Aliphatic Hydrosilanes via Nickel-Catalyzed Reductive Csp3-Si Coupling of Primary Alkyl Bromides and Chlorohydrosilanes

被引:1
作者
Wei, Xiao-Xue [1 ]
Zhao, Zhen-Zhen [1 ]
Pang, Xiaobo [1 ]
Shu, Xing-Zhong [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem SKLAOC, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
OXIDATIVE-ADDITION; HYDROSILYLATION; HALIDES;
D O I
10.1021/acs.orglett.4c01897
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reductive C-Si coupling of chlorosilanes offers efficient access to organosilanes, but its potential for constructing aliphatic ones remains largely unexplored. This manuscript presents a nickel-catalyzed Csp(3)-Si coupling reaction of unactivated alkyl-Br and R2Si(H)Cl. This work establishes a new approach for synthesizing highly functionalized aliphatic hydrosilanes from readily available chemical feedstocks. The reaction is easily scalable and can accommodate various functional groups, including carboxylic acids, which are usually incompatible with basic conditions.
引用
收藏
页码:6125 / 6129
页数:5
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