Skip to main content
Log in

Ethoxycarboxylation of methylpyridines

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The ethyl esters of pyridine carboxylic acids were obtained by reaction of the ethoxycarbonyl radical with methyl-substituted pyridines. A mechanism is proposed for the carboxylation reaction.

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. F. Minisci, Synthesis, 1, 1 (1973).

    Google Scholar 

  2. R. Bernardi, T. Caronna, R. Galli, F. Minisci, and M. Perchinunno, Tetrahedron Lett., 645 (1973).

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 224–225, February, 1976.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Min, R.S., Aksenov, V.S. Ethoxycarboxylation of methylpyridines. Chem Heterocycl Compd 12, 194–195 (1976). https://doi.org/10.1007/BF00523968

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00523968

Keywords

Navigation