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dc.contributor.authorSolas Luera, Marta 
dc.contributor.authorMuñoz Torres, Miguel Ángel 
dc.contributor.authorSuarez Pantiga, Samuel 
dc.contributor.authorSanz Díez, Roberto 
dc.date.accessioned2020-10-29T11:17:33Z
dc.date.available2020-10-29T11:17:33Z
dc.date.issued2020-10
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/10259/5533
dc.description.abstractSkipped diynones, efficiently prepared from biomass-derived ethyl lactate, undergo a tandem hydration− oxacyclization reaction under gold(I) catalysis. Reaction conditions have been developed for a switchable process that allows selective access to 4-pyrones or 3(2H)-furanones from the same starting diynones. Further application of this methodology in the total synthesis of polyporapyranone B was demonstrated.es
dc.description.sponsorshipMinisterio de Ciencia e Innovación and FEDER (CTQ2016-75023-C2-1-P) and Junta de Castilla y León and FEDER (BU291P18)es
dc.format.mimetypeapplication/pdf
dc.language.isospaes
dc.publisherAmerican Chemical Societyes
dc.relation.ispartofOrganic Letters. 2020, V. 22, n. 19, p. 7681–7687es
dc.subjectHydrocarbonses
dc.subjectCyclizationes
dc.subjectMixtureses
dc.subjectCatalystses
dc.subjectSelectivityes
dc.subject.otherQuímica orgánicaes
dc.subject.otherChemistry, Organicen
dc.titleRegiodivergent Hydration–Cyclization of Diynones under Gold Catalysises
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.relation.publisherversionhttps://doi.org/10.1021/acs.orglett.0c02892es
dc.identifier.doi10.1021/acs.orglett.0c02892
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/CTQ2016-75023-C2-1-P
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/BU291P18
dc.identifier.essn1523-7052
dc.journal.titleOrganic Letterses
dc.volume.number22es
dc.issue.number19es
dc.page.initial7681es
dc.page.final7687es
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersiones


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