Heck and suzuki reactions of aryl halides catalyzed by 1,3-dialkylimidazolinium/palladium

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dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridYaşar, Sedat/0000-0001-7285-2761
dc.authoridCetinkaya, Bekir/0000-0002-4551-8650
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidYaşar, Sedat/ABG-8356-2020
dc.contributor.authorYasar, Sedat
dc.contributor.authorOezdemir, Ismail
dc.contributor.authorCetinkaya, Bekir
dc.date.accessioned2024-08-04T20:30:44Z
dc.date.available2024-08-04T20:30:44Z
dc.date.issued2008
dc.departmentİnönü Üniversitesien_US
dc.description.abstractNew, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic carbene precursors were synthesized and characterized. These salts, combined with palladium acetate, provided active catalysts for Heck and suzuki cross-coupling of aryl chlorides and bromides under mild conditions.en_US
dc.identifier.doi10.1016/S1872-2067(08)60023-6
dc.identifier.endpage190en_US
dc.identifier.issn0253-9837
dc.identifier.issn1872-2067
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-40949148581en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage185en_US
dc.identifier.urihttps://doi.org/10.1016/S1872-2067(08)60023-6
dc.identifier.urihttps://hdl.handle.net/11616/94488
dc.identifier.volume29en_US
dc.identifier.wosWOS:000253932800017en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isozhen_US
dc.publisherScience Pressen_US
dc.relation.ispartofChinese Journal of Catalysisen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHeck reactionen_US
dc.subjectsuzuki reactionen_US
dc.subjectaryl halideen_US
dc.subjectimidazolinium salten_US
dc.subjectpalladiumen_US
dc.subjectcarbeneen_US
dc.titleHeck and suzuki reactions of aryl halides catalyzed by 1,3-dialkylimidazolinium/palladiumen_US
dc.typeArticleen_US

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