A convenient synthesis of an anti-helicobacter pylori agent, dehydrodiconiferyl alcohol

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Abstract

Potential anti-Helicobacter pylori agent dehydrodiconiferyl alcohol was synthesized in 44% overall yield, starting from vanillin which could be commercially available. Carbon extension of vanillin followed by the Horner-Wadsworth-Emmons reaction, a biomolecular radical coupling reaction and DIBAL-H reduction gave dehydrodiconiferyl alcohol.

Original languageEnglish
Pages (from-to)563-565
Number of pages3
JournalArchives of pharmacal research
Volume29
Issue number7
DOIs
Publication statusPublished - 2006 Jul 31

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Drug Discovery
  • Organic Chemistry

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