Skip to main content
Log in

Conclusions

In contrast to aminoboranes that contain a tricoordination boron atom, 9-amino-m-carboranes exhibit a reactivity that is close to that of aliphatic and aromatic amines: They are smoothly acylated, alkylated, form substituted ureas with phenyl isocyanate and Schiff bases with aldehydes, and enter into the carbylamine reaction.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Literature cited

  1. V. N. Kalinin, Usp. Khim.,49, 2188 (1980).

    Google Scholar 

  2. L. I. Zakharkin, V. N. Kalinin, and V. V. Gedymin, J. Organomet. Chem.,16, 371 (1969).

    Google Scholar 

  3. V. N. Kalinin, N. I. Kobel'kova, and L. I. Zakharkin, Zh. Obshch. Khim.,50, 919 (1980).

    Google Scholar 

  4. J. J. Bozell and L. S. Hegedus, J. Org. Chem.,46, 2561 (1981).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1200–1202, May, 1983.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kalinin, V.N., Kobel'kova, N.I., Krasnokutskaya, E.V. et al. Some reactions of 9-amino-m-carborane. Russ Chem Bull 32, 1084–1086 (1983). https://doi.org/10.1007/BF00956177

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00956177

Keywords

Navigation