Regioselective synthesis of o-methyl derivatives morindone and nataloe-emodnr of the trihydroxy anthraquinones
Cycloaddition chemistry of dichloronaphthoquinones has led to regioselective syntheses of all regioisomeric α-O-methyl derivatives of morindone (2) and nataloe-emodin (4), including the natural anthraquinone ethers (1) and (3).
Cameron, Donald W.,Coller, D. Ross
p. 941 - 948
(2007/10/03)
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