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Manganese dioxide oxidation of hydroxyamino-sym-triazines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The hydroxyamino group in sym-triazines is readily oxidized by the action of manganese dioxide. The stability of the nitrosotriazines formed in this oxidation depends on the electron donor properties of the other substituents in the molecule.

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 630090, Novosibirsk

    V. F. Sedova & O. P. Shkurko

Authors
  1. V. F. Sedova
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  2. O. P. Shkurko
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Additional information

For Previous Communication, see [1]

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 694–699, May, 1993.

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Sedova, V.F., Shkurko, O.P. Manganese dioxide oxidation of hydroxyamino-sym-triazines. Chem Heterocycl Compd 29, 593–597 (1993). https://doi.org/10.1007/BF00534476

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  • DOI: https://doi.org/10.1007/BF00534476

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