Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ludmila V. Osetrova"'
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
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