Camphor derived 1,4-oxathianes for carbonyl epoxidation

Autor:	J. Gair Ford, Ray V.H. Jones, Varinder K. Aggarwal, Robin Fieldhouse
Rok vydání:	1998
Předmět:	Inorganic Chemistry Camphor chemistry.chemical_compound Chemistry Yield (chemistry) Organic Chemistry Organic chemistry Physical and Theoretical Chemistry Catalysis
Zdroj:	Tetrahedron: Asymmetry. 9:1801-1807
ISSN:	0957-4166
DOI:	10.1016/s0957-4166(98)00028-7
Popis:	1,4-Oxathianes have been prepared in five steps from camphor and used to give stilbene oxides in excellent yield (81–100%) and with moderate enantioselectivity (54–64% ee).
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7cd69e79f509af8044ac1a3d5de4e90f https://doi.org/10.1016/s0957-4166(98)00028-7 Zobrazit plný text záznamu Full Text from ScienceDirect