Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L-amino acids by N-lauroyl L or D-histidine in CTABr micelles. |
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Authors: | Kimiho Yamada Hideto Shosenji Hirotaka Ihara Yonejiro Otsubo |
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Affiliation: | Department of Synthetic Chemistry, Faculty of Engineering, Kumamoto University, Kumamoto 860, Japan |
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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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