Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sergey Baykov"'
Autor:
Marina Tarasenko, Vera Sidneva, Alexandra Belova, Anna Romanycheva, Tatyana Sharonova, Sergey Baykov, Anton Shetnev, Eugeniy Kofanov, Mikhail Kuznetsov
Publikováno v:
ARKIVOC, Vol 2018, Iss 7, Pp 458-470 (2018)
Externí odkaz:
https://doaj.org/article/2dede4c59713482cb25a60f10021aee8
Autor:
Anton Shetnev, Sergey Baykov, Stanislav Kalinin, Alexandra Belova, Vladimir Sharoyko, Anton Rozhkov, Lev Zelenkov, Marina Tarasenko, Evgeny Sadykov, Mikhail Korsakov, Mikhail Krasavin
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 7, p 1699 (2019)
Replacement of amide moiety with the 1,2,4-oxadiazole core in the scaffold of recently reported efflux pump inhibitors afforded a novel series of oxadiazole/2-imidazoline hybrids. The latter compounds exhibited promising antibacterial activity on bot
Externí odkaz:
https://doaj.org/article/ddfc985590c44eab971047eeec1fdda5
Publikováno v:
International Journal of Chemical Engineering, Vol 2015 (2015)
Ribavirin is an important antiviral drug, which is used for treatment of many diseases. The pilot-scale chemoenzymatic process for synthesis of the active pharmaceutical ingredient Ribavirin was developed with 32% overall yield and more than 99.5% pu
Externí odkaz:
https://doaj.org/article/437d0559dff245c3b3a9080a37208b27
Autor:
Anton Shetnev, Marina Tarasenko, Valentina Kotlyarova, Sergey Baykov, Kirill Geyl, Svetlana Kasatkina, Nikolina Sibinčić, Vladimir Sharoyko, Elizaveta V. Rogacheva, Liudmila A. Kraeva
Publikováno v:
Molecular Diversity. 27:651-666
A new route to 5-amino-1,2,4-thiadiazole derivatives via reaction of N-chloroamidines with isothiocyanates has been proposed. The advantages of this method are high product yields (up to 93%), the column chromatography-free workup procedure, scalabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a40eee4da3caabd1424001cb4067957f
https://doi.org/10.1007/s11030-022-10445-1
https://doi.org/10.1007/s11030-022-10445-1
Autor:
Ekaterina Podrezova, Alina Okhina, Artem Rogachev, Sergey Baykov, Andreas Kirschning, Mekhman Yusubov, Natalia Soldatova, Pavel Postnikov
The arylation of azaheterocycles can be considered as one of the most important processes for the preparation of various biologically active compounds. In the present work, we describe a method for the copper-catalyzed N-arylation of hindered oxazoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b1a9a2507701b85b40b386c26b60cda
https://doi.org/10.26434/chemrxiv-2022-xnmf7
https://doi.org/10.26434/chemrxiv-2022-xnmf7
Autor:
Bartomeu Galmés, Giuseppe RESNATI, Antonio Frontera, Svetlana Kasatkina, Daniil Ivanov, Sergey Baykov, Vadim Kukushkin
Publikováno v:
Chemistry – A European Journal. 28
The co-crystallization of tetracyanobenzene (TCB) with haloarenes ArX provided six new co-crystals TCB ⋅ ArX (ArX=PhCl, PhBr, 4-MeC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b369b96cd6731b29b0e9784f0d7a3d21
https://doi.org/10.1002/chem.202201869
https://doi.org/10.1002/chem.202201869
Autor:
Sergey Baykov, Marina Tarasenko, Valentina Kotlyarova, Anton Shetnev, Lev E. Zelenkov, Irina A. Boyarskaya, Vadim P. Boyarskiy
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5aebcd558b011c6e20da12c569dd5b0
https://doi.org/10.1002/slct.202201201
https://doi.org/10.1002/slct.202201201
Autor:
Natalia Soldatova, Artem Semenov, Kirill Geyl, Sergey Baykov, Anton Shetnev, Anna Konstantinova, Mikhail Korsakov, Mekhman Yusubov, Pavel Postnikov
The direct N-arylation of cyclic amides can be considered a pivotal issue for modern organic chemistry. Here, we report the method for copper-catalyzed N-arylation of diverse oxadiazolones by diaryliodonium salts in mild conditions in high yields (up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e21012af50bac1d97a30627ddd1af3
https://doi.org/10.26434/chemrxiv.14368985
https://doi.org/10.26434/chemrxiv.14368985