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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1998 Volume 8, Issue 6, Pages 240–241 (Mi mendc4748)

This article is cited in 3 papers

2-Diazoacethydrazide derivatives and their ring-chain transformations

Yu. A. Rosina, E. A. Vorob'evaa, Yu. Yu. Morzherina, A. S. Yakimova, W. Dehaenb, V. A. Bakuleva

a Department of Technology of Organic Synthesis, Urals State Technical University, Ekaterinburg, Russian Federation
b Department of Chemistry, University of Leuven, Leuven, Belgium

Abstract: 1-Amino-1,2,3-triazol-5-olates 6, 13 and 14 have been obtained by the introduction of a diazo group into N-benzylidene-protected hydrazides of cyanoacetic and malonic acids. These compounds form open-chain isomers of 1-amino-5-hydroxy-1,2,3-triazoles upon acidification with an aqueous solution of HCl. Compounds 8, 15 and 16 are the first examples of the group of α-diazoacethydrazides

Language: English

DOI: 10.1070/MC1998v008n06ABEH001032



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