Stereoselectivity in micellar and vesicular reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. The Stereoselective Deacylation of Long-chain Amino Acid Esters by Comicelles ofN-Acyl-L-histidine and Various Cationic Surfactants
2. Syntheses of enterobactin and enantioenterobactin
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1. Mechanism of enantioselective ester cleavage by histidine-containing peptides at a micellar interface. 2. Effect of changing peptide chain length;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Asymmetric Catalysis Mediated by Synthetic Peptides;Chemical Reviews;2007-12-01
3. Recognition in Organized Aggregates Formed by a Chiral Amidic Surfactant;Langmuir;1999-09-14
4. A remarkably enhanced diastereoselectivity for the hydrolysis of dipeptide esters responding to pH and temperature in buffer solutions;Tetrahedron Letters;1996-05
5. Chiral Lipophilic Ligands. 3. Control of Enantioselectivity in Copper(II)-Catalyzed Cleavage of α-Amino Acid Esters by Aggregate Morphology;Langmuir;1996-01-01
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