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. 2017 Aug 11;7:7944. doi: 10.1038/s41598-017-06320-x

Table 2.

1H NMR (600 MHz) data of compounds 14 in CD3OD.

No. 1 2 3 4
δ H (J in Hz) δ H (J in Hz) δ H (J in Hz) δ H (J in Hz)
1a 3.71 (dd, 11.0, 5.8) 3.71 (dd, 11.0, 5.6) 2.70 (dd, 14.9, 5.7) 2.14 (m)
1b 2.17 (dd, 14.9, 1.9) 2.14 (m)
2a 2.86 (ddd, 13.9, 9.6, 5.8) 2.87 (ddd, 15.9, 9.6, 5.6) 2.97 (m) 2.62 (m)
2b 1.42 (m) 1.44 (m) 2.62 (m)
3 4.04 (dd, 9.6, 8.0) 4.04 (dd, 9.5, 8.2)
6a 2.05 (dd, 13.9, 3.7) 2.02 (m) 4.41 (dd, 3.8, 2.5) 5.91 (d, 6.2)
6b 1.94 (dd, 13.9, 10.9) 2.02 (m)
7 4.37 (dd, 10.9, 3.7) 4.51 (dd, 10.5, 4.2) 5.64 (brs) 6.17 (d, 6.2)
11a 2.30 (ddd, 14.0, 9.4, 7.6) 2.36 (td, 12.9, 11.9, 3.3) 5.75 (dd, 3.8, 3.7) 5.57 (m)
11b 1.63 (m) 1.79 (m)
12a 1.59 (m) 1.75 (m) 2.01 (m) 2.04 (m)
12b 1.59 (m) 1.75 (m) 2.01 (m) 2.04 (m)
15 5.78 (dd, 5.9, 3.4) 5.98 (s) 4.01 (dd, 11.1, 5.7) 4.10 (dd, 10.1, 6.7)
16a 2.15 (dd, 17.7, 3.4) 1.44 (m) 1.51 (m)
16b 1.99 (dd, 17.7, 5.9) 1.44 (m) 1.51 (m)
18 1.24 (d, 2.1) 1.73 (m) 1.32 (d, 2.2) 1.35 (brs)
19 1.37 (m) 1.33 (s) 1.17 (m) 1.15 (m)
20 1.53 (m) 1.61 (m) 1.54 (m) 1.56 (m)
21a 1.60 (m) 1.67 (m) 3.44 (ddd, 11.7, 9.8, 6.6) 3.44 (ddd, 11.4, 9.7, 6.6)
21b 1.21 (m) 1.28 (m)
22a 1.39 (m) 1.72 (m) 2.15 (m) 2.21 (dd, 14.9, 9.7)
22b 1.56 (m) 1.72 (m) 1.18 (m) 1.21 (m)
23 0.94 (s) 0.94 (s) 1.24 (s) 1.26 (s)
24 0.86 (s) 0.87 (s) 1.22 (s) 1.29 (s)
25 0.99 (s) 1.01 (s) 1.38 (s) 1.11 (s)
26 1.32 (s) 1.40 (s) 0.77 (s) 1.05 (s)
27 1.13 (s) 1.28 (s) 0.65 (s) 0.70 (s)
28 1.08 (s) 1.31 (s) 1.17 (s) 1.20 (s)
29 1.11 (d, 7.1) 1.17 (d, 6.8) 1.14 (d, 6.6) 1.14 (d, 6.7)
30 1.00 (d, 6.5) 1.00 (d, 6.5) 1.06 (d, 6.1) 1.06 (d, 6.1)