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Triazolium Salts as Appropriate Catalytic Scaffolds for 1,4-Additions toα,β-Unsaturated Carbonyls

dc.contributor.authorBratko, Ielyzaveta
dc.contributor.authorGuisado-Barrios, Gregorio
dc.contributor.authorFavier, Isabel
dc.contributor.authorMallet-Ladeira, Sonia
dc.contributor.authorTeuma, Emmanuelle
dc.contributor.authorPeris, Eduardo
dc.contributor.authorGómez, Montserrat
dc.date.accessioned2015-07-23T12:09:58Z
dc.date.available2015-07-23T12:09:58Z
dc.date.issued2014
dc.identifier.issn1434-193X
dc.identifier.urihttp://hdl.handle.net/10234/128866
dc.description.abstract1,2,3-Triazole derivatives containing a rigid dihydroanthracenyl skeleton are suitable precursors for both organometallic and organo-based catalysts. A Rh–carbene complex and the triazolium salt efficiently catalyzed the 1,4-additions of C- and heterodonor reagents to α,β-unsaturated carbonyl substrates, respectively.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherWiley Online Libraryca_CA
dc.relation.isPartOfEuropean Journal of Organic Chemistry, 2014, vol. 2014, nº 10ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/CNE/1.0/*
dc.subjectrhodiumca_CA
dc.subjectorganocatalysisca_CA
dc.subjectmesoionic carbeneca_CA
dc.subjectnitrogen heterocyclesca_CA
dc.subjectmichael additionca_CA
dc.titleTriazolium Salts as Appropriate Catalytic Scaffolds for 1,4-Additions toα,β-Unsaturated Carbonylsca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1002/ejoc.201301220
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://onlinelibrary.wiley.com/doi/10.1002/ejoc.201301220/abstractca_CA


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