| Literature DB >> 16092883 |
Eric Bacqué1, Myriem El Qacemi, Samir Z Zard.
Abstract
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. [reaction: see text]Entities:
Year: 2005 PMID: 16092883 DOI: 10.1021/ol051568l
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005