Palladium-catalyzed N-arylation of bis(ortho-substituted aryl)amines: An efficient method for preparing sterically congested triarylamines

Ryoichi Kuwano; Yasuhiro Matsumoto; Takenori Shige; Takeshi Tanaka; Shinichi Soga; Yasuaki Hanasaki

doi:10.1055/s-0030-1258125

Palladium-catalyzed N-arylation of bis(ortho-substituted aryl)amines: An efficient method for preparing sterically congested triarylamines

Ryoichi Kuwano, Yasuhiro Matsumoto, Takenori Shige, Takeshi Tanaka, Shinichi Soga, Yasuaki Hanasaki

Multidisciplinary chemistry

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

10 Citations (Scopus)

Abstract

Bis(ortho-substituted aryl)amines were arylated on the nitrogen atom with various haloarenes in high yields using the palladium catalyst, which was generated from palladium(II) acetate and tri(tert-butyl)phosphine.

Original language	English
Pages (from-to)	1819-1824
Number of pages	6
Journal	Synlett
Issue number	12
DOIs	https://doi.org/10.1055/s-0030-1258125
Publication status	Published - Jul 28 2010

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1055/s-0030-1258125

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title = "Palladium-catalyzed N-arylation of bis(ortho-substituted aryl)amines: An efficient method for preparing sterically congested triarylamines",

abstract = "Bis(ortho-substituted aryl)amines were arylated on the nitrogen atom with various haloarenes in high yields using the palladium catalyst, which was generated from palladium(II) acetate and tri(tert-butyl)phosphine.",

author = "Ryoichi Kuwano and Yasuhiro Matsumoto and Takenori Shige and Takeshi Tanaka and Shinichi Soga and Yasuaki Hanasaki",

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T1 - Palladium-catalyzed N-arylation of bis(ortho-substituted aryl)amines

T2 - An efficient method for preparing sterically congested triarylamines

AU - Kuwano, Ryoichi

AU - Matsumoto, Yasuhiro

AU - Shige, Takenori

AU - Tanaka, Takeshi

AU - Soga, Shinichi

AU - Hanasaki, Yasuaki

PY - 2010/7/28

Y1 - 2010/7/28

N2 - Bis(ortho-substituted aryl)amines were arylated on the nitrogen atom with various haloarenes in high yields using the palladium catalyst, which was generated from palladium(II) acetate and tri(tert-butyl)phosphine.

AB - Bis(ortho-substituted aryl)amines were arylated on the nitrogen atom with various haloarenes in high yields using the palladium catalyst, which was generated from palladium(II) acetate and tri(tert-butyl)phosphine.

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IS - 12

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Palladium-catalyzed N-arylation of bis(ortho-substituted aryl)amines: An efficient method for preparing sterically congested triarylamines

Abstract

All Science Journal Classification (ASJC) codes

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