Journal
GREEN CHEMISTRY
Volume 25, Issue 1, Pages 296-300Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2gc03703c
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A straightforward protocol for the electrochemical primary amination of imidazopyridines has been developed. This transformation utilizes TMSN3 as the nitrogen source and a trace amount of H2O as the hydrogen source. A wide range of imidazopyridines are compatible, providing the corresponding C3-amino substituted imidazopyridines in moderate to good yields.
A straightforward protocol involving electrochemical primary amination of imidazopyridines under mild conditions is described. This transformation utilizes TMSN3 as the nitrogen source and a trace amount of H2O as the hydrogen source. A wide range of imidazopyridines were found to be compatible, providing the corresponding C3-amino substituted imidazopyridines in moderate to good yields.
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