Table 3.
9 | ||||||||
---|---|---|---|---|---|---|---|---|
Entry | n | R1 | R2 | R3 | R4 | 10 | [%] Yielda | [%] ee |
1 | 1 | Me | H | H | H | 10a | 82 | 80 |
2 | 1 | Me | Cl | H | H | 10b | 62 | 63 |
3 | 1 | Me | H | Cl | H | 10c | 79 | 84 |
4 | 1 | Me | H | F | H | 10d | 81 | 79 |
5 | 1 | Me | H | MeO | H | 10e | 71 | 83 |
6 | 1 | Me | H | H | Br | 10f | 83 | 80 |
7 | 1 | Et | H | H | H | 10g | 57 | 79 |
8 | 1 | Et | H | H | Cl | 10h | 79 | 81 |
9 | 2 | Me | H | Cl | H | 10i | 79 | 93 |
Reactions performed over 48 h at 35 °C on a 0.1 mmol scale using 1.5 equiv. of 9 under illumination by a single HP LED (λmax = 420 nm)
aYield and ee measured on the isolated 10 (average of two runs per substrate)