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. Author manuscript; available in PMC: 2016 Jun 1.
Published in final edited form as: Phytochemistry. 2008 Sep 4;69(14):2627–2633. doi: 10.1016/j.phytochem.2008.07.010

Table 1.

1H (400 MHz) and 13C (100 MHz) NMR spectroscopic data of 2–4 (CDCl3, δ in ppm, J in Hz)a

Position 2 3 4
δH δC δH δC δH δC
1 6.50 s 104.4 6.39 s 103.9 - 140.2
2 - 152.0 - 150.3 - 140.2
3 - 136.4 - 134.5 6.15 s 107.6
4 - 147.2 - 146.8 - 161.5
4a - 114.9 - 114.7 - 124.2
4b - 121.1 - 107.8 - 117.4
5 - 141.7 8.02 s 111.5 - 156.6
6 -- 147.6 -- 147.2 6.93 d (2.0) 108.9
7 6.74 d (8.0) 109.2 147.1 - 161.0
8 6.79 d (8.0) 119.1 6.79 s 111.1 6.82 d (2.0) 102.0
8a - 132.6 - 125.4 - 129.0
9 2.64 s 30.6 2.74 s 29.5 8.06 d (8.4) 137.7
10 2.64 s 31.8 2.74 s 30.9 8.12 d (8.4) 122.9
10a - 136.4 - 130.1 - 132.7
OMe-2 3.89 s 56.3 3.88 s 56.2 - -
OMe-3 3.86 s 61.0 3.89 s 61.3 - -
OMe-4 - - - - 3.96 s 57.2
OMe-6 3.85 s 56.1 3.92 s 56.0 - -
OMe-7 - - 3.92 s 56.1 3.90 s 55.7
a

Assignments confirmed by APT, gHMQC, gCOSY and gHMBC experiments

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