Synthesis of indole alkaloid (−)-corynantheidol and formal synthesis of (−)-corynantheidine via one-pot asymmetric azaelectrocyclization

Abstract

The highly efficient asymmetric total synthesis of indole alkaloid, ( −)-corynantheidol, containing a 2,4,5-trisubstituted piperidine core, was achieved using a new version of the one-pot azaelectrocyclization reaction. The formal synthesis of ( −)-corynantheidine was also achieved using the common synthetic intermediate for these corynantheines.