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 | |
| 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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Cite this
Matsuo, G., Matsumura, S., & Toshima, K. (1996). Two-step synthesis of C-glycosyl juglones from unprotected sugars: A novel approach to angucycline antibiotics. Chemical Communications, (18), 2173-2174. https://doi.org/10.1039/cc9960002173