Enzyme catalysed hydrolysis of dialkylated propanedioic acid diesters, chain length dependent reversal of enantioselectivity
- 1 January 1985
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 41 (7) , 1347-1352
- https://doi.org/10.1016/s0040-4020(01)96536-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Preparation of chiral δ-lactones via enantiotopically specific pig liver esterase-catalysed hydrolyses of 3-substituted glutaric acid diestersJournal of the Chemical Society, Chemical Communications, 1984
- Preparations of bicyclic chiral lactone synthons via stereospecific pig liver esterase-catalysed hyderolyses of meso-diesters. Ring-size induced reversal of stereospecificityJournal of the Chemical Society, Chemical Communications, 1984
- A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver EsteraseHelvetica Chimica Acta, 1983
- New and improved methods for the radical decarboxylation of acidsJournal of the Chemical Society, Chemical Communications, 1983
- Resolution of α-methyl amino esters by chymotrypsinTetrahedron Letters, 1982
- Decarboxylations of β-Keto Acids and Related CompoundsPublished by Springer Nature ,1978
- Notes- A Modified Curtious ReactionThe Journal of Organic Chemistry, 1961