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. Author manuscript; available in PMC: 2022 Jan 1.
Published in final edited form as: Phytochemistry. 2020 Nov 17;181:112545. doi: 10.1016/j.phytochem.2020.112545

Table 2.

NMR spectroscopic data for compounds 3–6 in CD3OD.

no. 3
4
5
6
δC δH multi. J (Hz) δC δH multi. J (Hz) δC δH multi. J (Hz) δC δH multi. J (Hz)

1 170.1 170.1 170.1 170.7
2 120.7 5.96 d (15.6) 120.7 5.96 d (15.6) 117.3 5.86 d (15.6) 117.3 5.86 d (15.5)
3 146.4 7.25 d (15.5) 147.8 7.27 d (15.5) 148.9 7.30 d (15.5) 148.3 7.30 d (15.4)
4 135.9 134.7 131.4 132.3
5 137.4 5.88 d (8.9) 138.5 5.85 d (9.0) 138.3 6.41 d (11.3) 137.5 6.38 d (11.1)
6 70.9 4.33 dd (5.1, 8.9) 70.9 4.30 dd (5.9, 9.0) 127.0 6.51 t (11.9) 126.9 6.51 t (13.0)
7 74.2 3.55 m 74.3 3.48 m 139.3 5.97 m 137.7 5.97 m
8 32.3 1.55 m 32.3 1.38 m
1.50 m
32.4 2.20 m 27.0 2.46 m
9 25.2 1.35 m
1.55 m
25.2 1.36 m
1.51 m
22.9 1.70 m 40.9 2.62 t (7.2)
10 31.7 1.33 m 31.6 1.33 m 42.4 2.53 t (7.3) 212.3
11 22.3 1.34 m 22.2 1.34 m 210 35.3 2.50 m
12 13.0 0.92 t (6.6) 13.0 0.94 t (6.8) 28.7 2.14 s 6.77 1.05 t (7.3)
14 11.8 1.88 s 11.8 1.90 s 11.4 1.90 s 11.4 1.90 s