Kinetic resolution strategies II: Enhanced enantiomeric excesses and yields for the faster reacting enantiomer in lipase mediated kinetic resolutions.
- 31 May 1993
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (5), 813-822
- https://doi.org/10.1016/s0957-4166(00)80119-6
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Amplification of enantioselectivity in biocatalyzed kinetic resolution of racemic alcoholsThe Journal of Organic Chemistry, 1991
- Lipase-mediated homotopic and heterotopic double resolutions of a planar chiral organometallic alcoholBiotechnology Letters, 1991
- Resolution of binaphthols and spirobiindanols using cholesterol esteraseJournal of the American Chemical Society, 1989
- Catalytic asymmetric hydroboration of styrenesJournal of the American Chemical Society, 1989
- Chemoenzymic synthesis of chiral furan derivatives: useful building blocks for optically active structuresThe Journal of Organic Chemistry, 1988
- Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp.; an attractive alternative to ester hydrolysisJournal of the Chemical Society, Chemical Communications, 1988
- A highly selective ester hydrolase from Pseudomonas sp. for the enzymatic preparation of enantiomerically pure secondary alcohols; chiral auxiliaries in organic synthesisJournal of the Chemical Society, Chemical Communications, 1988
- Side chain hydroxylation of aromatic compounds by fungi.: 1. Products and stereochemistryCanadian Journal of Chemistry, 1987
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- Electron-rich aromatics. I. Solvolysis of 1-arylethyl acetatesJournal of the American Chemical Society, 1969