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Enyne ring-closing metathesis on heteroaromatic cations

dc.contributor.authorNúñez Ventura, Araceli 
dc.contributor.authorCuadro Palacios, Ana María 
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.contributor.authorVaquero López, Juan J.
dc.date.accessioned2009-06-19T03:35:49Z
dc.date.available2009-06-19T03:35:49Z
dc.date.issued2006
dc.identifier.bibliographicCitationChemical Communications, 2006, n. 25, p. 2690-2692en
dc.identifier.issn1359-7345
dc.identifier.urihttp://hdl.handle.net/10017/3215
dc.description.abstractCationic heteroaromatic enynes have been employed as substrates in enyne ring-closing metathesis, under an atmosphere of ethylene and using the Hoveyda-Grubbs catalyst, for the first time; the reaction affords new 1-vinyl- and 2-vinyl-substituted 3,4-dihydroquinolizinium salts, useful precursors for biologically relevant cations based on the quinolinizium system.
dc.description.sponsorshipThe authors acknowledge support for this work from the Plan Nacional de Investigación Científica, Desarrollo e Innovación Tecnológica, Ministerio de Ciencia y Tecnología through project BQU2002-03578 and a grant from the Comunidad de Madrid (A. N.).en
dc.description.sponsorshipMinisterio de Ciencia y Tecnologíaes_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherRoyal Society of Chemistryen
dc.rights(C) The Royal Society of Chemistry, 2006en
dc.subject1 Vinyl 3,4 dihydroquinolizinium derivativeen
dc.subject2 Vinyl 3,4 dihydroquinolizinium derivativeen
dc.subjectBerberine derivativeen
dc.subjectCationen
dc.subjectCoralyneen
dc.subjectDihydroquinoline derivativeen
dc.subjectEnyne derivativeen
dc.subjectEthyleneen
dc.subjectHeteroaromatic cationen
dc.subjectUnclassified drugen
dc.subjectArticleen
dc.subjectCation transporten
dc.subjectChemical structureen
dc.subjectProduct recoveryen
dc.subjectRing closing metathesisen
dc.subjectStructure activity relationen
dc.subjectStructure analysisen
dc.titleEnyne ring-closing metathesis on heteroaromatic cationsen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaCienciaes_ES
dc.subject.ecienciaQuímica orgánicaes_ES
dc.subject.ecienciaScienceen
dc.subject.ecienciaChemistry, organicen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Orgánicaes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1039/b602420c
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1039/b602420c
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICYT//BQU2002-03578/ES/NUEVOS CROMOFOROS CON PROPIEDADES INTERCALANTES DE ADN, AFINIDAD Y SELECTIVIDADes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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