Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Tetyana Beryozkina"'
Autor:
Vladimir Ilkin, Vera Berseneva, Tetyana Beryozkina, Tatiana Glukhareva, Lidia Dianova, Wim Dehaen, Eugenia Seliverstova, Vasiliy Bakulev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2937-2947 (2020)
N-Sulfonyl amidines bearing 1,2,3-triazole, isoxazole, thiazole and pyridine substituents were successfully prepared for the first time by reactions of primary, secondary and tertiary heterocyclic thioamides with alkyl- and arylsulfonyl azides. For e
Externí odkaz:
https://doaj.org/article/a4fcdef1bc294383ab11cf9ccbdfada8
Autor:
Konstantin L. Obydennov, Nadezhda A. Galieva, Vasiliy A. Bakulev, Tatiana V. Glukhareva, T. A. Kalinina, Tetyana Beryozkina, Zhijin Fan, Yue Zhang
Publikováno v:
Journal of Agricultural and Food Chemistry. 69:12048-12062
This work deals with the synthesis and evaluation of fungicidal activity of benzimidazole derivatives, which are structural analogues of commercial anti-tubulin fungicides. A number of N-acyl and N-thioacyl derivatives of 2-amino-1H-benzo[d]imidazole
Autor:
Tetyana Beryozkina, Nadezhda A. Galieva, Dmitriy A. Saveliev, Zhijin Fan, Gert Lubec, Jihong Xing, Oleg S. Eltsov, Vasiliy A. Bakulev
Publikováno v:
Mendeleev Communications. 31:495-497
The reactions of N-(benz[d]oxazol-2-yl)- or N-(benzo[d]-thiazol-2-yl)-substituted carbothioamides with sulfonyl azides proceed as replacement of thioxo substituent by the sulfonylimino group to afford the corresponding N'-sulfonylated amidines. Aceti
Autor:
Vladimir G. Ilkin, Vera S. Berseneva, Lidiya N. Dianova, Vasiliy A. Bakulev, Dmitry A. Saveliev, Tetyana Beryozkina
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1335-1340
The rearrangement of 5-amino-1-aryl-1,2,3-triazole-4-carbothioamides was investigated. The process was optimized by varying the solvent, temperature, and the type of base. The optimal reaction conditions were found, and new 1-unsubstituted 5-arylamin
Autor:
Valeriy O. Filimonov, Tetyana Beryozkina, Vasiliy А. Bakulev, Zhijin Fan, Pavel А. Slepukhin, Lidiya N. Dianova
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1341-1347
The reaction of 5-amino-1-aryl-1,2,3-triazole-4-carbothioamides with sulfonyl chlorides and acetyl and benzoyl chlorides is accompanied by the Dimroth rearrangement and proceeds regiospecifically with the formation of 5-arylamino-2-sulfonyl(acyl)-1,2
Publikováno v:
Journal of Heterocyclic Chemistry. 57:3173-3185
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c99869ec5b5da90f04dd5690ec83e81e
https://doi.org/10.1016/b978-0-12-409547-2.14792-4
https://doi.org/10.1016/b978-0-12-409547-2.14792-4
Autor:
Enrique Caldera‐Cruz, Kenan Zhang, Takuya Tsuda, Roman Tkachov, Tetyana Beryozkina, Nataliya Kiriy, Brigitte Voit, Anton Kiriy
Publikováno v:
Advanced Materials Interfaces
A pair of hole-conducting polymers comprising 3,6-linked carbazole and meta-linked anisole derivatives having solubilizing moieties to enable their solution processability, and complementarily reactive side-groups (azide and alkyne) for cross-linking
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e322e7b08d14eff79bf5cd7eb0f5ee35
https://hdl.handle.net/10995/118317
https://hdl.handle.net/10995/118317
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:704-715
Synthesis of 4-acetyl-substituted azoles (1,2,3-triazole, 1,2,3-thiadiazole, and 1,2-oxazole) is reported. Organocatalytic reactions of 4-acetyl-1,2,3-triazoles with aryl azides were used to obtain bis-1,2,3-triazoles containing directly linked ring
Autor:
Tatiana А. Pospelova, Dmitriy M. Mazur, Lidiya N. Dianova, Vasiliy А. Bakulev, Valeriy O. Filimonov, Tetyana Beryozkina, Pavel А. Slepukhin
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:547-553
Sulfonylation of 1,2,3-thiadiazolecarboxylic acid amidines in the presence of a base was found to be accompanied by the Cornforth rearrangement of the 1,2,3-thiadiazole ring into 1,2,3-triazole leading to the formation of 2-substituted 1,2,3-triazole