FeCl2-Catalyzed Rearrangement of Aryl Peroxyoxindole into 1,3-Benzooxazin-4-One

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Wiley

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We report an FeCl2-catalyzed radical rearrangement of aryl peroxyoxindoles into 1,3-benzooxazin-2-ones to obtain a variety of aryl substituted 1,3-benzooxazin-4-ones in moderate to good yields. Mechanistically, this skeletal rearrangement of peroxyoxindoles proceeded via radical pathway and was well supported with a series of experimental findings and DFT studies.

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Advanced Synthesis & Catalysis, 365(4), 515-521.

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