“…[2][3][4] Therefore, numerous methods have been developed for the preparation of these molecules, [1,5] and a powerful method constitutes the aldehyde C-H activation by direct acylation of aryl halides with aldehydes. [1] Several methods have been developed for the preparation of aryl ketones by the aldehydes C-H activation, using catalysts including Pd(dba) 2 , [6] N-heterocyclic carbenes, [7] Pd(OAc) 2 , [8] Pd(dba) 3 , [9] Ni(dppe)Br 2 /Zn, [10] Pdη 2 -(P-S)Cl 2 , [11] quaternary ammonium salt, [12] (N-heterocyclic carbene)Pd, [13] and others. [14] Unfortunately, most of these methods suffer from some lacks such as using expensive ligands, toxic reagents, harsh reaction conditions, tedious work-up, and difficulties recovering and recycling catalysts.…”