Reactivity and Steric Parameters from 2D to 3D Bulky Pyridines: Increasing Steric Demand at Nitrogen with Chiral Azatriptycenes

Sterically hindered pyridines embedded in a three‐dimensional triptycene framework have been synthesized, and their resolution by chiral HPLC enabled access to unprecedented enantiopure pyridines exceeding the known steric limits. The design principles for new axially chiral pyridine derivatives are then described. To rationalize their associations with Lewis acids and transition metals, a comprehensive determination of the steric and electronic parameters for this new class of pyridines was performed. This led to the general parameterization of the steric parameters (percent buried volume %VBur, Tolman cone angle θ, and He8_steric descriptor) for a large set of two‐ and three‐dimensional pyridine derivatives. These parameters are shown to describe quantitatively their interactions with carbon‐ and boron‐centered Lewis acids and were used to predict the ΔG° of association with the prototypical B(C6F5)3 Lewis acid widely used in frustrated Lewis pair catalysis. This first parameterization of pyridine sterics is a fundamental basis for the future development of predictive reactivity models and for guiding new applications of bulky and chiral pyridines in organocatalysis, frustrated Lewis pairs, and transition‐metal catalysis. Highly sterically hindered chiral pyridines were synthesized and resolved by HPLC. Their Brønsted/Lewis basicity were evaluated, and their reactivity was studied through their combination with Pd and B(C6F5)3 to generate new types of ligands/frustrated Lewis pairs. The study involved the first parameterization of the steric hindrance for a large set of pyridine derivatives.