Issue 0, 1982

Synthesis of sesquiterpenes, occidentalol, chamaecynone and related compounds characterised by a cis-eudesmane structure

Abstract

In continuation of our synthetic work for constructing the cis-decalin skeleton by a double Michael annulation using 3-methyl-4-methylenecyclohex-2-enone and its congeners with dimethyl 3-oxoglutarate, the sesquiterpenes, occidentalol, chamaecynone, and related compounds have been synthesised in a stereoselective manner.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 2849-2853

Synthesis of sesquiterpenes, occidentalol, chamaecynone and related compounds characterised by a cis-eudesmane structure

Y. Mizuno, R. Mori and H. Irie, J. Chem. Soc., Perkin Trans. 1, 1982, 2849 DOI: 10.1039/P19820002849

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