Copper-Catalyzed Borylative Methylation of Alkyl Iodides with CO as the C1 Source: Advantaged by Faster Reaction of CuH over CuBpin

被引:16
作者
Wu, Fu-Peng [1 ,2 ]
Wu, Xiao-Feng [1 ,2 ]
机构
[1] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China
关键词
alkyl iodides; borylmethylation; carbonylation; copper boryl; copper hydride; HYDROBORATION; HALIDES;
D O I
10.1002/anie.202102197
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CuH and CuBpin are versatile catalysts and intermediates in organic chemistry. However, studies that involve both CuH and CuBpin in the same reaction is still rarely reported due to their high reactivity. Now, a study on CuH- and CuBpin-catalyzed borylative methylation of alkyl iodides with CO as the C1 source is reported. Various one carbon prolongated alkyl boranes (RCH(2)Bpin and RCH(Bpin)(2)) were produced in moderate to good yields from the corresponding alkyl iodides (RI). In this cooperative system, CuH reacts with alkyl iodide faster than CuBpin.
引用
收藏
页码:11730 / 11734
页数:5
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