Abstract
Porcine liver esterase catalyses the reaction of -amino esters in water to give a mixture of the corresponding -lactam and the hydrolysis product, deacylation of the acyl enzyme intermediate by ring closure occurs with a high enantioselectivity giving an ee of 90% for the formation of (S)-5-phenyl-2-pyrrolidone from racemic ethyl 4-phenyl-4-aminobutanoate
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