Enantioselective preparation of the C1-C11 fragment of apoptolidin
- PMID: 14703361
- DOI: 10.1021/ol0361397
Enantioselective preparation of the C1-C11 fragment of apoptolidin
Abstract
[reaction: see text] A novel approach toward the synthesis of the triene portion of the biologically active polyketide apoptolidin is described. The use of an iterative thionyl chloride rearrangement/oxidation sequence to construct trisubstituted olefins is explored.
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