| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220521 | Tetrahedron | 2012 | 6 Pages |
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.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Morteza Shiri, Mohammad Ali Zolfigol, Mahtab Pirveysian, Roya Ayazi-Nasrabadi, Hendrik G. Kruger, Tricia Naicker, Iraj Mohammadpoor-Baltork,