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. Author manuscript; available in PMC: 2015 Oct 11.
Published in final edited form as: Chem Commun (Camb). 2014 Oct 11;50(79):11701–11704. doi: 10.1039/c4cc05650g

Fig. 2.

Fig. 2

Scope of the acetophenone-catalyzed photolytic C–H fluorination reaction. [a] Endo-2-fluoronorbornane was also formed in 4% NMR yield. [b] Isolated as the corresponding benzyl ester. [c] Substrate (1.0 equiv), Selectfluor (1.5 equiv). [d] Acetophenone (20 mol %).