BiCl3-catalyzed propargylic substitution reaction of propargylic alcohols with C-, O-, S- and N-centered nucleophiles

被引：147
|
作者：
Zhan, Zhuang-ping [1 ]
Yang, Wen-zhen
Yang, Rui-feng
Yu, Jing-liang
Li, Jun-ping
Liu, Hui-juan
机构：
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Key Lab Chem Biol Fujian Prov, Xiamen 361005, Fujian, Peoples R China
来源：
CHEMICAL COMMUNICATIONS | 2006年 / 31期
关键词：
D O I：
10.1039/b606470a
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
A general and efficient BiCl3-catalyzed substitution reaction of propargylic alcohols with carbon and heteroatom-centered nucleophiles such as allyl trimethylsilane, alcohols, aromatic compounds, thiols and amides, leading to the construction of C - C, C - O, C - S and C - N bonds, has been developed.
引用
收藏
页码：3352 / 3354
页数：3
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