Table 2. 1H (600 MHz) and 13C (100 MHz) NMR Data for Compounds 3–5 in DMSO-d6.
3 |
4 |
5 |
||||
---|---|---|---|---|---|---|
no. | δC | δH, mult. (J in Hz) | δC | δH, mult. (J in Hz) | δC | δH, mult. (J in Hz) |
1 | 198.9, C | 201.5, C | 203.2, C | |||
2 | 89.1, CH | 5.42, s | 93.5, CH | 5.41, s | 93.1, CH | 5.58, s |
3 | 168.4, C | 166.7, C | 168.0, C | |||
4 | 55.2, CH | 3.71, qd (6.7, 3.7) | 62.9, CH | 3.76, qd (6.9, 3.3) | 62.0, CH | 4.40, ddd (6.7, 2.2, 1.4) |
5 | 32.7, CH2 | 1.91, m; 1.74, m | 87.0, CH | 3.92, brs | 128.0, CH | 5.74, dd (6.0, 2.2) |
6 | 32.0, CH2 | 1.82, m; 1.71, m | 77.3, CH | 3.70, brs | 133.9, CH | 5.67, dd (6.0, 1.4) |
7 | 95.3, C | 78.4, C | 80.2, C | |||
8 | 22.0, CH3 | 1.30, d (6.6) | 23.2, CH3 | 1.31, s | 24.8, CH3 | 1.22, s |
9 | 16.4, CH3 | 1.20, d (6.9) | 17.9, CH3 | 1.19, d (6.6) | ||
1′ | 164.7, C | 163.9, C | 164.0, C | |||
2′ | 117.9, CH | 6.13, m | 117.7, CH | 5.99, m | 117.5, CH | 5.98, m |
3′ | 156.5, C | 156.0, C | 156.6, C | |||
4′ | 27.3, CH3 | 1.90, d (1.2) | 27.3, CH3 | 1.89, d (1.3) | 27.3, CH3 | 1.90, d (1.2) |
5′ | 20.1, CH3 | 2.13, d (1.2) | 20.0, CH3 | 2.14, d (1.3) | 20.0, CH3 | 2.15, d (1.2) |
NH | 9.90, s | 10.31, s | 10.49, s |