Organocatalytic atroposelective synthesis of axially chiral N,N′-pyrrolylindoles via de novo indole formation

The first organocatalytic atroposelective synthesis of axially chiral N,N '-pyrrolylindoles based on o-alkynylanilines was successfully established via de novo indole formation catalyzed by chiral phosphoric acid (CPA). This new synthetic strategy introduced CPA-catalyzed asymmetric 5-endo-dig cyclization of new well-designed o-alkynylanilines containing a pyrrolyl unit, resulting in a wide range of axially chiral N,N '-pyrrolylindoles in high yields with exclusive regioselectivity and excellent enantioselectivity (up to 99% yield, >20 : 1 rr, 95 : 5 er). Considering the potential biological significance of N-N atropisomers, preliminary biological activity studies were performed and revealed that these structurally important N,N '-pyrrolylindoles had a low IC50 value with promising impressive cytotoxicity against several kinds of cancer cell lines. DFT studies reveal that the N-nucleophilic cyclization mediated by CPA is the rate- and stereo-determining step, in which ligand-substrate dispersion interactions facilitate the axial chirality of the target products.

Automated summary

A novel organocatalytic method for the synthesis of axially chiral N,N'-pyrrolylindoles based on o-alkynylanilines has been successfully developed using chiral phosphoric acid as the catalyst. This strategy allows for the efficient and selective synthesis of N,N'-pyrrolylindoles with excellent yields and enantioselectivity. Preliminary biological activity studies show that these compounds exhibit promising cytotoxicity against various cancer cell lines.