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Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/38042
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dc.contributor.authorZink Lorre, Nathalie-
dc.contributor.authorFont-Sanchis, Enrique-
dc.contributor.authorSastre-Santos, Ángela-
dc.contributor.authorFernández-Lázaro, Fernando-
dc.contributor.otherDepartamentos de la UMH::Farmacología, Pediatría y Química Orgánicaes_ES
dc.date.accessioned2025-11-10T16:36:02Z-
dc.date.available2025-11-10T16:36:02Z-
dc.date.created2016-04-
dc.identifier.citationDyes and Pigments. Volume 127, April 2016, Pages 9-17es_ES
dc.identifier.issn1873-3743-
dc.identifier.issn0143-7208-
dc.identifier.urihttps://hdl.handle.net/11000/38042-
dc.description.abstractThe reaction of perylenediimides with alcohols in the presence of fluoride anions yields 1-alkoxy- or 1,6(7)-dialkoxyperylenediimides under very mild metal-free conditions. The reaction can also be applied to bay- and ortho-brominated perylenediimides.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent9es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/closedAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAreneses_ES
dc.subjectDyes/pigmentses_ES
dc.subjectAromatic substitutiones_ES
dc.subjectRadical reactiones_ES
dc.subjectSynthetic methodses_ES
dc.subjectPerylenediimideses_ES
dc.titleEasy and mild fluoride-mediated direct mono- and dialkoxylation of perylenediimideses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.dyepig.2015.12.011es_ES
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Artículos Farmacología, Pediatría y Química Orgánica


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