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. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: Phytochemistry. 2020 Feb 17;173:112278. doi: 10.1016/j.phytochem.2020.112278

Table 3.

1H NMR (600 MHz) and 13C NMR (150 MHz) data for compounds 11-13 in DMSO-d6.

Position 11 12 13
δC δH δCa δH δC δH
1 161.7 161.6 161.5
2 111.8 6.11, d (9.6) 112.1 6.13, d (9.6) 112.7 6.20, d (9.6)
3 149.0 7.40, d (9.6) 147.8 7.41, d (9.6) 144.7 7.56, d (9.6)
4 113.1 115.1 119.2
5 159.2 158.3 157.6
6 36.4 Hα: 2.39, dd (4.2, 14.4) 25.0 Hα: 2.30, m 66.2 4.47, t (6.6)
Hβ: 2.28, dd (8.4, 14.4) Hβ: 2.36, m
7 71.3 3.42, m 38.8 1.45, q (7.2) 39.1 Hα: 1.41, m
Hβ: 1.58, m
8 29.6 Hα: 1.42, m 64.8 3.55, m 18.3 Hα: 1.21, m
Hβ: 1.33, m Hβ: 1.32, m
9 10.1 0.89, dd (7.2, 7.8) 23.6 1.07, d (6.0) 13.9 0.87, t (7.2)
10 17.3 2.19, s 16.8 2.19, s 16.6 2.21, s
6-OH 5.16, br s
7-OH 4.56, d (5.4)
8-OH 4.48, d (4.8)
a

Determined from HSQC and HMBC spectra