Comparative esterification of phenylpropanoids versus hydrophenylpropanoids acids catalyzed by lipase in organic solvent media
Electron. j. biotechnol
;
10(4): 508-513, oct. 2007. ilus, tab
Article
Dans Anglais
| LILACS
| ID: lil-504124
ABSTRACT
The esterification of phenylpropanoid and hydrophenylpropanoid acids, catalyzed by candida antarctica lipase B (CAL-B), with several alcohols has demonstrated that the substitution pattern on the aromatic ring has a very significant influence on the reactivity of the carboxyl group due, mainly, to electronic effects, when compared to the unsaturated acids with the hydrogenated acids. It is also clear that in the saturated acids there still remain some unclear effects related to the aromatic substituents.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Phénylpropionates
/
Estérification
/
Triacylglycerol lipase
langue:
Anglais
Texte intégral:
Electron. j. biotechnol
Thème du journal:
Biotechnologie
Année:
2007
Type:
Article
/
descriptif de projet
Pays d'affiliation:
Mexique
Institution/Pays d'affiliation:
Universidad Autónoma Metropolitana/MX
/
Universidad Nacional Autónoma de México/MX
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