N-functionalized azolin-2-ylidene-palladium-catalyzed Heck reaction

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dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridGurbuz, Nevin/0000-0003-3201-3597
dc.authoridCetinkaya, Bekir/0000-0002-4551-8650
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidGök, Yetkin/AAA-5669-2021
dc.authorwosidGurbuz, Nevin/A-3069-2016
dc.contributor.authorOzdemir, Ismail
dc.contributor.authorGurbuz, Nevin
dc.contributor.authorGok, Yetkin
dc.contributor.authorCetinkaya, Bekir
dc.date.accessioned2024-08-04T20:30:39Z
dc.date.available2024-08-04T20:30:39Z
dc.date.issued2008
dc.departmentİnönü Üniversitesien_US
dc.description.abstractNovel 1,3-dialkylimidazolidinium, 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium, and 1,3-dialkyl-1H-4,5,6,7-tetrahydrodiazepinium hexafluorophosphates (la-c, 2a-c) as N-heterocyclic carbene precursors have been synthesized and characterized. The incorporation of saturated N-heterocyclic carbenes into palladium precatalysts gives high-catalyst activity in the Heck coupling of aryl bromide substrates in aqueous media. The complexes were generated in the presence of Pd(OAC)(2) by in situ deprotonation of 1,3-dialkylazolinium salts 1, 2. (C) 2008 Wiley Periodicals, Inc.en_US
dc.identifier.doi10.1002/hc.20415
dc.identifier.endpage86en_US
dc.identifier.issn1042-7163
dc.identifier.issn1098-1071
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-38449120716en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage82en_US
dc.identifier.urihttps://doi.org/10.1002/hc.20415
dc.identifier.urihttps://hdl.handle.net/11616/94438
dc.identifier.volume19en_US
dc.identifier.wosWOS:000252943900014en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherWiley-Hindawien_US
dc.relation.ispartofHeteroatom Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCross-Coupling Reactionsen_US
dc.subjectPalladium-Catalyzed Synthesisen_US
dc.subjectSuzuki-Miyaura Reactionen_US
dc.subjectAryl Chloridesen_US
dc.subjectHeterocyclic Carbenesen_US
dc.subjectEfficient Catalysten_US
dc.subjectC-Cen_US
dc.subjectComplexesen_US
dc.subjectLiganden_US
dc.subjectPalladacyclesen_US
dc.titleN-functionalized azolin-2-ylidene-palladium-catalyzed Heck reactionen_US
dc.typeArticleen_US

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