Recent Advances in Transition Metal-Catalyzed C-Si Bond Cleavage of Silacyclobutanes

被引:19
作者
Liu Min [1 ]
Qi Liping [1 ]
Zhao Dongbing [1 ]
机构
[1] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
transition metal catalysis; silacyclobutane; C-Si bond cleavage; H SILYLATION; ORGANOSILICON COMPOUNDS; 8-MEMBERED SILACYCLES; ACID-CHLORIDES; RING EXPANSION; PALLADIUM; EXCHANGE; DESYMMETRIZATION; CYCLOADDITION; ANNULATION;
D O I
10.6023/cjoc202306019
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Due to the widespread application of various organosilicon compounds in material science, electronic devices and pharmaceutical research, it is of great significance to develop green and efficient synthetic methods for diverse silicon-containing molecules. Silacyclobutane is an important kind of small-membered rings, which exhibits unique reactivities under transition metal catalysis to cleave the C-Si bond driven by the inherent ring strain and Lewis acidity. The resulting Si-M species can then be transformed into various organosilicon compounds. Herein, the recent advances of Pd, Rh, and Ni-catalyzed C-Si bond cleavage reactions of silacyclobutanes are summarized in detail, and the mechanism and development tendency of such reactions are briefly discussed.
引用
收藏
页码:3508 / 3525
页数:18
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