ELECTROREDUCTIVELY PROMOTED DIASTEREOSELECTIVE COUPLING OF KETONES WITH ALLYLIC ALCOHOLS - SYNTHESIS OF OPTICALLY-ACTIVE 1,4-DIOLS

Authors
SHONO T MORISHIMA Y MORIYOSHI N ISHIFUNE M KASHIMURA S
Citation
T. Shono et al., ELECTROREDUCTIVELY PROMOTED DIASTEREOSELECTIVE COUPLING OF KETONES WITH ALLYLIC ALCOHOLS - SYNTHESIS OF OPTICALLY-ACTIVE 1,4-DIOLS, Journal of organic chemistry, 59(2), 1994, pp. 273-275
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of organic chemistry → ACNP
ISSN journal
00223263
Volume
59
Issue
2
Year of publication
1994
Pages
273 - 275
Database
ISI
SICI code
0022-3263(1994)59:2<273:EPDCOK>2.0.ZU;2-Z
Abstract
Cathodic coupling of ketones with allylic alcohols has been found to t ake place with high regio- and stereoselectivities at the position gam ma to the hydroxyl group to afford the corresponding 1,4-diols.