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- W2090835768 abstract "The singlet oxygen oxygenation of 2-(α-C-glucopyranosyl)furans 1 leads readily and diastereoselectivity to the corresponding endoperoxides 2 whose fate can be controlled. Compounds 2 thermally rearrange into cis-dicarbonyl-α-O-glucosides 3 while by reduction they afford the cis-C-analogs 5. The latter readily convert to trans-8, which by silica gel chromatography tautomerize into β-anomers 9. Keywords: photooxygenation, 2-(c-glucopyranosyl)furans, o-glucopyranosides, c-glucopyranosides, furan-based synthesis, cis-1,4-dioxo-2-alkenyl glucopyranosides" @default.
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- W2090835768 date "2004-07-01" @default.
- W2090835768 modified "2023-10-09" @default.
- W2090835768 title "The First Dye-sensitized Photooxygenation of 2-(C-glycosyl)furans. One-Pot Stereoselective Approach to New Carbohydrate Derivatives" @default.
- W2090835768 doi "https://doi.org/10.2174/1570178043400839" @default.
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