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dc.contributor.authorCen-Pacheco, Franciscoes_ES
dc.contributor.authorNorte, Manueles_ES
dc.contributor.authorFernández, José J.es_ES
dc.contributor.authorHernández Daranas, Antonioes_ES
dc.date.accessioned2020-06-03T13:51:17Z-
dc.date.available2020-06-03T13:51:17Z-
dc.date.issued2014-05-15-
dc.identifier.citationOrganic Letters 16(11): 2880–2883 (2014)es_ES
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10261/213241-
dc.description.abstractChemical investigation of an Atlantic variety of Zoanthus sp. led to the isolation of two new metabolites, zoaramine and zoarenone. Their structures were deduced by the use of NMR spectroscopy and computational calculation of 1H and 13C chemical shifts. The core of these novel compounds resembles the structure of norzoanthamine alkaloids, and their isolation represents an important step toward a better understanding of the biogenetic origin of this group of antiosteoporotic molecules.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relation.isversionofPostprintes_ES
dc.rightsclosedAccesses_ES
dc.subjectChemical structurees_ES
dc.subjectCarbonylses_ES
dc.subjectOrganic compoundses_ES
dc.subjectMolecular structurees_ES
dc.subjectCarbones_ES
dc.titleZoaramine, a Zoanthamine-like Alkaloid with a New Skeletones_ES
dc.typeartículoes_ES
dc.identifier.doi10.1021/ol500860v-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1021/ol500860ves_ES
dc.identifier.e-issn1523-7052-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/es_ES
dc.relation.csicNoes_ES
oprm.item.hasRevisionno ko 0 false*
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