Enantioselective total synthesis of (+)-galbulin via organocatalytic domino Michael-Michael-aldol condensation.
Journal: Chemical Communications (Cambridge, England)
Published:
Abstract
A concise and practical enantioselective synthesis of (+)-galbulin has been achieved using organocatalytic domino Michael-Michael-aldol condensation and organocatalytic kinetic resolution as the key steps.
Authors
Bor-cherng Hong, Che-sheng Hsu, Gene-hsiang Lee