HYDRAZINOLYSIS OF COMPOUNDS CONTAINING OXAZOLIDINE RING

Authors

  • М. Мадесклер University of Auvergne, Pharmacy Department, 28 Place Henri Dunant, Clermont-Ferrand
  • Ж. Кукле University of Auvergne, Pharmacy Department, 28 Place Henri Dunant, Clermont-Ferrand
  • Ф. Леаль University of Auvergne, Pharmacy Department, 28 Place Henri Dunant, Clermont-Ferrand
  • В. П. Зайцев Samara State University, Samara 443011
  • С. Х. Шарипова Samara State University, Samara 443011

Keywords:

oxazolidines, perhydrooxazolo[3,4-c]oxazoles, hydrazinolysis

Abstract

We have studied hydrazinolysis of (4S,5S)-3-benzyl-4-hydroxymethyl-5-(4-nitrophenyl)oxazolidine, (1R,4S,5S)-1-(4-nitrophenyl)-1-aza-3,7-dioxabicyclo[3,3,0]octane, and (1R,4S,5S)-1-benzyl-4-(4-(1R,4S,5S)-1-(4-nitrophenyl)-1-aza-3,7-dioxabicyclo[3,3,0]octane, and (1R,4S,5S)-1-benzyl-4-(4-nitrophenyl)-1-azonia-3,7-dioxabicyclo[3,3,0]octane. We have shown that neutral compounds are decomposed with opening of the oxazolidine ring, while quaternary ammonium salts react with hydrazine in several directions.

How to Cite
Madesclaire, M.; Couquelet, J.; Leal, F.; Zaitsev, V. P.; Sharipova, S. Kh..  Chem. Heterocycl. Compd. 2002, 38, 71. [Khim. Geterotsikl. Soedin. 2002, 78.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1014807426609

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Published

2002-01-25

Issue

No. 1 (2002)

Section

Original Papers