An improvement of nickel catalyst for cross-coupling reaction of arylboronic acids with aryl carbonates by using a ferrocenyl bisphosphine ligand

Ryoichi Kuwano, Ryosuke Shimizu

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Aryl carbonates work as electrophilic substrates for the SuzukiMiyaura reaction in the presence of the nickel catalyst, which is generated from [Ni(cod)2] and ferrocenyl bisphosphine, DCyPF. The nickel catalyst allowed the cross-coupling reaction of arylboronic acids with non-benzo-fused aryl carbonates as well as naphthyl substrates.

Original languageEnglish
Pages (from-to)913-915
Number of pages3
JournalChemistry Letters
Volume40
Issue number9
DOIs
Publication statusPublished - Sep 14 2011

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Carbonates
Nickel
Ligands
Catalysts
Acids
Substrates

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

An improvement of nickel catalyst for cross-coupling reaction of arylboronic acids with aryl carbonates by using a ferrocenyl bisphosphine ligand. / Kuwano, Ryoichi; Shimizu, Ryosuke.

In: Chemistry Letters, Vol. 40, No. 9, 14.09.2011, p. 913-915.

Research output: Contribution to journalArticle

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