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[摘要]:The first synthesis of (+)-6'-hydroxyarenarol (I), the proposed biogenetic precursor to popolohuanone E, is described. An enantioselective route to a key iodide intermediate has been developed allowing the asym. synthesis of a known cis-decalin. Conditions which allow the removal of the Me ether protecting groups on the hydroxyarene leaving the exocyclic methylene moiety in tact have also been developed to complete this synthesis. |
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