Enantioselective hydrolysis of an α-amino acid ester in sugar-derived surfactant micelles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Stereoselective reaction of p-nitrophenyl N-acyl-phenylalanines with N-acyl-L-histidine in mixed micelles
2. THE HYDROLYSIS OFp-NITROPHENYL ESTERS OF α-AMINO ACIDS BYN-LAUROYL L OR D-HISTIDINE IN CATIONIC MICELLES
3. Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L or D-amino acids by optically active hydroxamic acid and dipeptides
4. ENANTIOSELECTIVE ESTER HYDROLYSIS CATALYZED BY A MICELLAR MODEL OF ZINC ENZYMES
5. Kinetics and molecular modelling studies on the stereoselective hydrolysis of enantiomeric esters by dipeptide catalysts
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hydrolysis of phenyl trifluoroacetate in mixed surfactant systems;Journal of Physical Organic Chemistry;2016-06-27
2. Sugar-Amide Surfactant Micelles as Effective Reaction Fields for Enantioselective Hydrolysis of α-Amino Acid Esters;Langmuir;2004-09-01
3. Water-Soluble Calixarenes as New Inverse Phase-Transfer Catalysts. Their Scope in Aqueous Biphasic Alkylations and Mechanistic Implications;Advanced Synthesis & Catalyis;2002-06
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