Russian Journal of Organic Chemistry

, Volume 45, Issue 8, pp 1214–1218 | Cite as

Oxidative coupling of substituted 1,2,3,4,4a,5-hexahydro-13H-benzimidazo[2,1-j]quinolines with methylene-active derivatives of carboxylic acids

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Abstract

The oxidative coupling of substituted 1,2,3,4,4a,5-hexahydro-13H-benzimidazo[2,1-j]quinolines with methylene-active derivatives of carboxylic acids led to the formation of p-methylenequinone imines of the mentioned series; in some events the reaction was accompanied with a hydrolytic cleavage of the exocyclic fragment.

Keywords

Oxidative Coupling Ethyl Cyanoacetate Diethyl Malonate Quinone Imine Compound IIIb 

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Copyright information

© Pleiades Publishing, Ltd. 2009

Authors and Affiliations

  • O. Yu. Slabko
    • 1
  • N. V. Ageenko
    • 1
    • 2
  • V. A. Kaminskii
    • 1
  1. 1.Far-Eastern State UniversityVladivostokRussia
  2. 2.Zhirmunskii Institute of Marine Biology, Far-Eastern DivisionRussian Academy of SciencesVladivostokRussia

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