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Chemistry of Heterocyclic Compounds

, Volume 28, Issue 11, pp 1264–1267 | Cite as

Planche rearrangement in indolines with acceptor substituents. 2. Pyrrolidone ring formation from the reaction between 1,3,3-trimethyl-ω-cyano-methyleneindoline and o-aminophenol

  • A. A. Tolmachev
  • L. N. Babichenko
  • A. K. Sheinkman
Article
  • 28 Downloads

Abstract

It was found that when 1,3,3-trimethyl-ω-cyanomethyleneindoline was condensed with o-aminophenol in polyphosphoric acid, a complex heterocyclic system containing a pyrrolidone ring was formed as a result of the Planche rearrangement.

Keywords

Organic Chemistry Pyrrolidone Ring Formation Heterocyclic System Indolines 
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

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Copyright information

© Plenum Publishing Corporation 1993

Authors and Affiliations

  • A. A. Tolmachev
    • 1
    • 2
  • L. N. Babichenko
    • 1
    • 2
  • A. K. Sheinkman
    • 1
    • 2
  1. 1.Dnepropetrovsk Construction Engineering InstituteDnepropetrovsk
  2. 2.Institute of Organic ChemistryUkrainian Academy of SciencesKiev

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