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 journalArticlepeer-review

28 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

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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