Affiliation:
1. Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Abstract
Nucleophilic substitution of hydrogen in 5-nitrobenzimidazole derivatives occurs upon reaction with 4-methylbenzyl cyanide under basic conditions and proceeds with concomitant cyclisation. This sequence offers a one-pot synthesis of new fluorescent heterocyclic compounds, 3-alkyl-8-methyl-3 H-imidazo[4,5- a]acridines.
Cited by
16 articles.
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1. Synthesis, photophysical, computational characterizations, electrochemical and photovoltaic characteristics of some new quinoline-based hybrid fluorescent dyes;Optical Materials;2024-02
2. Synthesis, Antiviral, Antibacterial, and Cytotoxicity Assessment of Some 3H-Benzo[a]imidazo[4,5-j]acridines and 3H-Benzo[a]pyrazolo[3,4-j]acridines;Russian Journal of Organic Chemistry;2020-08
3. Synthesis, Structure and Fluorescence Properties of Two Metal-Organic Frameworks Based on a Benzimidazole-Derived Ligand;Journal of Chemical Research;2018-08
4. Theoretical Investigation on the Kinetics and Mechanism of the Synthesis of Fluorescent 3,8-Disubstituted-3H-Imidazo [4,5-a] Acridine-11-Carbonitriles;Progress in Reaction Kinetics and Mechanism;2016-11
5. Kinetics and mechanism of producing 3,8-dimethyl-3H-imidazo[4,5-a]acridine-11-carbonitrile: a DFT investigation;Research on Chemical Intermediates;2016-09-19