Syntheses of DL-threo-thiamphenicol via green oxidation

Kai Liu*, Robert Franzén, Xiao Jing Yu, Jun Zhang, You Jun Xu

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Four methyl aryl thioethers related to thiamphenicol syntheses and methyl phenyl sulfide were cleanly oxidized into methyl sulfones in high to excellent yields via catalytic green oxidation with aqueous hydrogen peroxide in combination with sodium tungstate. When the same reactions were similarly performed in the absence of the catalyst, the corresponding sulfoxides could be obtained. This viable synthetic approach for the synthesis of DL-threo-thiamphenicol is a simple procedure, which has an economic advantage in view of its application for the large-scale synthesis because it can be carried out under mild conditions.

Original languageEnglish
Pages (from-to)602-605
Number of pages4
JournalChemical Research in Chinese Universities
Volume22
Issue number5
DOIs
Publication statusPublished - Sept 2006
MoE publication typeA1 Journal article-refereed

Keywords

  • Green oxidation
  • Hydrogen peroxide
  • Sodium tungstate
  • Thiamphenicol

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