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Russian Chemical Bulletin

, Volume 61, Issue 1, pp 59–63 | Cite as

Two directions in spiroheterocyclization of 1H-pyrrole-2,3-diones upon the action of 3-arylamino-1H-inden-1-ones

  • M. V. Dmitriev
  • P. S. Silaichev
  • Z. G. Aliev
  • S. M. Aldoshin
  • A. N. Maslivets
Full Articles

Abstract

4-Ethoxycarbonyl-5-phenyl-substituted 1H-pyrrole-2,3-diones react with 3-arylamino-1H-inden-1-ones in the ratios 1: 1 and 1: 2 to form substituted spiro{indeno[1,2-b]quinoline-10,3′-pyrroles} and substituted spiro{diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles}, respectively.

Key words

1H-pyrrole-2,3-diones spiroheterocyclization 3-arylamino-1H-inden-1-ones spiro{indeno[1,2-b]quinoline-10,3′-pyrroles} spiro{diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles} 

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Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  • M. V. Dmitriev
    • 1
  • P. S. Silaichev
    • 1
  • Z. G. Aliev
    • 2
  • S. M. Aldoshin
    • 2
  • A. N. Maslivets
    • 1
  1. 1.Perm State UniversityPermRussian Federation
  2. 2.Institute of Problems of Chemical PhysicsRussian Academy of SciencesChernogolovka, Moscow RegionRussian Federation

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