723-51-3Relevant articles and documents
A convenient preparation of heteroaryl sulfonamides and sulfonyl fluorides from heteroaryl thiols
Wright, Stephen W.,Hallstrom, Kelly N.
, p. 1080 - 1084 (2006)
Heteroaromatic thiols may be oxidized to the sulfonyl chloride at low temperature (-25 °C) by using 3.3 equiv of aqueous sodium hypochlorite. The reaction is rapid, avoids the use of chlorine gas, and succeeds with substrates that have previously been found to afford little or none of the sulfonamide product with other procedures. The method allows the preparation of the sulfonyl fluorides, which are stable enough to be purified and stored, making them potentially useful monomers in parallel chemistry efforts.
Metal-Free Intermolecular Aminoarylation of Alkynes
Rabet, Pauline T. G.,Boyd, Scott,Greaney, Michael F.
, p. 4183 - 4186 (2017)
A metal-free aminoarylation of internal alkynes is described, yielding tetrasubstituted enaminoates. The transformation proceeds in good to excellent yields through a tandem conjugate addition/Smiles rearrangement involving aryl and heteroaryl sulfonamide