Table 2.
The resonance assignments of 1H and 13C based on the NMR analysis of the novel MAGE.
| Position | 1H NMR δ (ppm) | 13C NMR δ (ppm) | ||||
|---|---|---|---|---|---|---|
| Isomer α | Isomer β | keto | Isomer α | Isomer β | keto | |
| 6 | 2.71 | 2.76 | 2.58 | 48.24 | 47.87 | 47.93 |
| 2-NH | 7.70 | 7.64 | 7.77 | |||
| 7 | 168.51 | 168.64 | ||||
| 8 | 1.8311 | 1.829 | 1.828 | 22.70 | ||
| 1′ | 2.85 | 2.94; 2.97 | 2.58 | 53.120 | 51.22 | 48.00 |
| 2′ | 100.54 | 102.30 | 205.74 | |||
| 3′ | 3.90 | 3.88 | 80.05 | 82.94 | ||
| 4′ | 3.82 | 3.80 | 76.57 | 77.81 | ||
| 5′ | 3.72 | 3.95 | 80.04 | 75.18 | ||
| 6′ |
3.67 3.403 |
3.63; 3.45 | 68.35 | 66.27 | ||
| 1″ | 4.67 (br) |
3.68 J = 3.7 Hz |
4.65 J = 4.12 Hz |
99.11 | 99.17 | 98.89 |
| 5″ | 3.08 | 70.98 | 71.07 | 70.87 | ||
| 6″ |
3.446 3.516 |
60.52 | 60.46 | 60.33 | ||