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. 2010 Sep 21;89(2):419–427. doi: 10.1007/s00253-010-2857-z

Table 1.

1H and 13C NMR data for DON and compound A (in CDCl3 at 30°C)

Position 1H-NMR δH, ppm (mult., J in Hz) 13C-NMR δC (ppm)
DON Compound A DON Compound A
2 3.6 (d, 4.5) 3.70 (s) 80.8 83.8
3 4.5 (ddd, 4.5, 4.5, 11.0) 4.33 (dd, 3.0, 7.5) 69.2 72.5
4 2.23 (dd, 4.0, 15.0) 2.93 (dd, 7.5, 15.5) 43.4 46.1
2.10 (dd, 11.0, 15.0) 1.60 (dd, 3.0, 15.5)
5 46.5 46.2
6 52.6 51.8
7 4.90 (br. s) 4.75 (s) 74.1 74.0
8 199.6 199.9
9 136.6 136.3
10 6.55 (d, 6.0) 6.53 (dd, 1.5, 6.0) 137.7 138.1
11 4.57 (d, 56.0) 4.19 (d, 6.0) 70.5 70.0
12 64.3 65.3
13 3.35 (d, 4.0) 3.16 (d, 4.5) 47.8 46.2
3.22 (d, 4.0) 3.11 (d, 4.5)
14 1.33 (3H, s) 1.22 (3H, s) 13.8 14.1
15 3.90 (d, 12.0) 3.80 (d, 12.0) 62.0 62.1
3.74 (d, 12.0) 3.72 (d, 12.0)
16 1.90 (br. s) 1.87 (3H, s) 15.2 15.3