Stereoselective total synthesis of racemic grandisol via 3-oximino-1,4,4-trimethylbicyclo[3.2.0]heptane. An improved practical procedure

@inproceedings{Rosini1986StereoselectiveTS,
  title={Stereoselective total synthesis of racemic grandisol via 3-oximino-1,4,4-trimethylbicyclo[3.2.0]heptane. An improved practical procedure},
  author={Goffredo Rosini and Monika Geier and Emanuela Marotta and Marino Petrini and Roberto Ballini},
  year={1986}
}
Abstract (±)Grandisol was stereoselectively obtained via 1,4,4-trimethylbicyclo¦3.2.0¦heptane-3-one and its oxime by an improved procedure. 2,5,5-Trimethylhept-1,6-dien-4-ol, the open chain molecule, was synthesized by two routes. Its conversion into ( )grandisol was performed emploing the photobicyclization as key step.