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. 2013 May 22;18(5):6092–6100. doi: 10.3390/molecules18056092

Table 1.

1H-NMR, 13C-NMR, and HMBC data of compound 5 in CD3OD.

1H δ (J in Hz) 13C HMBC
5a 5b 5a 5a
2 5.76 d (12.0) 5.76 d** 82.87 d C-1'
3 4.81 * 5.33 d (12.0) 51.21 d C-1', C-7'', C-9''
4 197.36 s
5 165.84 s
6 5.96 brs 5.96 brs 99.61 d C-8, C-10
7 164.92 s
8 5.96 brs 5.96 brs 96.65 d C-10
9 168.51 s
10 103.65 s
1' 130.55 s
2' 7.05 d (8.8) 7.11 d (8.0) 129.33 d C-2, C-4', C-6'
3' 6.35 d (8.4) 6.35 d (8.4) 115.51 d C-1', C-5'
4' 158.53 s
5' 6.35 d (8.4) 6.35 d (8.4) 115.51 d C-1', C-3'
6' 7.05 d (8.8) 7.11 d (8.0) 129.33 d C-2, C-2', C-4'
2'' 166.28 s
3'' 6.41 s 6.52 s 104.49 d C-1'''
4'' 184.04 s
5'' 162.75 s
6'' 6.66 s 6.56 s 100.01 d C-8'', C-10''
7'' 161.62 s
8'' 104.94 s
9'' 156.80 s
10'' 106.74 s
1''' 123.09 s
2''' 7.31 brs 7.26 brs 114.38 d C-6'''
3''' 146.92 s
4''' 151.35 s
5''' 6.88 d (8.4) 6.61 d (8.4) 116.97 d C-3'''
6''' 7.27 brd (8.0) 7.10 brd** 120.89 d C-2'', C-2''', C-4'''
1'''' 5.24 d (7.6) 5.17 d (8.0) 101.32 d C-7''
2'''' 3.34 m 3.34 m** 75.24 d
3'''' 3.38 dd (9.2, 8.8) 3.38 m** 78.22 d
4'''' 3.82 m 3.82 m** 75.73 d
5'''' 3.60 ddd (11.2, 6.2, 2.3) 3.60 m** 71.36 d
6''''a 4.27 dd (12.0, 2.3) 4.27 m** 64.54 t OCOMe
6''''b 4.13 dd (12.0, 6.4) 4.13 m**
OCOMe 172.75 s
Me 1.95 s 2.03 s 20.77 q OCOMe

Series a and b represent major and minor conformers at 25 °C, respectively. * Overlapping with solvent signals. ** Not identified due to overlapping.