Nickel(II)‐Catalyzed Oxidative Homocoupling of Terminal Alkynes

The homocoupling of terminal alkynes is a key approach for constructing 1,3‐diynes, typically relying on copper‐based bimetallic systems. Herein, a catalytic system is developed based on nickel chloride, using 1,10‐phenanthroline as the ligand and air as the oxidant, which successfully enables the homocoupling reactions of various terminal alkynes. This reaction is characterized by cheap and stable NiCl 2 as catalyst, mild reaction conditions, and excellent functional group compatibility, demonstrating great potential for practical applications.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-03-20
DOI
https://doi.org/10.1002/ejoc.202500207
Citations
3
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
2.81
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article

Nickel(II)‐Catalyzed Oxidative Homocoupling of Terminal Alkynes

Daofan Ma, Luying Cui, Guangwei Wang, Kai Yang et al.
3 citations
European Journal of Organic Chemistry
Catalytic Alkyne Reactions
2.81
article

Nickel(II)‐Catalyzed Oxidative Homocoupling of Terminal Alkynes

Daofan Ma, Luying Cui, Guangwei Wang, Kai Yang, Yingfan Yang, Xiangwei Ren
article en
3 citations

Abstract

The homocoupling of terminal alkynes is a key approach for constructing 1,3‐diynes, typically relying on copper‐based bimetallic systems. Herein, a catalytic system is developed based on nickel chloride, using 1,10‐phenanthroline as the ligand and air as the oxidant, which successfully enables the homocoupling reactions of various terminal alkynes. This reaction is characterized by cheap and stable NiCl 2 as catalyst, mild reaction conditions, and excellent functional group compatibility, demonstrating great potential for practical applications.

European Journal of Organic ChemistryVol. 28(22)
Tianjin University (CN)
Openalex Percentile: Top 11%
Catalytic Alkyne Reactions
2.81
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