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

Tetrahedron Letters

Volumn 26, Issue 17, 1985, Pages 2073-2076

  Laumen, Kurt ^a   Schneider, Manfred ^a  

^a UNIVERSITY OF WUPPERTAL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000881071     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)94782-8     Document Type: Article

References (13)

1. Enzymatic Syntheses of Chiral Building Blocks from Prochiralmeso-Substrates: Preparation of Methyl(hydrogen)-1,2-cycloalkanedicarboxylates
2. A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver Esterase
3. Preparations of bicyclic chiral lactone synthons via stereospecific pig liver esterase-catalysed hyderolyses of meso-diesters. Ring-size induced reversal of stereospecificity
4. Enzymatic Synthesis of Chiral Building Blocks from Prochiral Substrates: Enantioselective Synthesis of Monoalkyl Malonates
5. Preparation of chiral ?-lactones via enantiotopically specific pig liver esterase-catalysed hydrolyses of 3-substituted glutaric acid diesters