Asymmetric Syntheses of (−)-Malyngolide and (−)-Frontalin by Utilizing Bakers’ Yeast Reduction of S-Ethyl 2-Cyclopentanonecarboxylthioate

This publication has 20 references indexed in Scilit:

• Substrate modification as a means of enhancing the enantioselectivity of microbial reductions of .beta.-keto esters. A (R)- or (S)-1,3,5-trihydroxypentane synthon
  The Journal of Organic Chemistry, 1987
• Stereocontrol by introduction of a sulfur functional group in the asymmetric reduction of β-ketoesters with baker's yeast; preparation of optically pure 3s-hydroxydithioesters as a new chiral synthon of natural product synthesis
  Tetrahedron Letters, 1986
• Asymmetric reduction with baker's yeast.
  Journal of Synthetic Organic Chemistry, Japan, 1986
• Stereochemical control of yeast reductions. 5. Characterization of the oxidoreductases involved in the reduction of .beta.-keto esters
  Journal of the American Chemical Society, 1985
• Stereochemical control of microbial reduction. 2. Reduction of β-keto esters by immobilized bakers' yeast
  Tetrahedron Letters, 1985
• Enantiospecific synthesis of optically pure (3s)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters
  Tetrahedron Letters, 1984
• Stereochemical control in yeast reduction
  Tetrahedron Letters, 1984
• Stereoselektive Synthese von Alkoholen, XII. Synthese der C‐9/C‐13‐Teilstruktur des Methynolids
  European Journal of Inorganic Chemistry, 1983
• Stereospezifische Synthese von (+)‐(3R, 4R)‐4‐Methyl‐3‐heptanol, das Enantiomere eines Pheromons des kleinen Ulmensplintkäfers (Scolytus multistriatus)
  Helvetica Chimica Acta, 1979
• Specification of the stereospecificity of some oxido-reductases by diamond lattice sections
  Pure and Applied Chemistry, 1964