Cu-Catalyzed Three-Component Carbofunctionalization of 1,3-Dienes

The carboamination of 1,3-dienes provides direct and efficient access to allylic amines in a step-economical fashion. Herein, we disclose a three-component 1,3-diene carboamination reaction that provides modular access to a multitude of allylic amines. A representative scope of 1,3-dienes, activated alkyl halides, and amines is demonstrated to serve as components for this reaction, with yields ranging from up to 96%. High regioisomeric ratios are observed with both substituted and unsubstituted diene derivatives for either 1,2- or 1,4-carboamination (≥12:1). Mechanistic investigations demonstrate that the reaction proceeds via atom transfer radical addition to the diene, affording an isolable allylic halide intermediate. The scope was expanded to a general carbofunctionalization, by adding an exogenous O, S, P, or C nucleophile and base to the reaction upon formation of the allylic halide, in a two-step, one-pot process.

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Publication Details

Journal
ACS Catalysis
Published
2025-10-03
DOI
https://doi.org/10.1021/acscatal.5c04439
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81
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article

Cu-Catalyzed Three-Component Carbofunctionalization of 1,3-Dienes

Samuel N. Gockel, John A. Little, Matthew Barnett, Kami L. Hull et al.
3 citations
ACS Catalysis
Catalytic C–H Functionalization Methods
2.81
article

Cu-Catalyzed Three-Component Carbofunctionalization of 1,3-Dienes

Samuel N. Gockel, John A. Little, Matthew Barnett, Kami L. Hull, An T. Ho, Travis L. Buchanan, Andrei G. Popov, Vincent R. Viviani, Kira Q. McMahon
article en
3 citations

Abstract

The carboamination of 1,3-dienes provides direct and efficient access to allylic amines in a step-economical fashion. Herein, we disclose a three-component 1,3-diene carboamination reaction that provides modular access to a multitude of allylic amines. A representative scope of 1,3-dienes, activated alkyl halides, and amines is demonstrated to serve as components for this reaction, with yields ranging from up to 96%. High regioisomeric ratios are observed with both substituted and unsubstituted diene derivatives for either 1,2- or 1,4-carboamination (≥12:1). Mechanistic investigations demonstrate that the reaction proceeds via atom transfer radical addition to the diene, affording an isolable allylic halide intermediate. The scope was expanded to a general carbofunctionalization, by adding an exogenous O, S, P, or C nucleophile and base to the reaction upon formation of the allylic halide, in a two-step, one-pot process.

ACS CatalysisVol. 15(20)
The University of Texas at Austin (US)
Openalex Percentile: Top 9%
Catalytic C–H Functionalization Methods
2.81
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