利用 C-H 功能化化学的力量加速药物研发

Synlett Pub Date : 2024-01-15 DOI:10.1055/a-2245-6202
Bing Li, S. Tyagarajan, K. Dykstra, Timothy Cernak, Petr Vachal, S. Krska
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引用次数: 0

摘要

摘要 C-H 功能化化学领域在过去二十年中经历了快速发展,在有机合成中的应用日益强大。认识到这一新兴领域对药物发现的潜在影响,十多年前,我们实验室成立了专门的工作小组,目标是促进 C-H 功能化化学在活跃的药物化学项目中的应用。我们的方法以后期官能化(LSF)战略为中心,在该战略中,C-H 官能化化学被系统地、有针对性地用于从高级药物先导物中生成高价值的类似物。为了成功实现这一方法,我们开发了广泛实用的 LSF 化学平台和工作流程,从而提高了 C-H 功能化化学的成功率,并加速了新衍生物的获得。LSF 策略应用得当,可以快速合成解决特定药物化学问题的分子。本报告介绍了几个案例研究,并对研究小组的平台和工作流程进行了说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Harnessing the Power of C-H Functionalization Chemistry to Accelerate Drug Discovery

Harnessing the Power of C-H Functionalization Chemistry to Accelerate Drug Discovery
Abstract The field of C-H functionalization chemistry has experienced rapid growth in the past twenty years, with increasingly powerful applications in organic synthesis. Recognizing the potential of this emerging field to impact drug discovery, a dedicated effort was established in our laboratories more than ten years ago with a goal of facilitating the application of C-H functionalization chemistries to active medicinal chemistry programs. Our approach centered around the strategy of Late-Stage Functionalization (LSF) wherein C−H functionalization chemistry is employed in a systematic and targeted manner to generate high-value analogs from advanced drug leads. To successfully realize this approach, we developed broadly useful LSF chemistry platforms and workflows that increased the success rates of the C-H functionalization chemistries and accelerated access to new derivatives. The LSF strategy, when properly applied, enabled rapid synthesis of molecules designed to address specific medicinal chemistry issues. Several case studies are presented along with descriptions of the group’s platforms and workflows.
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