carbon atoms were defined to capture the features of the distal ring of the aryl substituents. The established statistical models of IDPi-catalyzed cyanosilylation reactions align well with the mechanistic understandings of the crucial role of C-H···π and cation-π interactions between the distal ring of IDPi and substrate in stereo-control. More selective catalysts for the challenging cyanosilylation reaction of 3-hexanone were successfully identified by using these descriptors to define and screen the chemical space of IDPi catalysts. This work not only enriches our understanding of the SSR of IDPi catalysts but also highlights the potential application of aryl fragment and remote site parameters as universal descriptors for IDPi in statistical modeling.
Zhou et al. (Wed,) studied this question.