Related Experiment Videos
[Lipoxygenase inhibitors. 3. Synthesis of tetrahydrobenzazepinone phenylhydrazones]
1Institut für Pharmazeutische Chemie, Martin-Luther-Universität Halle-Wittenberg.
Archiv Der Pharmazie
|February 1, 1994
Abstract:
Tetrahydro-2H-benz[b]azepin-2-ones as starting substances are synthesized by Beckmann rearrangement of Schmidt reaction. The tetrahydrobenzazepinones are transformed into the thiones, thiolactim ethers and phenylhydrazones. The compounds are tested as inhibitors of soja lipoxygenase.