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Статьи (122)

# Публикация
21 Larin A.A. , Dubasova E.V. , Ananyev I.V. , Monogarov K.A. , Gazieva G.A. , Fershtat L.L.
New energetic 1,2,4‐triazole‐nitrofuroxan hybrids
Journal of Heterocyclic Chemistry. 2024. V.61. N5. P.713-722. DOI: 10.1002/jhet.4797 WOS Scopus OpenAlex
22 Serkov S.A. , Sigay N.V. , Kostikova N.N. , Tyurin A.P. , Kolotyrkina N.G. , Gazieva G.A.
Synthesis of 5-oxo-1-[4-(aminosulfonyl)phenyl]pyrrolidine-3-carboxylic acids
Russian Chemical Bulletin. 2024. V.73. N5. P.1273-1279. DOI: 10.1007/s11172-024-4243-5 WOS Scopus OpenAlex
23 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
24 Lugovoi M.E. , Izmest’ev A.N. , Kolotyrkina N.G. , Izmalkova E.S. , Kravchenko A.N. , Gazieva G.A.
Synthesis of new heterylmethylidene derivatives of isomeric imidazo[4,5-e]thiazolo-fused [1,2,4]triazines
Mendeleev Communications. 2024. V.34. N4. P.558-560. DOI: 10.1016/j.mencom.2024.06.029 WOS Scopus OpenAlex
25 Serkov S.A. , Kostikova N.N. , Sigay N.V. , Tyurin A.P. , Kolotyrkina N.G. , Gazieva G.A.
The synthesis and study of antimicrobial activity of 5-oxo-1-(thiazol-2-yl)pyrrolidine-3-carboxylic acids
Chemistry of Heterocyclic Compounds. 2024. V.60. N7-8. P.365-370. DOI: 10.1007/s10593-024-03348-6 WOS Scopus OpenAlex
26 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
27 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
28 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
29 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
30 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
31 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
32 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
33 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
34 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
35 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
36 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
37 Izmest'ev A.N. , Motornov V.A. , Vinogradov D.B. , Ioffe S.L. , Kravchenko A.N. , Gazieva G.A.
Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes
Organic Chemistry Frontiers. 2022. V.9. N18. P.4998-5004. DOI: 10.1039/d2qo00911k 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 Serkov S.A. , Sigai N.V. , Kostikova N.N. , Fedorov A.E. , Gazieva G.A.
Synthesis and evaluation of cytotoxicity of S-substituted 5-sulfanylmethyl(ethyl)-1,3,4-thiadiazol-2-amines
Russian Chemical Bulletin. 2022. V.71. N8. P.1801-1805. DOI: 10.1007/s11172-022-3592-1 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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