A Simple, Efficient and Solvent-Free Protocol for the Friedländer Synthesis of Quinolines by Using SnCl2·2H2O

2005 ◽  
Vol 34 (3) ◽  
pp. 314-315 ◽  
Author(s):  
Pandurangan Arumugam ◽  
Ganesan Karthikeyan ◽  
Raji Atchudan ◽  
D. Muralidharan ◽  
Paramasivan T. Perumal
Keyword(s):  
Solvent Free ◽  
Friedlander Synthesis

ChemInform Abstract: ZrOCl2·8H2O Catalyzed Solvent-Free Friedlander Synthesis of 1,8-Naphthyridines.

ChemInform ◽  
2016 ◽  
Vol 47 (15) ◽  
pp. no-no
Author(s):  
K. Mogilaiah ◽  
A. Nageswara Rao ◽  
P. Koteswara Rao
Keyword(s):  
Solvent Free ◽  
Friedlander Synthesis

Dowex-50W Promoted Friedländer Synthesis of Substituted Quinolines under Solvent-Free Conditions

Heterocycles ◽  
2011 ◽  
Vol 83 (2) ◽  
pp. 331 ◽  
Author(s):  
Huey-Min Wang ◽  
Ling-Ching Chen ◽  
Rei-Sheu Hou ◽  
Hau-Dung Du ◽  
Iou-Jiun Kang
Keyword(s):  
Solvent Free ◽  
Solvent Free Conditions ◽  
Substituted Quinolines ◽  
Friedlander Synthesis

scholarly journals Highly efficient one-pot tandem Friedlander annulation and chemo-selective Csp3–H functionalization under calcium catalysis

RSC Advances ◽  
2017 ◽  
Vol 7 (31) ◽  
pp. 18874-18882 ◽  
Author(s):  
Garima Singh ◽  
Srinivasarao Yaragorla
Keyword(s):  
Solvent Free ◽  
One Pot ◽  
Highly Efficient ◽  
Solvent Free Conditions ◽  
Friedlander Synthesis ◽  
First Time ◽  
Calcium Catalysis

Highly efficient and regioselective Friedlander synthesis of 2-methyl-3-acyl quinolines and their chemoselective Csp3–H functionalization is described for the first time using Ca(OTf)2 as the sustainable catalyst under solvent free conditions with atom and step economy.

Iron(III) Chloride–Promoted, Solvent‐Free, Facile, and Efficient Friedländer Synthesis of Quinolines

2007 ◽  
Vol 37 (22) ◽  
pp. 4071-4078 ◽  
Author(s):  
Sanjay Kumar ◽  
Anil Saini ◽  
Jagir S. Sandhu
Keyword(s):  
Solvent Free ◽  
Friedlander Synthesis
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