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. Author manuscript; available in PMC: 2012 May 27.
Published in final edited form as: J Nat Prod. 2011 Mar 23;74(5):1117–1125. doi: 10.1021/np200051j

Table 3.

1H NMR Spectroscopic Data of Compounds 10, 16, and 19

position 10a 16b 19b
4
5 6.79 s 7.46 m 8.06 d (2.4)
6 7.46 m 7.58 m
8 7.94 brs 7.58 m
11 3.39 d (6.3) 3.28 brs 3.47 d (7.0)
12 5.26 m 5.14 m 5.25 m
14 1.67 s 1.67 s 1.75 s
15 1.79 s 1.76 s 1.84 s
16 4.12 d (6.3) 3.40 brs 3.58 d (6.9)
17 5.26 m 5.03 t (6.6) 5.25 m
19 1.65 s 1.83 s 1.87 s
20 1.83 s 2.04 m 2.10 m
21 2.00 m 2.10 m
22 5.14 m 5.04 m
24 1.57 s 1.66 s
25 1.53 s 1.56 s
OH-1 13.45 s 12.80 s 13.10 s
OH-3 6.50 s
OMe-3 3.78 s
OMe-6 3.97 s
OMe-7 3.77 s
Me-4 2.30 s
OAc 2.34 s
OAc 2.33 s
3' 8.22 d (7.5)
4' 7.58 m
5' 7.65 t (7.5)
6' 7.58 m
7' 8.22 d (7.5)
a

Data (δ) measured in CDCl3 at 400 MHz.

b

Data (δ) measured in CDCl3 at 300 MHz. s = singlet, brs = broad singlet, d = doublet, t = triplet, m = multiplet. J values presented in Hz and omitted if the signals overlapped as multiplets.