Facilitating Gold Redox Catalysis with Electrochemistry: An Efficient Chemical-Oxidant-Free Approach

被引:68
|
作者
Ye, Xiaohan [1 ]
Zhao, Pengyi [2 ]
Zhang, Shuyao [1 ]
Zhang, Yanbin [3 ]
Wang, Qilin [1 ]
Shan, Chuan [1 ]
Wojtas, Lukasz [1 ]
Guo, Hao [3 ]
Chen, Hao [2 ]
Shi, Xiaodong [1 ]
机构
[1] Univ S Florida, Dept Chem, Tampa, FL 33620 USA
[2] New Jersey Inst Technol, Dept Chem & Environm Sci, Newark, NJ 07102 USA
[3] Fudan Univ, Dept Chem, Shanghai 200438, Peoples R China
关键词
1,3-diynes; electrochemistry; gold; oxidative coupling; redox catalysis; OXIDATIVE COUPLING REACTIONS; TERMINAL ALKYNES; SELECTIVE SYNTHESIS; REACTIVITY;
D O I
10.1002/anie.201909082
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Due to the high oxidation potential between Au-I and Au-III, gold redox catalysis requires at least stoichiometric amounts of a strong oxidant. We herein report the first example of an electrochemical approach in promoting gold-catalyzed oxidative coupling of terminal alkynes. Oxidation of Au-I to Au-III was successfully achieved through anode oxidation, which enabled facile access to either symmetrical or unsymmetrical conjugated diynes through homo-coupling or cross-coupling. This report extends the reaction scope of this transformation to substrates that are not compatible with strong chemical oxidants and potentiates the versatility of gold redox chemistry through the utilization of electrochemical oxidative conditions.
引用
收藏
页码:17226 / 17230
页数:5
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