In this work, a detailed discussion of the design, synthesis, and structure-activity relationships of a novel class of axially chiral styrene-based organocatalysts was posted, successfully achieving the efficient asymmetric synthesis of sulfone-containing axially chiral styrenes. It was found that the dual chiral units in the catalyst operate through a synergistic mechanism: the R-configured axially chiral framework enables stereospatial recognition via π-π stacking, while the (S, S)-squaramide unit locks the conformation of the reaction intermediate through a multiple hydrogen-bonding network. Together, they confer excellent enantioselectivity to the key proton migration step, establishing the structural basis for the reaction's effective stereocontrol.
Li et al. (Fri,) studied this question.