Artificial metalloenzymes for enantioselective catalysis based on biotin-avidin

J Am Chem Soc. 2003 Jul 30;125(30):9030-1. doi: 10.1021/ja035545i.

Abstract

Homogeneous and enzymatic catalysis offer complementary means to generate enantiomerically pure compounds. Incorporation of achiral biotinylated rhodium-diphosphine complexes into (strept)avidin yields artificial metalloenzymes for the hydrogenation of N-protected dehydroamino acids. A chemogenetic optimization procedure allows one to produce (R)-acetamidoalanine with 96% enantioselectivity. These hybrid catalysts display features reminiscent both of enzymatic and of homogeneous systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylates / chemistry
  • Avidin / chemistry*
  • Biotin / chemistry*
  • Catalysis
  • Cinnamates / chemistry
  • Enzymes / chemistry*
  • Hydrogenation
  • Metalloproteins / chemistry*
  • Rhodium / chemistry*
  • Stereoisomerism
  • Streptavidin / chemistry
  • Substrate Specificity

Substances

  • Acrylates
  • Cinnamates
  • Enzymes
  • Metalloproteins
  • Avidin
  • Biotin
  • Streptavidin
  • Rhodium