Photoredox-catalyzed hydrogenation of alkenes assisted by an in situ generated PPh3(OH) radical and acetic acid

被引:2
|
作者
Xie, Zhen-Zhen [1 ]
Zheng, Yu [1 ,2 ]
Liao, Zi-Hao [1 ]
Yuan, Chu-Ping [1 ]
Li, Ming-Zhi [1 ]
Deng, Ke-Yi [1 ]
Xiang, Hao-Yue [1 ]
Chen, Kai [1 ]
Yang, Hua [1 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 15期
基金
中国国家自然科学基金;
关键词
COUPLED ELECTRON-TRANSFER; OXIDATIVE ADDITION; H BONDS; WATER; ACTIVATION; AMMONIA; REDUCTION; COMPLEXES; OLEFINS;
D O I
10.1039/d4qo00661e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, a practical, mild and convenient strategy was disclosed for the hydrogenation of alkenes under photocatalytic conditions through a HAT/protonation process. A combination of experimental and computational studies suggested that water was activated by a phosphine radical cation to generate the critical intermediate, the PR3(OH) radical, which acted as a "free" hydrogen atom to facilitate the initial HAT process.
引用
收藏
页码:4187 / 4193
页数:7
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