Nickel-Catalyzed Regioselective Hydroalkynylation of Nitrogen Heterocycle-Tethered Unactivated Alkenes
The hydroalkynylation of unactivated olefins presents a significant challenge, primarily due to difficulties in controlling the regioselectivity and competing reaction pathways. Herein, we report a practical NiH-catalyzed γ-selective hydroalkynylation of unactivated alkenes tethered to nitrogen heterocycles performed under external ligand-free conditions. This method provides structurally diverse alkynes in good to excellent yields with high regioselectivity and broad functional group tolerance. The synthetic utility of this approach is demonstrated through facile transformations of the products into other valuable scaffolds. Additionally, regioselectivity can be switched to the β position by employing DPPB/(TolSO<sub>3</sub>)<sub>2</sub>Ni·6H<sub>2</sub>O as a catalyst. Preliminary mechanistic studies offer insight into the reaction pathway.
Authors
- Yuanqing Xu
- L. Li
- Pengfei Zhang (ORCID: https://orcid.org/0000-0001-9859-0237)
- Shengnan Jin
- Hua-Feng Cao
- Zhong-Yan Cao
- Yi-Hui Li
Institutions
- Henan University (CN)
- Green Chemistry (PL)
- East China Normal University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-01-30
- DOI
- https://doi.org/10.1021/acs.orglett.5c05211
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00