Explores iron-catalyzed asymmetric synthesis of β-amino alcohols, suggesting efficient new pathways for synthesis.
Herein, we report an iron-catalyzed enantioselective intermolecular NH 2 -aminoesterification of alkenes employing O-carbonyl hydroxylammonium triflates as bifunctional reagents, enabled by newly developed N -Aryl-BIP ligands. The resulting β-amino esters are susceptible to intramolecular transacylation and hydrolysis, effectively providing an overall asymmetric aminohydroxylation (AA) of alkenes. This transformation accommodates both vinyl (hetero)arenes and 1,1-disubstituted alkenes, delivering a diverse array of β-amino free alcohols in good yields and with high enantioselectivity. Mechanistic studies reveal a stepwise pathway involving electrophilic addition of the amino group to the alkene, followed by rapid C–O bond formation. Crossover and linear relationship experiments support a monomeric iron species bearing both the amino and carboxylate groups as the key reactive intermediate, which is interpreted as an iron(III)-supported amino radical (•NH 2 ) species. DFT calculations indicate it undergoes a synchronous radical addition to the alkene coupled with ligand-to-metal single electron transfer, directly forming a benzylic carbocation. Subsequent C–O bond formation features a low kinetic barrier, which also represents the enantiodetermining step.
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Zhong et al. (2026) studied this question.
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