Stereoselective construction of an anti-β-alkoxy ether by Ireland–Claisen rearrangement for medium-ring ether synthesis

Abstract

The asymmetric synthesis of an acyclic anti-β-alkoxy ether was achieved by the Ireland–Claisen rearrangement of Z-3-alkoxy-2-propenyl glycolate ester, prepared from Garner’s aldehyde, a glycolic acid derivative, and ethynyl N, N-diisopropylcarbamate. The resulting acyclic ether was facilely converted to seven- and eight-membered cyclic ethers via processes involving ring-closing olefin metatheses.