Microbial deracemization of 1-arylethanol

This publication has 10 references indexed in Scilit:

• Deracemization of Cyclic Allyl Esters
  Journal of the American Chemical Society, 1994
• Deracemization of a Phosphine Oxide via Enantioselective Protonation
  The Journal of Organic Chemistry, 1994
• Enantioselective microbial oxidation of 1-arylethanol in an organic solvent
  Tetrahedron Letters, 1994
• Preparation of optically active cyclohexanediols and (+)-α- hydroxycycloheptanone by an enzyme catalysed stereoinversion/oxidation process
  Tetrahedron Letters, 1994
• A Study of the Stereocontrolled Reduction of Aliphatic β-Ketoesters by Geotrichum candidum
  Biocatalysis, 1992
• Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast
  The Journal of Organic Chemistry, 1991
• High-yield production of optically active 1,2-diols from the corresponding racemates by microbial stereoinversion.
  Agricultural and Biological Chemistry, 1990
• Effect of Allyl Alcohol on Reduction of β-Keto Esters by Bakers’ Yeast
  Chemistry Letters, 1987
• One-Step Microbial Conversion of a Racemic Mixture of Pantoyl Lactone to Optically Active d -(—)-Pantoyl Lactone
  Applied and Environmental Microbiology, 1987
• On the relation between elution order and absolute stereochemistry of alkylarylcarbinols from a Pirkle column
  The Journal of Organic Chemistry, 1983