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Heterocyclic bioantioxidants 4. Chlorolysis of 3-nitro-4-s-benzylcoumarin

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

3-Nitro-4-S-benzylcoumarin reacts with sulfuryl chloride to give an unstable compound, which in turn reacts with p-toluidine to give 3-nitro-4-p-tolylaminocoumarin.

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References

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Authors and Affiliations

  1. All-Union Scientific-Center for the Safety of Biologically Active Compounds, 142450, Kupavna

    E. A. Parfenov & L. D. Smirnov

Authors
  1. E. A. Parfenov
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  2. L. D. Smirnov
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Additional information

For Communication 3, see [1].

Translated from Khimiya Geterotsiklicheskikh Soednenii, No. 7, 888–889, July, 1992.

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Parfenov, E.A., Smirnov, L.D. Heterocyclic bioantioxidants 4. Chlorolysis of 3-nitro-4-s-benzylcoumarin. Chem Heterocycl Compd 28, 736–737 (1992). https://doi.org/10.1007/BF00474483

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  • DOI: https://doi.org/10.1007/BF00474483

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