Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marina V. Tarasenko"'
Autor:
Sofia I. Presnukhina, Marina V. Tarasenko, Kirill K. Geyl, Svetlana O. Baykova, Sergey V. Baykov, Anton A. Shetnev, Vadim P. Boyarskiy
Publikováno v:
Molecules, Vol 27, Iss 21, p 7508 (2022)
We have developed a simple and convenient method for the synthesis of 3-aryl- and 3-hetaryl-1,2,4-oxadiazin-5-ones bearing an easily functionalizable (methoxycarbonyl)methyl group at position 6 via the reaction of aryl or hetaryl amidoximes with male
Externí odkaz:
https://doaj.org/article/1cc162bff501443783ae687317da5ae2
Autor:
Sergey V. Baykov, Alexander S. Mikherdov, Alexander S. Novikov, Kirill K. Geyl, Marina V. Tarasenko, Maxim A. Gureev, Vadim P. Boyarskiy
Publikováno v:
Molecules, Vol 26, Iss 18, p 5672 (2021)
A series of N-pyridyl ureas bearing 1,2,4- (1a, 2a, and 3a) and 1,3,4-oxadiazole moiety (1b, 2b, 3b) was prepared and characterized by HRMS, 1H and 13C NMR spectroscopy, as well as X-ray diffraction. The inspection of the crystal structures of (1–3
Externí odkaz:
https://doaj.org/article/6c27243a3fb84fa9afb152b76eb94c68
Autor:
Anna S. Zalivatskaya, Dmitry S. Ryabukhin, Marina V. Tarasenko, Alexander Yu. Ivanov, Irina A. Boyarskaya, Elena V. Grinenko, Ludmila V. Osetrova, Eugeniy R. Kofanov, Aleksander V. Vasilyev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 883-894 (2017)
The metal-free reaction of 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles with arenes in neat triflic acid (TfOH, CF3SO3H), both under thermal and microwave conditions, leads to 5-(2,2-diarylethyl)-3-aryl-1,2,4-oxadiazoles. The products are formed throug
Externí odkaz:
https://doaj.org/article/d92cbb67843b4985b3c5af07f741d52c
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:349-353
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9c67bd43bb1e5f722f0bc696df2cf9e
https://doi.org/10.1007/s10593-022-03096-5
https://doi.org/10.1007/s10593-022-03096-5
Autor:
Sergey V. Baykov, Marina V. Tarasenko, Artem V. Semenov, Evgeniy A. Katlenok, Anton A. Shetnev, Vadim P. Boyarskiy
Publikováno v:
Journal of Molecular Structure. 1262:132974
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2de70a9100d65cf922243caaecf351e7
https://doi.org/10.1016/j.molstruc.2022.132974
https://doi.org/10.1016/j.molstruc.2022.132974
Autor:
Irina A. Boyarskaya, Marina V Tarasenko, Anna S. Zalivatskaya, Dmitry S. Ryabukhin, Elena V. Grinenko, Aleksander V. Vasilyev, Alexander Yu. Ivanov, Ludmila V Osetrova, E. R. Kofanov
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 883-894 (2017)
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 883-894 (2017)
The metal-free reaction of 5-(2-arylethenyl)-3-aryl-1,2,4-oxadiazoles with arenes in neat triflic acid (TfOH, CF3SO3H), both under thermal and microwave conditions, leads to 5-(2,2-diarylethyl)-3-aryl-1,2,4-oxadiazoles. The products are formed throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3952008a4d396e7624a1889f6a26c52c
https://pubmed.ncbi.nlm.nih.gov/28546846
https://pubmed.ncbi.nlm.nih.gov/28546846