Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

1. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
   Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
   Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
2. D. V. Reshetnikov, L. G. Burova, T. V. Rybalova, E. A. Bondareva, S. S. Patrushev, A. N. Evstropov, E. E. Shults
   Synthesis and Antibacterial Activity of Caffeine Derivatives Containing Amino-Acid Fragments
   Chemistry of Natural Compounds, 2022, V. 58, N 5, Pp 908-915 doi:10.1007/s10600-022-03826-3, IF=0.83
3. V.A. Stepanova, S.S. Patrushev, T.V. Rybalova, E.E. Shults
   Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
   Journal of Molecular Structure, V.1247, 5 January 2022, 131373 doi:10.1016/j.molstruc.2021.131373, IF=3.841

Reviews, articles

1. S.S. Patrushev, T.V. Rybalova, E.E. Shults
   Synthetic transformations of sesquiterpene lactones. Controllable synthesis of 11,13-dihydroisoalantolactone azides and 13-(1,2,3-triazolyl)eudesmanolides
   Chemistry of Heterocyclic Compounds, 2021, V.57, N 11, Pp 1116-1129, IF=1.277
2. Д.О. Васильева, С.С. Патрушев, Э.Э. Шульц, А.Н. Евстропов, Л.Г. Бурова, Е.А. Бондарева
   Изучение антибактериальной активности бис-(11,13-дигидро-изоалантолактонов) с азотсодержащими линкерами in vitro
   Проблемы медицинской микологии. 2021. Т. 23. № 2. С. 77.
3. 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, 2021, V. 18 , N 7 , Pp 686 - 700 doi:10.2174/1570180817999201211193151, IF=1.15

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

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.

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

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.

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

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