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

doi:10.1246/cl.2011.913

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

Multidisciplinary chemistry

Research output: Contribution to journal › Article › peer-review

38 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 language	English
Pages (from-to)	913-915
Number of pages	3
Journal	Chemistry Letters
Volume	40
Issue number	9
DOIs	https://doi.org/10.1246/cl.2011.913
Publication status	Published - 2011

All Science Journal Classification (ASJC) codes

Chemistry(all)

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10.1246/cl.2011.913

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

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.",

author = "Ryoichi Kuwano and Ryosuke Shimizu",

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journal = "Chemistry Letters",

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AU - Shimizu, Ryosuke

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Y1 - 2011

N2 - 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.

AB - 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.

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

Abstract

All Science Journal Classification (ASJC) codes

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