The Stereoselective Deacylation of Long-chain Amino Acid Esters by Comicelles of N-Acyl-l-histidine and Various Cationic Surfactants
- 1 February 1981
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 54 (2), 576-580
- https://doi.org/10.1246/bcsj.54.576
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- The Micelle-promoted Selective Hydrolysis of Anionic and Nonionic Ester Substrates by Hydroxamic Acids and Histidine DerivativesBulletin of the Chemical Society of Japan, 1980
- Micellar stereoselectivity. Cleavage of diastereomeric substrates by functional surfactant micellesJournal of the American Chemical Society, 1979
- The Catalytic Action of a Mixed Micelle of Lauroylamino Acid and a DetergentBulletin of the Chemical Society of Japan, 1976
- Micellar catalysis of ester hydrolysis. Influence of chirality and head group structure in simple surfactantsThe Journal of Organic Chemistry, 1974
- Nonpolar contributions to the rate of nucleophilic displacements of p-nitrophenyl esters in micellesJournal of the American Chemical Society, 1968
- Specificity and stereospecificity of α-chymotrypsinBiochemical Journal, 1967