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Stereoselective Synthesis of the C(1)-C(19) Fragment of Tetrafibricin
[Image: see text] A stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin has been accomplished via a highly diastereoselective double allylboration reaction of 6, 7, and 8, and an iodonium-ion promoted urethane cyclization for the installation of the C(15) alkoxy function in 3.
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2007
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2701644/ https://ncbi.nlm.nih.gov/pubmed/17249805 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol0629869 |
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