Eh good question. YOu mean something like this?
6-(tert-butyl)-1-(naphthalen-1-yl)-2-(trifluoromethyl)-1H-benzo[d]imidazole (7). To an oven dried 4 mL vial equipped with a magnetic stir bar was added N-(4-(tert-butyl)-2-(naphthalen-1-ylamino)phenyl)-2,2,2-trifluoroacetamide (6) (7.7 mg, 0.02 mmol, 1 equiv),(R)-CPA, pThr1, or pThr2 (0.002 mmol, 0.1 equiv), and toluene (0.2 mL, 0.1 M). The vial was sealed with a Teflon Cap and further secured with Parafilm M®. The reaction mixture was left to stir for 24 h at 60 ˚C, and then cooled to room temperature. The solvent was removed in vacuo and the crude product was used to 1 H NMR to determine the conversion and chiral HPLC to determine enantioselectivity.
Kwon, Y., Chinn, A. J., Kim, B., & Miller, S. J. (2018). Divergent Control of Point and Axial Stereogenicity: Catalytic Enantioselective C−N Bond-Forming Cross-Coupling and Catalyst-Controlled Atroposelective Cyclodehydration. Angewandte Chemie - International Edition, 57(21), 6251–6255.
https://doi.org/10.1002/anie.201802963