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Mild-base-promoted arylation of (hetero)arenes with anilines

dc.contributor.authorMartín García, Víctor Sotero 
dc.contributor.authorSantos, Tanausú
dc.contributor.authorMonzón, Diego M. 
dc.contributor.authorPinacho-Crisóstomo, F.
dc.contributor.authorCarrillo, Romen
dc.date.accessioned2019-09-19T13:45:16Z
dc.date.available2019-09-19T13:45:16Z
dc.date.issued2018
dc.identifier.urihttp://riull.ull.es/xmlui/handle/915/16139
dc.description.abstractTransition metal-free radical arylation of heteroarenes is achieved at room temperature by simply adding aqueous sodium carbonate to a solution of the corresponding heteroarene and arenediazonium salt, which can even be formed in situ. Such an easy, inexpensive and mild methodology has been optimized and applied to the expeditious modification of interesting molecular cores like naphthylimide or bisthienylcyclopentenes.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.relation.ispartofseriesChemistry, an Asian Journal, vol. 13, issue 3, 2018en
dc.rightsLicencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES
dc.titleMild-base-promoted arylation of (hetero)arenes with anilinesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/asia.201701585
dc.subject.keywordC−C couplingen
dc.subject.keyworddiazo compoundsen
dc.subject.keyworddyes/pigmentsen
dc.subject.keywordheterocyclesen
dc.subject.keywordradical reactionsen
dc.subject.keywordheterocicloses_ES
dc.subject.keywordreacciones radicaleses_ES


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Except where otherwise noted, this item's license is described as Licencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional)