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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 2.

13C NMR Spectroscopic Data for Compounds 25.

2 3 4 5

Position δC, mult.a,c δC, mult.a,c δC, mult.b,c δC, mult.b,c
1 34.0, CH 33.8, CH 35.6, CH 35.2, CH
2 25.1, CH2 25.4, CH2 26.2, CH2 26.0, CH2
3 26.2, CH2 30.3, CH2 30.8, CH2 31.5, CH2
4 138.3, qC 135.6, qC 133.7, qC 134.9, qC
5 124.3, CH 123.0, CH 126.6, CH 125.1, CH
6 35.5, CH 35.8, CH 36.9, CH 36.2, CH
7 40.0, CH 38.6, CH 47.2, CH 48.8, CH
8 25.4, CH2 28.0, CH2 29.7, CH2 68.7, CH
9 142.6, CH 142.1, CH 140.2, CH 143.7, CH
10 132.9, qC 133.1, qC 134.3, qC 134.3, qC
11 26.4, CH 35.3, CH 72.6, qC 27.3, CH
12 15.0, CH3 64.9, CH2 27.4, CH3 18.9, CH3
13 21.3, CH3 15.4, CH3 28.7, CH3 21.1, CH3
14 172.2, qC 172.0, qC 168.0, qC 168.0, qC
15 67.3, CH2 23.9, CH3 23.9, CH3 23.9, CH3
a

CDCl3, 75.5 MHz.

b

Acetone-d6, 75.5 MHz.

d

Implied multiplicities determined by DEPT.