Total synthesis of urdamycinone B via C-glycosidation of an unprotected sugar and Diels-Alder reaction of C-glycosyl juglone

Goh Matsuo, Yuko Miki, Masaya Nakata, Shuichi Matsumura, Kazunobu Toshima

Research output: Contribution to journalArticle

35 Citations (Scopus)


The total synthesis of C-glycosyl angucycline, urdamycinone B 1, was achieved via C-glycosidation of naphthol 6 and the unprotected D-olivose 7, and Diels-Alder reaction of the unprotected C-glycosyl juglone 9 and the diene 17 as the key steps.

Original languageEnglish
Pages (from-to)225-226
Number of pages2
JournalChemical Communications
Issue number2
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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