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. Author manuscript; available in PMC: 2010 Sep 16.
Published in final edited form as: J Am Chem Soc. 2009 Sep 16;131(36):12898–12899. doi: 10.1021/ja905768k

Table 3.

Conversion of aryl triflates and nonaflates to nitro aromatics.a

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a

ArX (1 mmol), NaNO2 (2.0 mmol), Pd2(dba)3 (0.5 mol%), 1 (1.2 mol%), t-BuOH (2 mL), 130 °C, 24 h; isolated yields, average of 2 runs.

b

Pd2(dba)3 (2.5 mol%), 1 (6 mol%).