Silicon-based cross-coupling reaction: an environmentally benign version

被引:643
作者
Nakao, Yoshiaki [1 ]
Hiyama, Tamejiro [2 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Chem Mat, Kyoto 6158510, Japan
[2] Chuo Univ, Res & Dev Initiat, Bunkyo Ku, Tokyo 1128551, Japan
关键词
CARBON BOND FORMATION; ORGANIC HALIDES; ARYL BROMIDES; ORGANOSILICON COMPOUNDS; SODIUM-HYDROXIDE; ROOM-TEMPERATURE; BIARYL SYNTHESIS; PALLADIUM; CHLORIDES; IODIDES;
D O I
10.1039/c1cs15122c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Much attention has been paid to the cross-coupling reaction of organosilicon compounds due to their stability, non-toxicity, and natural abundance of silicon. In addition, the silicon-based cross-coupling has many advantages over other cross-coupling protocols. Successful examples of the silicon-based cross-coupling reaction are reviewed, focusing especially on the advances made in the last decade. Having had a number of highly effective palladium catalysts developed mainly for other cross-coupling reactions, the development of the silicon-based protocol owes heavily to the design of organosilicon reagents which effectively undergo transmetalation, a key elemental step of the silicon-based cross-coupling reaction. This tutorial review thus classifies various organosilicon reagents depending on substituents on silicon and surveys their cross-coupling reactions with various electrophiles.
引用
收藏
页码:4893 / 4901
页数:9
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