O. N. Chupakhin, B. V. Rudakov, P. McDermott, S. G. Alexeev, V. N. Charushin, F. Hegarty, “An Unusually Easy Oxidative Dequaternization of N-Alkyl-1,2,4-triazinium Salts”, Mendeleev Commun., 5:3 (1995), 104

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Mendeleev Communications, 1995, Volume 5, Issue 3, Pages 104–105
DOI: https://doi.org/10.1070/MC1995v005n03ABEH000478 (Mi mendc5052)

This article is cited in 5 scientific papers (total in 5 papers)

An Unusually Easy Oxidative Dequaternization of N-Alkyl-1,2,4-triazinium Salts

O. N. Chupakhin^a, B. V. Rudakov^b, P. McDermott^c, S. G. Alexeev^b, V. N. Charushin^d, F. Hegarty^c

^a I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
^b Urals State Technical University, Ekaterinburg, Russian Federation
^c Department of Chemistry, University College Dublin, Belfield, Dublin, Ireland
^d Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation

Full-text PDF (298 kB) Citations (5)

DOI: https://doi.org/10.1070/MC1995v005n03ABEH000478

Abstract: Unusually easy dequaternization has been found to occur on treatment of 1-alkyl-3-morpholino-5-phenyl-1,2,4-triazinium iodides with triethylamine in alcohol or acetone solutions at room temperature; a plausible reaction mechanism has been advanced on the basis of NMR and kinetic studies.

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Document Type: Article

Language: English

Citation: O. N. Chupakhin, B. V. Rudakov, P. McDermott, S. G. Alexeev, V. N. Charushin, F. Hegarty, “An Unusually Easy Oxidative Dequaternization of N-Alkyl-1,2,4-triazinium Salts”, Mendeleev Commun., 5:3 (1995), 104–105

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This publication is cited in the following 5 articles:

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