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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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Multicomponent reactions

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Synthesis and herbicidal and fungistatic evaluation of Passerini adducts bearing phenoxyacetic moieties

TL;DR: In this paper, a new idea for the modification of a carboxylic group in phenoxyacetic herbicides is proposed, where the chalcogen analogs (arylthio and arylselenyl fragments instead of a phenoxy one) are used as carboxyl components in the tricomponent Passerini reaction.

SiO2.TTC: Efficient Catalyst for Synthesis of 3,4-Dihydropyrimidine-2(1H)-ones/Thiones

TL;DR: In this article, an efficient method has been developed to synthesize various 3,4-dihydropyrimidinones by using aldehyde, ethylacetoacetate and urea or thiourea with silica supported Titanium trichloride.
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N-Oxide-Induced Ugi Reaction: A Rapid Access to Quinoline-C2-amino Amides via Deoxygenative C(sp2)-H Functionalization.

TL;DR: In this article , a logic-based replacement of the carboxylic acid component of the Ugi reaction by quinoline N-oxides has been developed, which plays a vital role by shifting the equilibria toward the product side with irreversible addition onto the C2 position of the Noxide.
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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.