Abstract
AbstractAn efficient approach for the synthesis of quinazolinones from o‐aminobenzamides and alcohols by the combination of electrochemistry and redox‐metal catalysis has been developed. Taking manganese(II) sulfate as a redox catalyst, this transformation proceeded smoothly under ambient conditions in an undivided cell to afford quinazolinones in moderate to excellent yields with a wide substrate scope. Benzyl ethers were also suitable participants in the cascade cyclization sequence.
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