Reductions of keto esters with baker's yeast in organic solvents - a comparison with the results in water
- 1 January 1997
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 53 (3) , 935-938
- https://doi.org/10.1016/s0040-4020(96)01067-8
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- A novel method to synthesize (L)-β-hydroxyl esters by the reduction with bakers' yeastTetrahedron Letters, 1990
- A novel synthesis of trans-γ,δ-unsaturatedtrifluoromethyl ketonesTetrahedron Letters, 1990
- Reductive biotransformations of organic compounds by cells or enzymes of yeastEnzyme and Microbial Technology, 1990
- Purification and properties of two oxidoreductases catalyzing the enantioselective reduction of diacetyl and other diketones from baker's yeastEuropean Journal of Biochemistry, 1990
- Baker's Yeast as a Reagent in Organic SynthesisSynthesis, 1990
- Dehydrogenases for the synthesis of chiral compoundsEuropean Journal of Biochemistry, 1989
- Stereochemical control on yeast reduction of .alpha.-keto esters. Reduction by immobilized bakers' yeast in hexaneThe Journal of Organic Chemistry, 1988
- Diasterio‐ und enantioselektive Reduktion von β‐Ketoestern mit Cyclopentanon‐, Cyclohexanon‐, Piperidon‐ und Tetralon‐Struktur durch nicht fermentierende Bäcker‐HefeHelvetica Chimica Acta, 1987
- Effect of Allyl Alcohol on Reduction of β-Keto Esters by Bakers’ YeastChemistry Letters, 1987
- Regio- and enantio-selective reduction of .ALPHA.,.GAMMA.-diketones by fermenting bakers' yeast.Agricultural and Biological Chemistry, 1986