Highly enantioselective alkylation reaction of enamides by Brønsted-acid catalysis
- PMID: 19746916
- DOI: 10.1021/ol901892s
Highly enantioselective alkylation reaction of enamides by Brønsted-acid catalysis
Abstract
The H8-BINOL-derived, phosphoric acid catalyzed, highly enatioselective alkylation reaction of enamides with indolyl alcohols has been described. A phosphoric acid derived from H8-BINOL enabled an asymmetric alpha-alkylation of enamides with indolyl alcohols to give beta-aryl 3-(3-indolyl)propanones in high yields (up to 96%) and with excellent enantioselectivity (up to 96% ee).
LinkOut - more resources
Full Text Sources
Other Literature Sources