Diverse Synthesis of Alkenylsilanes via Pd-Catalyzed Alkenyl C-H Silylation

被引:11
作者
Ye, Zi-Hang [1 ,2 ]
Gou, Fei-Hu [2 ]
Wu, Yichen [2 ]
Li, Chuan-Ying [1 ]
Wang, Peng [2 ,3 ,4 ]
机构
[1] Zhejiang Sci Tech Univ, Dept Chem, Key Lab Surface & Interface Sci Polymer Mat Zhejia, Hangzhou 310018, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Energy Regulat Mat, Shanghai 200032, Peoples R China
[4] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, Hangzhou 310024, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CROSS-COUPLING REACTIONS; VINYLSILANES; ARYL; HYDROSILYLATION; PALLADACYCLES; ARYLATION; OXIDATION; OLEFINS; VINYL;
D O I
10.1021/acs.orglett.3c00633
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here, we disclose a general approach for the diverse synthesis of alkenylsilanes in a highly efficient, stereoselective, and atom-economic manner by leveraging the palladium-catalyzed disilylation reaction of 2-bromostyrene derivatives with hexame-thyldisilane, which is suitable for the preparation of a series of disubstituted, trisubstituted, and tetrasubstituted alkenylsilanes. Furthermore, the resulting tetrasubstituted alkenylsilanes could be readily transformed into the corresponding diarylated benzosiloles, which have been proven to be a potential AIE material and a fluorene material.
引用
收藏
页码:2145 / 2150
页数:6
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