Dynamic Kinetic Resolution of ß-Cyano α-Ketoesters via Asymmetric Transfer Hydrogenation.

ABSTRACT

An efficient rhodium-catalyzed asymmetric transfer hydrogenation of ß-cyano α-ketoesters via dynamic kinetic resolution has been developed. Despite the challenge posed by multiple functional groups, the reaction proceeded smoothly under mild conditions, generating versatile synthons with two adjacent stereocenters in high yields with excellent enantio- and diastereoselectivities. Furthermore, the power of this strategy is highlighted by the scale-up reaction and the follow-up synthesis of cytoxazone and paclitaxel intermediates.