A facile synthesis of 5(6)‐(chloromethyl)benzimidazoles: Replacement of a sulfonic acid functionality by chlorine
Author:
Affiliation:
1. Organic Chemical Technology Research Group of the Hungarian Academy of Sciences, Budapest University of Technology and Economics, H‐1521 Budapest, PO Box 91, Hungary
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.5570450208
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1. DNA binding ligands targeting drug-resistant Gram-positive bacteria. Part 1: Internal benzimidazole derivatives
2. Synthesis and structure–activity relationships of new antimicrobial active multisubstituted benzazole derivatives
3. Synthesis and biological evaluations of novel benzimidazoles as potential antibacterial agents
4. Synthesis of a novel dimeric bis-benzimidazole with site-selective DNA-binding properties
5. 2-Trifluoromethylbenzimidazoles: A New Class of Herbicidal Compounds
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1. Fe(OTf) 3 -catalyzed practical synthesis of 2-trifluoromethylarylimidazoles from o -arylenediamines and hexafluoroacetylacetone;Tetrahedron Letters;2016-07
2. Efficient syntheses of 2-fluoroalkylbenzimidazoles and -benzothiazoles;Tetrahedron Letters;2013-01
3. The current dye intermediate market – A cautionary tale and detective story; characterization and unambiguous synthesis of 5-amino-4-chloro-2,7-dimethyl-1H-benzimidazole;Dyes and Pigments;2009-05
4. ChemInform Abstract: A Facile Synthesis of 5(6)-(Chloromethyl)benzimidazoles: Replacement of a Sulfonic Acid Functionality by Chlorine.;ChemInform;2008-07-15
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