Synthesis of 4,7-phenanthroline derivatives by condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenone

Condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenones was used to synthesize 1,3-diaryl-4,7-phenanthrolines containing hydroxy and nitro groups in the phenyl rings.

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Bibliographic Details
Published inRussian journal of general chemistry Vol. 73; no. 6; pp. 964 - 967
Main Authors Gusak, KN, Kozlov, NG
Format Journal Article
LanguageEnglish
Published NEW YORK Springer Nature 01.06.2003
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Summary:Condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenones was used to synthesize 1,3-diaryl-4,7-phenanthrolines containing hydroxy and nitro groups in the phenyl rings.
ISSN:1070-3632
1608-3350
DOI:10.1023/A:1026321422453