Triphenylphosphine chalcogenides as efficient ligands for room temperature palladium(II)-catalyzed Suzuki–Miyaura reaction

Recent Advances in Metal Nanoparticles Stabilization into Nanopores of Montmorillonite and Their Catalytic Applications for Fine Chemicals Synthesis

“…The well-dispersed Ni o -nanoparticles with promising features for the reaction such as easy removal of the catalyst, solvent-free, shorter reaction time, high product yields (about 95%) and easy work-up procedure aroused much attraction. Palladium catalyzed cross-coupling reactions is a versatile tool for the generation of carbon-carbon bonds (300)(301)(302)(303)(304)(305). There are widespread interests to design heterogeneous Pd-catalyst system to increase the efficiency of the Heck and Sonogashira reactions (306-310).…”

Ligandless heterogeneous palladium: an efficient and recyclable catalyst for Suzuki‐type cross‐coupling reaction

“…Moreover, the catalytic system could be recycled repeatedly without any loss in activity and efficiency. Since 2010, our laboratory has emphasized the improvement of reactions involving easily accessible organoborons, and a series of transformations have been reported . According to accessible literatures, Pd/C has been demonstrated as an effective, commercially available heterogeneous catalyst for Suzuki–Miyaura cross‐coupling reactions, but have never been studied in Suzuki‐type cross‐coupling reactions of acid halides and arylboronic acids.…”

Iron(0), rhodium(I) and palladium(II) complexes with p‐(N,N‐dimethylaminophenyl) diphenylphosphine and the application of the palladium complex as a catalyst for the Suzuki–Miyaura cross‐coupling reaction

“…[29,30] In fact, there exist two reports in which P,N-based ligands containing a p-phenyl backbone resulted in dramatic performances in cross-coupling reactions. [31,32] Thus, as part of our ongoing research into Suzuki-Miyaura reactions, [33,34] we explored the catalytic potential of the palladium-phosphine complex 3 for the Suzuki-Miyaura reaction of aryl halides with arylboronic acids. The effects of different solvents, bases and catalyst quantities were also evaluated.…”