There is presented a synthetic process for the production of anthracyclinones, the aglycones of the anthracyclines. Also disclosed are novel intermediates in the above process. The end product aglycones may thereafter be utilized to produce biologically useful products such as carminomycin or adriamycin.
提出了一种合成
蒽环素酮的工艺,它是
蒽环素的无糖基化合物。同时还揭示了上述工艺中的新型中间体。然后,所得的无糖基化合物可用于生产
生物学上有用的产品,如氧化膦霉素或
阿霉素。