Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Study on the Reaction of Isoxazolidine-3-thione with Anhydrous Aluminum CHloride; Synthesis and Mechanism of the Formation of N-(p-Biphenylyl)-3-aryl-3-phenylpropanothioamides

  • Published : 1995.04.20
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Abstract

The reaction of 5-aryl-2-phenylisoxazolidine-3-thiones with more than 3 equivalents of anhydrous aluminum chloride in benzene at reflux gave N-(p-biphenylyl)-3-aryl-3-phenylpropanothioamides in good yields. It is conceived that the propanothioamides are formed via the formation of the corresponding N-phenyl-3-aryl-3-phenylpropanothiohydroxamic acids.

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References

  1. Synthesis Seo, Y.;Mun, K. R.;Kim, K.
  2. Advanced organic Chemistry(4th ed.) March, J.
  3. Chief v.Ⅴ Organic Reactions Berliner, E.;Adams, R.(ed.)
  4. Heterocycles v.22 Capozzi, G.;Grasso, A.;Romeo, G.
  5. Advanced Organic chemistry(4th ed.) March, J.
  6. J. Am. Chem. Soc. v.109 Fishbein, J. C.;McClelland, R. a.