Nickel-CatalyzedEnantioselective Arylative Cyclizationof Alkyne-Oxime Ethers: Access to Chiral Hydroxylamine Ethers
Chiral hydroxylamines serve as essential scaffolds in modern organic synthesis and are of significant interest in drug discovery. Although asymmetric hydrogenation of oximes is well-established, the development of metal-catalyzed asymmetric oxime ethers addition reactions, especially those employing earth-abundant metal catalysts, has remained limited. Herein, we report the first nickel-catalyzed asymmetric addition of oxime ethers, providing chiral hydroxylamine ethers in moderate to excellent yields (up to 94%) with generally excellent enantioselectivities (up to 99% ee). Moreover, this method enables the construction of chiral hydroxylamine ethers bearing multiple contiguous stereocenters via a substrate-controlled diastereoselective process.
Publication Details
- Journal
- Figshare
- Published
- 2025-03-27
- DOI
- https://doi.org/10.1021/acs.orglett.5c00539.s001
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00