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dc.contributor.authorPinacho Crisóstomo, Fernando R.-
dc.contributor.authorMartín, Tomás-
dc.contributor.authorCarrillo Fumero, Romen-
dc.date.accessioned2019-04-10T11:53:19Z-
dc.date.available2019-04-10T11:53:19Z-
dc.date.issued2014-02-17-
dc.identifierdoi: 10.1002/anie.201309761-
dc.identifierissn: 1433-7851-
dc.identifiere-issn: 1521-3773-
dc.identifier.citationAngewandte Chemie - International Edition 53(8): 2181-2185 (2014)-
dc.identifier.urihttp://hdl.handle.net/10261/179833-
dc.description.abstractAscorbic acid (vitamin C) has been used as a radical initiator in a metal-free direct CH arylation of (hetero)arenes. Starting from an aniline, the corresponding arenediazonium ion is generated in situ and immediately reduced by vitamin C to an aryl radical that undergoes a homolytic aromatic substitution with a (hetero)arene. Notably, neither heating nor irradiation is required. This procedure is mild, operationally simple, and constitutes a greener approach to arylation.-
dc.description.sponsorshipThis research was supported by the Spanish MINECO, cofinanced by the European Regional Development Fund (ERDF) (CTQ2011‐22653). F.P.C. thanks the CSIC for a JAE postdoctoral contract, cofinanced by the FSE.-
dc.publisherWiley-VCH-
dc.rightsclosedAccess-
dc.subjectMetal‐free reactions-
dc.subjectAscorbic acid-
dc.subjectAromatic substitution-
dc.subjectC-H arylation-
dc.subjectGreen chemistry-
dc.titleAscorbic Acid as an Initiator for the Direct C-H Arylation of (Hetero)arenes with Anilines Nitrosated In Situ-
dc.typeartículo-
dc.identifier.doi10.1002/anie.201309761-
dc.relation.publisherversionhttps://doi.org/10.1002/anie.201309761-
dc.date.updated2019-04-10T11:53:19Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderEuropean Commission-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderConsejo Superior de Investigaciones Científicas (España)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003339es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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