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Organoboron compounds Communication 20. N-substituted phenyldiaminoborons and B-phenylborazoles

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    The action of ethylamine, aniline or diethylamine on phenylboron dichloride leads to formation of N-substituted phenyldiaminoborons.

  2. 2.

    Heating of phenyldi(ethylamino)boron converts it into B-triphenyl-N-Uiethylborazole.

  3. 3.

    Heating of phenyldi(phenylamino)boron converts it into hexaphenylborazole.

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Literature cited

  1. R. Jones and C. Kinney, J. Am. Chem. Soc. 61, 1378 (1939).

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  2. B. M. Mikhailov and T. V. Kostroma, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1956; 1144.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry of the Academy of Sciences of the USSR, USSR

    V. M. Mikhailov & P. M. Aronovich

Authors
  1. V. M. Mikhailov
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  2. P. M. Aronovich
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Mikhailov, V.M., Aronovich, P.M. Organoboron compounds Communication 20. N-substituted phenyldiaminoborons and B-phenylborazoles. Russ Chem Bull 6, 1146–1148 (1957). https://doi.org/10.1007/BF01169396

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  • DOI: https://doi.org/10.1007/BF01169396

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