Journal
SYNLETT
Volume -, Issue 14, Pages 2089-2092Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-2008-1078019
Keywords
click chemistry; aromatic azides; Huisgen cycloaddition; chemoselectivity; 1,4-triazoles
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Funding
- EPSRC
- The University of Nottingham
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The practical and efficient one-pot azidation of anilines with the reagent combination t-BuONO and TMSN3 has become a useful addition to the click-chemistry toolbox. Herein we report a modification of this methodology, using microwave radiation to significantly enhance the rate of fori-nation of 1,4-triazoles from in situ generated azides.
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