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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: European J Org Chem. 2014 Oct 31;2015(1):109–121. doi: 10.1002/ejoc.201402984

Table 3.

NMR data for 7 and 8 (500 MHz for 1H, 125 MHz for 13C; chemical shifts in δ, coupling constants in Hz, CDCl3).

Position 7 8
δC δH mult (J in Hz) δC δH mult (J in Hz)
2 84.3 84.3
3 39.8 3.04, dd (17.2, 0.6) 40.7 3.07, d (17.2)
3.17, d (17.2) 3.48, d (17.2)
4 194.1 194.9
4a 107.7 107.5
5 162.0 161.9
6 110.7 6.55, dd (8.6, 0.6) 110.6 6.54, dd (8.6, 0.6)
7 139.2 7.42, t (8.6) 139.0 7.40, t (8.6)
8 107.7 6.54, dd (8.6, 0.6) 107.5 6.49, dd (8.6, 0.6)
8a 159.2 159.3
9 87.6 4.43, dd (4.0, 0.6) 86.5 4.36, dd (3.4, 0.6)
10 30.1 2.83, m 29.7 2.85, m
11 36.2 2.21, dd (17.8, 4.6) 36.4 2.21, dd (17.8, 4.6)
2.89, dd (17.8, 9.2) 3.01, dd (17.8, 9.2)
12 175.3 175.7
13 20.9 1.28, d (6.9) 20.7 1.18, d (6.9)
14 168.9 169.2
15 53.8 3.72, s 53.7 3.74, s
5-OH 11.43, s 11.45, s