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Radical arylation of thiourea and N,N'-diphenylthiourea using N-nitrosoacetanilides

  • B. V. Kopylova
  • I. I. Kandror
  • R. Kh. Freidlina
Brief Communications

Conclusions

  1. 1.

    The radical arylation of thiourea and N,N'-diphenylthiourea using N-nitrosoacetanilide and N-nitro-so(a cet-p-toluidide) as the source of aryl radicals gave the N-aryl-N,N'-diphenylisothiuronium compounds, which were isolated as the picrates.

     
  2. 2.

    The N-nitrosoacetanilides are more efficient arylating agents for N,N'-diphenylthiourea than phenylazotriphenylmethane.

     

Keywords

Thiourea Picrate Radical Arylation Diphenylthiourea 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Literature cited

  1. 1.
    I. I. Kandror, B. V. Kopylova, and R. Kh. Freidlina, Tetrahedron, Lett.,1978, 3087.Google Scholar
  2. 2.
    B. V. Kopylova, I. I. Kandror, and R. Kh. Freidlina, Dokl. Akad. Nauk SSSR,243, 1197 (1978).Google Scholar
  3. 3.
    D. C. Nonhebel and J. C. Walton, Free-Radical Chemistry, Cambridge Univ. Press (1973).Google Scholar
  4. 4.
    J. I. G. Cadogan, R. M. Paton, and C. Thomson, Chem. Communs.,1969, 614; 1970, 229.Google Scholar
  5. 5.
    H. France, I. M. Heilbron, and D. H. Hey, J. Chem. Soc.,1940, 369.Google Scholar

Copyright information

© Plenum Publishing Corporation 1979

Authors and Affiliations

  • B. V. Kopylova
    • 1
  • I. I. Kandror
    • 1
  • R. Kh. Freidlina
    • 1
  1. 1.Institute of Heteroorganic CompoundsAcademy of Sciences of the USSRMoscow

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