Highly polarized enamines 1. Synthesis and some properties of β-tetrazolylenamines

Authors

  • В. А. Макаров Center for the Chemistry of Medicinals, All-Russian Chemico-Pharmaceutical Scientific Research Institute, Moscow 119815
  • А. Л. Седов Center for the Chemistry of Medicinals, All-Russian Chemico-Pharmaceutical Scientific Research Institute, Moscow 119815
  • M. П. Немерюк Center for the Chemistry of Medicinals, All-Russian Chemico-Pharmaceutical Scientific Research Institute, Moscow 119815
  • Н. П. Соловьева Center for the Chemistry of Medicinals, All-Russian Chemico-Pharmaceutical Scientific Research Institute, Moscow 119815
  • T. C. Сафонова Center for the Chemistry of Medicinals, All-Russian Chemico-Pharmaceutical Scientific Research Institute, Moscow 119815

Abstract

A method has been developed for the synthesis of some β-tetrazolyl-β-nitroenamines containing various alkoxy or amino substituents in the α position. It is based on the transformation of a pyrimidine ring by sodium azide.

How to Cite
Makarov, V. A.; Sedov, A. L.; Nemeryuk, M. P.; Solov'eva, N. P.; Safonova, T. S. Chem. Heterocycl. Compd. 1994, 30, 846. [Khim. Geterotsikl. Soedin. 1994, 976.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169644

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Published

1994-07-25

Issue

No. 7 (1994)

Section

Original Papers