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Diels–Alder Cycloaddition Reactions in Sustainable Media
Diels–Alder cycloaddition reaction is one of the most powerful strategies for the construction of six-membered carbocyclic and heterocyclic systems, in most cases with high regio- and stereoselectivity. In this review, an insight into the most relevant advances on sustainable Diels–Alder reactions s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876200/ https://www.ncbi.nlm.nih.gov/pubmed/35209094 http://dx.doi.org/10.3390/molecules27041304 |
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author | Soares, Maria I. L. Cardoso, Ana L. Pinho e Melo, Teresa M. V. D. |
author_facet | Soares, Maria I. L. Cardoso, Ana L. Pinho e Melo, Teresa M. V. D. |
author_sort | Soares, Maria I. L. |
collection | PubMed |
description | Diels–Alder cycloaddition reaction is one of the most powerful strategies for the construction of six-membered carbocyclic and heterocyclic systems, in most cases with high regio- and stereoselectivity. In this review, an insight into the most relevant advances on sustainable Diels–Alder reactions since 2010 is provided. Various environmentally benign solvent systems are discussed, namely bio-based derived solvents (such as glycerol and gluconic acid), polyethylene glycol, deep eutectic solvents, supercritical carbon dioxide, water and water-based aqueous systems. Issues such as method’s scope, efficiency, selectivity and reaction mechanism, as well as sustainability, advantages and limitations of these reaction media, are addressed. |
format | Online Article Text |
id | pubmed-8876200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88762002022-02-26 Diels–Alder Cycloaddition Reactions in Sustainable Media Soares, Maria I. L. Cardoso, Ana L. Pinho e Melo, Teresa M. V. D. Molecules Review Diels–Alder cycloaddition reaction is one of the most powerful strategies for the construction of six-membered carbocyclic and heterocyclic systems, in most cases with high regio- and stereoselectivity. In this review, an insight into the most relevant advances on sustainable Diels–Alder reactions since 2010 is provided. Various environmentally benign solvent systems are discussed, namely bio-based derived solvents (such as glycerol and gluconic acid), polyethylene glycol, deep eutectic solvents, supercritical carbon dioxide, water and water-based aqueous systems. Issues such as method’s scope, efficiency, selectivity and reaction mechanism, as well as sustainability, advantages and limitations of these reaction media, are addressed. MDPI 2022-02-15 /pmc/articles/PMC8876200/ /pubmed/35209094 http://dx.doi.org/10.3390/molecules27041304 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Soares, Maria I. L. Cardoso, Ana L. Pinho e Melo, Teresa M. V. D. Diels–Alder Cycloaddition Reactions in Sustainable Media |
title | Diels–Alder Cycloaddition Reactions in Sustainable Media |
title_full | Diels–Alder Cycloaddition Reactions in Sustainable Media |
title_fullStr | Diels–Alder Cycloaddition Reactions in Sustainable Media |
title_full_unstemmed | Diels–Alder Cycloaddition Reactions in Sustainable Media |
title_short | Diels–Alder Cycloaddition Reactions in Sustainable Media |
title_sort | diels–alder cycloaddition reactions in sustainable media |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8876200/ https://www.ncbi.nlm.nih.gov/pubmed/35209094 http://dx.doi.org/10.3390/molecules27041304 |
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