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dc.contributor.authorHamdouchi, Chafiq
dc.contributor.authorEzquerra, Jesús
dc.contributor.authorVega Ramiro, Juan Antonio 
dc.contributor.authorVaquero López, Juan J.
dc.contributor.authorÁlvarez-Builla Gómez, Julio 
dc.contributor.authorHeinz, Beverly A.
dc.date.accessioned2009-06-05T15:20:57Z
dc.date.available2009-06-05T15:20:57Z
dc.date.issued1999
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, 1999, v. 9, n. 10, p. 1391-1394en
dc.identifier.issn0960-894X
dc.identifier.urihttp://hdl.handle.net/10017/3088
dc.description.abstractVarious 2-amino-3-acyl-6-[(E)-1-phenyl-2-N-methylcarbamoylvinyl]-imidazo[1,2-a]pyridines, structurally related to Enviroxime were prepared to determine the effect of acyl groups on the antirhinoviral activity. A short and efficient means for the construction of the imidazo nucleus as well as biological evaluation of the final compounds are disclosed.en
dc.description.sponsorshipThis research was supported by a CDTI program (Plan concertado 96/0036) and the Spanish Farma III programme (Ministerio de Industria y Ministerio de Sanidad). We are also grateful to the Lilly Rhinovirus Action Group for their advice and interest in this work.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherPergamonen
dc.rights(c) Elsevier, 1999en
dc.subjectEnviroximeen
dc.subjectChemistry, Medicinalen
dc.subjectChemistry, Organicen
dc.titleShort synthesis and anti-rhinoviral activity of imidazo[1,2-a]pyridines: the effect of acyl groups at 3-positionen
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/S0960-894X(99)00193-6
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/S0960-894X(99)00193-6
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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