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Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction

Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cy...

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Detalles Bibliográficos
Autores principales: Gahtory, Digvijay, Sen, Rickdeb, Kuzmyn, Andriy R., Escorihuela, Jorge, Zuilhof, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099469/
https://www.ncbi.nlm.nih.gov/pubmed/29542846
http://dx.doi.org/10.1002/anie.201800937
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author Gahtory, Digvijay
Sen, Rickdeb
Kuzmyn, Andriy R.
Escorihuela, Jorge
Zuilhof, Han
author_facet Gahtory, Digvijay
Sen, Rickdeb
Kuzmyn, Andriy R.
Escorihuela, Jorge
Zuilhof, Han
author_sort Gahtory, Digvijay
collection PubMed
description Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cycloaddition between cyclopropenes and o‐quinones in solution and on a surface. We demonstrate the “click character” of the reaction in solution and on surfaces for both monolayer and polymer brush functionalization.
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spelling pubmed-60994692018-08-24 Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction Gahtory, Digvijay Sen, Rickdeb Kuzmyn, Andriy R. Escorihuela, Jorge Zuilhof, Han Angew Chem Int Ed Engl Communications Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cycloaddition between cyclopropenes and o‐quinones in solution and on a surface. We demonstrate the “click character” of the reaction in solution and on surfaces for both monolayer and polymer brush functionalization. John Wiley and Sons Inc. 2018-04-17 2018-08-06 /pmc/articles/PMC6099469/ /pubmed/29542846 http://dx.doi.org/10.1002/anie.201800937 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Gahtory, Digvijay
Sen, Rickdeb
Kuzmyn, Andriy R.
Escorihuela, Jorge
Zuilhof, Han
Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title_full Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title_fullStr Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title_full_unstemmed Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title_short Strain‐Promoted Cycloaddition of Cyclopropenes with o‐Quinones: A Rapid Click Reaction
title_sort strain‐promoted cycloaddition of cyclopropenes with o‐quinones: a rapid click reaction
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099469/
https://www.ncbi.nlm.nih.gov/pubmed/29542846
http://dx.doi.org/10.1002/anie.201800937
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