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dc.contributor.authorVega Ramiro, Juan Antonio 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.contributor.authorEzquerra, Jesús
dc.contributor.authorHamdouchi, Chafiq
dc.date.accessioned2009-10-06T10:02:02Z
dc.date.available2009-10-06T10:02:02Z
dc.date.issued1999
dc.identifier.bibliographicCitationTetrahedron, 1999, v.55, n.8, p.2317-2326en
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/10017/4206
dc.description.abstractA microwave (focused waves) assisted N-alkylation of 2-halopyridines provides a convenient entry to 2-amino-imidazo[1,2-a]pyridine derivatives after reaction of the alkylated substrates with cyanamide under basic conditions.en
dc.description.sponsorshipCDTI program (Plan concertado 96/0036)es_ES
dc.description.sponsorshipPROFARMA program (Ministerio de Industria y Ministerio de Sanidad)es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherElsevieren
dc.rights© Elsevier, 1999en
dc.subjectFocused microwaveen
dc.subjectAlkylationen
dc.subject2-Halopyridinesen
dc.subjectImidazo[1,2-a]pyridinesen
dc.titleA new approach to the synthesis of 2-aminoimidazo[1,2-a]pyridine derivatives through microwave-assisted N-alkylation of 2-halopyridinesen
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(99)00012-5
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/S0040-4020(99)00012-5
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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