scholarly journals Direct Synthesis of Polysubstituted Quinoline Derivatives by InBr3-Promoted Dimerization of 2-Ethynylaniline Derivatives.

ChemInform ◽  
2006 ◽  
Vol 37 (38) ◽  
Author(s):  
Norio Sakai ◽  
Kimiyoshi Annaka ◽  
Takeo Konakahara
Synthesis ◽  
2017 ◽  
Vol 50 (06) ◽  
pp. 1350-1358 ◽  
Author(s):  
Cunde Wang ◽  
Xushun Qing ◽  
Ting Wang ◽  
Chenlu Dai ◽  
Zhenjie Su

An efficient iron/acetic acid system-mediated reductive cyclization reaction of substituted 2-aryl-3-nitro-2H-chromenes with substituted 2-nitrobenzaldehydes for the synthesis of 6-aryl-6H-chromeno[3,4-b]quinolines was developed. This reaction involves the sequential reduction, hydrolysis, aldol condensation, intramolecular addition, and the nucleophilic addition of substituted 2-aryl-3-nitro-2H-chromenes with substituted 2-nitrobenzaldehydes to give the corresponding 6H-chromeno[3,4-b]quinolines. This transformation provides a straightforward synthetic protocol for constructing substituted 6H-chromeno[3,4-b]quinoline derivatives. The structures of three typical products were confirmed by X-ray crystallography.


1966 ◽  
Vol 39 (1) ◽  
pp. 195-195 ◽  
Author(s):  
Yusuf Ahmad ◽  
Shamim Ahmad Shamsi

ChemInform ◽  
2015 ◽  
Vol 46 (27) ◽  
pp. no-no
Author(s):  
Guiyan Liu ◽  
Maocong Yi ◽  
Lu Liu ◽  
Jingjing Wang ◽  
Jianhui Wang

2015 ◽  
Vol 51 (14) ◽  
pp. 2911-2914 ◽  
Author(s):  
Guiyan Liu ◽  
Maocong Yi ◽  
Lu Liu ◽  
Jingjing Wang ◽  
Jianhui Wang

A one-pot procedure for the preparation of substituted quinolines from substituted o-nitrotoluenes with electron-withdrawing groups and olefins (acrylic esters and acrylonitriles) using a cesium catalyst under mild reaction conditions is reported. The process involves a [2+4] cycloaddition mechanism.


2006 ◽  
Author(s):  
Robert Musiol ◽  
Josef Jampilek ◽  
Katarina Kralova ◽  
Dominik Tabak ◽  
Barbara Podeszwa ◽  
...  

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