Abstract:
1,2,4-Triazine 4-oxides react with stable carbanions to form 5-substituted 1,2,4-triazines as the products of deoxygenation nucleophilic substitution of hydrogen.
Document Type:
Article
Language: English
Citation:
D. N. Kozhevnikov, A. M. Prokhorov, V. L. Rusinov, O. N. Chupakhin, “Auto-aromatization of the σH-adducts of 1,2,4-triazine 4-oxides with carbanions in reactions of nucleophilic substitution of hydrogen”, Mendeleev Commun., 10:6 (2000), 227–228
Linking options:
https://www.mathnet.ru/eng/mendc4471
https://www.mathnet.ru/eng/mendc/v10/i6/p227
This publication is cited in the following 5 articles:
Modern Nucleophilic Aromatic Substitution, 2013, 337
V. Charushin, V. Rusinov, O. Chupakhin, Comprehensive Heterocyclic Chemistry III, 2008, 95
O. N. Chupakhin, A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov, V. N. Kalinin, V. A. Ol'shevskaya, I. V. Glukhov, M. Yu. Antipin, “1,2,4-Triazinylcarboranes: a new approach to the synthesis and the crystal structures of 1-(3,6-ditolyl-1,2,4-triazin-5-yl)-2-phenyl-1,2-dicarba-closo-dodecaborane and 1,7-bis[6-phenyl-3-(4-chlorophenyl)-1,2,4-triazin-5-yl]-1,7-dicarba-closo-dodecaborane”, Mendeleev Commun., 13:4 (2003), 165–167
Dmitry N. Kozhevnikov, Anton M. Prokhorov, Vladimir L. Rusinov, Oleg N. Chupakhin, “ChemInform Abstract: Auto‐aromatization of the σH‐Adducts of 1,2,4‐Triazine 4‐Oxides with Carbanions in Reactions of Nucleophilic Substitution of Hydrogen.”, ChemInform, 32:17 (2001)
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