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- W2007085563 abstract "Abstract The 4,6-benzylidene acetal of methyl 2-deoxy-2-fluoro-α,β- d -glucopyranoside underwent inversion at C-3 via an oxidation–reduction sequence, and treatment of the derived 3-acetate with N -bromosuccinimide in carbon tetrachloride gave methyl 3- O -acetyl-4- O -benzoyl-6-bromo-2,6-dideoxy-2-fluoro-α- d -allopyranoside ( 6 ). Dehydrobromination of 6 and reduction of the resultant 5,6-ene gave the 5-epimer of 6 , which after removal of the ester substituents, afforded the title compound in good overall yield." @default.
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- W2007085563 date "1999-01-01" @default.
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- W2007085563 title "A concise synthesis of methyl 2,6-dideoxy-2-fluoro-β-l-talopyranoside" @default.
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- W2007085563 doi "https://doi.org/10.1016/s0008-6215(98)00325-5" @default.
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