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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...

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Detalles Bibliográficos
Autores principales: Spitzbarth, Benjamin, Eelkema, Rienk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
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.
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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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