Hydrophenoxylation of alkynes by cooperative gold catalysis

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Abstract

Double impact: The title method gives aryl vinyl ethers in high yields, short reaction times, Z-stereospecificity, and good regioselectivities. Insights into the reaction mechanism highlight the role of [{Au(NHC)} 2(μ-OH)][BF4] (NHC=N-heterocyclic carbene) as both a Lewis acid, [Au(NHC)][BF4], and a Brønsted base, [Au(NHC)(OH)], thereby generating a synergistic effect between the two gold moieties. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Oonishi, Y., Gõmez-Suárez, A., Martin, A. R., & Nolan, S. P. (2013). Hydrophenoxylation of alkynes by cooperative gold catalysis. Angewandte Chemie - International Edition, 52(37), 9767–9771. https://doi.org/10.1002/anie.201304182

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