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Mendeleev Communications, 2002, Volume 12, Issue 2, Pages 70–72
DOI: https://doi.org/10.1070/MC2002v012n02ABEH001570
(Mi mendc4097)
 

This article is cited in 13 scientific papers (total in 13 papers)

Interaction of diazoimidazoles and their diazonium salts with primary and secondary amines

E. V. Sadtchikova, V. S. Mokrushin

Department of Technology of Organic Synthesis, Urals State Technical University, Ekaterinburg, Russian Federation
Full-text PDF (76 kB) Citations (13)
Abstract: A number of 2- and 5-triazenoimidazoles were prepared by the coupling of diazo compounds with aliphatic amines; however, 4,5-dicyanoimidazole-2-diazonium chloride was transformed into 2-amino-1-methylimidazole-4,5-dicarbonitrile.
Document Type: Article
Language: English


Citation: E. V. Sadtchikova, V. S. Mokrushin, “Interaction of diazoimidazoles and their diazonium salts with primary and secondary amines”, Mendeleev Commun., 12:2 (2002), 70–72
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  • https://www.mathnet.ru/eng/mendc/v12/i2/p70
  • This publication is cited in the following 13 articles:
    1. Seynabou Sokhna, Natacha Mérindol, Marc Presset, Insa Seck, Marie-Pierre Girard, Seydou Ka, Samba Fama Ndoye, Aïcha Lalla Ba, Issa Samb, Lionel Berthoux, Erwan Le Gall, Isabel Desgagné-Penix, Matar Seck, “Potential of several triazene derivatives against DENGUE viruses”, Bioorganic & Medicinal Chemistry Letters, 101 (2024), 129646  crossref
    2. Seynabou Sokhna, Insa Seck, Ibrahima El Hadj Thiam, Marc Presset, Samba Fama Ndoye, Lalla Aïcha Ba, Issa Samb, Simon Coles, James Orton, Matar Seck, Erwan Le Gall, Mohamed Gaye, “Syntheses and crystal structure of 4-[(pyridin-3-yl)diazenyl]morpholine and 1-[(pyridin-3-yl)diazenyl]-1,2,3,4-tetrahydroquinoline”, Acta Crystallogr E Cryst Commun, 79:2 (2023), 74  crossref
    3. Rajesh Akkineni, Sarma V. Markandeya, Avvari N. Prasad, Bhaskar Yamajala, Venkateswara Rao B, Shankar Chaudhari, Deepak Kumar, Sandip T. Gadge, Bhalchandra M. Bhanage, “Rapid Synthesis of 1‐Aryl‐3, 3‐dimethyltriazenes by Using In Situ Generated Aryldiazonium Tetrafluoroborate Salts with “DMF‐DMA” under Ambient Conditions”, ChemistrySelect, 7:48 (2022)  crossref
    4. Jalal Isaad, Ahmida El Achari, “Synthesis and Spectroscopic Characterization of Water Soluble Triazene Dyes Based on Glyco-conjugated Pyrazolone Derivatives Catalyzed by an Acidic Ionic Liquid Supported on Silica-Coated Magnetite Nanoparticles”, Chemistry Africa, 3:4 (2020), 889  crossref
    5. Eugene V. Babaev, Studies in Natural Products Chemistry, 52, 2017, 69  crossref
    6. Siddappa Patil, Alejandro Bugarin, “Fifty Years of π‐Conjugated Triaz­enes”, Eur J Org Chem, 2016:5 (2016), 860  crossref
    7. Wanfang Li, Xiao-Feng Wu, “N2 Extrusion and CO Insertion: A Novel Palladium-Catalyzed Carbonylative Transformation of Aryltriazenes”, Org. Lett., 17:8 (2015), 1910  crossref
    8. Asadollah Mohammadi, “Novel triazene dyes based on N-phenylpiperazine: Synthesis, anti-bacterial activity and solvatochromic properties”, Journal of Molecular Liquids, 193 (2014), 69  crossref
    9. Amin Zarei, Leila Khazdooz, Hamidreza Aghaei, Ghobad Azizi, Alireza Najafi Chermahini, Abdol R. Hajipour, “Synthesis of triazenes by using aryl diazonium silica sulfates under mild conditions”, Dyes and Pigments, 101 (2014), 295  crossref
    10. Davit Jishkariani, C. Dennis Hall, Aydin Demircan, Blake J. Tomlin, Peter J. Steel, Alan R. Katritzky, “Push-Pull Triazenes Derived from 1-(Benzylideneamino)- and 1-(Sulfonimido)-azolylidenes”, J. Org. Chem., 78:7 (2013), 3349  crossref
    11. Jalal Isaad, Fouad Malek, Ahmida El Achari, “A facile route to the new triazene dyes based on substituted pyrazolidin-3,5-dione derivatives”, Dyes and Pigments, 92:3 (2012), 1212  crossref
    12. Dimitri M. Khramov, Christopher W. Bielawski, “Donor-Acceptor Triazenes:  Synthesis, Characterization, and Study of Their Electronic and Thermal Properties”, J. Org. Chem., 72:25 (2007), 9407  crossref
    13. Elena V. Sadtchikova, Vladimir S. Mokrushin, “Interaction of Diazoimidazoles and Their Diazonium Salts with Primary and Secondary Amines.”, ChemInform, 33:39 (2002), 119  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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