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dc.contributor.authorPonce de León Pintado, Jaime 
dc.contributor.authorEspinet Rubio, Pablo 
dc.date.accessioned2023-04-28T12:09:22Z
dc.date.available2023-04-28T12:09:22Z
dc.date.issued2021
dc.identifier.citationChemical Communications, 2021, 57, 10875–10878es
dc.identifier.issn1359-7345es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/59422
dc.descriptionProducción Científicaes
dc.description.abstractHighly selective cross-couplings to polyfluorinated assymmetric biaryls, including the symmetric biaryl C6F5–C6F5, are achieved at relatively low temperature (80 °C) and in short times using [MCl2(PhPEWO-F)] catalysts (M = Ni, Pd; PhPEWO-F = 1-(PPh2), 2-(CH[double bond, length as m-dash]CH–C(O)Ph)–C6F4), ArFI, and Zn(C6F5)2 as example of highly fluorinated nucleophile.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationNegishi cross-couplinges
dc.subject.classificationAcoplamiento de Negishies
dc.subject.classificationCross-coupling reaction catalyzedes
dc.subject.classificationReacción de acoplamiento cruzadoes
dc.titleSelective synthesis of fluorinated biaryls by [MCl2(PhPEWO-F)] (M = Ni, Pd) catalysed Negishi cross-couplinges
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2021 Royal Society of Chemistryes
dc.identifier.doi10.1039/d1cc04915aes
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2021/cc/d1cc04915aes
dc.identifier.publicationfirstpage10875es
dc.identifier.publicationissue83es
dc.identifier.publicationlastpage10878es
dc.identifier.publicationtitleChemical Communicationses
dc.identifier.publicationvolume57es
dc.peerreviewedSIes
dc.identifier.essn1364-548Xes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersiones
dc.subject.unesco23 Químicaes


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