Thioether-Facilitated Iridium-Catalyzed Hydrosilylation of Steric 1,1-Disubstituted Olefins

被引:3
作者
Zhang, Xueyan [1 ]
Gao, Chengpeng [1 ]
Xie, Xingze [1 ]
Liu, Yuanqi [1 ]
Ding, Shengtao [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, North Third Ring Rd 15, Beijing 100029, Peoples R China
[2] Fudan Univ, State Key Lab Mol Engn Polymers, 220 Handan Rd, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Iridium; Thioether; Hydrosilylation; Olefin; Polymerization; ALKENYL CARBONYL-COMPOUNDS; STEREOSELECTIVE HYDROSILYLATION; ASYMMETRIC HYDROSILYLATION; INTERNAL THIOALKYNES; UNACTIVATED ALKENES; ALLYLIC AMINES; METAL; HYDROACYLATION; ALKYNES; IRON;
D O I
10.1002/ejoc.201901513
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
One facile and efficient strategy for the hydrosilylation of steric 1,1-disubstituted terminal alkenes is demonstrated. Investigations on substrate scope and control experiments revealed the necessity of thioether in promoting this process under a simple iridium catalytic system. This convenient and feasible method is expected to be useful in the synthesis of sulfur-containing organosilicon polymers with different side-chains.
引用
收藏
页码:556 / 560
页数:5
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