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. Author manuscript; available in PMC: 2013 Jun 20.
Published in final edited form as: J Am Chem Soc. 2008 Mar 22;130(17):5636–5637. doi: 10.1021/ja8006534

Table 1. Pd-Catalyzed Hydroarylation of o-Alkynyl Biarylsa.

graphic file with name nihms382580u1.jpg

# Product Time, h Yield, %b # Product Time, h Yield, %b
1 graphic file with name nihms382580t1.jpg 2.5 10 graphic file with name nihms382580t10.jpg 3.0
98 93
2 graphic file with name nihms382580t2.jpg 3.0 11 graphic file with name nihms382580t11.jpg 3.0
95 94
3 graphic file with name nihms382580t3.jpg 1.5 12 graphic file with name nihms382580t12.jpg 4.0
96 89
4 graphic file with name nihms382580t4.jpg 2.0 13 graphic file with name nihms382580t13.jpg 5.0
96 87
5 graphic file with name nihms382580t5.jpg 0.5 14 graphic file with name nihms382580t14.jpg 1.0
79 85
6 graphic file with name nihms382580t6.jpg 3.0 15 graphic file with name nihms382580t15.jpg 1.5
92 77
7 graphic file with name nihms382580t7.jpg 4.0 16 graphic file with name nihms382580t16.jpg 24
95 47
8 graphic file with name nihms382580t8.jpg 1.0 17 graphic file with name nihms382580t17.jpg 48
93 30
9 graphic file with name nihms382580t9.jpg 0.5 18 graphic file with name nihms382580t18.jpg 6.0
98 86
a

Reaction conditions: 0.5 mmol of 1, 0.025 mmol of Pd(OAc)2, 0.035 mmol of 1,1′-bis(diisopropylphosphino)ferrocene, 1 mL of toluene, 120 °C.

b

Isolated yields.