Enantioselective hydrolysis of cis -1,2-diacetoxycycloalkanedimethanols:enzymatic preparation of chiral building blocks from prochiral meso -substrates.-Reference-Cited by-同舟云学术

Enantioselective hydrolysis of cis -1,2-diacetoxycycloalkanedimethanols:enzymatic preparation of chiral building blocks from prochiral meso -substrates.

Published:1985 Issue:17 Volume:26 Page:2073-2076
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Laumen Kurt,Schneider Manfred

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Immobilized porcine liver esterase: a convenient reagent for the preparation of chiral building blocks.

2. Enzymatic Syntheses of Chiral Building Blocks from Prochiralmeso-Substrates: Preparation of Methyl(hydrogen)-1,2-cycloalkanedicarboxylates

3. A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver Esterase

4. Preparations of bicyclic chiral lactone synthons via stereospecific pig liver esterase-catalysed hyderolyses of meso-diesters. Ring-size induced reversal of stereospecificity

5. Enzymatic Synthesis of Chiral Building Blocks from Prochiral Substrates: Enantioselective Synthesis of Monoalkyl Malonates

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