Asymmetric synthesis of (S)-arylalkanols by microbial reduction
- 31 October 1996
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (10), 3021-3024
- https://doi.org/10.1016/0957-4166(96)00392-8
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Lipase-Catalyzed Transesterification of Aryl-Substituted Alkanols in an Organic SolventBulletin of the Chemical Society of Japan, 1996
- Chemo-enzymatic synthesis of (R,R)-(-)-PyrenophorinTetrahedron, 1995
- Improvement of enantioselectivity of microbial reduction by using organic solvent redox coupler systemTetrahedron Letters, 1995
- Mechanistic study for stereochemical control of microbial reduction of α-keto esters in an organic solventTetrahedron, 1995
- Enantioselective Hydrosilylation of Ketones with a Chiral Titanocene CatalystJournal of the American Chemical Society, 1994
- Enantioselective microbial oxidation of 1-arylethanol in an organic solventTetrahedron Letters, 1994
- Asymmetric hydroboration of styrenes catalyzed by cationic chiral phosphine-rhodium(I) complexesTetrahedron: Asymmetry, 1991
- Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitineJournal of the American Chemical Society, 1983
- Production of (+)‐(S)‐Ethyl 3‐Hydroxybutyrate and (‐)‐(R)‐Ethyl 3‐Hydroxybutyrate by Microbial Reduction of Ethyl AcetoacetateHelvetica Chimica Acta, 1983