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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2004 Volume 14, Issue 2, Pages 76–77 (Mi mendc3814)

This article is cited 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

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.

Language: English

DOI: 10.1070/MC2004v014n02ABEH001891



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