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dc.contributor.authorFlores Giubi, Eugenia
dc.contributor.authorDurán Peña, María Jesús 
dc.contributor.authorBotubol Ares, José Manuel 
dc.contributor.authorEscobar Montaño, Felipe 
dc.contributor.authorZorrilla Cuenca, David 
dc.contributor.authorMacías Sánchez, Antonio José 
dc.contributor.authorHernández Galán, Rosario 
dc.contributor.otherQuímica Orgánicaes_ES
dc.date.accessioned2024-01-30T11:09:53Z
dc.date.available2024-01-30T11:09:53Z
dc.date.issued2017
dc.identifier.issn1520‐6025
dc.identifier.urihttp://hdl.handle.net/10498/30399
dc.description.abstractnovel diterpenoid, gaditanone (2), which possesses an unprecedented 5/6/4/6-fused gaditanane tetracyclic ring skeleton, and a new jatrophane (1) were isolated from the aerial parts of Euphorbia gaditana. The chemical structures and absolute configurations were determined by extensive spectroscopic NMR studies and ECD data analysis. A proposed biosynthetic pathway is presented for compound 2.es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherAMER CHEMICAL SOCes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceJournal of Natural Products, Vol. 80, Núm. 7, 2017, pp. 2161-2165es_ES
dc.subjecteuphorbiaes_ES
dc.subjectgaditanone skeletones_ES
dc.subjectnatural productses_ES
dc.titleGaditanone, a Diterpenoid Based on an Unprecedented Carbon Skeleton Isolated from Euphorbia gaditanaes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/ACS.JNATPROD.7B00332
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//BFU2015-68652-R/ES/REGENERACION DE LESIONES TRAUMATICAS EN EL SISTEMA NERVIOSO CENTRAL MEDIANTE MODULADORES DE LA ACTIVIDAD DE PKC/ es_ES
dc.type.hasVersionVoRes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This work is under a Creative Commons License Attribution-NonCommercial-NoDerivatives 4.0 Internacional