Shulʹts Élʹvira Éduardovna

Science activity

Articles - 274

Articles (274) More info

1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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 WOS РИНЦ
10	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 WOS РИНЦ
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	Gromova M.A. , Kharitonov Y.V. , Politanskaya L.,.V. , Tretyakov E.,.V. , Shults E.E. A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles Journal of Fluorine Chemistry. 2020. V.236. 109554 . DOI: 10.1016/j.jfluchem.2020.109554 WOS Scopus РИНЦ
33	Brusentseva O.I. , Kharitonov Y.V. , Dolgikh M.P. , Tolstikova T.G. , Shul'ts E.E. Synthesis and Analgesic Activity Assessment of Furanolabdanoid Conjugates with Glucuronic Acid Chemistry of Natural Compounds. 2020. V.56. N4. P.678-687. DOI: 10.1007/s10600-020-03119-7 WOS Scopus РИНЦ
34	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
35	Sirazhetdinova N.S. , Savelyev V.A. , Frolova T.S. , Baev D.S. , Klimenko L.S. , Chernikov I.V. , Oleshko O.S. , Sarojan T.A. , Pokrovskii A.G. , Shults E.E. 1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents Molecules. 2020. V.25. N11. 2547 . DOI: 10.3390/molecules25112547 WOS Scopus
36	Lipeeva A.V. , Dolgikh M.P. , Tolstikova T.G. , Shults E.E. A Study of Plant Coumarins. 18. Conjugates of Coumarins with Lupane Triterpenoids and 1,2,3-Triazoles: Synthesis and Anti-Inflammatory Activity Russian Journal of Bioorganic Chemistry. 2020. V.46. N2. P.125-132. DOI: 10.1134/S1068162020010161 WOS Scopus РИНЦ
37	Mironov M.E. , Poltanovich A.I. , Rybalova T.V. , Dolgikh M.P. , Tolstikova T.G. , Shults E.E. Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety Russian Chemical Bulletin. 2020. V.69. N3. P.537-546. DOI: 10.1007/s11172-020-2795-6 WOS Scopus РИНЦ
38	Lenskiy M.A. , Shul'ts E.E. , Korabel'nikov D.V. , Ozhogin A.V. , Novitskiy A.N. Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process Polymer. 2020. V.188. 122162 . DOI: 10.1016/j.polymer.2020.122162 WOS Scopus РИНЦ
39	Amanzhan A. , Zhanymkhanova P.Z. , Aidanuly B. , Shults E.E. , Turmukhambetov A.Z. , Adekenov S.M. SYNTHESIS AND STRUCTURE OF HYDRAZONE DERIVATIVES OF HARMINE NEWS OF THE NATIONAL ACADEMY OF SCIENCES OF THE REPUBLIC OF KAZAKHSTAN-SERIES CHEMISTRY AND TECHNOLOGY. 2020. N3. P.88-95. DOI: 10.32014/2020.2518-1491.48 WOS
40	Lenskiy M.A. , Shults E.E. , Korabel'nikov D.,.V. , Ozhogin A.,.V. , Novitskiy A.N. SYNTHESIS AND PROPERTIES OF BORON-CONTAINING OLIGOMERS BASED ON HYDROQUINONE AND BORIC ACID Известия высших учебных заведений. Серия: Химия и химическая технология. 2020. V.63. N4. P.4-11. DOI: 10.6060/ivkkt.20206304.6116 WOS Scopus РИНЦ
41	Popov S.A. , Semenova M.D. , Baev D.S. , Frolova T.S. , Shults E.E. , Wang C. , Turks M. Synthesis of cytotoxic urs-12-ene- and 28-norurs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles Steroids. 2020. V.153. 108524 . DOI: 10.1016/j.steroids.2019.108524 WOS Scopus РИНЦ
42	Brusentzeva O.I. , Kharitonov Y.V. , Fadeev D.S. , Shults E.E. Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020. V.96. N3-4. P.245-250. DOI: 10.1007/s10847-019-00965-z WOS Scopus
43	Urbagarova B.M. , Shults E.E. , Taraskin V.V. , Radnaeva L.D. , Petrova T.N. , Rybalova T.V. , Frolova T.S. , Pokrovskii A.G. , Ganbaatar J. Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity Journal of Ethnopharmacology. 2020. V.261. 112517 . DOI: 10.1016/j.jep.2019.112517 WOS Scopus РИНЦ
44	Popov S.A. , Semenova M.D. , Baev D.S. , Frolova T.S. , Shestopalov M.A. , Wang C. , Qi Z. , Shults E.E. , Turks M. Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole Steroids. 2020. V.162. 108698 . DOI: 10.1016/j.steroids.2020.108698 WOS Scopus РИНЦ
45	Gromova M.A. , Kharitonov Y.V. , Rybalova T.V. , Shults E.E. Synthetic studies on tricyclic diterpenoids: convenient synthesis of 16-arylisopimaranes Monatshefte für Chemie Chemical Monthly. 2020. V.151. N12. P.1817-1827. DOI: 10.1007/s00706-020-02713-3 WOS Scopus РИНЦ
46	Cheremnykh K.P. , Savelyev V.A. , Borisov S.A. , Ivanov I.D. , Baev D.S. , Tolstikova T.G. , Vavilin V.A. , Shults E.E. Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency Molecules. 2020. V.25. N23. 5578; . DOI: 10.3390/molecules25235578 WOS Scopus РИНЦ
47	Lipeeva A.V. , Zakharov D.O. , Gatilov Y.V. , Pokrovskii M.A. , Pokrovskii A.G. , Shults E.E. Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin ChemistrySelect. 2019. V.4. N34. P.10197-10201. DOI: 10.1002/slct.201901377 WOS Scopus РИНЦ
48	Savel'ev V.A. , Kotova A.A. , Rybalova T.V. , Shults E.E. Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles Containing an Anthranilic Acid Motif Chemistry of Heterocyclic Compounds. 2019. V.55. N10. P.943-955. DOI: 10.1007/s10593-019-02561-y WOS Scopus РИНЦ
49	Lenskiy M.A. , Shul'ts E.E. , Korabel'nikov D.,.V. , Ozhogin A.,.V. , Novitskiy A.N. Synthesis of Polyesters of Diatomic Phenols and Boric Acid and Their Interaction with Formaldehyde Polymer Science - Series B. 2019. V.61. N5. P.530-539. DOI: 10.1134/S1560090419050105 WOS Scopus РИНЦ
50	Krysin A.P. , Tolstikova T.G. , Dolgikh M.P. , Shul'ts E.E. , Pokrovskii L.M. SYNTHESIS AND ANTI-INFLAMMATORY ACTIVITY OF TYROSOL AND ITS STRUCTURAL ANALOGS Pharmaceutical Chemistry Journal. 2019. V.52. N11. P.907-911. DOI: 10.1007/s11094-019-01924-1 WOS Scopus РИНЦ

Identifiers

Scopus ID: 57218561188 , 57194489645 , 57220502258

ORCID: 0000-0002-0761-9696

ResearcherID: I-3916-2014

Elibrary ID: 44936