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Iodoetherification of unactivated alkenes catalyzed by diphosphine palladium(II) complexes
Authors:Todd A. Doroski
Affiliation:Department of Chemistry and Biochemistry, University of North Carolina Wilmington, Dobo Hall, Wilmington, NC 28403, USA
Abstract:A palladium-catalyzed intramolecular iodoetherification of alkenes is reported. The reaction is efficient and highly diastereoselective for disubstituted alkenes. The tether length between the alcohol and alkene can be varied to produce tetrahydrofuran and tetrahydropyran rings. Diphosphine palladium(II) salts are highly active catalysts enabling future studies on the development of an enantioselective process.
Keywords:Iodination   Palladium catalysis   Tetrahydrofurans   Tetrahydropyrans
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