Table 9.
1H and 13C NMR spectral data for compounds 15, 16, and 17
| Position | 15
|
16
|
17
|
|||
|---|---|---|---|---|---|---|
| δH | δC | δH | δC | δH | δC | |
| 2 | 7.1, br d | 131.4, d | 6.9, d(6) | 132.1, d | 7.0, br d | 131.5, d |
| 3 | 6.8, br d | 101.0, d | 6.8, d(6) | 101.2, d | 6.8, br d | 113.4, d |
| 3a | 149.2, s | 149.4, s | 149.2, s | |||
| 5 | 7.6, d(6) | 147.0, d | 8.0, d(7.6) | 146.4, d | 7.5, br d | 147.0, d |
| 6 | 7.5, br d | 118.3, d | 7.2, d(7.6) | 113.4, d | 7.5, br d | 124.8, d |
| 6a | 136.7, s | 135.5, s | 136.5, s | |||
| 7 | 6.8, s | 101.0, d | 6.7, s | 101.1, d | 6.8, s | 100.7, d |
| 8 | 151.6, s | 157.2, s | 158.5, s | |||
| 9 | 135.0, s | 135.0, s | 135.0, s | |||
| 9a | 123.8, s | 123.9, s | 124.0, s | |||
| 9b | 117.9, s | 118.1, s | 118.0, s | |||
| NCH3 | 3.9, s | 45.3, q | 3.8, s | 45.4, q | 3.9, s | 45.5, q |
| OCH3 | 3.9, s | 56.8, q | 3.9, s | 56.7, q | 3.9, s | 56.8, q |
| 1′ | 163.2, s | 164.9, s | 164.9, s | |||
| 2′ | 125.0, s | 125.3, s | 125.2, s | |||
| 3′ | 8.0, br d | 127.8, d | 8.1, d(8) | 130.5, d | 8.1, d(8) | 130.5, d |
| 4′ | 7.4, dd(8) | 113.6, d | 7.3, d(8) | 129.7, d | 7.6, d(8) | 126.0, d |
| 5′ | 157.2, s | 145.5, s | 157.3, s | |||
| 6′ | 149.0, s | 7.3, d(8) | 129.7, d | 7.6, d(8) | 126.0, d | |
| 7′ | 8.0, br d | 118.1, d | 8.1, d(8) | 130.5, d | 8.1, d(8) | 130.5, d |
| 8′ | 2.5, s | 21.8, q | 35.3, s | |||
| 9′ | 1.4, s | 31.0, q | ||||
| 10′ | 1.4, s | 31.0, q | ||||
| 11′ | 1.4, s | 31.0, q | ||||
Measured in CDCl3 at 400 MHz for 1H and 100 MHz for 13C, respectively. J values in Hz.