Tetrazoles. 33. New method for obtaining functionally substituted tetrazoles

Authors

  • М. А. Гольцберг St. Petersburg State Technological Institute, St. Petersburg 198013
  • Г. И. Колдобский St. Petersburg State Technological Institute, St. Petersburg 198013

Abstract

The interaction of 5-methylsulfonyl-1-phenyltetrazole with C-, N-, and O-nucleophiles at 18–20°C gives high yields of 1-phenyltetrazoles that are functionally substituted on the carbon atom of the heteroring. Prospects are examined for the use of 5-methylsulfonyl-1-phenyltetrazole as a universal synthon in the synthesis of tetrazoles with various types of structure.

How to Cite
Gol'tsberg, M. A.; Koldobskii, G. I. Chem. Heterocycl. Compd. 1996, 32, 1300. [Khim. Geterotsikl. Soedin. 1996, 1515.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169961

Published

1996-11-25

Issue

Section

Original Papers