γ-Ketoacid Derivatives

Ernest Wenkert Department of Chemistry, Indiana University Bloomington, Indiana, 47401

C. Allen McPherson Department of Chemistry, Indiana University Bloomington, Indiana, 47401

E. L. Sanchez Department of Chemistry, Indiana University Bloomington, Indiana, 47401

R. L. Webb Department of Chemistry, Indiana University Bloomington, Indiana, 47401

Abstract

It has been shown recently that β-oxycyclopropanecarboxylic esters, prepared by the cyclopropanation of enol ethers with diazoacetic esters, are cleaved easily on acid hydrolysis.^3,4 The following discussion illustrates further examples of this two-step procedure of γ-ketoacid synthesis and related reactions.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

γ-Ketoacid Derivatives

Information for

Open access

Opportunities

Help and information

γ-Ketoacid Derivatives

Abstract

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date

Your download is now in progress and you may close this window

Login or register to access this feature