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A general and efficient FeCl3-catalyzed nucleophilic substitution of propargylic alcohols
Authors:Zhan Zhuang-ping  Yu Jing-liang  Liu Hui-juan  Cui Yuan-yuan  Yang Rui-feng  Yang Wen-zhen  Li Jun-ping
Affiliation:Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, P. R. China. zpzhan@xmu.edu.cn
Abstract:A general and efficient FeCl3-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.
Keywords:
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