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- W2949650433 abstract "An efficient, high-yielding strategy has been developed for the asymmetric synthesis of 1-N-iminosugars (1-azasugars), a new class of glycosidase inhibitors with promising biomedical applications. A highly regioselective procedure for the 1,2-reduction of substituted pyridines was employed to transform methyl nicotinate into several representative 1-azasugars." @default.
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- W2949650433 date "2001-05-08" @default.
- W2949650433 modified "2023-09-28" @default.
- W2949650433 title "ChemInform Abstract: Selective Fowler Reductions: Asymmetric Total Syntheses of Isofagomine and Other 1-Azasugars from Methyl Nicotinate." @default.
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- W2949650433 doi "https://doi.org/10.1002/chin.200119123" @default.
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