Concise Stereoselective Total Synthesis of Leiocarpin C
A simple and highly concise strategy has been developed for the stereoselective total synthesis of leiocarpin C starting from commercially available mandelic ester. The strategy utilizes the OsO4‐catalyzed cis‐hydroxylation and selective reduction with K‐Selectride as key steps.
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Veröffentlicht in: | Helvetica chimica acta 2013-12, Vol.96 (12), p.2179-2184 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A simple and highly concise strategy has been developed for the stereoselective total synthesis of leiocarpin C starting from commercially available mandelic ester. The strategy utilizes the OsO4‐catalyzed cis‐hydroxylation and selective reduction with K‐Selectride as key steps. |
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ISSN: | 0018-019X 1522-2675 |
DOI: | 10.1002/hlca.201200656 |