Abstract
The enzymatic acylation of certain ω-hydroxycyanohydrins protected at the primary alcohol has been studied. The best enantioselectivities are obtained with Pseudomonas cepacia lipase (PSL-C) and Candida antarctica lipase A (CAL-A), for the ω- O-tritylated cyanohydrins. The effect of the protecting group in the enzymatic reactions has been studied using molecular modeling.
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