Table 1. Pd-Catalyzed Hydroarylation of o-Alkynyl Biarylsa.
| |||||
|---|---|---|---|---|---|
|
| |||||
| # | Product | Time, h Yield, %b | # | Product | Time, h Yield, %b |
| 1 |
|
2.5 | 10 |
|
3.0 |
| 98 | 93 | ||||
| 2 |
|
3.0 | 11 |
|
3.0 |
| 95 | 94 | ||||
| 3 |
|
1.5 | 12 |
|
4.0 |
| 96 | 89 | ||||
| 4 |
|
2.0 | 13 |
|
5.0 |
| 96 | 87 | ||||
| 5 |
|
0.5 | 14 |
|
1.0 |
| 79 | 85 | ||||
| 6 |
|
3.0 | 15 |
|
1.5 |
| 92 | 77 | ||||
| 7 |
|
4.0 | 16 |
|
24 |
| 95 | 47 | ||||
| 8 |
|
1.0 | 17 |
|
48 |
| 93 | 30 | ||||
| 9 |
|
0.5 | 18 |
|
6.0 |
| 98 | 86 | ||||
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.
Isolated yields.