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

被引：18

作者：

Huertas, I ^{[1
]}

Gallardo, I ^{[1
]}

Marquet, J ^{[1
]}

机构：

[1] Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, Spain

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 20期

关键词：

D O I：

10.1016/S0040-4039(01)00485-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

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. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：3439 / 3441

页数：3

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