@article{pittir18700,
          volume = {128},
          number = {42},
           month = {October},
          author = {DP Curran and AI Keller},
           title = {Radical additions of aryl iodides to arenes are facilitated by oxidative rearomatization with dioxygen},
         journal = {Journal of the American Chemical Society},
           pages = {13706 -- 13707},
            year = {2006},
             url = {http://d-scholarship-dev.library.pitt.edu/18700/},
        abstract = {Inter- and intramolecular additions of aryl radicals derived from aryl iodides to arenes are promoted by tris(trimethylsilyl)silane and occur under exceptionally mild conditions (15-30 min at 25 ?C) in nondegassed benzene. A chain mechanism involving reaction of the intermediate cyclohexadienyl radical with oxygen to directly generate the aromatized product and the hydroperoxy radical is proposed. Copyright {\copyright} 2006 American Chemical Society.}
}