Synthetic studies directed towards the potent cytotoxic natural product ottelione A: stereoselective construction of the complete framework
Data(s) |
07/11/1999
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Resumo |
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. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/38836/1/Synthetic_studies_directed.pdf 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. |
Publicador |
Royal Society of Chemistry |
Relação |
http://pubs.rsc.org/en/Content/ArticleLanding/1999/CC/a907273j http://eprints.iisc.ernet.in/38836/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |