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Synthesis of acyl-substituted S-butyne esters of prosphorus thioacids

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

Conclusions

  1. 1.

    Convenient methods were developed for the synthesis of S-(ω-chlorobutyn-2-yl) thioacetate and ω-chlorobutyn-2-yl acetate.

  2. 2.

    A number of S-butyne esters of phosphorus thioacids, containing either an acylmercapto or an acyloxy group in the alkthio moiety, was synthesized.

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Literature cited

  1. E. K. Balashova, A. P. Brestkin, L. A. Vikhreva, N. N. Godovikov, M. I. Kabachnik, T. A. Pudova, V. I. Rozengart, and O. E. Sherstobitov, Zh. Evolyuts. Biokhim. Fiziol.,4, 325 (1982).

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  2. L. A. Vikhreva, T. A. Pudova, N. N. Godovikov, S. A. Roslavtseva, E. K. Balashova, V. I. Rozengart, and O. E. Sherstobitov, in: Chemistry of Physiologically Active Compounds [in Russian], Nalchik (1980), Vol. 3, p. 118.

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Heteroorganic Compounds, Academy of Sciences of the USSR, Moscow

    N. N. Godovikov, L. A. Vikhreva, T. A. Pudova & M. I. Kabachnik

Authors
  1. N. N. Godovikov
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  2. L. A. Vikhreva
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  3. T. A. Pudova
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  4. M. I. Kabachnik
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 911–913, April, 1984.

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Godovikov, N.N., Vikhreva, L.A., Pudova, T.A. et al. Synthesis of acyl-substituted S-butyne esters of prosphorus thioacids. Russ Chem Bull 33, 838–841 (1984). https://doi.org/10.1007/BF00947848

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  • DOI: https://doi.org/10.1007/BF00947848

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