Abstract
A protocol for silver-catalyzed controlled intermolecular cross-coupling of silyl enolates is disclosed. The protocol displays good functional group tolerance and allows efficient preparation of a series of synthetically useful 1,4-diketones. Preliminary mechanistic investigations suggest that the reaction proceeds through a one-electron process involving free radical species in which PhBr acts as the oxidant. 2022 American Chemical Society.
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CITATION STYLE
Xu, L., Liu, X., Alvey, G. R., Shatskiy, A., Liu, J. Q., Kärkäs, M. D., & Wang, X. S. (2022). Silver-Catalyzed Controlled Intermolecular Cross-Coupling of Silyl Enol Ethers: Scalable Access to 1,4-Diketones. Organic Letters, 24(25), 4513–4518. https://doi.org/10.1021/acs.orglett.2c01477
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