Mehta, Goverdhan ; Srinivasa Reddy, D. (1999) Synthetic studies directed towards the potent cytotoxic natural product ottelione A: stereoselective construction of the complete framework Chemical Communications (21). pp. 2193-2194. ISSN 1359-7345
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Official URL: http://doi.org/10.1039/A907273J
Related URL: http://dx.doi.org/10.1039/A907273J
Abstract
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: | Article |
|---|---|
| Source: | Copyright of this article belongs to Royal Society of Chemistry 2021 |
| ID Code: | 122033 |
| Deposited On: | 27 Jul 2021 11:01 |
| Last Modified: | 30 Jul 2021 13:00 |
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