Abstract
In the synthesis of primary (hetero)aryl amines through copper-catalysis, the ammonia surrogates or aqueous ammonia nucleophilic partners can be replaced by sodium azide. Recent efforts in copper-mediated transformation of (hetero)aryl halides to (hetero) aryl amines using azide anion as the amino source are discussed in these highlights.
Keywords: Amination, Anilines, Aminoheterocycles, Sodium azide, copper, copper-catalysis
Mini-Reviews in Organic Chemistry
Title: Copper-Catalyzed Direct Amination of Halo(hetero)arenes with Sodium Azide as the Amino Source
Volume: 8 Issue: 4
Author(s): S. Messaoudi, J.-D. Brion and M. Alami
Affiliation:
Keywords: Amination, Anilines, Aminoheterocycles, Sodium azide, copper, copper-catalysis
Abstract: In the synthesis of primary (hetero)aryl amines through copper-catalysis, the ammonia surrogates or aqueous ammonia nucleophilic partners can be replaced by sodium azide. Recent efforts in copper-mediated transformation of (hetero)aryl halides to (hetero) aryl amines using azide anion as the amino source are discussed in these highlights.
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Cite this article as:
Messaoudi S., Brion J.-D. and Alami M., Copper-Catalyzed Direct Amination of Halo(hetero)arenes with Sodium Azide as the Amino Source, Mini-Reviews in Organic Chemistry 2011; 8 (4) . https://dx.doi.org/10.2174/157019311797440236
DOI https://dx.doi.org/10.2174/157019311797440236 |
Print ISSN 1570-193X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6298 |
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