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Mendeleev Communications, 2002, Volume 12, Issue 2, Pages 68–70
DOI: https://doi.org/10.1070/MC2002v012n02ABEH001560
(Mi mendc4096)
 

This article is cited in 11 scientific papers (total in 11 papers)

Synthesis of fused quinoxalines

M. G. Ponizovskya, A. M. Boguslavskya, M. I. Kodessb, V. N. Charushina, O. N. Chupakhinb

a Urals State Technical University, Ekaterinburg, Russian Federation
b I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Abstract: The intramolecular cyclization of NH and N-alkyl quaternary salts of 2-quinoxaline-2-carboxaldehyde hydrazones affords pyrazolo- [3,4-b]quinoxalines in good yields.
Document Type: Article
Language: English


Citation: M. G. Ponizovsky, A. M. Boguslavsky, M. I. Kodess, V. N. Charushin, O. N. Chupakhin, “Synthesis of fused quinoxalines”, Mendeleev Commun., 12:2 (2002), 68–70
Linking options:
  • https://www.mathnet.ru/eng/mendc4096
  • https://www.mathnet.ru/eng/mendc/v12/i2/p68
  • This publication is cited in the following 11 articles:
    1. Yuriy A. Kvashnin, Egor V. Verbitskiy, Ekaterina F. Zhilina, Gennady L. Rusinov, Oleg N. Chupakhin, Valery N. Charushin, “Synthesis of Heteroannulated Indolopyrazines through Domino N–H Palladium-Catalyzed/Metal-Free Oxidative C–H Bond Activation”, ACS Omega, 5:25 (2020), 15681  crossref
    2. Hui Tang, Juan Wu, Wen Zhang, Lei Zhao, Ya-Hui Zhang, Cheng-Wu Shen, “Design, synthesis and biological evaluation of novel non-azole derivatives as potential antifungal agents”, Chinese Chemical Letters, 26:9 (2015), 1161  crossref
    3. Valery N. Charushin, Oleg N. Chupakhin, Topics in Heterocyclic Chemistry, 37, Metal Free C-H Functionalization of Aromatics, 2014, 1  crossref
    4. Olga Yu. Bakulina, Alexander Yu. Ivanov, Pavel S. Lobanov, Dmitrii V. Dar'in, “Synthesis of novel peri-fused heterocyclic systems—pyrimido[4,5,6-de][1,8]naphthyridines, based on interaction of 4,6-dichloro-2-methylthiopyrimidine-5-carbaldehyde with geminal enediamines”, Tetrahedron, 70:43 (2014), 7900  crossref
    5. Antonio Guirado, José I. López Sánchez, Delia Bautista, “Reactions of 5,8-dichloro-2,3-dicyanoquinoxaline with amines and hydrazines. A new and efficient synthetic approach to 3-amino-5,8-dichloroflavazoles”, Tetrahedron, 67:22 (2011), 4123  crossref
    6. Anna V. Gulevskaya, Alexander F. Pozharskii, Advances in Heterocyclic Chemistry, 93, Advances in Heterocyclic Chemistry Volume 93, 2007, 57  crossref
    7. V. N. Charushin, O. N. Chupakhin, “Nucleophilic aromatic substitution of hydrogen and related reactions”, Mendeleev Commun., 17:5 (2007), 249–254  mathnet  crossref
    8. A. M. Boguslavskii, M. G. Ponizovskii, M. I. Kodess, V. N. Charushin, “Ring-Chain Transformations of Dihydroisoxazolo[4,5-b]quinoxaline”, Russ J Org Chem, 41:9 (2005), 1377  crossref
    9. S. K. Kotovskaya, V. N. Charushin, N. M. Perova, M. I. Kodess, O. N. Chupakhin, “Intramolecular Nucleophilic Substitution of Hydrogen in (Quinoxalinyl‐2)aminovinyl Derivatives as a New Approach to Pyrrolo‐ and Indolo[2,3‐b]quinoxalines”, Synthetic Communications, 34:14 (2004), 2531  crossref
    10. Michael P. Groziak, Progress in Heterocyclic Chemistry, 15, A critical review of the 2002 fiterature preceded by three chapters on current heterocyclic topics, 2003, 306  crossref
    11. Michail G. Ponizovsky, Artem M. Boguslavsky, Mikhail I. Kodess, Valery N. Charushin, Oleg N. Chupakhin, “Synthesis of Fused Quinoxalines.”, ChemInform, 33:39 (2002), 163  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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