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Formal synthesis of erythrodiene and spirojatamol via rhodium-catalysed Claisen rearrangement/hydroacylation
Authors:Tim Sattelkau  Peter Eilbracht
Affiliation:

Organische Chemie I (FB3), Universität Dortmund, Otto-Hahn-Str. 6, D-44227, Dortmund, Germany

Abstract:A novel procedure allows the synthesis of spiro[4.5]decane-1,6-dione 1, a key intermediate in the total synthesis of erythrodiene and spirojatamol. The key step is a combination of Claisen rearrangement of allyl vinyl ethers followed by an intramolecular hydroacylation catalysed by RhCl(cod)(dppe).
Keywords:Catalysis   Natural Products   Spiro Compounds
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