Dual-Co/Ni-Catalyzed Radical Hydroarylation of 1,3-Enynes: Selective Access to Tetrasubstituted Allenes
Metal hydride hydrogen atom transfer (MHAT) has emerged as a powerful strategy for alkene hydrofunctionalization, offering exceptional control over regio- and chemoselectivity. However, conventional MHAT reactions with 1,3-enynes remain limited to the 1,2-addition pathway. Herein, we report a regioselective 1,4-hydroarylation of 1,3-enynes with various aryl halides enabled by dual cobalt and nickel catalysis. This transformation proceeds through cobalt(III)-H-mediated HAT to the 1,3-enynes, followed by nickel-catalyzed cross-coupling with aryl halides, delivering a wide range of tetrasubstituted allenes in good to excellent yields. This work expands the scope of Co(III)H-mediated radical hydrofunctionalization reactions and offers a modular strategy for constructing valuable, highly substituted allene building blocks.
Authors
- Qi Meng (ORCID: https://orcid.org/0000-0002-6356-3762)
- Zhimeng Song
- Qian Zhang (ORCID: https://orcid.org/0000-0002-3136-841X)
- Dongliang Zhang (ORCID: https://orcid.org/0000-0002-9441-6781)
- Ge Zhang (ORCID: https://orcid.org/0000-0002-4904-3330)
- Ting Yin (ORCID: https://orcid.org/0009-0006-1719-3197)
Institutions
- Northeast Normal University (CN)
- Chinese Academy of Sciences (CN)
- Shanghai Institute of Organic Chemistry (CN)
- Laboratoire de Synthèse Organique (FR)
- State Key Laboratory of Organometallic Chemistry
Publication Details
- Journal
- Organic Letters
- Published
- 2025-11-03
- DOI
- https://doi.org/10.1021/acs.orglett.5c03596
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00