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

Goh Matsuo; Shuichi Matsumura; Kazunobu Toshima

doi:10.1039/cc9960002173

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

Goh Matsuo, Shuichi Matsumura, Kazunobu Toshima

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	2173-2174
Number of pages	2
Journal	Chemical Communications
Issue number	18
DOIs	https://doi.org/10.1039/cc9960002173
Publication status	Published - 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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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.",

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

Abstract

ASJC Scopus subject areas

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