Abstract
A synthetic approach to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented. Its most remarkable feature is the stereochemical diversification of a common precursor through the choice of different hydrogenation conditions.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Crystallography, X-Ray
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Hydrogenation
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Indans / chemical synthesis*
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Indans / chemistry
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Models, Molecular
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Molecular Conformation
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Sesterterpenes / chemical synthesis*
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Sesterterpenes / chemistry
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Stereoisomerism
Substances
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Indans
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Sesterterpenes
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hydrindane