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Stereoselective Synthesis of (–)-Heliannuol E by α-Selective Propargyl Substitution
Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry
AbstractThis paper describes a stereoselective synthesis of (–)-heliannuol E through intramolecular cyclization of a phenol mesylate. The introduction of the aromatic group was achieved by α-selective propargyl substitution of a propargylic phosphate.doi:10.1055/s-0040-1719844 fatcat:dprfbj73jnht7cwsnkhfiyo6rm