An efficient asymmetric biomimetic transamination of α-keto esters to chiral α-amino esters

Org Lett. 2012 Oct 19;14(20):5270-3. doi: 10.1021/ol302427d. Epub 2012 Oct 1.

Abstract

An efficient asymmetric biomimetic transamination of α-keto esters with quinine derivatives as chiral bases was described. A wide variety of α-amino esters containing various functional groups can be synthesized in high yield and enantioselectivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Biomimetics
  • Catalysis
  • Esters / chemistry*
  • Esters / metabolism
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Structure
  • Stereoisomerism
  • Transaminases / metabolism

Substances

  • Esters
  • Transaminases