Table 4.
| |
---|---|
entry | |
1) | 76% yield, 93% ee |
2) | R = Me (7d) 63% yield, 85% ee |
3) | R = allyl (7e) 68% yield, 85% ee |
4) | 4-Me (7f): 88% yield, 96% ee |
5) | 5-Me (7g): 83% yield, 95% ee |
6) | 6-Me (7h): 80% yield, 89% ee |
7) | 7-Me (7i): 94% yield, 94% ee |
7j |
|
8) | 85% yield, 91% ee |
7k |
|
9)b | 60% yield, 93% ee |
7l |
|
10)b | 63% yield, 92% ee |
11) | 4-Me (7m): 86% yield, 94% ee |
12) | 2-Me (7n): 26% yield, 87% ee |
7o |
|
13) | 75% yield, 93% ee |
14) | 4-F (7p): 78% yield, 93% ee |
15) | 3-F (7q): 76% yield, 92% ee |
16) | 2-F (7r): 35% yield, 92% ee |
7s |
|
17) | 88% yield, 92% ee |
18) | R = Me (7t): 61% yield, 85% ee |
19) | R = n-Bu (7u): 72% yield, 91% ee |
20) | R = i-Pr (7v): 66% yield, 92% ee |
21) | R = t-Bu (7w): 29% yield, 84% ee |
7x |
|
22) | 80% yield, 90% ee |
Reactions conducted under inert atmosphere on 0.1 or 0.2 mmol scale for 2 h. Isolated yields are reported. Enantiomeric excess was determined by chiral stationary phase SFC.
1.6 equiv SnCl4 were employed.