Mehta, Goverdhan and Islam, Kabirul (2000) An Eventful Synthetic Approach Towards the Biologically Potent Natural Product Ottelione A: Enantio-, Regio- and Stereoselective Construction of the Bicyclic Core. In: Synlett (10). 1473-1475 .
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Abstract
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural product ottelione A from the readily available Diels-Alder adduct of cyclopentadiene and p-benzoquinone is delineated. Our short strategy, besides being enantio-, regio- and stereoselective, charts an eventful course and is inherently well-suited for adaptation towards diverse synthetic analogues of this biologically potent natural product.
| Item Type: | Journal Article |
|---|---|
| Publication: | Synlett |
| Publisher: | Thieme Medical Publishers |
| Additional Information: | Copyright of this article belongs to Thieme Medical Publishers. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 30 Sep 2010 09:17 |
| Last Modified: | 30 Sep 2010 09:17 |
| URI: | http://eprints.iisc.ac.in/id/eprint/32556 |
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