Visible light-induced cobalt-catalyzed 1,3-diphosphination of alkenes

被引:5
|
作者
Shan, Wenlong [1 ]
Wang, Zemin [1 ]
Gao, Chenxia [1 ]
Li, Xiaowei [1 ]
Zhuang, Wenli [1 ]
Liu, Ruihua [1 ]
Shi, Cong [1 ]
Qin, Hongyun [1 ]
Li, Xiangqian [1 ]
Shi, Dayong [1 ,2 ]
机构
[1] Shandong Univ, State Key Lab Microbial Technol, Qingdao 266237, Shandong, Peoples R China
[2] Qingdao Marine Sci & Technol Ctr, Lab Marine Drugs & Bioprod, Qingdao 266237, Shandong, Peoples R China
关键词
PHOSPHINE-OXIDE; ACCEPTORLESS DEHYDROGENATION; LIGANDS; COMPLEXES; 1,3-DIFUNCTIONALIZATION; HYDROPHOSPHINATION; OXIDATION;
D O I
10.1039/d4gc02737j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
1,3-Difunctionalization of alkenes, as a novel route for the modern development of alkene transformations, has drawn significant research attention in recent years. Herein, we disclose a novel cobalt-catalyzed radical 1,3-diphosphination of alkenes, which enables straightforward access to 1,3-diphosphine skeleton compounds under mild conditions without additional oxidants and photosensitizers. This transformation features excellent functional group tolerance, operational simplicity, and high atom economy, and is amenable for late-stage functionalization of complex molecule skeletons. Preliminary bioactivity studies reveal that these valuable 1,3-diphosphine products show potential antitumor activity. A novel cobalt-catalyzed radical 1,3-diphosphination of alkenes was developed, which enables straightforward access to 1,3-diphosphine skeleton compounds under mild conditions.
引用
收藏
页码:9749 / 9756
页数:8
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