Аннотация:
New selective synthesis of 1-alkyl-5-nitro-1,2,3-triazoles and 1-alkyl-4-nitro-1,2,3-triazoles has been developed, involving acid N-dealkylation of the relative 4-nitro-1,2,3- and 3-nitro- 5-R-1,2,4-triazolium salts. The assortment of novel 1-alkyl- 4(5)-nitro-1,2,3-triazoles has been thus essentially expanded. Treatment of relative 3-nitro-1,2,4-triazolium salts with HCl or HBr proceeds mostly as SNipso-substitution of the nitro group.
Образец цитирования:
G. T. Sukhanov, Yu. V. Filippova, Yu. V. Gatilov, A. G. Sukhanova, K. K. Bosov, I. A. Krupnova, E. V. Pivovarova, “Acidic N-dealkylation in nitrotriazolium salts”, Mendeleev Commun., 32:2 (2022), 215–217
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc617
https://www.mathnet.ru/rus/mendc/v32/i2/p215
Эта публикация цитируется в следующих 1 статьяx:
Gennady T. Sukhanov, Yulia V. Filippova, Yuri V. Gatilov, Anna G. Sukhanova, Irina A. Krupnova, Konstantin K. Bosov, Ekaterina V. Pivovarova, Vyacheslav I. Krasnov, “Energetic Materials Based on N-substituted 4(5)-nitro-1,2,3-triazoles”, Materials, 15:3 (2022), 1119