Abstract
A range of different N- and S-containing heterocyclic bromides can be efficiently coupled with gaseous ammonia in the presence of copper(II) acetylacetonate [Cu(acac)2] as catalyst and in the absence of additional ligands. Unstable aminothiophenes and aminobenzothiophenes can be further reacted in situ to afford functionalized derivatives. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Fantasia, S., Windisch, J., & Scalone, M. (2013). Ligandless copper-catalyzed coupling of heteroaryl bromides with gaseous ammonia. Advanced Synthesis and Catalysis, 355(4), 627–631. https://doi.org/10.1002/adsc.201201010
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