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.

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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
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article

Nickel-Catalyzed Regioselective Hydroalkynylation of Nitrogen Heterocycle-Tethered Unactivated Alkenes

Yuanqing Xu, L. Li, Pengfei Zhang, Shengnan Jin et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Nickel-Catalyzed Regioselective Hydroalkynylation of Nitrogen Heterocycle-Tethered Unactivated Alkenes

Yuanqing Xu, L. Li, Pengfei Zhang, Shengnan Jin, Hua-Feng Cao, Zhong-Yan Cao, Yi-Hui Li
article en

Abstract

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.

Organic LettersVol. 28(6)
Henan University (CN), Green Chemistry (PL), East China Normal University (CN)
Openalex Percentile: Top 71%
Catalytic C–H Functionalization Methods
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