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Aminoarenethiolate−Copper(I)-Catalyzed Amination of Aryl Bromides
Aminoarenethiolate−copper(I) complexes are known to be efficient catalysts for carbon−carbon bond formation. Here, we show the first examples that these thiolate−copper(I) complexes are efficient for carbon−nitrogen bond formation reactions as well. N-Arylation of benzylamine and imidazole with brom...
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Published in: | Organic letters 2005-11, Vol.7 (23), p.5241-5244 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Aminoarenethiolate−copper(I) complexes are known to be efficient catalysts for carbon−carbon bond formation. Here, we show the first examples that these thiolate−copper(I) complexes are efficient for carbon−nitrogen bond formation reactions as well. N-Arylation of benzylamine and imidazole with bromobenzene was achieved either in NMP as solvent or under solvent-free conditions in the presence of 2.5 mol % of aminoarenethiolate−copper(I) complex only. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol052113z |