Skip to main content
. 2021 Mar 25;12:1875. doi: 10.1038/s41467-021-22084-5

Table 2.

Aminocarbonylation of indoles and their analogues with aromatic aminesa.

graphic file with name 41467_2021_22084_Tabb_HTML.jpg

aReaction conditions: KAP-Pd-PEPPSI-3 (5 mol%), indole (0.25 mmol), amine (1.25 mmol), I2 (0.5 mmol), DABCO (0.5 mmol), CsF (1.0 mmol), CO (2.0 MPa), DMF (2.0 mL), 80 °C, 24 h, isolated yield.

HHS Vulnerability Disclosure