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dc.contributor.authorLesieur, Mathieu
dc.contributor.authorLazreg, Faima
dc.contributor.authorCazin, Catherine S. J.
dc.date.accessioned2015-02-04T09:31:12Z
dc.date.available2015-02-04T09:31:12Z
dc.date.issued2014-08-18
dc.identifier159775493
dc.identifier2158ff5e-acf0-496c-88d7-a2b790f72e57
dc.identifier000339861700027
dc.identifier84904440448
dc.identifier000339861700027
dc.identifier.citationLesieur , M , Lazreg , F & Cazin , C S J 2014 , ' A cooperative Pd-Cu system for direct C-H bond arylation ' , Chemical Communications , vol. 50 , no. 64 , pp. 8927-8929 . https://doi.org/10.1039/c4cc03201ben
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/10023/6066
dc.descriptionThe authors are grateful to the Royal Society (University Research Fellowship to CSJC) for financial support.en
dc.description.abstractA novel and efficient method for C-H arylation using well-defined Pd- and Cu-NHC systems has been developed. This process promotes the challenging construction of C-C bonds from arenes or heteroarenes using aryl bromides and chlorides. Mechanistic studies show that [Cu(OH)(NHC)] plays a key role in the C-H activation and is involved in the transmetallation with the Pd-NHC co-catalyst.
dc.format.extent3
dc.format.extent1399661
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.subjectCross-coupling reactionsen
dc.subjectSuzuki-Miyauraen
dc.subjectVinyl halidesen
dc.subjectPalladiumen
dc.subjectComplexesen
dc.subjectReagentsen
dc.subjectCatalysten
dc.subjectSubstitutionsen
dc.subjectHeteroarenesen
dc.subjectActivationen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleA cooperative Pd-Cu system for direct C-H bond arylationen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1039/c4cc03201b
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.rsc.org/suppdata/cc/c4/c4cc03201b/c4cc03201b1.pdfen


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