ChemInform Abstract: Trifluoroacetylation of Ketone O-Vinyloximes

Autor:	D. S. D. Toryashinova, E. Yu. Shmidt, A. M. Vasil'tsov, Boris A. Trofimov, L. N. Il'icheva, Ol'ga A. Tarasova, Alexey B. Zaitsev, A. I. Mikhaleva, Andrei V. Afonin
Rok vydání:	2010
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Ketone chemistry Radical Pyridine Organic chemistry Stereoselectivity Ether General Medicine Trifluoroacetic anhydride Oxime Alkyl
Zdroj:	ChemInform. 32
ISSN:	1522-2667 0931-7597
DOI:	10.1002/chin.200141088
Popis:	Ketone oxime O-vinyl ethers having alkyl or phenyl radicals react with trifluoroacetic anhydride in ether in the presence of pyridine, yielding 43-54% of the corresponding ketone oxime O-(trans-4,4,4-trifluoro-3-oxo-1-butenyl) ethers with high stereoselectivity.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5f695980471e5b12389a9906aab8a8d6 https://doi.org/10.1002/chin.200141088 Zobrazit plný text záznamu Plný text