Abstract

Abstract The high enantioselective hydrolysis (ka,obsdL⁄ka,obsdD=27) of p-nitrophenyl N-dodecanoyl-d(l)-phenylalaninate with N-benzyloxycarbonyl-l-phenylalanyl-l-histidyl-l-leucine in the vesicular system (ditetradecyldimethylammonium bromide) was enhanced dramatically by the addition of micelles (hexadecyltrimethylammonium bromide) and attained to the enantiomer rate ratio (ka,obsdL⁄ka,obsdD)=71 at room temperature (25 °C).

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