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Journal ArticleDOI

"Multi-component reactions : emerging chemistry in drug discovery" 'from xylocain to crixivan'.

Christopher Hulme, +1 more
- 01 Jan 2003 - 
- Vol. 10, Iss: 1, pp 51-80
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TLDR
This review details developments of new, highly atom-economic MCR derived chemical methods, which enable the fast and efficient production of chemical libraries comprised of a variety of biologically relevant templates, and focuses on applications of isocyanide based MCR (IMCR) reactions.
Abstract
With the recent emergence of combinatorial chemistry and high-speed parallel synthesis for drug discovery applications, the multi-component reaction (MCR) has seen a resurgence of interest. Easily automated one-pot reactions, such as the Ugi and Passerini reactions, are powerful tools for producing diverse arrays of compounds, often in one step and high yield. Despite this synthetic potential, the Ugi reaction is limited by producing products that are flexible and peptide-like, often being classified as 'non drug-like'. This review details developments of new, highly atom-economic MCR derived chemical methods, which enable the fast and efficient production of chemical libraries comprised of a variety of biologically relevant templates. Representative examples will also be given demonstrating the successful impact of MCR combinatorial methods at different stages of the lead discovery, lead optimization and pre-clinical process development arenas. This will include applications spanning biological tools, natural products and natural product-like diversity, traditional small molecule and 'biotech' therapeutics respectively. In particular, this review will focus on applications of isocyanide based MCR (IMCR) reactions.

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Citations
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α-Acidic Isocyanides in Multicomponent Chemistry

TL;DR: The exceptional reactivity connected to isocyanides is unrivaled by other functional groups and has led to many synthetically useful novel reactions as mentioned in this paper, which can be easily combined in very short sequences with other complexity-generating processes, leading to yet other classes of heterocyclic motifs.
Journal ArticleDOI

A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives promoted by Ca(OTf)2

TL;DR: A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives has been reported using alkaline earth catalyst [Ca(OTf)2].
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Sulfonated magnetic nanocatalyst and application for synthesis of novel Spiro[acridine-9,5′-thiazole]-1,4′-dione derivatives

TL;DR: In this article, a new magnetic reusable nanocatalyst was prepared using chemical modification of magnetic nanoparticles (MNPs) surface with Sulfurol-SO3H, which act as acidic catalytic sites for catalysis purposes.
Journal ArticleDOI

Tandem three-component reaction of aldehyde, alkyl acrylate, and amide using ethyl diphenylphosphine as organocatalyst

TL;DR: In this article, the first chemoselective EtPPh2-catalyzed three-component reaction of aromatic aldehyde, alkyl acrylate, and phthalimide or methyl toluenesulfonamide has been achieved.
Journal ArticleDOI

Multicomponent reaction design: a one-pot route to substituted di-O-acylglyceric acid amides from α-diazoketones

TL;DR: In this article, a four-component assembly of substituted di-O-acylglyceric acid amides has been developed from α-diazoketones, which involves copper-catalyzed reaction of the α-doroketone with a carboxylic acid, and subsequent Passerini condensation of the in situ formed α-acylsoxyketone.
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How was synthetiside drug crixivan?

Crixivan, a synthetiside drug, was synthesized using multi-component reactions (MCR), specifically isocyanide based MCR (IMCR) reactions, showcasing efficient and cost-effective drug discovery methodologies.