37574-03-1Relevant articles and documents
STEREOSELECTIVE SYNTHESYS OF (+/-)-OCCIDENTALOL
Mizuno, Yukio,Tomita, Masako,Irie, Hiroshi
, p. 107 - 110 (1980)
Stereoselective synthesis of the sesquiterpene alcohol, occidentalol starting from methyl c-4,c-9-dimethyl-6-methoxycarbonyl-2,7-dioxo-cis-decalyl-r-8-carboxylate was described.
Synthesis of Sesquiterpenes, Occidentalol, Chamaecynone and Related Compounds Characterised by a cis-Eudesmane Structure
Mizuno, Yukio,Mori, Reiko
, p. 2849 - 2854 (2007/10/02)
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.