Abstract
Reaction of tetrafluoropyridazine with catechol gives a tricyclic 9,10-dioxa-1,2-diaza-anthracene system by a sequential nucleophilic aromatic substitution ring annelation process, further extending the use of perfluoroheteroaromatic derivatives for the synthesis of unusual polyfunctional heterocyclic architectures. The tricyclic scaffold reacts with amines and sodium ethoxide providing a short series of functional 9,10-dioxa-1,2-diaza-anthracene systems.
| Original language | English |
|---|---|
| Article number | 45 |
| Journal | Beilstein Journal of Organic Chemistry |
| Volume | 6 |
| DOIs | |
| Publication status | Published - 6 May 2010 |
Keywords
- 9,10-dioxa-1,2-diaza-anthracene
- Benzodioxinopyridazine
- Heterocyclic synthesis
- Nucleophilic aromatic substitution
- Perfluoroheteroaromatic
- Tetrafluoropyrazine
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