Regiospecific thermal C-acylation of imidazo [1,2-a] pyridines via an N-acylimidazolium intermediate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. A New Approach for the Synthesis of Fused Imidazoles: The Synthesis of 3-Acyl-Substituted Imidazo[1,2-x]azines
2. A Novel Method of Preparation of 3-Acylimidazo[1,2-a]pyridines
3. Bridgehead nitrogen heterocycles. II. Formation by reaction of .alpha.-amino nitrogen heterocyclic compounds with chlorothioformyl chloride
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1. 1-(Imidazo[1,2-a]pyridin-1-ium-1-yl)-2,3,4-trioxocyclobutan-1-ide;Molbank;2019-07-12
2. Metal‐Free Regioselective Carbonylation of Imidazo[1,2‐ a ]pyridines via Photoredox Catalysis using Nitrones;Asian Journal of Organic Chemistry;2019-05-03
3. Bicyclic Pyridines Containing Ring-Junction Nitrogen;Privileged Structures in Drug Discovery;2018-03-09
4. Recent synthetic scenario on imidazo[1,2-a]pyridines chemical intermediate;Research on Chemical Intermediates;2015-08-21
5. Non-classical donor–acceptor–donor chromophores. A strategy for high two-photon brightness;Journal of Materials Chemistry C;2014
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