Synthesis of the aglycon of scorzodihydrostilbenes B and D
Benzyl- and methyl-protected 2,4-dihydroxyacetophenones are added under ruthenium catalysis to 4-methoxy- and 3,4-dimethoxystyrene in a completely regioselective manner. Thus, oxygenated dihydrostilbenes are obtained that feature the skeleton of scorzodihydrostilbenes – antioxidative agents that were recently isolated from Scorzonera radiata. Selective deprotection liberates the corresponding phenols, among them the aglycon of scorzodihydrostilbenes B and D.
2009 ◽
Vol 74
(7-8)
◽
pp. 1023-1034
◽
Keyword(s):
2002 ◽
Vol 74
(1)
◽
pp. 19-24
◽
Keyword(s):
2020 ◽
Vol 59
(30)
◽
pp. 12392-12395
◽
Keyword(s):