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Chemistry of oxalyl derivatives of methyl ketones

V. Reaction of aroylpyruvic acids and their derivatives with o-aminothiophenol

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It was established by IR, UV, and PMR spectroscopy that 2-phenacylidenebenzo-1,4-thiazin-3-ones are formed in the reaction of o-aminothiophenol with aroylpyruvic acids or 5-arylfuran-2,3-diones. 2-Carbomethoxy-2-phenacyl-1,3-benzothiazolines were isolated in the reaction of o-aminothiophenol with aroylpyruvic acid esters.

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Literature cited

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Authors and Affiliations

  1. Perm Pharmaceutical Institute, 614600, Perm

    Yu. S. Andreichikov, S. P. Tendryakova, Yu. A. Nalimova & L. A. Voronova

Authors
  1. Yu. S. Andreichikov
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  2. S. P. Tendryakova
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  3. Yu. A. Nalimova
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  4. L. A. Voronova
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Additional information

See [1] for communication IV.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 755–757, June, 1977.

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Andreichikov, Y.S., Tendryakova, S.P., Nalimova, Y.A. et al. Chemistry of oxalyl derivatives of methyl ketones. Chem Heterocycl Compd 13, 611–613 (1977). https://doi.org/10.1007/BF00480663

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  • DOI: https://doi.org/10.1007/BF00480663

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