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Issue 9, 2012
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Retracted Article: Organocatalytic stereoselective synthesis of passifloricin A

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Abstract

The enantioselective synthesis of passifloricin A has been achieved in high diastereomeric excess. The 1,3-polyol moiety was constructed by iterative proline-catalyzed sequential α-aminoxylation and Horner–Wadsworth–Emmons (HWE) olefination of aldehydes while the synthesis of lactone moiety was achieved by ring-closing metathesis (RCM).

Graphical abstract: Retracted Article: Organocatalytic stereoselective synthesis of passifloricin A

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Article information


Submitted
10 Oct 2011
Accepted
01 Dec 2011
First published
05 Dec 2011

Org. Biomol. Chem., 2012,10, 1820-1825
Article type
Paper

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