Skip to main content
Log in

Chemistry of acetals

Communication 14. Preparation of polyenic aldehydic esters, their acetals, and symmetrical and unsymmetrical polyenic dicarboxylic esters

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

Summary

A new general method was developed for the synthesis of symmetrical and unsymmetrical polyenic dicarboxylic acids with even and odd numbers of double bonds, starting with glyoxal monoacetal and fumaraldehyde monoacetal.

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. V. F. Kucherov, B. G. Kovalev, G. A. Kogan, and L. A. Yanovskaya, Dokl. AN SSSR138, 1115 (1961).

    Google Scholar 

  2. B. G. Kovalev, L. A. Yanovskaya, V. F. Kucherov, and G. A. Kogan, Izv. AN SSSR. Otd. khim. n. 145 (1963).

  3. A. Cose and H. Johnson, J. Amer. Chem. Soc.80, 1504 (1958).

    Google Scholar 

  4. H. Fischer and E. Baer, Helv. chim. acta18, 514 (1935).

    Google Scholar 

  5. S. M. Makin and N. I. Telegina, Zh. obshch. khimii32, 1104 (1962).

    Google Scholar 

  6. L. A. Yanovskaya, B. A. Rudenko, V. F. Kucherov, R. N. Stepanova, and G. A. Kogan, Izv. AN SSSR. Otd. khim. n. 2189 (1962).

  7. K. Lunde and L. Zechmeister, J. Amer. Chem. Soc.77, 1647 (1955).

    Google Scholar 

  8. A. Wohl and F. Frank, Ber.35, 1906 (1902).

    Google Scholar 

  9. K. Zeile and H. Heusner, Chem. Ber.90, 1869 (1957).

    Google Scholar 

  10. U.S. Pat. 2116016; Chem. Abstrs.32, 4607 (1938).

  11. A. Funke and P. Karrer, Helv. chim. acta32, 1016 (1949).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yanovskaya, L.A., Stepanova, R.N., Kogan, G.A. et al. Chemistry of acetals. Russ Chem Bull 12, 774–780 (1963). https://doi.org/10.1007/BF01134723

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01134723

Keywords

Navigation