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Personal publicalions (DB NIOCh)
2021
Reviews, articles
- A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - A.S. Sokolova, K.S. Kovaleva, O.I. Yarovaya, N.I. Bormotov, L.N. Shishkina, O.A. Serova, A.A. Sergeev, A.P. Agafonov, R.A. Maksuytov, N.F. Salakhutdinov
(+)‐Camphor and (−)‐borneol derivatives as potential anti‐orthopoxvirus agents
ArchPharm, Online Version of Record before inclusion in an issue, e2100038 doi:10.1002/ardp.202100038, IF=2 - S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309 - S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309 - S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309 - S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309 - S.S. Borisevich, M.A. Gureev, О.I. Yarovaya, V.V. Zarubaev, G.A. Kostin, Yu.B. Porozov, N.F. Salakhutdinov
Can molecular dynamics explain decreased pathogenicity in mutant camphecene-resistant influenza virus?
Journal of Biomolecular Structure and Dynamics, Published Online: 22 Jan 2021 doi:10.1080/07391102.2020.1871414, IF=3.309 - N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81 - N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81 - N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81 - N.B. Asanbaeva, D.A. Rychkov, P.Yu. Tyapkin, S.G. Arkhipov, N.F. Uvarov
The unique structure of [(C4H9)4N]3[Pb(NO3)5]—one step forward in understanding transport properties in tetra-n-butylammonium-based solid electrolytes
Structural Chemistry, Published online 28 January 2021 doi:10.1007/s11224-021-01732-y, IF=2.81 - M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256 - M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256 - M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256 - M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256 - M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - V.А. Proshchenkova, V.Yu. Shuvalov, L.V. Glyzdinskaya, A.S. Fisyuk, S.A. Chernenko, M.V. Khvostov, T.G. Tolstikova, M.А. Vorontsova, G.P. Sagitullina
Synthesis of 4-Ethoxycarbonyl(cyano)-β-Carbolines via Thermolysis of 4-Aryl-3(5)-Azidopyridine Derivatives and the Study of their Optical and Hypoglycemic Properties
Chemistry of Heterocyclic Compounds (2021) Published: 03 March 2021 doi:10.1007/s10593-021-02892-9, IF=1.492 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
European Journal of Organic Chemistry, First published: 06 April 2021 doi:10.1002/ejoc.202100293, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - E. Tretyakov, K. Lomanovich, E. Bagryanskaya, G. Romanenko, A. Bogomyakov, E. Zueva, M. Petrova, A. Dmitriev, N. Gritsan
2‐(8‐Iodonaphthalen‐1‐yl)‐substituted Nitronyl Nitroxide: Suppressed Reactivity of Iodine Atom and Unusual Temperature Dynamics of the EPR Spectrum
European Journal of Organic Chemistry, First published: 10 March 2021 doi:10.1002/ejoc.202100138, IF=2.889 - Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Available online 8 April 2021, 104901, In Press doi:10.1016/j.bioorg.2021.104901, IF=4.567 - Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Available online 8 April 2021, 104901, In Press doi:10.1016/j.bioorg.2021.104901, IF=4.567 - Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Available online 8 April 2021, 104901, In Press doi:10.1016/j.bioorg.2021.104901, IF=4.567 - Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Available online 8 April 2021, 104901, In Press doi:10.1016/j.bioorg.2021.104901, IF=4.567 - Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
Bioorganic Chemistry, Available online 8 April 2021, 104901, In Press doi:10.1016/j.bioorg.2021.104901, IF=4.567 - A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.209 - A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.209 - A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.209 - A.D. Rogachev, V.P. Putilova, A.V. Zaykovskaya, O.I. Yarovaya, A.S. Sokolova, V.V. Fomenko, O.V. Pyankov, R.A. Maksyutov, A.G. Pokrovsky, N.F. Salakhutdinov
Biostability study, quantitation method and preliminary pharmacokinetics of a new antifilovirus agent based on borneol and 3-(piperidin-1-yl)propanoic acid
Journal of Pharmaceutical and Biomedical Analysis, 2021, V. 199, 114062 doi:10.1016/j.jpba.2021.114062, IF=3.209 - A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.006 - A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.006 - A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.006 - A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.006 - A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, O.V. Ardashov, J. Wärna, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Catalytic synthesis of terpenoid-derived hexahydro-2H-chromenes with analgesic activity over halloysite nanotubes
Applied Catalysis A: General, 2021, V. 618, 118144 doi:10.1016/j.apcata.2021.118144, IF=5.006 - M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=2.519 - M.A. Matsko, N.V. Semikolenova, V.A. Zakharov, I.E. Soshnikov, I.K. Shundrina, Wen-Hua. Sun
Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=2.519 - 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
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Formation of branched polyethylenes by ethylene homopolymerization using LNiBr2 homo- and heterogeneous precatalysts: Interpretation of the polymer structures in comparison with commercial LLDPE
Journal of Applied Polymer Science, 2021, V.138, N 20, 50436 doi:10.1002/app.50436, IF=2.519 - 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
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New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
Bioorganic & Medicinal Chemistry Letters, V. 40, 15 May 2021, 127926 doi:10.1016/j.bmcl.2021.127926, IF=2.572 - O.I. Yarovaya, K.S. Kovaleva, A.A. Zaykovskaya, L.N. Yashina, N.S. Scherbakova, D.N. Scherbakov, S.S. Borisevich, F.I. Zubkov, A.S. Antonova, R.Yu. Peshkov, I.V. Eltsov, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (-)-fenchone hydrazones
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Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - A.S. Sokolova, V.P. Putilova, O.I. Yarovaya, A.V. Zybkina, E.D. Mordvinova, A.V. Zaykovskaya, D.N. Shcherbakov, Ia.R. Orshanskaya, E.O. Sinegubova, Ia.L. Esaulkova, S.S. Borisevich, N.I. Bormotov, L.N. Shishkina, V.V. Zarubaev, O.V. Pyankov, R.A. Maksyutov, N.F. Salakhutdinov
Synthesis and Antiviral Activity of Camphene Derivatives against Different Types of Viruses
Molecules 2021, 26(8), 2235 doi:10.3390/molecules26082235, IF=3.267 - M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=3.83 - M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=3.83 - M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=3.83 - M.V. Khvostov, M.S. Borisova, N.V. Bulina, S.V. Makarova, N.B. Dumchenko, T.G. Tolstikova, N.Z. Lyakhov
The influence of zinc and silicate ions on biological properties of hydroxyapatite synthesized by a mechanochemical method
Ceramics International, 2021, V. 47, N 7, Part A, Pp 9495-9503 doi:10.1016/j.ceramint.2020.12.083, IF=3.83 - И.Е. Смирнова, Ю.В. Гатилов, И.Ю. Багрянская
Синтез и молекулярная структура гидрокси- и оксимино-производных холлонгдиона
Журнал органической химии. 2021. Т. 57. № 4. С. 592-596. DOI: 10.31857/S0514749221040169 doi:10.31857/S0514749221040169, IF=0.624 - E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=3.266 - E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=3.266 - E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=3.266 - E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=3.266 - E.D. Gladkova,A. A. Chepanova,E. S. Ilina,A. L. Zakharenko,J. Reynisson,O. A. Luzina,K. P. Volcho,O. I. Lavrik, N. F. Salakhutdinov
Discovery of Novel Sultone Fused Berberine Derivatives as Promising Tdp1 Inhibitors
Molecules 2021, 26(7), 1945 doi:10.3390/molecules26071945, IF=3.266 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - V.S. Glukhacheva, S.G. Il’yasov, I.V. Kazantsev, E.O. Shestakova, D.S. Il’yasov, I.V. Eltsov, A.A. Nefedov, Yu.V. Gatilov
New Reaction Products of Acetylacetone with Semicarbazide Derivatives
ACS Omega 2021, 6, 12, 8637-8645 doi:10.1021/acsomega.1c00518, IF=2.869 - E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
Bistricyclic aromatic enes annelated with nopinane fragment
Tetrahedron, V.83, 12 March 2021, 131979 doi:10.1016/j.tet.2021.131979, IF=2.233 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - Wei. Wei,V. I. Evseenko,M. V. Khvostov,S. A. Borisov,T. G. Tolstikova,N. E. Polyakov,A.V. Dushkin,Wenhao. Xu,Lu. Min ,Weike. Su
Solubility, Permeability, Anti-Inflammatory Action and In Vivo Pharmacokinetic Properties of Several Mechanochemically Obtained Pharmaceutical Solid Dispersions of Nimesulide
Molecules 2021, 26(6), 1513 doi:10.3390/molecules26061513, IF=3.267 - E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=3.137 - E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=3.137 - E. Shaydakov, V. Sannikov, V. Emelynenko, T. Tolstikova
First Experience of Using Russian Sulfacrylate Glue Clinical and Morphologic Study (In Vivo)
Journal of Vascular Surgery: Venous and Lymphatic Disorders, 2021, V. 9, N 2, Page 537 doi:10.1016/j.jvsv.2020.12.007, IF=3.137 - 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 - 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 - 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 - 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 - А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
Строение и стереохимия гидразонпроизводного гармина
Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 doi:10.26902/JSC_id69943, IF=0.745 - А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
Строение и стереохимия гидразонпроизводного гармина
Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 doi:10.26902/JSC_id69943, IF=0.745 - А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
Строение и стереохимия гидразонпроизводного гармина
Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 doi:10.26902/JSC_id69943, IF=0.745 - А. Аманжан, П.Ж. Жанымханова, И.Ю. Багрянская, Э.Э. Шульц, А.Ж. Турмухамбетов, С.М. Адекенов
Строение и стереохимия гидразонпроизводного гармина
Журнал структурной химии. 2021. Т. 62. № 3. С. 521-525. DOI: 10.26902/JSC_id69943 doi:10.26902/JSC_id69943, IF=0.745 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - A.D. Rogachev, N.A. Alemasov, V.A. Ivanisenko, N.V. Ivanisenko, E.V. Gaisler, O.S. Oleshko, S.V. Cheresiz, S.V. Mishinov, V.V. Stupak, A.G. Pokrovsky
Correlation of Metabolic Profiles of Plasma and Cerebrospinal Fluid of High-Grade Glioma Patients
Metabolites 2021, 11(3), 133 doi:10.3390/metabo11030133, IF=4.097 - I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.288 - I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.288 - I.V. Kulakov, A.L. Stalinskaya, S.Y. Chikunova, Yu.V. Gatilov
Synthesis of new representatives of 11,12-dihydro-5H-5,11-epoxybenzo[7,8]oxocino[4,3-b]pyridines – structural analogues of integrastatins A, B†
New J. Chem., 2021, V. 45, N 7, Pp 3559-3569 doi:10.1039/D0NJ06117D, IF=3.288 - A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=3.267 - A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=3.267 - A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=3.267 - О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// ) - О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// ) - О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// ) - О.А. Гурова, М.П. Сартаков, И.В. Ананьина, Д.И. Цветцых, Ю.М. Дерябина
Элементный состав бурого угля, битумов и гуминовых кислот оторьинского месторождения ХМАО-ЮГРЫ
Инновации и инвестиции. 2021. № 2. С. 107-109. ( ELEMENTAL COMPOSITION OF BROWN COAL, BITUMEN AND HUMIC ACIDS MOTORISCHE FIELD KHMAO-YUGRY/ GUROVA O.A., SARTAKOV M.P., ANANYINA I.V., COLORED D.I., DERYABINA YU.M// ) - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - Дырхеева Н.С., Захаренко А.Л., Новоселова Е.С., Чепанова А.А., Попова Н.А., Николин В.П., Лузина О.А., Салахутдинов Н.Ф., Рябчикова Е.И., Лаврик О.И.
Противоопухолевая активность комбинации топотекана и ингибитора тирозил-днк-фосфодиэстеразы 1 на модели асцитной карциномы кребс-2 мыши
Молекулярная биология. 2021. Т. 55. № 2. С. 312-317. doi:10.31857/S0026898421020051, IF=1.23 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857 - B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857 - B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Л.М. Горностаев, Д.С. Руденко, Т.А. Руковец, О.И. Фоминых, Ю.Г. Ромашкова, Ю.В. Гатилов, В.Н. Сильников
Реакции (4e)-3-ариламино-4-(гидроксиимино)нафталин-1(4h)-онов и (4e)-2-[ариламино(алкиламино)]-4-(гидроксиимино)нафталин-1(4h)-онов с 2,2-дигидрокси-1,3-индандионом
Журнал органической химии. 2021. Т. 57. № 2. С. 194-200. doi:10.31857/S0514749221020051, IF=0.624 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.288 - A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
Org. Biomol. Chem., 2021, V. 19, N 4, Pp 866-872 doi:10.1039/D0OB01893G, IF=3.411 - 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 - 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 - 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 - 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 - 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 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - V.V. Chernyshov, O.I. Yarovaya, S.Z. Vatsadze, S.S. Borisevich, S.N. Trukhan, Yu.V. Gatilov, R.Yu. Peshkov, I.V. Eltsov, O.N. Martyanov, N.F. Salakhutdinov
Unexpected ring opening during the imination of camphor-type bicyclic ketones
European Journal of Organic Chemistry, 2021, V. 2021, N 3, Pp 452-463 doi:10.1002/ejoc.202001397, IF=2.888 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.92 - T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.92 - T.Yu. Dranova, A.Yu. Vorobev, E.V. Pisarev, A.E. Moskalensky
Diaminorhodamine and Light-Activatable NO Donors: Photorelease Quantification and Potential Pitfalls
Journal of Fluorescence, 2021, V. 31, Pp.11-16 doi:10.1007/s10895-020-02643-7, IF=2.92 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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
- S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - S.V. Valiulin, A.A. Onischuk, S.N. Dubtsov, A.M. Baklanov, S.V. An’kov, M.E. Plokhotnichenko, T.G. Tolstikova, G.G. Dultseva, V.L. Rusinov, V.N. Charushin, V.M. Fomin
Aerosol inhalation delivery of triazavirin in mice: outlooks for advanced therapy against novel viral infections
Journal of Pharmaceutical Sciences, 2021б V. 110, N 3, Pp 1316-1322 doi:10.1016/j.xphs.2020.11.016, IF=2.996 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958 - N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958 - N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958 - N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958 - N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958 - L. Politanskaya, E. Tretyakov, Chanjuan. Xi
Synthesis of polyfluorinated 4-hydroxyquinolin-2(1H)-ones based on the cyclization of 2-alkynylanilines with carbon dioxide
Journal of Fluorine Chemistry, Available online 31 December 2020, 109720 doi:10.1016/j.jfluchem.2020.109720, IF=2.322 - Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
Биохимия. 2020. Т. 85. № 12. С. 1928-1938. DOI: 10.31857/S0320972520120155 (Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1/ D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova// Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159), IF=1.978 - Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
Биохимия. 2020. Т. 85. № 12. С. 1928-1938. DOI: 10.31857/S0320972520120155 (Autophagy as a Target for the Retinoprotective Effects of the Mitochondria-Targeted Antioxidant SkQ1/ D.V. Telegina, O.S. Kozhevnikova, A.Zh. Fursova, N.G. Kolosova// Biochemistry (Moscow), 2020, V. 85, N 12-13, Pp.1640-1649 doi:10.1134/S0006297920120159), IF=1.978 - Д.В. Телегина, О.С. Кожевникова, А.Ж. Фурсова, Н.Г. Колосова
Аутофагия как мишень ретинопротекторного действия митохондриального антиоксиданта SkQ1
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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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Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426 - N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
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Polymers 2020, 12(12), 3046 doi:10.3390/polym12123046, IF=3.426 - N.A. Chumakova, E.N. Golubeva, S.V. Kuzin, T.A. Ivanova, I.A. Grigoriev, S.V. Kostjuk, M.Ya. Melnikov
New Insight into the Mechanism of Drug Release from Poly(d,l-lactide) Film by Electron Paramagnetic Resonance
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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 - 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 - 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
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Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
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Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
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Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
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Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
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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 - 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
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Cyano Enone-Bearing Triterpenoid Soloxolone Methyl Inhibits Epithelial-Mesenchymal Transition of Human Lung Adenocarcinoma Cells in Vitro and Metastasis of Murine Melanoma in Vivo
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A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
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A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
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A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
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Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173 - 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 - 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
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A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
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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 - 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 - 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 - 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
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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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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
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
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Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
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Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(21), 7876 doi:10.3390/ijms21217876, IF=4.556 - A.V. Markov, A.V. Sen'kova, V.O. Babich, K.V. Odarenko, V.A. Talyshev, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
Dual Effect of Soloxolone Methyl on LPS-Induced Inflammation In Vitro and In Vivo
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Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
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Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
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Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
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Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
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Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
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Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A - T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
RSC Med. Chem., 2020,11, 1314-1325 doi:10.1039/C9MD00516A - T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
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NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
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Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
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Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745 - Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745 - Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745 - В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
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Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745 - В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745 - В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745 - В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
Журнал структурной химии. 2020. Т. 61. № 11. С. 1895-1905. doi:10.26902/JSC_id63266 (Structure and luminescent properties of coordination polymers containing lead(II) and thiophene ligands/ V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, V. A. Samsonov, A. A. Ryadun, D. N. Dybtsev & V. P. Fedin// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1800-1809 doi:10.1134/S002247662011013X), IF=0.745 - В.А. Дубских, А.А. Лысова, Д.Г. Самсоненко, В.А. Самсонов, А.А. Рядун, Д.Н. Дыбцев, В.П. Федин
Строение и люминесцентные свойства координационных полимеров, содержащих свинец(II) и тиофеновые лиганды
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Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
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Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
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Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
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Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
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Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
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Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
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Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
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Различия в жирнокислотных профилях мембран эритроцитов, связанные с локализацией опухоли при колоректальном раке (пилотное исследование)
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Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.Ф. Осипенко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Озможности использования жирных кислот мембран эритроцитов и сыворотки крови для диагностики болезни крона
Экспериментальная и клиническая гастроэнтерология. 2020. № 10 (182). С. 46-55. doi:10.31146/1682-8658-ecg-182-10-46-55 - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - T. Schulte, B. M. Sala, J. Nilvebrant, P.-Å. Nygren, A. Achour, A. Shernyukov, T. Agback, P. Agback
Assigned NMR backbone resonances of the ligand-binding region domain of the pneumococcal serine-rich repeat protein (PsrP-BR) reveal a rigid monomer in solution
Biomolecular NMR Assignments, 2020, V.14, N 2, Pp 195-200 doi:10.1007/s12104-020-09944-9, IF=0.677 - S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948 - S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948 - S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948 - S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948 - S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948 - S.A. Popov, M. D. Semenova, D. S. Baev, T. S. Frolova, E. E.Shults,Ch.Wang, M.Turks
Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
Steroids, 2020, V. 153, 108524 doi:10.1016/j.steroids.2019.108524, IF=1.948 - S.A. Popov, M. D. Semenova, D. S. Baev, T. S. Frolova, E. E.Shults,Ch.Wang, M.Turks
Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
Steroids, 2020, V. 153, 108524 doi:10.1016/j.steroids.2019.108524, IF=1.948 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
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Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
Application of EPR to porphyrin-protein agents for photodynamic therapy
Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383 - Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
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Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716 - Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716 - Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716 - Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716 - Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
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Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi: 10.31857/S0044460X20100054 (Synthesis, Molecular, and Crystal Structure of Tris(2-carbamoylmethoxyphenyl)phosphine Oxide/ T. V. Baulina, I. Yu. Kudryavtsev, A. V. Artem’ev, I. Yu. Bagryanskaya, M. P. Pasechnik, V. K. Brel// Russian Journal of General Chemistry, 2020, V. 90, N 10, Pp 1840-1844 doi:10.1134/S1070363220100059), IF=0.716 - A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613 - A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613 - А. Макубаева, Е.П. Романенко, С.М. Адекенов, А.В. Ткачев
Компонентный состав и биологическая активность эфирного масла ligularia heterophylla rupr.
Химия растительного сырья. 2020. № 3. С. 239-244. (COMPONENT COMPOSITION AND BIOLOGICAL ACTIVITY OF ESSENTIAL OIL OF LIGULARIA HETEROPHYLLA RUPR./ MAKUBAYEVA AIGERIM, ROMANENKO ELENA PETROVNA, ADEKENOV SERGAZY MYNZHASAROVICH, TKACHEV ALEKSEY VASIL'YEVICH// doi:10.14258/jcprm.2020038243) - А. Макубаева, Е.П. Романенко, С.М. Адекенов, А.В. Ткачев
Компонентный состав и биологическая активность эфирного масла ligularia heterophylla rupr.
Химия растительного сырья. 2020. № 3. С. 239-244. (COMPONENT COMPOSITION AND BIOLOGICAL ACTIVITY OF ESSENTIAL OIL OF LIGULARIA HETEROPHYLLA RUPR./ MAKUBAYEVA AIGERIM, ROMANENKO ELENA PETROVNA, ADEKENOV SERGAZY MYNZHASAROVICH, TKACHEV ALEKSEY VASIL'YEVICH// doi:10.14258/jcprm.2020038243) - Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745 - Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745 - Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745 - Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745 - Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, Е.С. Васильев, Л.А. Шелудякова, М.И. Рахманова, А.В. Ткачев
Комплекс Zn(ii) с хиральным нопинан-аннелированным 9,9-би-4,5-диазафлуоренилиденом: синтез, структура, свойства
Журнал структурной химии. 2020. Т. 61. № 10. С. 1690-1699., doi:10.26902/JSC_id61853 (A complex of Zn(II) with chiral nopinane-annelated 9,9′-bi-4,5-diazafluorenylidene: synthesis, structure, and properties/ T. E. Kokina, L. A. Glinskaya, D. A. Piryazev, E. S. Vasiliev, L. A. Sheludyakova, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry volume 61, pages1606–1614(2020) doi:10.1134/S0022476620100133), IF=0.745 - Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745 - Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745 - Н.А. Шеховцов, К.А. Виноградова, Е.Б. Николаенкова, В.П. Кривопалов, М.Б. Бушуев
Двойная эмиссия 2-амино-4-метилпиримидина: теоретическое исследование
Журнал структурной химии. 2020. Т. 61. № 10. С. 1605-1613., doi:10.26902/JSC_id61806 (Dual emission of 2-amino-4-methylpyrimidine: a theoretical study/ N. A. Shekhovtsov, K. A. Vinogradova, E. B. Nikolaenkova, V. P. Krivopalov & M. B. Bushuev// Journal of Structural Chemistry, 2020, V. 61, N/ 10, Pp 1521-1529 doi:10.1134/S0022476620100042), IF=0.745 - Н.Ф. Салахутдинов, С.С. Лаев, Д.С. Сергеевичев
Модуляторы нарушения гемопоэза (обзор)
Химия в интересах устойчивого развития. 2020. Т. 28. № 4. С. 343-365. (Modulators of hematopoiesis disorders (a review)/ Salakhutdinov N. F., Laev S. S., Sergeevichev D. S.// Chemistry for Sustainable Development, 2020, V. 28, N 4, Pp. 343-365 doi:10.15372/KhUR2020239) - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556 - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556 - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556 - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556 - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
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The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
Int. J. Mol. Sci. 2020, 21(19), 7162 doi:10.3390/ijms21197162, IF=4.556 - E.D. Gladkova, I.V. Nechepurenko, R.A. Bredikhin, A.A. Chepanova, A.L. Zakharenko, O.A. Luzina, E.S. Ilina, N.S. Dyrkheeva, E.M. Mamontova, R.O. Anarbaev, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
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The First Berberine-Based Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), an Important DNA Repair Enzyme
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Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
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The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
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The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
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The Comparative Immunotropic Activity of Carrageenan, Chitosan and Their Complexes
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Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
Catalysts 2020, 10(9), 1002 doi:10.3390/catal10091002, IF=3.519 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, I.V. Oleynik, G.A. Solan, Ya. Ma, T. Liang, Wen-Hua. Sun
Adjusting Ortho-Cycloalkyl Ring Size in a Cycloheptyl-Fused N,N,N-Iron Catalyst as Means to Control Catalytic Activity and Polyethylene Properties
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Biomass Ashes for Acid Mine Drainage Remediation
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Biomass Ashes for Acid Mine Drainage Remediation
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Biomass Ashes for Acid Mine Drainage Remediation
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A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
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A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
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A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
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A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
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Primary Radical Cations in Irradiated Poly(isobutylene)
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Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267 - S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
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Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
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J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71 - D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71 - D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71 - D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71 - D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
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Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
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Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
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Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
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Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
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Betulinic Acid-Azaprostanoid Hybrids: Synthesis and Pharmacological Evaluation as Anti-inflammatory Agents
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Betulinic Acid-Azaprostanoid Hybrids: Synthesis and Pharmacological Evaluation as Anti-inflammatory Agents
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P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
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P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
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P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
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P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
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Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762 - L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762 - L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
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Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762 - L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
Thermochimica Acta, 2020, V. 689, 178639 doi:10.1016/j.tca.2020.178639, IF=2.762 - L.N. Zelenina, K.V. Zherikova, T.P. Chusova, S.V. Trubin, R.A. Bredikhin, N.V. Gelfond, N.B. Morozova
Comprehensive thermochemical study of sublimation, melting and vaporization of scandium(III) beta-diketonates
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Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687 - И.К. Шундрина, И.В. Олейник, В.И. Пастухов, Л.А. Шундрин, В.С. Черноносова, П.П. Лактионов
Синтез полимеров уретанового типа с полидиметилсилоксановыми блоками для изготовления волокнистых матриксов методом электроформования
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Синтез полимеров уретанового типа с полидиметилсилоксановыми блоками для изготовления волокнистых матриксов методом электроформования
Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 4. С. 306-314, doi: 10.31857/S2308113920040099 (Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090), IF=0.976 - Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719 - Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719 - Е.Ю. Яковлева, Е.Е. Барановская, И.К. Шундрина, Е.Ю. Герасимов
Влияние способа синтеза высокофторированного полиимида на свойства адсорбента, приготовленного на его основе
Журнал физической химии. 2020. Т. 94. № 7. С. 1099-1104. DOI: 10.31857/S0044453720070328 (Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328), IF=0.719 - A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
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Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
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Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - О.Ю. Мазурков, Л.Н. Шишкина, Н.И. Бормотов, М.О. Скарнович, О.А. Серова, Н.А. Мазуркова, А.А. Черноносов, А.Я. Тихонов, Б.А. Селиванов
Оценка абсолютной биодоступности химической субстанции противооспенного препарата НИОХ-14 в экспериментах на мышах
Бюллетень экспериментальной биологии и медицины. 2020. Т. 170. № 8. С. 173-177. (Estimation of absolute bioavailability of the chemical substance of the anti-smallpox preparation NIOCH-14 in experiments with mice/ MAZURKOV O. YU.1, SHISHKINA L. N.1, BORMOTOV N. I.1, SKARNOVICH M. O.1, SEROVA O. A.1, MAZURKOVA N. A.1, CHERNONOSOV A. A.2, TIKHONOV A. YA.3, SELIVANOV B. A.3// Bulletin of Experimental Biology and Medicine, 2020, V. 170, N 2, Pp 207-210 doi:10.1007/s10517-020-05034-x), IF=0.774 - A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
A new Сu(i) iodide complex showing deep-red luminescence
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A new Сu(i) iodide complex showing deep-red luminescence
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A new Сu(i) iodide complex showing deep-red luminescence
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A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745 - A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745 - A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745 - В.Н. Ковтонюк, Х. Хань, Ю.В. Гатилов
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Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174 - T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174 - T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174 - T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174 - T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174 - P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
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Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267 - P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
Synthesis of Nitroxide Diradical Using a New Approach
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Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267 - N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267 - N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267 - N. Sannikova, I. Timofeev, E. Bagryanskaya, M. Bowman, M. Fedin, O. Krumkacheva
Electron Spin Relaxation of Photoexcited Porphyrin in Water-Glycerol Glass
Molecules 2020, 25(11), 2677 doi:10.3390/molecules25112677, IF=3.267 - A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
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Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
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Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
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Новые подходы к повышению эффективности нестероидных противовоспалительных средств с использованием наноразмерных систем доставки
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Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
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Optical uncaging of adp reveals the early calcium dynamics in single, freely moving platelets
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Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
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Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183 - E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183 - E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183 - E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183 - E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
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Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567 - S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567 - S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567 - S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567 - S.O. Kuranov, O.A. Luzina, O. Onopchenko, I. Pishel, S. Zozulya, M. Gureev, N.F. Salakhutdinov, M. Krasavin
Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40)
Bioorganic Chemistry Volume 99, June 2020, 103830 doi:10.1016/j.bioorg.2020.103830, IF=4.567 - Полосьмак Н.В., Карпова Е.В., Амосов Е.В.
Уникальная ткань с городища Джеты-Асар-2 (Восточное Приаралье) в контексте центрально-азиатской текстильной традиции
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Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
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Особенности липидомического профиля мембран эритроцитов и сыворотки крови у пациентов с жировой болезнью печени
Атеросклероз. 2020. Т. 16. № 2. С. 16-33. doi:10.15372/ATER20200202 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
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The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
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The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - I.А. Novakov, L.L. Brunilina, I.А. Kirillov, M.B. Nawrozkij, M.D. Robinovich, E.S. Titova, D.S. Sheikin, E.А. Ruchko, A.V. Pavlova, A.А. Kotlyarova, T.G. Tolstikova
The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 6, Pp 769-775 doi:10.1007/s10593-020-02729-x, IF=1.519 - V.V. Chernyshov, O.I. Yarovaya, R.Yu. Peshkov, N.F. Salakhutdinov
Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity
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Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - А.А. Бажина, С.В. Валиулин, А М. Бакланов, С.Н. Дубцов, С.В. Аньков, М.Е. Плохотниченко, Т.Г. Толстикова, А.А. Онищук
Метод генерации аэрозоля антибактериального лекарственного вещества цефазолина
Оптика атмосферы и океана. 2020. Т. 33. № 6 (377). С. 459-462 doi:10.15372/AOO20200607. (A Method for Generating an Aerosol of the Antibacterial Medicine Cefazolin/ A. A. Bazhina, S. V. Valiulin, A. M. Baklanov, S. N. Dubtsov, S. V. An’kov, M. E. Plokhotnichenko, T. G. Tolstikova, A. A. Onischuk// Atmospheric and Oceanic Optics, 2020, V. 33, N 6, Pp 555-558 doi:10.1134/S1024856020050048) - M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745 - M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745 - M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745 - M.P. Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, A.V. Artem'ev
A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties
Журнал структурной химии, 2020, Т. 61, N 6, Сс. 947-951 DOI: 10.26902/JSC_id57701 (A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086), IF=0.745 - M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694 - M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694 - M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694 - L. A.Shundrin,I.A.Os'kina,I. G.Irtegova,A. F.Poveshchenko
9H-Thioxanthen-9-one S,S-dioxide based redox active labels for electrochemical detection of DNA duplexes immobilized on Au electrodes
Mendeleev Communications, 2020, V. 30, N 3, Pp 296-298 doi:10.1016/j.mencom.2020.05.011, IF=1.694 - N.Yu. Adonin, V.V. Bardin
Polyfluorinated arylboranes as catalysts in organic synthesis
Mendeleev Communications, 2020, V. 30, N 3, Pp 262-272 doi:10.1016/j.mencom.2020.05.002, IF=1.694 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267 - A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267 - A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267 - A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267 - A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267 - A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556 - A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556 - A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556 - A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556 - A.V. Markov, A.V. Sen'kova, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.I. Komarova, A.A. Ilyina, N.F. Salakhutdinov, M.A. Zenkova
Novel 3'-Substituted-1'2',4'-Oxadiazole Derivatives of 18βH-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
Int. J. Mol. Sci. 2020, 21(10), 3511 doi:10.3390/ijms21103511, IF=4.556 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
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Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
ChemCatChem, 2020, V. 12, N. 9, Pp 2605- 2609 doi:10.1002/cctc.202000070, IF=4.853 - A. Sidorenko, N. Li-Zhulanov, P. Mäki-Arvela, T. Sandberg, A. Kravtsova, A. Peixoto, C. Freire, K. Volcho, N. Salakhutdinov, V. Agabekov, D. Murzin
Stereoselectivity inversion by water addition in the -SO3H catalyzed tandem Prins-Ritter reaction for synthesis of 4-amidotetrahydropyran derivatives
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Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216) - А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216) - А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216) - А.П. Крысин, В.А. Солошенко, Ю.Г. Юшков, Н.А. Донченко, О.Г. Мерзлякова
Снижение смертности на всех этапах жизни животных и получение продуктивного долголетия с использованием аурола (п-тирозола)
Химия в интересах устойчивого развития. 2020. Т. 28. № 2. С. 171-179. doi:10.15372/KhUR2020216 (Reduction in Mortality at All Stages of Animal Life and the Ways to Achieve Productive Longevity Using Aurol (p-Tyrosol)/ KRYSIN A. P., SOLOSHENKO V. A. YUSHKOV YU. G.2, DONSHENKO N. A., MERZLYAKOVA O. G.// Chemistry for Sustainable Development, 2020, V. 28, N 2, Pp 166-173 doi:10.15372/CSD2020216) - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - M. Han, Q. Zhang, I.I. Oleynik, H. Suo, G.A. Solan, I.V. Oleynik, Ya. Ma, T. Liang, Wen-Hua. Sun
High molecular weight polyethylenes of narrow dispersity promoted using bis(arylimino)cyclohepta[b]pyridine-cobalt catalysts ortho-substituted with benzhydryl & cycloalkyl groups
Dalton Trans., 2020, V. 49, N 15, Pp 4774-4784 doi:10.1039/d0dt00576b, IF=4.174 - A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758 - A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758 - D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
Biophotonics approach for the study of leukocyte activation
Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325 - D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
Biophotonics approach for the study of leukocyte activation
Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325 - D.N. Chernova, S.G. Sokolovski, A.Y. Vorobev, A.E. Moskalensky
Biophotonics approach for the study of leukocyte activation
Proceedings of SPIEE, 2020, V. 11457, Saratov Fall Meeting 2019: Optical and Nano-Technologies for Biology and Medicine; 114570G doi:10.1117/12.2560325 - S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267 - S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267 - S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267 - S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267 - S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267 - A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426 - A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426 - A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426 - A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426 - A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426 - Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174 - Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174 - Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174 - Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174 - D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889 - D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889 - D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889 - D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889 - D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632 - D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
Study of calcium signaling dynamics in single platelets using optical activation methods.
Proceedings of SPIE, 2020, V. 11359, #113590U doi:10.1117/12.2559414 - D.V. Spiryova, A.Y. Vorob'ev, A.E. Moskalensky
Study of calcium signaling dynamics in single platelets using optical activation methods.
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Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
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Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
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Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
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Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
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Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
Reaction Kinetics, Mechanisms and Catalysis, 2020, V. 129, N 2, Pp 627-644 doi:10.1007/s11144-020-01740-9, IF=1.52 - M. Laluc, P. Maki-Arvela, A.F. Peixoto, N. Li-Zhulanov, T. Sandberg, N.F. Salakhutdinov, K. Volcho, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Catalytic synthesis of bioactive 2H-chromene alcohols from (-)-isopulegol and acetone on sulfonated clays
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Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744 - E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
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Room temperature synthesis of fluorinated graphite intercalation compounds with low fluorine loading of host matrix
Journal of Fluorine Chemistry, 2020, V. 232, 109482 doi:10.1016/j.jfluchem.2020.109482, IF=2.332 - G.N. Chekhova, D.V. Pinakov, Yu.V. Shubin, V.P. Fadeeva, V.D. Tikhova, A.V. Okotrub, L.G. Bulusheva
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Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
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Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
(Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267 - E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
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Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6 - E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6 - E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
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Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6 - E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6 - E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6 - E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
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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 - 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 - 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 - E.F. Khusnutdinova, A.V. Petrova, A.N. Lobov, O.S. Kukovinets, D.S. Baev, O.B. Kazakova
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A search for synthetic routes to tetrabenzylglycoluril
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Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
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Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857 - V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857 - V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
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Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
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Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - N.N. Fishman, N.N. Lukzen, K.L. Ivanov, M.V. Edeleva, S.V. Fokin, G.V. Romanenko, V.I. Ovcharenko
Multifrequency NMR as an Efficient Tool to Investigate Heterospin Complexes in Solutions
The Journal of Physical Chemistry A, 2020, 124, 7, 1343-1352 doi:10.1021/acs.jpca.9b11104, IF=2.6 - I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
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Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
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ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758 - A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
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Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
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Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
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Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
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Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
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Study of Sirolimus Adsorption and Preparation of Its Samples in Methanol, Acetonitrile and Their Mixtures with Water for HPLC-MS/MS Analysis
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Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
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Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061 - Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061 - Д.А. Рудаков, А.М. Генаев, Ю.В. Гатилов, Е.А. Дикусар, Т.Д. Зверева, З.П. Зубрейчук, В.И. Поткин
Синтез и структура 9-гидрокси-1,2-дикарба-клозо-додекаборана(11)
Известия Академии наук. Серия химическая. 2020. № 2. С. 320-324. (Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1), IF=1.061 - A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38 - A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38 - A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
Minerals 2020, 10(2), 88 (This article belongs to the Special Issue Genesis of Hydrocarbons in the Upper Mantle) doi:10.3390/min10020088, IF=2.38 - A. Sokol, A. Tomilenko, I. Sokol, P. Zaikin, T. Bul'bak
Formation of Hydrocarbons in the Presence of Native Iron under Upper Mantle Conditions: Experimental Constraints
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Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996 - N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
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Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996 - N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
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Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996 - N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
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Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
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Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
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Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - Н.Е. Костина, А.В. Спасельникова, А.А. Егорова, Е.В. Колосовская, Д.В. Домрачев, А.В. Романова, С.Р. Туманян, С. Хамас, Й. Кумлен, И.М. Дубовский, С.В. Герасимова
Создание линии табака со сниженными анти-фидантными свойствами по отношению к колорадскому жуку
Биотехнология и селекция растений. 2020. Т. 3. № 1. С. 24-30. doi:10.30901/2658-6266-2020-l-o5 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753 - A.Yu. Vorobev, A.E. Moskalensky
Long-wavelength photoremovable protecting groups: On the way to in vivo application
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Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - Y.I. Ragino, V.S. Shramko, E.M. Stakhneva, E.I. Chernyak, S.V. Morozov, E.V. Shakhtshneider, Y.V. Polonskaya, L.V. Shcherbakova, A.M. Chernyavskiy
Changes in the blood fatty-acid profile associated with oxidative-antioxidant disturbances in coronary atherosclerosis
Journal of Medical Biochemistry, 2020, V. 39, N 1, Pp 46-53 doi:10.2478/jomb-2019-0010, IF=1.109 - В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
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Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24) - В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24) - В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
Комплексные проблемы сердечно-сосудистых заболеваний. 2020. Т. 9. № 1. С. 15-24. (CLINICAL CHARACTERISTICS OF PATIENTS WITH CORONARY ATHEROSCLEROSIS DEPENDING ON BLOOD FATTY ACIDS/ Shramko V.S., Morozov S.V., Chernyak E.I., Shcherbakova L.V., Kurguzov A.V., Chernyavskyi A.M., Ragino Yu.I.// doi:10.17802/2306-1278-2020-9-1-15-24) - В.С. Шрамко, С.В. Морозов, Е.И. Черняк, Л.В. Щербакова, А.В. Кургузов, А.М. Чернявский, Ю.И. Рагино
Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
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Клинические характеристики пациентов с атеросклерозом коронарных артерий в зависимости от жирно-кислотного спектра крови
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Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174 - J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174 - J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174 - J. Guo, W. Zhang, I. I. Oleynik, G. A. Solan, I.V. Oleynik, T. Liang.Wen-Hua Sun
Probing the effect of ortho-cycloalkyl ring size on activity and thermostability in cycloheptyl-fused N,N,N-iron ethylene polymerization catalysts
Dalton Trans., 2020, V. 49, N 1, Pp 136-146 doi:10.1039/C9DT04325J, IF=4.174 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
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Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
Bioorganic & Medicinal Chemistry, 2020, V. 28, N 1, 115234 doi:10.1016/j.bmc.2019.115234, IF=3.073 - E.M. Mamontova, A.L. Zakharenko, O.D. Zakharova, N.S. Dyrkheeva, K.P. Volcho, J. Reynisson, H.J. Arabshahi, N.F. Salakhutdinov, O.I. Lavrik
Identification of novel inhibitors for the tyrosyl-DNA-phosphodiesterase 1 (Tdp1) mutant SCAN1 using virtual screening
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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 - 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 - 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 - С.А. Низомов, И.В. Сорокина, Н.А. Жукова, С.А. Борисов, Т.Г. Толстикова, Д.Е. Семенов, М.А. Бакарев
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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 - Т.П. Кукина, Д.Н. Щербаков, Н.В. Пантелеева, О.И. Сальникова, П.В. Колосов
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Качественный и количественный состав продукта дистилляции алифатических кислот подсолнечного масла
Химия растительного сырья. 2020. № 1. С. 199-206. (QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909) - 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
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Ионные жидкости с фторсодержащими анионами как новый класс функциональных материалов: особенности синтеза, физико-химических свойств и примеры использования
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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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - D. Spiryova, A. Vorob'ev, A.E. Moskalensky
Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621 - D. Spiryova, A. Vorob'ev, A.E. Moskalensky
Dual-agonist Optical Stimulation of Platelets Results in Increased and Reliable Activation
Proceedings - 2020 Cognitive Sciences, Genomics and Bioinformatics, CSGB 2020, pp 106-109 doi:10.1109/CSGB51356.2020.9214621
2019
Reviews, articles
- 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - S.V. Nikitin, J. Sanchez-Marquez, I.I. Oleynik, I. Oleynik, E.G. Bagryanskaya
A screening DFT study of the para-substituent effect on local hyper-softness in bis(phenoxy-imine) titanium complexes to get insights about their catalytic activity in ethylene polymerization
Molecular Catalysis, 2019, V. 469, Pp 57-67 doi:10.1016/j.mcat.2019.02.024, IF=2.938 - V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923 - V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923 - 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 - 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 - 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 - 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 - 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 - A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971 - A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971 - A.G. Maryasov, M.K. Bowman, M.V. Fedin, S.L. Veber
Theoretical Basis for Switching a Kramers Single Molecular Magnet by Circularly-Polarized Radiation
Materials 2019, 12(23), 3865 doi:10.3390/ma12233865, IF=2.971 - A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147 - V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997 - V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997 - V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997 - V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997 - V.A. Bagryansky, V.I. Borovkov, A.O. Bessmertnykh, I.S. Tretyakova, I.V. Beregovaya, Yu.N. Molin
Interaction of spin-correlated radical pair with a third radical: Combined effect of spin-exchange interaction and spin-selective reaction
Journal of Chemical Physics, , 2019, V. 151, N 22, 224308 doi:10.1063/1.5127812, IF=2.997 - E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59 - E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11 - A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723 - A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723 - A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723 - A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723 - A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723 - A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049 - A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049 - A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049 - A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049 - G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491 - G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491 - G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491 - G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491 - V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (–)-fenchone and anthranilamide
Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93 - V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
The first example of the stereoselective synthesis and crystal structure of a spirobicycloquinazolinone based on (–)-fenchone and anthranilamide
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Физическая активация процессов экстракции и органического синтеза
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Физическая активация процессов экстракции и органического синтеза
Химия в интересах устойчивого развития. 2019. Т. 27. № 6. С. 704-715. (Physical Activation of Extraction and Organic Synthesis Processes/ Pankrushina N. A., Lomovsky O. I., Shakhtshneider T. P// Chemistry for Sustainable Development, 2019, V. 27, № 6, P. 704-715. (In Russian) doi:10.15372/KhUR2019194) - A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953 - A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953 - A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953 - A. Kulikov, N. Sinyakova, E. Kulikova, T. Khomenko, N. Salakhutdinov, V. Kulikov, K. Volcho
Effects of Acute and Chronic Treatment of Novel Psychotropic Drug, 8- (Trifluoromethyl)-1, 2, 3, 4, 5-benzopentathiepin-6-amine Hydrochloride (TC-2153), on the Behavior of Zebrafish (Danio Rerio): A Comparison with Fluoxetine
Letters in Drug Design & Discovery, 2019, V.16, N 12, Pp.1321-1328 doi:10.2174/1570180816666190221162952, IF=0.953 - O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447 - O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447 - O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447 - O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447 - O.I. Yarovaya, A.S. Sokolova, I.Ya. Mainagashev, A.S. Volobueva, K. Lantseva, S.S. Borisevich, A.A. Shtro, V.V. Zarubaev, N.F. Salakhutdinov
Synthesis and structure-activity relationships of novel camphecene analogues as anti-influenza agents
Bioorganic & Medicinal Chemistry Letters, 1019, V. 29, N 23, 126745 doi:10.1016/j.bmcl.2019.126745, IF=2.447 - A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052 - A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052 - A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052 - A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052 - A.V. Artem'ev, M.P. Davydova, A.S. Berezin, V.K. Brel, V.P. Morgalyuk, I.Yu. Bagryanskaya, D.G. Samsonenko
Luminescence of the Mn2+ ion in non-Oh and Td coordination environments: the missing case of square pyramid
Dalton Trans., 2019, V. 48, N 43, Pp 16448-16456 doi:10.1039/C9DT03283E, IF=4.052 - V.I. Borovkov, L.N. Shchegoleva
Magnetic Resonance Characteristics of Negative Polarons in Neat Poly(3-hexyl-thiophene)
Journal of Physical Chemistry C, 2019, 123, 46, 28058-28065 doi:10.1021/acs.jpcc.9b08331, IF=4.309 - I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25 - I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25 - I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25 - I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25 - A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789 - A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789 - A. V.Lastovka,A. D.Rogachev,I. V.Il'ina,A.Kabir,K.P.Volcho,V. P.Fadeeva,A.G.Pokrovsky,N. F.Salakhutdinov,K. G.Furtonc
Comparison of dried matrix spots and fabric phase sorptive extraction methods for quantitation of highly potent analgesic activity agent (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol in rat whole blood and plasma using LC–MS/MS
Journal of Chromatography B, 2019, V. 1132, Art. Number 121813 doi:10.1016/j.jchromb.2019.121813, IF=2.789 - S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595 - S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
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Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025 - E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025 - E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025 - E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
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Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
UNITED EUROPEAN GASTROENTEROLOGY JOURNAL, 2019, V. 7, N S8, P. 387 (27th United European Gastroenterology Week Barselona 2019) doi:10.1177/2050640619854671, IF=3.453 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, S.A. Kurilovich, V.N. Kruchinin, V.M. Generalov, M.V. Shashkov, A.S. Sokolova, I.N. Yakovina, N.A. Bannova, G.V. Shuvalov
Electrical and viscoelastic parameters of erythrocytes in combination with the fatty acid profile of their membranes and serum as potentialbiomarkers for the diagnosis of colorectal cancer
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Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965 - S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965 - S.A. Kremis, D.S. Baev, A.V. Lipeeva, E.E. Shults, T.G. Tolstikova, O.I. Sinitsyna, A.V. Kochetov, T.S. Frolova
Genotoxic activity of 1,2,3-triazolyl modified furocoumarins and 2,3-dihydrofurocoumarins
Journal of biochemical and molecular toxicology, 2019, V. 33, N 11, e22396 doi:10.1002/jbt.22396, IF=2.965 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
Molecular Catalysis, 2019, V. 478, 110569 doi:10.1016/j.mcat.2019.110569, IF=2.937 - N. Li-Zhulanov, P. Maki-Arvela, M. Laluc, A.F. Peixoto, E. Kholkina, T. Sandberg, A. Aho, K. Volcho, N. Salakhutdinov, C. Freire, A.Yu. Sidorenko, D.Yu. Murzin
Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays
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6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
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Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - O.I. Artyushin, A.A. Moiseeva, V.V. Zarubaev, A.V. Slita, A.V. Galochkina, A.A. Muryleva, S.S. Borisevich, O.I. Yarovaya, N.F. Salakhutdinov, V.K. Brel
Synthesis of Camphecene and Cytisine Conjugates Using Click Chemistry Methodology and Study of Their Antiviral Activity
Chemistry & Biodiversity, 2019, V. 16, N 11, e1900340 doi:10.1002/cbdv.201900340, IF=1.449 - A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
Synthesis of benzo[c][1,7]naphthyridine derivatives
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Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492 - A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492 - A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492 - M.A. Bazhenov, A.V. Shernyukov, M.S. Kupryushkin, D.V. Pyshnyi
Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
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Study of the Staudinger Reaction and Reveal of Key Factors Affecting the Efficacy of Automatic Synthesis of Phosphoryl Guanidinic Oligonucleotide Analogs
Russian Journal of Bioorganic Chemistry, 2019, V. 45, N 6, Pp 699-708 doi:10.1134/S1068162019060074, IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - А.А. Чепанова, Н.С. Ли-Жуланов, А.С. Сухих,, A. Zafar, J. Reynisson, А.Л. Захаренко, О.Д. Захарова, Д.В. Корчагина, К.П. Волчо, Н.А. Салахутдинов, О.И. Лаврик
Эффективные ингибиторы тирозил-днк-фосфодиэстеразы 1 на основе монотерпеноидов как потенциальные агенты для противоопухолевой терапии
Биоорганическая химия, 2019, т. 45, №6, С. 647-655 (Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104), IF=0.794 - М.В. Хвостов, Т.Г. Толстикова, С.А. Борисов, А.В. Душкин
Применение природных полисахаридов в фармацевтике
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Липофильные компоненты мытников PEDICULARIS STRIATA PALLAS и PEDICULARIS FLAVA PALLAS
Химия растительного сырья. 2019. № 4. С. 113-118. (Lipophilic constituents of pedicularis striata pallas и pedicularis flava pallas/ Kukina, T.P., Khan, I.V.// Khimiya Rastitel'nogo Syr'ya, Issue 4, 1 January 2020, Pages 113-118 doi:10.14258/jcprm.2019044952) - П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541 - П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541 - П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541 - П.М. Васильев, О.А. Лузина, Д.А. Бабков, Д.Т. Аппазова, Н.Ф. Салахутдинов, А.А. Спасов
Исследование зависимости между структурой хемотипов некоторых природных соединений и спектром их таргетных активностей, соотносимых с гипогликемическим действием
Журнал структурной химии. 2019. Т. 60. № 11. С. 1901-1906 DOI: 10.26902/JSC_id48260. (Studying dependences between the chemotype structure of some natural compounds and the spectrum of their targeted activities correlated with the hypoglycemic effect/ P.M. Vasilyev, O.A. Luzina, D.A. Babkov, D.T. Appazova, N.F. Salakhutdinov, A.A. Spasov// J Struct Chem., 2019, V. 60, N 11, Pp 1827-1832 doi:10.1134/S0022476619110179), IF=0.541 - Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751 - Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751 - Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751 - Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751 - Л.М. Горностаев, О.И. Фоминых, Т.И. Лаврикова, Ю.Г. Халявина, Ю.В. Гатилов, Г.А. Сташина
Особенности взаимодействия 2-амино-1,4-нафтохинонов с 2,2-дигидрокси-1h-инден-1,3(2h)-дионом
Журнал органической химии. 2019. Т. 55. № 11. С. 1751-1761. (Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125), IF=0.751 - L. Politanskaya, N. Troshkova, E. Tretyakov, Ch. Xi
Synthesis of polyfluorinated bezofurans
Journal of Fluorine Chemistry, Volume 227, November 2019, 109371 doi:10.1016/j.jfluchem.2019.109371, IF=2.055 - M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65 - M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65 - M.M. Shmakov, V.V. Bardin, S.A. Prikhod'ko, N.Yu. Adonin
Preparation of heptafluoronaphthyllithiums and -magnesiums: An unexpected difference in the reactivity of isomers C10F7H and C10F7Br towards organolithium and organomagnesium compounds
Journal of Organometallic Chemistry, 2019, V. 899, 120889 doi:10.1016/j.jorganchem.2019.120889, IF=2.65 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.S. Filimonov, A.A. Chepanova, O.A. Luzina, A.L. Zakharenko, O.D. Zakharova, E.S. Ilina, N.S. Dyrkheeva, M.S. Kuprushkin, A.V. Kolotaev, D.S. Khachatryan, J. Patel, I.K. H. Leung, R. Chand, D.M. Ayine-Tora, J. Reynisson, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
New Hydrazinothiazole Derivatives of Usnic Acid as Potent Tdp1 Inhibitors
Molecules 2019, 24(20), 3711 doi:10.3390/molecules24203711, IF=3.59 - A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716 - A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716 - O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861 - O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861 - S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136 - S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136 - A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934 - A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934 - A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934 - A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934 - A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934 - M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394 - M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394 - M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394 - M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394 - M.F. Kasakin, A.D. Rogachev, E.V. Predtechenskaya, V.J. Zaigraev, V.V. Koval, A.G. Pokrovsky
Targeted metabolomics approach for identification of relapsing–remitting multiple sclerosis markers and evaluation of diagnostic models
Med. Chem. Commun., 2019, N. 10, 1803-1809 doi:10.1039/C9MD00253G, IF=2.394 - N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69 - N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69 - N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69 - N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69 - N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69 - М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907 - М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907 - М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907 - М.А. Ленский, Э.Э. Шульц, Д.В. Корабельников, А.В. Ожогин, А.Н. Новицкий
Синтез полиэфиров двухатомных фенолов и борной кислоты и их взаимодействие с формальдегидом
Высокомолекулярные соединения. Серия Б. 2019. Т. 61. № 5. С. 335-344 (Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy// Polymer Science, Series B, 2019, V. 61, N 5, pp 530-539 doi:10.1134/S1560090419050105), IF=0.907 - Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238 - Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238 - Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541 - Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541 - Т.В. Родионова, Д.С. Одинцов, А.Ю. Манаков, В.Ю. Комаров
Ионные клатратные гидраты нитрата тетра-н-бутиламмония (TBANO3) и смешанного TBA(NO3,OH): новые сверхструктуры тетрагональной структуры I
Журнал структурной химии, 2019, Т. 60, N 10, Сс 1726-1735 DOI: 10.26902/JSC_id48002 (Ionic Clathrate Hydrates of Tetra-n-Butylammonium Nitrate (TBANO3) and Mixed TBA(NO3,OH): Novel Superstructures of Tetragonal Structure I/ T. V. Rodionova, D. S. Odintsov, A. Yu. Manakov, V. Yu. Komarov// Journal of Structural Chemistry, V. 60, N 10, pp 1660-1669 doi:10.1134/S0022476619100123), IF=0.541 - Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751 - Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751 - Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751 - Рудаков Д.А., Генаев А.М., Дикусар Е.А., Зверева Т.Д., Зубрейчук З.П., Поткин В.И.
Галогенирование и μh-таутомерия 7-бензил-7,8-дикарба-нидо-ундекаборат(-1) аниона
Журнал органической химии. 2019. Т. 55. № 10. С. 1540-1550 (Halogenation and μH-Tautomerism of 7-Benzyl-7,8-dicarba-nido-undecaborate(-1) Anion/ D.A. Rudakov, A.M. Genaev, E.A. Dikusar, T.D. Zvereva, Z.P. Zubreichuk, V.I.Potkin// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1495-1503 doi:10.1134/S1070428019100075), IF=0.751 - В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751 - В.В. Шелковников, Н.А. Орлова, И.Ю. Каргаполова, К.Д. Ерин, А.М. Максимов, А.А. Черноносов
Формильные производные аминозамещенных полифтортрифенил-4,5-дигидро-1H-пиразолов: синтез и использование в качестве донорных блоков в структурах нелинейно-оптических хромофоров
Журнал органической химии. 2019. Т. 55. № 10. С. 1551-1566 (Formyl Derivatives of Amino Substituted Polyfluorotriphenyl4,5-dihydro-1H-pyrazoles: Synthesis and Use as Donor Blocks in the Structures of Nonlinear Optical Chromophores/ V.V. Shelkovnikov, N.A, Orlova, I.Yu. Kargapolova, K.D. Erin, A.M. Maksimov, A.A.Chernonosov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1504-1517 doi:10.1134/S1070428019100087), IF=0.751 - O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055 - O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055 - O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055 - E.S. Vasilyev, S.N. Bizyaev, V.Yu. Komarov, A.V. Tkachev
Syntheses of chiral fused 4,5-diazafluorene–bis(nopinane) derivatives
Mendeleev Commun., 2019, V. 29, N 5, Pp 584-586 doi:10.1016/j.mencom.2019.09.036, IF=2.01 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131 - A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11 - A.Yu. Vorob'ev, T.Yu. Dranova, A.E. Moskalensky
Photolysis of dimethoxynitrobenzyl-"caged" acids yields fluorescent products
SCIENTIFIC REPORTS, 2019, V. 9, Art.num 13421 doi:10.1038/s41598-019-49845-z, IF=4.11 - O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256 - O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256 - O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256 - O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256 - T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381 - T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381 - A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649 - A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649 - A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649 - A. Predtetchinski, E. Predtechenskaya, I. Sorokina, A. Guzev, S. Aydagulova
Morphologic changes and protective role of prolactin in experimental multiple sclerosis animal model
MULTIPLE SCLEROSIS JOURNAL, 2019, V.25, S2, Pp 435-435 (P845) (35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019 Конференция: 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual MULTIPLE SCLEROSIS JOURNAL Том: 25 Специальный выпуск: SI Приложение: 2 Стр.: 435-435 Аннотация к встрече: P845 Conference of Rehabilitation in MS Местоположение: Stockholm, SWEDEN публ.: SEP 11-13, 2019, IF=5.649 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - M.Y. Myshkin, R. Mannikko, O.A. Krumkacheva, D.S. Kulbatskii, A.O. Chugunov, A.A. Berkut, A.S. Paramonov, M.A. Shulepko, M.V. Fedin, M.G. Hanna, D.M. Kullmann, E.G. Bagryanskaya, A.S. Arseniev, M.P. Kirpichnikov, E.N. Lyukmanova, A.A. Vassilevski, Z.O. Shenkarev
Cell-free expression of sodium channel domains for pharmacology studies. noncanonical spider toxin binding site in the second voltage-sensing domain of human nav1.4 channel
Front. Pharmacol., 2019, V. 10, Art. number 953 doi:10.3389/fphar.2019.00953, IF=3.845 - A.V. Markov, A.E. Kel, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, E.B. Logashenko
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Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: A transcriptome analysis
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Oxidative addition of verdazyl halogenides to Pd(PPh3)4
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Oxidative addition of verdazyl halogenides to Pd(PPh3)4
New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69 - P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
Oxidative addition of verdazyl halogenides to Pd(PPh3)4
New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69 - P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
Oxidative addition of verdazyl halogenides to Pd(PPh3)4
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The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544 - E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544 - E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
IBRO Reports, V. 6, Supplement, September 2019, Page S492. P32.59 doi:10.1016/j.ibror.2019.07.1544 - E. Kulikova, N. Khotskin, N. Illarionova, I. Sorokin, K. Volcho, A. Kulikov
The antidepressant effect of STEP inhibitor (TC-2153) and its influence on the serotoninergic 5-HT2A receptors in the brain
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Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368 - A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368 - A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368 - A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368 - A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
IBRO Reports, 2019, V. 6, Supplement, Page S115 doi:10.1016/j.ibror.2019.07.368 - A. Kulikov, V. Moskaliuk, R. Kozhemyakina, D. Bazovkina, E. Terenina, K. Volcho, V. Naumenko, E. Kulikova
Effects of drug TC-2153 on the behavior and striatal-enriched tyrosine protein phosphatase in the brain of rats selectively bred for high and low aggression towards humans
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Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291 - E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291 - E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291 - E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291 - E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291 - E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
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Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - K. Kovaleva, O. Oleshko, E. Mamontova, O. Yarovaya, O. Zakharova, A. Zakharenko, A. Kononova, N. Dyrkheeva, S. Cheresiz, A. Pokrovsky, O. Lavrik, N. Salakhutdinov
Dehydroabietylamine Ureas and Thioureas as Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Enhance the Antitumor Effect of Temozolomide on Glioblastoma Cells
Journal of Natural Products, 2019, V. 82, N 9, Pp 2443-2450 doi:10.1021/acs.jnatprod.8b01095, IF=4.256 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868 - М.В. Кручинина, А.В. Азгалдян, И.О. Светлова, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот сыворотки крови и мембран эритроцитов у пациентов с воспалительными заболеваниями кишечника (пилотное исследование)
Современные проблемы науки и образования. 2019. № 3. С. 127. doi:10.17513/spno.28868 - A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795 - A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795 - A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795 - A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795 - A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018 - О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
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Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567 - О.П. Молодых, И.В. Сорокина, Е.В. Виноградова, В.И. Капустина, А.А. Ходаков
Ультраструктура печени при воздействии циклофосфамида и тритерпеноидов
Бюллетень экспериментальной биологии и медицины. 2019. Т. 168. № 9. С. 376-382. (Ultrastructure of the liver exposed to cyclophosphamide and triterpenoids/ O.P. Molodykh, I.V. Sorokina, E.V. Vinogradova, V.I. Kapustina, A.A. Khodakov// Bulletin of Experimental Biology and Medicine, 2020, V. 168, N 3, Pp 400-405 doi:10.1007/s10517-020-04718-8), IF=0.567 - Т.П. Кукина, И.А. Елшин, О.И. Сальникова, И.В. Ельцов
Алифатические и тритерпеновые продукты омыления эфирных экстрактов POPULUS NIGRA L
Химия растительного сырья. 2019. № 3. С. 109-118. (Aliphatic and triterpenoic products of ether extracts saponification of POPULUS NIGRA L/ T. P. Kukina, I. A. Elshin , O. I. Salnikova , I. V. Eltsov// doi:10.14258/jcprm.2019034951) - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641 - B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056 - B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056 - B.M. Urbagarova, V.V. Taraskin, E.E. Shults, L.D. Radnaeva
Development of assay method by HPLC-DAD for the quantitative determination of chromones in Saposhnikovia divaricata radices and its validation
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012056 (Conference Paper) doi:10.1088/1755-1315/320/1/012056 - D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052 - D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052 - D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052 - D.M. Mognonov, S.V. Morozov, O. Zh. Ayurova, E.I. Chernyak, V.I. Rodionov, M.N. Grigor'eva, S.A. Stelmakh
Thermal stability of polymer mixtures based on oxidized cellulose and polyguanidine hydrochloride
IOP Conference Series: Earth and Environmental Science, 2019, V. 320, N 1, art. Num. 012052 (Conference Paper) doi:10.1088/1755-1315/320/1/012052 - Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595 - D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279 - D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279 - D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279 - G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049 - G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049 - G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049 - G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - O.A. Chinak, A.V. Shernyukov, S.S. Ovcherenko, E.A. Sviridov, V.M. Golyshev, A.S. Fomin, I.A. Pyshnaya, E.V. Kuligina, V.A. Richter, E.G. Bagryanskaya
Structural and Aggregation Features of a Human k-Casein Fragment with Antitumor and Cell-Penetrating Properties
Molecules 2019, 24(16), 2919 doi:10.3390/molecules24162919, IF=3.59 - K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035 - K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035 - K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035 - K. Volcho, A. Zakharenko, O. Luzina, T. Khomenko, E. Suslov, O. Salomatina, O. Zakharova, N. Li-Zhulanov, J. Reynisson, O. Lavrik, N. Salakhutdinov
Tdp1 Inhibition as a Promising Approach to New Anticancer Drugs
Proceedings 2019, 22(1), 35 (This article belongs to the Proceedings of The Molecules Medicinal Chemistry Symposium-Challenges in Drug Discovery Barcelona, Spain | 15-17 May 2019) doi:10.3390/proceedings2019022035 - V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255 - V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255 - V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255 - V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255 - V. Shramko, Y. Ragino, E. Kashtanova, Y. Polonskaya, S. Morozov, E. Chernyak, A. Chernyavskyi
The fatty acids composition in patients with coronary atherosclerosis and unstable atherosclerotic plaques
Aterosclerosis, 2019, V. 287, E163-E163 Аннотация к встрече: EAS19-0489 doi:10.1016/j.atherosclerosis.2019.06.491, IF=4.255 - V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255 - V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255 - V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255 - V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255 - V. Shramko, Y. Polonskaya, E. Kashtanova, S. Morozov, A. Chernyavskyi, Y. Ragino
Associations of polyunsaturated fatty acids with oxidative-antioxidant parameters of the blood serum in coronary atherosclerosis
Aterosclerosis, 2019, V. 287, E286-E286 Аннотация к встрече: EAS19-1098 doi:10.1016/j.atherosclerosis.2019.06.886, IF=4.255 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Data for isolation and properties analysis of diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide
Data in Brief, 2019, V. 25, August 2019, Article number 104148 doi:10.1016/j.dib.2019.104148 - A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429 - A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429 - A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429 - A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - М.В. Кручинина, А.А. Громов, М.В. Паруликова, А.В. Рабко, М.В. Шашков, А.С. Соколова, В.Н. Кручинин
Особенности состава жирных кислот мембран эритроцитов у пациентов с резистентной артериальной гипертензией (пилотное исследование)
Атеросклероз. 2019. Т. 15. № 2. С. 24-31. doi:10.15372/ATER20190204 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689 - E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78 - E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78 - E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78 - E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78 - E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - Ю.А. Брылева, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.С. Богомяков, Т.С. Сухих, Е.А. Горбунова, А.В. Ткачев, С.В. Ларионов
Синтез, структура, магнитные и фотолюминесцентные свойства комплексов лантанидов(iii) с лигандом на основе 1,10-фенантролина и (+)-3-карена
Журнал структурной химии, 2019, V. 60, N 8, pp 1366-1378 (Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)-3-Carene/ Yu.A. Bryleva, L.A. Glinskaya, A.M. Agafontsev, M.I. Rakhmanova, A.S. Bogomyakov, T.S. Sukhikh, E.A. Gorbunova, A.V. Tkachev, S.V. Larionov// Journal of Structural Chemistry, 2019, V. 60, N 8, pp 1314-1326 doi:10.1134/S0022476619080110), IF=0.541 - A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59 - A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59 - A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59 - A.V. Markov, V.O. Babich, I.I. Popadyuk, O.V. Salomatina, E.B. Logashenko, N.F. Salakhutdinov, M.A. Zenkova
Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
Molecules 2019, 24(14), 2644 doi:10.3390/molecules24142644, IF=3.59 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217 - A. Ochkasova, M. Meschaninova, A. Venyaminova, A. Ivanov, D. Graifer, G. Karpova
The human ribosome as a possible mRNA quality controller that recognizes the abasic site by protein uS3
FEBS OPEN BIO, V. 9, Pp 163-163, Suppl. 1 Аннотация к встрече: P-11-010, WOS:000486972402108, IF=1.958 - M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97 - M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97 - M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97 - M.V. Kruchinina, A.A. Gromov, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin
Peculiarities of fatty acid profile of erythrocyte membranes in patients with resistant arterial hypertension: possible contribution to pathogenesis of the disease
JOURNAL OF HYPERTENSION, 2019, V. 37 , Pp E108-E108, Sup. 1 (29th European Meeting of Hypertension and Cardiovascular Protection of the European-Society-of-Hypertension (ESH), Milan, ITALY, JUN 21-24, 2019) doi:10.1097/01.hjh.0000571388.53224.97 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O.G. Tomilova, O.N. Yaroslavtseva, M.D. Ganina, M.V. Tyurin, E.I. Chernyak, I.V. Senderskiy, Yu.A. Noskov, O.V. Polenogova, Yu.B. Akhanaev, V.Yu. Kryukov, V.V. Glupov, S.V. Morozov
Changes in antifungal defence systems during the intermoult period in the Colorado potato beetle
Journal of Insect Physiology, 2019, V. 116, Pp 106-117 doi:10.1016/j.jinsphys.2019.05.003, IF=2.862 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733 - T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136 - T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136 - T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136 - T.S. Khlebnicova, Yu.A. Piven, A.V. Baranovsky, F.A. Lakhvich, I.V. Sorokina, T.G. Tolstikova
Fluorine-containing lupane triterpenoid acid derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory agents
Steroids, V.147, July 2019, Pp 62-69 doi:10.1016/j.steroids.2018.10.001, IF=2.136 - M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882) - M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882) - M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882) - M.A. Lenskiy, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy, E.E. Shul'ts
Синтез и свойства полиметилен-п-трифенилового эфира борной кислоты
Известия ВУЗов. "Серия Химия и химические технологии", 2019, Т. 62, N 7, Сс 31-37 (Synthesis and properties of polyethylene-p-triphenylboron ester of boric acid/ M. A. Lenskiy, E. E. Shul'ts, D. V. Korabel'nikov, A. V. Ozhogin, A. N. Novitskiy,// Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 2019, V. 62, N 7, Pp 31-37 doi:10.6060/ivkkt20196207.5882) - A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849 - A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849 - A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849 - A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849 - A.S. Poryvaev, D.M. Polyukhov, E. Gjuzi, F. Hoffmann, M. Froba, M.V. Fedin
Radical-Doped Metal–Organic Framework: Route to Nanoscale Defects and Magnetostructural Functionalities
Inorganic Chemistry 2019, 58, 13, 8471-8479 doi:10.1021/acs.inorgchem.9b00696, IF=4.849 - А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129) - А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129) - А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129) - А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, М.В. Хвостов, Н.Э. Поляков, Н.З. Ляхов
Супрамолекулярные системы доставки молекул лекарственных веществ на основе водорастворимых растительных метаболитов. физико-химические, фармакологические свойства и особенности механохимического получения
Химия в интересах устойчивого развития. 2019. Т. 27, № 3. С. 233-244. (Supramolecular systems for the delivery of the molecules of medicinal substances based on water-soluble plant metabolites. physicochemical, pharmacological properties and the features of mechanochemical preparation/ Dushkin A.V., Meteleva E.S., Tolstikova T.G., Khvostov M.V., Polyakov N.E., Lyakhov N.Z.// Chemistry for Sustainable Development, 2019. V. 27, № 3. P. 233-244. (in Russian) doi:10.15372/KhUR2019129) - Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636 - Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636 - Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636 - Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636 - Т.Е. Кокина, О.В. Саломатина, И.И. Попадюк, Л.А. Глинская, И.В. Корольков, Л.А. Шелудякова, М.И. Рахманова, Н.Ф. Салахутдинов
Комплексы ZN(II) и СU(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия. 2019. Т. 45. № 7. С. 420-426. (DOI: 10.1134/S0132344X1907003X ) (Complexes of Zn(II) and Сu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties/ T. E. Kokina, O. V. Salomatina, I. I. Popadyuk, L. A. Glinskaya, I. V. Korol'kov, L. A. Sheludyakova, M. I. Rakhmanova, N. F. Salakhutdinov// Russian Journal of Coordination Chemistry, July 2019, V. 45, N 7, pp 505-511 doi:10.1134/S1070328419070030), IF=0.636 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.Yu. Sosorev, M.K. Nuraliev, E.V. Feldman, D.R. Maslennikov, O.V. Borshchev, M.S. Skorotetcky, N.M. Surin, M.S. Kazantsev, S.A. Ponomarenko, D.Yu. Paraschuk
Impact of terminal substituents on the electronic, vibrational and optical properties of thiophene-phenylene co-oligomers
Physical Chemistry Chemical Physics, 2019, V. 21, N 22, Pp 11578-11588 doi:10.1039/C9CP00910H, IF=3.567 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - A.A. Lomzov, M.S. Kupryushkin, A.V. Shernyukov, M.D. Nekrasov, I.S. Dovydenko, D.A. Stetsenko, D.V. Pyshnyi
Diastereomers of a mono-substituted phosphoryl guanidine trideoxyribonucleotide: Isolation and properties
Biochemical and Biophysical Research Communications, 2019, V. 513, N 4, Pp 807-811 doi:10.1016/j.bbrc.2019.04.024, IF=2.705 - N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52 - N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52 - N.A. Muraleva, O.S. Kozhevnikova, A.Z. Fursova, N.G. Kolosova
Suppression of AMD-Like Pathology by Mitochondria-Targeted Antioxidant SkQ1 Is Associated with a Decrease in the Accumulation of Amyloid β and in mTOR Activity
Antioxidants 2019, 8(6), 177 doi:10.3390/antiox8060177, IF=4.52 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - A.G. Sokol, A.A. Tomilenko, T.A. Bul'bak, I.A. Sokol, P.A. Zaikin, G.A. Palyanova, Yu.N. Palyanov
Hydrogenation of carbon at 5.5-7.8 GPa and 1100-1400°C: Implications to formation of hydrocarbons in reduced mantles of terrestrial planets
Physics of the Earth and Planetary Interiors, 2019, V. 291, Pp 12-23 doi:10.1016/j.pepi.2019.04.002, IF=2.615 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - D. Avgustinovich, M. Tsyganov, G. Vishnivetskaya, А. Кovner, I. Sorokina, I. Orlovskaya, L. Toporkova, E. Goiman, T. Tolstikova, A. Dushkin, N. Lyakhov, V. Mordvinov
Effects of supramolecular complexation of praziquantel with disodium glycyrrhizinate on the liver fluke Opisthorchis felineus: an in vitro and in vivo study
Acta Tropica, 2019, V.194, Pp 1-12 doi:10.1016/j.actatropica.2019.03.017, IF=2.629 - V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
Journal of Soils and Sediments, 2019, V. 19, N 6, pp 2697-2707 doi:10.1007/s11368-018-2097-x, IF=2.669 - V.D. Tikhova, Yu.M. Deryabina, R.S. Vasilevich, E.D. Lodygin
Structural features of tundra and taiga soil humic acids according to IR EXPERT analytical system data
Journal of Soils and Sediments, 2019, V. 19, N 6, pp 2697-2707 doi:10.1007/s11368-018-2097-x, IF=2.669 - T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929 - T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929 - T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929 - T.S. Frolova, A.V. Lipeeva, D.S. Baev, S.I. Baiborodin, К.E. Orishchenko, A.V. Kochetov, O.I. Sinitsyna
Fluorescent labeling of ursolic acid with FITC for investigation of its cytotoxic activity using confocal microscopy
Bioorganic Chemistry, 2019, V. 87, Pp 876-887 doi:10.1016/j.bioorg.2018.11.052, IF=3.929 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723 - С.А. Низомов, И.В. Сорокина, Н.А. Жукова, Т.Г. Толстикова, Д.Е. Семенов, А.Е. Просенко
Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
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Морфологическая оценка простатотропной активности (3,5-диметил-4-гидрокси)бензилтиододекана на модели доброкачественной гиперплазии предстательной железы у крыс
Бюллетень экспериментальной биологии и медицины. 2019. Т. 167. № 6. С. 772-776. (Morphological analysis of prostatotropic activity of (3,5-dimethyl-4-hydroxy) benzyltiodyododecan in the model of benign prostatic hyperplasia in rats/ S.A. Nizomov, I.V. Sorokina, N.A. Zhukova, T.G. Tolstikova, D.E. Semenov, A.E. Prosenko// Bulletin of Experimental Biology and Medicine, 2019, V. 167, N 6, pp 809-812 doi:10.1007/s10517-019-04628-4), IF=0.567 - A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541 - A.V. Artem'v, A.S. Beresin, I.Yu. Bagryanskaya
Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine
Журнал структурной химии. 2019. Т. 60. № 6. С. 1008-1012. (DOI:10.26902/JSC_id40732) (Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118), IF=0.541 - A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
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Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
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Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, T.G. Tolstikova, M.E. Plokhotnichenko, G.G. Dultseva, P.S. Mazunina
Excipient-free isoniazid aerosol administration in mice: Evaporation-nucleation particle generation, pulmonary delivery and body distribution
International Journal of Pharmaceutics, 2019, V. 563, Pp 101-109 doi:10.1016/j.ijpharm.2019.03.050, IF=4.213 - T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
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Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
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Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
Proceedings of SPIE - The International Society for Optical Engineering, 2019, V. 11030, Num.art 110301D doi:10.1117/12.2521139 - S.V. Derevyashkin, E.A. Soboleva, V.V. Shelkovnikov, V.P. Korolkov, A.I. Malyshev, E.V. Spesivtsev
Triacrylamide polyfluorinated chalcone derivative as high resistant light-sensitive material for technology of diffractive optical elements
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Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802 - T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802 - T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802 - T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802 - T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
Bioorganic & Medicinal Chemistry, 2019, V. 27, N 10, Pp 1942-1951 doi:10.1016/j.bmc.2019.03.029, IF=2.802 - T. Yamasaki, D. Buric, C. Chacon, G. Audran, D. Braguer, S.R-A. Marque, M. Carre, P. Bremond
Chemical modifications of imidazole-containing alkoxyamines increase C–ON bond homolysis rate: effects on their cytotoxic properties in glioblastoma cells
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Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
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Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694 - I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
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Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831 - I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831 - I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831 - I.Yu. Fleitlikh, N.A. Grigorieva, N.I. Pavlenko, A.A. Kondrasenko, A.Ya. Tikhonov, O.A. Logutenko
Synergistic Silver Extraction from Hydrochloric Acid Solutions with Triisobutylphosphine Sulfide in the Presence of Organic Proton-Donor Additives
Solvent Extraction and Ion Exchange, 2019, V. 37, N 1, Pp 96-109 doi:10.1080/07366299.2019.1592925, IF=1.831 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - P. Maki-Arvela, N. Shcherban, Ch. Lozachmeur, K. Eranen, A. Aho, A. Smeds, N. Kumar, J. Peltonen, M. Peurla, V. Russo, K.P. Volcho, D.Yu. Murzin
Aldol Condensation of Cyclopentanone with Valeraldehyde Over Metal Oxides
Catalysis Letters, 2019, V. 149, N 5, pp 1383-1395 doi:10.1007/s10562-019-02701-1, IF=2.372 - N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08 - N.A. Muraleva, N.G. Kolosova, N.A. Stefanova
p38 MAPK–dependent alphaB-crystallin phosphorylation in Alzheimer's disease-like pathology in OXYS rats
Experimental Gerontology, Volume 119, May 2019, Pp 45-52 doi:10.1016/j.exger.2019.01.017, IF=3.08 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
International Journal of Biological Macromolecules, V. 128, 1 May 2019, Pp 158-166 doi:10.1016/j.ijbiomac.2019.01.079, IF=4.784 - Q. Zhang, L. Suntsova, Yu.S. Chistyachenko, V. Evseenko, M.V. Khvostov, N.E. Polyakov, A.V. Dushkin, W. Su
Preparation, physicochemical and pharmacological study of curcumin solid dispersion with an arabinogalactan complexation agent
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Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
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Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06 - A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06 - A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06 - A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06 - T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
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Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284 - T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
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Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
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Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
Polyhedron, 2019, V. 163, Pp 121-130 doi:10.1016/j.poly.2019.02.020, IF=2.284 - T.E. Kokina, L.A. Glinskaya, L.A. Sheludyakova, Yu.A. Eremina, L.S. Klyushova, V. Yu. Komarov, D.A. Piryazev, A.V. Tkachev, S.V. Larionov
Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (-)-camphor thiosemicarbazone
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Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
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Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014 - И.В. Нечепуренко, Е.Д. Широкова, М.В. Хвостов, Т.С. Фролова, О.И. Синицина, А.М. Максимов, Р.А. Бредихин, Н.И. Комарова, Д.С. Фадеев, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014 - А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
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Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014 - А.С. Соколова, Д.В. Баранова, О.И. Яровая, Д.С. Баев, О.А. Полежаева, А.В. Зыбкина, Д.Н. Щербаков, Т.Г. Толстикова, Н.Ф. Салахутдинов
Синтез производных (1S)-(+)-камфора-10-сульфокислоты и изучение их противовирусной активности в качестве ингибиторов филовирусных инфекций in vitro и in silico
Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1041-1046 (Synthesis of (1S)-(+)-camphor-10-sulfonic acid derivatives and investigations in vitro and in silico of their antiviral activity as the inhibitors of fi lovirus infections/ A. S. Sokolova, D. V. Baranova, O. I. Yarovaya, D. S. Baev, O. A. Polezhaeva, A. V. Zybkina, D. N. Shcherbakov, T. G. Tolstikova, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V 68, N 5, pp 1041-1046 doi:10.1007/s11172-019-2517-0), IF=1.014 - А.Г. Потапов, И.К. Шундрина
Влияние алифатических диолов и дикарбоновых кислот на свойства сополиэфиров этиленсукцината
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О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
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О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751 - Л.М. Горностаев, Э.В. Нуретдинова, Т.И. Лаврикова, Ю.Г. Халявина, О.И. Фоминых, Ю.В. Гатилов
О реакции 2-бензиламино-1,4-нафтохинонов с нитрозилсерной кислотой
Журнал органической химии. 2019. Т. 55. № 5. С. 700-707. (DOI: 10.1134/S0514749219050069) (On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051), IF=0.751 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418 - V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418 - V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418 - V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418 - V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953 - E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
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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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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18 - E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Disodium salt of glycyrrhizic acid - A novel supramolecular delivery system for anthelmintic drug praziquantel
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Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
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Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061 - V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061 - V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
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Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
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Structural diversity of zinc(II) coordination polymers with octafluorobiphenyl-4,4'-dicarboxylate based on mononuclear, paddle wheel and cuboidal units
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Effect of chiral polyhydrochromenes on cannabinoid system
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Effect of chiral polyhydrochromenes on cannabinoid system
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Mechanism of action of an old antibiotic revisited: Role of calcium ions in protonophoric activity of usnic acid
Biochimica et Biophysica Acta (BBA) - Bioenergetics, V. 1860, N 4, 1 April 2019, Pp 310-316 doi:10.1016/j.bbabio.2019.01.005, IF=4.441 - Yu.N. Antonenko, L.S. Khailova, T.I. Rokitskaya, E.S. Nosikova, P.A. Nazarov, O.A. Luzina, N.F. Salakhutdinov, E.A. Kotova
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Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - J. Guo, Z. Wang, W. Zhang, I.I. Oleynik, A. Vignesh, I.V. Oleynik, X. Hu, Ya. Sun, Wen-Hua. Sun
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
Molecules 2019, 24(6), 1176 doi:10.3390/molecules24061176, IF=3.06 - Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259 - Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
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Oxygen-guided radiation therapy
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Oxygen-guided radiation therapy
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Oxygen-guided radiation therapy
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Oxygen-guided radiation therapy
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Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
Oxygen-guided radiation therapy
International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203 - A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16 - A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16 - A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16 - A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16 - D. V. Telegina, N.G. Kolosova, O. S. Kozhevnikova
Immunohistochemical localization of NGF, BDNF, and their receptors in a normal and AMD-like rat retina
BMC Medical Genomics, March 2019, 12(Supp. 2):48 (From 11th International Multiconference “Bioinformatics of Genome Regulation and StructureSystems Biology” - BGRSSB-2018 Novosibirsk, Russia. 20-25 August 2018) doi:10.1186/s12920-019-0493-8, IF=2.568 - D. V. Telegina, N.G. Kolosova, O. S. Kozhevnikova
Immunohistochemical localization of NGF, BDNF, and their receptors in a normal and AMD-like rat retina
BMC Medical Genomics, March 2019, 12(Supp. 2):48 (From 11th International Multiconference “Bioinformatics of Genome Regulation and StructureSystems Biology” - BGRSSB-2018 Novosibirsk, Russia. 20-25 August 2018) doi:10.1186/s12920-019-0493-8, IF=2.568 - Ju.A. Sidorova, K.P. Volcho, N.F. Salakhutdinov
Neuroregeneration in Parkinson’s Disease: From Proteins to Small Molecules
Current Neuropharmacology, 2019,V. 17 , N 3 , Pp. 268 - 287 doi:10.2174/1570159X16666180905094123, IF=4.568 - V. Morozov, E. Tretyakov
Spin polarization in graphene nanoribbons functionalized with nitroxide
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Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
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Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934 - A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934 - A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934 - A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934 - V.E. Evtushok, A.Yu. Vorob'ev
Synthesis of pyrazolo- and [1,2,4]triazolo-[1,5-а]quinolin-9-ols by cycloaddition to 8-hydroxyquinoline N-imide
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Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014 - П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014 - П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014 - П.А. Никитина, Н.И. Бормотов, Л.Н. Шишкина, А.Я. Тихонов, В.П. Перевалов
Синтез и противовирусная активность в отношении вируса осповакцины 1-гидрокси-2-(2-гидроксифенил)имидазолов
Известия Академии наук. Серия химическая. 2019. № 3. С. 634-637. (Synthesis and antiviral activity of 1-hydroxy-2-(2-hydroxyphenyl)imidazoles against vaccinia virus/ P.A. Nikitina, N.I. Bormotov, L.N. Shishkina, A.Ya. Tikhonov, V.P. Perevalov// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 634-637 doi:10.1007/s11172-019-2467-6), IF=1.014 - И.В. Береговая, Л.Н. Щеголева, В.И. Боровков, В.М. Карпов
Анион-радикал перфторбензоциклобутена - структурно нежесткая частица
Журнал структурной химии. 2019. Т. 60. № 3. С. 392-395. DOI:10.26902/JSC_id39468 (Perfluorobenzocyclobutene radical anion: A structurally flexible particle/ I.V. Beregovaya, L.N. Shchegoleva, V.I. Borovkov, V.M. Karpov// Journal of Structural Chemistry, 2019, V. 60, N 3, pp 373-376 doi:10.1134/S0022476619030041), IF=0.541 - Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751 - Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751 - D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716 - D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716 - D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716 - M. Edeleva, G. Audran, S. Marque, E. Bagryanskaya
Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
Materials, 2019, V. 12, N 5, Pp. 688-707 doi:10.3390/ma12050688, IF=2.972 - M. Edeleva, G. Audran, S. Marque, E. Bagryanskaya
Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations
Materials, 2019, V. 12, N 5, Pp. 688-707 doi:10.3390/ma12050688, IF=2.972 - A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
Molecular receptors for recognition and sensing of nucleotides
Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16 - A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
Molecular receptors for recognition and sensing of nucleotides
Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16 - A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
Molecular receptors for recognition and sensing of nucleotides
Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16 - A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
Molecular receptors for recognition and sensing of nucleotides
Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - 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 - V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716 - V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716 - V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716 - V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716 - V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606 - A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V.