A series of 3-aryl-7-propenoates including cinnamates, (E)-methyl/ethyl 3-[
2-(1, 1-dimethoxy-5,8-dione)naphthalenyl]-2- propenoates (8ba, 8bb) and (E3
)-methyl/ethyl 3-[2-(1,4-dihydroxy-9,10-dione)anthracenyl]-2-propenoates (9
aa, 9ab) was synthesized and evaluated for antitumor cytotoxicity. It was f
ound that the or ortho- or para-dihydroxy functionality on the aryl ring wa
s essential for the cytotoxicity of cinnamates. Compounds 8ba, 8bb and 9aa,
9ab showed potent cytotoxicity against various tumor cell lines. (C) 2001
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