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. Author manuscript; available in PMC: 2012 Nov 15.
Published in final edited form as: Bioorg Med Chem. 2011 Jun 1;19(22):6604–6607. doi: 10.1016/j.bmc.2011.05.046

Table 1.

NMR data for compound 1 (1H 500 MHz, 13C 125 MHz, δ ppm) in methanol-d4

position δC δH mult. (J in Hz) 1H-1H COSY HMBC
1 127.5 CH 7.80 m H-2 C-3, C-4a, C-13
1a 138.0 C
2 135.0 CH 7.82 m C-1a, C-4
3 125.8 C
4 119.2 CH 8.54 d (1.2) H-2 C-4a, C-1a, C-2, C-3
4a 144.1 C
6 125.3 CH 9.26 d (6.8) H-7 C-12b, C-4a, C-7a, C-7
7 118.7 CH 8.77 d (6.8) C-12a, C-7b, C-6, C-12b
7a 137.5 C
7b 121.9 C
8 124.8 CH 8.43 d (8.4) H-9, H-10 C-11a, C-10, C-7b
9 124.0 CH 7.49 dd (8.4, 7.6) H-10 C-10, C-7b, C-11
10 134.6 CH 7.83 m H-11 C-11a, C-8, C-9
11 114.5 CH 7.82 m C-11a, C-9
11a 147.5 C
12a 132.4 C
12b 145.0 C
13 79.6 C
14 51.6 CH2 4.16 d (18.4) C-15, C-12b, C-1a, C-13
15 206.7 C 4.26 d (18.4)
16 30.4 CH3 1.99 s C-15, C-14, C-13