Сотрудник:
Патрушева Оксана Станиславовна
Занимаемые должности:
нс(кхн) ЛФАВ
Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- E.V. Suslov, K.Yu. Ponomarev, O.S. Patrusheva, S.O. Kuranov, A.A. Okhina, A.D. Rogachev, A.A. Munkuev, R.V. Ottenbacher, A.I. Dalinger, M.A. Kalinin, S.Z. Vatsadze, K.P. Volcho, N.F. Salakhutdinov
Novel Bispidine-Monoterpene Conjugates—Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones
Molecules, 2021, 26(24), 7539 doi:10.3390/molecules26247539, IF=4.411
- О.С. Патрушева, К.П. Волчо, Н.Ф. Салахутдинов
Подходы к синтезу кислородсодержащих гетероциклических соединений на основе монотерпеноидов
Успехи химии, 2018, Т. 87, N 8, Сc 771-796 (Synthesis of oxygen-containing heterocyclic compounds based on monoterpenoids/ O S Patrusheva, K P Volcho, N F Salakhutdinov// RUSS CHEM REV, 2018, V. 87, N 8, Pp 771-796 doi:10.1070/RCR4810), IF=3.991
- M.N. Timofeeva, V.N. Panchenko, K.P. Volcho, S.V. Zakusin, V.V. Krupskaya, A. Gil, O.S. Mikhalchenko, M.A. Vicente
Effect of acid modification of kaolin and metakaolin on Bronsted acidity and catalytic properties in the synthesis of octahydro-2H-chromen-4-ol from vanillin and isopulegol
Journal of Molecular Catalysis A: Chemical, , V. 414, April 2016, Pp 160-166 doi:10.1016/j.molcata.2016.01.010, IF=3.957
- 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.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
- I.V. Ilyina, O.S. Patrusheva, V.V. Zarubaev, M.A. Misiurina, A.V. Slita, Ia.L. Esaulkova, D.V. Korchagina, Yu.V. Gatilov, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
Influenza antiviral activity of F- and OH-containing isopulegol-derived octahydro-2H-chromenes
Bioorganic & Medicinal Chemistry Letters, 2021, V. 31, 127677 doi:10.1016/j.bmcl.2020.127677, IF=2.823
- S. Yu. Kurbakova, I. V. Il'ina, O. S. Mikhalchenko, M. A. Pokrovsky, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov
The short way to chiral compounds with hexahydrofluoreno[9,1-bc]furan framework: Synthesis and cytotoxic activity
Bioorganic & Medicinal Chemistry, V. 23, N 7, 2015, Pp 1472-1480. doi:10.1016/j.bmc.2015.02.013, IF=2.793
- O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
A practical way to synthesize chiral fluoro-containing polyhydro-2H-chromenes from monoterpenoids
Beilstein J. Org. Chem. 2016, 12, 648-653 doi:10.3762/bjoc.12.64, IF=2.697
- N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
Effect of chiral polyhydrochromenes on cannabinoid system
Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
- O. Mikhalchenko, I. Il’ina, A. Pavlova, E. Morozova, D. Korchagina, T. Tolstikova, E. Pokushalov, K. Volcho, N.Salakhutdinov
Synthesis and analgesic activity of new heterocyclic compounds derived from monoterpenoids
Medicinal Chemistry Research, 2013, V. 22, N 6, P. 3026-3034. doi:10.1007/s00044-012-0310-9, IF=1.611
- I.V. Il'ina, O.S. Patrusheva, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3˙Et2O-H2O Catalytic System
Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 867-874 doi:10.1007/s10593-020-02743-z, IF=1.519
- I. Il’ina, O. Mikhalchenko, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov, E. Pokushalov
Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
Medicinal Chemistry Research, 2014, V. 23, N 12, pp 5063-5073 doi:10.1007/s00044-014-1071-4, IF=1.402
- A. Pavlova, O. Mikhalchenko, A. Rogachev, I. Il'ina, D. Korchagina, Yu. Gatilov, T. Tolstikova, K. Volcho, N. Salakhutdinov
Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
Medicinal Chemistry Research, 2015, V 24, N 11, pp 3821-3830 doi:10.1007/s00044-015-1426-5, IF=1.401
- O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
Formation of the Compounds with an Epoxychromene Framework: Role of the Methoxy Groups
Helvetica Chimica Acta, 2014, vol. 97, N 10, p. 1406-1421 doi:10.1002/hlca.201300461, IF=1.394
- I.V. Il’ina, K.P. Volcho, O.S. Mikhalchenko, D.V. Korchagina, N.F. Salakhutdinov
Reactions of Verbenol Epoxide with Aromatic Aldehydes Containing Hydroxy or Methoxy Groups in the Presence of Montmorillonite Clay
Helv. Chim. Acta, 2011, V. 94, N 3, 502-513. doi:10.1002/hlca.201000269, IF=1.284
- A. Pavlova, O. Patrusheva, I. Il'ina, K. Volcho, T. Tolstikova, N. Salakhutdinov
The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8ahexahydro- 2H-chromene-4,8-diols in their Biological Activity
Letters in Drug Design & Discovery, 2017, V. 14, N 5, pp. 508-514 doi:10.2174/1570180813666161102142642, IF=1.169
- Е.С. Можайцев, К.Ю. Пономарев, О.С. Патрушева, А.В. Медведько, А.И. Далингер, А.Д. Рогачев, Н.И. Комарова, Д.В. Корчагина, Е.В. Суслов, К.П. Волчо, Н.Ф. Салахутдинов, С.З. Вацадзе
Конъюгаты биспидина и монотерпеноидов как лиганды металлокомплексных катализаторов реакции Анри
Журнал органической химии. 2020. Т. 56. № 11. С. 1768-1783 doi:10.31857/S0514749220110129. (Conjugates of Bispidine and Monoterpenoids as Ligands of Metal Complex Catalysts for the Henry Reaction/ E. S. Mozhaitsev, K. Y. Ponomarev, O. S. Patrusheva, A. V. Medvedko, A. I. Dalinger, A. D. Rogachev, N. I. Komarova, D. V. Korchagina, E. V. Suslov, K. P. Volcho, N. F. Salakhutdinov, S. Z. Vatsadze// Russian Journal of Organic Chemistry, 2020, V.56, N 11, Pp 1969-1981 doi:10.1134/S1070428020110123), IF=0.624
- И.В. Ильина, М.А. Покровский, О.С. Михальченко, Д.В. Корчагина, К.П. Волчо, А.Г. Покровский, Н.Ф. Салахутдинов
Синтез и цитотоксическая активность замещенных гексагидро-2 H-4,6-(эпоксиметано)хромен-8(5 H)-онов, получаемых из (-)-вербенона
Известия Академии наук. Серия химическая, 2015, № 9, С. 2257. (Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone/ I. V. Il'ina, M. A. Pokrovsky, O. S. Mikhalchenko, D. V. Korchagina, K. P. Volcho, A. G. Pokrovsky, N. F. Salakhutdinov// Russian Chemical Bulletin, 2018, V. 64, N 9, pp 2257-2260 doi:10.1007/s11172-015-1148-3), IF=0.481
- A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
- O.S. Patrusheva, A.V. Pavlova, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties
Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1066-1071 doi:10.1007/s10600-017-2202-1, IF=0.46
