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Copper-catalyzed rearrangement of vinyl oxiranes.

Journal of the American Chemical Society (2006-12-15)
Lindsay A Batory, Christine E McInnis, Jon T Njardarson
ABSTRACT

A novel copper-catalyzed vinyl oxirane ring expansion protocol has been developed. A wide range of vinyl oxiranes can be rearranged to 2,5-dihydrofurans in excellent yields in the presence of electrophilic copper(II) acetylacetonate catalysts. Regioisomeric vinyl oxiranes can be converted to a single dihydrofuran product using these conditions. This method uses low catalyst loadings (0.5-5 mol %), has good tolerance of substitution patterns, and can be done in the absence of solvent.

MATERIALS
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Brand
Product Description

Sigma-Aldrich
3,4-Epoxy-1-butene, 98%