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N-arylsulfinyl-1,4-benzoquinonimines

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Abstract

Stable N-arylsulfinyl-1,4-benzoquinonimines were synthesized by acylation of the corresponding 1,4-benzoquinone monooximes with arenesulfenyl chlorides. The process involves transformation of sulfur(II) into sulfur(IV).

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Authors and Affiliations

  1. Donbass State Machine Building Academy, ul. Shkadinova 72, 84313, Kramatorsk, Ukraine

    A. P. Avdeenko, M. V. Stanovskii, S. A. Konovalova & A. L. Yusina

  2. Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Ukraine

    V. V. Pirozhenko

Authors
  1. A. P. Avdeenko
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  2. V. V. Pirozhenko
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  3. M. V. Stanovskii
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  4. S. A. Konovalova
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  5. A. L. Yusina
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Additional information

Translated from Zhurnal Organicheskoi Khimii, Vol. 40, No. 9, 2004, pp. 1340–1343.

Original Russian Text Copyright © 2004 by Avdeenko, Pirozhenko, Stanovskii, Konovalova, Yusina.

This study was performed under financial support by the ES INTAS program (grant no. 00 157–1999) and by the Ministry of Education and Science of Ukraine.

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Avdeenko, A.P., Pirozhenko, V.V., Stanovskii, M.V. et al. N-arylsulfinyl-1,4-benzoquinonimines. Russ J Org Chem 40, 1291–1294 (2004). https://doi.org/10.1007/s11178-005-0008-2

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  • DOI: https://doi.org/10.1007/s11178-005-0008-2

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