The coupling of aryl or vinyl halides with terminal acetylenes catalysed by palladium and
other transition metals, commonly termed as Sonogashira cross-coupling reaction, is one of …

Micelles generated upon dissolving surfactants in water can be employed as nanovessels
for catalytic transformations, in the so-called micellar catalysis methodology. This review is …

The in vogue N-heterocyclic carbenes (NHCs) have attracted attention largely for its new
found popularity in chemical catalysis and also for displaying promising traits in biomedical …

This review is a critical presentation of catalysts based on palladium and ruthenium bearing
N-heterocyclic carbene ligands that have enabled a more sustainable approach to catalysis …

The use of aqueous media in palladium‐catalyzed reactions has become popular because
water‐based synthetic processes are inherently safer as well as being inexpensive …

The cross-coupling of terminal acetylenes for the construction of alkyne motives is a reaction
type that is frequently required in the assembly of pharmaceuticals and natural products that …

A template consisting of a melamine‐based microporous polymer network was synthesized
and utilized as a solid support to stabilize palladium nanoparticles; the resulting Pd/SNW1 …

The high surface area of 2D-hexagonal periodic mesoporous organosilica (PMO) containing
a phloroglucinol-diimine moiety inside the pore wall has been utilized for grafting Pd (II) at …

The palladium-catalyzed coupling reaction of aryl halides with terminal alkynes, the
Sonogashira coupling, took place in water under copper-free conditions by use of an …

Micellar reaction conditions, in a predominantly aqueous medium, have been developed for
transformations commonly used by synthetic chemists working in the pharmaceutical …