Abstract
An asymmetric synthesis of the tricyclic core (-)-1 of the marine diterpene bielschowskysin is described. In particular, a methodology was developed to introduce the crucial quaternary center at C-12.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Diterpenes / chemical synthesis*
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Diterpenes / chemistry*
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Heptanes / chemistry
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Molecular Structure
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Stereoisomerism
Substances
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Diterpenes
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Heptanes
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bielschowskysin