Abstract

Lipase from Pseudomonas cepacia was used to prepare esters of hydrocinnamic acid by direct esterification of the carboxylic acid in good yields (70–83%). For some esters, transesterification gave better yields (92%). Optimization of the reaction conditions resulted in a dramatic increase in the yield of the product ester. The role of solvents was studied. Notably, cinnamic acid esters are not formed under these conditions.

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