β‑Stereoselective Mannosylation Using 2,6-Lactones

β-Stereoselective mannosylation using donors bearing the 2,6-lactone moiety is described. In general, glycosylation is a nucleophilic substitution reaction between an alcoholic nucleophile and a sugar moiety containing a leaving group at the anomeric position. Owing to stereoelectronic effects, the reaction tends to proceed via an S_N1 mechanism to afford α-glycosides. We found that the introduction of a 2,6-lactone bridge can circumvent the competing S_N1 reaction, affording β-glycosides with stereoinversion via S_N2­(-like) mechanisms. Glycosyl trichloroacetimidates are particularly efficient when activated by a combined catalyst of AuCl₃ and 3,5-bis­(trifluoromethyl)­phenyl thiourea. In addition, the product stereoselectivity was highly dependent on the concentration of the reaction. Moreover, even when the reaction proceeds via an S_N1 mechanism, the corresponding glycosyl cation appears to present sterically a β-directing nature. Overall, 2,6-lactones were promising structures for achieving β-mannosylations.