Abstract
An efficient and simple synthesis of various N-sulfonylimino quinolines and pyridines had been achieved via monofunctionalization of quinoliniums and pyridiniums, which could regioselectively favor in nucleophilic attack at the C-2 position. This base-promoted methodology has been directly to form the 2-sulfonylimino derivatives with simple available starting materials, metal-free conditions, and high regioselectivity.
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