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- W2896782261 endingPage "14000" @default.
- W2896782261 startingPage "13991" @default.
- W2896782261 abstract "A copper-mediated direct C3 amination of imidazopyridines has been disclosed under additive-free conditions in short reaction times. This methodology utilizes commercially available N-fluorobenzenesulfonimide (NFSI) as the amino source, which exhibits broad substrate scope and good functional group tolerance. The obtained C3-aminated imidazopyridines can undergo further desulfonylation transformations. Control experiments suggest that this reaction probably proceeds via a free-radical mechanism. Moreover, NFSI also shows potential application in C-H fluorination of imidazopyridines." @default.
- W2896782261 created "2018-10-26" @default.
- W2896782261 creator A5005256512 @default.
- W2896782261 creator A5014725026 @default.
- W2896782261 creator A5015725187 @default.
- W2896782261 creator A5026014655 @default.
- W2896782261 creator A5036584872 @default.
- W2896782261 creator A5052692366 @default.
- W2896782261 creator A5060802281 @default.
- W2896782261 date "2018-10-23" @default.
- W2896782261 modified "2023-10-17" @default.
- W2896782261 title "Copper-Mediated C–H Amination of Imidazopyridines with <i>N</i>-Fluorobenzenesulfonimide" @default.
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