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. Author manuscript; available in PMC: 2015 Oct 6.
Published in final edited form as: Angew Chem Int Ed Engl. 2014 Aug 25;53(41):11056–11059. doi: 10.1002/anie.201406393

Figure 2.

Figure 2

Scope studies for the oxidative [3+2] cycloaddition[a] All reactions conducted on 0.40 mmol phenol, 0.52 mmol alkene, 0.80 mmol (NH4)2S2O8, and 0.02 mmol 2•(PF6)2, unless otherwise noted. Yields represent the averaged isolated yields of two reproducible experiments.[b] Reactions conducted with 0.80 mmol alkene.