N-Heterocyclic Carbenes: Useful Ligands for the Palladium-Catalysed Direct C5 Arylation of Heteroaromatics with Aryl Bromides or Electron-Deficient Aryl Chlorides

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dc.authoridKaloğlu, Murat/0000-0002-2770-5532
dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridbruneau, christian/0000-0002-2220-1458
dc.authoridDoucet, Henri/0000-0002-1410-3663
dc.authorwosidKaloğlu, Murat/AAA-3956-2021
dc.authorwosidBruneau, Christian/AAL-4582-2020
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidGök, Yetkin/AAA-5669-2021
dc.contributor.authorOzdemir, Ismail
dc.contributor.authorGok, Yetkin
dc.contributor.authorOzeroglu, Oezlem
dc.contributor.authorKaloglu, Murat
dc.contributor.authorDoucet, Henri
dc.contributor.authorBruneau, Christian
dc.date.accessioned2024-08-04T20:32:23Z
dc.date.available2024-08-04T20:32:23Z
dc.date.issued2010
dc.departmentİnönü Üniversitesien_US
dc.description.abstractNew Pd-N-heterocyclic carbene complexes have been prepared and employed for palladium-catalysed direct arylation of heteroaromatic derivatives by using aryl halides. These catalyst precursors promote the coupling of challenging aryl halides such as deactivated or congested aryl bromides and also activated aryl chlorides. This procedure employs only 1 mol-% of an air-stable palladium complex. This is a practical advantage over the procedures that employ palladium attached to air-sensitive phosphane ligands, which are often used to promote the coupling of such aryl halides.en_US
dc.description.sponsorshipCentre National de la Recherche Scientifique; Rennes Metropole, Inonu University [BAP 2009/13]; Technological and Scientific Research Council of Turkiye TUBITAK [107T419, 108T411]en_US
dc.description.sponsorshipWe thank the Centre National de la Recherche Scientifique and Rennes Metropole, Inonu University Research Fund (BAP 2009/13) and Technological and Scientific Research Council of Turkiye TUBITAK (107T419 and 108T411) for providing financial support.en_US
dc.identifier.doi10.1002/ejic.200901195
dc.identifier.endpage1805en_US
dc.identifier.issn1434-1948
dc.identifier.issn1099-0682
dc.identifier.issue12en_US
dc.identifier.scopus2-s2.0-77951913165en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage1798en_US
dc.identifier.urihttps://doi.org/10.1002/ejic.200901195
dc.identifier.urihttps://hdl.handle.net/11616/95029
dc.identifier.wosWOS:000277631900005en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherWiley-V C H Verlag Gmbhen_US
dc.relation.ispartofEuropean Journal of Inorganic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAryl halidesen_US
dc.subjectAtom economyen_US
dc.subjectC-H activationen_US
dc.subjectCarbenesen_US
dc.subjectHeteroaromaticsen_US
dc.subjectPalladiumen_US
dc.titleN-Heterocyclic Carbenes: Useful Ligands for the Palladium-Catalysed Direct C5 Arylation of Heteroaromatics with Aryl Bromides or Electron-Deficient Aryl Chloridesen_US
dc.typeArticleen_US

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