Asymmetric Wacker-Type Oxyallenylation and Azaallenylation of Cyclic Alkenes

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Abstract

Palladium-catalyzed three-component carboetherification of cyclic alkenes proceeded to give trans adducts exclusively with excellent enantioselectivity through a Wacker-type pathway. The reaction is also applicable to other oxygen nucleophiles, such as water, phenols, and carboxylic acids, as well as some electron-poor aryl amines.

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Teng, S., Jiao, Z., Chi, Y. R., & Zhou, J. S. (2020). Asymmetric Wacker-Type Oxyallenylation and Azaallenylation of Cyclic Alkenes. Angewandte Chemie - International Edition, 59(6), 2246–2250. https://doi.org/10.1002/anie.201911961

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