Progress toward the total synthesis of cassaine via the transannular diels-alder strategy
Phoenix1, Bourque, Deslongchamps
1Laboratoire de synthese organique, Departement de Chimie, Institut de Pharmacologie, Universite de Sherbrooke, 3001, 12(e) ave nord, Sherbrooke, Quebec, Canada J1H 5N4.
Abstract:
The transannular Diels-Alder reaction of trans-trans-trans macrocyclic triene A, bearing two cis substiuents in C(12) and C(13) as well as a gem-dimethyl in C(4), was studied. Under thermal conditions, only the desired trans-anti-cis tricycle B was obtained. This tricycle represents an advanced intermediate toward the total synthesis of cassaine C.
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