Literature DB >> 17763363

Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes.

Gian Cesare Tron1, Tracey Pirali, Richard A Billington, Pier Luigi Canonico, Giovanni Sorba, Armando A Genazzani.   

Abstract

In recent years, there has been an ever-increasing need for rapid reactions that meet the three main criteria of an ideal synthesis: efficiency, versatility, and selectivity. Such reactions would allow medicinal chemistry to keep pace with the multitude of information derived from modern biological screening techniques. The present review describes one of these reactions, the 1,3-dipolar cycloaddition ("click-reaction") between azides and alkynes catalyzed by copper (I) salts. The simplicity of this reaction and the ease of purification of the resulting products have opened new opportunities in generating vast arrays of compounds with biological potential. The present review will outline the accomplishments of this strategy achieved so far and outline some of medicinal chemistry applications in which click-chemistry might be relevant in the future. (c) 2007 Wiley Periodicals, Inc.

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Year:  2008        PMID: 17763363     DOI: 10.1002/med.20107

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  105 in total

1.  Targeting tuberculosis through a small focused library of 1,2,3-triazoles.

Authors:  Guillermo R Labadie; Agustina de la Iglesia; Héctor R Morbidoni
Journal:  Mol Divers       Date:  2011-06-02       Impact factor: 2.943

2.  Copper(II)-Catalyzed Conversion of Aryl/Heteroaryl Boronic Acids, Boronates, and Trifluoroborates into the Corresponding Azides: Substrate Scope and Limitations.

Authors:  Kimberly D Grimes; Amol Gupte; Courtney C Aldrich
Journal:  Synthesis (Stuttg)       Date:  2010-05-01       Impact factor: 3.157

3.  α-Azido ketones. Part 7: synthesis of 1,4-disubstituted triazoles by the "click" reaction of various terminal acetylenes with phenacyl azides or α-azidobenzo(hetera)cyclanones.

Authors:  Krisztina Kónya; Szabolcs Fekete; Anita Abrahám; Tamás Patonay
Journal:  Mol Divers       Date:  2012-02-04       Impact factor: 2.943

4.  Highly efficient click labeling using 2-[¹⁸F]fluoroethyl azide and synthesis of an ¹⁸FN-hydroxysuccinimide ester as conjugation agent.

Authors:  Dong Zhou; Wenhua Chu; Carmen S Dence; Robert H Mach; Michael J Welch
Journal:  Nucl Med Biol       Date:  2012-07-04       Impact factor: 2.408

5.  Conformational remodeling of femtomolar inhibitor-acetylcholinesterase complexes in the crystalline state.

Authors:  Yves Bourne; Zoran Radić; Palmer Taylor; Pascale Marchot
Journal:  J Am Chem Soc       Date:  2010-11-19       Impact factor: 15.419

6.  Inhibition of siderophore biosynthesis by 2-triazole substituted analogues of 5'-O-[N-(salicyl)sulfamoyl]adenosine: antibacterial nucleosides effective against Mycobacterium tuberculosis.

Authors:  Amol Gupte; Helena I Boshoff; Daniel J Wilson; João Neres; Nicholas P Labello; Ravindranadh V Somu; Chengguo Xing; Clifton E Barry; Courtney C Aldrich
Journal:  J Med Chem       Date:  2008-12-11       Impact factor: 7.446

Review 7.  Computational studies on the regioselectivity of metal-catalyzed synthesis of 1,2,3 triazoles via click reaction: a review.

Authors:  Tayebeh Hosseinnejad; Bahareh Fattahi; Majid M Heravi
Journal:  J Mol Model       Date:  2015-09-18       Impact factor: 1.810

8.  Regioselective intramolecular dipolar cycloaddition of azides and unsymmetrical alkynes.

Authors:  Ryan A Brawn; Morgan Welzel; Jason T Lowe; James S Panek
Journal:  Org Lett       Date:  2010-01-15       Impact factor: 6.005

9.  Expedient Synthesis of SMAMPs via Click Chemistry.

Authors:  Tsung-Hao Fu; Yan Li; Hitesh D Thaker; Richard W Scott; Gregory N Tew
Journal:  ACS Med Chem Lett       Date:  2013-07-22       Impact factor: 4.345

10.  Beta-lactam-based approach for the chemical programming of aldolase antibody 38C2.

Authors:  Julia I Gavrilyuk; Ulrich Wuellner; Carlos F Barbas
Journal:  Bioorg Med Chem Lett       Date:  2009-01-15       Impact factor: 2.823

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