Table 1.
1H- and 13C—NMR chemical shift values of compound 1 (ppm, CD3OD, 600 and 150 MHz respectively).
C. No. | δC | δH (J, Hz) | C. No. | δC | δH (J, Hz) |
---|---|---|---|---|---|
1 | 220.4 | - | 18 | 20.7 | 1.35 s |
2 | 40.5 | 2.31, 2.12 | 19 | 18.2 | 1.27 s |
3 | 75.0 | 3.84 br m, (W1/2 = 14.5) | 20 | 78.1 | - |
4 | 41.0 | 2.04, 2.01 m | 21 | 21.1 | 1.59 |
5 | 136.3 | - | 22 | 83.1 | 4.23 dd (13.2, 3.4) |
6 | 123.6 | 4.58 br s | 23 | 32.9 | 1.60, 1.84 overlap |
7 | 32.6 | 1.77, 1.75 m | 24 | 160.1 | - |
8 | 22.1 | 1.63 m | 25 | 126.4 | - |
9 | 21.0 | 1.61 m | 26 | 168.0 | - |
10 | 52.7 | - | 27 | 62.7 | 4.30 d (11.4), 4.31 d (11.7) |
11 | 21.1 | 1.27, 1.35 m | 28 | 18.0 | 2.01 s |
12 | 20.8 | 1.61, 2.01 m | 1′ | 104.0 | 4.36 d (7.6) |
13 | 49.0 | - | 2′ | 75.0 | 3.31 t (8.1) |
14 | 85.5 | - | 3′ | 74.0 | 3.65 overlap |
15 | 22.3 | 1.63, 1.75 m | 4′ | 71.6 | 3.33 overlap |
16 | 32.8 | 1.35, 1.09 m | 5′ | 78.0 | 3.33 overlap |
17 | 50.5 | 2.30 t (9.4) | 6′ | 63.5 | 3.64 dd (11.8, 4.8), 3.84 d (11.8) |