Radical alkylation and protonation induced anti-Markovnikov hydroalkylation of unactivated olefins via cobalt catalysis.

Although strategies of olefin hydroalkylation continue to emerge rapidly, the precise control of the regio- or chemoselectivity and the expansion of the reaction range are still challenges. Herein, a straightforward route for cobalt-catalyzed anti-Markovnikov hydroalkylation of unactivated olefins with alkyl iodides has been achieved. The developed reaction is compatible with oxa-, aza-, cyclo- and a series of other functional groups as well as the frameworks of some bioactive compounds. Mechanism studies confirm that an alkyl radical is involved and cobalt–alkyl insertion followed by protonation with water are possible pathways in this reaction. [ABSTRACT FROM AUTHOR]