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Process for asymmetic total synthesis of camptothecln analogues and intermediates prepared thereby

机译:喜树碱类似物和由此制备的中间体的不对称全合成方法

摘要

The present invention provides a process for the asymmetric synthesis of camptothecin analogues as well as novel chemical intermediates of Formula I, II, and III. In general, the present process comprises conversion of a cis dioxolanone, having the same desired absolute configuration as the desired camptothecin analogue, to a compound of Formula I, II, or III, which compound is then converted to the desired camptothecin analogue. IMAGE (I)
机译:本发明提供了喜树碱类似物以及式I,II和III的新型化学中间体的不对称合成方法。通常,本发明方法包括将具有与所需喜树碱类似物相同的所需绝对构型的顺式二氧杂戊环酮转化为式I,II或III的化合物,然后将该化合物转化为所需喜树碱类似物。 <图像>(I)

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