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- W2801362900 endingPage "3131" @default.
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- W2801362900 abstract "An unprecedented copper-catalyzed aminative aza-annulation of enynyl azide using commercially available N-fluorobenzenesulfonimide (NFSI) as an amination reagent is described. The reaction proceeds via regioselective inter-/intramolecular diamination, incorporating one nitrogen from the NFSI and the other from the azide, to provide amino-substituted nicotinate derivatives in a single step with moderate to high yield. This method represents an efficient way to access diverse aminonicotinates through direct C-N bond-coupling processes." @default.
- W2801362900 created "2018-05-17" @default.
- W2801362900 creator A5007684250 @default.
- W2801362900 creator A5075830234 @default.
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- W2801362900 date "2018-04-30" @default.
- W2801362900 modified "2023-10-15" @default.
- W2801362900 title "Cu(I)-Catalyzed Aminative Aza-Annulation of Enynyl Azide using <i>N</i>-Fluorobenzenesulfonimide: Synthesis of 5-Aminonicotinates" @default.
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- W2801362900 doi "https://doi.org/10.1021/acs.orglett.8b01228" @default.
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