The ligand-assisted palladium (Pd)-catalyzed Suzuki–Miyaura cross-coupling reaction is
one of the most attractive protocols in organic chemistry and phosphines have been …

Remarkable developments have been accomplished in silica-supported palladium
nanoparticles (PdNPs)-mediated organic transformations for the generation of Suzuki (C–C) …

Cross‐coupling reactions, namely, the Suzuki–Miyaura, Heck, Sonogashira, Hiyama,
Negishi, Kumada, and Hartwig–Buchwald, are the most powerful approaches in the …

The development of a green and sustainable synthetic methodology still remains a
challenge across the globe. Encouraging the prevailing challenge, herein, we have …

The synthesis of a new Schiff base ligand “4-((Z)-((Z)-3-hydroxy-1, 3-diphenylallylidene)
amino)-1, 5-dimethyl-2-phenyl-1H-pyrazol-3 (2H)-one (APD)” and its palladium complex [Pd …

A bis-N-heterocyclic carbene (NHC) functionalized with chloropropyltriethoxysilane over
silica was used to synthesize a well-defined immobilized palladium complex. This complex …

As a continuation of our efforts to develop new heterogeneous nanomagnetic catalysts for
greener reactions, we identified a Schiff base–palladium (II) complex anchored on magnetic …

Oxime-palladacycle catalyzed Suzuki–Miyaura cross-coupling reaction of acid chlorides and
arylboronic acids to yield aryl ketones was developed. The remarkable benefit of this …

The Pd catalyzed cross-coupling reactions have played a crucial role in accomplishing
different valuable organic transformations. These transformations involve the use of …

A new heterogeneous palladium catalyst was prepared by covalent anchoring of a
palladium-(II)-Schiff base complex onto the mesoporous cage-like material SBA-16. Several …