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. Author manuscript; available in PMC: 2014 Apr 26.
Published in final edited form as: J Nat Prod. 2013 Mar 21;76(4):710–714. doi: 10.1021/np400042q

Table 2.

1H and 13C NMR data (600 MHz and 150 MHz, CDCl3) for compounds 5 and 9

5 9

δH (m, J Hz) δ C δH(m, J Hz) δ C
1 - 202.6 - 202.5
2a 2.73 (dd, 17.0, 12.6) 45.8 2.72 (dd, 17.0, 12.3) 45.7
2b 2.81 (dd, 17.1, 3.4) - 2.81 (dd, 17.1, 3.4) -
3 3.30 (m) 40.2 3.24 (m) 40.1
4 3.01 (m) 38.7 3.00 (m) 38.1
5 6.23 (s) 101.8 6.25 (brs) 107.2
6 - 167.2 - 166.3
7 - 111.8 6.28 (d, 2.1) 99.1
8 - 160.8 - 165.9
9 - 110.9 - 111.3
10 - 147.5 - 146.3
1' - 135.6 - 136.5
2' 7.12 (d, 8.4) 128.8 6.77 (d, 1.7) 114.0
3' 6.79 (d, 8.4) 115.7 - 146.3
4' - 154.6 - 142.5
5' 6.79 (d, 8.4) 115.7 6.81 (d, 8.1) 115.8
6' 7.12 (d, 8.4) 128.8 6.66 (dd, 8.1, 1.7) 119.2
2” 5.26 (t, 8.2) 88.1 - -
3”a 2.94 (dd, 15.4, 7.6) 30.9 - -
3”b 3.28 (dd, 15.6, 10.0) - - -
1”'a 4.90 (brs) 112.8 - -
1”'b 5.05 (brs) - - -
2”' - 143.4 - -
3”' 1.74 (s) 17.2 - -
OMe - - 3.81 (s) 55.7