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. 2019 Winter;18(1):406–411.

Table 1.

1H and 13C NMR data of compounds 1 and 2 in CDCl /CD OD (500 MHz for δ ; 125 MHz for δ )

1
2
position δ C δ H (J in Hz) δ C δ H (J in Hz)
1α 1β 41.6 0.85b
1.52b
40.0 0.88b
1.53b
2α 2β 18.3 1.60b
1.33b
18.4 1.53b
1.35b
3α 3β 44.1 1.05b
1.22b
41.8 1.07b
1.28b
4 33.4 32.9
56.7 0.83b 56.7 0.83b
6α 6β 67.6 4.39 brd (2.6) 20.6 1.57b
1.18b
7α 7β 51.3 1.55b
1.91 dd (13.5, 2.0)
43.8 1.34b
1.75 dt (12.5,3.0)
8 73.4 74.5
62.1 1.03b 62.3 1.00 t (3.5)
10 38.9 39.2
11α 11β 17.9 1.49
1.28
18.0 1.46b
1.26b
12α 12β 40.9 1.60b
1.41b
40.8 1.60b
1.38b
13 73.1 73.8
14β 75.1 3.55 dd (8.5, 2.5) 77.8 3.39 dd (7.5, 3.5)
15a 15b 66.2 3.96 dd (11.5, 8.5)
4.22 dd (11.5, 2.5)
62.5 3.50 dd (11.5, 7.5)
3.65 dd (11.5, 3.5)
16 22.6 1.10 s 22.0 1.08 s
17 24.8 1.32 s 23.6 1.09 s
18 32.8 0.89 s 33.4 0.79 s
19 24.2 1.10 s 21.5 0.71 s
20 16.1 1.08 s 14.9 0.73 s
CH3CO CH3CO 19.8
171.3
1.99 s
a

δ values were extracted from COSY, HSQC and HMBC experiments.

b

Overlapping signals.