Palladium‐Catalyzed Cross‐Coupling of Ynones with Aryl Bromides Enabled by C(O)‐C(sp) Bond Activation

Transition metal-catalyzed cross-coupling reactions have emerged as one of the most attractive methods in organic synthesis in recent years. However, due to the inertness of C-C bonds, C-C bond activation enabled cross-coupling reactions are far less common. In this work, the first example of palladium-catalyzed cross-coupling of ynones with aryl bromides for the synthesis of diarylacetylenes via C(O)-C(sp) bond activation was described. The reaction exhibited directing group-free unstrained C-C bond activation, wide substrate scope, and good functional group tolerance. Preliminary mechanistic studies suggested that a cross-electrophile coupling reaction pathway might be involved rather than the conventional nucleophilic addition/β-C elimination pathway.

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Journal
Chemistry - An Asian Journal
Published
2025-02-11
DOI
https://doi.org/10.1002/asia.202401768
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Palladium‐Catalyzed Cross‐Coupling of Ynones with Aryl Bromides Enabled by C(O)‐C(sp) Bond Activation

Yanqiong Zhang, Zewei Jin, Xiangge Zhou, Yang Long et al.
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
article

Palladium‐Catalyzed Cross‐Coupling of Ynones with Aryl Bromides Enabled by C(O)‐C(sp) Bond Activation

Yanqiong Zhang, Zewei Jin, Xiangge Zhou, Yang Long, Qiang Li, Qinyue Tao
article en

Abstract

Transition metal-catalyzed cross-coupling reactions have emerged as one of the most attractive methods in organic synthesis in recent years. However, due to the inertness of C-C bonds, C-C bond activation enabled cross-coupling reactions are far less common. In this work, the first example of palladium-catalyzed cross-coupling of ynones with aryl bromides for the synthesis of diarylacetylenes via C(O)-C(sp) bond activation was described. The reaction exhibited directing group-free unstrained C-C bond activation, wide substrate scope, and good functional group tolerance. Preliminary mechanistic studies suggested that a cross-electrophile coupling reaction pathway might be involved rather than the conventional nucleophilic addition/β-C elimination pathway.

Chemistry - An Asian JournalVol. 20(10)
North Sichuan Medical University (CN), Sichuan University (CN)
Openalex Percentile: Top 98%
Catalytic C–H Functionalization Methods
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