Hydrolyse enzymatique: 1 - approche dans l'etude de l'hydrolyse de diesters: selectivite par competition intermoleculaire
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (49), 6063-6064
- https://doi.org/10.1016/s0040-4039(00)95125-6
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- An extremely facile ring opening of substituted 1-(alkylthio)cyclopropene via vinylcarbene intermediateThe Journal of Organic Chemistry, 1985
- Enzymatic hydrolysis of prochiralTetrahedron Letters, 1984
- Lipase-catalyzed hydrolysis as a route to esters of chiral epoxy alcoholsJournal of the American Chemical Society, 1984
- Enzymatic Syntheses of Chiral Building Blocks from Prochiral meso‐Substrates: Preparation of Methyl(hydrogen)‐1,2‐cycloalkanedicarboxylatesAngewandte Chemie International Edition in English, 1984
- Enzymatic Synthesis of Chiral Building Blocks from Prochiral Substrates: Enantioselective Synthesis of Monoalkyl MalonatesAngewandte Chemie International Edition in English, 1984
- A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver EsteraseHelvetica Chimica Acta, 1983