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. Author manuscript; available in PMC: 2018 May 7.
Published in final edited form as: Angew Chem Int Ed Engl. 2018 Feb 27;57(13):3488–3492. doi: 10.1002/anie.201800699

Table 1.

C–N sulfonamidation control experiments.[a]

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Entry Conditions Yield [%]
1 as shown 99
2 no light 0
3 no nickel 0
4 no photocatalyst 11
5 benzophenone (0.5%) as photocatalyst 18
6 no photocatalyst, no light 0
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[a]

Performed with Ir(ppy)2(bpy)PF6 (0.05 mol%), Ni(cod)2 (5 mol%), TMG (1.5 equiv), aryl halide (1.0 equiv), and benzenesulfonamide (1.5 equiv).

[b]

Yields were obtained by 1H NMR analysis.