Issue 11, 1994

Total synthesis of the novel sesquiterpenes of Eremophila georgei Diels

Abstract

The first stereoselective total synthesis of the natural sesquiterpenes 4 and 5, having the tricyclo[6.2.1.01,5]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.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1303-1304

Total synthesis of the novel sesquiterpenes of Eremophila georgei Diels

N. Selvakumar and G. S. R. S. Rao, J. Chem. Soc., Chem. Commun., 1994, 1303 DOI: 10.1039/C39940001303

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