1,2-Eliminations in a novel reductive coupling of nitroarenes to give azoxy arenes by sodium bis(trimethylsilyl)amide

Ru Hwu Jih, Asish R. Das, Wei Yang Chia, Jiann Jyh Huang, Ming Hua Hsu

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

(Chemical Equation Presented) Symmetric azoxy arenes were successfully prepared in one step from 2 equiv of the corresponding nitroarenes by use of sodium bis-(trimethylsilyl)amide as the deoxygenating agents in THF at 150°C in a sealed tube.

Original languageEnglish
Pages (from-to)3211-3214
Number of pages4
JournalOrganic Letters
Volume7
Issue number15
DOIs
Publication statusPublished - 2005 Jul 21

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Amides
amides
elimination
Sodium
sodium
tubes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Jih, Ru Hwu ; Das, Asish R. ; Chia, Wei Yang ; Huang, Jiann Jyh ; Hsu, Ming Hua. / 1,2-Eliminations in a novel reductive coupling of nitroarenes to give azoxy arenes by sodium bis(trimethylsilyl)amide. In: Organic Letters. 2005 ; Vol. 7, No. 15. pp. 3211-3214.
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1,2-Eliminations in a novel reductive coupling of nitroarenes to give azoxy arenes by sodium bis(trimethylsilyl)amide. / Jih, Ru Hwu; Das, Asish R.; Chia, Wei Yang; Huang, Jiann Jyh; Hsu, Ming Hua.

In: Organic Letters, Vol. 7, No. 15, 21.07.2005, p. 3211-3214.

Research output: Contribution to journalArticle

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AU - Hsu, Ming Hua

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