Functional Group Transposition Enabled by Palladium and Photo Dual Catalysis
Menghua Xu1, Chengjun Wu1, Ming Chen1
1Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24061, United States.
Journal of the American Chemical Society
|October 27, 2025
Summary
This study introduces a novel functional group transposition reaction. Palladium and photo dual catalysis enable the conversion of iodoarenes to arylboronates, creating new molecular structures.
Area of Science:
- Synthetic organic chemistry
- Medicinal chemistry
- Catalysis
Background:
- Molecular structure modification is crucial for synthetic and medicinal chemistry.
- Functional group transposition offers a novel strategy for molecular editing.
- Existing methods may require significant changes to synthesis routes.
Purpose of the Study:
- To disclose an unusual functional group transposition reaction.
- To develop a method for accessing novel chemical entities.
- To enable molecular editing without altering established synthesis routes.
Main Methods:
- Utilizing palladium and photo dual catalysis.
- Employing a radical-induced process.
- Investigating the transposition between iodo and boryl groups.
Main Results:
- Successfully converted iodoarenes appended with an alkylboronate group.
- Achieved the formation of arylboronates appended with an alkyl iodide.
- Demonstrated an unusual functional group transposition.
Conclusions:
- The developed method provides a powerful strategy for molecular editing.
- This reaction expands the toolkit for synthetic organic chemists.
- The dual catalysis approach offers a unique pathway for functional group interconversion.
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