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

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.

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