Skip to main content
SpringerLink
Log in

Chemistry of acetals

Communication 9. Mechanism of the trimerization of acrolein acetal

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

Summary

The structure of the cyclic product formed by the action of boron trifluoride on acrolein diethyl acetal is proved. This results confirm the scheme proposed earlier for the trimerization of the acetal.

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

Literature cited

  1. S. S. Yufit and V. F. Kueherov, Izv. AN SSSR. Otd. khim. n. 1522(1961).

  2. J. Mathieu and J. Valls Uspekhi khimii28, 1915 (1959).

    Google Scholar 

Download references

Author information

Authors and Affiliations

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

    S. S. Yufit & V. F. Kucherov

Authors
  1. S. S. Yufit
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. V. F. Kucherov
    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

Yufit, S.S., Kucherov, V.F. Chemistry of acetals. Russ Chem Bull 10, 2040–2041 (1961). https://doi.org/10.1007/BF01182950

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01182950

Keywords

Search

Navigation