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.
Authors
- Samuel N. Gockel (ORCID: https://orcid.org/0000-0003-3584-066X)
- John A. Little (ORCID: https://orcid.org/0000-0001-5896-138X)
- Matthew Barnett (ORCID: https://orcid.org/0000-0001-8287-9044)
- Kami L. Hull (ORCID: https://orcid.org/0000-0003-3102-2686)
- An T. Ho
- Travis L. Buchanan (ORCID: https://orcid.org/0000-0001-9038-9790)
- Andrei G. Popov (ORCID: https://orcid.org/0009-0001-7385-4838)
- Vincent R. Viviani
- Kira Q. McMahon
Institutions
- The University of Texas at Austin (US)
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