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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

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Personal publicalions (DB NIOCh)


2021

Reviews, articles

  1. 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, Version of Record online:06 January 2021 doi:10.1002/app.50436, IF=2.519
  2. 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, Version of Record online:06 January 2021 doi:10.1002/app.50436, IF=2.519
  3. 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, Version of Record online:06 January 2021 doi:10.1002/app.50436, IF=2.519
  4. 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, Version of Record online:06 January 2021 doi:10.1002/app.50436, IF=2.519
  5. 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, Version of Record online:06 January 2021 doi:10.1002/app.50436, IF=2.519
  6. A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
    Org. Biomol. Chem., 2021, Advance Article doi:10.1039/D0OB01893G, IF=3.411
  7. 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=2.303
  8. 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=2.303
  9. 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=2.303
  10. 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=2.303
  11. 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=3.55
  12. 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=3.55
  13. 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=3.55
  14. 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=2.303
  15. 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=2.303
  16. 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=2.303
  17. 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=2.303
  18. 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=4.612
  19. 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=4.612
  20. 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=4.612
  21. 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=4.612
  22. 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=4.612
  23. 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=4.612
  24. 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=4.612
  25. 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=4.612
  26. 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=4.612
  27. 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=3.426
  28. 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=3.426
  29. 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=3.426
  30. 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=3.426
  31. 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=3.426
  32. 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=3.763
  33. 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=3.763
  34. 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=3.763
  35. 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=3.763
  36. 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=3.763
  37. 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=3.763
  38. 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=3.763
  39. 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=3.763
  40. 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=3.763
  41. 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=5.88
  42. 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=5.88
  43. 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=5.88
  44. 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=5.88
  45. 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=5.88
  46. 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=5.88
  47. 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=5.88
  48. 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=5.88
  49. 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=5.88
  50. 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=5.88
  51. 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=1.947
  52. 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=1.947
  53. 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=1.947
  54. 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=1.947
  55. 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=1.947
  56. 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=1.947
  57. 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=1.947
  58. 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=3.267
  59. 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=3.267
  60. 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=3.267
  61. 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=3.267
  62. 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=3.267
  63. 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.31,127677 doi:10.1016/j.bmcl.2020.127677, IF=2.303
  64. 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.31,127677 doi:10.1016/j.bmcl.2020.127677, IF=2.303
  65. 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.31,127677 doi:10.1016/j.bmcl.2020.127677, IF=2.303
  66. 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.31,127677 doi:10.1016/j.bmcl.2020.127677, IF=2.303
  67. 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.31,127677 doi:10.1016/j.bmcl.2020.127677, IF=2.303
  68. 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=3.72
  69. 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=3.72
  70. 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=3.72
  71. 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=2.572
  72. 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=2.572
  73. 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=2.572
  74. 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=2.572
  75. 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=2.572
  76. 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 (E-pub Ahead of Print) doi:10.2174/1570180817999201211193151, IF=1
  77. 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 (E-pub Ahead of Print) doi:10.2174/1570180817999201211193151, IF=1
  78. 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 (E-pub Ahead of Print) doi:10.2174/1570180817999201211193151, IF=1
  79. 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 (E-pub Ahead of Print) doi:10.2174/1570180817999201211193151, IF=1

2020

Reviews, articles

  1. 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, Available online 10 December 2020 doi:10.1016/j.ceramint.2020.12.083, IF=3.83
  2. 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, Available online 10 December 2020 doi:10.1016/j.ceramint.2020.12.083, IF=3.83
  3. 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, Available online 10 December 2020 doi:10.1016/j.ceramint.2020.12.083, IF=3.83
  4. 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, Available online 10 December 2020 doi:10.1016/j.ceramint.2020.12.083, IF=3.83
  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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  10. 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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  11. 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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  12. 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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  13. 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 , Available online 26 November 2020 doi:10.1016/j.xphs.2020.11.016, IF=2.996
  14. 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, First published 06 Nov 2020 doi:10.1007/s10895-020-02643-7, IF=2.92
  15. 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, First published 06 Nov 2020 doi:10.1007/s10895-020-02643-7, IF=2.92
  16. 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, First published 06 Nov 2020 doi:10.1007/s10895-020-02643-7, IF=2.92
  17. 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 (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13
  18. 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 (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13
  19. 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 (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13
  20. 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 (2020), Published: 24 August 2020 doi:10.1007/s11030-020-10132-z, IF=2.13
  21. 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 ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
  22. 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 ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
  23. 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 ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
  24. 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 ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
  25. 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 ), Published online: 28 Mar 2020 doi:10.1080/14786419.2020.1744139, IF=2.158
  26. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  27. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  28. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  29. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  30. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  31. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  32. 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, Published online: 03 Aug 2020 doi:10.1080/14786419.2020.1795655, IF=2.157
  33. 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
  34. 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
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    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
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    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
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    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
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    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
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    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
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    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
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    Chemistry - A European Journal, Accepted manuscript online: 16 November 2020 doi:10.1002/chem.202004606, IF=4.857
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    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, Accepted manuscript online: 16 November 2020 doi:10.1002/chem.202004606, IF=4.857
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    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, Accepted manuscript online: 16 November 2020 doi:10.1002/chem.202004606, IF=4.857
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    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
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    Unexpected ring opening during the imination of camphor-type bicyclic ketones
    European Journal of Organic Chemistry, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
  47. 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, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
  48. 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, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
  49. 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, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
  50. 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, First online 19 November 2020 doi:10.1002/ejoc.202001397, IF=2.888
  51. D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova
    Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1
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  52. D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova
    Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1
    Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159, IF=1.978
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    Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1
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    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
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    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
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    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
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    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
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    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
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    New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
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    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
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    New type of anti-influenza agents based on benzo[d][1,3]dithiol core
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    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
  64. 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
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    Nanoscale, 2020,12 (48), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
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    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (48), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
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    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (48), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
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    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (48), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
  70. 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
  71. 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
  72. 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
  73. 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
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    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
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    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
  76. 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
  77. 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
  78. 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
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    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
  80. 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
  81. 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
  82. 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
  83. 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
  84. 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
  85. 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
  86. 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
  87. 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
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    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
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    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
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    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
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    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
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    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
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    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
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    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. 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
  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. 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.
    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)
  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.
    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.
    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. 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
  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. 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
  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. 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
  785. 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
  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

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
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    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
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    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
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    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
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    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
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    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
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    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
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    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
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    Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
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    Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
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  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
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  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
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    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
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    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
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    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
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    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
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    Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
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    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
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    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
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    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
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    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
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    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
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    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
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    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
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    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
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    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
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    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
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    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
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    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
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    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
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    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
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    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
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    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
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    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
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    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
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    Физическая активация процессов экстракции и органического синтеза
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    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
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    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
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    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
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    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
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    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
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    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
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    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
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    Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
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    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
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    Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
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    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
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    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
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    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
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    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
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    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
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    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
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    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
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    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
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    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
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    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
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    Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
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    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
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    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
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    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
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    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
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    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
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    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
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    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
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    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
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    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
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    Effects of acute and chronic treatment of STEP inhibitor, TC-2153, on the nervous system and behaviour of zebrafish (Danio rerio)
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    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
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    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
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    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
  756. 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
  757. 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
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    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
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    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
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    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
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    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
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    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
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    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
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    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
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    A near-infra-red emitting manganese(II) complex with a pyrimidine-based ligand
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    Оценка корректности результатов обращенной газовой хроматографии при определении термодинамической совместимости полимерных смесей
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    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
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    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
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    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
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    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
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    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
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    Inhibitory Effect of New Semisynthetic Usnic Acid Derivatives on Human Tyrosyl-DNA Phosphodiesterase 1
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    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
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    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
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    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
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    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
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    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
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    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
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    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
  801. 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
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    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
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    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
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    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
  805. 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
  806. А.Б. Будаев, А.В. Иванов, О.В. Петрова, А.Я. Тихонов, В.А. Самсонов, Л.Н. Собенина, Б.А. Трофимов
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    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
  807. 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
  808. 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
  809. 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
  810. 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
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  811. 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
  812. 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
  813. 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
  814. 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
  815. 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
  816. 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
  817. 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
  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. 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
  823. 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
  824. 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
  825. 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
  826. 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
  827. 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
  828. 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
  829. 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
  830. 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
  831. 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
  832. 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
  833. 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
  834. 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
  835. 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
  836. 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
  837. 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
  838. 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
  839. 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
  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. 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
  843. 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
  844. 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
  845. 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
  846. 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
  847. 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
  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. 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
  856. 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
  857. 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
  858. 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
  859. 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
  860. 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
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    Маскирующие свойства структур на основе триакриламидного производного полифторхалкона при жидкостном и реактивном ионном травлении
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    Результаты исследований золотых изделий из погребений Хунну Ноин-Ула (Монголия)
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    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)
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    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
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    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
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    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
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    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
  874. 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
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    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
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    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
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    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
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    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
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    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. 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
  883. 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
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    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
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    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
  886. 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
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    European Journal of Medicinal Chemistry, 2019, V. 161, Pages 581-593 doi:10.1016/j.ejmech.2018.10.055, IF=4.833
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    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
  888. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
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    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
  889. 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
  890. 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
  891. 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
  892. 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
  893. 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
  894. 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
  895. 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
  896. 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
  897. 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
  898. 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
  899. 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
  900. 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
  901. 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
  902. 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)
  903. 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)
  904. 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)
  905. 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)
  906. 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)
  907. 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)
  908. 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
  909. 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
  910. 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
  911. 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
  912. 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
  913. 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
  914. 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
  915. 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
  916. 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
  917. 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
  918. 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.