Despite notable progress in catalytic olefin isomerization processes enabling distal Csp3 -H functionalization, most methods depend on complex metal-based catalytic systems and face inherent challenges in achieving regiodivergent outcomes1–3 . Herein, we present a conceptually distinct approach in which we leverage cationic olefin isomerization for regiodivergent Csp³–H functionalization, wherein the selectivity results from a ketone-assisted process we term “cation sampling” . This method enables site-selective, on-demand regiodivergent functionalization of Csp³ carbons, allowing the formation of C– heteroatom bonds in challenging positions and unlocking access to products that were previously unattainable through metal-based methodologies. Remarkably, this platform is not limited to olefinic substrates, also offering a versatile framework for alcohol transposition reactions, a formal migratory Appel reaction, and an effective solution for resolving regioisomeric bromohydrin mixtures.
No takes yet. Share an insight, caveat, or question.
Spieß et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: