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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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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Abstract 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.
AbstractList 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.
Author Gusak, KN
Kozlov, NG
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CLAR E (WOS:000185978200025.4) 1964; 1
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Snippet Condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenones was used to synthesize 1,3-diaryl-4,7-phenanthrolines...
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Physical Sciences
Science & Technology
Title Synthesis of 4,7-phenanthroline derivatives by condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenone
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