The Catalytic Action of a Mixed Micelle of Lauroylamino Acid and a Detergent
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/49/3/49_3_719/_pdf
Reference6 articles.
1. Kinetics of organic reactions in micellar systems
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3. Reactivity of Sulfhydryl Groups in Micelles. A Model for Protein
4. Use of esters of N-hydroxysuccinimide in the synthesis of N-acylamino acids
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1. Asymmetric Catalysis Mediated by Synthetic Peptides;Chemical Reviews;2007-12-01
2. Stereoselective hydrolysis of amino acid esters in branched or linear poly(ethylenimine) derivatives;Macromolecules;1988-08
3. Deacylation Effect in the Hydrolysis ofp-Nitrophenyl Esters by Bifunctional Comicelles Containing Imidazolyl and Hydroxyl Groups;Bulletin of the Chemical Society of Japan;1987-02
4. Substrate specificity on hydrolysis by dipeptide derivatives containing l-histidine in micellar systems;Journal of Colloid and Interface Science;1987-02
5. Efficient stereoselective hydrolysis of enantiomeric amino acid esters by bilayer vesicular systems which include di- or tri-peptide histidine catalysts;Journal of the Chemical Society, Perkin Transactions 2;1987
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