A metal- and ligand-free Cs2CO3-promoted protocol for the N-(hetero)aryl functionalization of sulfoximines. The synthetic methodology exhibits a broad substrate scope, and the mild reaction conditions enable the functionalization of chiral sulfoximines with complete retention of configuration.
No takes yet. Share an insight, caveat, or question.
Adhav et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: