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dc.contributor.authorCano, M. José
dc.contributor.authorBouanou, Hanane
dc.contributor.authorTapia, Rubén
dc.contributor.authorAlvarez, Esteban
dc.contributor.authorAlvarez-Manzaneda Roldán, Ramón Jesús 
dc.contributor.authorChahboun, Rachid
dc.contributor.authorAlvarez-Manzaneda, Enrique
dc.date.accessioned2024-04-12T13:28:17Z
dc.date.available2024-04-12T13:28:17Z
dc.date.issued2013-08-28
dc.identifier.citationJ. Org. Chem. 2013, 78, 9196−9204es_ES
dc.identifier.issn0022-3263
dc.identifier.urihttp://hdl.handle.net/10835/16351
dc.description.abstractTreatment of o-allyl phenols with catalytic NIS−PPh3 affords the corresponding spirodihydrobenzofuran derivatives in high yield with high regio- and total stereoselectivity under mild conditions. These results were utilized to achieve the first total synthesis of the protein kinase C inhibitor corallidictyal D starting from α-ionone.es_ES
dc.language.isoenes_ES
dc.publisherAmerican Chemical Societyes_ES
dc.titleNIS−PPh3: A Selective Reagent for the Spiroannulation of o‑Allyl Phenols. Total Synthesis of Corallidictyal Des_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/jo4014047es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.1021/jo4014047


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