## Abstract Some by‐products of the carbazolation of di‐(1‐anthraquinonyl)‐amine in aluminium chloride‐pyridine fusions rich in aluminium chloride are shown to result from pyridiniosubstitution and higher condensation of the 1, 2; 7, 8‐diphthaloyl‐carbazole primarily formed.
✦ LIBER ✦
Schmelzreaktionen mit Aluminiumchlorid. 6. Mitteilung [1]. Zur kenntnis der carbazolierung von anthrimiden in aluminiumchlorid-schmelzen
✍ Scribed by A. K. Wick
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- German
- Weight
- 904 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The behaviour of di‐(1‐anthraquinonyl)‐amine, when cyclised in pyridine‐aluminium chloride or pure aluminium chloride fusions, has been compared. The formation of blue educt complexes with aluminium chloride in the latter case has been revealed as a factor which inhibits cyclisation. The results are discussed and generalised, classifying carbazolation of anthrimides as an intramolecular Scholl‐type reaction.
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