Three-Component 1,2-Carboalkynylation of Alkenes Via Cooperative Nickel/Photoredox Catalysis

A photoredox/nickel dual catalytic system was developed for the three-component 1,2-carboalkynylation of alkenes. This redox-neutral protocol enables the efficient and divergent synthesis of aliphatic alkynes in high yields with excellent regioselectivity, using readily available starting materials. The resulting adducts can be readily transformed into terminal alkynes, facilitating diverse downstream transformations. Mechanistic studies were performed to elucidate the preferred pathway of this alkene difunctionalization process.

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Publication Details

Journal
Organic Letters
Published
2025-03-24
DOI
https://doi.org/10.1021/acs.orglett.5c00471
Citations
3
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
2.81

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article

Three-Component 1,2-Carboalkynylation of Alkenes Via Cooperative Nickel/Photoredox Catalysis

Meiqi Zhu, Lanfen Wang, Dingyi Wang, L. L. Niu et al.
3 citations
Organic Letters
Synthesis of Indole Derivatives
2.81
article

Three-Component 1,2-Carboalkynylation of Alkenes Via Cooperative Nickel/Photoredox Catalysis

Meiqi Zhu, Lanfen Wang, Dingyi Wang, L. L. Niu, Shengzhou Jin
article en
3 citations

Abstract

A photoredox/nickel dual catalytic system was developed for the three-component 1,2-carboalkynylation of alkenes. This redox-neutral protocol enables the efficient and divergent synthesis of aliphatic alkynes in high yields with excellent regioselectivity, using readily available starting materials. The resulting adducts can be readily transformed into terminal alkynes, facilitating diverse downstream transformations. Mechanistic studies were performed to elucidate the preferred pathway of this alkene difunctionalization process.

Organic LettersVol. 27(13)
College of Medical Sciences (NP), CAS Key Laboratory of Urban Pollutant Conversion (CN), Hubei Normal University (CN), Universidad del Noreste (MX), Nanjing University (CN)
National Natural Science Foundation of China, Northeastern University, Zhejiang Normal University, Natural Science Foundation of Liaoning Province
Openalex Percentile: Top 11%
Synthesis of Indole Derivatives
2.81
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