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. Author manuscript; available in PMC: 2022 Dec 15.
Published in final edited form as: J Am Chem Soc. 2021 Nov 30;143(49):21024–21036. doi: 10.1021/jacs.1c10932

Figure 7.

Figure 7.

Dual-catalyzed XEC of medicinally relevant aryl halides with 1-bromo-3-phenylpropane using TPiE and TME as the reductants. Reaction conditions: aryl halides (0.0300 mmol), 1-bromo-3phenylpropane (0.0480 mmol), reductant (0.0480 mmol), (dtbbpy)NiIIBr2 (Y mol%), CoII(Pc) (Z mol%) in DMAc (0.3 mL) at 80 °C for 24 h. The yields were determined by integration of 1H NMR spectra against a hexamethylbenzene external standard.