Lewis Acid-Mediated Deoxygenative Synthesis of Trivalent Sterically Hindered Phosphines from Aldehydes
The efficient synthesis of trisubstituted trivalent phosphines remains challenging. Herein, we report a novel approach for rapid construction of these compounds from aldehydes under Lewis acid-mediated conditions. By using sterically hindered disubstituted phosphines, aldehydes can undergo a deoxygenative reaction to afford trivalent phosphorus compounds. This modular and practical method is characterized by operational simplicity, a broad substrate scope, and excellent functional group tolerance, which holds great potential for applications in organic synthesis.
Authors
- Tao Xu (ORCID: https://orcid.org/0000-0002-4228-4895)
- Wei Zhong (ORCID: https://orcid.org/0000-0002-2880-8736)
- Xiaoqiang Wu (ORCID: https://orcid.org/0009-0004-1797-8766)
- Abuduwaili Alimu
Institutions
- Tongji University (CN)
- Jiaxing University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-05-29
- DOI
- https://doi.org/10.1021/acs.orglett.5c01581
- Citations
- 4
- Primary Topic
- Organophosphorus compounds synthesis
- Type
- article
- Field-Weighted Citation Impact
- 3.74
Funders
- National Natural Science Foundation of China
- Jiaxing University
- Fundamental Research Funds for the Central Universities