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. Author manuscript; available in PMC: 2010 Jul 29.
Published in final edited form as: J Am Chem Soc. 2009 Jul 29;131(29):9886–9887. doi: 10.1021/ja903573p

Table 1.

Directing Group Screeninga,b

graphic file with name nihms132640f3.jpg
X = OMe
a 0%
b 0%
graphic file with name nihms132640t1.jpg
a 3%
b 0%
graphic file with name nihms132640t2.jpg
a 0%
b 0%
graphic file with name nihms132640t3.jpg
a 12%
b 0%
graphic file with name nihms132640t4.jpg
a 10%
b 0%
graphic file with name nihms132640t5.jpg
a 24%
b 12%
graphic file with name nihms132640t6.jpg
a 18%
b 8%
graphic file with name nihms132640t7.jpg
a 30%
b 22%
graphic file with name nihms132640t8.jpg
a 34%
b 54%
a

Conditions: 0.2 mmol of substrate, 10 mol% Pd(OAc)2, 20 mol% ligand, 3.0 equiv of CsF, 3.0 equiv of aryl iodide, 100 mg 3Å MS, 1 mL toluene, 100 °C, N2, 24 h.

b

Yield was determined by 1H NMR analysis of crude product using CH2Br2 as the internal standard.