期刊
SYNTHETIC COMMUNICATIONS
卷 51, 期 5, 页码 720-726出版社
TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2020.1850796
关键词
Aryldiazo sulfones; diaryl selenides; diselenides; photoredox reaction
资金
- Soonchunhyang University Research Fund
- Basic Science Research Program through the National Research Foundation of Korea [NRF2019R1F1A1059821]
A photcatalyst-free photoredox synthesis of diaryl selenides has been developed by coupling reaction of diselenides with aryldiazo sulfones. The reaction was accelerated under visible light irradiation without using a photocatalyst or photosensitizer. This approach facilitates the synthesis of diaryl selendes with a wide range of functional group tolerance.
A photcatalyst-free photoredox synthesis of diaryl selenides has been developed by coupling reaction of diselenides with aryldiazo sulfones. The reaction was accelerated under visible light irradiation without using a photocatalyst or photosensitizer. This approach facilitates the synthesis of diaryl selendes with a wide range of functional group tolerance.
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