Reactions of substituted 7-aminoindoles with 1,3-diketones

Authors

  • С. А. Ямашкин M. E. Evsev'ev Mordovian State Pedagogical Institute, Saransk 430007
  • И. А. Батанов M. E. Evsev'ev Mordovian State Pedagogical Institute, Saransk 430007

Abstract

The condensation of 2,3-dimethyl and 1,2,3-trimethyl-7-aminoindoles with β-dicarbonyl compounds leads to enaminoketones, which undergo cyclization by the action of trifluoroacetic acid giving substituted pyrrolo[3,2-h]quinolines.

How to Cite
Yamashkin, S. A.; Batanov, I. A. Chem. Heterocycl. Compd. 1995, 31, 50. [Khim. Geterotsikl. Soedin. 1995, 58.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171290

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Published

1995-01-25

Issue

No. 1 (1995)

Section

Original Papers