Abstract
Stereoselective glycosylation remains the main challenge in the chemical synthesis of oligosaccharides. Herein we report a simple method to convert thioglycosides into β-sulfonium ions via an intramolecular alkylation reaction, leading to highly α-selective glycosylations for a variety of glycosyl acceptors. The influence of the thioglycoside substituent and the protecting group pattern on the glycosyl donor was investigated and showed a clear correlation with the observed stereoselectivity.
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CITATION STYLE
Moons, S. J., Mensink, R. A., Bruekers, J. P. J., Vercammen, M. L. A., Jansen, L. M., & Boltje, T. J. (2019). α-Selective Glycosylation with β-Glycosyl Sulfonium Ions Prepared via Intramolecular Alkylation. Journal of Organic Chemistry, 84(7), 4486–4500. https://doi.org/10.1021/acs.joc.9b00022
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