Skip to main content
. 2016 Mar 14;21(3):336. doi: 10.3390/molecules21030336

Table 1.

1H-NMR (400 MHz) and 13C-NMR (100 MHz) data for compound 1 and 2 in DMSO-d6.

Position Compound 1 Compound 2
δH δC δH δC
2 163.5 163.2
3 6.83 (s) 103.4 7.03 (s) 104.0
4 182.0 182.1
5 157.1 157.2
6 110.4 110.4
7 162.5 162.6
8 6.58 (s) 94.8 6.63 (s) 95.0
9 156.1 156.2
10 103.2 103.5
1′ 121.2 123.9
2′ 7.79 (d, J = 1.8 Hz) 114.4 7.63 (d, J = 2.4 Hz) 110.2
3′ 145.6 149.8
4′ 150.7 149.2
5′ 6.96 (d, J = 8.4 Hz) 121.9 7.25 (d, J = 8.8 Hz) 115.0
6′ 7.65 (dd, J = 1.8, 8.4 Hz) 116.4 7.66 (dd, J = 2.4, 8.8 Hz) 120.5
boivinose
1′′ 5.30 (dd, J = 2.7, 12.3 Hz) 67.3 5.34 (dd, J = 2.8, 12.4 Hz) 67.4
2′′ 1.48 (d, J = 13.8 Hz) 31.4 1.50 (d, J = 14.0 Hz) 31.4
2.19 (ddd, J = 2.7, 4.2, 13.8 Hz) 2.21 (ddd, J = 2.4, 3.2, 14.0 Hz)
3′′ 3.83 (br.s) 66.5 3.85 (br.s) 66.5
4′′ 3.23 (br.s) 68.6 3.25 (br.s) 68.7
5′′ 4.02 (q, J = 6.6 Hz) 70.6 3.90 (q, J = 6.0 Hz) 70.6
6′′ 1.14 (d, J = 6.6 Hz) 17.1 1.16 (d, J = 6.0 Hz) 17.1
glucose
1′′′ 4.89 (d, J = 7.2 Hz) 101.9 5.08 (d, J = 7.2 Hz) 99.5
2′′′ 3.32 (m) 73.3 3.33 (m) 73.1
3′′′ 3.30 (m) 75.9 3.30 (m) 76.8
4′′′ 3.15 (m) 70.1 3.17 (m) 69.6
5′′′ 3.47 (m) 77.4 3.36 (m) 77.1
6′′′ 3.77 (m) 60.9 3.47 (m) 60.6
3.48 (m) 3.68 (m)
-OCH3 3.90 (s) 56