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Synlett 2014; 25(20): 2903-2907
DOI: 10.1055/s-0034-1378903
DOI: 10.1055/s-0034-1378903
letter
Selective Azidation of Aryl Halides to Aryl Azides Promoted by Proline and CuFeO2
Further Information
Publication History
Received: 16 July 2014
Accepted after Revision: 30 September 2014
Publication Date:
29 October 2014 (online)
Abstract
An efficient and selective azidation of aryl halides by reacting sodium azide with aryl halides is described. The heterogeneous nature of the copper(Ι) catalyst, which catalyzes the cross-coupling reactions, and the antiviral and antibacterial properties of the products are features of this methodology. It is also worth noting that no aryl amines are produced as byproducts under these conditions.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/products/ejournals/journal/ 10.1055/s-00000083.
- Supporting Information
-
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