Table 5. NMR Spectroscopic Data (1H at 800 MHz, 13C at 200 MHz, CD3OD) of 2,3-Dehydro-3″-hydroxychamanetin (5).
| position | δC, type | δH | J (Hz) | HMBC, H→C |
|---|---|---|---|---|
| 2 | 165.8, C–O | |||
| 3 | 105.6, CH | 6.69 | s | C-2, C-4, C-4a, C-1′ |
| 4 | 184.3, C=O | |||
| 4a | 105.7, C | |||
| 5 | 161.2, C–O | |||
| 6 | 99.9, CH | 6.36 | s | C-4, C-4a, C-5, C-7, C-8 |
| 7 | 164.3, C–O | |||
| 8 | 107.4, C | |||
| 8a | 157.0, C–O | |||
| 1′ | 132.6, C | |||
| 2′/6′ | 127.6, CH | 7.80 | m | C-2, C-2′/6′, C-4′ |
| 3′/5′ | 130.2, CH | 7.47 | m | C-1′, C-2′/6′, C-3′/5′ |
| 4′ | 132.9, CH | 7.51 | m | C-2′/6′ |
| 1″ | 128.3, C | |||
| 2″ | 144.2, C–O | |||
| 3″ | 146.0, C–O | |||
| 4″ | 113.9, CH | 6.62 | dd, (7.8, 1.6) | C-2″, C-3″, C-5″ C-6″ |
| 5″ | 120.3, CH | 6.47 | dd, (7.9, 7.8) | C-1″, C-3″, C-4″, C-6″ |
| 6″ | 120.4, CH | 6.34 | dd, (7.9, 1.6) | C-2″, C-4″, C-7″ |
| 7″ | 22.8, CH2 | 4.16 | s | C-7, C-8, C-8a, C-1″, C-2″, C-6″ |