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dc.contributor.authorFernández, Antonio
dc.contributor.authorAlvarez, Esteban
dc.contributor.authorAlvarez-Manzaneda Roldán, Ramón Jesús 
dc.contributor.authorChahboun, Rachid
dc.contributor.authorAlvarez-Manzaneda, Enrique
dc.date.accessioned2024-04-12T13:30:21Z
dc.date.available2024-04-12T13:30:21Z
dc.date.issued2014-09-03
dc.identifier.citationChem. Commun., 2014, 50, 13100es_ES
dc.identifier.issn1359-7345
dc.identifier.urihttp://hdl.handle.net/10835/16355
dc.description.abstractA short synthetic sequence for the preparation of merosesquiterpenes with a benzoxanthene skeleton starting from commercial (-)-sclareol is reported. The D ring of the target compound is obtained through a Diels–Alder cycloaddition, involving a dienoldiether derived from a tricyclic α,β-enone synthesized in two steps from the starting diterpene. Utilizing this procedure, the preparation of (+)-hongoquercin A and the first synthesis of (+)-cyclospongiaquinone-1 were achieved.es_ES
dc.language.isoenes_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.titleA short route towards merosesquiterpenes with a benzoxanthene skeletones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2014/cc/c4cc05116ees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1039/c4cc05116e


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