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. Author manuscript; available in PMC: 2015 Dec 7.
Published in final edited form as: Bioorg Med Chem Lett. 2011 Jun 17;21(15):4397–4399. doi: 10.1016/j.bmcl.2011.06.044

Table 1.

NMR data (CDCl3) for nothospondin (1)a

No. δ C δH (J in Hz) gHMBC
1 209.1
2 76.9 4.71 d (8.7) 1, 3, 19
3 83.7 2.93 dd (10.1, 8.7) 2, 4, 18
4 34.7 1.96 m 3, 5, 18
5 41.6 1.30 m 19
6a 25.7 1.82 ddd (14.8, 12.4, 2.1) 5, 10
6b 2.10 dt (14.8, 3.6) 4, 5, 8, 10
7 82.1 4.29 brt (2.9) 5, 9
8 36.9
9 47.5 3.15 s 1, 7, 8, 10, 11, 17, 18
10 48.1
11 190.8
12 148.4
13 140.5
14 47.3 2.42 dd (12.1, 7.0) 8, 9, 12, 13, 17, 20
15a 31.7 2.55 dd (18.6, 12.1) 12, 13, 14
15b 2.97 dd (18.6, 7.0) 8, 9, 16
16 169.0
17 23.2 1.20 s 7, 8, 9, 14
18 14.9 1.04 d (6.5) 3, 4, 5
19 15.6 1.46 s 1, 5, 9, 10
20 16.0 1.89 s 12, 13, 14
OCH3 60.0 3.67 s 12
a

Data were acquired with a Bruker Avance 111 600 MHz spectrometer; chemical shifts are in ppm and referenced to the residual solvent signal; J in Hz; HMBC correlations are from the proton(s) stated to the indicated carbon.