Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Vera S. Berseneva"'
Autor:
Pavel S. Silaichev, Lidia N. Dianova, Tetyana V. Beryozkina, Vera S. Berseneva, Andrey N. Maslivets, Vasiliy A. Bakulev
Publikováno v:
Molecules, Vol 28, Iss 8, p 3576 (2023)
The reaction of 3,3-diaminoacrylonitriles with DMAD and 1,2-dibenzoylacetylene was studied. It is shown that the direction of the reaction depends on the structure both of acetylene and of diaminoacrylonitrile. In the reaction of DMAD with acrylonitr
Externí odkaz:
https://doaj.org/article/8f62331778c240da8aec6a85ccfe7ad2
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a771357ab12d2af49c315975fc448c1
https://doi.org/10.1007/s10593-020-02819-w
https://doi.org/10.1007/s10593-020-02819-w
Autor:
Leila K. Sadieva, Igor S. Kovalev, Olga S. Taniya, Vadim A. Platonov, Alexander S. Novikov, Vera S. Berseneva, Sougata Santra, Grigory V. Zyryanov, Brindaban C. Ranu, Valery N. Charushin
Publikováno v:
Dyes and Pigments. 210:111014
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b72c64ae0a220a3db19853aeace5ee2f
https://doi.org/10.1016/j.dyepig.2022.111014
https://doi.org/10.1016/j.dyepig.2022.111014
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:1153-1160
A three-step method was designed and developed on the basis of retrosynthetic analysis for the synthesis of hybrid molecules containing a thiazole ring and an N-sulfonyl amidine fragment, connected by a methylene linker. The mechanism of the last ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::755600ab3718456ae8d409af96efcf78
https://doi.org/10.1007/s10593-019-02407-7
https://doi.org/10.1007/s10593-019-02407-7
Autor:
Wim Dehaen, Vera S. Berseneva, Tatiana V. Glukhareva, Vasiliy A. Bakulev, Vladimir G. Ilkin, Lidia Dianova, Eugenia Seliverstova, Tetyana Beryozkina
Publikováno v:
Beilstein J. Org. Chem.
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2937-2947 (2020)
Beilstein Journal of Organic Chemistry
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::113aa38cd1e8e555d00afda0f66dc56e
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098581931&doi=10.3762/BJOC.16.243&partnerID=40&md5=b1f1f0316806f1a0c034b46e936aae18
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098581931&doi=10.3762/BJOC.16.243&partnerID=40&md5=b1f1f0316806f1a0c034b46e936aae18
Autor:
Igor S. Kovalev, O. S. Ermakova, M. I. Kodess, Yu. A. Azev, Vera S. Berseneva, Marina A. Ezhikova
Publikováno v:
Chemistry of Natural Compounds. 53:519-522
6,7-Difluoroquinoxaline (1) reacted with 1- and 2-methylindoles (2a and 2b) with heating in AcOH to give products from substitution of H in the heterocyclic fragment (3a and 3b) and tris(indol-3-yl)methane derivatives (4a and 4b).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7125196a818aec87cd98257261d55a54
https://doi.org/10.1007/s10600-017-2036-x
https://doi.org/10.1007/s10600-017-2036-x
Autor:
Yu. A. Azev, Marina A. Ezhikova, Vera S. Berseneva, Vasiliy A. Bakulev, M. I. Kodess, O. S. Ermakova
Publikováno v:
Russian Journal of Organic Chemistry. 53:90-95
6,7-Difluoroquinoxalin-2-one reacted with indoles, 5,5-dimethylcyclohexane-1,3-dione, 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one, resorcinol, and pyrogallol on heating in acetic acid to give products of hydrogen substitution in the heterocyclic fragment.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::131dae360f81bad1bf4ed7ba7aabc3c0
https://doi.org/10.1134/s107042801701016x
https://doi.org/10.1134/s107042801701016x
Publikováno v:
Russian Journal of General Chemistry. 86:2442-2445
Reaction of benzocaine with indane-1,3-dione-2-carbaldehyde afforded the corresponding azomethine. Ethoxymethylenemalonate reacted with benzocaine to form ethyl 4-{[2-(ethoxycarbonyl)-4-methoxy-3-oxobuten-1-yl]amino}benzoate, which was converted to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f93243f3aaaa8b18474666d4a59f234
https://doi.org/10.1134/s1070363216110074
https://doi.org/10.1134/s1070363216110074
Autor:
Maria A. Kostenko, Pavel A. Slepukhin, Vera S. Berseneva, Valeriy O. Filimonov, Tetyana Beryozkina, Kristina A. Galata, Vladimir T. Abaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:721-726
The reaction of 2-azidobenzaldehydes with 2-thioamides of cyanoacetic acid proceeds without a solvent and base at 80–90°C selectively by one of the possible routes to form tetrazolo[1,5-a]quinolines. The proposed mechanism of the reaction involves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c18f631e6d50d806ce3483db64e7711a
https://doi.org/10.1007/s10593-016-1954-z
https://doi.org/10.1007/s10593-016-1954-z
Autor:
Vera S. Berseneva, Gert Lubec, Predrag Kalaba, Tetyana Beryozkina, Lidia Dianova, Pavel A. Slepukhin, Johann Leban, Vasiliy A. Bakulev, Harald H. Sitte, Marija Ilic, Nilima Y. Aher
Publikováno v:
Synthesis. 48:1046-1054
A design and a convenient approach for the synthesis of novel N-sulfonyl-2-diphenylmethylsulfinylacetamidines have been demonstrated by starting from benzhydrylsulfanylacetic (BSA) acid. This approach involves a sequential amidation with amines, thio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5958e3bd51e44fc3051d1ea5acb0501
https://doi.org/10.1055/s-0035-1561350
https://doi.org/10.1055/s-0035-1561350