Literature DB >> 12470248

The application of multi-component reactions in drug discovery.

Lutz Weber1.   

Abstract

Multi-component reactions (MCRs) enable the facile, automated and high throughput generation of small organic molecules. MCRs have been used to create diversity oriented and biased combinatorial libraries, to accomplish the synthesis of highly complex natural products as well as for the large-scale production of drug candidates. This provides medicinal chemists with a powerful tool to create novel chemical diversity, matching the space of biological targets with relevant chemistry. The discovery of novel MCRs has become an increasingly active area of research, yielding novel chemical scaffolds for drug discovery efforts.

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Year:  2002        PMID: 12470248     DOI: 10.2174/0929867023368719

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  28 in total

1.  Microwave-assisted Mannich-type three-component reactions.

Authors:  Nicholas E Leadbeater; Hanna M Torenius; Heather Tye
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

2.  Local neighborhood behavior in a combinatorial library context.

Authors:  Dragos Horvath; Christian Koch; Gisbert Schneider; Gilles Marcou; Alexandre Varnek
Journal:  J Comput Aided Mol Des       Date:  2011-02-12       Impact factor: 3.686

Review 3.  Synthesis of Biologically Active Molecules through Multicomponent Reactions.

Authors:  Daniel Insuasty; Juan Castillo; Diana Becerra; Hugo Rojas; Rodrigo Abonia
Journal:  Molecules       Date:  2020-01-24       Impact factor: 4.411

4.  Synthesis of Constrained Heterocycles Employing Two Post-Ugi Cyclization Methods for Rapid Library Generation with In Cellulo Activity.

Authors:  Nicholas McConnell; Zhigang Xu; Vishnu Kumarasamy; Daekyu Sun; Brendan Frett; Hong-Yu Li
Journal:  ChemistrySelect       Date:  2017-12-19       Impact factor: 2.109

5.  A three component one-pot procedure for the synthesis of [1,2,4]triazolo/benzimidazolo-quinazolinone derivatives in the presence of H6P2W18O(62).18H2O as a green and reusable catalyst.

Authors:  Majid M Heravi; Leila Ranjbar; Fatemeh Derikvand; Behnoush Alimadadi; Hossien A Oskooie; Fatemeh F Bamoharram
Journal:  Mol Divers       Date:  2008-09-09       Impact factor: 2.943

6.  Multicomponent reactions of dimethyl methoxymalonate and dialkyl acetylenedicarboxylate in the presence of N-nucleophiles: one-pot synthesis of 2H-pyridinyl-2-butenedioates in water.

Authors:  Mohammad A Khalilzadeh; Zinatossadat Hossaini; Samaneh Kharian
Journal:  Mol Divers       Date:  2009-09-11       Impact factor: 2.943

7.  Cerium ammonium nitrate (CAN)-catalyzed four-component one-pot synthesis of multi-substituted pyrano[2,3-c] pyrazoles under ultrasound irradiation.

Authors:  Keyume Ablajan; Wang Liju; Yakefujiang Kelimu; Feng Jun
Journal:  Mol Divers       Date:  2013-08-06       Impact factor: 2.943

8.  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.

Authors:  Majid M Heravi; Leila Ranjbar; Fatemeh Derikvand; Behnoush Alimadadi
Journal:  Mol Divers       Date:  2008-10-01       Impact factor: 2.943

9.  An efficient synthesis of 2,5-diketopiperazine derivatives by the Ugi four-center three-component reaction.

Authors:  Sangwon Cho; Gyochang Keum; Soon Bang Kang; So-Yeop Han; Youseung Kim
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

10.  Ruthenium-Catalyzed Multicomponent Reactions: Access to α-Silyl-β-Hydroxy Vinylsilanes, Stereodefined 1,3-Dienes, and Cyclohexenes.

Authors:  Barry M Trost; Dennis C Koester; Ehesan U Sharif
Journal:  Chemistry       Date:  2016-01-25       Impact factor: 5.236

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