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

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Employee:  Patrushev Sergey Sergeevich
Positions:  Researcher (Cand. Chem.), LMCh


 


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Personal publicalions (DB NIOCh)


2021

Reviews, articles

  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

  1. D.V. Reshetnikov, S.S. Patrushev, E.E. Shults
    Synthetic Transformations of Sesquiterpene Lactones. 11.* Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers
    Chemistry of Natural Compounds, 2020, V. 56, N 5, Pp 855-860 doi:10.1007/s10600-020-03169-x, IF=0.652

2017

Reviews, articles

  1. S.S. Patrushev, T.V. Rybalova, I. D. Ivanov, V.A. Vavilin, E.E. Shults
    Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines
    Tetrahedron, 2017, V. 73, N 19, Pp 2717-2726 In Press, Accepted Manuscript - Note to users doi:10.1016/j.tet.2017.03.016, IF=2.651
  2. Л.Г. Бурова, И.В. Широких, С.С. Патрушев, Т.Г. Толстикова, Э.Э. Шульц
    Взаимосвязь структура-антибактериальная активность в ряду производных изоалантолактона
    Фундаментальная и клиническая медицина. 2017. Т. 2. № 1. С. 28-34.

2016

Reviews, articles

  1. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
    Synthetic Transformations of Sesquiterpene Lactones 10*. Synthesis of 13-Arylguaianolides
    Chemistry of Heterocyclic Compounds, October 2016, V. 52, N 10, pp 788-796 doi:10.1007/s10593-016-1967-7, IF=0.815
  2. S.S. Patrushev, M.M. Shakirov, E.E. Shults
    Synthetic transformations of sesquiterpene lactones 9.*Synthesis of 13-(pyridinyl)eudesmanolides
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N 3, pp 165-171 doi:10.1007/s10593-016-1855-1, IF=0.814

2014

Reviews, articles

  1. S.S. Patrushev, M.M. Shakirov, T.V. Rybalova, E.E. Shults
    Synthetic Transformations of Sesquiterpene Lactones. 8*. Synthesis of 13-(2-Oxofuro- [2,3-d]pyrimidin-3(2H)-yl)eudesmanolides
    Chemistry of Heterocyclic Compounds, November 2014, V. 50, N 8, pp 1063-1080 doi:10.1007/s10593-014-1566-4, IF=0.698
  2. Э.Э. Шульц, А.С. Кишкентаева, C.C. Патрушев, Г.А. Атажанова, С.М. Адекенов
    Модификации cесквитерпеновых лактонов c помощью реакции Хека. Некоторые результаты и перспективы.
    Фармацевтический бюллетень. 2014, №1-3, с. 20-28.

2013

Reviews, articles

  1. С.С. Патрушев, М.М. Шакиров, Т.В. Рыбалова, Э.Э. Шульц
    Синтетические трансформации сесквитерпеновых лактонов. VII.. Катализируемое соединениями палладия кросс-сочетание изоалантолактона с 5-галогенурацилами
    Журнал органической химии, 2013, Т. 49, N 12, С.1802-1815. (Synthetic transformations of sesquiterpene lactones: VII. Palladium-catalyzed cross-coupling of isoalantolactone with 5-halouracils/ S. S. Patrushev, M. M. Shakirov, T. V. Rybalova, E. E. Shul’ts// Russian Journal of Organic Chemistry, 2013, V.49, N 12, pp 1783-1797 doi:10.1134/S1070428013120130), IF=0.513
  2. A. E. Esenbaeva, E. E. Shul’ts, Yu. V. Gatilov, M. M. Shakirov, S. S. Patrushev, G. A. Atazhanova, A. B. Kenesheva, S. M. Adekenov
    Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity
    Chemistry of Natural Compounds, 2013, V. 49, N 5, P. 875-881. doi:10.1007/s10600-013-0768-9, IF=0.598

2012

Reviews, articles

  1. E.E. Shul'ts, S.S. Patrushev, A.V. Belovodskii, M.M. Shakirov, T.V. Rybalova, A.G. Pokrovskii, M.A. Pokrovskii, G.A. Tolstikov, S.M. Adekenov
    Synthetic transformations of sesquiterpene lactones. V.* Synthesis and cytotoxicity of 13-aryl-substituted tourneforin derivatives
    Chem. Nat. Compd., 2012, V. 48, N 2, pp. 245-249. doi:10.1007/s10600-012-0214-4, IF=1.29



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