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Chin. J. Org. Chem. ›› 1990, Vol. 10 ›› Issue (1): 30-36. Previous Articles Next Articles
Original Articles
俞菊荣;蔡俊超;高怡生
发布日期:
YU JURONG;CAI JUNCHAO;GAO YISHENG
Published:
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The title compound I and derivatives were prepared from 4-acetoxy-3-bromophthalide and dimethoxytoluene in 9 steps. I showed antitumor activity against leukemia P388 cell in vitro. The inhibitory rates were 85.7%, 58.7%, and 42.9% at 100, 10 and 1 mg/mL, resp.
Key words: ANTHRAQUINONE P, ETHOXY GROUP, METHOXY GROUP, DIHYDROXY GROUP, ANTITUMOR DRUGS, RUBIA CORDIFOLIA
CLC Number:
R914
O629
YU JURONG;CAI JUNCHAO;GAO YISHENG. Synthesis f 3,8-dihydroxy-2-ethoxymethyl-1-methoxyanthraquinone[J]. Chin. J. Org. Chem., 1990, 10(1): 30-36.
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