Tempo-mediated oxidation of primary alcohols to carboxylic acids by exploitation of ethers inan aqueous-organicbiphase system

Zhen Wu Mei, Li Jian Ma, Hiroyuki Kawafuchi, Takumi Okihara, Tsutomu Inokuchi

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Expeditious and benign methods for primary alcohol- carboxylicacid conversions with TEMPO were developed in abiphasic system composed of aslightlymiscible ether (THP) and aqueous layer. Easily available co-oxidants such as Py-HBr3, Bu4NBr3, and electrooxidation were successfully applied to generate N-oxoammonium species as a recyclable catalyst.

Original languageEnglish
Pages (from-to)1000-1002
Number of pages3
JournalBulletin of the Chemical Society of Japan
Volume82
Issue number8
DOIs
Publication statusPublished - 2009

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Ethers
Electrooxidation
Carboxylic Acids
Oxidants
Ether
Alcohols
Oxidation
Catalysts
TEMPO

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Tempo-mediated oxidation of primary alcohols to carboxylic acids by exploitation of ethers inan aqueous-organicbiphase system. / Mei, Zhen Wu; Ma, Li Jian; Kawafuchi, Hiroyuki; Okihara, Takumi; Inokuchi, Tsutomu.

In: Bulletin of the Chemical Society of Japan, Vol. 82, No. 8, 2009, p. 1000-1002.

Research output: Contribution to journalArticle

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