Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Vera V. Astakhova"'
Publikováno v:
Molecules, Vol 27, Iss 20, p 6910 (2022)
Allyl halides with triflamide under oxidative conditions form halogen-substituted amidines. Allyl cyanide reacts with triflamide in acetonitrile or THF solutions in the presence of NBS to give the products of bromotriflamidation with a solvent interc
Externí odkaz:
https://doaj.org/article/cfd6a7a7fb964977b95d7784f049bca1
Autor:
Mikhail Y. Moskalik, Vera V. Astakhova
Publikováno v:
Molecules, Vol 27, Iss 16, p 5201 (2022)
Among the variety of sulfonamides, triflamides (CF3SO2NHR, TfNHR) occupy a special position in organic chemistry. Triflamides are widely used as reagents, efficient catalysts or additives in numerous reactions. The reasons for the widespread use of t
Externí odkaz:
https://doaj.org/article/0492febf73ef498fa1c5d1358823b091
Autor:
Bagrat A. Shainyan, Nina N. Chipanina, Larisa P. Oznobikhina, Irina V. Sterkhova, Mikhail Yu. Moskalik, Vera V. Astakhova, Anton S. Ganin
Publikováno v:
Structural Chemistry. 34:139-152
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c27a2bcdb3e32498b5df3bf971c05ad3
https://doi.org/10.1007/s11224-022-02032-9
https://doi.org/10.1007/s11224-022-02032-9
Autor:
Bagrat A. Shainyan, Nina N. Chipanina, Larisa P. Oznobikhina, Irina V. Sterkhova, Vera V. Astakhova, Mikhail Yu. Moskalik
Publikováno v:
Structural Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea143703506a03974ab89db4d970d12d
https://doi.org/10.1007/s11224-023-02127-x
https://doi.org/10.1007/s11224-023-02127-x
Autor:
Ivan A. Garagan, Mikhail Yu. Moskalik, Vera V. Astakhova, Irina V. Sterkhova, Alexander V. Vashchenko, Alexander I. Albanov, Bagrat A. Shainyan
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fa47f500a5c49dcc66c8845d7cf9795
https://doi.org/10.1002/slct.202202231
https://doi.org/10.1002/slct.202202231
Publikováno v:
RSC Advances. 10:40514-40528
Oxidative sulfonamidation of divinylsilanes with various sulfonamides in different solvents is reported. With t-BuOI as an oxidant, halogenation is the main process, whereas aziridines are the minor products. With NBS in CH2Cl2 the products of bromin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68fd02cb0b9f7120ec29da5df7441deb
https://doi.org/10.1039/d0ra07469a
https://doi.org/10.1039/d0ra07469a
Publikováno v:
Journal of Organometallic Chemistry. 978:122473
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b61d689402663079d624e740b7b8f367
https://doi.org/10.1016/j.jorganchem.2022.122473
https://doi.org/10.1016/j.jorganchem.2022.122473
Publikováno v:
Tetrahedron. 75:4531-4541
The reaction of trimethyl(vinyl)silane 1 and dimethyl(divinyl)silane 2 with various sulfonamides in the oxidative system (tert-BuOCl + NaI) has been studied and shown to be an efficient approach for the synthesis of silylated N-heterocycles. Triflami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84995656a17140008ebacf66e55eac4c
https://doi.org/10.1016/j.tet.2019.06.045
https://doi.org/10.1016/j.tet.2019.06.045
Autor:
Yanina V. Burgart, Mikhail Yu. Moskalik, A. A. Tyutyunov, Valery N. Charushin, Victor I. Saloutin, Galina N. Lipunova, Lyubov N. Sobenina, Pavel V. Nikul'Shin, Andrei B. Koldobskii, Vera V. Astakhova, Daria V. Vorobyeva, Nicolay Yu. Adonin, Salekh M. Masoud, Larisa V. Politanskaya, Vasiliy M. Muzalevskiy, Bagrat A. Shainyan, E. V. Panteleeva, Sema L. Ioffe, Evgeny V. Shchegolkov, Aleksey Yu. Aksinenko, Emiliya V. Nosova, Vyacheslav Ya. Sosnovskikh, Sergei M. Igumnov, Vadim V. Bardin, Evgeny V. Tretyakov, Vladimir Eduardovich Boiko, Tatyana V. Mezhenkova, Sergey N. Osipov, Galina A. Selivanova, Dmitrii L. Obydennov, Sergey A. Usachev, Valentine G. Nenajdenko, Boris A. Trofimov, Arkady G. Makarov, Vyacheslav E. Platonov, E. S. Balenkova, Victor M. Karpov, Aleksander V. Vasilyev, Andrey V. Zibarev, Kseniya V. Belyaeva, Alexey V. Shastin, Darya O. Prima, Andrey S. Vinogradov, V. B. Sokolov, Sofia M. Morozova, Alexander D. Dilman, Yaroslav V. Zonov, Andrey A. Tabolin, Olga S. Shilova
Publikováno v:
Russian Chemical Reviews. 88:425-569
Currently, the chemistry of organofluorine compounds is a leading and rapidly developing area of organic chemistry. Fluorine present in a molecule largely determines its specific chemical and biological properties. This thematic issue covers the tren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1e3c713e514b517dfee714264b81884
https://doi.org/10.1070/rcr4871
https://doi.org/10.1070/rcr4871
Publikováno v:
Organic & Biomolecular Chemistry. 17:7927-7937
The reaction of trimethyl(vinyl)silane with sulfonamides in the presence of N-bromosuccinimide was shown to proceed regioselectively in methylene chloride under mild conditions and led to the products of bromosulfamidation in up to 88% yield. The obt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb885ca7dea30fdc906b4e36e4f2b73
https://doi.org/10.1039/c9ob01689a
https://doi.org/10.1039/c9ob01689a