Nickel-Catalyzed\nNarasaka–Heck Cyclization\nCarbonylation of Unsaturated Oxime Esters with Arylboronic Acids
The Narasaka–Heck reaction is one of the most\nstraightforward\nmethods for constructing pyrroline derivatives. Herein, we report\na novel nickel-catalyzed three-component carbonylation reaction, which\ncleverly realizes the continuous construction of C(sp<sup>3</sup>)–N\nbonds and C(sp<sup>3</sup>)–C(sp<sup>2</sup>) bonds and effectively\npromotes the synthesis of acyl-substituted pyrroline derivatives.\nFurthermore, this strategy not only expands the conversion pathway\nof γ,δ-unsaturated oxime esters but also provides a new\nmethod for the synthesis of nitrogen-containing heterocyclic compounds.
Publication Details
- Journal
- Figshare
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1021/acs.orglett.4c02647.s001
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00