A facile method for regioselective synthesis of new N-acetyl/thioacetyl-<i>(E</i>)-stilbene benzenesulfonamide derivatives via N-acetyl/thioacetyl sulfonamide formation

<p>A series of new N-acetyl/thioacetyl-(<i>E</i>)-stilbene benzenesulfonamide derivatives were synthesized regioselectively in moderate to high yields by following a convenient, three-step procedure. The procedure consists of the direct oxidative conversion of a thiol compound to the corresponding sulfonyl chloride using TMSCl/KNO₃, followed by a room temperature reaction in a one-pot transformation of the resultant sulfonyl chloride into N-acetyl/thioacetyl sulfonamide, which undergoes a further Pd-catalyzed coupling reaction, giving rise to the stilbene compounds reported for the first time.</p