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. Author manuscript; available in PMC: 2008 Sep 9.
Published in final edited form as: J Nat Prod. 2007 Jul 31;70(8):1317–1320. doi: 10.1021/np070251m

Table 3.

1H NMR data [δH (mult, JH)] for compound 2a

position 2 position 2
2 2.79 (br m) 12minor 5.91 (s)
3 5.29 (dt, 10, 2.0) 16 0.76 (d, 7.4)
4 5.57 (dt, 10, 3.4) 17major 8.27 (d, 13)
5 2.39 (br m) 17minor 8.42 (d, 15)
6eq 1.72 (m) 18 0.98 (d, 7.4)
6ax 1.23 (m) 19 1.04 (s)
7eq 1.50 (m) 20major 3.60 (q, 5.3)
7ax 1.50 (m) 20minor 3.66 (q, 5.3)
8eq 1.34 (br d, 12) 21 3.86 (br t, 5.3)
8ax 1.50 (m) NHmajor 11.88 (br s)
9 1.51 (m) NHminor 10.16 (br s)
10 2.21 (br d, 7.2) OHmajor 2.00 (br s)
12major 5.86 (s) OHminor 2.03 (br s)
a

CDCl3, 300 MHz. 1H NMR signals for the major and minor forms were not clearly resolved for the modified decalin portion of the molecule or for H2-21, but some of the corresponding signals did appear to be broadened.