The air- and water-stable iodonium salt phenyl(trifluoroethyl)iodonium triflimide is shown to activate thioglycosides for glycosylation at room temperature. Both armed and disarmed thioglycosides rapidly undergo glycosylation in 68-97% yield. The reaction conditions are mild and do not require strict exclusion of air and moisture. The operational simplicity of the method should allow experimentalists with a limited synthetic background to construct glycosidic linkages. © 2014 American Chemical Society.
CITATION STYLE
Chu, A. H. A., Minciunescu, A., Montanari, V., Kumar, K., & Bennett, C. S. (2014). An Air- and water-stable iodonium salt promoter for facile thioglycoside activation. Organic Letters, 16(6), 1780–1782. https://doi.org/10.1021/ol5004059
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