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Δ2-isoxazolines from arylcyclopropanes: III. Phenylcyclopropanes substituted in three-membered ring in reaction with nitrosyl chloride activated with oxides of sulfur(IV, VI)

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Abstract

The reaction of phenylcyclopropanes substituted in the three-membered ring with nitrosyl chloride activated with sulfur(IV, VI) oxides provided in good yield substituted 5-phenylisoxazolines as a mixture of structural isomers.

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Authors and Affiliations

  1. Moscow State University, Moscow, 119991, Russia

    O. B. Bondarenko, A. Yu. Gavrilova, L. G. Saginova, N. V. Zyk & N. S. Zefirov

Authors
  1. O. B. Bondarenko
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  2. A. Yu. Gavrilova
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  3. L. G. Saginova
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  4. N. V. Zyk
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  5. N. S. Zefirov
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Corresponding author

Correspondence to O. B. Bondarenko.

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Original Russian Text © O.B. Bondarenko, A.Yu. Gavrilova, L.G. Saginova, N.V. Zyk, N.S. Zefirov, 2009, published in Zhurnal Organicheskoi Khimii, 2009, Vol. 45, No. 2, pp. 230–237.

For communication II, see [1].

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Bondarenko, O.B., Gavrilova, A.Y., Saginova, L.G. et al. Δ2-isoxazolines from arylcyclopropanes: III. Phenylcyclopropanes substituted in three-membered ring in reaction with nitrosyl chloride activated with oxides of sulfur(IV, VI). Russ J Org Chem 45, 218–225 (2009). https://doi.org/10.1134/S1070428009020110

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  • DOI: https://doi.org/10.1134/S1070428009020110

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