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dc.contributor.authorValenciano Martínez, Jesús 
dc.contributor.authorCuadro Palacios, Ana María 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.date.accessioned2009-07-07T01:33:09Z
dc.date.available2009-07-07T01:33:09Z
dc.date.issued1999
dc.identifier.bibliographicCitationTetrahedron Letters, 1999, v. 40, p. 763-766en
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10017/3479
dc.description.abstract2-Alkoxycarbonylpyridinium N-aminides behave as 1,3-dipoles when reacted with Michael accepters, giving rise to the corresponding cycloadducts which, depending on their regioisomeric nature, subsequently undergo a ring expansion to give pyrido[1,2-b]pyridazinium inner salts.en
dc.description.sponsorshipComisión Interministerial de Ciencia y Tecnología - CICYTEes_ES
dc.description.sponsorshipMinisterio de Educación y Cienciaes_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherPergamonen
dc.rights© Elsevier Science, 1999en
dc.subjectN-aminidesen
dc.subjectBetainesen
dc.subjectRearrangementen
dc.subject1,3/1,4-dipolesen
dc.subjectWestphal condensationen
dc.subjectAs-triazinesen
dc.subjectDerivativesen
dc.titleNew route to pyrido[1,2-b]pyridazinium inner salts. Evidence of a 1,3-dipolar cycloaddition-ring expansion processen
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 Orgánica
dc.relation.publisherversionhttp://dx.doi.org/10.1016/S0040-4039(98)02406-X
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/S0040-4039(98)02406-X
dc.relation.projectIDinfo:eu-repo/grantAgreement/CICYT//PM97-004/ESes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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