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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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| 出版年: | Beilstein J Org Chem |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Beilstein-Institut
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4685925/ https://ncbi.nlm.nih.gov/pubmed/26734108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.11.282 |
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