Issue 18, 2023

Electrochemically enabled C(sp3)–C(sp) cross-coupling of alkyl iodides, N-hydroxyphthalimide esters, and Katritzky salts with acetylenic sulfones

Abstract

An electrochemically enabled C(sp3)–C(sp) cross-coupling reaction is herein described for the synthesis of internal alkynes. This method is suitable not only for a diverse range of acetylenic sulfones, but also for a wide range of alkyl radical precursors, such as alkyl iodides, N-hydroxyphthalimide esters and Katritzky salts. This method can also be applied to vinylation, thioetherification, selenation and hydrogenation reactions. This reaction has a lot of significant advantages such as mild conditions, broad functional group tolerance, simple operation and easy purification and scale-up.

Graphical abstract: Electrochemically enabled C(sp3)–C(sp) cross-coupling of alkyl iodides, N-hydroxyphthalimide esters, and Katritzky salts with acetylenic sulfones

Supplementary files

Article information

Article type
Research Article
Submitted
06 Jun 2023
Accepted
05 Aug 2023
First published
07 Aug 2023

Org. Chem. Front., 2023,10, 4679-4686

Electrochemically enabled C(sp3)–C(sp) cross-coupling of alkyl iodides, N-hydroxyphthalimide esters, and Katritzky salts with acetylenic sulfones

J. Yin, X. Zhang, L. Zhao, M. Luo, L. Guo, C. Yang and W. Xia, Org. Chem. Front., 2023, 10, 4679 DOI: 10.1039/D3QO00844D

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