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. 2014 Nov 20;12(11):5563–5575. doi: 10.3390/md12115563

Table 1.

1H (400 MHz) and 13C (100 MHz) NMR data for compounds 13.

NO. 1 a 2 a 3 b
δH (J in Hz) δC δH (J in Hz) δC δH (J in Hz) δC
1 167.8 167.0
2 4.21, m 68.8
3 1.68, ddd (4.1,12.0, 14.4)
2.01, dt (1.9, 14.4)
38.9 155.9 156.7
4 5.04, dd (1.9, 4.1) 60.1 6.31, s 105.8 6.40, s 106.7
4a 116.1 141.2 140.5
5 158.6 6.58, d (1.8) 104.5 6.70, d (2.1) 104.3
6 6.72, d (8.2) 107.9 166.1 165.9
7 7.12, t (8.2) 130.5 6.62, d (1.8) 103.9 6.89, d (2.1) 103.7
8 6.49, d (8.2) 112.0 164.5 164.1
8a 157.4 101.4 101.5
9 1.40, d (6.3) 21.6 2.22, s 19.4 2.67, dd (4.9, 14.3)
2.74, dd (7.8, 14.3)
44.3
10 4.45, m 65.4
11 1.40, d (6.2) 24.4
1′ 5.70, d (4.5) 103.4 5.74, d (4.4) 101.8 6.17, d (4.2) 102.1
2′ 4.23, dd (4.5, 6.4) 73.9 4.24, dd (4.4, 6.2) 73.6 4.87, m 74.1
3′ 4.10, dd (2.6, 6.4) 71.4 4.12, dd (3.0, 6.2) 71.2 4.85, m 71.3
4′ 4.20, m 88.5 4.15, m 88.3 4.88, m 89.0
5′ 3.64, dd (3.9, 12.1)
3.69, dd (3.6, 12.1)
63.5 3.65, dd (3.8, 12.1)
3.72, dd (3.3, 12.1)
63.3 4.12, dd (3.8, 12.0)
4.17, dd (3.7, 12.0)
63.4

a Measured in CD3OD; b measured in C5D5N.