ENZYMES IN ORGANIC SYNTHESIS .19. THE ENZYME-CATALYZED SEQUENTIAL ESTERIFICATION OF (PLUS-OR-MINUS)-ANTI-2,4-DIMETHYLGLUTARIC ANHYDRIDE - AN EFFICIENT ROUTE TO ENANTIOMERICALLY ENRICHED MONOESTERS AND DIESTERSOF ANTI-2,4-DIMETHYLGLUTARIC ACID

Citation
R. Ozegowski et al., ENZYMES IN ORGANIC SYNTHESIS .19. THE ENZYME-CATALYZED SEQUENTIAL ESTERIFICATION OF (PLUS-OR-MINUS)-ANTI-2,4-DIMETHYLGLUTARIC ANHYDRIDE - AN EFFICIENT ROUTE TO ENANTIOMERICALLY ENRICHED MONOESTERS AND DIESTERSOF ANTI-2,4-DIMETHYLGLUTARIC ACID, Liebigs Annalen der Chemie, (2), 1994, pp. 215-217
Citations number
19
Categorie Soggetti
Chemistry
Journal title
ISSN journal
01702041
Issue
2
Year of publication
1994
Pages
215 - 217
Database
ISI
SICI code
0170-2041(1994):2<215:EIOS.T>2.0.ZU;2-9
Abstract
(+/-)-anti-2,4-Dimethylpentanedioic anhydride (rac-1) was converted in good yields and with enantiomeric excess by an enzyme-catalyzed seque ntial esterification into the (2R,4R)-monoester 2 and the (2S,4S)-dies ter ent-3. Best results were obtained with Novozym 435, a lipase from Candida antarctica.