46248-01-5Relevant articles and documents
Synthesis and immunocorrector activity of aromatic sulfonic acid azolides
Purygin,Dragunova,Limareva,Danil'chenko
, p. 247 - 248 (1998)
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Sulfonamide Synthesis through Electrochemical Oxidative Coupling of Amines and Thiols
Laudadio, Gabriele,Barmpoutsis, Efstathios,Schotten, Christiane,Struik, Lisa,Govaerts, Sebastian,Browne, Duncan L.,No?l, Timothy
supporting information, p. 5664 - 5668 (2019/04/17)
Sulfonamides are key motifs in pharmaceuticals and agrochemicals, spurring the continuous development of novel and efficient synthetic methods to access these functional groups. Herein, we report an environmentally benign electrochemical method which enables the oxidative coupling between thiols and amines, two readily available and inexpensive commodity chemicals. The transformation is completely driven by electricity, does not require any sacrificial reagent or additional catalysts and can be carried out in only 5 min. Hydrogen is formed as a benign byproduct at the counter electrode. Owing to the mild reaction conditions, the reaction displays a broad substrate scope and functional group compatibility.
Sulfonamide Synthesis via Calcium Triflimide Activation of Sulfonyl Fluorides
Mukherjee, Paramita,Woroch, Cristian P.,Cleary, Leah,Rusznak, Mark,Franzese, Ryan W.,Reese, Matthew R.,Tucker, Joseph W.,Humphrey, John M.,Etuk, Sarah M.,Kwan, Sabrina C.,Am Ende, Christopher W.,Ball, Nicholas D.
supporting information, p. 3943 - 3947 (2018/07/15)
A method using calcium triflimide [Ca(NTf2)2] as a Lewis acid to activate sulfonyl fluorides toward nucleophilic addition with amines is described. The reaction converts a wide array of sterically and electronically diverse sulfonyl fluorides and amines into the corresponding sulfonamides in good yield.