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• W2152072192 endingPage "3675" @default.
• W2152072192 startingPage "3675" @default.
• W2152072192 abstract "The Johnson–Claisen rearrangement of D-gluco and L-ido-derived allylic orthoesters afforded γ,δ-unsaturated ester that on ester reduction, epoxidation, regioselective oxirane opening by sodium azide and hydrogenation led to sugar amino alcohols—immediate precursors for 1-deoxy-homonojirimycin 3a,b and polyhydroxylated homoazepanes 4a,b. Our synthetic approach and glycosidase inhibitory activity is reported." @default.
• W2152072192 created "2016-06-24" @default.
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• W2152072192 date "2006-01-01" @default.
• W2152072192 modified "2023-10-03" @default.
• W2152072192 title "Polyhydroxylated homoazepanes and 1-deoxy-homonojirimycin analogues: synthesis and glycosidase inhibition study" @default.
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• W2152072192 doi "https://doi.org/10.1039/b609000a" @default.
• W2152072192 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16990944" @default.
• W2152072192 hasPublicationYear "2006" @default.
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