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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Phytochemistry. 2016 Apr 2;126:4–10. doi: 10.1016/j.phytochem.2016.03.013

Table 1.

1H NMR spectroscopic data (400 MHz) for 1–4 in CDCl3.

# 1 2 3 4




δH (mult., J) δH (mult., J) δH (mult., J) δH (mult., J)
1 3.70 (br s)
3.35 (dd, 13.5, 3.2) 2.19 (dt, 13.5, 2.5) 3.48 (d, 3.3) 5.76 (d, 10.3)
2.22 (dd, 13.5, 3.7) 1.96 (dt, 13.5, 2.7)
3 3.88 (br s) 3.52 (br s) 3.27 (d, 3.3) 6.17 (d, 10.3)
5 1.81 (dd, 12.7, 2.0) 1.78 (dd, 12.6, 2.0)
1.69 (m) 1.74 (m) 1.75 (dt, 13.9, 3.5) 1.79 (dd, 14.4, 3.6)
1.50 (m) 1.41 (m) 1.60 (m) 1.73 (ddd, 14.4, 4.1, 3.3)
2.04 (m) 2.06 (m) 2.21 (m) 2.19 (dt, 4.9, 14.1)
1.66 (m) 1.70 (m) 1.70 (dt, 12.8, 3.4) 1.82 (m)
9 2.04 (m) 2.21 (dd, 13.0, 4.9) 2.64 (dd, 12.8, 4.5) 2.60 (dd, 12.8, 4.5)
11α 2.96 (dd, 15.5, 4.5) 2.37 (dd, 15.2, 4.9) 3.04 (dd, 15.3, 4.5) 3.15 (dd, 15.5, 4.5)
11β 1.91 (dd, 15.5, 12.7) 1.99 (dd, 15.2, 13.0) 1.98 (dd, 15.3, 12.8) 2.01 (dd, 15.5, 12.8)
12 1.26 (s) 1.25 (s) 1.25 (s) 1.33 (s)
13 1.02 (s) 1.01 (s) 1.29 (s) 1.25 (s)
14 1.08 (s) 0.83 (s) 1.27 (s) 1.13 (s)
15 1.24 (s) 0.83 (s) 1.23 (s) 1.297 (s)
4′α 2.48 (dd, 16.9, 14.0) 2.49 (dd, 16.8, 14.0) 2.48 (dd, 16.9, 14.4) 2.49 (dd, 16.9, 14.0)
4′β 2.35 (dd, 16.9, 3.2) 2.32 (dd, 16.8, 3.1) 2.36 (dd, 16.9, 2.9) 2.36 (dd, 16.9, 3.2)
5′ 4.57 (dqd, 14.0, 6.3, 3.2) 4.54 (ddq, 14.0, 3.1, 6.3) 4.60 (ddq, 14.4, 2.9, 6.3) 4.60 (ddq, 14.0, 3.2, 6.3)
6′ 1.43 (d, 6.3) 1.42 (d, 6.3) 1.43 (d, 6.3) 1.44 (d, 6.3)
3-OH 1.54 (br s)
5-OH 2.68 (br d, 2.0) 1.44 (s)