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Chemistry of Heterocyclic Compounds

, Volume 33, Issue 7, pp 823–827 | Cite as

Synthesis of pyrroloquinolines from 2,3-dimethyl-5-methoxy-6-aminoindole

  • S. A. Yamashkin
  • N. Ya. Kucherenko
  • M. A. Yurovskaya
Article
  • 46 Downloads

Abstract

Formation of enaminoketones, enaminocrotonate, and aminomethylenemalonate from 2,3-dimethyl-5-methoxy-6-aminoindole occurs significantly less easily than for the 7-methoxy analog. A similar dependence is observed in the reaction of enamines to the corresponding pyrroloquinolines independently of the cyclization conditions.

Keywords

Organic Chemistry Cyclization Condition Similar Dependence Enamine Pyrroloquinolines 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    S. A. Yamashkin, N. Ya. Kucherenko, and M. A. Yurovskaya, Khim. Geterotsikl. Soedin., No. 1, 75 (1997).Google Scholar
  2. 2.
    S. A. Yamashkin, L. G. Yudin, and A. N. Kost, Khim. Geterotsikl. Soedin., No. 4, 493 (1983).Google Scholar

Copyright information

© Plenum Publishing Corporation 1998

Authors and Affiliations

  • S. A. Yamashkin
  • N. Ya. Kucherenko
  • M. A. Yurovskaya

There are no affiliations available

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