Research Article
Cycloaddition Reaction of Ethyl Thioxoacetate and the Dienamine Derived from Pummerer's Ketone
Table 1
200 MHz 1H N.M.R spectrum of the cycloadduct (21).
| |
| Protons | δ P.P.m. | Coupling constants (Hz) |
| 7 | 6.93 | ddq, j 8.2, 1.9 and 0.6 | 9 | 6.86 | dP, j1,9 and 0.6 | 6 | 6.61 | dm, j 8.2 and <0.4 | 4a | 4.86 | dd, j 4.0 and 0,7 | OCH2CH3 | 4.21 | q, j 7.2 | de 11 | 4.11 | dd, j 2.9 and1.3 | 4 | 3.35 | d, j 4.0 | 1 | 2.92 | qd, j 3.1 and 0.8 | 2β | 2.57 | dd, j 19.8 and 3.1 | 8-Me | 2.26 | S, with fine splitting | 2α | 1.97 | ddd, j 19.8, 3.3 and 1.3 | 9b-CH3 | 1.63 | S | OCH2CH3 | 1.28 | t, j 7.2 |
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