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Synthesis of uniform cyclodextrin thioethers to transport hydrophobic drugs
Methyl and ethyl thioether groups were introduced at all primary positions of α-, β-, and γ-cyclodextrin by nucleophilic displacement reactions starting from the corresponding per-(6-deoxy-6-bromo)cyclodextrins. Further modification of all 2-OH positions by etherification with iodo terminated trieth...
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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
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4273231/ https://ncbi.nlm.nih.gov/pubmed/25550759 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.310 |
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