STEREOSELECTIVE ESTEROLYSIS OF DIPEPTIDE-TYPE AMINO-ACID ESTERS WITH DI-PEPTIDE-TYPE AND TRI-PEPTIDE-TYPE L-HISTIDINE DERIVATIVES IN THE SOLUTION OF A CHIRAL CATIONIC SURFACTANT

被引：3

作者：

OHKUBO, K

OGATA, H

YAMAKI, K

机构：

来源：

JOURNAL OF MOLECULAR CATALYSIS | 1984年 / 26卷 / 01期

关键词：

D O I：

10.1016/0304-5102(84)85014-2

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

引用

页码：1 / 5

页数：5

共 10 条

[1]

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[6] A CRITICAL CONCENTRATION FOR MICELLAR DIASTEREOSELECTIVITY [J].

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[7] MICELLAR DIASTEREOSELECTIVITY - TRIPEPTIDE SUBSTRATES [J].

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[8] STEREOSELECTIVE DEACYLATION OF LONG-CHAIN AMINO-ACID ESTERS WITH MIXED MICELLES OF L-HISTIDINE DERIVATIVES AND CATIONIC SURFACTANTS [J].

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[9] ENANTIOSELECTIVE DEACYLATION OF LONG-CHAIN PARA-NITROPHENYL N-ACYLPHENYLALANATES BY N-(N-DODECANOYL-L-HISTIDYL)-L-LEUCINE AND A CATIONIC CHIRAL SURFACTANT [J].

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[10]

OHKUBO K, 1983, J MOL CATAL, V23, P29

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