. 2016 Sep 22;49(10):2146–2157. doi: 10.1021/acs.accounts.6b00247

Table 12. Pd-Catalyzed Fluorination of 2-Substituted 3-Bromothiophenes^a.

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Yields determined by ¹⁹F NMR spectroscopy are shown. Values in parentheses indicate % conversion of the starting material.

Isolated yield.

Toluene was used as the reaction solvent.

Table 12. Pd-Catalyzed Fluorination of 2-Substituted 3-Bromothiophenesa.