Synthesis of Sesquiterpenes, Occidentalol, Chamaecynone and Related Compounds Characterised by a cis-Eudesmane Structure
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.
Mizuno, Yukio,Mori, Reiko
p. 2849 - 2854
(2007/10/02)
Total synthesis of dl-chamaecynone, a termiticidal norsesquiterpene
-
Harayama,Cho,Inubushi
p. 1201 - 1214
(2007/10/10)
Total synthesis of dl chamaecynone, a termiticidal norsesquiterpene
-
Harayama,Cho,Inubushi
p. 3273 - 3276
(2007/10/10)
More Articles about upstream products of 55220-87-6