Total Synthesis of Cytotoxic Natural Product (2R,3S)-Rubiginone A2 and Absolute Configuration Reassi

来源 :第九届IUPAC化学生物学国际研讨会暨第八届世界华人药物化学研讨会 | 被引量 : 0次 | 上传用户:seraph72
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  Rubiginones are a family of the natural products that have been isolated from the fermentation broth of Streptomyces griseorubiginosus.Rubiginone A2 1 was claimed to be useful in the treatment of AIDS and Alzheimers disease.The absolute stereochemistry has been determined by the O-methyl mandelate method.Its analogue,benzopyrenomycin(2) has a unique benzo[a]pyrene-type skeleton and shows strong cytotoxic activity against various tumor-cell lines.For instance,benzopyrenomycin exhibited GIs0 of 3.2 μg/mL and 4.2 μg/mL for L-929 and K562 cell lines,respectively.2 The absolute configuration of benzopyrenomycin(2) was reported by Hertweck et al.,which is the same as that of rubiginone A2(1)(2R,3S),based on their similar molecular structures and close OR values(+50°for 1 and+38° for 2 in chloroform),including the evidences that assigning its absolute configuration of 3using Mosher methods,3 in which 3 can be converted into 2.
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The ideal synthesis is pursued actively by organic chemists since it encompasses the ideas of atom,step,redox-economy,as well as economies of time,labor,resource management,and waste generation.As suc
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