Iridium-catalyzed enantioselective allylic substitution of unstabilized enolates derived from α,β-unsaturated ketones

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Abstract

We report Ir-catalyzed, enantioselective allylic substitution reactions of unstabilized silyl enolates derived from α,β-unsaturated ketones. Asymmetric allylic substitution of a variety of allylic carbonates with silyl enolates gave allylated products in 62-94% yield with 90-98% ee and >20:1 branched-to-linear selectivity. The synthetic utility of this method was illustrated by the short synthesis of an anticancer agent, TEI-9826. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Chen, M., & Hartwig, J. F. (2014). Iridium-catalyzed enantioselective allylic substitution of unstabilized enolates derived from α,β-unsaturated ketones. Angewandte Chemie - International Edition, 53(33), 8691–8695. https://doi.org/10.1002/anie.201403844

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