Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C−H Functionalization

Giacomo Crisenza

doi:10.1002/anie.201808299

Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C−H Functionalization

Giacomo Crisenza

Organic Chemistry Group

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

Abstract

An IrI-system modified with a ferrocene derived bisphosphine ligand promotes α-selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd-catalyzed Fujiwara–Moritani reaction.

Original language	English
Pages (from-to)	14198-14202
Number of pages	5
Journal	Angewandte Chemie International Edition
Volume	57
Issue number	43
DOIs	https://doi.org/10.1002/anie.201808299
Publication status	Published - 31 Aug 2018

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title = "Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C−H Functionalization",

abstract = "An IrI-system modified with a ferrocene derived bisphosphine ligand promotes α-selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd-catalyzed Fujiwara–Moritani reaction.",

author = "Giacomo Crisenza",

year = "2018",

month = aug,

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doi = "10.1002/anie.201808299",

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AB - An IrI-system modified with a ferrocene derived bisphosphine ligand promotes α-selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd-catalyzed Fujiwara–Moritani reaction.

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DO - 10.1002/anie.201808299

M3 - Article

SN - 1433-7851

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JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

IS - 43

ER -

Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C−H Functionalization

Abstract

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