Cu(II)/I2 Mediated Synthesis of α-Keto Esters via Csp2 -Csp Bond Cleavage of 1,2-Alkynediones Followed by C-O Bond Formation

Abstract

Herein, we disclose an efficient method for the synthesis of α-keto esters through a copper(II)/iodine-mediated reaction. The transformation involves the selective cleavage of the C(sp²)–C(sp) bond of 1,2-alkynediones, which is subsequently followed by C–O bond formation with alcohols. This protocol offers a broad substrate scope, accommodating a wide range of substrates to furnish the desired α-keto esters in good yields.

Supplementary files

Article information

Article type
Communication
Submitted
22 Jan 2026
Accepted
02 Mar 2026
First published
03 Mar 2026

New J. Chem., 2026, Accepted Manuscript

Cu(II)/I2 Mediated Synthesis of α-Keto Esters via Csp2 -Csp Bond Cleavage of 1,2-Alkynediones Followed by C-O Bond Formation

A. Naveed and S. D. Sawant, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D6NJ00240D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements