Chiral amine-silyl triflate complex mediated asymmetric intramolecular Michael-aldol reaction via a novel enantioselective enol silylation process

Citation
K. Takasu et al., Chiral amine-silyl triflate complex mediated asymmetric intramolecular Michael-aldol reaction via a novel enantioselective enol silylation process, CHEM COMMUN, (18), 2000, pp. 1739-1740
Citations number
15
Categorie Soggetti
Chemistry
Journal title
CHEMICAL COMMUNICATIONS
ISSN journal
13597345 → ACNP
Issue
18
Year of publication
2000
Pages
1739 - 1740
Database
ISI
SICI code
1359-7345(2000):18<1739:CATCMA>2.0.ZU;2-P
Abstract
An asymmetric intramolecular Michael-aldol reaction of a C-s symmetric keto ne using chiral amine and silyl triflate is described as a new methodology of chiral induction; nonracemic tricyclic cyclobutanes were obtained from a 4-substituted cyclohexanone in high yields with moderate enantioselectivit ies in one step.