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 |
| Publication status | Published - 1996 |
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ASJC Scopus subject areas
- Chemistry(all)
Cite this
Two-step synthesis of C-glycosyl juglones from unprotected sugars : A novel approach to angucycline antibiotics. / Matsuo, Goh; Matsumura, Shuichi; Toshima, Kazunobu.
In: Chemical Communications, No. 18, 1996, p. 2173-2174.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Two-step synthesis of C-glycosyl juglones from unprotected sugars
T2 - A novel approach to angucycline antibiotics
AU - Matsuo, Goh
AU - Matsumura, Shuichi
AU - Toshima, Kazunobu
PY - 1996
Y1 - 1996
N2 - 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.
AB - 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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UR - http://www.scopus.com/inward/citedby.url?scp=0029761762&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0029761762
SP - 2173
EP - 2174
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 18
ER -