A simple and efficient method for the synthesis of highly substituted imidazoles using 3-aroylquinoxalin-2(1H)-ones-Reference-Cited by-同舟云学术

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A simple and efficient method for the synthesis of highly substituted imidazoles using 3-aroylquinoxalin-2(1H)-ones

Published:2011-08 Issue:33 Volume:52 Page:4280-4284
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mamedov Vakhid A.,Zhukova Nataliya A.,Beschastnova Tat′yana N.,Gubaidullin Aidar T.,Rakov Dimitry V.,Rizvanov Il’dar Kh.

Funder

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. Antimycotic imidazoles. Part 4. Synthesis and antifungal activity of ketoconazole, a new potent orally active broad-spectrum antifungal agent

2. Selective antagonists of benzodiazepines

3. Cimetidine—A Non-Thiourea H2-Receptor Antagonist

4. genotype–related efficacy of omeprazole for the treatment of infection caused by

5. Electroencephalographic study of the short-acting hypnotics etomidate and methohexital in dogs

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3. One-Pot Synthesis of 7-(Benzimidazol-2-yl)thioxolumazine and -lumazine Derivatives via H2SO4-Catalyzed Rearrangement of Quinoxalinones When Exposed to 5,6-Diamino-2-mercapto- and 2,5,6-Triaminopyrimidin-4-ols;The Journal of Organic Chemistry;2018-11-15

4. The rearrangement of 1H,1′H-spiro[quinoline-4,2′-quinoxaline]-2,3′ (3H,4′H)-diones – a new and efficient method for the synthesis of 4-(benzimidazol-2-yl)quinolin-2(1H)-ones;Tetrahedron;2018-11

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