A substrate model for the enzymatic resolution of esters of bicyclic alcohols by candida cylindracea lipase
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 45 (6) , 1679-1682
- https://doi.org/10.1016/s0040-4020(01)80032-6
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Structural requirements in the enzymic optical resolution of bicyclic esters using pig liver esteraseTetrahedron Letters, 1988
- Enantioselective hydrolysis of dimethyl 2.alpha.,3.alpha.-[(dimethylmethylene)dioxy]-5.beta.-hydroxy-1.beta.,4.beta.-cyclopentanedicarboxylate with pig liver esterase. Stereoselective synthesis of methyl 2(R),3(S)-[(dimethylmethylene)dioxy]-5(R)-hydroxy-1(S)-carboxy-4(R)-cyclopentanecarboxylate. A cyclopentane synthone with all ring atoms chiralThe Journal of Organic Chemistry, 1988
- Enzymatic preparation of optically active 7-oxabicyclo[2.2.1] heptane derivativesTetrahedron, 1988
- Facile enolate alkylation of norbornenonesTetrahedron Letters, 1988
- Enzymatic resolution of norbornane-type estersTetrahedron, 1987
- Large scale preparation of (+)- and (−)-endo-norbornenol by enzymatic hydrolysisTetrahedron Letters, 1986
- Tetrahedron report number 203Tetrahedron, 1986
- A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver EsteraseHelvetica Chimica Acta, 1983
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- SECTION OF CHEMICAL SCIENCES: ON THE ACTIVE SITE AND SPECIFICITY OF α‐CHYMOTRYPSIN*Transactions of the New York Academy of Sciences, 1969