Facile synthesis of the cyclohexane fragment of enacloxins, a series of antibiotics isolated from Frateuria sp. W-315

Aki Saito, Wataru Igarashi, Hiroyuki Furukawa, Teiko Yamada, Shigefumi Kuwahara, Hiromasa Kiyota

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

An efficient and good yield synthesis of the cyclohexane moiety of enacyloxins, a series of antibiotics isolated from Frateuria sp. W-315, was achieved from D-quinic acid using a successive Barton - McCombie deoxygenation.

Original languageEnglish
Pages (from-to)766-769
Number of pages4
JournalBioscience, Biotechnology and Biochemistry
Volume78
Issue number5
DOIs
Publication statusPublished - Jan 1 2014

Keywords

  • Antibiotics
  • Barton-McCombie deoxygenation
  • D-quinic acid
  • Enacyloxin

ASJC Scopus subject areas

  • Biotechnology
  • Analytical Chemistry
  • Biochemistry
  • Applied Microbiology and Biotechnology
  • Molecular Biology
  • Organic Chemistry

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