Issue 43, 2023

Light-mediated sulfonyl-iodination of ynamides and internal alkynes

Abstract

We synthesized tetrasubstituted olefins regioselectively and stereoselectively from ynamides and internal alkynes with sulfonyl iodides under blue LEDs in few minutes. The key features are being metal-free, easy to handle, simple, broad in scope, and environmentally friendly. Furthermore, a gram-scale experiment was conducted, and the synthesized corresponding sulfonyl-iodinated products were smoothly altered into various other products.

Graphical abstract: Light-mediated sulfonyl-iodination of ynamides and internal alkynes

Supplementary files

Article information

Article type
Communication
Submitted
22 Feb 2023
Accepted
26 Apr 2023
First published
26 Apr 2023

Chem. Commun., 2023,59, 6584-6587

Light-mediated sulfonyl-iodination of ynamides and internal alkynes

M. R. Mutra, J. Li and J. Wang, Chem. Commun., 2023, 59, 6584 DOI: 10.1039/D3CC00842H

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