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

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Employee:  Patrusheva Oxana Stanislavovna
Positions:  Researcher (Cand. Chem.), LPhAC


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Personal publicalions (DB NIOCh)


Reviews, articles

  1. 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


Reviews, articles

  1. 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
  2. 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


Reviews, articles

  1. 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


Reviews, articles

  1. 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
  2. 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
  3. E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46


Reviews, articles

  1. 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
  2. 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
  3. 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
  4. 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


Reviews, articles

  1. 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
  2. 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
  3. 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


Reviews, articles

  1. 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
  2. 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
  3. K. Volcho, Ardashov, O. Mikhalchenko, I. Il'ina, N. Salakhutdinov
    Synthetic Transformations of para-Menthane Monoterpenoids: New Way to Elaboration of Medicines for Mental Health
    Chem. Listy, 108, s120-s121 (2014)., IF=0.195


Reviews, articles

  1. 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
  2. О.В. Ардашов, Е.В. Хаид, О.С. Михальченко, Д.В. Корчагина, К.П. Волчо, Н.Ф. Салахутдинов
    Первый синтез пара-мента-1,8-диенового триола
    Известия АН. Серия химическая, 2013, N 1, С. 172-175. (First synthesis of p-mentha-1,8-diene triol/ O. V. Ardashov, E. V. Khaid, O. S. Mikhal’chenko, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2013, V. 62, N 1, pp 171-174 doi:10.1007/s11172-013-0025-1), IF=0.423


Reviews, articles

  1. О.С. Михальченко, К.П. Волчо, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез гетероциклических соединений взаимодействием альдегидов с монотерпеноидами в присутствии монтмориллонитовых глин
    Известия Уфимского научного центра РАН, 2012, № 4, 53-79.


Reviews, articles

  1. 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

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