Enantioselectivity in microbial reduction of prochiral carbonyl groups: A wide screening toward R and S isomers

This publication has 10 references indexed in Scilit:

• Baker's Yeast as a Reagent in Organic Synthesis
  Synthesis, 1990
• Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates
  The Journal of Organic Chemistry, 1989
• Synthesis of (-)-talaromycins a and b
  Tetrahedron, 1987
• Characterization of thiocarbonyl ylides in the reaction of triplet carbenes with thioketones
  Tetrahedron Letters, 1986
• Trifunctional Chiral Synthons via Stereocontrolled Yeast Reduction. Preparation of Chiral Pentane-1,3,5-triol Derivatives
  Chemistry Letters, 1986
• Role of lipase activators produced by Saccharomycopsis lipolytica and calcium ion in its lipase reaction.
  Agricultural and Biological Chemistry, 1986
• Tetrahedron report number 203
  Tetrahedron, 1986
• Chelation- and non-chelation-controlled additions to 2-O-benzyl-3-O-(tert-butyldimethylsilyl)glyceraldehyde
  The Journal of Organic Chemistry, 1985
• Metal ion controlled addition to .alpha.,.beta.-dialkoxy carbonyl compounds
  The Journal of Organic Chemistry, 1985
• Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]
  Angewandte Chemie International Edition in English, 1984