Palladium nanoparticles for aerobic oxidative Heck arylation of alkenes

Abstract Herein, we report a palladium nanoparticle-catalyzed aerobic oxidative Heck arylation of alkenes with aryl boronic acids, yielding a range of (E)-β-aryl acrylates and (E)-stilbene derivatives. This reaction uses molecular oxygen as the terminal oxidant, requiring no base or additional oxidants. The catalyst displays notable tolerance to unprotected amide groups, surpassing conventional strategies.

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Publication Details

Journal
Chemistry Letters
Published
2025-03-27
DOI
https://doi.org/10.1093/chemle/upaf068
Citations
2
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
1.87
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article

Palladium nanoparticles for aerobic oxidative Heck arylation of alkenes

Yasushi Obora, Kazuki Tabaru, Takeyuki Suzuki, Haruka Nishimura
2 citations
Chemistry Letters
Catalytic Cross-Coupling Reactions
1.87
article

Palladium nanoparticles for aerobic oxidative Heck arylation of alkenes

Yasushi Obora, Kazuki Tabaru, Takeyuki Suzuki, Haruka Nishimura
article en
2 citations

Abstract

Abstract Herein, we report a palladium nanoparticle-catalyzed aerobic oxidative Heck arylation of alkenes with aryl boronic acids, yielding a range of (E)-β-aryl acrylates and (E)-stilbene derivatives. This reaction uses molecular oxygen as the terminal oxidant, requiring no base or additional oxidants. The catalyst displays notable tolerance to unprotected amide groups, surpassing conventional strategies.

Chemistry LettersVol. 54(4)
Kansai University (JP)
Openalex Percentile: Top 17%
Catalytic Cross-Coupling Reactions
1.87
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