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3-Phenyl- and 3-carbomethoxyisoxazoline-N-oxides in the 1,3-dipolar cycloaddition reaction

  • Organic and Biological Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    A method of synthesis for 3-phenylisoxazoline-N-oxide and 3-earbomethoxyisoxazoline-N-oxide has been worked out.

  2. 2.

    With respect to increase in reactivity of isoxazoline-N-oxides in the 1,3-cycloaddition reaction, substituents in the 3-position can be arranged in the order: NO2 > COOCH3 > C6H5.

  3. 3.

    Inclusion of the nitrone ether 1,3-system in a 5-membered ring reduces its reactivity in the 1,3-cycloaddition reaction.

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Literature cited

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Authors and Affiliations

  1. N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, USSR

    I. E. Chlenov, V. I. Khudak, V. A. Tartakovskii & S. S. Novikov

Authors
  1. I. E. Chlenov
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  2. V. I. Khudak
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  3. V. A. Tartakovskii
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  4. S. S. Novikov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2266–2269, Ocotober, 1969.

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Chlenov, I.E., Khudak, V.I., Tartakovskii, V.A. et al. 3-Phenyl- and 3-carbomethoxyisoxazoline-N-oxides in the 1,3-dipolar cycloaddition reaction. Russ Chem Bull 18, 2113–2116 (1969). https://doi.org/10.1007/BF00906630

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  • DOI: https://doi.org/10.1007/BF00906630

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