Enantioselective biocatalytic formal α-amination of hexanoic acid to l-norleucine

Org Biomol Chem. 2018 Nov 7;16(43):8030-8033. doi: 10.1039/c8ob02212g.

Abstract

A three-step one-pot biocatalytic cascade was designed for the enantioselective formal α-amination of hexanoic acid to l-norleucine. Regioselective hydroxylation by P450CLA peroxygenase to 2-hydroxyhexanoic acid was followed by oxidation to the ketoacid by two stereocomplementary dehydrogenases. Combination with final stereoselective reductive amination by amino acid dehydrogenase furnished l-norleucine in >97% ee.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Bacteria / enzymology
  • Biocatalysis*
  • Caproates / chemistry*
  • Cytochrome P-450 Enzyme System / metabolism*
  • Norleucine / chemistry*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Caproates
  • hexanoic acid
  • Norleucine
  • Cytochrome P-450 Enzyme System