Table 2.
13C NMR spectroscopic data of compounds 1–4
| No | 1*a | 2*b | 3*c | 4*b |
|---|---|---|---|---|
| 1 | 162.3 | 163.1 | 162.2 | 162.2 |
| 2 | 117.3 | 117.1 | 117.1 | 117.6 |
| 3 | 146.8 | 146.4 | 146.3 | 147.1 |
| 4 | 121.8 | 121.1 | 121.4 | 121.8 |
| 5 | 112.5 | 112.2 | 112.0 | 110.9 |
| 6 | 164.6 | 163.6 | 163.9 | 165.7 |
| 7 | 107.7 | 106.6 | 107.2 | 105.9 |
| 8 | 161.9 | 161.8 | 161.9 | 161.6 |
| 9 | 188.5 | 188.2 | 188.2 | 188.6 |
| 10 | 57.7 | 57.2 | 57.2 | 58.0 |
| 1a | 117.5 | 116.8 | 117.4 | 118.1 |
| 4a | 143.0 | 142.2 | 140.7 | 141.1 |
| 5a | 146.4 | 145.9 | 146.1 | 146.5 |
| 8a | 117.1 | 116.3 | 116.7 | 117.6 |
| 3-Me | 21.8 | 21.8 | 21.7 | 21.9 |
| 1′ | 162.6 | 162.6 | 162.8 | 162.8 |
| 2′ | 117.7 | 117.3 | 117.3 | 117.4 |
| 3′ | 148.3 | 147.8 | 147.7 | 147.5 |
| 4′ | 122.2 | 122.1 | 122.0 | 122.2 |
| 5′ | 109.7 | 108.3 | 108.9 | 110.7 |
| 6′ | 166.4 | 166.4 | 166.8 | 167.8 |
| 7′ | 100.7 | 101.5 | 101.1 | 103.3 |
| 8′ | 165.7 | 165.4 | 165.3 | 165.7 |
| 9′ | 191.3 | 191.4 | 191.2 | 191.0 |
| 10′ | 56.7 | 56.4 | 56.3 | 56.7 |
| 1a′ | 116.0 | 115.2 | 114.7 | 115.3 |
| 4a′ | 140.0 | 140.7 | 139.7 | 140.3 |
| 5a′ | 143.1 | 144.4 | 145.4 | 145.8 |
| 8a′ | 111.5 | 111.4 | 112.2 | 111.1 |
| 3′-Me | 22.1 | 22.0 | 22.2 | 22.3 |
| 1″ | 106.1 | 105.1 | 106.5 | 105.9 |
| 2″ | 74.9 | 74.5 | 74.9 | 74.9 |
| 3″ | 78.8 | 78.4 | 78.6 | 78.9 |
| 4″ | 71.2 | 71.3 | 71.3 | 71.5 |
| 5″ | 77.4 | 77.1 | 77.1 | 77.4 |
| 6″ | 62.7 | 62.8 | 62.9 | 62.7 |
| 6′-0Me | 56.5 | 56.2 | 56.2 | 56.4 |
a 13CNMR data were measured in CD3OD at 125 MHz
b 13CNMR data were measured in CD3COCD3 or CD3OD at 150 MHz
c 13CNMR data were measured in CD3COCD3 at 125 MHz