Employing phenols and phenol derivatives as electrophiles for cross-coupling reactions has
numerous advantages over commonly used aryl halides in terms of environmental …

In the transition-metal-catalyzed cross-coupling reactions, the use of the first row transition
metals as catalysts is much more appealing than the precious metals owing to the apparent …

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 …

This review describes our laboratory's efforts to develop transition metal-catalyzed cross-
couplings of several unconventional phenol-based electrophiles. Specifically, we highlight …

Nickel catalysis for biaryl coupling reactions has received significant attention as a less
expensive and less toxic alternative to “standard” palladium catalysis. Here we describe …

A Schiff base ligand (SBL), N2, N3-bis (anthracen-9-ylmethylene) pyridine-2, 3-diamine, was
synthesized through the condensation of 2, 6-diaminopyridine and anthracene-9 …

The first Suzuki− Miyaura cross-coupling reactions of the synthetically versatile aryl O-
carbamate and O-sulfamate groups are described. The transformations utilize the …

One of the rapidly develo** fields now a days in medicine is the application of inorganic
chemistry, elegantly it is seen that the novel therapeutic and diagnostic metals and metal …

The use of temperature‐controlled mechanochemistry to enable the mechanochemical
nickel‐catalyzed Suzuki–Miyaura coupling is herein described. Transitioning from a …

The nickel-catalyzed Suzuki–Miyaura coupling of aryl halides and phenol-derived
substrates with aryl boronic acids using green solvents, such as 2-Me-THF and tert-amyl …