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Reaction of some amines with unsaturated N-acylbenzoxazolones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It is shown that the addition of aniline proceeds at the carbon-carbon double bond of N-acryloyl-, N-chloroacryloyl-, and N-methylacryloylbenzoxazolones. The basicity of the amine has a substantial effect on the course of the reaction with various amines. Transamidation of the acryloyl residue occurs with strongly basic amines.

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Literature cited

  1. N. A. Aliev and N. N. Mel'nikov, in: Chemical Agents for the Protection of Plants [in Russian], Vol. 4, Moscow (1973), p. 61.

  2. V. Kalcheva and D. Simov, Khim. Geterotsikl. Soedin., 1333 (1971).

  3. S. D. Danilov, Author's Abstract of Master's Dissertation, Moscow (1973).

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1044–1048, August, 1974.

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Aliev, N.A., Razakov, R., Abdullaev, N.D. et al. Reaction of some amines with unsaturated N-acylbenzoxazolones. Chem Heterocycl Compd 10, 909–912 (1974). https://doi.org/10.1007/BF00487107

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  • DOI: https://doi.org/10.1007/BF00487107

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