P.P., Шаяхметова А., Яковлева М., Шитикова О.В., Ишмуратов Г.Ю., Толстиков Г.А.
    Исследование реакции гидроборирования-окисления производных рицинолевой кислоты
    Журнал органической химии, 2008, Т. 44, N 8. С. 1145-1148. (Hydroboration-oxidation of ricinoleic acid derivatives/ R.R. Muslukhov, A.K. Shayakhmetova, M.P. Yalkovleva, O.V. Shitikova, G.Y. Ishmuratov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, pp 1130-1133 doi:10.1134/S1070428008080046), IF=0.51
  135. G.I. Roshchupkina, A.A. Bobko, A. Bratasz, V.A. Reznikov, P. Kuppusamy, V.V. Khramtsov
    In vivo EPR measurement of glutathione in tumor-bearing mice using improved disulfide biradical probe
    Free Rad. Biol. Med., 2008, V.45, N 3,312-320. doi:10.1016/j.freeradbiomed.2008.04.019, IF=4.813
  136. G.I. Roshchupkina, A.A. Bobko, A. Bratasz, V.A. Reznikov, P. Kuppusamy, V.V. Khramtsov
    In vivo EPR measurement of glutathione in tumor-bearing mice using improved disulfide biradical probe
    Free Rad. Biol. Med., 2008, V.45, N 3,312-320. doi:10.1016/j.freeradbiomed.2008.04.019, IF=4.813
  137. G.I. Roshchupkina, A.A. Bobko, A. Bratasz, V.A. Reznikov, P. Kuppusamy, V.V. Khramtsov
    In vivo EPR measurement of glutathione in tumor-bearing mice using improved disulfide biradical probe
    Free Rad. Biol. Med., 2008, V.45, N 3,312-320. doi:10.1016/j.freeradbiomed.2008.04.019, IF=4.813
  138. G.I. Roshchupkina, A.A. Bobko, A. Bratasz, V.A. Reznikov, P. Kuppusamy, V.V. Khramtsov
    In vivo EPR measurement of glutathione in tumor-bearing mice using improved disulfide biradical probe
    Free Rad. Biol. Med., 2008, V.45, N 3,312-320. doi:10.1016/j.freeradbiomed.2008.04.019, IF=4.813
  139. Y.V. Gerasimova, I.A. Erchenko, M.M. Shakirov, T.S. Godovikova
    Interaction of human serum albumin and its clinically relevant modification with oligoribonucleotides
    Bioorg. Med. Chem. Lett., 2008, V. 18, N 16, 4511-4514. doi:10.1016/j.bmcl.2008.07.060, IF=2.604
  140. Y.V. Gerasimova, I.A. Erchenko, M.M. Shakirov, T.S. Godovikova
    Interaction of human serum albumin and its clinically relevant modification with oligoribonucleotides
    Bioorg. Med. Chem. Lett., 2008, V. 18, N 16, 4511-4514. doi:10.1016/j.bmcl.2008.07.060, IF=2.604
  141. Y.V. Gerasimova, I.A. Erchenko, M.M. Shakirov, T.S. Godovikova
    Interaction of human serum albumin and its clinically relevant modification with oligoribonucleotides
    Bioorg. Med. Chem. Lett., 2008, V. 18, N 16, 4511-4514. doi:10.1016/j.bmcl.2008.07.060, IF=2.604
  142. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  143. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  144. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  145. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  146. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  147. S.N. Konchenko, N.P. Gritsan, I.G. Irtegova, A.V. Lonchakov, R. Mews, V.I. Ovcharenko, U. Radius, A.V. Zibarev
    Cobaltocenium [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
    Eur. J. Inorg. Chem., 2008, N 24, 3833-3838. doi:10.1002/ejic.200800390, IF=2.596
  148. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  149. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  150. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  151. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  152. V.S. Minkov, A.S. Krylov, E.V. Boldyreva, S.V. Goryainov, S.N. Bizyaev, A.N. Vtyurin
    Pressure-induced phase transitions in crystalline l- and DL-cysteine
    J. Phys. Chem. B, 2008, V. 112, N 30, 8851-8854. doi:10.1021/jp8020276, IF=4.85
  153. E. Bagryanskaya, D. Bertin, D. Gigmes, I. Kirilyuk, S.R. A. Marque, V. Reznikov, G. Roshchupkina, I. Zhurko, D. Zubenko
    Can the first addition of alkyl radicals play a role in the fate of NMP?
    Macromol. Chem. Phys. 2008, V. 209, N 13, 1345–1357. doi:10.1002/macp.200800099, IF=2.46
  154. E. Bagryanskaya, D. Bertin, D. Gigmes, I. Kirilyuk, S.R. A. Marque, V. Reznikov, G. Roshchupkina, I. Zhurko, D. Zubenko
    Can the first addition of alkyl radicals play a role in the fate of NMP?
    Macromol. Chem. Phys. 2008, V. 209, N 13, 1345–1357. doi:10.1002/macp.200800099, IF=2.46
  155. E. Bagryanskaya, D. Bertin, D. Gigmes, I. Kirilyuk, S.R. A. Marque, V. Reznikov, G. Roshchupkina, I. Zhurko, D. Zubenko
    Can the first addition of alkyl radicals play a role in the fate of NMP?
    Macromol. Chem. Phys. 2008, V. 209, N 13, 1345–1357. doi:10.1002/macp.200800099, IF=2.46
  156. E. Bagryanskaya, D. Bertin, D. Gigmes, I. Kirilyuk, S.R. A. Marque, V. Reznikov, G. Roshchupkina, I. Zhurko, D. Zubenko
    Can the first addition of alkyl radicals play a role in the fate of NMP?
    Macromol. Chem. Phys. 2008, V. 209, N 13, 1345–1357. doi:10.1002/macp.200800099, IF=2.46
  157. И.В. Зибарева, И.В. Курбангалеева, Н.С. Редькина, Б.С. Елепов
    Некоторые аспекты библиометрических исследований в Сибирском отделении Российской академии наук
    Библиотековедение, 2008, № 3, 39-45.
  158. И.В. Зибарева, И.В. Курбангалеева, Н.С. Редькина, Б.С. Елепов
    Некоторые аспекты библиометрических исследований в Сибирском отделении Российской академии наук
    Библиотековедение, 2008, № 3, 39-45.
  159. И.В. Зибарева, И.В. Курбангалеева, Н.С. Редькина, Б.С. Елепов
    Некоторые аспекты библиометрических исследований в Сибирском отделении Российской академии наук
    Библиотековедение, 2008, № 3, 39-45.
  160. Т.А. Асташова, Ю.Э. Бергман, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркер лимфотоксикоза и его коррекции
    Вестник лимфологии, 2008, №2, 34-35.
  161. Т.А. Асташова, Ю.Э. Бергман, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркер лимфотоксикоза и его коррекции
    Вестник лимфологии, 2008, №2, 34-35.
  162. Т.А. Асташова, Ю.Э. Бергман, С.В. Морозов, В.В. Асташов
    Свободные жирные кислоты как маркер лимфотоксикоза и его коррекции
    Вестник лимфологии, 2008, №2, 34-35.
  163. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  164. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  165. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  166. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  167. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  168. Е.М. Стахнева, В.А. Вавилин, Н.Ф. Салахутдинов, О.Г. Сафронова, С.И. Макарова, М.В. Иванова, Ю.И. Рагино
    Липидснижающий и антиоксидантный эффекты симваглизина при экспериментальной гиперхолестеринемии
    Регионарное кровообращение и микроциркуляция, 2008, Т. 7, № 2, 52-53.
  169. E.M. Suleimenov, V.A. Raldugin, S.M. Adekenov
    Anhydroaustricin from Artemisia albida
    Chemistry of Natural Compounds, 2008, V. 44, N 4, 541-542. doi:10.1007/s10600-008-9118-8, IF=0.442
  170. E.M. Suleimenov, V.A. Raldugin, S.M. Adekenov
    Anhydroaustricin from Artemisia albida
    Chemistry of Natural Compounds, 2008, V. 44, N 4, 541-542. doi:10.1007/s10600-008-9118-8, IF=0.442
  171. E. N. Shmidt, G. F. Chernenko, T. P. Kukina, L. M. Pokrovskii
    Extractable Substances from Needles of Siberian Fir Picea obovata
    Chemistry of Natural Compounds, 2008, V. 44, N 4, pp 508-509. doi:10.1007/s10600-008-9115-y, IF=0.442
  172. T.N. Drebushchak, S.N. Bizyaev, E.V. Boldyreva
    Bis(DL-cysteinium) oxalate
    Acta Crystallogr. C, 2008, V. 64, N 6, O313-O315. doi:10.1107/S0108270108012341, IF=0.718
  173. T.N. Drebushchak, S.N. Bizyaev, E.V. Boldyreva
    Bis(DL-cysteinium) oxalate
    Acta Crystallogr. C, 2008, V. 64, N 6, O313-O315. doi:10.1107/S0108270108012341, IF=0.718
  174. Г.Ю. Ишмуратов, М.П. Яковлева, А.Х. Шаяхметова, Н.М. Ишмуратова, Г.А. Толстиков
    Асимметрическое эпоксидирование и дигидроксилирование олефинов в синтезе феромонов насекомых
    Химия растительного сырья, 2008, N 3, 5-32.
  175. Г.Ю. Ишмуратов, М.П. Яковлева, А.Х. Шаяхметова, Н.М. Ишмуратова, Г.А. Толстиков
    Асимметрическое эпоксидирование и дигидроксилирование олефинов в синтезе феромонов насекомых
    Химия растительного сырья, 2008, N 3, 5-32.
  176. Г.Ю. Ишмуратов, М.П. Яковлева, А.Х. Шаяхметова, Н.М. Ишмуратова, Г.А. Толстиков
    Асимметрическое эпоксидирование и дигидроксилирование олефинов в синтезе феромонов насекомых
    Химия растительного сырья, 2008, N 3, 5-32.
  177. Г.Ю. Ишмуратов, М.П. Яковлева, А.Х. Шаяхметова, Н.М. Ишмуратова, Г.А. Толстиков
    Асимметрическое эпоксидирование и дигидроксилирование олефинов в синтезе феромонов насекомых
    Химия растительного сырья, 2008, N 3, 5-32.
  178. И.А. Кирилюк, Д.А. Морозов, Ю.С. Табатчикова, В.С. Медведев, А.В. Лебедев, Г.В. Романенко, Т.В. Рыбалова, И.А. Григорьев
    Синтез 4Н-имидазол-5-карбальдоксим-3-оксидов и 4Н-имидазол-5-карбонитрил-3-оксидов
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 7, 1487–1503. (Synthesis of 4Н--imidazole-5-carbaldoxime 3-oxides and 4Н--imidazole-5- carbonitrile 3-oxides/ I.A. Kirilyuk, D.A. Morozov, Yu.S. Tabatchikova, V.S. Medvedev, A.V. Lebedev, T.V. Rybalova, I.A. Grigor'Ev, G.V. Romanenko// Russian Chemical Bulletin, 2008, V. 57, N 7, Pp 1516-1533 doi:10.1007/s11172-008-0196-3), IF=0.537
  179. И.А. Кирилюк, Д.А. Морозов, Ю.С. Табатчикова, В.С. Медведев, А.В. Лебедев, Г.В. Романенко, Т.В. Рыбалова, И.А. Григорьев
    Синтез 4Н-имидазол-5-карбальдоксим-3-оксидов и 4Н-имидазол-5-карбонитрил-3-оксидов
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 7, 1487–1503. (Synthesis of 4Н--imidazole-5-carbaldoxime 3-oxides and 4Н--imidazole-5- carbonitrile 3-oxides/ I.A. Kirilyuk, D.A. Morozov, Yu.S. Tabatchikova, V.S. Medvedev, A.V. Lebedev, T.V. Rybalova, I.A. Grigor'Ev, G.V. Romanenko// Russian Chemical Bulletin, 2008, V. 57, N 7, Pp 1516-1533 doi:10.1007/s11172-008-0196-3), IF=0.537
  180. И.А. Кирилюк, Д.А. Морозов, Ю.С. Табатчикова, В.С. Медведев, А.В. Лебедев, Г.В. Романенко, Т.В. Рыбалова, И.А. Григорьев
    Синтез 4Н-имидазол-5-карбальдоксим-3-оксидов и 4Н-имидазол-5-карбонитрил-3-оксидов
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 7, 1487–1503. (Synthesis of 4Н--imidazole-5-carbaldoxime 3-oxides and 4Н--imidazole-5- carbonitrile 3-oxides/ I.A. Kirilyuk, D.A. Morozov, Yu.S. Tabatchikova, V.S. Medvedev, A.V. Lebedev, T.V. Rybalova, I.A. Grigor'Ev, G.V. Romanenko// Russian Chemical Bulletin, 2008, V. 57, N 7, Pp 1516-1533 doi:10.1007/s11172-008-0196-3), IF=0.537
  181. Е.В. Суслов, Д.В. Корчагина, В.В. Самуков, К.П. Волчо, Н.Ф. Салахутдинов
    Влияние модификации цеолита Csβ хиральными веществами на ход реакции 5,5,8-триметилнона-3,7-диен-2-она с малононитрилом
    Химия в инстересах устойчивого развития, 2008, Т. 16, № 4, 441–447.
  182. N.E. Polyakov, T.V. Leshina, A.V. Tkachev, I.A. Nikitina, N.A. Pankrushina
    Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study
    J. Photochem. Photobiol. A: Chem., 2008, V. 197, N 2-3, 290-294. doi:10.1016/j.jphotochem.2008.01.006, IF=1.911
  183. N.E. Polyakov, T.V. Leshina, A.V. Tkachev, I.A. Nikitina, N.A. Pankrushina
    Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study
    J. Photochem. Photobiol. A: Chem., 2008, V. 197, N 2-3, 290-294. doi:10.1016/j.jphotochem.2008.01.006, IF=1.911
  184. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  185. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  186. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  187. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  188. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  189. N.Yu. Adonin, D.E. Babushkin, V.N. Parmon, V.V. Bardin, G.A. Kostin, V.I. Mashukov, H.J. Frohn
    The effect of N-heterocyclic carbene ligands in the palladium - catalyzed cross-coupling reaction of K[C6F5BF3] with aryl iodides and aryl bromides
    Tetrahedron, 2008, V. 64, N 25, 5920-5924. doi:10.1016/j.tet.2008.04.043, IF=2.868
  190. А. Ермакова, А.М. Чибиряев, И.В. Кожевников, П.Е. Микенин, В.И. Аникеев
    Особенности фазового равновесия бинарных смесей «α-пинен-вода» в до- и сверхкритическом состоянии
    Журнал физической химии. 2008, Т. 82, N 6, С. 1059-1063. (The special features of phase equilibria in α-pinene-water binary mixtures in the sub- and supercritical states/ A. Ermakova, A. M. Chibiryaev, I. V. Kozhevnikov, P. E. Mikenin, V. I. Anikeev// Russian Journal of Physical Chemistry A. 2008. V. 82. № 6. С. 928-932 doi:10.1134/S0036024408060101), IF=0.476
  191. А. Ермакова, А.М. Чибиряев, И.В. Кожевников, П.Е. Микенин, В.И. Аникеев
    Особенности фазового равновесия бинарных смесей «α-пинен-вода» в до- и сверхкритическом состоянии
    Журнал физической химии. 2008, Т. 82, N 6, С. 1059-1063. (The special features of phase equilibria in α-pinene-water binary mixtures in the sub- and supercritical states/ A. Ermakova, A. M. Chibiryaev, I. V. Kozhevnikov, P. E. Mikenin, V. I. Anikeev// Russian Journal of Physical Chemistry A. 2008. V. 82. № 6. С. 928-932 doi:10.1134/S0036024408060101), IF=0.476
  192. А. Ермакова, А.М. Чибиряев, И.В. Кожевников, П.Е. Микенин, В.И. Аникеев
    Особенности фазового равновесия бинарных смесей «α-пинен-вода» в до- и сверхкритическом состоянии
    Журнал физической химии. 2008, Т. 82, N 6, С. 1059-1063. (The special features of phase equilibria in α-pinene-water binary mixtures in the sub- and supercritical states/ A. Ermakova, A. M. Chibiryaev, I. V. Kozhevnikov, P. E. Mikenin, V. I. Anikeev// Russian Journal of Physical Chemistry A. 2008. V. 82. № 6. С. 928-932 doi:10.1134/S0036024408060101), IF=0.476
  193. М.М. Вьюшкова, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычный комплекс с переносом протона от катион-радикала к молекуле 2,2,6,6-тетраметилпиперидина
    Доклады АН, 2008, Т. 420, № 4, 500-503. (Unusual proton-transfer complex between the 2,2,6,6-tetramethylpiperidine radical cation and neutral molecule/ M. M. Vyushkova, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2008, V. 420, N 2, pp 125-127 doi:10.1134/S001250160806002X), IF=0.442
  194. М.М. Вьюшкова, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычный комплекс с переносом протона от катион-радикала к молекуле 2,2,6,6-тетраметилпиперидина
    Доклады АН, 2008, Т. 420, № 4, 500-503. (Unusual proton-transfer complex between the 2,2,6,6-tetramethylpiperidine radical cation and neutral molecule/ M. M. Vyushkova, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2008, V. 420, N 2, pp 125-127 doi:10.1134/S001250160806002X), IF=0.442
  195. М.М. Вьюшкова, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычный комплекс с переносом протона от катион-радикала к молекуле 2,2,6,6-тетраметилпиперидина
    Доклады АН, 2008, Т. 420, № 4, 500-503. (Unusual proton-transfer complex between the 2,2,6,6-tetramethylpiperidine radical cation and neutral molecule/ M. M. Vyushkova, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2008, V. 420, N 2, pp 125-127 doi:10.1134/S001250160806002X), IF=0.442
  196. М.М. Вьюшкова, В.И. Боровков, Л.Н. Щеголева, И.В. Береговая, В.А. Багрянский, Ю.Н. Молин
    Необычный комплекс с переносом протона от катион-радикала к молекуле 2,2,6,6-тетраметилпиперидина
    Доклады АН, 2008, Т. 420, № 4, 500-503. (Unusual proton-transfer complex between the 2,2,6,6-tetramethylpiperidine radical cation and neutral molecule/ M. M. Vyushkova, V. I. Borovkov, L. N. Shchegoleva, I. V. Beregovaya, V. A. Bagryanskii, Yu. N. Molin// Doklady Physical Chemistry, 2008, V. 420, N 2, pp 125-127 doi:10.1134/S001250160806002X), IF=0.442
  197. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  198. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  199. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  200. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  201. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  202. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, Г.А. Толстиков, Н.Э. Поляков, Н.А. Неверов, Е.Н. Медведева, В.А. Бабкин
    Механохимическое получение и фармакологическая активность водорастворимых межмолекулярных комплексов арабиногалактана и лекарственных веществ
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1274-1282 (Mechanochemical preparation and pharmacological activities of water-soluble intermolecular complexes of arabinogalactan with medicinal agents/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, G. A. Tolstikov, N. E. Polyakov, N. A. Neverova, E. N. Medvedeva, V. A. Babkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1299-1307 doi:10.1007/s11172-008-0167-8), IF=0.537
  203. Т.А. Кропачева, В.К. Хлесткин
    Получение эфиров 1-гидрокси-3-фенил-1Н-хиноксалин-2-он-4-оксида по реакции Митсунобу
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 6, 1240-1244. (The Mitsunobu 1-O-esterification of 1-hydroxy-3-phenyl-1H-quinoxalin-2-one 4-oxide/ T. A. Kropacheva, V. K. Khlestkin// Russian Chemical Bulletin, 2008, V. 57, N 6, Pp 1264-1267 doi:10.1007/s11172-008-0162-0), IF=0.537
  204. И.В. Зибарева, В.В. Писляков, Т.Н. Теплова, О.М. Нефедов
    Библиометрический анализ журнала Успехи химии
    Вестник РАН, 2008, Т. 78, № 6, 490-499. (Bibliometric analysis of the journal Uspekhi Khimii (Russian Chemical Reviews)/ I. V. Zibareva, V. V. Pislyakov, T. N. Teplova, O. M. Nefedov// Herald of the Russian Academy of Sciences, 2008, V. 78, N 3, pp 247-256. doi:10.1134/S101933160803012X), IF=0.317
  205. И.В. Зибарева, В.В. Писляков, Т.Н. Теплова, О.М. Нефедов
    Библиометрический анализ журнала Успехи химии
    Вестник РАН, 2008, Т. 78, № 6, 490-499. (Bibliometric analysis of the journal Uspekhi Khimii (Russian Chemical Reviews)/ I. V. Zibareva, V. V. Pislyakov, T. N. Teplova, O. M. Nefedov// Herald of the Russian Academy of Sciences, 2008, V. 78, N 3, pp 247-256. doi:10.1134/S101933160803012X), IF=0.317
  206. И.В. Зибарева, В.В. Писляков, Т.Н. Теплова, О.М. Нефедов
    Библиометрический анализ журнала Успехи химии
    Вестник РАН, 2008, Т. 78, № 6, 490-499. (Bibliometric analysis of the journal Uspekhi Khimii (Russian Chemical Reviews)/ I. V. Zibareva, V. V. Pislyakov, T. N. Teplova, O. M. Nefedov// Herald of the Russian Academy of Sciences, 2008, V. 78, N 3, pp 247-256. doi:10.1134/S101933160803012X), IF=0.317
  207. И.И. Олейник, А.И. Кочнев, И.В. Олейник, С.С. Иванчев, Г.А. Толстиков
    Препаративное получение салицилальдиминов 4-тритиланилина в условиях микроволнового облучения
    Журнал органической химии, 2008, Т. 44, N 6, 934-935. (Preparative microwave-assisted synthesis of N-salicylidene-4-triphenylmethylanilines/ I. I. Oleinik, A. I. Kochnev, I. V. Oleinik, S. S. Ivanchev, G. A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 6, pp 927-928 doi:10.1134/S1070428008060249), IF=0.51
  208. H.J. Frohn, M. Hirschberg, A. Wenda, V.V. Bardin
    Polyvalent perfluoroorgano- and selected polyfluoroorgano- halogen(III and V) compounds
    J. Fluor. Chem., 2008, V. 129, N 6, 459-473. doi:10.1016/j.jfluchem.2008.04.001, IF=1.513
  209. H.J. Frohn, M. Hirschberg, A. Wenda, V.V. Bardin
    Polyvalent perfluoroorgano- and selected polyfluoroorgano- halogen(III and V) compounds
    J. Fluor. Chem., 2008, V. 129, N 6, 459-473. doi:10.1016/j.jfluchem.2008.04.001, IF=1.513
  210. H.J. Frohn, M. Hirschberg, A. Wenda, V.V. Bardin
    Polyvalent perfluoroorgano- and selected polyfluoroorgano- halogen(III and V) compounds
    J. Fluor. Chem., 2008, V. 129, N 6, 459-473. doi:10.1016/j.jfluchem.2008.04.001, IF=1.513
  211. O.A. Snytnikova, A.Zh. Fursova, E.I. Chernyak, V.G. Vasiliev, S.V. Morozov, N.G. Kolosova, Yu.P. Tsentalovich
    Deaminated UV filter 3-hydroxykynurenine O-β-D-glucoside is found in cataractous human lenses
    Exp. Eye Res, 2008, V.86, N 6, 951-956. doi: 10.1016/j.exer.2008.03.013, IF=2.651
  212. O.A. Snytnikova, A.Zh. Fursova, E.I. Chernyak, V.G. Vasiliev, S.V. Morozov, N.G. Kolosova, Yu.P. Tsentalovich
    Deaminated UV filter 3-hydroxykynurenine O-β-D-glucoside is found in cataractous human lenses
    Exp. Eye Res, 2008, V.86, N 6, 951-956. doi: 10.1016/j.exer.2008.03.013, IF=2.651
  213. O.A. Snytnikova, A.Zh. Fursova, E.I. Chernyak, V.G. Vasiliev, S.V. Morozov, N.G. Kolosova, Yu.P. Tsentalovich
    Deaminated UV filter 3-hydroxykynurenine O-β-D-glucoside is found in cataractous human lenses
    Exp. Eye Res, 2008, V.86, N 6, 951-956. doi: 10.1016/j.exer.2008.03.013, IF=2.651
  214. O.A. Snytnikova, A.Zh. Fursova, E.I. Chernyak, V.G. Vasiliev, S.V. Morozov, N.G. Kolosova, Yu.P. Tsentalovich
    Deaminated UV filter 3-hydroxykynurenine O-β-D-glucoside is found in cataractous human lenses
    Exp. Eye Res, 2008, V.86, N 6, 951-956. doi: 10.1016/j.exer.2008.03.013, IF=2.651
  215. M.A. Voinov, A. Ruuge, V.A. Reznikov, I.A. Grigor'ev, A.I. Smirnov
    Mapping Local Protein Electrostatics by EPR of pH-Sensitive Thiol-Specific Nitroxide
    Biochemistry, 2008, V. 47, N 20, 5626-5637. doi:10.1021/bi800272f, IF=3.368
  216. M.A. Voinov, A. Ruuge, V.A. Reznikov, I.A. Grigor'ev, A.I. Smirnov
    Mapping Local Protein Electrostatics by EPR of pH-Sensitive Thiol-Specific Nitroxide
    Biochemistry, 2008, V. 47, N 20, 5626-5637. doi:10.1021/bi800272f, IF=3.368
  217. V. Levenshtein, E. Konstantinova, E. Konstantinov, S. Molodtsov
    Reconstruction of a graph from 2-vicinities of its vertices
    Discrete Applied Mathematics 2008, V.156, N 9, 1399-1406. doi:10.1016/j.dam.2006.11.016, IF=0.625
  218. V. Levenshtein, E. Konstantinova, E. Konstantinov, S. Molodtsov
    Reconstruction of a graph from 2-vicinities of its vertices
    Discrete Applied Mathematics 2008, V.156, N 9, 1399-1406. doi:10.1016/j.dam.2006.11.016, IF=0.625
  219. V. Levenshtein, E. Konstantinova, E. Konstantinov, S. Molodtsov
    Reconstruction of a graph from 2-vicinities of its vertices
    Discrete Applied Mathematics 2008, V.156, N 9, 1399-1406. doi:10.1016/j.dam.2006.11.016, IF=0.625
  220. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    The kinetics of thermal isomerization of β-pinene and a mixture of β- and α-pinenes in supercritical ethanol.
    J. Supercrit. Fluids, 2008, V. 45, N 1, 74-79. doi:10.1016/j.supflu.2007.12.005, IF=2.188
  221. A. Yermakova, A.M. Chibiryaev, I.V. Kozhevnikov, V.I. Anikeev
    The kinetics of thermal isomerization of β-pinene and a mixture of β- and α-pinenes in supercritical ethanol.
    J. Supercrit. Fluids, 2008, V. 45, N 1, 74-79. doi:10.1016/j.supflu.2007.12.005, IF=2.188
  222. E.M. Suleimenov, V.A. Raldugin, S.M. Adekenov
    Cirsimaritin from Stizolophus balsamita
    Chemistry of Natural Compounds, 2008, V. 44, N 3, 398. doi:10.1007/s10600-008-9077-0, IF=0.442
  223. E.M. Suleimenov, V.A. Raldugin, S.M. Adekenov
    Cirsimaritin from Stizolophus balsamita
    Chemistry of Natural Compounds, 2008, V. 44, N 3, 398. doi:10.1007/s10600-008-9077-0, IF=0.442
  224. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  225. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  226. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  227. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  228. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  229. N. V. Korobko, Ya. A. Turko, V. V. Shokun, E. N. Chernyak, L. M. Pokrovskii, O. N. Smetankina, B. F. Kerimzhanova, U. A. Baltaev
    GC-MS investigations. II. Lipid composition of Stevia rebaudiana
    Chemistry of Natural Compounds, 2008, V. 44, N 3, pp 359-360. doi:10.1007/s10600-008-9061-8, IF=0.442
  230. Б.А. Радбиль, С.Р. Кушнир, А.Б. Радбиль, Э.Н. Шмидт, В.Ф. Смирнов, Н.Б. Мельникова
    Четвертичные аммониевые соединения на основе смоляных кислот и канифоли и их коллоидно-химические и биоцидные свойства
    Журнал прикладной химии, 2008, Т. 81, N 5, 837-842. (Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297), IF=0.268
  231. Б.А. Радбиль, С.Р. Кушнир, А.Б. Радбиль, Э.Н. Шмидт, В.Ф. Смирнов, Н.Б. Мельникова
    Четвертичные аммониевые соединения на основе смоляных кислот и канифоли и их коллоидно-химические и биоцидные свойства
    Журнал прикладной химии, 2008, Т. 81, N 5, 837-842. (Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297), IF=0.268
  232. Б.А. Радбиль, С.Р. Кушнир, А.Б. Радбиль, Э.Н. Шмидт, В.Ф. Смирнов, Н.Б. Мельникова
    Четвертичные аммониевые соединения на основе смоляных кислот и канифоли и их коллоидно-химические и биоцидные свойства
    Журнал прикладной химии, 2008, Т. 81, N 5, 837-842. (Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297), IF=0.268
  233. Б.А. Радбиль, С.Р. Кушнир, А.Б. Радбиль, Э.Н. Шмидт, В.Ф. Смирнов, Н.Б. Мельникова
    Четвертичные аммониевые соединения на основе смоляных кислот и канифоли и их коллоидно-химические и биоцидные свойства
    Журнал прикладной химии, 2008, Т. 81, N 5, 837-842. (Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297), IF=0.268
  234. Б.А. Радбиль, С.Р. Кушнир, А.Б. Радбиль, Э.Н. Шмидт, В.Ф. Смирнов, Н.Б. Мельникова
    Четвертичные аммониевые соединения на основе смоляных кислот и канифоли и их коллоидно-химические и биоцидные свойства
    Журнал прикладной химии, 2008, Т. 81, N 5, 837-842. (Quaternary ammonium compounds based on resin acids and rosin and their colloidal-chemical and biocidal properties/ B. A. Radbil’, S. R. Kushnir, A. B. Radbil’, E. N. Shmidt, V. F. Smirnov, N. B. Mel’nikova// Russian Journal of Applied Chemistry, 2008, V. 81, N 5, pp 874-879. doi:10.1134/S1070427208050297), IF=0.268
  235. Г.Ю. Иишуратов, Э.Р. Латыпова, Р.Я. Харисов, P.P. Муслухов, А.В. Баннова, Р.Ф. Талипов, Г.А. Толстиков
    (R)-4-ментенон в реакциях 1,4-сопря-женного и 1,3-диполярного присоеди-нения
    Журнал органической химии, 2008, Т. 44, N 5, 663-665. ((R)-4-menthenone in reactions of 1,4-conjugate and 1,3-dipolar addition/ G.Y. Ishmuratov, E.R. Latypova, P.Y. Kharisov, R.R. Muslukhov, A.A. Bannova, R.F. Talipov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 5, 652-656. doi:10.1134/S1070428008050035), IF=0.51
  236. Г.Ю. Иишуратов, Э.Р. Латыпова, Р.Я. Харисов, P.P. Муслухов, А.В. Баннова, Р.Ф. Талипов, Г.А. Толстиков
    (R)-4-ментенон в реакциях 1,4-сопря-женного и 1,3-диполярного присоеди-нения
    Журнал органической химии, 2008, Т. 44, N 5, 663-665. ((R)-4-menthenone in reactions of 1,4-conjugate and 1,3-dipolar addition/ G.Y. Ishmuratov, E.R. Latypova, P.Y. Kharisov, R.R. Muslukhov, A.A. Bannova, R.F. Talipov, G.A. Tolstikov// Russian Journal of Organic Chemistry, 2008, V. 44, N 5, 652-656. doi:10.1134/S1070428008050035), IF=0.51
  237. Г.Ю. Ииш