Özdemir, IGök, YGürbüz, NÇetinkaya, EÇetinkaya, B2024-08-042024-08-0420041042-71631098-1071https://doi.org/10.1002/hc.20034https://hdl.handle.net/11616/94778From readily available starting compounds, six functionalized 1,3-dialkylbenzimidazolium salts (2a-c and 4a-c) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. A highly effective, easy to handle, and environmentally benign process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component systems Pd(OAc)(2)/1,3-dialkylbenzimidazolium chlorides and Cs2CO3 catalyze quantitatively the Suzuki cross-coupling of deactivated aryl chlorides. (C) 2004 Wiley Periodicals, Inc.eninfo:eu-repo/semantics/openAccessCross-Coupling ReactionsN-Heterocyclic CarbenesAryl ChloridesEfficient CatalystsArylboronic AcidsComplexesHeckConvenientPhosphinesChemistryPalladium-catalyzed Suzuki reaction using 1,3-dialkylbenzimidazol-2-ylidene ligands in aqueous mediaArticle15641942310.1002/hc.200342-s2.0-6344282398Q4WOS:000224013200001Q3