Remote substituent effects in microbial reductions of 3-ketoglutarate and 3-ketoadipate esters

This publication has 12 references indexed in Scilit:

• Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
  Journal of the American Chemical Society, 1983
• Enantiospecific syntheses of trifunctional (R)-3-hydroxy esters by baker's yeast reduction
  Journal of the Chemical Society, Chemical Communications, 1983
• Reaktion von α‐Lithioessigsäureestern mit Bernsteinsäureanhydriden
  Angewandte Chemie, 1979
• C‐Acylation under Virtually Neutral Conditions
  Angewandte Chemie International Edition in English, 1979
• Meldrum's acid
  Chemical Society Reviews, 1978
• Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivatives
  Australian Journal of Chemistry, 1976
• Eine einfache Synthese von Malonsäure-mono- und -bis-phenylestern¹
  Synthesis, 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
• Asymmetric Reductions. XII. Stereoselective Ketone Reductions by Fermenting Yeast^*
  Biochemistry, 1964
• Specification of the stereospecificity of some oxido-reductases by diamond lattice sections
  Pure and Applied Chemistry, 1964