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Volumn 202, Issue 1-2, 2003, Pages 17-22
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Hydrolytic metalloenzyme models enantioselective hydrolysis of long chain α-amino acid esters by chiral metallomicelles composed of lipophilic L-histidinol
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Author keywords
Chiral metallomicelles; Enantioselective hydrolysis; L Histidinol; Synthesis; Amino acid esters
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Indexed keywords
AMINO ACIDS;
ESTERS;
HYDROLYSIS;
MICELLES;
SUPRAMOLECULAR CHEMISTRY;
ENANTIOSELECTIVITY;
CATALYSTS;
ALPHA AMINO ACID;
HISTIDINOL;
HYDROXYL GROUP;
N ALPHA LAUROYLHISTIDINOL;
UNCLASSIFIED DRUG;
ZINC;
ARTICLE;
CATALYSIS;
CHEMICAL ANALYSIS;
CHEMICAL COMPOSITION;
CHEMICAL REACTION KINETICS;
CHIRALITY;
DEACYLATION;
ENANTIOSELECTIVITY;
HYDROLYSIS;
LIPOPHILICITY;
MICELLE;
PKA;
SUPRAMOLECULAR CHEMISTRY;
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EID: 0038450204
PISSN: 13811169
EISSN: None
Source Type: Journal
DOI: 10.1016/S1381-1169(03)00199-7 Document Type: Article |
Times cited : (55)
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References (30)
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