Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar

Exploring architectures displaying multimeric presentations of a trihydroxypiperidine iminosugar

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 sc...

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Bibliographic Details
Main Authors: Camilla Matassini, Stefania Mirabella, Andrea Goti, Inmaculada Robina, Antonio J. Moreno-Vargas, Francesca Cardona
Format: Article
Language:English
Published: Beilstein-Institut 2015-12-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
dendrimers
glycosidase inhibitors
iminosugars
multivalency
piperidine alkaloids
Online Access:https://doi.org/10.3762/bjoc.11.282

Internet

https://doi.org/10.3762/bjoc.11.282

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