Palladium/copper Co-catalyzed oxidative C-H/C-H carbonylation of diphenylamines: A way to access acridones

Jiangwei Wen; Shan Tang; Fan Zhang; Renyi Shi; Aiwen Lei

doi:10.1021/acs.orglett.6b03356

Palladium/copper Co-catalyzed oxidative C-H/C-H carbonylation of diphenylamines: A way to access acridones

Jiangwei Wen
, Shan Tang
, Fan Zhang
, Renyi Shi
, Aiwen Lei

Wuhan University
CAS - Lanzhou Institute of Chemical Physics

科研成果: 期刊稿件 › 文章 › 同行评审

63 引用（Scopus）

摘要

An efficient palladium/copper co-catalyzed oxidative double C(sp²)-H functionalization/carbonylation of diphenylamines for synthesis of acridones has been developed. This method utilizes readily available starting materials and mild reaction conditions. The protocol provides a simple, efficient, and atomeconomic way to access acridones. Notably, the present protocol has excellent functional group tolerance and application value.

源语言	英语
页（从-至）	94-97
页数	4
期刊	Organic Letters
卷	19
期	1
DOI	https://doi.org/10.1021/acs.orglett.6b03356
出版状态	已出版 - 6 1月 2017
已对外发布	是

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abstract = "An efficient palladium/copper co-catalyzed oxidative double C(sp2)-H functionalization/carbonylation of diphenylamines for synthesis of acridones has been developed. This method utilizes readily available starting materials and mild reaction conditions. The protocol provides a simple, efficient, and atomeconomic way to access acridones. Notably, the present protocol has excellent functional group tolerance and application value.",

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AU - Lei, Aiwen

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AB - An efficient palladium/copper co-catalyzed oxidative double C(sp2)-H functionalization/carbonylation of diphenylamines for synthesis of acridones has been developed. This method utilizes readily available starting materials and mild reaction conditions. The protocol provides a simple, efficient, and atomeconomic way to access acridones. Notably, the present protocol has excellent functional group tolerance and application value.

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Palladium/copper Co-catalyzed oxidative C-H/C-H carbonylation of diphenylamines: A way to access acridones

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