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dc.contributor.authorMinguez Ortega, José Miguel
dc.contributor.authorCastellote Álvaro, María Isabel 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorGarcía Navío, José Luis 
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.contributor.authorCastaño González, Obis Dionisio 
dc.contributor.authorAndrés, José L. de
dc.date.accessioned2009-10-01T12:27:36Z
dc.date.available2009-10-01T12:27:36Z
dc.date.issued1997
dc.identifier.bibliographicCitationTetrahedron, 1997, v.53, n.27, p.9341-9356en
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/10017/4174
dc.description.abstractThe structure of 3,4-dihydropyrrolo[1,2-a]pyrazine and its N-protonated form is studied by ab initio calculations. Examples of the reactivity of this poorly studied system are presented in which it is shown that the imino moiety does not react with dienes but does undergo inter- and intramolecular 1,3-dipolar cycloadditions by reaction of azomethine ylides of this bicyclic system with suitable dipolarophiles.en
dc.description.sponsorshipMinisterio de Educación y Cienciaes_ES
dc.description.sponsorshipCentro de Computación de Galixia (CESGA)es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherElsevieren
dc.rights© Elsevier, 1997en
dc.subjectPyrrolodiazinesen
dc.subjectDipolarophilesen
dc.titlePyrrolodiazines. 4. Structure and chemistry of 3,4-dihydropyrrolo[1,2-a]pyrazineen
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/S0040-4020(97)00587-5
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/S0040-4020(97)00587-5
dc.relation.projectIDQFN94-4619 (Comisió Interdepartamental de Reçerca i Innovació Técnologica-CIRIT)
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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