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9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine
- Source :
- Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 45 (2010), Beilstein Journal of Organic Chemistry
- Publication Year :
- 2010
- Publisher :
- Beilstein-Institut, 2010.
-
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.
- Subjects :
- chemistry.chemical_classification
Catechol
Annulation
Anthracene
Sodium ethoxide
tetrafluoropyrazine
Organic Chemistry
nucleophilic aromatic substitution
heterocyclic synthesis
Ring (chemistry)
Medicinal chemistry
benzodioxinopyridazine
Full Research Paper
perfluoroheteroaromatic
lcsh:QD241-441
Chemistry
chemistry.chemical_compound
chemistry
lcsh:Organic chemistry
Nucleophilic aromatic substitution
Organic chemistry
9,10-dioxa-1,2-diaza-anthracene
lcsh:Q
lcsh:Science
Tricyclic
Subjects
Details
- Language :
- English
- ISSN :
- 18605397
- Volume :
- 6
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Beilstein Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....1e0ff20360f107044c06c2bb884eaa18