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Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors
Over the last few decades, the study of more complex, chemical systems closer to those found in nature, and the interactions within those systems, has grown immensely. Despite great efforts, the need for new, versatile, and robust chemistry to apply in CRNs remains. In this Feature Article, we give...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508045/ https://www.ncbi.nlm.nih.gov/pubmed/37529876 http://dx.doi.org/10.1039/d3cc02126b |
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author | Spitzbarth, Benjamin Eelkema, Rienk |
author_facet | Spitzbarth, Benjamin Eelkema, Rienk |
author_sort | Spitzbarth, Benjamin |
collection | PubMed |
description | Over the last few decades, the study of more complex, chemical systems closer to those found in nature, and the interactions within those systems, has grown immensely. Despite great efforts, the need for new, versatile, and robust chemistry to apply in CRNs remains. In this Feature Article, we give a brief overview over previous developments in the field of systems chemistry and how β′-substituted Michael acceptors (MAs) can be a great addition to the systems chemist's toolbox. We illustrate their versatility by showcasing a range of examples of applying β′-substituted MAs in CRNs, both as chemical signals and as substrates, to open up the path to many applications ranging from responsive materials, to pathway control in CRNs, drug delivery, analyte detection, and beyond. |
format | Online Article Text |
id | pubmed-10508045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-105080452023-09-20 Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors Spitzbarth, Benjamin Eelkema, Rienk Chem Commun (Camb) Chemistry Over the last few decades, the study of more complex, chemical systems closer to those found in nature, and the interactions within those systems, has grown immensely. Despite great efforts, the need for new, versatile, and robust chemistry to apply in CRNs remains. In this Feature Article, we give a brief overview over previous developments in the field of systems chemistry and how β′-substituted Michael acceptors (MAs) can be a great addition to the systems chemist's toolbox. We illustrate their versatility by showcasing a range of examples of applying β′-substituted MAs in CRNs, both as chemical signals and as substrates, to open up the path to many applications ranging from responsive materials, to pathway control in CRNs, drug delivery, analyte detection, and beyond. The Royal Society of Chemistry 2023-07-26 /pmc/articles/PMC10508045/ /pubmed/37529876 http://dx.doi.org/10.1039/d3cc02126b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Spitzbarth, Benjamin Eelkema, Rienk Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title | Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title_full | Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title_fullStr | Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title_full_unstemmed | Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title_short | Chemical reaction networks based on conjugate additions on β′-substituted Michael acceptors |
title_sort | chemical reaction networks based on conjugate additions on β′-substituted michael acceptors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508045/ https://www.ncbi.nlm.nih.gov/pubmed/37529876 http://dx.doi.org/10.1039/d3cc02126b |
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