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A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors
A versatile one‐step photopolymerization approach for the immobilization of enantioselective organocatalysts is presented. Chiral organocatalyst‐containing monoliths based on polystyrene divinylbenzene copolymer were generated inside channels of microfluidic chips. Exemplary performance tests were p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693110/ https://www.ncbi.nlm.nih.gov/pubmed/32453458 http://dx.doi.org/10.1002/chem.202002063 |
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author | Warias, Rico Ragno, Daniele Massi, Alessandro Belder, Detlev |
author_facet | Warias, Rico Ragno, Daniele Massi, Alessandro Belder, Detlev |
author_sort | Warias, Rico |
collection | PubMed |
description | A versatile one‐step photopolymerization approach for the immobilization of enantioselective organocatalysts is presented. Chiral organocatalyst‐containing monoliths based on polystyrene divinylbenzene copolymer were generated inside channels of microfluidic chips. Exemplary performance tests were performed for the monolithic Hayashi–Jørgensen catalyst in continuous flow, which showed good results for the Michael addition of aldehydes to nitroalkenes in terms of stereoselectivity and catalyst stability with minimal consumption of reagents and solvents. |
format | Online Article Text |
id | pubmed-7693110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76931102020-12-11 A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors Warias, Rico Ragno, Daniele Massi, Alessandro Belder, Detlev Chemistry Communications A versatile one‐step photopolymerization approach for the immobilization of enantioselective organocatalysts is presented. Chiral organocatalyst‐containing monoliths based on polystyrene divinylbenzene copolymer were generated inside channels of microfluidic chips. Exemplary performance tests were performed for the monolithic Hayashi–Jørgensen catalyst in continuous flow, which showed good results for the Michael addition of aldehydes to nitroalkenes in terms of stereoselectivity and catalyst stability with minimal consumption of reagents and solvents. John Wiley and Sons Inc. 2020-09-17 2020-10-15 /pmc/articles/PMC7693110/ /pubmed/32453458 http://dx.doi.org/10.1002/chem.202002063 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Warias, Rico Ragno, Daniele Massi, Alessandro Belder, Detlev A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title | A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title_full | A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title_fullStr | A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title_full_unstemmed | A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title_short | A Visible‐Light‐Powered Polymerization Method for the Immobilization of Enantioselective Organocatalysts into Microreactors |
title_sort | visible‐light‐powered polymerization method for the immobilization of enantioselective organocatalysts into microreactors |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693110/ https://www.ncbi.nlm.nih.gov/pubmed/32453458 http://dx.doi.org/10.1002/chem.202002063 |
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