4.8 Article

An unusual radical smiles rearrangement

Journal

ORGANIC LETTERS
Volume 7, Issue 17, Pages 3817-3820

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol051568l

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Radicals derived from N-(alpha-xanthyl)acetanilides or N-(alpha-xanthyl)acetylaminopyridines possessing a substituent next to the nitrogen undergo a hitherto undocumented Smiles rearrangement proceeding through a four-membered ring. It was also found that under certain conditions the amidyl radical produced by cleavage of the four-membered ring intermediate can undergo fragmentation to give an isocyanate. Such fragmentations are unprecedented at temperatures corresponding to refluxing benzene or chlorobenzene.

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