PEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous media

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dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.contributor.authorKaloglu, Nazan
dc.contributor.authorOzdemir, Ismail
dc.date.accessioned2024-08-04T20:45:45Z
dc.date.available2024-08-04T20:45:45Z
dc.date.issued2019
dc.departmentİnönü Üniversitesien_US
dc.description.abstractA series of unsymmetrical 1,3-disubstituted benzimidazolium chlorides were synthesized as N-heterocyclic carbene (NHC) precursors. These compounds were used to synthesize of the PEPPSI-type palladium NHC complexes. The structures of all compounds were characterized by H-1 NMR, C-13 NMR, FT-IR spectroscopy and elemental analyses. The catalytic activity of the PEPPSI-type palladium-NHC complexes has been evaluated with respect to the Suzuki-Miyaura cross-coupling reactions of phenyl boronic acid with various aryl halides in aqueous media. (C) 2019 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.tet.2019.02.062
dc.identifier.endpage2313en_US
dc.identifier.issn0040-4020
dc.identifier.issue15en_US
dc.identifier.scopus2-s2.0-85062443667en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage2306en_US
dc.identifier.urihttps://doi.org/10.1016/j.tet.2019.02.062
dc.identifier.urihttps://hdl.handle.net/11616/98675
dc.identifier.volume75en_US
dc.identifier.wosWOS:000463288100009en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofTetrahedronen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectN-Heterocyclic carbeneen_US
dc.subjectPEPPSI-type palladium complexen_US
dc.subjectSuzuki-Miyaura cross-coupling reactionen_US
dc.titlePEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous mediaen_US
dc.typeArticleen_US

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