Chemistry, regioselective and stereoselective electrochemical dearomatization-multifunctionalization reactions of pyridine
Peer-Reviewed Publication
Updates every hour. Last Updated: 22-May-2026 15:15 ET (22-May-2026 19:15 GMT/UTC)
A research team led by Ke-Yin Ye and Yuqi Lin at Fuzhou University developed an electrochemically mediated dearomatization saturation strategy, successfully achieving chemo, regio, and stereoselective multifunctionalization reactions of pyridine. This strategy provides an efficient synthetic route for the one-step construction of complex three-dimensional piperidine skeletons with four convertible functional groups. Mechanistic studies show that cyanogen bromide generated in situ by electrochemical processes can initiate the dearomatization of pyridine, thereby generating a dihydropyridine intermediate. This intermediate, through intramolecular anodic carbon effects and CH···π interactions, synergistically regulates the stereochemical selectivity of the subsequent electrochemical ortho-bifunctionalization process, thus achieving highly selective transformation. The article was published as an open access Research Article in CCS Chemistry, the flagship journal of the Chinese Chemical Society.
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