Issue 7, 1995

Synthesis based on cyclohexadienes. Part 17. Total synthesis of the sesquiterpenes of Eremophila georgei diels

Abstract

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]octene skeleton via a bicyclo[2.2.2]octane derivative.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 839-846

Synthesis based on cyclohexadienes. Part 17. Total synthesis of the sesquiterpenes of Eremophila georgei diels

N. Selvakumar, S. N. Janaki, K. Pramod and G. S. R. S. Rao, J. Chem. Soc., Perkin Trans. 1, 1995, 839 DOI: 10.1039/P19950000839

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