13C NMR data (100 MHz) of compounds 5–9a.
| Position | 5b | 6b | 7b | 8c | 9b |
|---|---|---|---|---|---|
| 1 | 144.0 | 147.9 | 154.3 | 150.6 | 150.0 |
| 1a | 119.0 | 127.1 | 110.4 | 115.3 | 129.8 |
| 1b | 126.5 | 129.0 | 123.3 | 119.9 | 133.8 |
| 2 | 148.9 | 153.1 | 148.3 | 147.7 | 145.4 |
| 3 | 107.6 | 117.6 | 102.7 | 143.7 | 123.8 |
| 3a | 127.5 | 128.5 | 137.9 | 132.6 | 131.9 |
| 4 | 29.7 | 27.7 | 125.8 | 107.9 | 31.4 |
| 5 | 55.0 | 43.4 | 144.9 | 156.6 | 43.5 |
| 6a | 63.9 | 54.9 | 147.1 | 132.6 | 52.7 |
| 7 | 27.5 | 36.1 | 184.1 | 174.7 | 35.0 |
| 7a | 123.3 | 135.7 | 126.3 | 126.9 | 138.4 |
| 8 | 143.5 | 129.6 | 152.0 | 108.1 | 129.9 |
| 9 | 146.6 | 129.6 | 157.9 | 150.8 | 129.7 |
| 10 | 114.5 | 129.1 | 126.3 | 113.4 | 129.5 |
| 11 | 120.7 | 129.9 | 125.9 | 123.0 | 128.7 |
| 11a | 124.6 | 133.2 | 124.9 | 120.3 | 132.7 |
| OCH2O | 102.4 | 104.4 | 102.8 | ||
| 1-OCH3 | 61.7 | 61.3 | |||
| 3-OCH3 | 61.3 | ||||
| 5-OCH3 | 56.2 | ||||
| 8-OCH3 | 61.7 | ||||
| 9-OCH3 | 56.2 | ||||
|
22.7 | ||||
|
171.4 | ||||
| N–CH3 | 44.0 | ||||
|
21.1 | ||||
|
172.5 | ||||
| 1′ | 103.0 | ||||
| 2′ | 75.4 | ||||
| 3′ | 78.8 | ||||
| 4′ | 71.9 | ||||
| 5′ | 78.8 | ||||
| 6′ | 63.1 |
Assignments were based on 1H–1H COSY, HMQC, HMBC, and NOESY experiments; chemical shifts (δ) are given in ppm.
Recorded in CDCl3.
Recorded in CD3OD.