Manganese‐catalyzed Electro‐oxidative Azidation‐annulation Cascade to Access Oxindoles and Quinolinones

Abstract An environmentally benign and proficient electro‐oxidative tandem azidation‐radical cyclization strategy is reported. Manganese‐catalyzed electrochemical reaction in an undivided cell at room temperature and the use of NaN 3 as the cheapest azide source are the key features of this protocol. Using this approach, a series of oxindole and quinolinone derivatives are synthesized in high yields. The synthesized azide functionality was efficiently converted to various valuable derivatives.