Mehta, Goverdhan and Reddy, Srinivasa D (1999) Synthetic studies directed towards the potent cytotoxic natural product ottelione A: stereoselective construction of the complete framework. In: Chemical Communications (21). pp. 2193-2194.
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Abstract
A stereoselective strategy for the rapid acquisition of the complete framework (dideoxyottelione A) of the promising cytotoxic agent ottelione A, with four contiguous stereogenic centres on a hydrindane skeleton and a sensitive 4-methylenecyclohex-2-enone functionality, from the readily available Diels-Alder adduct of 1,2,3,4-tetrachloro-5,5-dimethoxycyclopentadiene and norbornadiene, is delineated.
| Item Type: | Journal Article |
|---|---|
| Publication: | Chemical Communications |
| Publisher: | Royal Society of Chemistry |
| Additional Information: | Copyright of this article belongs to Royal Society of Chemistry. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 02 Jul 2011 06:19 |
| Last Modified: | 02 Jul 2011 06:19 |
| URI: | http://eprints.iisc.ac.in/id/eprint/38836 |
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