Development of N-centered radical scavengers that enables photoredox-catalyzed transition-metal-free radical amination of alkyl pinacol boronates
In recent years, amination of alkylboronates through ionic copper catalysis or boron-ate complex 1,2-metalation has been well established, but complementary radical processes remain less studied before. Herein, based on rational design, we develop several imine-type N-centered radical scavengers and apply them to the radical amination of alkylboronates. The reaction proceeds under mild photoredox-catalyzed transition-metal-free conditions and features excellent functional group tolerance. It also enables the preparation of a range of medicinally valuable amine derivatives from complex natural products. Further application of this reagent in C-H amination, deoxygenative amination, decarboxylative amination and three component trifluoromethylative/sulfonylative aminations are also realized. Further mechanistic studies and DFT calculations are conducted to provide detailed evidence for the mechanism.
Authors
- Jingjing Wu (ORCID: https://orcid.org/0000-0001-8401-065X)
- Jiaxin Lin (ORCID: https://orcid.org/0000-0002-4218-7059)
- Changlei Zhu (ORCID: https://orcid.org/0000-0003-2486-2513)
- Xiaoguang Bao (ORCID: https://orcid.org/0000-0001-7190-8866)
Institutions
- Shanghai Innovative Research Center of Traditional Chinese Medicine (CN)
- Soochow University (CN)
- Shanghai Institute of Organic Chemistry (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-04-04
- DOI
- https://doi.org/10.1038/s41467-025-58347-8
- Citations
- 8
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 7.49
Funders
- National Natural Science Foundation of China
- Shanghai Jiao Tong University
- Recruitment Program of Global Experts
- Fundamental Research Funds for the Central Universities