| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273655 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
A total synthesis of the bioactive meroterpenoid natural products frondosin B and frondosin A (formal) from readily available cyclohexanone and gentisic aldehyde dimethyl ether, involving RCM as the key step to generate the bicyclic 6,7-fused core structure, is outlined.
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