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
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article

Nickel-CatalyzedEnantioselective Arylative Cyclizationof Alkyne-Oxime Ethers: Access to Chiral Hydroxylamine Ethers

Figshare
Radical Photochemical Reactions
article

Nickel-CatalyzedEnantioselective Arylative Cyclizationof Alkyne-Oxime Ethers: Access to Chiral Hydroxylamine Ethers

article en

Abstract

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.

Figshare
Openalex Percentile: Top 63%
Radical Photochemical Reactions
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