Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols

Photolysis of 1-arylthio-2-azidoanthraquinones in DMSO in the presence of phenols leads to the formation of 5 H -naphtho[2,3- c ]phenothiazine-8,13-diones, in which the nitrogen atom is covalently bonded with the phenyl ring of the introduced phenol. As a result, poorly available polycyclic phenothi...

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Veröffentlicht in:Russian chemical bulletin Jg. 65; H. 7; S. 1814 - 1819
Hauptverfasser: Klimenko, L. S., Sirazhetdinova, N. S., Savel’ev, V. A., Martyanov, T. P., Korchagin, D. V.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: New York Springer US 01.07.2016
Springer Nature B.V
Schlagworte:
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Full Articles
Inorganic Chemistry
Organic Chemistry
Phenols
Photolysis
phenothiazine-8,13-diones
phenols
thermolysis
5
photolysis
naphtho[2,3
azides
X-ray diffraction analysis
photocyclization
9,10-anthraquinones
ISSN:1066-5285, 1573-9171
Online-Zugang:Volltext
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Zusammenfassung:Photolysis of 1-arylthio-2-azidoanthraquinones in DMSO in the presence of phenols leads to the formation of 5 H -naphtho[2,3- c ]phenothiazine-8,13-diones, in which the nitrogen atom is covalently bonded with the phenyl ring of the introduced phenol. As a result, poorly available polycyclic phenothiazine derivatives were obtained in one step in high yields. The cyclo-condensation with phenols was found to proceed only photochemically.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-016-1515-8