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.

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Journal
Organic Letters
Published
2025-11-03
DOI
https://doi.org/10.1021/acs.orglett.5c03596
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Dual-Co/Ni-Catalyzed Radical Hydroarylation of 1,3-Enynes: Selective Access to Tetrasubstituted Allenes

Qi Meng, Zhimeng Song, Qian Zhang, Dongliang Zhang et al.
Organic Letters
Radical Photochemical Reactions
article

Dual-Co/Ni-Catalyzed Radical Hydroarylation of 1,3-Enynes: Selective Access to Tetrasubstituted Allenes

Qi Meng, Zhimeng Song, Qian Zhang, Dongliang Zhang, Ge Zhang, Ting Yin
article en

Abstract

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.

Organic LettersVol. 27(45)
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
Openalex Percentile: Top 75%
Radical Photochemical Reactions
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Dual-Co/Ni-Catalyzed Radical Hydroarylation of 1,3-Enynes: Selective Access to Tetrasubstituted Allenes — Qi Meng, Zhimeng Song, et al. · Organic Letters (2025) | TGRS Research Map | TGRS