Asymmetric Transamination of α-Keto Acids Catalyzed by Chiral Pyridoxamines

Org Lett. 2016 Aug 5;18(15):3658-61. doi: 10.1021/acs.orglett.6b01714. Epub 2016 Jul 20.

Abstract

A new type of novel chiral pyridoxamines 3a-g containing a side chain has been developed. The pyridoxamines displayed catalytic activity and promising enantioselectivity in biomimetic asymmetric transamination of α-keto acids, to give various α-amino acids in 47-90% yields with up to 87% ee's under very mild conditions. An interesting effect of the side chain on enantioselectivity was observed in the reaction.

Publication types

  • Research Support, Non-U.S. Gov't