Total Synthesis of Isokidamycin
The synthesis of isokidamycin, which represents the first total synthesis of a bis-C-aryl glycoside natural product in the pluramycin family, has been completed. The synthesis features the use of a silicon tether as a disposable regiocontrol element in an intramolecular Diels−Alder reaction between...
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Veröffentlicht in: | Journal of the American Chemical Society 2010-11, Vol.132 (44), p.15528-15530 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The synthesis of isokidamycin, which represents the first total synthesis of a bis-C-aryl glycoside natural product in the pluramycin family, has been completed. The synthesis features the use of a silicon tether as a disposable regiocontrol element in an intramolecular Diels−Alder reaction between a substituted naphthyne and a glycosyl furan and a subsequent O→C-glycoside rearrangement. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja107926f |