Enantioselective synthesis of phenylacetamides in the presence of high organic cosolvent concentrations catalyzed by stabilized penicillin G acylase. Effect of the acyl donor

Biotechnology Progress

Volumn 20, Issue 3, 2004, Pages 984-988

  Abian, Olga ^a   Mateo, César ^a   Palomo, José M ^a   Fernández Lorente, Gloria ^a   Guisán, José M ^a   Fernández Lafuente, Roberto ^a  

^a CSIC   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; CARBOXYLIC ACIDS; CONDENSATION; MOLECULAR ORIENTATION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ENANTIOSELECTIVITY; IMMOBILIZATION; QUANTITATIVE TRANSFORMATIONS; REACTION CONDITIONS;

BIOTECHNOLOGY;

ACETAMIDE DERIVATIVE; IMMOBILIZED ENZYME; ORGANIC COMPOUND; PENICILLIN AMIDASE; PHENETHYLAMINE DERIVATIVE; SOLVENT;

ACYLATION; ARTICLE; CHEMISTRY; COMPARATIVE STUDY; ENZYME ACTIVATION; ENZYME SPECIFICITY; ENZYME STABILITY; ENZYMOLOGY; ESCHERICHIA COLI; EVALUATION; KINETICS; OXIDATION REDUCTION REACTION; REPRODUCIBILITY; SENSITIVITY AND SPECIFICITY; STEREOISOMERISM; SYNTHESIS;

ACETAMIDES; ACYLATION; ENZYME ACTIVATION; ENZYME STABILITY; ENZYMES, IMMOBILIZED; ESCHERICHIA COLI; KINETICS; ORGANIC CHEMICALS; OXIDATION-REDUCTION; PENICILLIN AMIDASE; PHENETHYLAMINES; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SOLVENTS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 2942756031     PISSN: 87567938     EISSN: None     Source Type: Journal    
DOI: 10.1021/bp034354g     Document Type: Article

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