Suzuki-Miyaura reaction of unactivated aryl chlorides using benzimidazol-2-ylidene ligands

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dc.authoridGurbuz, Nevin/0000-0003-3201-3597
dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridCetinkaya, Bekir/0000-0002-4551-8650
dc.authorwosidGurbuz, Nevin/A-3069-2016
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidGök, Yetkin/AAA-5669-2021
dc.contributor.authorÖzdemir, I
dc.contributor.authorGök, Y
dc.contributor.authorGürbüz, N
dc.contributor.authorÇetinkaya, E
dc.contributor.authorÇetinkaya, B
dc.date.accessioned2024-08-04T20:56:13Z
dc.date.available2024-08-04T20:56:13Z
dc.date.issued2004
dc.departmentİnönü Üniversitesien_US
dc.description.abstractFour functionalized bis(benzimidazolium) salts (2a-d) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. A highly effective, easy to handle, and environmentally bengin process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component system Pd(OAc)(2)/bis(benzimidazolium) bromides (2a-d) and Cs2CO3 catalyzes quantitatively the Suzuki cross-coupling of deactivated aryl chloride in aqueous media.en_US
dc.identifier.doi10.1081/SCC-200036594
dc.identifier.endpage4144en_US
dc.identifier.issn0039-7911
dc.identifier.issn1532-2432
dc.identifier.issue22en_US
dc.identifier.scopus2-s2.0-8644290061en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage4135en_US
dc.identifier.urihttps://doi.org/10.1081/SCC-200036594
dc.identifier.urihttps://hdl.handle.net/11616/102133
dc.identifier.volume34en_US
dc.identifier.wosWOS:000225241500011en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofSynthetic Communicationsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSuzukien_US
dc.subjectcarbeneen_US
dc.subjectpalladiumen_US
dc.subjectbenz imidazol-2-ylideneen_US
dc.subjectaryl chloridesen_US
dc.subjectphenylboronic aciden_US
dc.titleSuzuki-Miyaura reaction of unactivated aryl chlorides using benzimidazol-2-ylidene ligandsen_US
dc.typeArticleen_US

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