Copper-Catalyzed Oxidative α-Double Bond Construction in α-Amino Carbonyl Compounds via Homocoupling with Arylamine Release

Herein, we present a copper-catalyzed method for oxidative α-double bond formation in α-amino ketone compounds using DTBP as the oxidant. This process, involving homocoupling of α-amino radicals and arylamine release, efficiently produces a series of enaminone skeletons. The strategy has a broad substrate scope and functional group tolerance. In particular, arylamines bearing electron-rich substituents exhibit a pronounced reactivity. This approach facilitates the synthesis of diverse enaminones, enabling the efficient construction of nitrogen-containing heterocycles.

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Publication Details

Journal
Organic Letters
Published
2024-09-17
DOI
https://doi.org/10.1021/acs.orglett.4c03044
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.75

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article

Copper-Catalyzed Oxidative α-Double Bond Construction in α-Amino Carbonyl Compounds via Homocoupling with Arylamine Release

Yiting Zhu, Huan Wang, Ming Chen, Yan Jiang et al.
3 citations
Organic Letters
Catalytic C–H Functionalization Methods
0.75
article

Copper-Catalyzed Oxidative α-Double Bond Construction in α-Amino Carbonyl Compounds via Homocoupling with Arylamine Release

Yiting Zhu, Huan Wang, Ming Chen, Yan Jiang, Yibin Wang, Sen Yang, Yan-fang Zhan
article en
3 citations

Abstract

Herein, we present a copper-catalyzed method for oxidative α-double bond formation in α-amino ketone compounds using DTBP as the oxidant. This process, involving homocoupling of α-amino radicals and arylamine release, efficiently produces a series of enaminone skeletons. The strategy has a broad substrate scope and functional group tolerance. In particular, arylamines bearing electron-rich substituents exhibit a pronounced reactivity. This approach facilitates the synthesis of diverse enaminones, enabling the efficient construction of nitrogen-containing heterocycles.

Organic LettersVol. 26(38)
Changzhou University (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Changzhou University
Openalex Percentile: Top 32%
Catalytic C–H Functionalization Methods
0.75
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