Control of dynamic sp3-C stereochemistry

Stereogenic sp(3)-hybridized carbon centres are fundamental building blocks of chiral molecules. Unlike dynamic stereogenic motifs, such as sp(3)-nitrogen centres or atropisomeric biaryls, sp(3)-carbon centres are usually fixed, requiring intermolecular reactions to undergo configurational changes. Here we report the internal enantiomerization of fluxional carbon cages and the consequences of their adaptive configurations for the transmission of stereochemical information. The sp(3)-carbon stereochemistry of the rigid tricyclic cages is inverted through strain-assisted Cope rearrangements, emulating the low-barrier configurational dynamics typical for sp(3)-nitrogen inversion or conformational isomerism. This dynamic enantiomerization can be stopped, restarted or slowed by external reagents, while the configuration of the cage is controlled by neighbouring, fixed stereogenic centres. As part of a phosphoramidite-olefin ligand, the fluxional cage acts as a conduit to transmit stereochemical information from the ligand while also transferring its dynamic properties to chiral-at-metal coordination environments, influencing catalysis, ion pairing and ligand exchange energetics.

Automated summary

In this study, the enantiomerization of fluxional carbon cages and its consequences for stereochemical information transmission were reported. Strain-assisted Cope rearrangements were used to invert the sp(3)-carbon stereochemistry of rigid tricyclic cages, emulating the low-barrier configurational dynamics seen in sp(3)-nitrogen inversion or conformational isomerism. This dynamic enantiomerization could be controlled by external reagents and the configuration of the cage was controlled by neighboring, fixed stereogenic centers. The fluxional cage acted as a conduit to transmit stereochemical information from the ligand and also transferred its dynamic properties to chiral-at-metal coordination environments, influencing catalysis, ion pairing, and ligand exchange energetics.