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Reactions of arylsulfonyl compounds with an excess of an organolithium reagent 13. Synthesis of o-mercapto sulfones and o-bissulfones of the benzene, naphthalene, and thiophene series from o-lithio sulfones

  • Organic Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    Methods have been developed for obtaining o-mercapto sulfones of the benzene, naphthalene, and thiophene series, and derivatives with transition-metal salts have been obtained for them.

  2. 2.

    The presence of an intramolecular hydrogen bond in the o-mercapto sulfones has been shown by IR spectroscopy, and spectral confirmation has been shown of the participation of the sulfonyl group in coordination with the metal in their metal derivatives.

  3. 3.

    A number of o-bissulfones and trissulfones of the benzene and thiophene series have been synthesized. The basic possibility of nucleophilic substitution of one of the sulfone groups in them has been shown.

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Literature cited

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For Communication 12, see [1].

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2760–2767, December, 1978.

The authors express their gratitude to I. P. Yakovlev for a discussion of the spectral results.

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Gol'dfarb, Y.L., Stoyanovich, F.M., Chermanova, G.B. et al. Reactions of arylsulfonyl compounds with an excess of an organolithium reagent 13. Synthesis of o-mercapto sulfones and o-bissulfones of the benzene, naphthalene, and thiophene series from o-lithio sulfones. Russ Chem Bull 27, 2462–2469 (1978). https://doi.org/10.1007/BF00941097

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  • DOI: https://doi.org/10.1007/BF00941097

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