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Microwave-Assisted Amination from Aryl Triflates without Base and Catalyst
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Abstract

Aryl triflates are effectively converted to the corresponding anilines under microwave irradiation in 1-methyl-2-pyridone (NMP) without base and catalyst. Aryl triflates substituted with both electron-poor and electron-rich groups give good to excellent yields. It is noteworthy that the halogenated aryl triflates can chemoselectively react with amines to afford halogenated anilines.
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Younis Baqi and Christa E. MüllerThe Journal of Organic Chemistry2007 72 (15), 5908-5911The synthesis of N-substituted 5-nitroanthranilic acid derivatives 3a-w was achieved by a new, mild, microwave-assisted, regioselective amination reaction of 5-nitro-2-chlorobenzoic acid (1a) with a diverse range of aliphatic and aromatic amines 2a-w ...
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History
- Published In Issue March 18, 2004
- Received January 6, 2004
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