Carbonylation reactions typically rely on toxic carbon monoxide gas, often under pressurized conditions. Herein, we report an enantioselective nickel-catalyzed carbonylative difunctionalization of activated olefins using formic acid as a safe and operationally simple CO surrogate under mild conditions. The reaction employs a chiral phosphine-based ferrocene ligand to furnish ester-functionalized oxindoles bearing stereogenic quaternary carbon centers in high yields and enantioselectivities. Isotopic-labeling and XPS studies support in situ CO generation and trapping by an alkyl-nickel intermediate.
No takes yet. Share an insight, caveat, or question.
Kathirvel et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: