Abstract
Figure represented. An improved method for the preparation of 3-formyl-1,4-dimethylcarbazole, a key intermediate in the synthesis of ellipticine, is presented. Conditions of the Vilsmeier-Haack reaction have been modified to facilitate the production of 3-formyl-1,4-dimethylcarbazole as a major product leading to an overall improvement in yield of ellipticine from 3% to 14%. This approach was also applied to the synthesis of 6-methylellipticine and 9-methoxyellipticine.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 814-823 |
| Number of pages | 10 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 48 |
| Issue number | 4 |
| Publication status | Published - Jul 2011 |