Skip to main content
Log in

New hydrogenating systems for ionic hydrogenation

  • Organic Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

Ethyldichlorosilane and alkylisopropylbenzenes in the presence of aluminum halides are hydride ion donors in the ionic hydrogenation of olefins, alkyl halides, and trifluoroacetate derivatives of alcohols.

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.

Similar content being viewed by others

Literature cited

  1. D. N. Kursanov, Z. N. Parnes, and N. M. Loim, Synthesis, 633 (1974).

  2. D. N. Kursanov, Z. N. Parnes, M. I. Kalinkin, and N. M. Loim, Ionic Hydrogenation [in Russian], Izd. Khimiya, Moscow (1979). p. 85.

    Google Scholar 

  3. V. N. Ipatieff, H. Pines, and R. C. Olberg, J. Am. Chem. Soc.,70, 2123 (1948).

    Google Scholar 

  4. N. Zelinsky, Chem. Ber.,34, 2877 (1901).

    Google Scholar 

  5. M. Mousseron, G. Manon, and G. Combes, Bull. Soc. Chim. Fr., 399 (1949).

  6. V. N. Setkina, D. N. Kursanov, and E. V. Bykova, Izv. Akad. Nauk SSSR, Otd. Khim. Nauk, 1367 (1962).

  7. Huang-Minlon, J. Am. Chem. Soc.,68, 2487 (1946).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1322–1326, June, 1982.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bolestova, G.I., Latypova, F.M., Parnes, Z.N. et al. New hydrogenating systems for ionic hydrogenation. Russ Chem Bull 31, 1179–1182 (1982). https://doi.org/10.1007/BF00955973

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00955973

Keywords

Navigation