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

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Abstract

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. © 2001 Elsevier Science Ltd.
Original languageEnglish
Pages (from-to)3439-3441
JournalTetrahedron Letters
Volume42
Issue number20
DOIs
Publication statusPublished - 14 May 2001

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