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. Author manuscript; available in PMC: 2009 Jan 5.
Published in final edited form as: J Am Chem Soc. 2007 Sep 22;129(41):12404–12405. doi: 10.1021/ja075802+

Table 2.

Arylation scope with respect to aryl iodidesa

graphic file with name nihms-64156-t0003.jpg
Entry ArI Product Yield, %
1 4-CF3C6H4I graphic file with name nihms-64156-t0004.jpg 91
2 4-FC6H4I graphic file with name nihms-64156-t0005.jpg 90
3 4-MeOC6H4I graphic file with name nihms-64156-t0006.jpg 80
4 3,5-Me2C6H3I graphic file with name nihms-64156-t0007.jpg 85
5 2-MeC6H4I graphic file with name nihms-64156-t0008.jpg 91
6 2,4,6-Me3C6H2I graphic file with name nihms-64156-t0009.jpg 55
7 1-Iodonaphthalene graphic file with name nihms-64156-t0010.jpg 90
8 2-Iodopyridine graphic file with name nihms-64156-t0011.jpg 89
a

Substrate (1 equiv), aryl iodide (3 equiv), base (2 equiv). Yields are isolated yields.