dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T14:21:04Z
dc.date.available2014-05-20T14:21:04Z
dc.date.created2014-05-20T14:21:04Z
dc.date.issued2004-12-01
dc.identifierQuímica Nova. Sociedade Brasileira de Química, v. 27, n. 6, p. 878-881, 2004.
dc.identifier0100-4042
dc.identifierhttp://hdl.handle.net/11449/26308
dc.identifier10.1590/S0100-40422004000600007
dc.identifierS0100-40422004000600007
dc.identifierS0100-40422004000600007.pdf
dc.identifier1308042794786872
dc.identifier4484083685251673
dc.description.abstractPhytochemical studies with leaves of Uncaria guianensis resulted in the isolation of the oxindole alkaloids isomitraphylline (1), 3-isoajmalicine (2) mitraphylline (3), and isomitraphylinic acid (4). Structural assignments of these alkaloids, including relative configurations and conformations, were performed through spectral data and physical properties. 1D and 2D homonuclear and heteronuclear NMR spectroscopy was a valuable tool for the establishment of the relative stereochemistry of those compounds.
dc.languagepor
dc.publisherSociedade Brasileira de Química
dc.relationQuímica Nova
dc.relation0.646
dc.relation0,255
dc.rightsAcesso aberto
dc.sourceSciELO
dc.subjectUncaria guianensis
dc.subjectRubiaceae
dc.subjectoxindole alkaloids
dc.subjectstereochemistry
dc.titleDeterminação por RMN das configurações relativas e conformações de alcalóides oxindólicos isolados de Uncaria guianensis
dc.typeArtículos de revistas


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