Reactions involving an azido group where the azide remains intact are rare and largely underexplored. In this issue of Chem, Bi and co-workers disclose a mild, functional-group-tolerant strategy for the… Click to show full abstract
Reactions involving an azido group where the azide remains intact are rare and largely underexplored. In this issue of Chem, Bi and co-workers disclose a mild, functional-group-tolerant strategy for the synthesis of β-difluoroalkyl azides from readily accessible α-vinyl azides via an unusual 1,2-azide migration pathway.
               
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