6/22/2021 – Congratulations to Dylan, Diana, and Minji on their work on aziridine synthesis through coupling unactivated alkenes and primary amines via metastable dicationic intermediates. Out in Nature now!

Aziridines, three-membered nitrogen-containing cyclic molecules, are important synthetic targets. Their significant ring strain and resultant proclivity towards ring opening reactions makes them versatile precursors to diverse amine products and, in some cases, the aziridine functional group itself imbues important …

6/10/2021 – Congratulations to Alyah, Oliver, and Colleen on their work exploiting non-innocent radical anion intermediates in photoredox catalysis for promoting diverse coupling reactions of classically inert aryl chlorides. Out on JACS now!

We describe a photocatalytic system that elicits potent photoreductant activity from conventional photocatalysts by leveraging radical anion intermediates generated in situ. The combination of isophthalonitrile and sodium formate promotes diverse aryl radical coupling reactions from abundant …