Skip to main content
SpringerLink
Log in

Formation of dihydroperoxide derivatives during the oxidation of cyclohexene and tetralin by dioxygen

  • Published:
Reaction Kinetics and Catalysis Letters Aims and scope Submit manuscript

Abstract

1H- and13C-NMR investigations revealed that prolonged oxidation of unsubstituted cyclohexene and tetralin, containing symmetrical and weak allylic and benzylic CH bonds, results in the formation of both mono- and dihydroperoxo derivatives.

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

Access this article

Log in via an institution

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

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. B. Yeomans, D. P. Young:J. Chem. Soc., 2288 (1958).

  2. K. Asakura, N. Tanaka, Sh. Matsumura, S. Yoshikawa:Chemistry Letters, 1997 (1989).

Download references

Author information

Authors and Affiliations

  1. Institute of Pharmaceutical Chemistry, A. Szent-Györgyi Medical University, Szeged, Hungary

    György Dombi & Ferenc Evanics

  2. Institute of Inorganic and Analytical Chemistry, A. József University, P.O. Box 44, 6701, Szeged, Hungary

    Károly Jáky & László J. Csányi

Authors
  1. György Dombi
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Ferenc Evanics
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Károly Jáky
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. László J. Csányi
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dombi, G., Evanics, F., Jáky, K. et al. Formation of dihydroperoxide derivatives during the oxidation of cyclohexene and tetralin by dioxygen. React Kinet Catal Lett 63, 241–244 (1998). https://doi.org/10.1007/BF02475394

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02475394

Keywords

Search

Navigation