“Double enantioselection” by a lipase-catalyzed transesterification of a meso-Diol with a racemic carboxylic ester
- 1 June 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (24) , 3457-3460
- https://doi.org/10.1016/s0040-4039(00)92662-5
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Lipase-catalyzed transesterification of meso-cyclopentane diolsTetrahedron, 1991
- Esterolytic and Lipolytic Enzymes in Organic SynthesisSynthesis, 1991
- Highly diastereoselective inter-esterification reactions involving a racemic acetate and a racemic carboxylic acid catalysed by lipase enzymesJournal of the Chemical Society, Chemical Communications, 1991
- Asymmetric transformations catalyzed by enzymes in organic solventsAccounts of Chemical Research, 1990
- Enzymatic synthesis of amides with two chiral centresJournal of the Chemical Society, Chemical Communications, 1990
- Enzymatic Catalysts in Organic SynthesisScience, 1989
- Enantioselektive Biokatalyse in organischen Solventien am Beispiel Lipase‐katalysierter ReaktionenAngewandte Chemie, 1989
- Resolution of Enantiomers via BiocatalysisTopics in Stereochemistry, 1989
- Tetrahedron report number 203Tetrahedron, 1986