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. Author manuscript; available in PMC: 2018 Jul 3.
Published in final edited form as: Angew Chem Int Ed Engl. 2017 Jun 9;56(28):8183–8186. doi: 10.1002/anie.201704411

Table 2.

Scope of aryl iodides.[a,b]

graphic file with name nihms886224f4.jpg
[a]

Reaction conditions: 1a (0.1 mmol), Aryl iodide 2 (3.0 equiv), Pd(OAc)2 (10 mol %), Isoquinoline (20 mol%), NBE-CO2Me (1.5 equiv), AgOAc (3.0 equiv), DCE (1.0 mL), 100 °C, 24 h.

[b]

Isolated yield.