Khusimone (1), one of the main odor-donating compounds of vetiver oil,
is subject of the following study on structure/odor relationship. Rin
g opening of the carbonyl-functionalized bridge of the tricyclic khusi
mone leads to the bicyclic structures 2a/b. The enantioselective appro
ach to these degraded structures is described, and the olfactory conse
quences are studied. Starting point of the synthesis is an enantiomeri
cally pure enone ester which is easily obtainable from camphorsulfonic
acid.