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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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Detalles Bibliográficos
Autores principales: Matassini, Camilla, Mirabella, Stefania, Goti, Andrea, Robina, Inmaculada, Moreno-Vargas, Antonio J, Cardona, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685925/
https://www.ncbi.nlm.nih.gov/pubmed/26734108
http://dx.doi.org/10.3762/bjoc.11.282