Skip to main content
Log in

N,N-Bis(tert-butyldimethylsilyloxy)aminobenzene as a new synthetic equivalent of nitrosobenzene

  • Letters to the Editor
  • Published:
Russian Chemical Bulletin Aims and scope

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.

References

  1. The Chemistry of Amino, Nitroso, Nitro and Related Groups, Ed. S. Patai, Wiley, Chichester, 1996, Parts 1 and 2.

    Google Scholar 

  2. A. D. Dilman, A. A. Tishkov, I. M. Lyapkalo, S. L. Ioffe, Yu. A. Strelenko, and V. A. Tartakovsky,Synthesis 1998, 181.

  3. A. D. Dilman, I. M. Lyapkalo, S. L. Joffe, Yu. A. Strelenko, and V. A. Tartakovsky,Synthesis, 1999, 1767.

  4. A. J. Bloom and J. M. Mellor,J. Chem. Soc., Perkin Trans. 1, 1987, 2737.

  5. I. M. Lyapkalo, S. L. Ioffe, Yu. A. Strelenko, and V. A. Tartakovsky,Izv. Akad. Nauk, Ser. Khim., 1996, 901 [Russ. Chem. Bull., 1996,45, 856 (Engl. Transl.)].

    Google Scholar 

  6. T. Severin, R. Shmitz, and H. Temme,Chem. Ber., 1964,97, 467.

    CAS  Google Scholar 

  7. V. F. Rudchenko,Chem. Rev., 1993,93, 725.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

I-Nitro-1,3-cyclohexadiene (2) was synthesized by the nitration of 1,3-cyclohexadiene according to the previously described procedure.

Published inIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1659–1660, September, 2000.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dilman, A.D., Lyapkalo, I.M., Belyakov, P.A. et al. N,N-Bis(tert-butyldimethylsilyloxy)aminobenzene as a new synthetic equivalent of nitrosobenzene. Russ Chem Bull 49, 1649–1650 (2000). https://doi.org/10.1007/BF02495178

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02495178

Keywords

Navigation