Synthesis and enantiomeric excess measurements of optically active N- acetyl tetramic acids

Petroliagi, M; Igglessi-Markopoulou, O

dc.contributor.author	Petroliagi, M	en
dc.contributor.author	Igglessi-Markopoulou, O	en
dc.date.accessioned	2014-03-01T01:15:16Z
dc.date.available	2014-03-01T01:15:16Z
dc.date.issued	1999	en
dc.identifier.issn	0957-4166	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/13401
dc.subject	Optical Activity	en
dc.subject	Physical Characteristic	en
dc.subject	Amino Acid	en
dc.subject	Enantiomeric Excess	en
dc.subject.classification	Chemistry, Inorganic & Nuclear	en
dc.subject.classification	Chemistry, Organic	en
dc.subject.classification	Chemistry, Physical	en
dc.subject.other	tetramic acid derivative	en
dc.subject.other	acylation	en
dc.subject.other	article	en
dc.subject.other	chemical modification	en
dc.subject.other	chemical reaction	en
dc.subject.other	cyclization	en
dc.subject.other	enantiomer	en
dc.subject.other	optical rotation	en
dc.subject.other	priority journal	en
dc.subject.other	synthesis	en
dc.title	Synthesis and enantiomeric excess measurements of optically active N- acetyl tetramic acids	en
heal.type	journalArticle	en
heal.identifier.primary	10.1016/S0957-4166(99)00192-5	en
heal.identifier.secondary	http://dx.doi.org/10.1016/S0957-4166(99)00192-5	en
heal.language	English	en
heal.publicationDate	1999	en
heal.abstract	A facile route to chiral functionalised tetramic acids through C-acylation-cyclisation reactions of active methylene compounds with N-hydroxysuccinimide esters of N-acetyl-L-amino acids is described. Enantiomeric excesses and physical characteristics of all compounds are reported. (C) 1999 Elsevier Science Ltd. All rights reserved.	en
heal.publisher	PERGAMON-ELSEVIER SCIENCE LTD	en
heal.journalName	Tetrahedron Asymmetry	en
dc.identifier.doi	10.1016/S0957-4166(99)00192-5	en
dc.identifier.isi	ISI:000081389700010	en
dc.identifier.volume	10	en
dc.identifier.issue	10	en
dc.identifier.spage	1873	en
dc.identifier.epage	1875	en