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Mendeleev Communications, 2015, Volume 25, Issue 4, Pages 257–259
DOI: https://doi.org/10.1016/j.mencom.2015.07.007
(Mi mendc2371)
 

This article is cited in 28 scientific papers (total in 28 papers)

Communications

Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes

L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The [3 + 2] cycloaddition of azidofuroxans to internal and terminal acetylenes was found to occur only in ionic liquids on heating and afford (1H-1,2,3-triazol-1-yl)furoxans in moderate to good yields. The reaction with terminal acetylenes proceeds with high regio- selectivity.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (192.6 Kb)


Citation: L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259
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  • This publication is cited in the following 28 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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