Rapid construction of imidazopyridines from ortho-haloaminopyridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. DNA binding ligands targeting drug-resistant Gram-positive bacteria. Part 2: C-terminal benzimidazoles and derivatives
2. New polyfunctional imidazo[4,5-C]pyridine motifs: Synthesis, crystal studies, docking studies and antimicrobial evaluation
3. C-3 halo and 3-methyl substituted 5′-nor-3-deazaaristeromycins: Synthesis and antiviral properties
4. Imidazopyridine-Based Fatty Acid Synthase Inhibitors That Show Anti-HCV Activity and in Vivo Target Modulation
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2. Conversion of oxadiazolo[3,4-b]pyrazines to imidazo[4,5-b]pyrazines via a tandem reduction-cyclization sequence generates new mitochondrial uncouplers;Bioorganic & Medicinal Chemistry Letters;2022-10
3. Experimental, Density Functional Theory, and Dynamic Molecular Studies of Imidazopyridine Derivatives as Corrosion Inhibitors for Mild Steel in Hydrochloric Acid;Surface Engineering and Applied Electrochemistry;2021-03
4. Review of Application of Imidazole and Imidazole Derivatives as Corrosion Inhibitors of Metals;New Challenges and Industrial Applications for Corrosion Prevention and Control;2020
5. Crystal structure of 2-tert-butyl-1H-imidazo[4,5-b]pyridine, C10H13N3;Zeitschrift für Kristallographie - New Crystal Structures;2019-09-25
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