Rapid Synthesis of the 7-Deoxy Zaragozic Acid Core

We have developed an efficient synthesis of the 7-deoxy zaragozic acid core. The synthesis begins with a Feist−Bénary reaction that assembles all three carbons of the polycarboxylic acid portion of the core. This reaction is followed by highly diastereoselective aldol and dihydroxylation reactions t...

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Veröffentlicht in:Organic letters 2002-01, Vol.4 (2), p.209-212
Hauptverfasser: Calter, Michael A, Zhu, Cheng, Lachicotte, Rene J
Format: Artikel
Sprache:eng
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Zusammenfassung:We have developed an efficient synthesis of the 7-deoxy zaragozic acid core. The synthesis begins with a Feist−Bénary reaction that assembles all three carbons of the polycarboxylic acid portion of the core. This reaction is followed by highly diastereoselective aldol and dihydroxylation reactions that set the remaining stereocenters of the core. The synthesis finishes with lactol oxidation and lactone alcoholysis/ketal formation reactions to construct the bicyclic ring system of the core.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol0169980