Abstract
A mild and efficient method for photoredox-catalyzed bromonitroalkylation of alkenes is described herein. In this reaction, bromonitromethane serves as a source of both nitroalkyl and bromine for direct and regioselective formation of C–Br and C–C bonds from alkenes, and additional cyclization provides C–C bonds to the cyclopropylamine core as an LSD1 inhibitor.
PMID: 38174236