Progress on Iridium-Catalyzed Hydrosilylation of Alkenes and Alkynes

被引:28
|
作者
Gao, Weiwei [1 ]
Ding, Shengtao [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
来源
SYNTHESIS-STUTTGART | 2020年 / 52卷 / 23期
基金
中国国家自然科学基金;
关键词
OXIDATIVE ADDITION; TERMINAL ALKYNES; STEREOSELECTIVE HYDROSILYLATION; DEHYDROGENATIVE SILYLATION; HOMOGENEOUS CATALYSIS; CRYSTAL-STRUCTURES; CARBENE COMPLEXES; SILICON HYDRIDES; DONOR LIGAND; REACTIVITY;
D O I
10.1055/s-0040-1707239
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hydrosilylation of multiple carbon-carbon bonds is a well-known process for the construction of organosilicon compounds. Nowadays, precious metal catalysts, especially platinum complexes, still occupy dominant positions in such processes. However, one important member of the precious metal family, iridium, is less used in this field. As early research mainly focused on developing stable and effective iridium catalysts, recent advances have disclosed the specific efficiency of simple iridium catalytic systems in the synthesis of functional organo-silicon compounds. This short review summarizes the utilization of iridium complexes for the hydrosilylation of alkenes and alkynes, with an emphasis on the recent advances published in the last decade.
引用
收藏
页码:3549 / 3563
页数:15
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