Site-selective desaturation of C(sp3)-C(sp3) bonds via photoinduced ruthenium catalysis

被引:2
|
作者
Wang, Chuanyong [1 ]
Xing, Zhongqiu [1 ]
Ge, Qiangqiang [1 ]
Yu, Yangyang [1 ]
Wang, Minyan [2 ]
Duan, Wei-Liang [1 ]
机构
[1] Yangzhou Univ, Coll Chem & Chem Engn, 180 Siwangting Rd, Yangzhou 225002, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
VISIBLE-LIGHT PHOTOCATALYSIS; LATE-STAGE FUNCTIONALIZATION; C-H FUNCTIONALIZATION; PHOTOREDOX CATALYSIS; ELECTRON-TRANSFER; ALKYLATION; ARYLATION; RADICALS; HETEROARYLATION; DEHYDROGENATION;
D O I
10.1039/d2qo00332e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Ruthenium(ii) photocatalysis has emerged as one of the most advanced tools in modern synthetic chemistry, but its catalytic mode is generally limited to single-electron transfer and triplet energy transfer events. Herein, we introduce a dual function ruthenium(ii) catalytic system by intertwining single-electron transfer with its innate transition metal catalytic activity. This approach allows for the efficient desaturation of various amide and alcohol derivatives in a highly regio- and stereoselective fashion under mild conditions. Further, an interesting radical-triggered cascade 1,5-HAT/Heck-type coupling could also be achieved through this photoinduced Ru catalysis.
引用
收藏
页码:4316 / 4327
页数:12
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