Stereoselective reduction with NADH model BNAH through chiral induction in cyclodextrins

Bioorg Chem. 2001 Feb;29(1):14-8. doi: 10.1006/bioo.2000.1185.

Abstract

Stereoselective reductive debromination-cyclopropanation of 2-bromo-1-phenylethylidene-malononitrile and 2-bromo-1-beta-naphthylethylidenemalononitrile by coenzyme NADH model BNAH through chiral induction in cyclodextrins is reported. The matching between substrates and cyclodextrins, the substituent effect, and the effect of cyclodextrin concentration on the optical yields have been investigated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclodextrins / chemistry*
  • Magnetic Resonance Spectroscopy
  • NAD / analogs & derivatives
  • NAD / metabolism*
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • 1-benzyl-1,4-dihydronicotinamide
  • Cyclodextrins
  • NAD