Abstract
The first enantiospecific total synthesis of the tricyclic sesquiterpene (+)-seychellene, starting from ( R)-carvone via ( S)-3-methylcarvone, has been accomplished employing a combination of an intermolecular Michael addition–intramolecular Michael addition sequence and an intramolecular alkylation reaction for the generation of the two vicinal quaternary carbon atoms.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
