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9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine

Authors :
Dmitrii S. Yufit
John A. Christopher
Graham Pattison
Graham Sandford
Judith A. K. Howard
David D. Miller
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.

Details

Language :
English
ISSN :
18605397
Volume :
6
Issue :
1
Database :
OpenAIRE
Journal :
Beilstein Journal of Organic Chemistry
Accession number :
edsair.doi.dedup.....1e0ff20360f107044c06c2bb884eaa18