Enantioselective Synthesis of Azoniahelicenes by Rh-Catalyzed C-H Annulation with Alkynes

A rhodium(III)-catalyzed enantioselective C-H activation/annulation process is disclosed. With a catalyst derived from a chiral CpRh(III) complex and a chiral acid, the direct annulation reactions between 1-aryl isoquinoline derivatives and alkynes take place smoothly to afford a series of chiral azoniahelicenes in excellent yields and enantioselectivity (up to 99% yield and 96% ee). Mechanistic studies suggest that C-H bond cleavage may be the turnover-limiting step.

Automated summary

This study reveals a rhodium(III)-catalyzed enantioselective C-H activation/annulation process for the synthesis of chiral azoniahelicenes with high yields and enantioselectivity. Mechanistic studies suggest that C-H bond cleavage may be the turnover-limiting step.