Complementary lipase-mediated desymmetrization processes of 3-Aryl-1,5-disubstituted fragments. enantiopure synthetic valuable carboxylic acid derivatives

Journal of Organic Chemistry

Volumn 76, Issue 3, 2011, Pages 811-819

  Ríos Lombardía, Nicolás ^a   Gotor Fernández, Vicente ^a   Gotor, Vicente ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVES; CHIRAL BUILDING BLOCKS; DESYM-METRIZATION; DIESTERS; ENANTIOPURE; ENZYMATIC PROCESS; HYDROLYSIS REACTION; MONOESTERS; OPTICAL PURITY; OPTIMAL METHODS; REACTION PARAMETERS; REACTION TIME;

ACETYLATION; CARBOXYLIC ACIDS;

OPTIMIZATION;

3 (2 METHOXYPHENYL)PENTANE 1,5 DIOL; 3 PHENYLPENTANE 1,5 DIOL; ACETOACETIC ACID; ALKANE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; COMPLEMENTARY LIPASE; PENTANE 1,5 DIOL; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; VINYL ACETATE;

ACETYLATION; ARTICLE; BIOCATALYST; CHEMICAL REACTION; CHIRALITY; DESYMMETRIZATION; ENANTIOMER; ENANTIOSELECTIVITY; HYDROLYSIS; REACTION TIME; SOLVENT EFFECT; SUBSTITUTION REACTION; SYNTHESIS; TEMPERATURE SENSITIVITY;

CARBOXYLIC ACIDS; CATALYSIS; LIPASE; MOLECULAR STRUCTURE; OPTICAL ROTATION; SOLVENTS; STEREOISOMERISM; TEMPERATURE;

EID: 79851488812     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101962v     Document Type: Article

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