Enzymatic synthesis of hydrophilic and hydrophobic derivatives of natural phenolic acids in organic media

Stamatis, H; Sereti, V; Kolisis, FN

dc.contributor.author	Stamatis, H	en
dc.contributor.author	Sereti, V	en
dc.contributor.author	Kolisis, FN	en
dc.date.accessioned	2014-03-01T02:41:52Z
dc.date.available	2014-03-01T02:41:52Z
dc.date.issued	2001	en
dc.identifier.issn	1381-1177	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/30643
dc.subject	Cinnamic acids	en
dc.subject	Esterification	en
dc.subject	Lipase	en
dc.subject	Organic media	en
dc.subject	Phenolic antioxidants	en
dc.subject.classification	Biochemistry & Molecular Biology	en
dc.subject.classification	Chemistry, Physical	en
dc.subject.other	antioxidant	en
dc.subject.other	benzoic acid derivative	en
dc.subject.other	cinnamic acid derivative	en
dc.subject.other	esterase	en
dc.subject.other	triacylglycerol lipase	en
dc.subject.other	acylation	en
dc.subject.other	conference paper	en
dc.subject.other	drug identification	en
dc.subject.other	drug purification	en
dc.subject.other	drug synthesis	en
dc.subject.other	enzyme activity	en
dc.subject.other	esterification	en
dc.subject.other	high performance liquid chromatography	en
dc.subject.other	in vitro study	en
dc.subject.other	infrared spectrometry	en
dc.subject.other	nuclear magnetic resonance spectroscopy	en
dc.subject.other	reaction analysis	en
dc.subject.other	technique	en
dc.subject.other	thin layer chromatography	en
dc.title	Enzymatic synthesis of hydrophilic and hydrophobic derivatives of natural phenolic acids in organic media	en
heal.type	conferenceItem	en
heal.identifier.primary	10.1016/S1381-1177(00)00016-3	en
heal.identifier.secondary	http://dx.doi.org/10.1016/S1381-1177(00)00016-3	en
heal.language	English	en
heal.publicationDate	2001	en
heal.abstract	The enzymatic esterification of natural phenolic antioxidants such as cinnamic acid and benzoic acid derivatives, with aliphatic alcohols, monosaccharides as well as alkylglucosides, using various lipases and esterases in non-aqueous media, was investigated. Reaction rate and esterification yield seems to be Linked to the structural characteristics of the substrates (aromatic acids and alcohols or sugars) used. (C) 2001 Elsevier Science B.V. All rights reserved.	en
heal.publisher	ELSEVIER SCIENCE BV	en
heal.journalName	Journal of Molecular Catalysis - B Enzymatic	en
dc.identifier.doi	10.1016/S1381-1177(00)00016-3	en
dc.identifier.isi	ISI:000167014100026	en
dc.identifier.volume	11	en
dc.identifier.issue	4-6	en
dc.identifier.spage	323	en
dc.identifier.epage	328	en