Selective enzymatic hydrolysis of (Z,E)-dimethyl-2,4-hexadienedioate. Preparation of (Z,E)difunctionalized dienes
摘要:
Enzymatic hydrolysis of (Z,E)-dimethyl-2,4-hexadienedioate 6 by Pig Liver Esterase mainly led to (2E,4Z)-5-methoxycarbonyl-2,4-pentadienoic acid 2a. This compound was a starting material for the preparation of other difunctionalized dienes.