Kaloglu, NazanOzdemir, Ismail2024-08-042024-08-0420190040-4020https://doi.org/10.1016/j.tet.2019.02.062https://hdl.handle.net/11616/98675A 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.eninfo:eu-repo/semantics/closedAccessN-Heterocyclic carbenePEPPSI-type palladium complexSuzuki-Miyaura cross-coupling reactionPEPPSI-Pd-NHC catalyzed Suzuki-Miyaura cross-coupling reactions in aqueous mediaArticle75152306231310.1016/j.tet.2019.02.0622-s2.0-85062443667Q2WOS:000463288100009Q2