Photoinduced, Redox-Neutral Decyanative and Defluorinative Phosphination of (Hetero)Arenes

Triarylphosphines play a crucial role in organic synthesis as versatile components serving as ligands, catalysts, and reactants. This study introduces a metal-free, visible-light-induced method for the cross-coupling of cyanopyridines or polyfluoroarenes with diarylphosphines. This approach facilitates the formation of C(sp<sup>2</sup>)-P bonds through redox-neutral decyanative or defluorinative process, enabling the convenient synthesis of diverse triarylphosphines.

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Publication Details

Journal
Organic Letters
Published
2024-09-16
DOI
https://doi.org/10.1021/acs.orglett.4c03049
Citations
5
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.25

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article

Photoinduced, Redox-Neutral Decyanative and Defluorinative Phosphination of (Hetero)Arenes

Lan‐Gui Xie, Meizhong Tang, Shenlin Huang, Yating Wang et al.
5 citations
Organic Letters
Radical Photochemical Reactions
1.25
article

Photoinduced, Redox-Neutral Decyanative and Defluorinative Phosphination of (Hetero)Arenes

Lan‐Gui Xie, Meizhong Tang, Shenlin Huang, Yating Wang, Conghui Wang
article en
5 citations

Abstract

Triarylphosphines play a crucial role in organic synthesis as versatile components serving as ligands, catalysts, and reactants. This study introduces a metal-free, visible-light-induced method for the cross-coupling of cyanopyridines or polyfluoroarenes with diarylphosphines. This approach facilitates the formation of C(sp<sup>2</sup>)-P bonds through redox-neutral decyanative or defluorinative process, enabling the convenient synthesis of diverse triarylphosphines.

Organic LettersVol. 26(38)
Nanjing Normal University (CN), Nanjing Forestry University (CN)
National Key Research and Development Program of China
Clean water and sanitation
Openalex Percentile: Top 23%
Radical Photochemical Reactions
1.25
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