Sulfinic acids and their salts have recently emerged as versatile coupling partners to
efficiently access a wide variety of hetero-and carbocyclic compounds, under relatively mild …

Needless to say that organosulfur compounds with sulfur–nitrogen bonds have found
various applications in diverse fields such as pharmaceuticals, agrochemicals, polymers …

An efficient I2-mediated approach for the synthesis of sulfonamides at room temperature
using water as the solvent has been developed. This method for the synthesis of …

This review focuses on the reactive intermediates (disulfides, sulfenyl halides, thiyl radicals,
sulfenium cations, and metal–organosulfur species) and the mechanisms of the recently …

Oxidative strategies are a powerful tool in organic synthesis for the formation of heteroatom–
heteroatom, carbon–heteroatom, and carbon–carbon bonds. Among these processes the …

Sulfonamides, with the general formula R-SO2NR1R2, have attracted great attention since
the early discovery of sulfonamide-containing antibacterial drugs. The combinations of …

A simple, practical and metal-free method has been developed for the synthesis of
sulfonamides and β-arylsulfonyl enamines via the selective cleavage of C–N and C–H …

Sulfonamide moiety is the backbone of various antimicrobial, anticancer, antiglaucoma,
anticonvulsant, uricosuric agents, and numerous other drugs. The age-old demand of …

A continuous flow metal‐free protocol for the synthesis of sulfonyl chlorides from thiols and
disulfides in the presence of nitric acid, hydrochloric acid and oxygen was developed. The …

The hydrosulfamoylation of diverse aryl olefins provides facile access to alkylsulfonamides.
Here we report a novel protocol utilizing radical-mediated addition and a thiol-assisted …