Kinetic resolution of racemic 1-phenyl 1-propanol by lipase catalyzed enantioselective esterification reaction

Artificial Cells, Blood Substitutes, and Biotechnology

Volumn 38, Issue 5, 2010, Pages 288-293

  Karadeniz, Fatma ^a   Bayraktar, Emine ^a   Mehmetoglu, Ülkü ^a  

^a ANKARA UNIVERSITY   (Turkey)

Author keywords

1 phenyl 1 propanol; Enantioselectivity; Esterification; Kinetic resolution; Lipase; Racemic

Indexed keywords

1-PROPANOL; ACYL DONORS; CARBON LENGTH; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE ESTERIFICATION; KINETIC RESOLUTION; LAURIC ACID; LIPASE-CATALYZED; LOG P-VALUE; MOLAR RATIO; NOVOZYM435; RACEMIC; REACTION CONDITIONS; REACTION TIME; S-ENANTIOMERS;

CATALYSIS; ENANTIOMERS; ESTERIFICATION; ESTERS; FATTY ACIDS; LIPASES; MOLECULAR SIEVES; ORGANIC SOLVENTS; PROPANOL; SIEVES; TOLUENE;

ENANTIOSELECTIVITY;

1 PHENYL 1 PROPANOL; ALCOHOL DERIVATIVE; AMONA LIPASE AK; AMONA LIPASE PS; CARBON; ENZYME; FATTY ACID; HEPTANE; HEXANE; LAURIC ACID; MYRISTIC ACID; NOVOZYM 435; OCTANE; PALMITIC ACID; TETRAHYDROFURAN; TOLUENE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION KINETICS; ENANTIOMER; ENANTIOSELECTIVITY; ENZYME KINETICS; ENZYME MECHANISM; ESTERIFICATION; REACTION TIME;

BIOCATALYSIS; CANDIDA; ESTERIFICATION; KINETICS; LIPASE; PROPANOLS; PSEUDOMONAS; SOLVENTS; STEREOISOMERISM; SUBSTRATE SPECIFICITY; TEMPERATURE;

EID: 77956570485     PISSN: 10731199     EISSN: 15324184     Source Type: Journal    
DOI: 10.3109/10731199.2010.494579     Document Type: Article

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