(R)-(+) and (S)-(−) ethyl 4,4,4-trifluoro-3-hydroxy butanoate by enantioselective Baker’s yeast reduction

This publication has 16 references indexed in Scilit:

• Stereoselective synthesis and absolute configuration of (1′R,3R,4R)-4-acetoxy-3-(2′,2′,2′-trifluoro-1′-hydroxyethyl)azetidin-2-one
  Tetrahedron: Asymmetry, 1998
• Some influences of fluorine in bioorganic chemistry
  Chemical Communications, 1997
• Stereoselective reduction of thiocarbonyl compounds with baker's yeast
  Tetrahedron: Asymmetry, 1994
• Stereodivergent synthesis of fluorinated threonine derivatives in high optical purity
  Tetrahedron: Asymmetry, 1993
• Allyl bromide, a powerful inhibitor against R-enzyme activities in Bakers' yeast reduction of ethyl 3-oxoalkanoates
  Enzyme and Microbial Technology, 1993
• Preparation of both enantiomers of ethyl 4,4,4-trifluoro-3-hydroxy butanoate by enantioselective microbial reduction
  Bioorganic & Medicinal Chemistry Letters, 1991
• Stereochemical Control in Microbial Reduction. 8. Stereochemical Control in Microbial Reduction of β-Keto Esters
  Bulletin of the Chemical Society of Japan, 1989
• A microbially based approach for the preparation of chiral molecules possessing the trifluoromethyl group
  The Journal of Organic Chemistry, 1987
• Effect of Allyl Alcohol on Reduction of β-Keto Esters by Bakers’ Yeast
  Chemistry Letters, 1987
• Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
  Journal of the American Chemical Society, 1983