An Efficient and Recyclable Oxidation System for Pd(II)‐Catalyzed <i>Remote</i> ‐CH Alkenylation

The development of cheap and efficient oxidation strategies to replace excessive and expensive metal salt oxidants remains of great significance in the field of organic synthesis. Herein, we report an efficient and recyclable oxidation system for Pd(II)‐catalyzed remote ‐CH functionalization, in which the loading of the nonmetallic salt oxidant is reduced to 10 mol% and air serves as a co‐oxidant. The control experiments and XPS results demonstrated that Pd(0) can be repeatedly oxidized to generate active Pd(II) species; thus, with extended reaction time, the loading of Pd(OAc) 2 can be reduced to as low as 1 mol%.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-06-16
DOI
https://doi.org/10.1002/adsc.70600
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

An Efficient and Recyclable Oxidation System for Pd(II)‐Catalyzed Remote ‐CH Alkenylation

X X Li, Hua‐Jin Xu, Yi Hu, Ziyan Wang et al.
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

An Efficient and Recyclable Oxidation System for Pd(II)‐Catalyzed Remote ‐CH Alkenylation

X X Li, Hua‐Jin Xu, Yi Hu, Ziyan Wang, Chen‐Yu Lu, Ke‐Xu Ren, Long‐Jia Fan, Xu Yang
article en

Abstract

The development of cheap and efficient oxidation strategies to replace excessive and expensive metal salt oxidants remains of great significance in the field of organic synthesis. Herein, we report an efficient and recyclable oxidation system for Pd(II)‐catalyzed remote ‐CH functionalization, in which the loading of the nonmetallic salt oxidant is reduced to 10 mol% and air serves as a co‐oxidant. The control experiments and XPS results demonstrated that Pd(0) can be repeatedly oxidized to generate active Pd(II) species; thus, with extended reaction time, the loading of Pd(OAc) 2 can be reduced to as low as 1 mol%.

Advanced Synthesis & CatalysisVol. 368(12)
Nanjing Tech University (CN)
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
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