Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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