2-Aryl-7,7-dimethyl-5,6,7,8-tetrahydrothieno[3,2-c]azepin-4-ones from 5,5-dimethyl-1,3-cyclohexanedione
✍ Scribed by Roberto Martinez; Ma. Esther Durán L; César Cortés L; J. Gustavo Avila Z
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 300 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A novel synthesis of substituted thieno[3,2‐c]azepinones is described. This new approach uses 5,5‐dimethyl‐1,3‐cyclohexanedione (dimedone) as the starting material. Oxime intermediates are obtained in three steps from the aforementioned diketone. Using these intermediates, the title compounds are synthesized in moderate yields.
📜 SIMILAR VOLUMES
The selenious acid oxidation of 2-aryl-7,7-dimethyl-5,6,7,8-formation of an intramolecular unsymmetrical diselenide by selenious acid oxidation and reports the first derivatives of tetrahydro-5-quinazolones 2a-c leads to the corresponding 2-aryl-7,7-dimethyl-6,8-epidiseleno-5,6,7,8-tetrahydro-5-the