Skip to main content
Log in

Regiospecific cleavage of 1,3-dioxanes by organoaluminum compounds

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Organoaluminum compounds react with 4-methyl-2-phenyl-1,3-dioxane with cleavage of the O1-C2 bond to give monoethers with a primary alcohol group.

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. L. N. Zakharkin and I. M. Khorina, Izv. Akad. Nauk SSSR, Ser. Khim., 6, 2255 (1959).

    Google Scholar 

  2. W. Zajac and K. Byrne, J. Org. Chem., 38., 384 (1973).

    Google Scholar 

  3. B. A. Trofimov and S. E. Korostova, Usp. Khim., 44, 75 (1975).

    Google Scholar 

  4. Takahiro Kosokawa, Chem. Commun., 1245 (1983).

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1036–1037, August, 1985.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Volkov, A.A., Zlot-skii, S.S., Kravets, É.K. et al. Regiospecific cleavage of 1,3-dioxanes by organoaluminum compounds. Chem Heterocycl Compd 21, 861–863 (1985). https://doi.org/10.1007/BF00519809

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00519809

Keywords

Navigation