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用于富sp片段模块化推进的紧急合成方法。

Emergent synthetic methods for the modular advancement of sp-rich fragments.

作者信息

Caplin Max J, Foley Daniel J

机构信息

School of Physical and Chemical Sciences, University of Canterbury Christchurch New Zealand

出版信息

Chem Sci. 2021 Mar 2;12(13):4646-4660. doi: 10.1039/d1sc00161b.

Abstract

Fragment-based drug discovery is an important and increasingly reliable technology for the delivery of clinical candidates. Notably, however, sp-rich fragments are a largely untapped resource in molecular discovery, in part due to the lack of general and suitably robust chemical methods available to aid their development into higher affinity lead and drug compounds. This Perspective describes the challenges associated with developing sp-rich fragments, and succinctly highlights recent advances in C(sp)-H functionalisations of high potential value towards advancing fragment hits by 'growing' functionalised rings and chains from unconventional, carbon-centred vectors.

摘要

基于片段的药物发现是一种用于提供临床候选药物的重要且日益可靠的技术。然而,值得注意的是,富含sp的片段在分子发现中很大程度上是未被开发的资源,部分原因是缺乏通用且足够稳健的化学方法来帮助将它们开发成具有更高亲和力的先导化合物和药物化合物。本综述描述了开发富含sp的片段所面临的挑战,并简要强调了具有高潜在价值的C(sp)-H官能团化的最新进展,这些进展通过从非常规的、以碳为中心的载体“生长”官能化环和链来推进片段命中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8683/8179648/db6f0d1ab4f9/d1sc00161b-f1.jpg

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