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Abstract The stereoselective glycosylation of alcohols and their silyl ethers has been achieved using O ‐alkyl‐, O ‐acyl‐, and acetal‐protected glycosyl fluorides of the pyranose and furanose series and boron trifluoride etherate in CH 2 Cl 2 .
Kunz et al. (Wed,) studied this question.