BiCl3-Catalyzed propargylic substitution reaction of propargylic alcohols with C-, O-, S- and N-centered nucleophiles
- 27 June 2006
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 37 (31), 3352-3354
- https://doi.org/10.1039/b606470a
Abstract
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.Keywords
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