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21
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Finke A.O.
, Pavlova A.V.
, Morozova E.A.
, Tolstikova T.G.
, Shults E.E.
Synthesis of 1,2,3-Triazolyl-Substituted Derivatives of the Alkaloids Sinomenine and Tetrahydrothebaine on Ring A and Their Analgesic Activity
Chemistry of Natural Compounds. 2022.
V.58. N5. P.895-902. DOI: 10.1007/s10600-022-03824-5
WOS
РИНЦ
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22
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Kharitonov Y.V.
, Shults E.E.
An Approach toward 17-Arylsubstituted Marginatafuran-Type Isospongian Diterpenoids via a Palladium-Catalyzed Heck–Suzuki Cascade Reaction of 16-Bromolambertianic Acid
Molecules. 2022.
V.27. N9. P.2643. DOI: 10.3390/molecules27092643
WOS
РИНЦ
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23
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Amanzhan A.
, Zhanymkhanova P.Z.
, Bagryanskaya I.Y.
, Shults E.E.
, Turmukhambetov A.Z.
, Adekenov S.M.
STRUCTURE AND STEREOCHEMISTRY OF A HYDRAZONE DERIVATIVE OF HARMINE
Journal of Structural Chemistry. 2021.
V.62. N3. P.491-495. DOI: 10.1134/S0022476621030161
WOS
Scopus
РИНЦ
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24
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Qi Z.
, Yang G.
, Deng T.
, Wang J.
, Zhou H.
, Popov S.A.
, Shults E.E.
, Wang C.
Design and linkage optimization of ursane-thalidomide-based PROTACs and identification of their targeted-degradation properties to MDM2 protein
Bioorganic Chemistry. 2021.
V.111. 104901
. DOI: 10.1016/j.bioorg.2021.104901
WOS
Scopus
РИНЦ
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25
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Аманжан А.
, Жанымханова П.Ж.
, Багрянская И.Ю.
, Шульц Э.Э.
, Турмухамбетов А.Ж.
, Адекенов С.М.
Строение и стереохимия гидразонпроизводного гармина
Журнал структурной химии (J STRUCT CHEM+). 2021.
Т.62. №3. С.521-525. DOI: 10.26902/JSC_id69943
РИНЦ
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26
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Gromova M.A.
, Kharitonov Y.V.
, Borisov S.A.
, Baev D.S.
, Tolstikova T.G.
, Shul’ts E.E.
Synthetic Transformations of Higher Terpenoids. 39.∗ Synthesis and Analgesic Activity of Isopimaric Acid Derivatives
Chemistry of Natural Compounds. 2021.
V.57. P.474–481. DOI: 10.1007/s10600-021-03391-1
WOS
Scopus
РИНЦ
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27
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Adekenov S.M.
, Kishkentayeva A.S.
, Khasenova A.B.
, Shul’ts E.E.
, Gatilov Y.V.
, Bagryanskaya I.Y.
New Arylhalo-Derivatives of Grosshemin
Chemistry of Natural Compounds. 2021.
V.57. N4. P.685-690. DOI: 10.1007/s10600-021-03450-7
WOS
Scopus
РИНЦ
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28
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Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations
Macroheterocycles. 2021.
V.14. N1. P.105-111. DOI: 10.6060/mhc200817s
WOS
Scopus
РИНЦ
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29
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Sirazhetdinova N.S.
, Savelyev V.A.
, Baev D.S.
, Golubeva T.S.
, Klimenko L.S.
, Tolstikova T.G.
, Ganbaatar J.
, Shults E.E.
Synthesis, characterization and anticancer evaluation of nitrogen-substituted 1-(3-aminoprop-1-ynyl)-4-hydroxyanthraquinone derivatives
Medicinal Chemistry Research. 2021.
V.30. P.1541–1556. DOI: 10.1007/s00044-021-02754-1
WOS
Scopus
РИНЦ
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30
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Avdeeva E.
, Porokhova E.
, Khlusov I.
, Rybalova T.
, Shults E.
, Litvinova L.
, Shupletsova V.
, Khaziakhmatova O.
, Sukhodolo I.
, Belousov M.
Calcium chelidonate: Semi‐synthesis, crystallography, and osteoinductive activity in vitro and in vivo
Pharmaceuticals. 2021.
V.14. N6. 579
. DOI: 10.3390/ph14060579
WOS
Scopus
РИНЦ
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31
|
Popov S.A.
, Wang C.
, Qi Z.
, Shults E.E.
, Turks M.
Synthesis of water-soluble ester-linked ursolic acid–gallic acid hybrids with various hydrolytic stabilities
Synthetic Communications. 2021.
V.51. N16. P.2466-2477. DOI: 10.1080/00397911.2021.1939057
WOS
Scopus
РИНЦ
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32
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Semenova M.D.
, Popov S.A.
, Golubeva T.S.
, Baev D.S.
, Shults E.E.
, Turks M.
Synthesis and Cytotoxicity of Sulfanyl, Sulfinyl and Sulfonyl Group Containing Ursane Conjugates with 1,3,4-Oxadiazoles and 1,2,4-Triazoles
ChemistrySelect. 2021.
V.6. N25. P.6472-6477. DOI: 10.1002/slct.202101594
WOS
Scopus
РИНЦ
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33
|
Cheremnykh K.P.
, Savelyev V.A.
, Shults E.E.
An Efficient Access to 3,5-Disubstituted Isoxazoles with Anthranilate Ester Moiety: Alkaloid Lappaconitine - Aryl Conjugates with an Isoxazole Linker
Asian Journal of Organic Chemistry. 2021.
V.10. N10. P.2638-2643. DOI: 10.1002/ajoc.202100474
WOS
Scopus
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34
|
Kharitonov Y.V.
, Shul'ts E.E.
, Rybalova T.V.
, Pavlova A.V.
, Tolstikova T.G.
Synthetic Transformations of Higher Terpenoids. 40. Synthesis and Assessment of Analgesic Activity of N-Containing Derivatives of Lambertianic Acid
Chemistry of Natural Compounds. 2021.
V.57. N5. P.879-886. DOI: 10.1007/s10600-021-03502-y
WOS
Scopus
РИНЦ
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35
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Finke A.O.
, Ravaeva M.Y.
, Krasnov V.I.
, Cheretaev I.V.
, Chuyan E.N.
, Baev D.S.
, Shults E.E.
Cross-Coupling-Cyclocondensation Reaction Sequence to Access a Library of Ring-C Bridged Pyrimidino-tetrahydrothebaines and Pyrimidinotetrahydrooripavines
ChemistrySelect. 2021.
V.6. N29. P.7391-7397. DOI: 10.1002/slct.202101790
WOS
Scopus
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36
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Luginina J.
, Linden M.
, Bazulis M.
, Kumpins V.
, Mishnev A.
, Popov S.A.
, Golubeva T.S.
, Waldvogel Siegfried R. S.R.
, Shults E.E.
, Turks M.
Electrosynthesis of Stable Betulin-Derived Nitrile Oxides and their Application in Synthesis of Cytostatic Lupane-Type Triterpenoid-Isoxazole Conjugates
European Journal of Organic Chemistry. 2021.
V.2021. N17. P.2557-2577. DOI: 10.1002/ejoc.202100293
WOS
Scopus
РИНЦ
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37
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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
WOS
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РИНЦ
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38
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Ivanov I.D.
, Mosalev K.I.
, Lipeeva A.V.
, Shul'Ts E.E.
, Vavilin V.A.
ИССЛЕДОВАНИЕ МЕХАНИЗМОВ ПРОТИВОВОСПАЛИТЕЛЬНОЙ И ИММУНОМОДУЛИРУЮЩЕЙ АКТИВНОСТИ СОЕДИНЕНИЙ БЕТУЛИНОВОЙ КИСЛОТЫ С ФУРОКУМАРИНАМИ
Экспериментальная и клиническая фармакология/Eksperimental'naya i Klinicheskaya Farmakologiya. 2021.
Т.84. №6. С.28-34. DOI: 10.30906/0869-2092-2021-84-6-28-34
Scopus
РИНЦ
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39
|
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
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40
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Липеева А.В.
, Долгих М.П.
, Толстикова Т.Г.
, Шульц Е.Е.
ИССЛЕДОВАНИЕ РАСТИТЕЛЬНЫХ КУМАРИНОВ. 18. КОНЪЮГАТЫ КУМАРИНОВ С ЛУПАНОВЫМИ ТРИТЕРПЕНОИДАМИ И 1,2,3-ТРИАЗОЛАМИ: СИНТЕЗ И ПРОТИВОВОСПАЛИТЕЛЬНАЯ АКТИВНОСТЬ
Биоорганическая химия (RUSS J BIOORG CHEM+). 2020.
Т.46. №2. С.115-123. DOI: 10.31857/S0132342320010194
РИНЦ
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