Table 2. 1H (600 MHz) and 13C (150 MHz) NMR Spectroscopic Data for Caulamidine C (2) and Isocaulamidine C (3) in CD3OD.
| no. | caulamidine C (2) |
isocaulamidine C (3) |
|||
|---|---|---|---|---|---|
| , type | (mult., J in Hz) | no. | , type | (mult., J in Hz) | |
| 2 | 168.9, C | 2 | 168.9, C | ||
| 4 | 149.8, C | 4 | 145.4, C | ||
| 5 | 125.7, CH | 7.29 (d, 7.5) | 5 | 126.5, CH | 7.34a |
| 6 | 132.5, CH | 7.55 (t, 7.5) | 6 | 132.3, CH | 7.57 (td, 7.5, 1.5) |
| 7 | 116.1, CH | 7.34a | 7 | 114.5, CH | 7.31a |
| 8 | 125.5, CH | 7.27 (d, 7.5) | 8 | 126.5, CH | 7.30a |
| 9 | 127.1, C | 9 | 126.5, C | ||
| 10 | 60.3, C | 10 | 61.4, C | ||
| 11 | 47.9, CH | 5.48 (dd, 10.3, 6.6) | 11 | 49.8, CH | 5.26 (dd, 9.9, 6.3) |
| 12a | 54.6, CH2 | 4.38 (dd, 14.0, 6.6) | 12a | 51.53, CH2 | 4.41 (dd, 17.4, 6.3) |
| 12b | 4.07 (dd, 14.0, 10.3) | 12b | 3.94 (dd, 17.4, 9.9) | ||
| 14 | 158.1, C | 14 | 153.8, C | ||
| 16 | 140.3, C | 16 | 143.5, C | ||
| 17 | 123.7, CH | 7.53 (d, 1.7) | 17 | 118.8, CH | 7.31a |
| 18 | 123.1, C | 18 | 123.3, C | ||
| 19 | 129.4, CH | 7.31a | 19 | 125.7, CH | 7.14 (dd, 8.0, 1.8) |
| 20 | 131.9, CH | 7.08 (d, 8.1) | 20 | 131.8, CH | 7.00 (8.0) |
| 21 | 121.1, C | 21 | 120.6, C | ||
| 22a | 34.1, CH2 | 2.73 (d, 16.3) | 22a | 34.8, CH2 | 2.62 (d, 15.5) |
| 22b | 2.59 (d, 16.3) | 22b | 2.40 (d, 15.5) | ||
| 23 | 48.3, C | 23 | 48.2, C | ||
| 24 | 51.1, CH | 4.49 (dd, 8.4, 7.3) | 24 | 51.46, CH | 4.21 (t, 8.5) |
| 25a | 55.5, CH2 | 4.40 (dd, 15.0, 7.3) | 25a | 55.7, CH2 | 4.44 (dd, 15.1, 8.5) |
| 25b | 4.32 (dd, 15.0, 8.4) | 25b | 4.35 (dd, 15.1, 8.5) | ||
| 26 | 39.8, CH3 | 3.45 (s) | 26 | 40.3, CH3 | 3.53 (s) |
| 27 | 39.2, CH3 | 3.61 (s) | 27 | 32.9, CH3 | 3.55 (s) |
Signals overlapped.