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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...

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Autores principales: Soares, Maria I. L., Cardoso, Ana L., Pinho e Melo, Teresa M. V. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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