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dc.contributor.authorVencato, Ivo-
dc.contributor.authorCunha, Silvio do Desterro-
dc.contributor.authorFerrari, Jailton-
dc.contributor.authorNapolitano, Hamilton B.-
dc.contributor.authorLariucci, Carlito-
dc.creatorVencato, Ivo-
dc.creatorCunha, Silvio do Desterro-
dc.creatorFerrari, Jailton-
dc.creatorNapolitano, Hamilton B.-
dc.creatorLariucci, Carlito-
dc.date.accessioned2012-09-05T16:51:09Z-
dc.date.available2012-09-05T16:51:09Z-
dc.date.issued2004-
dc.identifier.issn1600-5368-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/6695-
dc.descriptionp. 2479-2481pt_BR
dc.description.abstractThe solid-state structure of the title enaminone, C15H17N1O7, the C adduct obtained from the reaction of 4-aminopent-3-en- 2-one with methoxymethylene Meldrum's acid, has been investigated by X-ray diffraction, and several structural features are different from the previously described structure of the corresponding N adduct. The carbonyl group of the enaminone moiety of the C adduct is not coplanar with the enamine fragment. One bifurcated intramolecular NÐH O hydrogen bond [2.688 (2) and 2.668 (2) A Ê ] and two intermolecular CÐH O hydrogen bonds [3.339 (3) and 3.379 (3) A Ê ] are observed. The structure packs in a linear fashion along the [100] direction.pt_BR
dc.language.isoenpt_BR
dc.publisherInternational Union of Crystallographypt_BR
dc.sourcehttp://dx.doi.org/10.1107/S1600536804030211pt_BR
dc.subjectSingle-crystal X-ray studypt_BR
dc.subjectMean (C±C) = 0.003 AÊpt_BR
dc.subjectR factor = 0.056pt_BR
dc.subjectwR factor = 0.162pt_BR
dc.subjectData-to-parameter ratio = 12.9pt_BR
dc.titleThe polyfunctionalized enaminone ethyl [(Z)-2-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl- idenemethyl)-1-methyl-3-oxo-but-1-enylamino]- acetatept_BR
dc.title.alternativeActa Crystallographica Section Ept_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 60, n. 12pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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