Intermolecular Iodofluoroalkylation of Unactivated Alkynes and Alkenes Mediated by Manganese Catalysts

被引:30
|
作者
Ji, Yun-Xing [1 ]
Wang, Lu-Jun [1 ]
Guo, Wei-Si [2 ]
Bi, Qirui [1 ]
Zhang, Bo [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, State Key Lab Base Ecochem Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Radicals; Iodofluoroalkylation; Manganese; Visible light; Synthetic methods; RADICAL-ADDITION; ATOM-TRANSFER; DIMANGANESE DECACARBONYL; PERFLUOROALKYL IODIDES; FLEXIBLE APPROACH; TRIFLUOROMETHYLATION; FLUORINE; IODOPERFLUOROALKYLATION; FLUOROALKYLATION; HYDROSILYLATION;
D O I
10.1002/adsc.201901556
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An approach for iodofluoroalkylation of unactivated alkynes and alkenes facilitated by an earth-abundant and inexpensive manganese catalyst, Mn-2(CO)(10), is reported. This protocol employs visible light as the energy input and shows a wide substrate scope and high functional-group compatibility. A variety of synthetically useful fluoroalkylated alkyl and alkenyl iodides can be prepared in moderate to excellent yields. The reaction features high efficiency, operational simplicity, scalability, as well as excellent chemo-, regio-, and E/Z selectivities.
引用
收藏
页码:1131 / 1137
页数:7
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