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Chemistry of Heterocyclic Compounds

, Volume 30, Issue 6, pp 683–691 | Cite as

Synthesis, alkylation, and structural studies of 2-vinylpyrrolo[1,2-a]indoles

  • N. Z. Tugusheva
  • S. Yu. Ryabova
  • N. P. Solov'eva
  • V. G. Granik
Article
  • 31 Downloads

Abstract

2-Piperidinomethylene-2H pyrrolo[l,2-a]indole-3,9-dione can readily react with substances having an. active methylene unit to form piperidinium salts which are converted to 2-vinyl pyrrolojl,2-a]indoles. They can also undergo O-methylation using dimethyl sulfate in polar and non polar solvents to form the 9-alkoxy derivatives.

Keywords

Sulfate Methylene Organic Chemistry Dimethyl Indole 
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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Copyright information

© Plenum Publishing Corporation 1995

Authors and Affiliations

  • N. Z. Tugusheva
  • S. Yu. Ryabova
  • N. P. Solov'eva
  • V. G. Granik

There are no affiliations available

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