Kinetic resolution of racemic secondary alcohols via oxidation with Yarrowia lipolytica strains
- 1 June 2000
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 11 (11) , 2367-2373
- https://doi.org/10.1016/s0957-4166(00)00185-3
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Asymmetric Reduction of α,β-Unsaturated Cyclic Ketones by a YeastChemistry Letters, 1998
- Microbial reduction of methyl-substituted bicyclo[3.2.0]hept-3-en-6-ones : a screening to homochiral endo- and exo-alcoholsTetrahedron: Asymmetry, 1996
- Enantiomerically Pure 4-Methyl- and 1,4-Dimethyl-bicyclo[3.2.0]hept-3-en-6-ols and Ones by Microbial RedoxChemistry Letters, 1996
- Bacillus stearothermophilus alcohol dehydrogenase: A new catalyst to obtain enantiomerically pure bicyclic octen- and hepten-ols and -ones.Tetrahedron, 1996
- Combined microbial oxidation and reduction: a new approach to the highyield synthesis of homochiral unsaturated secondary alcohols from racematesTetrahedron: Asymmetry, 1995
- Kinetic resolution via oxidation of endo-bicyclic octen- and heptenols with Bacillus stearothermophilusTetrahedron: Asymmetry, 1994
- Enantioselective hydrolysis of 2-methylcyclohexanyl acetates with the cultured cells of Marchantia polymorphaTetrahedron: Asymmetry, 1993
- Microbial oxidation with Bacillus stearothermophilus: High enantioselective resolution of 1-heteroaryl and 1-aryl alcoholsTetrahedron: Asymmetry, 1993
- Kinetic resolution of 1-aryl- and 1-heteroaryl ethanols by oxidation with Baker's yeastTetrahedron Letters, 1993
- CHIRAL DRUGSChemical & Engineering News, 1992