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Mendeleev Communications, 2011, Volume 21, Issue 4, Pages 198–200
DOI: https://doi.org/10.1016/j.mencom.2011.07.009
(Mi mendc2915)
 

This article is cited in 4 scientific papers (total 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
Full-text PDF (246 kB) Citations (4)
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.
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Document Type: Article
Language: English


Citation: M. B. Gazizov, R. A. Khairullin, A. A. Minnikhanova, A. I. Alekhina, R. Z. Musin, O. G. Sinyashin, “Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles”, Mendeleev Commun., 21:4 (2011), 198–200
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  • https://www.mathnet.ru/eng/mendc/v21/i4/p198
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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