Diastereo- and enantioselective microbiological reduction of 2-methyl 3-oxoalkanoates

This publication has 20 references indexed in Scilit:

• Improved enantioselective synthesis of anti α-methyl-β-hydroxyesters through TiCl4-PPh3 mediated aldol condensation
  Tetrahedron Letters, 1986
• An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction
  Accounts of Chemical Research, 1984
• The use of microorganisms in oraganic synthesis. V. Microbiological asymmetric reduction of methyl 2-methyl-3-(2-thienyl)-3-oxopropionate.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
• The use of microorganisms in organic synthesis. III. Microbiological asymmetric reduction of methyl 3-(2-furyl)-2-methyl-3-oxopropionate.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
• The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereof
  Tetrahedron, 1984
• Production of (+)‐(S)‐Ethyl 3‐Hydroxybutyrate and (‐)‐(R)‐Ethyl 3‐Hydroxybutyrate by Microbial Reduction of Ethyl Acetoacetate
  Helvetica Chimica Acta, 1983
• Synthesis of functionalized chiral synthons via microbiological reduction
  Tetrahedron Letters, 1982
• Über die Stereospezifität der α‐Alkylierung von β‐Hydroxycarbonsäureestern. Vorläufige Mitteilung
  Helvetica Chimica Acta, 1979
• Stereospezifische Synthese von (+)‐(3R, 4R)‐4‐Methyl‐3‐heptanol, das Enantiomere eines Pheromons des kleinen Ulmensplintkäfers (Scolytus multistriatus)
  Helvetica Chimica Acta, 1979
• Asymmetric reductinon of carbonyl compounds by yeast. II. Preparation of optically active α- and β-hydroxy carboxylic acid derivatives
  Australian Journal of Chemistry, 1976