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

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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 http://hdl.handle.net/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.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

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