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. Author manuscript; available in PMC: 2016 May 25.
Published in final edited form as: J Nat Prod. 2015 May 22;78(6):1271–1276. doi: 10.1021/acs.jnatprod.5b00065

Table 1.

1H NMR Spectroscopic Data for Compounds 1–7 in CDCl3.

position 1
2
3
4
5
6
7
δH (J in Hz) δH (J in Hz) δH (J in Hz) δH (J in Hz) δH (J in Hz) δH (J in Hz) δH (J in Hz)
2 6.11, s 6.15, s 6.12 s 6.12 s 6.23, s 6.25, s
4 6.27, s 6.24, s 6.30 s 6.27, s 6.15, s 6.25, s 6.25, s
6a 1.81, m 1.80, m 1.85, m 1.85, m 1.75, dt (10.6, 3.6) 1.85 m 1.62 m
7 2.41, m 2.41, m 2.10, m 2.38, m 1.86, m 1.56, m 1.94, m 1.35, m
8 4.10, d (4.8) 4.31, bt 5.68, d (5.6) 5.62, bs 2.21, m 1.82, m 2.26, m
10 6.66, bs 6.54, bs 4.27, d (8.4) 5.08, d (2.4) 4.22, d (8.8) 3.88, bs 6.79, s
10a 3.11, d (11.2) 3.30, d (10) 2.77, t (8.1) 2.70, m 2.69, t (10.2) 2.79, d (12.0) 3.27, m
11 1.80 s 1.76 s 1.76 s 1.84 s 5.10 bs 1.36 s 4.48 s
4.94 bs
12 1.42, s 1.39, s 1.37, s 1.40, s 1.35, s 1.39, s 1.45, s
13 1.09, s 1.09, s 1.04, s 1.11, s 1.01, s 1.03, s 1.11, s
1′ 2.41, dd (6.4, 8.4) 2.41, dd (6, 8.4) 2.42, m 2.40, m 2.43, dd (8.4, 6.0) 2.44, m 2.93, m
2′ 1.55, m 1.54, m 1.55, m 1.55, m 1.56, m 1.54, m 1.58, m
3′ 1.29, m 1.29, m 1.29, m 1.29, m 1.30, m 1.31, m 1.23, m
4′ 1.29, m 1.29, m 1.29, m 1.29, m 1.30, m 1.31, m 1.23, m
5′ 0.87, t (6.8) 0.87, t (7.1) 0.89, t (6.8) 0.89, t (6.8) 0.87, t (6.4) 0.88, t (6.8) 0.89, t (6.9)
OCOCH3 2.07, s