Nickel-catalyzed arylative telomerization of isoprene

Developing new transformations of bulky chemicals is an important approach to expand the reaction boundary of current chemistry. Instead of traditional hydroarylation of dienes, we herein demonstrate a nickel-catalyzed arylative telomerization of isoprene with high chemo- and regioselectivities. By utilizing a bulky mono-phosphine ligand, a range of structurally diverse aryl substituted terpenes are created efficiently under redox-neutral conditions. Preliminary mechanistic studies suggest this telomerization proceeds through an oxidative cyclometallation of isoprene with Ni(0) species followed by arylation with organoboron reagents. Beyond enabling efficient isoprene transformation, this work also provides a supplementary approach for the monoterpenoids synthesis.

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Publication Details

Journal
Nature Communications
Published
2025-11-12
DOI
https://doi.org/10.1038/s41467-025-64893-y
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Nickel-catalyzed arylative telomerization of isoprene

Qing‐An Chen, Ding‐Wei Ji, Bingzhi Chen, Yan Liu et al.
1 citations
Nature Communications
Radical Photochemical Reactions
0.94
article

Nickel-catalyzed arylative telomerization of isoprene

Qing‐An Chen, Ding‐Wei Ji, Bingzhi Chen, Yan Liu, Xiaoyu Wang, Xueting Li, Su-Yang Xu
article en
1 citations

Abstract

Developing new transformations of bulky chemicals is an important approach to expand the reaction boundary of current chemistry. Instead of traditional hydroarylation of dienes, we herein demonstrate a nickel-catalyzed arylative telomerization of isoprene with high chemo- and regioselectivities. By utilizing a bulky mono-phosphine ligand, a range of structurally diverse aryl substituted terpenes are created efficiently under redox-neutral conditions. Preliminary mechanistic studies suggest this telomerization proceeds through an oxidative cyclometallation of isoprene with Ni(0) species followed by arylation with organoboron reagents. Beyond enabling efficient isoprene transformation, this work also provides a supplementary approach for the monoterpenoids synthesis.

Nature CommunicationsVol. 16(1)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 20%
Radical Photochemical Reactions
0.94
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