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Russian Journal of Organic Chemistry

, Volume 48, Issue 5, pp 694–698 | Cite as

Five-membered 2,3-dioxoheterocycles: LXXXVI. Spiro-heterocyclization of 1-aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones under the action of 3-arylamino-1H-inden-1-ones. Crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H-spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione

  • N. V. Bubnov
  • E. S. Denislamova
  • P. S. Silaichev
  • P. A. Slepukhin
  • A. N. Maslivets
Article

Abstract

1-Aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones react with 3-arylamino-1H-inden-1-ones affording 1,1′-diaryl-3′-aroyl-4′-hydroxy-1H-spiro[indeno[1,2-b]pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-triones. The crystal and molecular structure of 4′-hydroxy-3′-(2,4-dimethylbenzoyl)-1,1′-diphenyl-1H-spiro[indeno[1,2-b] pyrrole-3,2′-pyrrole]-2,4,5′(1′H)-trione.

Keywords

Diones Pyrrole Spiro Trione Indeno 
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

© Pleiades Publishing, Ltd. 2012

Authors and Affiliations

  • N. V. Bubnov
    • 1
  • E. S. Denislamova
    • 2
  • P. S. Silaichev
    • 1
    • 2
  • P. A. Slepukhin
    • 3
  • A. N. Maslivets
    • 1
    • 2
  1. 1.Institute of Natural Sciences at Perm State UniversityPermRussia
  2. 2.Perm State UniversityPermRussia
  3. 3.Postovskii Institute of Organic Synthesis, Ural DivisionRussian Academy of SciencesYekaterinburgRussia

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