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...
Shranjeno v:
| Principais autores: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Beilstein-Institut
2015-12-01
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| Serija: | Beilstein Journal of Organic Chemistry |
| Teme: | |
| Online dostop: | https://doi.org/10.3762/bjoc.11.282 |
| Oznake: |
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