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dc.contributor.authorIrastorza Epelde, Aitziber
dc.contributor.authorAizpurua Iparraguirre, Jesús María
dc.contributor.authorCorrea Navarro, Arkaitz
dc.date.accessioned2018-01-25T15:39:29Z
dc.date.available2018-01-25T15:39:29Z
dc.date.issued2016-02-24
dc.identifier.citationOrganic Letters 18 (5) : 1080–1083 (2016)es_ES
dc.identifier.issn1523-7052
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/10810/24693
dc.description.abstractSelective Pd-catalyzed C(sp2)–H oxygenation of 4-substituted 1,2,3-triazoles is described. Unlike previous metal-catalyzed C–H functionalization events, which preferentially occur at the activated heterocyclic C–H bond, the regioselective oxygenation of the arene/alkene moiety is now achieved featuring the unconventional role of a simple triazole scaffold as a modular and selective directing group.es_ES
dc.description.sponsorshipMINECO for a Ramon y Cajal research contract (RYC-2012-09873).es_ES
dc.language.isoenges_ES
dc.publisherACS Publicationses_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/RYC-2012-09873es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectacetoxylationes_ES
dc.subjectclickes_ES
dc.subjectpalladiumes_ES
dc.subjectC-H activationes_ES
dc.subjectTriazoleses_ES
dc.titleTriazole-Directed Pd-Catalyzed C(sp2)–H Oxygenation of Arenes and Alkeneses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderCopyright © 2016 American Chemical Societyes_ES
dc.relation.publisherversionhttp://pubs.acs.org/doi/abs/10.1021/acs.orglett.6b00195es_ES
dc.identifier.doi10.1021/acs.orglett.6b00195
dc.contributor.funderMINECO
dc.departamentoesQuímica orgánica Ies_ES
dc.departamentoeuKimika organikoa Ies_ES


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