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.
UR - http://www.scopus.com/inward/record.url?scp=0029761762&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029761762&partnerID=8YFLogxK
U2 - 10.1039/cc9960002173
DO - 10.1039/cc9960002173
M3 - Article
AN - SCOPUS:0029761762
SP - 2173
EP - 2174
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 18
ER -