Abstract:
5-Cyano-1,2,4-triazines enter into the Ritter reaction with secondary and tertiary alcohols to form N-alkylated 1,2,4-triazine-5-carboxamides.
Document Type:
Article
Language: English
Citation:
D. N. Kozhevnikov, T. V. Nikitina, V. L. Rusinov, O. N. Chupakhin, “The Ritter reaction in the 5-cyano-1,2,4-triazine series”, Mendeleev Commun., 10:3 (2000), 117–118
Linking options:
https://www.mathnet.ru/eng/mendc4413
https://www.mathnet.ru/eng/mendc/v10/i3/p117
This publication is cited in the following 6 articles:
Ya. K. Shtaitz, E. D. Ladin, N. V. Slovesnova, K. D. Krasnoperova, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, “Synthesis of Novel Memantine and Rimantadine Derivatives as Promising Drug Candidates”, Russ J Gen Chem, 93:S1 (2023), S100
R. Bishop, Comprehensive Organic Synthesis II, 2014, 239
Comprehensive Organic Name Reactions and Reagents, 2010, 2399
V. Charushin, V. Rusinov, O. Chupakhin, Comprehensive Heterocyclic Chemistry III, 2008, 95
Carmen Ochoa, Pilar Goya, Progress in Heterocyclic Chemistry, 13, A critical review of the 2000 literature preceded by two chapters on current heterocyclic topics, 2001, 296
Dmitry N. Kozhevnikov, Tatiana V. Nikitina, Vladimir L. Rusinov, Oleg N. Chupakhin, “ChemInform Abstract: The Ritter Reaction in the 5‐Cyano‐1,2,4‐triazine Series.”, ChemInform, 31:44 (2000)
Contact us: