Copper-catalyzed four-component reaction of alkenes, Togni's reagent, amines and CO2: stereoselective synthesis of (Z)-enol carbamates

被引:7
|
作者
Wang, Lu [1 ]
Wang, Pan [2 ]
Guo, Tianzuo [1 ]
Xiong, Wenfang [1 ]
Kang, Bangxiong [1 ]
Qi, Chaorong [1 ]
Luo, Gen [2 ,3 ,4 ]
Luo, Yi [2 ]
Jiang, Huanfeng [1 ]
机构
[1] South China Univ Technol, Key Lab Funct Mol Engn Guangdong Prov, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China
[2] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[3] Anhui Univ, Inst Phys Sci, Hefei 230601, Peoples R China
[4] Anhui Univ, Inst Informat Technol, Hefei 230601, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2021年 / 8卷 / 08期
基金
中国国家自然科学基金;
关键词
CARBON-DIOXIDE; FUNCTIONALIZATION; DIETHYLAMINE; ACTIVATION; CHEMICALS; ALKYNES; ACCESS;
D O I
10.1039/d0qo01607a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A copper-catalyzed four-component reaction of alkenes, Togni's reagent, amines and CO2 has been successfully developed for the first time, which provides an efficient and straightforward method for the synthesis of a range of stereodefined (Z)-enol carbamates. Easily available starting materials and cheap catalyst, high stereoselectivity, good functional group tolerance and broad substrate scope are the features of the transformation. The mechanistic aspects of this transformation have been elucidated by control experiments and density functional theory calculations.
引用
收藏
页码:1851 / 1857
页数:7
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