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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2004 Volume 14, Issue 5, Pages 212–214 (Mi mendc3881)

This article is cited in 12 papers

Reaction of 2-acetyl-5-methyl-2H-1,2,3-diazaphosphole with butane-2,3-diol

N. G. Khusainovaa, O. A. Mostovayaa, N. M. Azancheevb, I. A. Litvinovb, D. B. Krivolapovb, R. A. Cherkasova

a Department of Chemistry, V.I. Ul'yanov-Lenin Kazan State 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: The reaction of 2-acetyl-5-methyl-2H-1,2,3-diazaphosphole with (rac)-butane-2,3-diol at temperatures below 0 °C leads to the formation of a hydrospirophosphorane containing both a diazaphospholene and a dioxaphospholane ring system and a β-hydroxyalkoxy-1,2,3-diazaphospholene. On heating, these products form a hydrospirotetraoxaphosphorane, its tautomeric monocyclic β-hydroxyalkylphosphite and N-acetyl-N’-isopropylidene-hydrazine.

Language: English

DOI: 10.1070/MC2004v014n05ABEH001926



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