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- W2227647904 endingPage "2640" @default.
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- W2227647904 abstract "The synthesis of new multivalent architectures based on a trihydroxypiperidine α-fucosidase inhibitor is reported herein. Tetravalent and nonavalent dendrimers were obtained by means of the click chemistry approach involving the copper azide-alkyne-catalyzed cycloaddition (CuAAC) between suitable scaffolds bearing terminal alkyne moieties and an azido-functionalized piperidine as the bioactive moiety. A preliminary biological investigation is also reported towards commercially available and human glycosidases." @default.
- W2227647904 created "2016-06-24" @default.
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- W2227647904 date "2015-12-16" @default.
- W2227647904 modified "2023-10-18" @default.
- W2227647904 title "Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar" @default.
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- W2227647904 doi "https://doi.org/10.3762/bjoc.11.282" @default.
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