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Russian Chemical Bulletin

, Volume 61, Issue 1, pp 74–77 | Cite as

4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide

  • S. Yu. Pechenkin
  • A. M. Starosotnikov
  • M. A. Bastrakov
  • I. V. Glukhov
  • S. A. Shevelev
Full Articles

Abstract

A number of new tetrahydroisoindole derivatives fused with the furazan ring were synthesized based on the 1,3-dipolar cycloaddition of N-methylazomethine ylide with substituted 4-nitrobenzofurazans. Substituents in the benzene ring were found to affect the cycloaddition process.

Key words

1,3-dipolar cycloaddition azomethine ylides benzofurazans nitro compounds polycyclic systems 

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Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  • S. Yu. Pechenkin
    • 1
  • A. M. Starosotnikov
    • 1
  • M. A. Bastrakov
    • 1
  • I. V. Glukhov
    • 2
  • S. A. Shevelev
    • 1
  1. 1.N. D. Zelinsky Institute of Organic ChemistryRussian Academy of SciencesMoscowRussian Federation
  2. 2.A. N. Nesmeyanov Institute of Organoelement CompoundsRussian Academy of SciencesMoscowRussian Federation

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