Mehta, Goverdhan and Roy, Subhrangsu (2004) Enantioselective Total Synthesis of (+)-Eupenoxide and (+)-Phomoxide: Revision of Structures and Assignment of Absolute Configuration. In: Organic Letters, 6 (14). pp. 2389-2392.
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Official URL: http://pubs.acs.org/doi/abs/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: | Journal Article |
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Publication: | Organic Letters |
Publisher: | American Chemical Society |
Additional Information: | Copyright for this article belongs to American Chemical Society. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 25 Jan 2005 |
Last Modified: | 19 Jan 2012 05:55 |
URI: | http://eprints.iisc.ac.in/id/eprint/2661 |
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