CONVERSION OF BICYCLIC C-AZOAZIRIDINES TO 2-SUBSTITUTED 2H-1,2,3-TRIAZOLES

Authors

  • С. М. Бучака St. Petersburg State University, St. Petersburg 198504
  • М. А. Кузнецов St. Petersburg State University, St. Petersburg 198504
  • Й. Г. Шантль Institute of Organic Chemistry, University of Innsbruck, Innsbruck A-6020

DOI:

https://doi.org/10.1007/8174

Keywords:

C-azoaziridines, 2H-1, 2, 3-triazoles

Abstract

In an acidified chloroform solution, bicyclic C-azo-N-(N-hetaryl)aziridines are converted to bicyclic 2H-1,2,3-triazoles. This transformation can occur on the surface of silica gel, and also during storage of these compounds at room temperature.

How to Cite
Buchaka, S. M.; Kuznetsov, M. A.; Schantl, J. G.  Chem. Heterocycl. Compd. 2005, 41, 1321. [Khim. Geterotsikl. Soedin. 2005, 1573.]

For this article in the English edition, see DOI 10.1007/s10593-005-0319-9


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Published

2023-10-19

Issue

No. 10 (2005)

Section

Original Papers