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Total synthesis of the potent antifungal agents bengazole C and E

Álvaro Enríquez-García and Steven V. Ley

Jazyk angličtina Země Česko

Perzistentní odkaz   https://www.medvik.cz/link/bmc09004750
E-zdroje Online

NLK ProQuest Central od 2005-01-01 do 2011

The bengazoles are marine natural products with unique structure, containing two oxazole rings flanking a single carbon. They show very potent antifungal activity. The total syntheses of bengazole C and E are described following a convergent route which involves diastereoselective cycloaddition of an appropriately substituted nitrile oxide with a butane-1,2-diacetal-protected alkenediol as the key step.

Bibliografie atd.

Lit.: 7

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$a The bengazoles are marine natural products with unique structure, containing two oxazole rings flanking a single carbon. They show very potent antifungal activity. The total syntheses of bengazole C and E are described following a convergent route which involves diastereoselective cycloaddition of an appropriately substituted nitrile oxide with a butane-1,2-diacetal-protected alkenediol as the key step.
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