Mehta, Goverdhan ; Roy, Subhrangsu (2004) Enantioselective total synthesis of (+)-eupenoxide and (+)-phomoxide: revision of structures and assignment of absolute configuration Organic Letters, 6 (14). pp. 2389-2392. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol0492288
Related URL: http://dx.doi.org/10.1021/ol0492288
Abstract
Stereo- and enantioselective total syntheses of the novel, polyketide natural products ent-eupenoxide and ent-phomoxide have been accomplished from the readily available Diels-Alder adduct of cyclopentadiene and p-benzoquinone. These synthetic studies necessitate the revision of the assigned stereostructures of the natural products and reveal their absolute configuration.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 29354 |
| Deposited On: | 17 Dec 2010 08:11 |
| Last Modified: | 17 Dec 2010 08:11 |
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