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)

Abstract

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

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Naphthols
Naphthol
Sugars
urdamycinone B
juglone
olivose

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Total synthesis of urdamycinone B via C-glycosidation of an unprotected sugar and Diels-Alder reaction of C-glycosyl juglone. / Matsuo, Goh; Miki, Yuko; Nakata, Masaya; Matsumura, Shuichi; Toshima, Kazunobu.

In: Chemical Communications, No. 2, 1996, p. 225-226.

Research output: Contribution to journalArticle

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