4.7 Article

Total synthesis of (±)-asteriscanolide

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 66, Issue 22, Pages 7443-7448

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo010623a

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The total synthesis of asteriscanolide (1) has been achieved by taking advantage on an intermolecular Pauson-Khand cycloaddition and a ring-closing metathesis as key bond-forming transformations. The approach incorporates the cyclooctane stereogenic center prior to ring formation. Interestingly, the ring-closing metathesis generates a new eight-membered ring with an in-out intrabridgehead relationship.

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