Issue 98, 2024

Nickel-catalyzed silylation of aryl thianthrenium salts with silylzinc pivalates

Abstract

A nickel-catalyzed C–S silylation of aryl thianthrenium salts with salt-stabilized silylzinc pivalates is disclosed, thus allowing us to rapidly incorporate silyl motifs into aromatics in a site- and chemoselective fashion. This method is distinguished by its ample scope and facile derivatizations of the aryl silanes for increasing functional molecular complexity. Moreover, modular installation of silyl groups into pharmaceutically active molecules provides a new platform for the synthesis of sila-drugs.

Graphical abstract: Nickel-catalyzed silylation of aryl thianthrenium salts with silylzinc pivalates

Supplementary files

Article information

Article type
Communication
Submitted
12 Oct 2024
Accepted
15 Nov 2024
First published
15 Nov 2024

Chem. Commun., 2024,60, 14593-14596

Nickel-catalyzed silylation of aryl thianthrenium salts with silylzinc pivalates

Z. Tian, Z. Cui, Y. Hu, J. Zhang, L. Ruan and J. Li, Chem. Commun., 2024, 60, 14593 DOI: 10.1039/D4CC05395H

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