Two-step synthesis of C-glycosyl juglones from unprotected sugars: A novel approach to angucycline antibiotics

Goh Matsuo, Shuichi Matsumura, Kazunobu Toshima

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

The two-step synthesis of C-glycosyl juglones, versatile synthetic intermediates for angucycline antibiotics, has been developed by the C-glycosidation of naphthalene-1,5-diol with an unprotected sugar and the subsequent regioselective photooxygenation of the resultant C-glycosyl naphthalenediol.

Original languageEnglish
Pages (from-to)2173-2174
Number of pages2
JournalChemical Communications
Issue number18
DOIs
Publication statusPublished - 1996 Jan 1

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

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