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 …

The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and
an organic halide or pseudo-halide in the presence of a palladium or nickel catalyst and a …

Organoselenium compounds have been used extensively as building blocks for the
development of catalysts for several chemical transformations during the last two decades …

A highly efficient green protocol for palladium acetate-catalysed ligand-free Suzuki–Miyaura
cross-coupling reactions in neat 'water extract of banana (WEB)'was developed. This …

Organoselenium ligands have attracted great attention among researchers during the past
two decades. Various homogeneous, heterogeneous and nanocatalytic systems have been …

Organoselenium ligands are building blocks of several transition metal complexes which
catalyze various organic reactions efficiently in solution. In this review the survey of …

During the last two decades, several research groups across the globe have utilized
organochalcogen compounds as:(i) ligands for developing homogeneous, ie chalcogen …

Palladium (II) complexes of organochalcogen ligands have emerged as viable alternatives
to complexes of phosphine/carbene ligands for Suzuki–Miyaura and Heck C–C cross …

Suzuki–Miyaura C–C cross coupling (SMC), an important synthetic strategy for many
organic molecules, has several advantages such as mild reaction conditions, high tolerance …

Organochalcogen compounds have been used as the building blocks for the development
of a variety of catalysts that have been studied comprehensively during the last two decades …