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A single crystal X-ray study of the products of halogen mercury cyclization of 8-allylthioquinoline

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Abstract

The reaction products of 8-allylthioquinoline with mercury halides are studied by single crystal X-ray diffraction. It is shown that the products are organomercury derivatives of salts of 2,3-dihydro[1,4]-thiazino[2,3,4-ij]quinoliniuim.

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Authors and Affiliations

  1. I. Ya. Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, Ekaterinburg, Russia

    P. A. Slepukhin & V. N. Charushin

  2. South Ural State University, Chelyabinsk, Russia

    V. I. Batalov & D. G. Kim

Authors
  1. P. A. Slepukhin
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  2. V. I. Batalov
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  3. D. G. Kim
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  4. V. N. Charushin
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Corresponding author

Correspondence to P. A. Slepukhin.

Additional information

Original Russian Text Copyright © 2012 by P. A. Slepukhin, V. I. Batalov, D. G. Kim, and V. N. Charushin

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Translated from Zhurnal Strukturnoi Khimii, Vol. 53, No. 1, pp. 149–154, January–February, 2012.

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Slepukhin, P.A., Batalov, V.I., Kim, D.G. et al. A single crystal X-ray study of the products of halogen mercury cyclization of 8-allylthioquinoline. J Struct Chem 53, 145–150 (2012). https://doi.org/10.1134/S0022476612010192

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  • DOI: https://doi.org/10.1134/S0022476612010192

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