A facile one-pot Friedländer synthesis of quinoline derivatives
Author:
Affiliation:
1. Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 607, India
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823408X375151
Reference26 articles.
1. A New Series of PDGF Receptor Tyrosine Kinase Inhibitors: 3-Substituted Quinoline Derivatives
2. 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
3. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives
4. Potent In vitro methicillin-resistant Staphylococcus aureus activity of 2-(1H-indol-3-yl)quinoline derivatives
5. Synthesis of Carbocyclic and Heterocyclic Fused Quinolines by Cascade Radical Annulations of Unsaturated N-Aryl Thiocarbamates, Thioamides, and Thioureas
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2. A mild and highly efficient Friedländer synthesis of quinolines in the presence of heterogeneous solid acid nano-catalyst;Arabian Journal of Chemistry;2016-09
3. Preparation and characterization of ZrO2 supported Fe3O4 MNPs as an effective and reusable superparamagnetic catalyst for the riedländer synthesis of quinoline derivatives;Journal of the Serbian Chemical Society;2015
4. Solvent-free synthesis of quinoline derivatives via the Friedländer reaction using 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and recyclable ionic liquid catalyst;Comptes Rendus Chimie;2014-04
5. CuFe2O4 nanoparticles: a magnetically recoverable and reusable catalyst for the synthesis of quinoline and quinazoline derivatives in aqueous media;RSC Advances;2014
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