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Direct coupling of nucleophiles with nitroaromatic compounds via fluoride-promoted oxidative nucleophilic aromatic substitution for hydrogen

✍ Scribed by Inma Huertas; Iluminada Gallardo; Jordi Marquet

Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
59 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis

Useful yields are achieved in the regioselective direct coupling of amines, amides, and ketones with m-dinitrobenzene, 1-nitronaphthalene, and 1,3-dinitronaphthalene, through oxidatively activated nucleophilic aromatic substitution for hydrogen promoted by fluoride anions.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Direct Coupling of
ChemInform Abstract: Direct Coupling of Nucleophiles with Nitroaromatic Compounds via Fluoride-Promoted Oxidative Nucleophilic Aromatic Substitution for Hydrogen.
✍ Inma Huertas; Iluminada Gallardo; Jordi Marquet πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 2 views

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