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dc.contributor.authorCañeque Cobo, Tatiana
dc.contributor.authorCuadro Palacios, Ana María 
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.contributor.authorVaquero López, Juan J.
dc.date.accessioned2009-04-29T11:55:45Z
dc.date.available2009-04-29T11:55:45Z
dc.date.issued2009
dc.identifier.bibliographicCitationTetrahedron Letters, 2009, v.50 n.13, p.1419-1422en
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10017/2678
dc.description.abstractAn efficient functionalization of the quinolizinium system is reported. The reaction of the four isomeric bromoquinolizinium salts with different organotrifluoroborates afforded alkyl-, vinyl-, aryl-, and heteroaryl quinolizinium derivatives in moderate or good yields. Reactions are carried out in water using a counterion exchange for the isolation of the cationic-coupled compounds.en
dc.description.sponsorshipComunidad de Madrid
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherElsevieren
dc.rights© Elsevier, 2009en
dc.subjectQuinoliziniumen
dc.subjectEfficient functionalizationen
dc.subjectOrganotrifluoroboratesen
dc.subjectWateren
dc.titleEfficient functionalization of quinolizinium cations with organotrifluoroborates in wateren
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaBioquímicaes_ES
dc.subject.ecienciaBiochemistryen
dc.subject.ecienciaSCIENCEen
dc.subject.ecienciaCIENCIAes_ES
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Orgánica
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tetlet.2009.01.040
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/j.tetlet.2009.01.040
dc.relation.projectIDCTQ2005/011060/BQU (Ministerio de Educación y Ciencia)
dc.relation.projectIDCCG-UAH/SAL-0660 (Universidad de Alcalá)
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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