The efficient generation of biaryl compounds and heterocycles via the advent of the
transition-metal-free coupling reaction constitutes an important development in the last few …

Potassium hydroxide (KOH) in dimethyl sulfoxide (DMSO) forms a superbasic medium that
allows one to access cross‐coupling products from reactions between aryl halides with …

A series of amine-substituted aryl sulfides have been synthesized from nitroaryl halides via a
simple one-pot procedure involving metal-free C− S cross-coupling and in situ nitro group …

The excellent advantages of cesium such as short reaction times, small amount of reagent
used, high yields of the products, milder reaction conditions, and easy work-up procedures …

Transition-Metal-Free Acid-Mediated Synthesis of Aryl Sulfides from Thiols and Thioethers |
The Journal of Organic Chemistry ACS ACS Publications C&EN CAS Find my institution …

Microwave irradiation promotes the rapid and efficient reaction of a thiophenol and aryl or
heteroaryl halide using a copper or palladium catalyst and a range of ligands, depending …

Potassium tert-butoxide mediated carbon–chalcogen C–E (E= O, S and Se) coupling
reaction has been studied from aryl bromide and phenol/aryl disulfide/diselenide substrates …

Abstract Ceric ammonium nitrate (3 mol%) efficiently catalyzes the aza-Michael reaction of
amines with α, β-unsaturated carbonyl compounds in water to produce the corresponding β …

A highly efficient and simple route for the synthesis of benzo-5-membered heterocycles
sulfides has been developed by the cross-coupling reaction of 2-mercaptobenzo-5 …

(E)-Alkenyl halides were transformed into (E)-alkenyl sulfides by the nickel (0) triethyl
phosphite complex-catalyzed reaction with thiols, whereas (Z)-alkenyl halides gave alkynes …