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 …

A novel, rapid, and environmentally-friendly protocol for the synthesis of sulfonamides using
iodine as catalyst under solvent-free conditions is described. This method involves the …

An efficient electrochemical synthesis of sulfonamides (yields 56–98%) from
arenesulfonohydrazides or sodium p-methylbenzenesulfinate and amines was performed in …

An intermolecular alkylation of sulfonamides with trichloroacetimidates is reported. This
transformation does not require an exogenous acid, base, or transition metal catalyst; …

An iodine-induced synthesis of sulfonate esters via cross-coupling reactions of sodium
sulfinates with phenols is reported. This synthetic route is low-cost, facile, green and …

We demonstrate here a rapid and comfortable synthetic sequence to benzothiadiazinone
dioxide (six-membered cyclic sulfamide) derivatives, analogues of Monastrol, which is …

With H2O as the solvent and NaI as the supporting electrolyte, a green and efficient
electrochemical route has been developed to synthesize arylsulfonamides via I2 …

This study provides a direct, sustainable and eco-friendly method for the synthesis of various
sulfonamides via the sulfonylation of sulfonyl hydrazides with tert-amines. The method …

A protocol for three-component reactions of cyclic ethers, α-diazo esters, and weak nitrogen,
oxygen, carbon, and sulfur nucleophiles (p K a= 2.2–14.8) to afford a variety of structurally …

Air-stable N-sulfonyl and N-phosphonyl DBN hexafluorophosphate salts have been
synthesised under mild conditions as sulfonylating and phosphonylating agents. These salts …