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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2011 Volume 21, Issue 4, Pages 198–200 (Mi mendc2915)

This article is cited in 4 papers

Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles

M. B. Gazizova, R. A. Khairullina, A. A. Minnikhanovaa, A. I. Alekhinaa, R. Z. Musinb, O. G. Sinyashinb

a Kazan National Research Technological University, Kazan, Russian Federation
b A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation

Abstract: Treatment of 1-tert-butyl-2-dimethoxyphosphoryl-3,3-dimethylaziridine with picric, perchloric or fluoboric acid affords the stable corresponding aziridinium salts, which are prone to undergo ring opening on reaction with alcohols, carboxylate and thiocyanate ions.

Language: English

DOI: 10.1016/j.mencom.2011.07.009



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