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Stereoselective Synthesis of Quaternary Carbons via the Dianionic Ireland–Claisen Rearrangement

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posted on 2015-12-17, 01:57 authored by Michael T. Crimmins, John D. Knight, Philip S. Williams, Yan Zhang
A dianionic Ireland–Claisen rearrangement of chiral, nonracemic α-methyl-β-hydroxy allylic esters has been developed that proceeds with high diastereoselectivity and provides products containing three contiguous stereogenic carbons, including a quaternary center. The potential utility of the rearrangement for complex molecule synthesis is also demonstrated.

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