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A novel strategy for the solid-phase synthesis of cyclic lipodepsipeptides
A rapid and efficient Fmoc solid-phase synthesis of cyclic lipodepsipeptide analogue 1 to antibiotic fusaricidin A is described. Our synthetic approach includes resin attachment of the first amino acid via side chain, successful use of combination of four quasi-orthogonal removable protecting groups...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2006
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1852459/ https://ncbi.nlm.nih.gov/pubmed/17440603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2006.09.116 |
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