Issue 29, 2024

Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes

Abstract

Free radical initiated bicyclization of 1,6-enynes with chloralkanes, is achieved via selective activation of the C(sp3)–H bond of the chloralkane, resulting in diverse polychlorinated/chlorinated polyheterocycles. Two kinds of transformations and a scaled-up experiment were performed to test the synthetic importance of the organic chlorides. Finally, a range of radical inhibition operations and radical clock tests were explored to support the reaction process.

Graphical abstract: Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes

Supplementary files

Article information

Article type
Communication
Submitted
07 Feb 2024
Accepted
07 Mar 2024
First published
11 Mar 2024

Chem. Commun., 2024,60, 3938-3941

Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes

H. Zhou, L. Li, Q. Yan, J. Ma, Y. Wang, Y. Gao, Z. Liu and Z. Li, Chem. Commun., 2024, 60, 3938 DOI: 10.1039/D4CC00651H

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