Oxidative C-H homodimerization of phenylacetamides

Didier G. Pintori; Michael F. Greaney

doi:10.1021/ol202212f

Oxidative C-H homodimerization of phenylacetamides

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

Abstract

A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates. © 2011 American Chemical Society.

Original language	English
Pages (from-to)	5713-5715
Number of pages	2
Journal	Organic Letters
Volume	13
Issue number	21
DOIs	https://doi.org/10.1021/ol202212f
Publication status	Published - 4 Nov 2011

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title = "Oxidative C-H homodimerization of phenylacetamides",

abstract = "A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates. {\textcopyright} 2011 American Chemical Society.",

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AU - Pintori, Didier G.

AU - Greaney, Michael F.

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N2 - A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates. © 2011 American Chemical Society.

AB - A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates. © 2011 American Chemical Society.

U2 - 10.1021/ol202212f

DO - 10.1021/ol202212f

M3 - Article

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SP - 5713

EP - 5715

JO - Organic Letters

JF - Organic Letters

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Oxidative C-H homodimerization of phenylacetamides

Abstract

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