Table 1.
Position | δH (J in Hz) | δC, Mult. | HMBC | NOESY |
---|---|---|---|---|
1 | 1.51, ddd (13.6, 5.6, 5.6) | 39.0 CH | C-2, C-4, C-5, C-10, C-14,C-15 | H-3, H-4, H-7 |
2 | Hα: 1.82, m | 31.5 CH2 | C-1, C-3 | |
Hβ: 2.01, m | C-1, C-3 | |||
3 | 5.45, ddd (8.1, 7.5, 5.0) | 71.0 CH | C-1, C-4, C-5, C-16 | Hα-2, Hβ-2, H-4 |
4 | 3.64, d (7.5) | 75.9 CH | C-3, C-5, C-6, C-15 | H-1, H-3, H-7 |
5 | – | 43.3 qC | ||
6 | Hα: 1.94, br d (14.3) | 30.5 CH2 | C-5, C-7, C-15 | H-4, H-7 |
Hβ: 1.16, overlapped | Hβ-9 | |||
7 | 2.51, m | 36.7 CH | C-5, C-6, C-11, C12 | H-1, H-4, H-8, H-11 |
8 | 4.58, ddd (13.2, 8.6, 2.8) | 79.7 CH | C-7 | H-7, Hα-9, Hβ-9, H-11 |
9 | Hα: 2.07, m | 36.4 CH2 | C-1, C-7, C-8, C-10, C-14 | |
Hβ: 1.66, br d (12.7) | C-1, C-7, C-8, C-10 | Hβ-6, H-14, H-15, | ||
10 | 1.80, m | 28.5 CH | C-1, C-5, C-14 | |
11 | 2.94, m | 37.5 CH | C-6, C-7, C-12, C-13 | H-7, H-8, H-13 |
12 | – | 177.8 qC | ||
13 | 1.02, d (7.4) | 9.7 CH3 | C-7, C-11, C-12 | Hβ-6, H-7, H-11 |
14 | 0.90, d (7.0) | 16.4 CH3 | C-1, C9, C-10 | Hα-9 |
15 | 1.18, s | 17.5 CH3 | C-1, C-4, C-5, C-6 | Hβ-9, H-10 |
16 | – | 169.8 qC | ||
17 | 2.04, s | 20.3 CH3 | C-16 | H-3 |
Note: a 1H (400 MHz) and 13C (100 MHz) NMR; δ in ppm.