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1
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Omarova B.A.
, Shults E.E.
, Zhakipbekov K.S.
, Abekova А.О.
, Ishmuratova M.Y.
, Petrova T.N.
, Kartbayeva E.B.
Biological effects and phytochemical study of the underground part of Iris scariosa Willd. ex Link extract: A new source of bioactive constituents
Fitoterapia. 2024.
P.105920. DOI: 10.1016/j.fitote.2024.105920
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2
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Qi Z.
, Xie P.
, Wang Z.
, Zhou H.
, Tao R.
, Popov S.A.
, Yang G.
, Shults E.E.
, Wang C.
Synthesis of novel ursolic acid-gallate hybrids via 1,2,3-triazole linkage and its anti-oxidant and anti-inflammatory activity study
Arabian Journal of Chemistry. 2024.
105762
:1-27. DOI: 10.1016/j.arabjc.2024.105762
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3
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Kharitonov Y.V.
, Antipova V.I.
, Marenina M.K.
, Meshkova Y.V.
, Tolstikova T.G.
, Shults E.E.
Synthetic Transformations of Higher Terpenoids. 44#. Synthesis of New Derivatives of 18-Nor-4-Amino-8(17),13,14-Labdatriene and Evaluation of Their Cytotoxicity for MCF7, HepG2, and HeLa Tumor Cell Lines
Chemistry of Natural Compounds. 2024.
V.60. N2. P.252-262. DOI: 10.1007/s10600-024-04299-2
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4
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Finke A.O.
, Krasnov V.I.
, Rybalova T.V.
, Chirkova V.Y.
, Belenkaya S.V.
, Volosnikova E.A.
, Shcherbakov D.N.
, Shults E.E.
A straightforward trifluoromethylation at the C6 position of morphinane alkaloids, their modification and evaluation of inhibition of the SARS-CoV-2 main protease
Journal of Fluorine Chemistry. 2023.
V.271. 110189
:1-10. DOI: 10.1016/j.jfluchem.2023.110189
WOS
РИНЦ
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5
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Миронов М.Е.
, Шульц Э.Э.
Синтез и превращения 2,4-диокса- и 2,4-диазаспиро[5.5]ундеканонов, содержащих дитерпеноидный заместитель
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2023.
Т.72. №10. С.2453-2465.
РИНЦ
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6
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Kharitonov Y.V.
, Antipova V.I.
, Marenina M.K.
, Meshkova Y.V.
, Tolstikova T.G.
, Shults E.E.
Synthetic Transformations of Higher Terpenoids. 43. Synthesis and Cytotoxic Properties of New Lambertianic Acid Derivatives at the Carboxylic Group
Chemistry of Natural Compounds. 2023.
№6. С.936–947. DOI: 10.1007/s10600-023-04206-1
WOS
РИНЦ
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7
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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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8
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Popov S.A.
, Qi Z.
, Wang C.
, Shults E.E.
Synthesis of ursane-derived isothiocyanates and study of their reactions with series of amines and ammonia
Journal of Sulfur Chemistry. 2023.
V.44. N5. P.523-541. DOI: 10.1080/17415993.2023.2193669
WOS
РИНЦ
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9
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Cheremnykh K.P.
, Bryzgalov A.O.
, Baev D.S.
, Borisov S.A.
, Sotnikova Y.S.
, Savelyev V.A.
, Tolstikova T.G.
, Sagdullaev S.S.
, Shults E.E.
Synthesis, Pharmacological Evaluation, and Molecular Modeling of Lappaconitine–1,5-Benzodiazepine Hybrids
Molecules. 2023.
Т.28. №10. 4234
:1-20. DOI: 10.3390/molecules28104234
WOS
РИНЦ
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10
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Finke A.O.
, Mironov M.E.
, Pokrovskii M.A.
, Shults E.E.
Mannich Reaction of Solasodine with Acetylenes and Formaldehyde. Cytotoxicity of N-Propargyl-Substituted Alkaloid Derivatives
Chemistry of Natural Compounds. 2023.
V.59. N1. P.87-93. DOI: 10.1007/s10600-023-03924-w
WOS
РИНЦ
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11
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Mironov M.E.
, Rybalova T.V.
, Pokrovskii M.A.
, Emaminia F.
, Gandalipov E.R.
, Pokrovskii A.G.
, Shults E.E.
Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents
Steroids. 2023.
V.190. P.109133. DOI: 10.1016/j.steroids.2022.109133
WOS
РИНЦ
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12
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Mironov M.E.
, Shults E.E.
Synthesis and transformations of 2,4-dioxa- and 2,4-diazaspiro[5.5]undecanones equipped with a diterpenoid substituent
Russian Chemical Bulletin. 2023.
V.72. N10. P.2453-2465. DOI: 10.1007/s11172-023-4047-z
WOS
Scopus
РИНЦ
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13
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Черемных К.П.
, Савельев В.А.
, Скорова А.Б.
, Шульц Э.Э.
Синтез 2,4-диарилзамещенных 3H-1,5-бензодиазепинов последовательной трехкомпонентной реакцией 5-(этинил)метилантранилата, бензоилхлоридов и о-фенилендиамина
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
№6. С.746-752. DOI: 10.15372/KhUR2023522
РИНЦ
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14
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Харитонов Ю.В.
, Петрова Д.А.
, Шульц Э.Э.
, Покровский М.А.
, Покровский А.Г.
Синтез и оценка цитотоксичности фуранолабданоидов, содержащих 3-аминопропаноильный заместитель в фурановом цикле
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
№6. С.737-745. DOI: 10.15372/KhUR2023521
РИНЦ
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15
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CHEREMNYKH K.P.
, SAVELYEV V.A.
, SKOROVA A.B.
, SHULTS E.E.
SYNTHESIS OF 2,4-DIARYLSUBSTITUTED 3H-1,5-BENZODIAZEPINES BY A CONSECUTIVE THREE-COMPONENT REACTION OF 5-(ETHYNYL)METHYLANTHRANILATE WITH BENZOYL CHLORIDES AND O-PHENYLENEDIAMINE
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
V.31. N6. P.724-730. DOI: 10.15372/CSD2023522
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РИНЦ
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16
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KHARITONOV Y.V.
, PETROVA D.A.
, SHULTS E.E.
, POKROVSKII M.A.
, POKROVSKII A.G.
SYNTHESIS AND EVALUATION OF THE CYTOTOXICITY OF FURANOLABDANOIDS CONTAINING A 3-AMINOPROPANOYL SUBSTITUENT IN THE FURAN RING
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2023.
V.31. N6. P.715-723. DOI: 10.15372/CSD2023521
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РИНЦ
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17
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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
WOS
Scopus
РИНЦ
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18
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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
WOS
Scopus
РИНЦ
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19
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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
WOS
РИНЦ
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20
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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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РИНЦ
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