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Peculiarities of the reactivities of 3-carboxyalkylsydnones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

In contrast to the 3-alkyl analogs, the heteroring in 3-carboxyalkylsydnones is cleaved by the action of hydrogen chloride in alcohols. The kinetics of the previously known alkaline cleavage of the ring in 3-carboxyalkylsydnones and sydnoneimines were studied by a spectrophotometric method.

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Literature cited

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Authors and Affiliations

  1. Institute of Biophysics, Ministry of Public Health of the USSR, Moscow

    I. S. Slyusarenko, V. V. Ogorodnikova & V. G. Yashunskii

Authors
  1. I. S. Slyusarenko
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  2. V. V. Ogorodnikova
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  3. V. G. Yashunskii
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 450–453, April, 1976.

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Slyusarenko, I.S., Ogorodnikova, V.V. & Yashunskii, V.G. Peculiarities of the reactivities of 3-carboxyalkylsydnones. Chem Heterocycl Compd 12, 378–381 (1976). https://doi.org/10.1007/BF00480418

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  • DOI: https://doi.org/10.1007/BF00480418

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