Abstract
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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Soares, M. I. L., Cardoso, A. L., & Pinho E Melo, T. M. V. D. (2022, February 1). Diels–Alder Cycloaddition Reactions in Sustainable Media. Molecules. MDPI. https://doi.org/10.3390/molecules27041304
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