Journal
CHEM
Volume 6, Issue 4, Pages 823-825Publisher
CELL PRESS
DOI: 10.1016/j.chempr.2020.03.007
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Activation of ubiquitous organic halides into radical intermediates has been a challenging topic. In a recent paper published in Science, Leonori, Julia, and co-workers disclosed a new and robust strategy for halogen-atom-transfer activation of alkyl and aryl halides with the use of alpha-aminoalkyl radicals, easily generated from simple tertiary amines via single-electron transfer (SET) oxidation.
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