Progress in asymmetric biomimetic transamination of carbonyl compounds

Chem Soc Rev. 2015 Apr 7;44(7):1740-8. doi: 10.1039/c4cs00507d. Epub 2015 Feb 3.

Abstract

Transamination of α-keto acids with transaminases and pyridoxamine phosphate is an important process to form optically active α-amino acids in biological systems. Various biomimetic transamination systems have been developed for carbonyl compounds including α-keto acid derivatives, fluoroalkyl ketones, and unactivated ketones with chiral vitamin B6 analogues, artificial transaminase mimics, chiral nitrogen sources, and chiral catalysts. This review provides a brief summary of this area.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amination
  • Amino Acids / chemistry
  • Biomimetics*
  • Catalysis
  • Ketones / chemistry*
  • Transaminases / chemistry
  • Vitamin B 6 / analogs & derivatives

Substances

  • Amino Acids
  • Ketones
  • Vitamin B 6
  • Transaminases