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Chemistry of Heterocyclic Compounds

, Volume 47, Issue 11, pp 1415–1429 | Cite as

N-acylaminophenylcyclopropanes in reaction with nitrous acid generated in situ

  • S. S. MochalovEmail author
  • R. A. Gazzaeva
  • A. Z. Kadzhaeva
  • A. N. Fedotov
  • E. V. Trofimova
Article

The reaction of N-acylaminophenylcyclopropanes with HNO2 proceeds regioselectively with introduction of an N = O fragment into the three-membered ring and formation of the corresponding Δ2-isoxazolines. For ortho-substituted N-acylaminophenylcyclopropanes side processes were observed, caused by the intramolecular participation of the N-acyl group in conversions of the carbenium ions formed on opening the cyclopropane ring under the action of the nitrosating reagent, and by direct insertion of the modified ortho substituent into the three-membered ring.

Keywords

N-acylaminophenylcyclopropanes 3,1-benzoxazines Δ2-isoxazolines heterocyclization 

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Copyright information

© Springer Science+Business Media, Inc. 2012

Authors and Affiliations

  • S. S. Mochalov
    • 1
    Email author
  • R. A. Gazzaeva
    • 2
  • A. Z. Kadzhaeva
    • 1
  • A. N. Fedotov
    • 1
  • E. V. Trofimova
    • 1
  1. 1.Moscow M. V. Lomonosov State UniversityMoscowRussia
  2. 2.North-Ossetiian K. L. Khetagurov State UniversityNorth-OssetiyaRussia

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