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. Author manuscript; available in PMC: 2020 Aug 19.
Published in final edited form as: Angew Chem Int Ed Engl. 2019 Jul 11;58(34):11704–11708. doi: 10.1002/anie.201905247

Table 2.

Substrate Scope for 1,2-(Bis)trifluoromethylationa,b

graphic file with name nihms-1037062-t0006.jpg
a

All reactions were with 1 (0.16 mmol) and 2 (0.16 mmol) in 2.8 mL of solvent for 1 h.

b

The 19F NMR yield determined by 19F NMR spectroscopy with 1-fluoro-4-methylbenzene as the internal standard, with the isolated yields given in parentheses. The E/Z ratios were determined by 19F NMR spectroscopy of the crude product mixtures.