Abstract Direct conversion of [1] benzothieno [3, 2-b] pyridine (IVa), thieno [3, 2-b: 4, 5-b'] dipyridine (Va), and thieno [2, 3-b: 4, 5-b'] dipyridine (VIa) into their sulfoxides was effected by means of an equimolar quantity of iodobenzene dichloride in aqueous acetonitrile. Treatment of IVa-VIa with excess chlorine gas in carbon tetrachloride and then with water gave the corresponding sulfones, IVc-VIc. Hydrogen peroxide in glacial acetic acid ...