scispace - formally typeset
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
Reads0
Chats0
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.

read more

Citations
More filters
Journal ArticleDOI

Lewis acid-catalyzed formation of Ugi four-component reaction product from Passerini three-component reaction system without an added amine

TL;DR: In this article, the phenol-Passerini three-component reaction (phenol-P-3CR) was shown to be amine equivalent in isocyanide-based multicomponent reactions (IMCRs).
Journal ArticleDOI

Novel Copper-Catalyzed Multicomponent Cascade Synthesis of Iminocoumarin Aryl Methyl Ethers

TL;DR: A copper(I)-catalyzed one-pot synthesis of iminocoumarin aryl methyl ethers has been developed from ynal, phenol, and sulfonyl azide at ambient conditions via a cascade of 1,3-pseudopericyclic ketenimine rearrangement, 1,4-conjugate addition, and aldol-type condensation.
Journal ArticleDOI

Three-component one-pot synthesis of 4,6-diarylpyrimidin- 2(1H)-ones under solvent-free conditions in the presence of sulfamic acid as a green and reusable catalyst

TL;DR: The condensation of acetophenone derivatives, aldehydes and urea in the presence of sulfamic acid was employed to synthesize a variety of pyrimidinones in moderate to excellent yields.
Journal ArticleDOI

Synthesis of Structurally Diverse Polyfunctional Pyrrolo[1,2-a]quinolines by Sequential Iron-Catalyzed Three-Component Coupling and Gold-Catalyzed Hydroarylation Reactions

TL;DR: In this paper, a simple and efficient synthesis of complex pyrrolo[1,2-a]quinoline derivatives was achieved through sequential reactions that involved an iron(III)-catalyzed synthesis of N-(2-alkynylaryl)pyrroles and a gold(III) catalyzed intramolecular hydroarylation reaction.
Related Papers (5)
Trending Questions (1)
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.