Use of bis(benzimidazolium) -: palladium system as a convenient catalyst for Heck and Suzuki coupling reactions of aryl bromides and chlorides

dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridDüşünceli, Serpil Demir/0000-0001-8765-4039
dc.authoridCetinkaya, Bekir/0000-0002-4551-8650
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidDemir, Serpil/AAI-1740-2019
dc.authorwosidDüşünceli, Serpil Demir/AAA-7160-2021
dc.contributor.authorDemir, S
dc.contributor.authorÖzdemir, I
dc.contributor.authorÇetinkaya, B
dc.date.accessioned2024-08-04T20:15:23Z
dc.date.available2024-08-04T20:15:23Z
dc.date.issued2006
dc.departmentİnönü Üniversitesien_US
dc.description.abstractSix new, sterically demanding bis(benzimidazolium) salts (2a-f) as NHC precursors have been synthesized and characterized. These salts, in combination with palladium acetate, provide active catalysts for the cross-coupling of aryl chlorides and bromides under mild conditions in aqueous media. Copyright (c) 2006 John Wiley & Sons, Ltd.en_US
dc.identifier.doi10.1002/aoc.1039
dc.identifier.endpage259en_US
dc.identifier.issn0268-2605
dc.identifier.issn1099-0739
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-33645782787en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage254en_US
dc.identifier.urihttps://doi.org/10.1002/aoc.1039
dc.identifier.urihttps://hdl.handle.net/11616/94349
dc.identifier.volume20en_US
dc.identifier.wosWOS:000236916700003en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofApplied Organometallic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHecken_US
dc.subjectSuzukien_US
dc.subjectcarbeneen_US
dc.subjectpalladiumen_US
dc.subjectbenzimidazol-2-ylideneen_US
dc.titleUse of bis(benzimidazolium) -: palladium system as a convenient catalyst for Heck and Suzuki coupling reactions of aryl bromides and chloridesen_US
dc.typeArticleen_US

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