A general and efficient FeCl3-catalyzed nucleophilic substitution of propargylic alcohols.

J Org Chem

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.

Published: October 2006

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.

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http://dx.doi.org/10.1021/jo061234pDOI Listing

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