The Suzuki–Miyaura (SM) reaction is one of the most widely used synthetic protocols for synthesizing biaryl compounds through a palladium (Pd)-catalyzed coupling reaction between an aryl halide and an arylboronic acid.[1–5] The Suzuki reaction is typically performed with a homogeneous Pd catalyst, phosphorus derivatives as ligands and an inorganic bases (ie carbonate, bicarbonate and hydroxide) in aqueous organic solvents.[5 ...