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Reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with 2-mercapto- and 2-hydroxy-ethanolamines: The products and some of their transformations

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It was found that the nature of the SH and OH groups in 2-mercapto- and 2-hydroxyethanolamines plays a decisive role in the reactions between these compounds and methyl 3-phenyl-3-chloro-2-oxopropionate, the products comprising 1,4-thiazine and 1,4-oxazane derivatives, respectively. Some of the reactions of these products were investigated.

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References

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center, Russian Academy of Sciences, Kazan

    V. A. Mamedov, V. N. Valeeva, F. G. Sibgatullina, L. A. Antokhina & I. A. Nuretdinov

Authors
  1. V. A. Mamedov
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  2. V. N. Valeeva
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  3. F. G. Sibgatullina
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  4. L. A. Antokhina
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  5. I. A. Nuretdinov
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 250–252, February, 1993.

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Mamedov, V.A., Valeeva, V.N., Sibgatullina, F.G. et al. Reaction of methyl 3-phenyl-3-chloro-2-oxopropionate with 2-mercapto- and 2-hydroxy-ethanolamines: The products and some of their transformations. Chem Heterocycl Compd 29, 219–221 (1993). https://doi.org/10.1007/BF00531670

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  • DOI: https://doi.org/10.1007/BF00531670

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