Semisynthesis of linarin, acacetin, and 6-iodoapigenin derivatives from diosmin
Semisynthesis of linarin and acacetin from the Citrus flavonoid diosmin was performed via, as first intermediate, the 3′-O-phenyltetrazolyl ether of diosmin. This paper relates also a semisynthetic access to 6-iodoapigenin derivatives, which are key compounds in the synthesis of some biflavonoids such as robustaflavone.
Quintin, Jerome,Lewin, Guy
p. 1624 - 1627
(2007/10/03)
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