Construction of Chiral Tricyclic Indoles through a Rhodium-Catalyzed Asymmetric Arylation Protocol

A rhodium/diene complex
catalyzed asymmetric 1,4-addition of arylboronic
acids to indole-derived α,β-unsaturated esters to access
highly enantioenriched 3-(1H-indol-2-yl)-3-arylpropanoates
has been developed. By taking advantage of the nucleophilic character
of indole at C3 and N1 positions, construction of a series of valuable
chiral tricyclic indole frameworks such as 2,3-dihydro-1H-pyrrolo­[1,2-a]­indoles and cyclopenta­[b]­indoles can be efficiently achieved.