Literature DB >> 18174988

Dynamic combinatorial chemistry: on the road to fulfilling the promise.

Sylvain Ladame1.   

Abstract

Dynamic combinatorial chemistry makes use of reversible reactions between functionalised monomeric building blocks to generate a mixture of products (dimers or oligomers) under thermodynamic equilibrium. This system reorganises upon addition of a target so that species that bind to, and are therefore stabilised by the target, are favourably formed and are thus amplified. Since the mid-1990's, dynamic combinatorial chemistry has been successfully applied to the identification/selection of ion receptors, enzyme inhibitors, catalysts, materials and nucleic acid ligands. Although it is now established as a powerful tool with broad applications some intrinsic limitations appeared when working on systems of increasing complexity. We present here the most recent advances in the field of dynamic combinatorial chemistry that have been developed to overcome these limitations and explore new areas of application.

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Year:  2007        PMID: 18174988     DOI: 10.1039/b714599c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  24 in total

1.  Synthesis and ring-chain-ring tautomerism of bisoxazolidines, thiazolidinyloxazolidines, and spirothiazolidines.

Authors:  Cecilia Saiz; Peter Wipf; Graciela Mahler
Journal:  J Org Chem       Date:  2011-06-14       Impact factor: 4.354

2.  Hierarchical functional gradients of pH-responsive self-assembled monolayers using dynamic covalent chemistry on surfaces.

Authors:  Lara Tauk; André P Schröder; Gero Decher; Nicolas Giuseppone
Journal:  Nat Chem       Date:  2009-10-23       Impact factor: 24.427

3.  Nucleophilic catalysis of acylhydrazone equilibration for protein-directed dynamic covalent chemistry.

Authors:  Venugopal T Bhat; Anne M Caniard; Torsten Luksch; Ruth Brenk; Dominic J Campopiano; Michael F Greaney
Journal:  Nat Chem       Date:  2010-05-16       Impact factor: 24.427

4.  Dynamic covalent chemistry enables formation of antimicrobial peptide quaternary assemblies in a completely abiotic manner.

Authors:  James F Reuther; Justine L Dees; Igor V Kolesnichenko; Erik T Hernandez; Dmitri V Ukraintsev; Rusheel Guduru; Marvin Whiteley; Eric V Anslyn
Journal:  Nat Chem       Date:  2017-08-21       Impact factor: 24.427

5.  Dynamic thiol exchange with β-sulfido-α,β-unsaturated carbonyl compounds and dithianes.

Authors:  Gururaj Joshi; Eric V Anslyn
Journal:  Org Lett       Date:  2012-08-30       Impact factor: 6.005

6.  Dynamic combinatorial selection of molecules capable of inhibiting the (CUG) repeat RNA-MBNL1 interaction in vitro: discovery of lead compounds targeting myotonic dystrophy (DM1).

Authors:  Peter C Gareiss; Krzysztof Sobczak; Brian R McNaughton; Prakash B Palde; Charles A Thornton; Benjamin L Miller
Journal:  J Am Chem Soc       Date:  2008-12-03       Impact factor: 15.419

7.  Reversible thiazolidine exchange: a new reaction suitable for dynamic combinatorial chemistry.

Authors:  Cecilia Saiz; Peter Wipf; Eduardo Manta; Graciela Mahler
Journal:  Org Lett       Date:  2009-08-06       Impact factor: 6.005

8.  Discovering Echinococcus granulosus thioredoxin glutathione reductase inhibitors through site-specific dynamic combinatorial chemistry.

Authors:  Cecilia Saiz; Valerie Castillo; Pablo Fontán; Mariana Bonilla; Gustavo Salinas; Alejandra Rodríguez-Haralambides; S Graciela Mahler
Journal:  Mol Divers       Date:  2013-10-18       Impact factor: 2.943

9.  Generation of a Multicomponent Library of Disulfide Donor-Acceptor Architectures Using Dynamic Combinatorial Chemistry.

Authors:  Wojciech Drożdż; Michał Kołodziejski; Grzegorz Markiewicz; Anna Jenczak; Artur R Stefankiewicz
Journal:  Int J Mol Sci       Date:  2015-07-17       Impact factor: 5.923

10.  A dynamic combinatorial approach for identifying side groups that stabilize DNA-templated supramolecular self-assemblies.

Authors:  Delphine Paolantoni; Sonia Cantel; Pascal Dumy; Sébastien Ulrich
Journal:  Int J Mol Sci       Date:  2015-02-06       Impact factor: 5.923

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