Artigo Acesso aberto Revisado por pares

Highly Reactive, Single‐Component Nickel Catalyst Precursor for Suzuki–Miyuara Cross‐Coupling of Heteroaryl Boronic Acids with Heteroaryl Halides

2012; Wiley; Volume: 51; Issue: 51 Linguagem: Inglês

10.1002/anie.201207428

ISSN

1521-3773

Autores

Shaozhong Ge, John F. Hartwig,

Tópico(s)

Organoboron and organosilicon chemistry

Resumo

One for all: The coupling of a range of nitrogen- and sulfur-containing heteroaryl halides with five-membered nitrogen-, oxygen-, and sulfur-containing heteroaryl boronic acids were achieved in high yields with only 0.5 mol % of the single-component nickel precatalyst [(dppf)NiCl(cinnamyl)] (dppf=1,1′-bis(diphenylphosphanyl)ferrocene). The reaction demonstrates good functional group compatibility, and is easily conducted on a large scale without a dry box. Detailed facts of importance to specialist readers are published as "Supporting Information". Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

Referência(s)