Three-Component Copper-Catalyzed 1,4-Carboamination of 1,3-Dienes

We herein report a highly selective copper-catalyzed three-component 1,4-carboamination of 1,3-dienes with activated alkyl bromides and amines, providing a general and practical route to functionalized allylamine derivatives. This operationally simple protocol demonstrates a broad substrate scope (>45 examples), good functional group tolerance, and high <i>E</i>/<i>Z</i> ratio selectivity. The synthetic utility of this method was further exemplified by its successful application in the late-stage functionalization of various bioactive molecules.

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Publication Details

Journal
Organic Letters
Published
2025-10-17
DOI
https://doi.org/10.1021/acs.orglett.5c03922
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

Three-Component Copper-Catalyzed 1,4-Carboamination of 1,3-Dienes

Suhua Shi, Zonglei Guo, Yanyan Li, Hui Wang et al.
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Three-Component Copper-Catalyzed 1,4-Carboamination of 1,3-Dienes

Suhua Shi, Zonglei Guo, Yanyan Li, Hui Wang, Chengdong Wang
article en

Abstract

We herein report a highly selective copper-catalyzed three-component 1,4-carboamination of 1,3-dienes with activated alkyl bromides and amines, providing a general and practical route to functionalized allylamine derivatives. This operationally simple protocol demonstrates a broad substrate scope (>45 examples), good functional group tolerance, and high <i>E</i>/<i>Z</i> ratio selectivity. The synthetic utility of this method was further exemplified by its successful application in the late-stage functionalization of various bioactive molecules.

Organic LettersVol. 27(43)
Qingdao University of Science and Technology (CN)
Openalex Percentile: Top 75%
Asymmetric Hydrogenation and Catalysis
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