An Efficient Method for The Synthesis of 4-Arylfuro[2,3-a][4,7]phenanthroline Derivatives Catalyzed by Iodine
Author:
Affiliation:
1. School of Chemistry and Chemical Engineering; Xuzhou Normal University, The Key Laboratory of Biotechnology on Medical Plant; Xuzhou Jiangsu 221116 People's Republic of China
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.824/fullpdf
Reference24 articles.
1. Strategies for Heterocyclic Construction via Novel Multicomponent Reactions Based on Isocyanides and Nucleophilic Carbenes
2. Domino Reactions in Organic Synthesis
3. Multicomponent Domino Reaction from β-Ketoamides: Highly Efficient Access to Original Polyfunctionalized 2,6-Diazabicyclo[2.2.2]octane Cores
4. An Unexpected Triethylbenzylammonium Chloride Catalyzed Ring Opening of 2-Pyrones in the Synthesis of 1-Arylbenzo[f]quinoline-2-carboxamide Derivatives in Aqueous Media
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1. Synthesis and Antioxidant Properties of Novel Polycycles with Tetrahydroquinoline and Chromane Fragments;Russian Journal of Organic Chemistry;2022-02
2. Synthesis, structure, antimycobacterial and anticancer evaluation of new pyrrolo-phenanthroline derivatives;Journal of Enzyme Inhibition and Medicinal Chemistry;2015-05-06
3. Molecular iodine-catalyzed multicomponent reactions: an efficient catalyst for organic synthesis;RSC Advances;2013
4. ChemInform Abstract: An Efficient Method for the Synthesis of 4-Arylfuro[2,3-a][4,7]phenanthroline Derivatives Catalyzed by Iodine.;ChemInform;2012-11-19
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