Stereoselective Synthesis of Ribofuranoid -Glycals by One-Pot Julia Olefination Using Ribofuranosyl Sulfones.

One-pot Julia olefination using ribofuranosyl sulfones is described. The α-anomers of the ribofuranosyl sulfones were synthesized with complete α-selectivity via the glycosylation of heteroarylthiols using ribofuranosyl iodides as glycosyl donors and the subsequent oxidation of the resulting heteroaryl 1-thioribofuranosides with magnesium monoperphthalate (MMPP). The Julia olefination of the α-ribofuranosyl sulfones with aldehydes proceeded smoothly in one pot to afford the thermodynamically less stable ()--glycals with modest-to-excellent stereoselectivity (up to / = 94:6) under the optimized conditions. The selectivity was especially high for aromatic aldehydes. In contrast, the ()--glycal was obtained as the main product with low stereoselectivity when the corresponding β-ribofuranosyl sulfone was used (/ = 41:59). The remarkable impact of the anomeric configuration of the ribofuranosyl sulfones on the stereoselectivity of the Julia olefination has been rationalized using density functional theory (DFT) calculations. The protected ribose moiety of the resulting -glycals induced completely α-selective cyclopropanation on the exocyclic carbon-carbon double bond via the Simmons-Smith-Furukawa reaction. The 2-cyanoethyl group was found to be useful for the protection of the -glycals, as it could be removed without affecting the exocyclic C═C bond.