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Stereoselective addition of diorganyl chalcogenides to cyclohexene catalyzed with tin(IV) chloride

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Abstract

The addition of diorganyl disulfides and dimethyl diselenide to cyclohexene in the presence of tin(IV) chloride proceeded stereoselectively affording trans-adducts of 1:1 composition. No reaction occurs in the absence of tin(IV) chloride.

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Authors and Affiliations

  1. Faworsky Irkutsk Institute of Chemistry, Siberian Division, Russian Academy of Sciences, Irkutsk, 664033, Russia

    A. V. Martynov, A. R. Zhinkin & S. V. Amosova

Authors
  1. A. V. Martynov
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  2. A. R. Zhinkin
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  3. S. V. Amosova
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Correspondence to A. V. Martynov.

Additional information

Original Russian Text © A.V. Martynov, A.R. Zhinkin, S.V. Amosova, 2006, published in Zhurnal Organicheskoi Khimii, 2006, Vol. 42, no. 2, pp. 207–209.

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Martynov, A.V., Zhinkin, A.R. & Amosova, S.V. Stereoselective addition of diorganyl chalcogenides to cyclohexene catalyzed with tin(IV) chloride. Russ J Org Chem 42, 190–192 (2006). https://doi.org/10.1134/S1070428002120059

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  • DOI: https://doi.org/10.1134/S1070428002120059

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