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. 2021 Sep 6;11(47):29684–29689. doi: 10.1039/d1ra05760j

NMR data for compounds 1 and 2 (400 MHz for 1H, and 100 MHz for 13C)a,b.

No. 1 (DMSO-d6) 2 (DMSO-d6)
δ H δ C δ H δ C
1 1.70 (m, H-1a) 36.6 1.76 (m, H-1a) 36.8
2.21 (m, H-1b) 2.52 (m, H-1b)
2 1.28 (m, H-2a) 28.2 2.43 (m, H-2a) 34.6
1.62 (m, H-2b) 2.67 (m, H-2b)
3 3.08 (br t, 7.2) 77.0 216.1
4 39.1 47.1
5 1.18 (dd, 2.2, 12.4) 49.7 1.86 (dd, 2.0, 12.4) 49.7
6 1.84 (m, H-6a) 18.8 1.72 (m, H-6a) 19.8
1.87 (m, H-6b) 1.82 (m, H-6b)
7 2.77 (m, H-7a) 33.7 2.81 (m, H-7a) 33.5
2.89 (dd, 5.6, 18.2, H-7b) 2.93 (dd, 5.6, 18.0, H-7b)
8 154.6 154.1
9 141.5 140.0
10 37.1 36.6
11 7.48 (d, 8.1) 133.2 7.62 (d, 8.2) 147.0
12 6.94 (d, 8.1) 121.0 7.03 (d, 8.2) 121.5
13 154.6 154.9
16 2.33 (s, 3H) 24.0 2.37 (s, 3H) 23.7
18 0.98 (s, 3H) 28.7 1.08 (s, 3H) 26.8
19 0.77 (s, 3H) 16.3 1.03 (s, 3H) 21.3
20 1.07 (s, 3H) 25.1 1.19 (s, 3H) 24.4
3-OH 4.45 (br s)
a

Chemical shift values were in ppm and J values (in Hz) were presented in parentheses.

b

The assignments were based on HMQC, HMBC, and 1H–1H COSY experiments.