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. Author manuscript; available in PMC: 2020 Oct 14.
Published in final edited form as: J Am Chem Soc. 2019 Apr 18;141(17):6853–6858. doi: 10.1021/jacs.9b03024

Table 2.

Scope of the Copper-Catalyzed Trifluoromethylation Reaction of Alkyl Bromides via Metallophotoredoxa,b

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a

Performed with CuCl2 (20 mol %), 8 (2 equiv), 4 (2 equiv), Na2CO3 (4 equiv), and with either 1 (1 mol %) or 17 (5 mol %) in MeCN or DMSO, respectively (see Supporting Information for full experimental details).

b

Due to the volatility of a number of products, yields are reported on the basis of 19F NMR analysis using PhCF3 as an internal standard. Isolated yields are in parentheses.

c

Performed with 17 in DMSO for 1 h.

d

Performed with 1 in MeCN for 4 h.

e

Performed with 17 in DMSO for 30 min.