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dc.contributor.authorde la Hoz, A.-
dc.contributor.authorDíaz-Ortiz, A.-
dc.contributor.authorMateo, María del Carmen-
dc.contributor.authorMoral, Mónica-
dc.contributor.authorMoreno, Andrés-
dc.contributor.authorElguero, José-
dc.contributor.authorFoces-Foces, Concepción-
dc.contributor.authorRodríguez, Matias L.-
dc.contributor.authorSánchez-Migallón, A.-
dc.date.accessioned2013-03-26T10:18:27Z-
dc.date.available2013-03-26T10:18:27Z-
dc.date.issued2006-
dc.identifierdoi: 10.1016/j.tet.2006.04.020-
dc.identifierissn: 0040-4020-
dc.identifier.citationTetrahedron 62: 5868- 5874 (2006)-
dc.identifier.urihttp://hdl.handle.net/10261/72952-
dc.description.abstractA series of 2-imidazolines and imidazoles has been synthesized using green synthetic methodologies. The preparation of 2-imidazolines was performed by cyclization of nitriles with ethylenediamine. The use of microwave irradiation in solvent-free conditions enabled 2-imidazolines to be obtained in high yields within short reaction times. Aromatization of imidazoles was performed under microwave irradiation in toluene and using Magtrieve™ as the oxidant. The X-ray structures for five of these derivatives are provided. In all cases, the molecules are assembled into chains through N-H⋯N hydrogen bonds. © 2006 Elsevier Ltd. All rights reserved.-
dc.language.isoeng-
dc.publisherPergamon Press-
dc.rightsclosedAccess-
dc.titleMicrowave assisted synthesis and crystal structures of 2-imidazolines and imidazoles-
dc.typeartículo-
dc.identifier.doi10.1016/j.tet.2006.04.020-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.tet.2006.04.020-
dc.date.updated2013-03-26T10:18:27Z-
dc.description.versionPeer Reviewed-
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