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dc.contributor.authorBouanou, Hanane
dc.contributor.authorTapia, Rubén
dc.contributor.authorCano, M. José
dc.contributor.authorRamos, Jose M.
dc.contributor.authorAlvarez, Esteban
dc.contributor.authorBoulifa, Ettahir
dc.contributor.authorDahdouh, Abdelaziz
dc.contributor.authorIbn Mansour, Ahmed
dc.contributor.authorAlvarez-Manzaneda Roldán, Ramón Jesús 
dc.contributor.authorChahboun, Rachid
dc.contributor.authorAlvarez-Manzaneda, Enrique
dc.date.accessioned2024-04-12T13:29:09Z
dc.date.available2024-04-12T13:29:09Z
dc.date.issued2013-11-19
dc.identifier.citationOrg. Biomol. Chem., 2014, 12, 667es_ES
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/10835/16354
dc.description.abstractA very efficient method for synthesizing spirolactones is reported. Treatment of δ,ε-unsaturated carboxylic acids with iodine and triphenylphosphine under mild conditions leads to the corresponding spiro γ-lactones in high yield and with complete stereoselectivity. Utilizing this, the first synthesis of the terpene spirolactones (−)-isoambreinolide, (+)-vitexifolin D and (+)-vitedoin B has been achieved.es_ES
dc.language.isoenes_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.titleThe first synthesis of (−)-isoambreinolide, (+)-vitexifolin D and (+)-vitedoin Bes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2014/ob/c3ob42122hes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1039/c3ob42122h


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