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- W3205730718 abstract "Abstract A convenient protocol for the β-stereoselective synthesis of 2-deoxy-C-arylglycosides has been developed. This reaction takes place in one step by using I2/Et3SiH to activate a glycosyl acetate to generate a glycosyl iodide intermediate in situ, which is captured by a naphthol; this is followed by a Fries-like O-to-C glycoside rearrangement to afford a β-C-aryl glycoside selectively. The approach is applicable to a wide range of naphthol moieties, and its utility was demonstrated in syntheses of 5-aza analogues of aquayamycin." @default.
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- W3205730718 date "2021-10-15" @default.
- W3205730718 modified "2023-09-23" @default.
- W3205730718 title "A Metal-Free β-Stereoselective Synthesis of 2-Deoxy-C-arylglycosides: Synthesis of 5-Aza Analogues of Aquayamycin" @default.
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- W3205730718 doi "https://doi.org/10.1055/a-1670-2290" @default.
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