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1
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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
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РИНЦ
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2
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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.
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3
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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
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4
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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
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РИНЦ
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5
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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
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РИНЦ
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6
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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
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7
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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
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РИНЦ
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8
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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
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РИНЦ
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9
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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
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РИНЦ
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10
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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.
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11
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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
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РИНЦ
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12
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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
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РИНЦ
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13
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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
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РИНЦ
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14
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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
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РИНЦ
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15
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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
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РИНЦ
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16
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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
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17
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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
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РИНЦ
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