Copper-catalyzed reaction enables selective C(sp3)–H esterification, suggesting azidobenziodoxole enhances selectivity and expands functional group compatibility.
An efficient and selective copper-catalyzed secondary C(sp3)-H esterification has been developed. The reaction of various alkane substrates with azidobenziodoxole derivatives, in the presence of a cuprous iodide catalyst and trifluoromethanesulfonic acid additive, afforded inert aliphatic C-H esterification products. These reactions are selective and compatible with a wide range of functional groups. Mechanistic studies suggest that the azidobenziodoxole derivatives not only function as hydrogen-abstracting reagents to selectively activate C(sp3)-H bonds but also serve as ester donors in the esterification reaction.
No takes yet. Share an insight, caveat, or question.
Nong et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: