摘要

A rhodium(III)-catalyzed CH direct allylation reaction with 4-vinyl-1,3-dioxolan-2-ones has been developed. The reaction provides a facile and stereoselective access to substituted-(E)-allylic alcohols under mild and redox-neutral reaction conditions. Olefinic CH activation is applicable, giving multifunctionalized skipped dienes in good yields. Minimal double-bond migration was observed.