Nickel-Catalyzed Silylation of Aryl Thianthrenium Salts with Silylzinc Pivalates DOI

Tian Zhenfeng,

Zhili Cui,

Ying Hu

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

A modular nickel-catalyzed silylation of aryl thianthrenium salts with salt-stabilized silylzinc pivalates is disclosed, thus providing an expedient route to rapidly incorporate silyl motifs into aromatics.

Language: Английский

Pyrrolylsulfonium salts: stable, accessible and versatile pseudohalides for Stille couplings DOI Creative Commons
Jodie L. Hann, Catherine L. Lyall, Gabriele Kociok‐Köhn

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Pyrroles functionalised with a thianthrenium or diphenylsulfonium group undergo Stille couplings aryl alkynyl stannanes in good yields, avoiding the issues of instability that can hamper use analogous pyrrolyl halides.

Language: Английский

Citations

0

Nickel-Catalyzed Silylation of Aryl Thianthrenium Salts with Silylzinc Pivalates DOI

Tian Zhenfeng,

Zhili Cui,

Ying Hu

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

A modular nickel-catalyzed silylation of aryl thianthrenium salts with salt-stabilized silylzinc pivalates is disclosed, thus providing an expedient route to rapidly incorporate silyl motifs into aromatics.

Language: Английский

Citations

0