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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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Journal ArticleDOI

Synthesis of substituted imidazolines by an Ugi/Staudinger/aza-Wittig sequence

TL;DR: A series of 2-(acetamide-2-yl)-imidazolines (II) with 5 points of diversity were prepared by an Ugi-4CR-Staudinger-aza-Wittig-sequence starting from simple azidoalkylamines.
Journal ArticleDOI

Synthesis of 1-(Cyclohexylamino)-2-(aryl)pyrrolo[1,2-a]quinoline-3-carbonitrile Derivatives Using a Mild, Four-Component Reaction

TL;DR: In this article, 1-(Cyclohexylamino)-2-(aryl)pyrrolo[1,2-a]quinoline-3-carbonitrile derivatives were synthesized in an efficient method from four-component condensation reaction between cyclohexyl isocyanide, quinoline, malononitrile, and aromatic aldehydes in the presence of a catalytic amount of titanium dioxide (TiO2) in CH2Cl2 at ambient temperature in good yields.
Journal ArticleDOI

An asymmetric hydrocyanation/Michael reaction of α-diazoacetates via Cu(I)/chiral guanidine catalysis

TL;DR: An asymmetric one-pot hydrocyanation/Michael reaction of α-aryl diazoacetates with trimethylsilyl cyanide, tert-butanol, and N-phenylmaleimides has been realized in good yields with excellent diastereo- and enantioselectivities.
Journal ArticleDOI

Uniting Amide Synthesis and Activation by PIII/PV-Catalyzed Serial Condensation: Three-Component Assembly of 2-Amidopyridines.

TL;DR: In this paper, an organophosphorus (PIII/PV redox) catalyzed method for the three-component condensation of amines, carboxylic acids, and pyridine Noxides to generate 2-amidopyridines via serial dehydration is reported.
Journal ArticleDOI

Solvent free preparation of amidophosphonates from isocyanides

TL;DR: In this paper, a two-step Mannich/Ugi one-pot procedure from isocyanides was used to synthesize Aminophosphonates from primary amines, dialkyl phosphites and carbonyl compounds under LiClO 4 catalysis.
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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.