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
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
(+/-)-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.