Enantioselective Ni–Al Bimetal-Catalyzed Cycloaddition of Cyclopropyl Ketones with Alkynes under Mild Conditions

Transition metal-catalyzed enantioselective intermolecular cycloaddition of cyclopropyl ketones and π-unsaturated compounds represents a long-standing challenge in the asymmetric C-C bond activation of cyclopropanes. Developed strategies rely on substrate modifications to mitigate racemization or to stabilize radical intermediates. In contrast, an efficient approach governed by transition-metal catalysts for general cyclopropyl ketones remains an elusive challenge. Herein, we report a highly active chiral diamine-phosphine oxide-ligated Ni-Al bimetallic catalyst that promotes enantioselective C-C cycloaddition under mild conditions. This system effectively suppresses product racemization and affords a diverse range of cyclopentyl ketones bearing a chiral α-tertiary carbon center in up to 99% yield and 99% ee.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-11
DOI
https://doi.org/10.1021/jacs.5c18087
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
1.87
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article

Enantioselective Ni–Al Bimetal-Catalyzed Cycloaddition of Cyclopropyl Ketones with Alkynes under Mild Conditions

Mengchun Ye, Hao-Rui Wang, Yinpeng Wang, Xing Gao et al.
2 citations
Journal of the American Chemical Society
Cyclopropane Reaction Mechanisms
1.87
article

Enantioselective Ni–Al Bimetal-Catalyzed Cycloaddition of Cyclopropyl Ketones with Alkynes under Mild Conditions

Mengchun Ye, Hao-Rui Wang, Yinpeng Wang, Xing Gao, Ligong Ji, Qi‐Lin Zhou, Yi Li, Yu Fu, Weiwei Xu
article en
2 citations

Abstract

Transition metal-catalyzed enantioselective intermolecular cycloaddition of cyclopropyl ketones and π-unsaturated compounds represents a long-standing challenge in the asymmetric C-C bond activation of cyclopropanes. Developed strategies rely on substrate modifications to mitigate racemization or to stabilize radical intermediates. In contrast, an efficient approach governed by transition-metal catalysts for general cyclopropyl ketones remains an elusive challenge. Herein, we report a highly active chiral diamine-phosphine oxide-ligated Ni-Al bimetallic catalyst that promotes enantioselective C-C cycloaddition under mild conditions. This system effectively suppresses product racemization and affords a diverse range of cyclopentyl ketones bearing a chiral α-tertiary carbon center in up to 99% yield and 99% ee.

Journal of the American Chemical SocietyVol. 147(51)
Nankai University (CN), Institute of Organic Chemistry (HU)
Openalex Percentile: Top 13%
Cyclopropane Reaction Mechanisms
1.87
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