Articles - Sciact

Articles (17)

#	Публикация
1	Patrushev S.S. , Vasil’eva D.O. , Burova L.G. , Bondareva E.A. , Zakharova L.N. , Evstropov A.N. , Shults E.E. Synthesis and evaluation of antibacterial activity of bis-eudesmanolides connected by nitrogen-containing linkers Russian Chemical Bulletin. 2023. V.72. N10. P.2513-2524. DOI: 10.1007/s11172-023-4054-0 WOS Scopus РИНЦ OpenAlex
2	Патрушев С.С. , Васильева Д.О. , Бурова Л.Г. , Бондарева Е.А. , Захарова Л.Н. , Евстропов А.Н. , Шульц Э.Э. Синтез и оценка антибактериальной активности бис-эудесманолидов с азотсодержащими линкерами Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2023. Т.72. №10. С.2513-2524.
3	Reshetnikov D.V. , Burova L.G. , Rybalova T.V. , Bondareva E.A. , Patrushev S.S. , Evstropov A.N. , Shults E.E. Synthesis and Antibacterial Activity of Caffeine Derivatives Containing Amino-Acid Fragments Chemistry of Natural Compounds. 2022. V.58. N5. P.908-915. DOI: 10.1007/s10600-022-03826-3 WOS РИНЦ OpenAlex
4	Reshetnikov D.V. , Ivanov I.D. , Baev D.S. , Rybalova T.V. , Mozhaitsev E.S. , Patrushev S.S. , Vavilin V.A. , Tolstikova T.G. , Shults E.E. Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors Molecules. 2022. V.27. N24. P.8787. DOI: 10.3390/molecules27248787 WOS РИНЦ OpenAlex
5	Stepanova V.A. , Patrushev S.S. , Rybalova T.V. , Shults E.E. Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent Journal of Molecular Structure. 2022. V.1247. 131373 . DOI: 10.1016/j.molstruc.2021.131373 WOS Scopus РИНЦ OpenAlex
6	Patrushev S.S. , Rybalova T.V. , Shults E.E. Synthetic transformations of sesquiterpene lactones. Controllable synthesis of 11,13-dihydroisoalantolactone azides and 13-(1,2,3-triazolyl)eudesmanolides based on sesquiterpene lactones Chemistry of Heterocyclic Compounds. 2021. V.57. N11. P.1116–1129. DOI: 10.1007/s10593-021-03030-1 WOS Scopus OpenAlex
7	Patrushev S.S. , Burova L.G. , Shtro A.A. , Rybalova T.V. , Baev D.S. , Shirokikh I.V. , Evstropov A.N. , Shults E.E. Modifications of isoalantolactone leading to effective anti-bacterial and anti-viral compounds Letters in Drug Design and Discovery. 2021. V.18. N7. P.686-700. DOI: 10.2174/1570180817999201211193151 WOS Scopus РИНЦ OpenAlex
8	Reshetnikov D.V. , Patrushev S.S. , Shults E.E. *Synthetic Transformations of Sesquiterpene Lactones. 11. Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers** Chemistry of Natural Compounds. 2020. V.56. N5. P.855-860. DOI: 10.1007/s10600-020-03169-x WOS Scopus РИНЦ OpenAlex
9	Patrushev S.S. , Rybalova T.V. , Ivanov I.D. , Vavilin V.A. , Shults E.E. Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines Tetrahedron. 2017. V.73. N19. P.2717-2726. DOI: 10.1016/j.tet.2017.03.016 WOS Scopus РИНЦ OpenAlex
10	Бурова Л.Г. , Широких И.В. , Патрушев С.С. , Толстикова Т.Г. , Шульц Э.Э. ВЗАИМОСВЯЗЬ СТРУКТУРА-АНТИБАКТЕРИАЛЬНАЯ АКТИВНОСТЬ В РЯДУ ПРОИЗВОДНЫХ ИЗОАЛАНТОЛАКТОНА ФУНДАМЕНТАЛЬНАЯ И КЛИНИЧЕСКАЯ МЕДИЦИНА. 2017. Т.2. №1. С.28-34.
11	Kihkentayeva A.S. , Shults E.E. , Gatilov Y.V. , Patrushev S.S. , Karim S. , Atazhanova G.A. , Adekenov S.M. *Synthetic Transformations of Sesquiterpene Lactones 10. Synthesis of 13-Arylguaianolides** Chemistry of Heterocyclic Compounds. 2016. V.52. N10. P.788-796. DOI: 10.1007/s10593-016-1967-7 WOS Scopus РИНЦ OpenAlex
12	Patrushev S.S. , Shakirov M.M. , Shults E.E. *Synthetic transformations of sesquiterpene lactones 9.() Synthesis of 13-(pyridinyl)eudesmanolides** Chemistry of Heterocyclic Compounds. 2016. V.52. N3. P.165-171. DOI: 10.1007/s10593-016-1855-1 WOS Scopus РИНЦ OpenAlex
13	Patrushev S.S. , Shakirov M.M. , Rybalova T.V. , Shults E.E. *Synthetic Transformations of Sesquiterpene Lactones. 8. Synthesis of 13-(2-Oxofuro- [2,3-d]pyrimidin-3(2H)-yl)eudesmanolides** Chemistry of Heterocyclic Compounds. 2014. V.50. N8. P.1063-1080. DOI: 10.1007/s10593-014-1566-4 WOS Scopus РИНЦ OpenAlex
14	Patrushev S.S. , Shakirov M.M. , Rybalova T.V. , Shul'ts E.E. Synthetic transformations of sesquiterpene lactones: VII. Palladium-catalyzed cross-coupling of isoalantolactone with 5-halouracils Russian Journal of Organic Chemistry. 2013. V.49. N12. P.1783-1797. DOI: 10.1134/S1070428013120130 WOS Scopus РИНЦ OpenAlex
15	Esenbaeva A.E. , Shul'ts E.E. , Gatilov Y.V. , Shakirov M.M. , Patrushev S.S. , Atazhanova G.A. , Kenesheva A.B. , Adekenov S.M. Synthesis of 13-Aryl Derivatives of the Sesquiterpene Lactone Argolide and their Analgesic Activity Chemistry of Natural Compounds. 2013. V.49. N5. P.875-881. DOI: 10.1007/s10600-013-0768-9 WOS Scopus РИНЦ OpenAlex
16	Патрушев С.С. , Шакиров М.М. , Рыбалова Т.В. , Шульц Э.Э. Синтетические трансформации сесквитерпеновых лактонов. vii. катализируемое соединениями палладия кросс-сочетание изоалантолактона с 5-галогенурацилами Журнал органической химии (RUSS J ORG CHEM+). 2013. Т.49. №12. С.1802-1815. РИНЦ
17	Shul'ts E.E. , Patrushev S.S. , Belovodskii A.V. , Shakirov M.M. , Rybalova T.V. , Pokrovskii A.G. , Pokrovskii M.A. , Tolstikov G.A. , Adekenov S.M. *Synthetic transformations of sesquiterpene lactones. V. Synthesis and cytotoxicity of 13-aryl-substituted tourneforin derivatives** Chemistry of Natural Compounds. 2012. V.48. N2. P.245-249. DOI: 10.1007/s10600-012-0214-4 WOS Scopus РИНЦ OpenAlex

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