Title of article :
A new and facile access to the 2-(indol-3-yl)-3-nitriloquinolines based on Friedländer annulations
Author/Authors :
Morteza Shiri، نويسنده , , Mohammad Ali Zolfigol، نويسنده , , Mahtab Pirveysian، نويسنده , , Roya Ayazi-Nasrabadi، نويسنده , , Hendrik G. Kruger، نويسنده , , Tricia Naicker، نويسنده , , Iraj Mohammadpoor-Baltork، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
6
From page :
6059
To page :
6064
Abstract :
Preparation of 2-(indol-3-yl)-3-nitriloquinolines via Friedländer quinoline synthesis using 3-cyanoacetylindoles possessing an α-methylene group and ortho-amino arylketones have been described. This reaction took place in PEG-400 as a green solvent and it is catalyzed with polyphosphoric acid (PPA) to give novel types of quinolines containing both indoles and cyano functions in one step under thermal and microwave conditions.
Keywords :
Quinolines , Indoles , Friedl?nder quinoline synthesis , Ethylene glycol
Journal title :
Tetrahedron
Serial Year :
2012
Journal title :
Tetrahedron
Record number :
1104728
Link To Document :
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