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Synthesis and spectroscopic studies of 5-arylidene-3-substituted tetramic acids as possible substrates for catalytic asymmetric hydrogenation

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dc.contributor.author Athanasellis, G en
dc.contributor.author Gavrielatos, E en
dc.contributor.author Igglessi-Markopoulou, O en
dc.date.accessioned 2014-03-01T01:17:13Z
dc.date.available 2014-03-01T01:17:13Z
dc.date.issued 2001 en
dc.identifier.issn 0022-152X en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/14392
dc.subject.classification Chemistry, Organic en
dc.subject.other 4' nitro 3 butanoyltetramic acid derivative en
dc.subject.other 5 benzylidene 3 acetyltetramic acid en
dc.subject.other 5 benzylidene 3 ethoxycarbonyltetramic acid en
dc.subject.other tetramic acid derivative en
dc.subject.other unclassified drug en
dc.subject.other acylation en
dc.subject.other article en
dc.subject.other carbon nuclear magnetic resonance en
dc.subject.other catalysis en
dc.subject.other chemical analysis en
dc.subject.other cyclization en
dc.subject.other finite element analysis en
dc.subject.other hydrogenation en
dc.subject.other spectroscopy en
dc.subject.other synthesis en
dc.title Synthesis and spectroscopic studies of 5-arylidene-3-substituted tetramic acids as possible substrates for catalytic asymmetric hydrogenation en
heal.type journalArticle en
heal.identifier.primary 10.1002/jhet.5570380527 en
heal.identifier.secondary http://dx.doi.org/10.1002/jhet.5570380527 en
heal.language English en
heal.publicationDate 2001 en
heal.abstract A new series of 5-arylidene-3-substituted tetramic acids 6-19 have been synthesized by a condensation reaction of 3-butanoyl tetramic acid 3, 3-ethoxycarbonyl tetramic acid 4 and 3-acetyl tetramic acid 5 with a variety of substituted benzaldehydes. The structures of the isolated compounds 6-19 have been elucidated using FT-IR, H-1 and C-13-NMR spectroscopy, FAB-MS spectroscopy as well as elemental analyses. en
heal.publisher HETERO CORPORATION en
heal.journalName Journal of Heterocyclic Chemistry en
dc.identifier.doi 10.1002/jhet.5570380527 en
dc.identifier.isi ISI:000171704700027 en
dc.identifier.volume 38 en
dc.identifier.issue 5 en
dc.identifier.spage 1203 en
dc.identifier.epage 1208 en


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