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Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L-amino acids by N-lauroyl L or D-histidine in CTABr micelles.
Authors:Kimiho Yamada  Hideto Shosenji  Hirotaka Ihara  Yonejiro Otsubo
Affiliation:Department of Synthetic Chemistry, Faculty of Engineering, Kumamoto University, Kumamoto 860, Japan
Abstract:Remarkable dependencies of the rate constants and enantioselectivities on the substituents and protecting groups were demonstrated by the catalyzed hydrolysis of p-nitrophenyl esters of various N-protected L-amino acids by L or D-LauHis in the presence of mixed micelles with CTABr.
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