Total synthesis of the novel sesquiterpenes of Eremophila georgei Diels
Data(s) |
07/06/1994
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Resumo |
The first stereoselective total synthesis of the natural sesquiterpenes 4 and 5, having the tricyclo[6.2.1.0(1,5)]undecane skeleton with a bridgehead methyl group, is reported via the intermediate 9, which was obtained by the acid catalysed rearrangement of the alcohols 7 and 8. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/36915/1/Total_Synthesis_of_the_Novel.pdf Selvakumar, Natesan and Rao, Subba GSR (1994) Total synthesis of the novel sesquiterpenes of Eremophila georgei Diels. In: Journal of the Chemical Society - Series Chemical Communications (11). pp. 1303-1304. |
Publicador |
Royal society of chemistry |
Relação |
http://pubs.rsc.org/en/Content/ArticleLanding/1994/C3/c39940001303 http://eprints.iisc.ernet.in/36915/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |