Table 1.
NMR data of compounds 1 and 2 in CDCl3 (1H: 500 MHz; 13C: 125 MHz; δ in ppm, J in Hz).
Position | 1 | 2 | ||
---|---|---|---|---|
δ H | δ C | δ H | δ C | |
1 | - | 67.5 | - | 67.5 |
2 | 3.27 (1 H, dd, 6.8, 7.7) | 59.4 | 3.15 (dd, 1 H, 1.6, 4.8) | 61.8 |
3 | 2.16 (1 H, ddd, 3.1, 7.7, 14.2) | 27.0 | 2.15 (ddd, 1 H, 3.1, 4.8, 15.6) | 26.8 |
1.53 (1 H, ddd, 6.8, 13.3, 14.2) | 1.53 (ddd, 1 H, 1.6, 13.3, 15.6) | |||
4 | 1.88 (1 H, m) | 48.3 | 2.25 (ddd, 1 H, 3.1, 13.3, 13.5) | 46.1 |
5 | - | 43.3 | - | 41.8 |
6 | 1.85 (1 H, dd, 12.6, 16.3) | 50.1 | 1.87 (1 H,dd, 5.0, 16.3) | 48.4 |
1.66 (1 H, dd, 1.6, 16.3) | 1.46 (1 H, dd, 11.6, 16.3) | |||
7 | 3.85 (1 H,dd, 1.6, 12.6) | 72.6 | 4.29 (1 H,dd, 5.0, 11.6) | 68.2 |
8 | 1.61 (1 H, m) | 42.9 | 1.47 (1 H, m) | 43.3 |
1.41 (1 H, m) | 1.40 (1 H, m) | |||
9 | 1.92 (1 H, m) | 29.9 | 1.85 (1 H, m) | 29.6 |
1.77 (1 H, m) | 1.76 (1 H, m) | |||
10 | 2.95 (1 H, ddd, 2.2, 13.5, 13.6) | 50.0 | 2.92 (1 H, ddd, 2.2, 13.4, 14.3) | 50.7 |
11 | - | 149.0 | - | 148.3 |
12 | 4.79 (1 H, d, 1.3) | 113.4 | 4.85 (1 H, d, 1.3) | 113.9 |
4.68 (1 H, d, 1.3) | 4.74 (1 H, d, 1.3) | |||
13 | 1.66 (3 H, s) | 23.2 | 1.73 (3 H, s) | 23.4 |
14 | 3.90 (1 H, d, 12.9) | 60.6 | 4.07 (1 H, d, 12.5) | 61.8 |
3.75 (1 H, d, 12.9) | 3.30 (1 H, d, 12.5) | |||
15 | 0.99 (3 H, s) | 18.3 | 0.85 (3 H, s) | 18.3 |