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. 2012 Jun 25;17(7):7637–7644. doi: 10.3390/molecules17077637

Table 1.

1H (500 MHz), 13C (125 MHz) and 2D-NMR (500 MHz) data of 1 in CDCl3.

Position δH J(Hz) δC HMBC COSY NOE
2 4.51 dd (6.5, 10) 90.5 C-12, 13 H-3 H-3, 12, 13, 14
3 2.16 m 30.6 C-2,3a, 4, 7a, 11, 14 H-2 H-13
3a 60.6
4 175.1
5 107.3
6 192.3
7 106.5
7a 195.7
8(-OH) 18.84 s 198.2 C-6, 7, 8, 9
9 3.18 m 40.0 C-7, 8, 10, 1′
3.10 m
10 2.92 m 31.0 C-8, 9, 1′, 2′, 6′
2.85 m
1′ 133.3
2′ 7.19 d (8.5) 113.7 C-10, 3′, 4′, 6′
3′ 6.82 d (8.5) 129.4 C-1′, 4′, 5′ OCH3-4′
4′ 158.0
5′ 6.82 d (8.5) 129.4 C-1′, 3′, 4′ OCH3-4′
6′ 7.19 d (8.5) 113.8 C-10, 2′, 4′, 5′
11 71.2
12 1.33 s 26.6 C-2, 11, 13 H-2
13 1.16 s 23.8 C-2, 11, 12 H-2
14 2.50 dd (7.5, 14.0) 38.7 C-3a, 4, 7a, 3, 15, 16 H-15 H-2
2.39 dd (7.5, 14.0)
15 4.96 t (7.5) 117.1 C-17, 18 H-14, 17, 18 H-17
16 137.0
17 1.66 s 25.8 C-15, 16, 18 H-15 H-15
18 1.52 s 17.8 C-15, 16, 17 H-15
19 3.10 m 21.5 C-4, 5, 6, 20, 21 H-20, 23
3.00 dd (7.5, 14.5)
20 5.11 t (7.5) 121.5 C-19, 22, 23 H-19, 23 H-23
21 132.1
22 1.72 s 17.8 C-20, 21, 23
23 1.68 s 25.6 C-20, 21, 22 H-19, 20
4′(-OCH3) 3.77 s 55.2 C-4′ H-3′, 5′