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. 2021 Aug 6;26(16):4777. doi: 10.3390/molecules26164777

Table 3.

Data 1H-NMR and 13C-NMR of compound 13 recorded in CD3OD.

Position δC (Type) δH (J in Hz)
1 94.1 (CH) 5.82 (brs)
3 141.5 (CH) 6.20 (dd, J = 6.3, 2.7 Hz)
4 103.2 (CH) 4.73 (m)
5 41.3 (CH) 2.80 (m)
6 76.8 (CH) 4.00 (m)
7 48.5 (CH2) 2.14 m
8 90.3 (C)
9 49.4 (CH) 2.89 (m)
10 22.4 (CH3) 1.58 (s)
1′ 99.8 (CH) 4.63 (d, J = 7.8 Hz)
2′ 74.6 (CH) 3.20 (t, J = 7.8 Hz)
3′ 77.8 (CH) 3.28 ov
4′ 71.4 (CH) 3.28 ov
5′ 77.9 (CH) 3.36 ov
6′ 62.7 (CH2) 3.83 (d, J = 12.0 Hz)
3.60 m
1″ 135.9 (C)
2′ 126.8 (CH) 7.39 ov
3″ 121.9 (CH) 7.33 ov
4″ 131.8 (CH) 7.58 ov
5″ 126.8 (CH) 7.39 ov
6″ 121.9 (CH) 7.39 ov
7″ 142.4 (CH) 6.93 (d, J = 12.6 Hz)
8″ 122.3 (CH) 5.95 (d, J = 12.6 Hz)
9″ 168.2 (C)

brs = broad singlet = doublet, m = multiplet; ov = overlapped; s = singlet; t = triplet, J values (Hz) are reported in brackets