Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eugenia A. Silyanova"'
Autor:
Dmitry V. Tsyganov, Alexander V. Samet, Eugenia A. Silyanova, Vladimir I. Ushkarov, Alexander E. Varakutin, Natalia B. Chernysheva, Roman N. Chuprov-Netochin, Andrey A. Khomutov, Anna S. Volkova, Sergey V. Leonov, Marina N. Semenova, Victor V. Semenov
Publikováno v:
ACS Omega, Vol 7, Iss 4, Pp 3369-3383 (2022)
Externí odkaz:
https://doaj.org/article/16dffba4f2bf43e6a6b374523bb38672
Autor:
Daniil A. Rusanov, Samah Mutasim Alfadul, Ekaterina Yu. Portnyagina, Eugenia A. Silyanova, Nikita A. Kuznetsov, Kirill E. Podpovetny, Alexander V. Samet, Victor V. Semenov, Maria V. Babak
Publikováno v:
ChemBioChem.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2eedb3797b1b038a334fbfaf12b6265
https://doi.org/10.1002/cbic.202300161
https://doi.org/10.1002/cbic.202300161
Publikováno v:
Russian Chemical Bulletin. 70:498-509
A series of 3,4-diarylpyrrole-2-carboxamides was synthesized using the Barton—Zard reaction of nitrostilbenes with ethyl isocyanoacetate in the key stage. The antiproliferative properties of these compounds were studied on a sea urchin embryo model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::159e1d22888f94fcd8212515196674db
https://doi.org/10.1007/s11172-021-3115-5
https://doi.org/10.1007/s11172-021-3115-5
Autor:
Victor V. Semenov, Victor N. Khrustalev, Alexander V. Samet, Eugenia A. Silyanova, Lev K. Salamandra
Publikováno v:
European Journal of Organic Chemistry. 2020:2093-2100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cbb00ae924fde429d5b8b783219ba52
https://doi.org/10.1002/ejoc.202000099
https://doi.org/10.1002/ejoc.202000099
Autor:
Leonid D. Konyushkin, Delphine Gorses, Alexander V. Samet, Victor V. Semenov, Marina N. Semenova, Arkady A. Dudinov, Evgenii N Khodot, Mikhail M. Krayushkin, Eugenia A. Silyanova, Alexei S. Karpov, Boris V. Lichitsky, Thomas Radimerski, Alex S. Kiselyov, Andrey N. Komogortsev
Publikováno v:
ACS Combinatorial Science. 21:805-816
1,3-Substituted pyrazolo[3,4-b]pyridinones 11-18 were synthesized by a three-component condensation of Meldrum's acid with aryl aldehydes and 1,3-substituted 5-aminopyrazoles. Their biological activity was evaluated using the in vivo phenotypic sea u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5709419948b56c9ec086d82231691b
https://doi.org/10.1021/acscombsci.9b00135
https://doi.org/10.1021/acscombsci.9b00135
Publikováno v:
Russian Chemical Bulletin. 67:2316-2319
Barton-Zard reaction of nitrostilbenes with ethyl isocyanoacetate carried out in EtOH in the presence of K2CO3 allowed us to minimize the formation of side products and to obtain 3,4-diarylpyrrole-2-carboxylates in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceca6c38d3e4b6be2a17f8a742319752
https://doi.org/10.1007/s11172-018-2375-1
https://doi.org/10.1007/s11172-018-2375-1
Autor:
Dmitry V. Demchuk, Alexander E. Varakutin, Anna S. Maksimenko, Alex S. Kiselyov, N. B. Chernysheva, Marina N. Semenova, V. P. Kislyi, Leonid D. Konyushkin, Eugenia A. Silyanova, Mikhail M. Raihstat, Victor V. Semenov, Dmitry V. Tsyganov, Alexander V. Samet
Publikováno v:
ACS Combinatorial Science. 20:700-721
A series of both novel and reported combretastatin analogues, including diarylpyrazoles, -isoxazoles, -1,2,3-triazoles, and -pyrroles, were synthesized via improved protocols to evaluate their antimitotic antitubulin activity using in vivo sea urchin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9201a126c9cf575c8c1bfb403f8a709
https://doi.org/10.1021/acscombsci.8b00113
https://doi.org/10.1021/acscombsci.8b00113
Autor:
Victor V. Semenov, Eugenia A. Silyanova, Daniil A. Rusanov, Andrey B. Myshlyavtsev, Alexander V. Samet
Publikováno v:
Mendeleev Communications. 30:485-486
3-Aryl-4-methylpyrrole-2-carboxylates were prepared via the Barton–Zard reaction using pseudonitrosites as a source of the corresponding nitroalkenes. The starting pseudonitrosites were, in turn, obtained via addition of N2O3 to propenylbenzenes av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0088dbf80cd137174065a73f485c92c7
https://doi.org/10.1016/j.mencom.2020.07.026
https://doi.org/10.1016/j.mencom.2020.07.026
Autor:
Boris V, Lichitsky, Andrey N, Komogortsev, Arkady A, Dudinov, Mikhail M, Krayushkin, Evgenii N, Khodot, Alexander V, Samet, Eugenia A, Silyanova, Leonid D, Konyushkin, Alexei S, Karpov, Delphine, Gorses, Thomas, Radimerski, Marina N, Semenova, Alex S, Kiselyov, Victor V, Semenov
Publikováno v:
ACS combinatorial science. 21(12)
1,3-Substituted pyrazolo[3,4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f31200d714d9547f6e1612bdcaa16a9e
https://pubmed.ncbi.nlm.nih.gov/31689077
https://pubmed.ncbi.nlm.nih.gov/31689077