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. 2015 Mar 10;20(3):4450–4459. doi: 10.3390/molecules20034450

Table 1.

NMR assignments of 1 by DEPT, HSQC, HMBC, and NOESY experiments in C5D5N a.

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.