Abstract
AbstractA practical and mild electrochemical dehydrogenative regioselective cyclization method has been established for the synthesis of 4‐pyrrolin‐2‐ones using 3‐aza‐1,5‐dienes and 1,3‐dicarbonyl compounds as substrates. This protocol is catalyst‐free, metal‐free, and does not require oxidizing agents. It exhibits wide substrate compatibility and can be easily scaled up to the gram scale.
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