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Mendeleev Communications, 2010, Volume 20, Issue 1, Pages 50–51
DOI: https://doi.org/10.1016/j.mencom.2010.01.019
(Mi mendc2988)
 

This article is cited in 10 scientific papers (total in 10 papers)

An efficient one-pot synthesis of 3-aryl-1,2,4-oxadiazol-5-amines under solvent-free conditions

M. Adiba, Sh. Bagherzadeha, M. Mahdavia, H. R. Bijanzadehb

a Department of Chemistry, Faculty of Science, University of Tehran, Tehran, Iran
b Department of Chemistry, Tarbiat Modarres University, Tehran, Iran
Abstract: The in situ prepared amidoximes from the reaction between nitriles and hydroxylamine are condensed with carbodiimides in the presence of molecular sieves under solvent-free conditions to produce the title compounds in excellent yields.
Document Type: Article
Language: English


Citation: M. Adib, Sh. Bagherzadeh, M. Mahdavi, H. R. Bijanzadeh, “An efficient one-pot synthesis of 3-aryl-1,2,4-oxadiazol-5-amines under solvent-free conditions”, Mendeleev Commun., 20:1 (2010), 50–51
Linking options:
  • https://www.mathnet.ru/eng/mendc2988
  • https://www.mathnet.ru/eng/mendc/v20/i1/p50
  • This publication is cited in the following 10 articles:
    1. Valentina Nascimento Melo de Oliveira, Franciane Gonçalves dos Santos, Vanessa Pinheiro Gonçalves Ferreira, Héverton Mendes Araújo, Cláudia do Ó Pessoa, Roberto Nicolete, Ronaldo Nascimento de Oliveira, “Focused microwave irradiation-assisted synthesis of N-cyclohexyl-1,2,4-oxadiazole derivatives with antitumor activity”, Synthetic Communications, 48:19 (2018), 2522  crossref
    2. P. A. Volkov, N. I. Ivanova, K. O. Khrapova, A. A. Telezhkin, T. N. Borodina, N. K. Gusarova, B. A. Trofimov, “Solvent-free synthesis of 4-chalcogenophosphorylpyridines via SHNAr reaction of pyridines with secondary phosphine chalcogenides”, Mendeleev Commun., 28:6 (2018), 582–583  mathnet  crossref
    3. Mehdi Adib, Sara Saeedi, Mehdi Soheilizad, Maryam Bayanati, Mahmood Tajbakhsh, Massoud Amanlou, “An Efficient One-Pot Synthesis of 3-Aryl-5-(Dialkoxymethyl)-1,2,4-Oxadiazoles under Solvent-Free Conditions”, Journal of Chemical Research, 40:5 (2016), 314  crossref
    4. Marion Donnier-Maréchal, David Goyard, Vincent Folliard, Tibor Docsa, Pal Gergely, Jean-Pierre Praly, Sébastien Vidal, “3-Glucosylated 5-amino-1,2,4-oxadiazoles: synthesis and evaluation as glycogen phosphorylase inhibitors”, Beilstein J. Org. Chem., 11 (2015), 499  crossref
    5. Robert R. P. Torregrosa, Encyclopedia of Reagents for Organic Synthesis, 2015, 1  crossref
    6. Arif Kivrak, Metin Zora, “A novel synthesis of 1,2,4-oxadiazoles and isoxazoles”, Tetrahedron, 70:4 (2014), 817  crossref
    7. Metin Zora, Arif Kivrak, Yilmaz Kelgokmen, “A novel one-pot synthesis of ferrocenyl-substituted 1,2,4-oxadiazoles”, Journal of Organometallic Chemistry, 759 (2014), 67  crossref
    8. Dongshan Su, Haifeng Duan, Zhonglin Wei, Jungang Cao, Dapeng Liang, Yingjie Lin, “Condensation of Vilsmeier salts, derived from tetraalkylureas, with amidoximes: a novel approach to access N,N-dialkyl-1,2,4-oxadiazol-5-amines”, Tetrahedron Letters, 54:50 (2013), 6959  crossref
    9. Mehdi Adib, Sharareh Bagherzadeh, Mohammad Mahdavi, Hamid R. Bijanzadeh, “ChemInform Abstract: An Efficient One‐Pot Synthesis of 3‐Aryl‐1,2,4‐oxadiazol‐5‐amines under Solvent‐Free Conditions.”, ChemInform, 41:25 (2010)  crossref
    10. Maria Ispikoudi, Michalis Amvrazis, Christos Kontogiorgis, Alexandros E. Koumbis, Konstantinos E. Litinas, Dimitra Hadjipavlou-Litina, Konstantina C. Fylaktakidou, “Convenient synthesis and biological profile of 5-amino-substituted 1,2,4-oxadiazole derivatives”, European Journal of Medicinal Chemistry, 45:12 (2010), 5635  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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