A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions.

ABSTRACT: A convergent and enantioselective synthesis of the natural product amurensinine is described. The synthetic strategy takes advantage of mild and selective C-H and C-C bond insertion reactions, in addition to the palladium-catalyzed aerobic oxidative kinetic resolution recently developed in these laboratories.

SUBMITTER: Tambar UK 

PROVIDER: S-EPMC2529249 | biostudies-literature | 2006 Sep

REPOSITORIES: biostudies-literature