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. Author manuscript; available in PMC: 2011 Mar 26.
Published in final edited form as: J Nat Prod. 2010 Mar 26;73(3):476–478. doi: 10.1021/np900608d

Table 1.

1H NMR Spectroscopic Data for Compounds 25.

2 3 4 5

Position δHa (J in Hz) δHa (J in Hz) δHb (J in Hz) δHb (J in Hz)
1 2.58, br d (11.4) 2.58, br d (10.2) 2.54, br d (10.6) 2.43, br d (10.6)
2 a: 1.99, m a: 1.91, m a: 1.89, m a: 1.93, m
b: 1.37, qd (11.4, 5.4) b: 1.42, qd (11.7, 5.4) b: 1.50, qd (11.7, 5.5) b: 1.45, qd (11.7, 5.4)
3 2.08, m a: 2.06, m a: 1.98, m a: 2.08, m
b: 1.88, m b: 1.95, m b: 1.93, m
5 5.79, d (4.1) 5.52, br s 5.71, br d (5.1) 5.57, br d (4.4)
6 2.04, m 2.10, m 2.11, m 2.10, m
7 1.53, tt (10.2, 5.1) 1.65, tt (10.2, 5.1) 1.68, td (10.3, 5.1) 1.52, ddd (3.2, 8.7, 10.7)
8 a: 2.15, dt (19.8, 5.1) a: 2.27, dt (19.8, 5.1) a: 2.38, dt (19.6, 5.1) 4.13, br d (8.7)
b: 1.97, m b: 2.02, m b: 2.01, m
9 7.14, br s 7.10, br s 6.95, br t (3.9) 6.79, d (1.8)
11 2.03, m 2.05, m 2.25, m
12 0.83, d (6.8) a: 3.77 (dd, 4.8, 10.6) 1.23, s 1.00, d (7.1)
13 0.90, d (6.8) 1.03, d (7.0) 1.18, s 1.10, d (7.1)
14
15 4.03, br s 1.68, br s 1.66, br s 1.68, br s
a

CDCl3, 300 MHz.

b

Acetone-d6, 300 MHz.