A convergent synthetic study of biologically active benzofuran derivatives

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

In order to construct a benzofuran library, we developed a model study of benzbromarone. Synthesis has been achieved in 53% overall yield, starting from phenol via the key intermediate 2-ethylbenzofuran which was afforded by intramolecular Wittig reaction.

Original languageEnglish
Pages (from-to)476-478
Number of pages3
JournalArchives of pharmacal research
Volume29
Issue number6
DOIs
Publication statusPublished - 2006 Jun 30

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Benzbromarone
Phenol
Libraries
Derivatives
benzofuran

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Drug Discovery
  • Organic Chemistry

Cite this

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title = "A convergent synthetic study of biologically active benzofuran derivatives",
abstract = "In order to construct a benzofuran library, we developed a model study of benzbromarone. Synthesis has been achieved in 53{\%} overall yield, starting from phenol via the key intermediate 2-ethylbenzofuran which was afforded by intramolecular Wittig reaction.",
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A convergent synthetic study of biologically active benzofuran derivatives. / Hu, Kun; Jeong, Jin-Hyun.

In: Archives of pharmacal research, Vol. 29, No. 6, 30.06.2006, p. 476-478.

Research output: Contribution to journalArticle

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