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Mendeleev Communications, 2004, Volume 14, Issue 2, Pages 76–77
DOI: https://doi.org/10.1070/MC2004v014n02ABEH001891
(Mi mendc3814)
 

This article is cited in 23 scientific papers (total in 23 papers)

Synthesis and Dimroth rearrangement of 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles

V. Yu. Rozhkov, L. V. Batog, E. K. Shevtsova, M. I. Struchkova

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (88 kB) Citations (23)
Abstract: The cycloaddition of 4-amino-3-azido-1,2,5-oxadiazole to nitriles with activated methylene groups has been studied, and 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles and the products of their Dimroth rearrangement, viz, N-(4-R-1H-1,2,3-triazol-5-yl)-1,2,5-oxadiazole-3,4-diamines, have been synthesised.
Document Type: Article
Language: English


Citation: V. Yu. Rozhkov, L. V. Batog, E. K. Shevtsova, M. I. Struchkova, “Synthesis and Dimroth rearrangement of 3-amino-4-(5-amino-1H-1,2,3-triazol-1-yl)-1,2,5-oxadiazoles”, Mendeleev Commun., 14:2 (2004), 76–77
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  • This publication is cited in the following 23 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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