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.
![[img]](http://eprints.iisc.ernet.in/style/images/fileicons/application_pdf.png) |
PDF
Enantioselective.pdf - Published Version Restricted to Registered users only Download (93Kb) | Request a copy |
|
PDF
Supporting_Information.pdf - Supplemental Material Restricted to Registered users only Download (2096Kb) | Request a copy |
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 |
|---|---|
| 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.ernet.in/id/eprint/2661 |
Actions (login required)
 |
View Item |
