Synthesis based on cyclohexadienes. Part 17. Total synthesis of the sesquiterpenes of Eremophila georgei diels
| Data(s) |
07/04/1995
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|---|---|
| Resumo |
The first stereoselective total synthesis of the novel sesquiterpenes 1 and 2 is described. The preparation of the key intermediate 27 involved a rearrangement of a bicyclo[3.2.1] octane framework to an isomeric bicyclo[3.2.1]octane skeleton via a bicyclo[2.2.2]octane derivative. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/37947/1/Synthesis_based_on_cyclohexadienes.pdf Selvakumar, Natesan and Janaki, Seenivasaga N and Pramod, Kakumanu and Rao, Subba GSR (1995) Synthesis based on cyclohexadienes. Part 17. Total synthesis of the sesquiterpenes of Eremophila georgei diels. In: Perkin Transactions 1 (7). pp. 839-846. |
| Publicador |
Royal Society of Chemistry |
| Relação |
http://pubs.rsc.org/en/Content/ArticleLanding/1995/P1/p19950000839 http://eprints.iisc.ernet.in/37947/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
