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Reaction of benzoyl and trichloroacetyl isocyanates with quinoline

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Conclusions

Trichoroacetyl isocyanate under the influence of quinoline forms ditrichloroacetylcarbodiimide, which adds to the C=N bond of quinoline on the type of a 2+4-cycloaddition. Benzoyl isocyanate under the influence of quinoline forms the dimer.

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Literature cited

  1. 1.

    R. Huisgen, K. Herbig, and M. Morikawa, Chem. Ber.,100, 1107 (1967).

  2. 2.

    R. Huisgen, M. Morikawa, K. Herbig, and E. Brunn, Chem. Ber.,100, 1094 (1967).

  3. 3.

    B. A. Arbuzov, N. N. Zobova, and F. B. Balabanova, Izv. Akad. Nauk SSSR, Ser. Khim., 1570 (1970).

  4. 4.

    T. W. Campbell, J. I. Monagle, and V. S. Foldi, J. Am. Chem. Soc.,84, 3673 (1962).

  5. 5.

    L. A. McGrew, W. Sweeny, T. W. Campbell, and V. S. Foldi, J. Org. Chem.,29, 3002 (1964).

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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No.2, pp.456–458, February, 1973.

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Arbuzov, B.A., Zobova, N.N., Balabanova, F.B. et al. Reaction of benzoyl and trichloroacetyl isocyanates with quinoline. Russ Chem Bull 22, 440–441 (1973). https://doi.org/10.1007/BF00851013

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Keywords

  • Quinoline
  • Isocyanate
  • Benzoyl
  • Trichloroacetyl
  • Trichloroacetyl Isocyanate