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. Author manuscript; available in PMC: 2021 Jan 7.
Published in final edited form as: Angew Chem Int Ed Engl. 2019 Nov 22;59(2):658–662. doi: 10.1002/anie.201909983

Table 2.

Scope of the electrophotocatalytic arylation of heteroaromatics.[a]

graphic file with name nihms-1054273-t0007.jpg
[a]

See SI for detailed procedures. Reactions performed with 5 equiv. aryl fluoride and 1 equiv. nucleophile under constant voltage and irradiation for 36 h at rt. Percentages in parentheses indicate yield of C-H/N–H coupling products.

[b]

2.0 ml CH2Cl2 used as co-solvent.