Аннотация:
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
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4748
https://www.mathnet.ru/rus/mendc/v8/i6/p240
Эта публикация цитируется в следующих 3 статьяx:
Monalisa Akter, Kavuri Rupa, Pazhamalai Anbarasan, “1,2,3-Triazole and Its Analogues: New Surrogates for Diazo Compounds”, Chem. Rev., 122:15 (2022), 13108
Nazariy T. Pokhodylo, Olga Ya. Shyyka, Vasyl S. Matiychuk, Mykola D. Obushak, Volodymyr V. Pavlyuk, “A Novel Base‐Solvent Controlled Chemoselective Azide Attack on an Ester Group versus Keto in Alkyl 3‐Substituted 3‐Oxopropanoates: Mechanistic Insights”, ChemistrySelect, 2:21 (2017), 5871
Yury A. Rosin, Elena A. Vorob'eva, Yury Yu. Morzherin, Alexander C. Yakimov, Wim Dehaen, Vasiliy A. Bakulev, “ChemInform Abstract: 2-Diazoacethydrazide Derivatives and Their Ring-Chain Transformations.”, ChemInform, 30:18 (2010), no
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