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

Inma Huertas; Iluminada Gallardo; Jordi Marquet

doi:10.1016/S0040-4039(01)00485-3

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

Inma Huertas, Iluminada Gallardo, Jordi Marquet

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

20 Citations (Scopus)

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 language	English
Pages (from-to)	3439-3441
Journal	Tetrahedron Letters
Volume	42
Issue number	20
DOIs	https://doi.org/10.1016/S0040-4039(01)00485-3
Publication status	Published - 14 May 2001

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

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. {\textcopyright} 2001 Elsevier Science Ltd.",

author = "Inma Huertas and Iluminada Gallardo and Jordi Marquet",

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T1 - Direct coupling of nucleophiles with nitroaromatic compounds via fluoride-promoted oxidative nucleophilic aromatic substitution for hydrogen

AU - Huertas, Inma

AU - Gallardo, Iluminada

AU - Marquet, Jordi

PY - 2001/5/14

Y1 - 2001/5/14

N2 - 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.

AB - 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.

U2 - 10.1016/S0040-4039(01)00485-3

DO - 10.1016/S0040-4039(01)00485-3

M3 - Article

SN - 0040-4039

VL - 42

SP - 3439

EP - 3441

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 20

ER -

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

Abstract

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