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 Okt. 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

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