Biocatalytic transformation of racemates into chiral building blocks in 100% chemical yield and 100% enantiomeric excess
- 1 January 1999
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 10 (1) , 107-117
- https://doi.org/10.1016/s0957-4166(98)00490-x
Abstract
No abstract availableKeywords
This publication has 51 references indexed in Scilit:
- SYNTHESIS OF ENANTIOPURE EPOXIDES THROUGH BIOCATALYTIC APPROACHESAnnual Review of Microbiology, 1997
- Deracemization of (±)-2,3-disubstituted oxiranes via biocatalytic hydrolysis using bacterial epoxide hydrolases: kinetics of an enantioconvergent processJournal of the Chemical Society, Perkin Transactions 1, 1997
- Dynamic resolutions in asymmetric synthesisChemical Society Reviews, 1996
- Biocatalytic Ways to Optically Active 2-Amino-1-phenylethanols.Acta Chemica Scandinavica, 1996
- Microbial Epoxide Hydrolases.Acta Chemica Scandinavica, 1996
- Microbial production of (2R, 4R)-2,4-pentanediol by enatioselective reduction of acetylacetone and stereoinversion of 2,4-pentanediolBiotechnology Letters, 1994
- Highly efficient conversion of (±)-mandelic acid to its (R)-(−)-enantiomer by combination of enzyme-mediated oxidation and reductionBiotechnology Letters, 1992
- Kinetics study on absorption of carbon dioxide into solutions of activated methyldiethanolamineIndustrial & Engineering Chemistry Research, 1992
- Preparative separation of ?- and ?-naphthols catalyzed by immobilized sulfataseBiotechnology & Bioengineering, 1983
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981