Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions
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Ruff, Yves and Berst, Frederic (2018) Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions. MedChemComm. ISSN 2040-2511; 2040-2503
Official URL: http://pubs.rsc.org/en/content/articlelanding/2018...
Abstract
Herein, we describe the development of a copper-catalyzed N-arylation of DNA-conjugated aryl iodides with aliphatic amines. This protocol leverages a novel ligand, 2-((2,6-dimethoxyphenyl)amino)-2-oxoacetic acid, to effect the transformation in aqueous DMSO, under mild conditions, in air, making it an ideal candidate for the synthesis of DNA-encoded libraries.
Item Type: | Article |
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Date Deposited: | 31 Jul 2018 00:45 |
Last Modified: | 31 Jul 2018 00:45 |
URI: | https://oak.novartis.com/id/eprint/35390 |