Diastereo- and enantio-selective reduction of 2-methyl-3-oxobutanoate by bakers' yeast

This publication has 7 references indexed in Scilit:

• An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction
  Accounts of Chemical Research, 1984
• The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereof
  Tetrahedron, 1984
• Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
  Journal of the American Chemical Society, 1983
• The use of microorganisms in organic synthesis. I. Microbiological asymmetric reduction of 2-methyl-3-oxobutyrates.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
• Stereoselektive Synthese von Alkoholen, IX. Absolute Konfiguration von Stegobinon
  European Journal of Inorganic Chemistry, 1981
• Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivatives
  Australian Journal of Chemistry, 1976
• .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
  The Journal of Organic Chemistry, 1969