Asymmetric syntheses of benzaldehyde and o-anisaldehyde methyl isopropyl acetals

Asymmetric syntheses of (+)-(αR)-benzaldehyde and (+)-(αR)-o-anisaldehyde methyl isopropyl acetals in 93 and > 95% ee respectively using methodology based on the stereoselective reactions of enantiopure (ortho-substituted benzaldehyde) chromium tricarbonyl complexes are described.

Библиографические подробности
Главные авторы: Davies, S, Correia, L
Формат: Journal article
Язык:English
Опубликовано: 1996
Описание
Итог:Asymmetric syntheses of (+)-(αR)-benzaldehyde and (+)-(αR)-o-anisaldehyde methyl isopropyl acetals in 93 and > 95% ee respectively using methodology based on the stereoselective reactions of enantiopure (ortho-substituted benzaldehyde) chromium tricarbonyl complexes are described.