AMINATION OF 4-AZAFLUORENE UNDER CHICHIBABIN REACTION CONDITIONS. SOME CHEMICAL TRANSFORMATIONS OF 1-AMINO-4-AZAFLUORENE

Authors

  • А. B. Варламов Russian People's Friendship University, Moscow 117198
  • А. И. Левов Russian People's Friendship University, Moscow 117198
  • Ф. Тозе Russian People's Friendship University, Moscow 117198
  • А. И. Чернышев Russian People's Friendship University, Moscow 117198
  • B. B. Дaвыдов Russian People's Friendship University, Moscow 117198
  • M. А. Рябов Russian People's Friendship University, Moscow 117198
  • O. А. Егорова Russian People's Friendship University, Moscow 117198

Keywords:

1-amino-4-azafluorene, diazotization, nucleophilic substitution

Abstract

4-Azafluorene is aminated by sodium amide in dimethylaniline at C(1). The oxidation of 1-amino-4-azafluorene was studied along with the condensation of this compound with acetic anhydride and its diazotization.

How to Cite
Varlamov, A. V.; Levov, A. N.; Toze, F.; Chernyshev, A. I.; Davydov, V. V.; Ryabov, M. A.; Egorova, O. A. Chem. Heterocycl. Compd. 2002, 38, 1484. [Khim. Geterotsikl. Soedin. 2002, 1682.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1022645511984

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Published

2002-12-25

Issue

No. 12 (2002)

Section

Original Papers