In-situ generated functionalized benzimidazol-2-ylidene-palladium catalyst for Suzuki reaction

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dc.contributor.authorÖzdemir I.
dc.contributor.authorGök Y.
dc.contributor.authorGürbüz N.
dc.contributor.authorYaşar S.
dc.contributor.authorÇetinkaya E.
dc.contributor.authorÇetinkaya B.
dc.date.accessioned2019-10-27T00:13:07Z
dc.date.available2019-10-27T00:13:07Z
dc.date.issued2004
dc.departmentEge Üniversitesien_US
dc.description.abstractFrom readily available starting materials functionalized 1,3-dialkylbenzimidazolium salts (1a-g) have been prepared and characterized by conventional spectroscopic methods and elemental analysis. The in situ prepared three component system Pd(OAc)2/1,3-dialkylbenzimidazolium halides (1a-g) and Cs2CO3 catalyses Suzuki cross-coupling of aryl chloride substrates. These concepts for making catalysts in situ open the way for the discovery of many new catalysts via the interaction of commercially available metal complexes and suitable electron releasing ligands.en_US
dc.identifier.endpage2147en_US
dc.identifier.issn0137-5083
dc.identifier.issn0137-5083en_US
dc.identifier.issue11.Decen_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage2141en_US
dc.identifier.urihttps://hdl.handle.net/11454/22428
dc.identifier.volume78en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofPolish Journal of Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAryl chloridesen_US
dc.subjectFunctional carbeneen_US
dc.subjectPhenylboronic aciden_US
dc.subjectSuzukien_US
dc.titleIn-situ generated functionalized benzimidazol-2-ylidene-palladium catalyst for Suzuki reactionen_US
dc.typeArticleen_US

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