Metal ion and micellar triggering of enantioselectivity in the hydrolysis of N-protected amino acid esters
Author:
Publisher
Elsevier BV
Subject
General Engineering
Reference17 articles.
1. Experimental and computer modeling studies of micellar diastereoselectivity
2. Remarkable substituent effects on the micellar enantioselective hydrolysis of amino acid esters
3. Kinetics and molecular modelling studies on the stereoselective hydrolysis of enantiomeric esters by dipeptide catalysts
4. Membrane matrix for the hydrolysis of amino acid esters with marked enantioselectivity
5. Chiral reaction field for highly stereoselective hydrolysis of enantiomeric esters
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1. Hydrolysis of 4-nitrophenyl esters of picolinic acid and N-protected amino acids by metalloenzyme models in vesicular assemblies;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Facile Synthesis of Substituted Phenanthroline Ligands by Samarium-Promoted Coupling of Phenanthroline with Ketones;Organic Letters;1999-10-10
3. Influence of Transition-Metal Ions on the Aggregation Behavior of a Single-Chained Ammonium Amphiphile Carrying ano-Hydroxyazobenzene Unit;European Journal of Organic Chemistry;1999-03
4. Micellar solutions as reaction media;Tetrahedron;1996-08
5. Reaction rate enhancement by addition of anionic surfactant SDS in the ruthenium catalyzed hydrogen transfer from a 1,4-diol to 4-phenyl-3-buten-2-one;Journal of Organometallic Chemistry;1994-06
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