化学
天然产物
模块化设计
组合化学
立体化学
药物发现
多样性(政治)
转化(遗传学)
生物化学
计算机科学
人类学
基因
操作系统
社会学
作者
Vunnam Srinivasulu,Scott McN. Sieburth,Monther A. Khanfar,Imad A. Abu‐Yousef,Amin F. Majdalawieh,Mani Ramanathan,Anusha Sebastian,Taleb H. Al‐Tel
标识
DOI:10.1021/acs.joc.1c01523
摘要
The indolo[2,3-a]quinolizines, canthines, and arborescidines natural products exhibit a wide range of bioactivities including anticancer, antiviral, antibacterial, and anti-inflammatory, among others. Therefore, the development of modular and efficient strategies to access the core scaffolds of these classes of natural products is a remarkable achievement. The Complexity-to-Diversity (CtD) strategy has become a powerful tool that transforms natural products into skeletal and stereochemical diversity. However, many of the reactions that could be utilized in this process are limited by the type of functional groups present in the starting material, which restrict transformations into a variety of products to achieve the desired diversity. In the course of employing a (CtD) strategy en route to the synthesis of nature-inspired compounds, unexpected stereoelectronic-driven rearrangement reactions have been discovered. These reactions provided a rapid access to indolo[2,3-a]quinolizines-, canthines-, and arborescidines-inspired alkaloids in a modular and diastereoselective manner. The disclosed strategies will be widely applicable to other late-stage natural product transformation programs and drug discovery initiatives.
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