Abstract
AbstractA series of 4‐aryl‐2‐imino‐1,3‐dithiolanes was synthesized by means of a straightforward strategy starting from readily available precursors: reactions of dithiocarbamates and arylsulfonium salts, at room temperature in water/CH2Cl2 as biphasic medium, afforded the five‐membered cyclic products in good yields. The reaction mechanism was investigated by DFT calculations.
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