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. 2012 Feb 27;10(3):539–550. doi: 10.3390/md10030539

Table 2.

1H and 13C NMR data of compounds 45.

Position 4 b 5 a
δC, mult. δH ( J in Hz) δC, mult. δH ( J in Hz)
1 24.8, CH2 1.55, 2m 29.1, CH2 1.63, 2m
2 18.9, CH2 1.61, 2m 17.9, CH2 1.67, 2m
3 38.7, CH2 1.64, m; 1.11, m 36.3, CH2 1.71, m; 1.53, m
4 37.4, C 36.7, C
5 80.0, C 82.6, C
6 107.2, C 210.9, C
7 74.6, CH 4.48, s 74.6, CH 5.23, s
8 132.6, C 131.8, C
9 141.7, C 139.8, C
10 52.1, C 50.7, C
11α 21.7, CH2 2.19, ddd (13.6, 5.8, 2.9) 21.2, CH2 2.15, m
11β 1.92, m 1.90, m
12α 28.0, CH2 1.80, m 30.2, CH2 1.83, m
12β 1.41, m 1.49, m
13 39.6, C 39.7, C
14 70.6, CH 4.01, s 72.4, CH 4.13, s
15 146.2, CH 6.07, dd (17.5, 11.1) 142.0, CH 6.03, dd (17.3, 1.4)
16a 112.1, CH2 5.07, dd (17.5, 1.5) 114.8, CH2 5.23, dd (17.3, 1.4)
16b 5.05, dd (11.1, 1.5) 5.21, dd (11.4, 1.4)
Position 4 b 5 a
δC, mult. δH (J in Hz) δC, mult.
17 21.3, CH3 0.93, s 22.8, CH3 1.08, s
18 24.3, CH3 1.46, s 23.8, CH3 1.46, s
19 28.9, CH3 1.23, s 27.8, CH3 1.07, s
20 72.4, CH2 4.13, d (9.2) 23.5, CH3 1.07, s
3.40, d (9.2)

a Measured in CDCl3; b Measured in CD3OD. 500 MHz for 1H NMR; 125 MHz for 13C NMR.