Abstract
A new synthesis of diaryl sulfones is achieved from N,N'-disulfonylhydrazines and diaryliodonium salts. Its key advantage is that N,N'-disulfonylhydrazines carry out an efficient base-promoted evolution of nitrogen to generate in situ ammonium sulfinates with good solubility and high reactivity. N,N'-Disulfonylhydrazines prove to be an excellent synthetic equivalent of sulfinic acids and their salts with none of their drawbacks.
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