Table 1.
NMR data of acremonidin E (1, DMSO-d6)a
| No. | δc, mult.b | δH (J in Hz) | COSY | HMBC |
|---|---|---|---|---|
| 1 | 167.9, qC | |||
| 2 | 112.3, qC | |||
| 3 | 141.2, CH | |||
| 4 | 117.4, CH | 6.93, d (J = 8.8 Hz) | 5 | 2 |
| 5 | 122.1, CH | 6.81, d (J = 8.8 Hz) | 4 | 3,7 |
| 6 | 146.5, CH | |||
| 7 | 131.1, qC | |||
| 8 | 199.9, qC | |||
| 9 | 108.9, qC | |||
| 10 | 162.2, CH | 12 | ||
| 11 | 107.4, qC | 6.11, s | 15 | |
| 12 | 147.4, qC | |||
| 13 | 107.4, CH | 6.11, s | 15 | |
| 14 | 162.2, CH | 12 | ||
| 15 | 22.3, CH3 | 2.17, s | ||
| 16 | 52.5, OCH3 | 3.55, s | 1 | |
| 3-OH | 11.37, br s | |||
| 6-OH | 11.37, br s | |||
| 10-OH | 9.20, br s | |||
| 14-OH | 9.70, br s |
300 MHz for 1H NMR and 125 MHz for 13C NMR.
Multiplicity was determined by analysis of 2D spectra.