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Stereoselective Total Synthesis of the Nonenolide (+)-Microcarpalide

Banwell, Martin; Loong, David

Description

The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.

CollectionsANU Research Publications
Date published: 2004
Type: Journal article
URI: http://hdl.handle.net/1885/78446
Source: Heterocycles

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