Articles - Sciact

Articles (121)

#	Публикация
21	Gazieva G.A. , Chegaev K. Special Issue “Development and Synthesis of Biologically Active Compounds” International Journal of Molecular Sciences. 2024. V.25. N7. 4015 . DOI: 10.3390/ijms25074015 WOS Scopus OpenAlex
22	Izmest’ev A.N. , Isakov S.S. , Kravchenko A.N. , Gazieva G.A. The synthesis and antitumor activity of novel 1-alkyl-3-phenyland 3-alkyl-1-phenylimidazothiazolotriazines Chemistry of Heterocyclic Compounds. 2024. V.60. P.196-204. DOI: 10.1007/s10593-024-03318-y WOS Scopus OpenAlex
23	Izmest'ev A.N. , Svirshchevskaya E.V. , Akopov S.B. , Kravchenko A.N. , Gazieva G.A. Recognition of arylmetylidene derivatives of imidazothiazolotriazinones as novel tubulin polymerization inhibitors RSC Medicinal Chemistry. 2024. V.15. N4. P.1258-1273. DOI: 10.1039/d4md00027g WOS Scopus OpenAlex
24	Vinogradova E. , Karnoukhova V. , Kravchenko A.N. , Gazieva G.A. Construction of New Heterocyclic System, Imidazo[4,5‐d]thiazolo[4,3‐b]oxazole, via Cascade Reaction of Thioglycolurils with α‐Bromoketones Asian Journal of Organic Chemistry. 2024. V.13. N11. e202400369 . DOI: 10.1002/ajoc.202400369 WOS Scopus OpenAlex
25	Vinogradov D.B. , Izmest'ev A.N. , Kravchenko A.N. , Strelenko Y.A. , Gazieva G.A. Synthesis of imidazo[4,5-e][1,3]thiazino[2,3-c][1,2,4]triazines via a base-induced rearrangement of functionalized imidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazines Beilstein Journal of Organic Chemistry. 2023. V.19. P.1047-1054. DOI: 10.3762/bjoc.19.80 WOS Scopus OpenAlex
26	Vinogradova E.E. , Kravchenko A.N. , Gazieva G.A. One‐pot regioselective synthesis of new imidazo[4,5‐e]thiazolo[3,2‐b][1,2,4]triazines by reaction of imidazotriazines with propargyl bromide Journal of Heterocyclic Chemistry. 2023. V.60. N9. P.1609-1618. DOI: 10.1002/jhet.4706 WOS Scopus OpenAlex
27	Izmest’ev A.N. , Streltsov A.A. , Kravchenko A.N. , Gazieva G.A. 5-Arylmethylidene-2-iminothiazolidin-4-ones in the synthesis of novel dispiro-fused oxindolepyrrolidineiminothiazolidinones Chemistry of Heterocyclic Compounds. 2023. V.59. N4-5. P.309-316. DOI: 10.1007/s10593-023-03198-8 WOS Scopus OpenAlex
28	Vinogradova E.E. , Alekseenko A.L. , Popkov S.V. , Kolotyrkina N.G. , Kravchenko A.N. , Gazieva G.A. Synthesis and Evaluation on the Fungicidal Activity of S-Alkyl Substituted Thioglycolurils International Journal of Molecular Sciences. 2023. V.24. N6. 5756 . DOI: 10.3390/ijms24065756 WOS Scopus OpenAlex
29	Izmest′ev A.N. , Vinogradov D.B. , Kravchenko A.N. , Kolotyrkina N.G. , Gazieva G.A. Diastereoselective Synthesis of Dispiro[Imidazothiazolotriazine-Pyrrolidin-Oxindoles] and Their Isomerization Pathways in Basic Medium International Journal of Molecular Sciences. 2023. V.24. N22. 16359 . DOI: 10.3390/ijms242216359 WOS Scopus OpenAlex
30	Izmest'ev A.N. , Kravchenko A.N. , Gazieva G.A. A new reversible transformation of oxindolylidene derivatives of imidazothiazolotriazine into 3-[(imidazotriazin-3-yl)thio]-2-oxoquinoline-4-carboxylates Organic & Biomolecular Chemistry. 2023. V.21. N8. P.1827-1834. DOI: 10.1039/d2ob02242g WOS Scopus OpenAlex
31	Belen’kii L.I. , Gazieva G.A. , Evdokimenkova Y.B. , Soboleva N.O. The literature of heterocyclic chemistry, Part XX, 2020 Advances in Heterocyclic Chemistry. 2023. P.201-274. DOI: 10.1016/bs.aihch.2022.10.005 WOS Scopus OpenAlex
32	Serkov S.A. , Sigay N.V. , Kostikova N.N. , Tyurin A.P. , Kolotyrkina N.G. , Gazieva G.A. Synthesis of 5-oxo-1-(5-R-1,3,4-thiadiazol-2-yl)pyrrolidine-3-carboxylic acids Russian Chemical Bulletin. 2023. V.72. N8. P.1837-1843. DOI: 10.1007/s11172-023-3966-z WOS Scopus OpenAlex
33	Izmest’ev A.N. , Kravchenko A.N. , Gazieva G.A. A 1,3-dipolar cycloaddition of azomethine ylides to imidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazine oxindolylidene derivatives in the synthesis of novel spirooxindole derivatives Chemistry of Heterocyclic Compounds. 2023. V.59. N8. P.594-603. DOI: 10.1007/s10593-023-03238-3 WOS Scopus OpenAlex
34	Izmest'ev A.N. , Anikina L.V. , Zanin I.E. , Kolotyrkina N.G. , Ekaterina I.S. , Kravchenko A.N. , Gazieva G.A. Design, synthesis and in vitro evaluation of the hybrids of oxindolylidene and imidazothiazolotriazine as efficient antiproliferative agents New Journal of Chemistry. 2022. V.46. N24. P.11632-11647. DOI: 10.1039/d2nj01454h WOS Scopus OpenAlex
35	Larin A.A. , Ananyev I.V. , Dubasova E.V. , Teslenko F.E. , Monogarov K.A. , Khakimov D.V. , He C-l. , Pang S-p. , Gazieva G.A. , Fershtat L.L. Simple and energetic: Novel combination of furoxan and 1,2,4-triazole rings in the synthesis of energetic materials Energetic Materials Frontiers. 2022. V.3. N3. P.146-153. DOI: 10.1016/j.enmf.2022.08.002 Scopus OpenAlex
36	Izmest'ev A.N. , Streltsov A.A. , Karnoukhova V.A. , Kolotyrkina N.G. , Strelenko Y.A. , Kravchenko A.N. , Gazieva G.A. 5‐Indolylidene‐2‐iminothiazolidin‐4‐ones – Convenient Starting Compounds for Stereoselective Synthesis of Novel Dispirooxindole Derivatives ChemistrySelect. 2022. V.7. N2. e202104128 . DOI: 10.1002/slct.202104128 WOS Scopus OpenAlex
37	Kuptsova A.O. , Vinogradova E.E. , Kravchenko A.N. , Gazieva G.A. Methods for substitution of the thioxo group with the oxo group in imidazolidine-2-thione derivatives Russian Chemical Bulletin. 2022. V.71. N5. P.885-904. DOI: 10.1007/s11172-022-3488-0 WOS Scopus OpenAlex
38	Izmest’ev A.N. , Streltsov A.А. , Kravchenko A.N. , Gazieva G.А. The Chemo- and Regioselectivity of the Cyclization of Thiosemicarbazides with Haloacetic Acids and their Derivatives Chemistry of Heterocyclic Compounds. 2022. V.58. N10. P.483-492. DOI: 10.1007/s10593-022-03117-3 WOS Scopus OpenAlex
39	Vinogradov D.B. , Izmest’ev A.N. , Kravchenko A.N. , Gazieva G.А. A regioselective synthesis of imidazothiazolotriazines based on the cyclization of imidazotriazinethiones with phenacyl bromides Chemistry of Heterocyclic Compounds. 2022. V.58. N10. P.524-530. DOI: 10.1007/s10593-022-03123-5 WOS Scopus OpenAlex
40	Izmest’ev A.N. , Karnoukhova V.A. , Larin A.A. , Kravchenko A.N. , Fershtat L.L. , Gazieva G.A. Synthesis, Structure and Stereochemistry of Dispirocompounds Based on Imidazothiazolotriazine and Pyrrolidineoxindole International Journal of Molecular Sciences. 2022. V.23. N22. 13820 . DOI: 10.3390/ijms232213820 WOS Scopus OpenAlex

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