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Oxidation products of nitroxyl radicals of isoindoline series

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

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 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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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
  2. 2.
    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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    G. R. Delpierre and M. Lamchen, Quart. Rev.,19, 329 (1965).Google Scholar
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    O. H. Wheeler and P. H. Gore, J. Am. Chem. Soc.,78, 3363 (1956).Google Scholar

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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