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
Document Type:
Article
Language: English
Citation:
Yu. A. Rosin, E. A. Vorob'eva, Yu. Yu. Morzherin, A. S. Yakimov, W. Dehaen, V. A. Bakulev, “2-Diazoacethydrazide derivatives and their ring-chain transformations”, Mendeleev Commun., 8:6 (1998), 240–241
Linking options:
https://www.mathnet.ru/eng/mendc4748
https://www.mathnet.ru/eng/mendc/v8/i6/p240
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