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dc.creatorGUZMÁN,M
dc.creatorORTEGA,P
dc.creatorVERA,L
dc.creatorASTUDILLO,E
dc.date2005-03-01
dc.date.accessioned2020-02-17T15:35:34Z
dc.date.available2020-02-17T15:35:34Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-97072005000100003
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/131968
dc.descriptionThe synthesis of derivatives of dihydroeuparin, a secondary metabolite of the shrub Senecio graveolens, is described. The main modifications were the introduction of a hydrocarbon branch and the transformation of a ketone group into its oxime. Structure identification was carried out by IR, ¹H-NMR and 13C-NMR spectroscopy. These compounds may have application in the process of copper extraction
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0717-97072005000100003
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceJournal of the Chilean Chemical Society v.50 n.1 2005
dc.subjectDihydroeuparin
dc.subjectSolvent Extraction
dc.subjectSenecio Graveolens
dc.titleOxime-Derivatives of Dihydroeuparin


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