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Synlett 2013; 24(18): 2340-2344
DOI: 10.1055/s-0033-1339860
DOI: 10.1055/s-0033-1339860
synpacts
One-Pot Procedures for the Formation of Secondary Aryl Amines from Nitro Aryls
Further Information
Publication History
Received: 24 July 2013
Accepted after revision: 03 September 2013
Publication Date:
30 September 2013 (online)
![](https://www.thieme-connect.de/media/synlett/201318/lookinside/thumbnails/10.1055-s-0033-1339860-1.jpg)
Abstract
Strategies for the one-pot formation of secondary aryl amines from the corresponding nitro aryls by utilizing reductive amination procedures are discussed. The extension of this chemistry where a Suzuki–Miyaura cross-coupling is conducted between a boronic acid and bromonitrobenzene prior to the reductive amination in one-pot is also presented.
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For reviews discussing heterogeneous palladium-catalyzed Suzuki–Miyaura cross-coupling reactions, see: