Abstract
Starting from 4-methylcyclohexanone (7), a concise total synthesis of the pinguisane-type sesquiterpenoid acutifolone A, in racemic form, has been accomplished in 14 steps with an overall yield of 14.5%.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Cyclization
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Cyclohexanes / chemistry*
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Diazonium Compounds / chemistry*
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Molecular Structure
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Oxygen / chemistry*
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Stereoisomerism
Substances
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Cyclohexanes
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Diazonium Compounds
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Cyclohexane
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Oxygen