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Journal ArticleDOI

Late-stage C-H functionalization offers new opportunities in drug discovery

TLDR
In this paper, the authors provide a toolbox for chemists in academia as well as industrial practitioners, and introduce guiding principles for the application of late-stage functionalization strategies to access new molecules of interest.
Abstract
Over the past decade, the landscape of molecular synthesis has gained major impetus by the introduction of late-stage functionalization (LSF) methodologies. C–H functionalization approaches, particularly, set the stage for new retrosynthetic disconnections, while leading to improvements in resource economy. A variety of innovative techniques have been successfully applied to the C–H diversification of pharmaceuticals, and these key developments have enabled medicinal chemists to integrate LSF strategies in their drug discovery programmes. This Review highlights the significant advances achieved in the late-stage C–H functionalization of drugs and drug-like compounds, and showcases how the implementation of these modern strategies allows increased efficiency in the drug discovery process. Representative examples are examined and classified by mechanistic patterns involving directed or innate C–H functionalization, as well as emerging reaction manifolds, such as electrosynthesis and biocatalysis, among others. Structurally complex bioactive entities beyond small molecules are also covered, including diversification in the new modalities sphere. The challenges and limitations of current LSF methods are critically assessed, and avenues for future improvements of this rapidly expanding field are discussed. We, hereby, aim to provide a toolbox for chemists in academia as well as industrial practitioners, and introduce guiding principles for the application of LSF strategies to access new molecules of interest. Late-stage C–H functionalization of complex molecules has emerged as a powerful tool in drug discovery. This Review classifies significant examples by reaction manifold and assesses the benefits and challenges of each approach. Avenues for future improvements of this fast-expanding field are proposed.

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Citations
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Journal ArticleDOI

Bioisosteres of the Phenyl Ring: Recent Strategic Applications in Lead Optimization and Drug Design.

TL;DR: In this paper, the design and applications of bioisosteric replacements for a phenyl ring that have provided practical solutions to a range of developability problems frequently encountered in lead optimization campaigns are discussed.
Journal ArticleDOI

A Perspective on Late-Stage Aromatic C–H Bond Functionalization

TL;DR: In this Perspective, aromatic C–H LSF is evaluated on the basis of four criteria—reactivity, chemoselectivity, site-selectivity, and substrate scope—and the author's views on current challenges as well as promising strategies and areas of growth going forward are provided.
Journal ArticleDOI

Radical C(sp3)–H functionalization and cross-coupling reactions

TL;DR: This Review highlights the diverse approaches for C(sp3)–H functionalization and cross-coupling reactions, emphasizing radical-relay reactions.
Journal ArticleDOI

Electrooxidative palladium- and enantioselective rhodium-catalyzed [3 + 2] spiroannulations

TL;DR: In this article , a palladaelectro-catalyzed C-H activation/[3 + 2] spiroannulation of alkynes by 1-aryl-2-naphthols was described.
Journal ArticleDOI

The emergence of the C–H functionalization strategy in medicinal chemistry and drug discovery

TL;DR: In this paper, the authors discuss the recent trends of C-H activation methodologies such as synthesis of medicinal scaffolds through a cascade of cascade-based activation and activation/annulation cascade, arylation for sp2sp2 and sp2-sp3 cross-coupling, borylation/silylation to introduce a functional linchpin for further manipulation, amination for N-heterocycles and hydrogen bond acceptors, C-h fluorination/fluoroalkylation to tune polarity and lipophilicity, peptide modification and
References
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Journal ArticleDOI

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TL;DR: This Review provides an overview of C-H bond functionalization strategies for the rapid synthesis of biologically active compounds such as natural products and pharmaceutical targets.
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