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dc.contributor.authorBallesteros-Garrido, R.-
dc.contributor.authorBlanco, F.-
dc.contributor.authorBallesteros, R.-
dc.contributor.authorLeroux, Frédérc R.-
dc.contributor.authorAbarca, B.-
dc.contributor.authorColobert, François-
dc.contributor.authorAlkorta, Ibon-
dc.contributor.authorElguero, José-
dc.date.accessioned2013-01-30T12:15:13Z-
dc.date.available2013-01-30T12:15:13Z-
dc.date.issued2009-
dc.identifierdoi: 10.1002/ejoc.200900818-
dc.identifierissn: 1434-193X-
dc.identifiere-issn: 1099-0690-
dc.identifier.citationEuropean Journal of Organic Chemistry: 5765- 5778 (2009)-
dc.identifier.urihttp://hdl.handle.net/10261/65474-
dc.description.abstractIn the course of the synthesis of new fluorophores for molecular recognition an experimental (1H NMR) and theoretical (DFT) study of the ring-chain isomerism of 3-(pyridin-2-yl )[1,2,3]triazolo[1,5-a]quinoline derivatives (A) into 2-([1,2,3]triazolo[1,5-a]pyridin-3-yl)quinoline derivatives (B) has been carried out. The rearrangement is influenced by steric and electronic effects of the substituents present on the quinoline ring. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.-
dc.language.isoeng-
dc.publisherJohn Wiley & Sons-
dc.rightsclosedAccess-
dc.title3-(pyridin-2-yl)[l,2,3]triazolo[l,5-a]quinoline: A theoretical and experimental analysis of ring-chain isomerisation-
dc.typeArtículo-
dc.identifier.doi10.1002/ejoc.200900818-
dc.date.updated2013-01-30T12:15:13Z-
dc.description.versionPeer Reviewed-
Appears in Collections:(IQM) Artículos
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