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Ugi four-component reaction with tandem deprotection, cyclization and pictet-spengler reaction: A concise route to N-fused polycyclic indoledi-ketopiperazine alkaloid analogues

机译:具有串联脱保护,环化和pictet-spengler反应的Ugi四组分反应:简捷的路线,可得到N稠合的多环吲哚酮-酮戊哌嗪生物碱类似物

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摘要

Aza-fused polycyclic indolediketopiperazine alkaloids are of potential interest due to their broad range of biological activities. Traditionally, a number of methods have been used to generate N-fused polycyclic indolediketopiperazine skeletons, but the need to develop novel, concise methods with which to modify the substitution pattern continues. Herein, we describe the two-step formation of N-fused polycyclic indolediketopiperazine alkaloid analogues by the application of the Ugi four-component reaction with tandem deprotection, cyclization and Pictet-Spengler reaction.
机译:氮杂稠合的多环吲哚二酮哌嗪生物碱由于其广泛的生物活性而备受关注。传统上,已经使用了许多方法来生成N稠合的多环吲哚二酮哌嗪骨架,但是仍然需要开发新颖,简洁的方法来修饰取代模式。在这里,我们描述了Ugi四组分反应与串联脱保护,环化和Pictet-Spengler反应的应用,介绍了N稠合的多环吲哚二酮哌嗪生物碱类似物的两步形成。

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