Karaca, Emine OzgeGurbuz, NevinOzdemir, IsmailDoucet, HenriSahin, OnurBuyukgungor, OrhanCetinkaya, Bekir2024-08-042024-08-0420150276-73331520-6041https://doi.org/10.1021/om501201rhttps://hdl.handle.net/11616/96859The synthesis and characterization of novel 1,3-benzyl-3,4,5,6-tetrahydropyrimidin-2-ylidene-based N-hetero-cyclic carbene palladium(II) complexes (1a-d) were described. The crystal structure of trans-dichlorobis[1,3-bis(4-methylbenzyl)-3,4,5,6-tetrahydropyrimidin-2-ylidend- palladium(II) was presented. Pd(II) complexes 1a-d were tested as catalysts in the direct C5 or C2 arylation of furans, thiophenes, and thiazoles, with various aryl bromides at 150 degrees C for 1 h. These complexes exhibited moderate to high catalytic activities under the given conditions.eninfo:eu-repo/semantics/closedAccessN-Heterocyclic-CarbeneC-H FunctionalizationCross-Coupling ReactionsDirect C-2 ArylationBond FormationAryl HalidesRoom-TemperatureAzolesEfficientChloridesPalladium Complexes with Tetrahydropyrimidin-2-ylidene Ligands: Catalytic Activity for the Direct Arylation of Furan, Thiophene, and Thiazole DerivativesArticle34112487249310.1021/om501201r2-s2.0-84935870521Q1WOS:000356841800051Q1