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. 2012 Aug 24;17(9):10046–10051. doi: 10.3390/molecules170910046

Table 1.

NMR data of compounds 1 and 2 in CDCl3 (1H: 500 MHz; 13C: 125 MHz; δ in ppm, J in Hz).

Position 1 2
δ H δ C δ H δ C
1 - 67.5 - 67.5
2 3.27 (1 H, dd, 6.8, 7.7) 59.4 3.15 (dd, 1 H, 1.6, 4.8) 61.8
3 2.16 (1 H, ddd, 3.1, 7.7, 14.2) 27.0 2.15 (ddd, 1 H, 3.1, 4.8, 15.6) 26.8
1.53 (1 H, ddd, 6.8, 13.3, 14.2) 1.53 (ddd, 1 H, 1.6, 13.3, 15.6)
4 1.88 (1 H, m) 48.3 2.25 (ddd, 1 H, 3.1, 13.3, 13.5) 46.1
5 - 43.3 - 41.8
6 1.85 (1 H, dd, 12.6, 16.3) 50.1 1.87 (1 H,dd, 5.0, 16.3) 48.4
1.66 (1 H, dd, 1.6, 16.3) 1.46 (1 H, dd, 11.6, 16.3)
7 3.85 (1 H,dd, 1.6, 12.6) 72.6 4.29 (1 H,dd, 5.0, 11.6) 68.2
8 1.61 (1 H, m) 42.9 1.47 (1 H, m) 43.3
1.41 (1 H, m) 1.40 (1 H, m)
9 1.92 (1 H, m) 29.9 1.85 (1 H, m) 29.6
1.77 (1 H, m) 1.76 (1 H, m)
10 2.95 (1 H, ddd, 2.2, 13.5, 13.6) 50.0 2.92 (1 H, ddd, 2.2, 13.4, 14.3) 50.7
11 - 149.0 - 148.3
12 4.79 (1 H, d, 1.3) 113.4 4.85 (1 H, d, 1.3) 113.9
4.68 (1 H, d, 1.3) 4.74 (1 H, d, 1.3)
13 1.66 (3 H, s) 23.2 1.73 (3 H, s) 23.4
14 3.90 (1 H, d, 12.9) 60.6 4.07 (1 H, d, 12.5) 61.8
3.75 (1 H, d, 12.9) 3.30 (1 H, d, 12.5)
15 0.99 (3 H, s) 18.3 0.85 (3 H, s) 18.3