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. Author manuscript; available in PMC: 2009 Oct 1.
Published in final edited form as: Phytochemistry. 2008 Aug 29;69(13):2495–2500. doi: 10.1016/j.phytochem.2008.07.005

Table 1.

1H and 13C NMR spectral data of 1-2 (in CD3OD)

Position 1 2
δc DEPT δH (mult., J in Hz) δc DEPT δH (mult., J in Hz)
1 179.0, s 177.0, s
2 35.3, t 2.25 (2H, m) 37.4, t 2.34 (1H, m)
1.52 (1H, m)
3 72.3, t 4.10 (1H, dd, 6.5, 13) 72.4, d 4.06 (1H, dd, 6.5, 13)
4 135.7, d 5.62 (1H, dd, 6.5, 15.5) 136.3, d 5.60 (1H, dd, 6.5, 15)
5 125.7, d 6.49 (1H, dd, 11, 15.5) 125.5, d 6.49 (1H, dd, 11, 15)
6 128.3, d 5.95 (1H, t, 11) 128.4, d 5.96 (1H, t, 11)
7 132.1, d 5.41 (1H, dt, 8.0, 11) 131.9, d 5.41 (1H, m)
8 27.6, t 2.18 (2H, m) 27.6, t 2.20 (2H, m)
9 25.7, t 1.59 (2H, m) 25.3, t 1.60 (1H, m)
1.41 (1H, m)
10 29.7, t 1.32 (2H, m) 29.8, t 1.33 (2H, m)
11 29.4, t 1.32 (2H, m) 29.6, t 1.33 (2H, m)
12 29.3, t 1.32 21H, m) 29.5, t 1.33 21H, m)
13 29.2, t 1.32 (2H, m) 29.1, t 1.33 (2H, m)
14 20.7, t 2.05 (2H, m) 32.0, t 1.33 (2H, m)
15 124.5, d 5.35 (1H, m) 22.7, t 1.33 (2H, m)
16 133.6, d 5.46 (1H, m) 13.4, t 0.91 (3H, t, 7.5)
17 20.7, t 2.05 (2H, m)
18 13.5, q 0.95 (3H, t, 7.5)