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.
Authors
- Mengchun Ye (ORCID: https://orcid.org/0000-0002-2019-5365)
- Hao-Rui Wang (ORCID: https://orcid.org/0000-0002-9765-6203)
- Yinpeng Wang (ORCID: https://orcid.org/0000-0001-5370-0404)
- Xing Gao (ORCID: https://orcid.org/0000-0002-3279-2984)
- Ligong Ji (ORCID: https://orcid.org/0009-0000-6383-3008)
- Qi‐Lin Zhou (ORCID: https://orcid.org/0000-0002-4700-3765)
- Yi Li (ORCID: https://orcid.org/0000-0001-7252-0281)
- Yu Fu (ORCID: https://orcid.org/0000-0002-3000-0496)
- Weiwei Xu (ORCID: https://orcid.org/0009-0008-2373-9138)
Institutions
- Nankai University (CN)
- Institute of Organic Chemistry (HU)
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