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 .Full text not available from this repository.
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|
|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|
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