Cobalt-catalyzed highly diastereoselective [3 + 2] carboannulation reactions: facile access to substituted indane derivatives

Efficient oxidative [3 + 2] annulation reaction involving aryl hydrazones and heterobicyclic alkenes has been realized with inexpensive and earth-abundant cobalt salts under aerobic conditions. The reaction proceeds via directing-group-assisted C-H activation and exo -selective migratory insertion, followed by the intramolecular nucleophilic attack of the alkylcobalt( iii ) species onto the imine with high anti -diastereoselectivity to provide complex indane derivatives. The generation of three contiguous stereogenic centers within the indanyl unit and the avoidance of the use of stoichiometric amounts of metal oxidants make this transformation more valuable and appealing. Cobalt( ii )-catalyzed oxidative annulation of hydrazones with heterobicyclic alkenes has been accomplished for accessing functionalized indane derivatives under aerobic conditions.