Oxidation products of nitroxyl radicals of isoindoline series

  • V. A. Golubev
  • V. D. Sholle
  • É. G. Rozantsev
Brief Communications
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Conclusions

  1. 1.

    The primary reaction products of isoindolineoxyls with SbCl5 are oxoisoindolinium hexachloro-antimonates.

     
  2. 2.

    The 1,1,3,3-tetraethyl-2-oxoisoindolinium salts easily cleave ethylene and are converted to nitrone salts.

     

Keywords

Oxidation Ethylene Oxidation Product Nitroxyl Nitrone 

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Literature cited

  1. 1.
    V. A. Golubev, G. N. Voronina, and E. G. Rozantsev, Izv. Akad. Nauk SSSR, Ser. Khim., 2605 (1970).Google Scholar
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    V. A. Golubev, R. I. Zhdanov, I. T. Protsishin, and E. G. Rozantsev, Dokl. Akad. Nauk SSSR,195, 1139 (1970).Google Scholar
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    V. D. Sholle, L. A. Krinitskaya, and E. G. Rozantsev, Izv. Akad. Nauk SSSR, Ser. Khim., 149 (1969).Google Scholar
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Copyright information

© Consultants Bureau 1972

Authors and Affiliations

  • V. A. Golubev
    • 1
  • V. D. Sholle
    • 1
  • É. G. Rozantsev
    • 1
  1. 1.Institute of Chemical PhysicsAcademy of Sciences of the USSRUSSR

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