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. Author manuscript; available in PMC: 2010 May 1.
Published in final edited form as: Adv Synth Catal. 2009 May 1;351(7-8):1101–1114. doi: 10.1002/adsc.200800765

Table 1.

Pd-catalyzed hydroarylation of o-alkynyl biaryls.a

graphic file with name nihms148089u1.jpg
# Product Time, h Yield, %b # Product Time, h Yield%b # Product Time, h Yield, %b
1 graphic file with name nihms148089t1.jpg
2a
2.5
98
7 graphic file with name nihms148089t2.jpg
2g
4.0
95
13 graphic file with name nihms148089t3.jpg
2m
5.0
87
2 graphic file with name nihms148089t4.jpg
2b
3.0
95
8 graphic file with name nihms148089t5.jpg
2h
1.0
93
14 graphic file with name nihms148089t6.jpg
2n
1.0
85
3 graphic file with name nihms148089t7.jpg
2c
1.5
96
9 graphic file with name nihms148089t8.jpg
2i
0.5
98
15 graphic file with name nihms148089t9.jpg
2o
1.5
77
4 graphic file with name nihms148089t10.jpg
2d
2.0
96
10 graphic file with name nihms148089t11.jpg
2j
3.0
93
16 graphic file with name nihms148089t12.jpg
2p
24
47
5 graphic file with name nihms148089t13.jpg
2e
0.5
79
11 graphic file with name nihms148089t14.jpg
2k
3.0
94
17 graphic file with name nihms148089t15.jpg
2q
48
30
6 graphic file with name nihms148089t16.jpg
2f
3.0
92
12 graphic file with name nihms148089t17.jpg
2l
4.0
89
18 graphic file with name nihms148089t18.jpg
2r
6.0
86
a

Reaction conditions: 0.5 mmol of 1, 0.025 mmol of Pd(OAc)2, 0.035 mmol of d-i-Prpf, 1ml of toluene, 120°C.

b

Isolated yields.