Towards the development of continuous, organocatalytic, and stereoselective reactions in deep eutectic solvents

Scholarly Works

• Ahmer, M. F.; Ullah, Q. Development and applications of deep eutectic solvents in different chromatographic techniques. JPC – Journal of Planar Chromatography – Modern TLC 2022, 35, 549–570. doi:10.1007/s00764-022-00216-x
• Cicco, L.; Roggio, M.; López-Aguilar, M.; Ramos-Martín, M.; Perna, F. M.; García-Álvarez, J.; Vitale, P.; Capriati, V. Selective Aerobic Oxidation of Alcohols in Low Melting Mixtures and Water and Use for Telescoped One-Pot Hybrid Reactions. ChemistryOpen 2022, 11, e202200160. doi:10.1002/open.202200160
• Boldrini, C. L.; Quivelli, A. F.; Manfredi, N.; Capriati, V.; Abbotto, A. Deep Eutectic Solvents in Solar Energy Technologies. Molecules (Basel, Switzerland) 2022, 27, 709. doi:10.3390/molecules27030709
• Pandey, A.; Tiwari, B.; Vuppaladadiyam, A. K.; Varsha Vuppaladadiyam, S. S.; Leu, S.-Y.; Pandey, S. Deep eutectic solvents—An Introduction. Current Developments in Biotechnology and Bioengineering; Elsevier, 2022; pp 1–20. doi:10.1016/b978-0-323-99905-2.00003-0
• Saavedra, B.; Meli, A.; Rizzo, C.; Ramón, D. J.; D'Anna, F. Natural eutectogels: sustainable catalytic systems for C–C bond formation reactions. Green Chemistry 2021, 23, 6555–6565. doi:10.1039/d1gc01647d
• Wang, Y.; Yao, Q.-X.; He, J.-R.; Liang, Z.-H.; Li, X.; Cheng, H.; Li, L.-L. L-proline-catalyzed Knoevenagel reaction promoted by choline chloride-based deep eutectic solvents. Biomass Conversion and Biorefinery 2021, 12, 87–93. doi:10.1007/s13399-021-01747-9
• Wang, Y.; Yao, Q.-X.; He, J.-R.; Liang, Z.-H.; Li, X.; Cheng, H.; Li, L.-L. L-proline-catalyzed Knoevenagel reaction promoted by choline chloride-based deep eutectic solvents. Biomass Conversion and Biorefinery 2021, 1–7.
• Alonso, D. A.; Burlingham, S.-J.; Chinchilla, R.; Guillena, G.; Ramón, D. J.; Tiecco, M. Asymmetric Organocatalysis in Deep Eutectic Solvents. European Journal of Organic Chemistry 2021, 2021, 4065–4071. doi:10.1002/ejoc.202100385
• Faverio, C.; Boselli, M. F.; Gonzalez, P. C.; Puglisi, A.; Benaglia, M. Nitroalkene reduction in deep eutectic solvents promoted by BH3NH3. Beilstein journal of organic chemistry 2021, 17, 1041–1047. doi:10.3762/bjoc.17.83
• Fanjul-Mosteirín, N.; del Amo, V. Organocatalytic transformations in deep eutectic solvents: Green methodologies made greener. Tetrahedron 2021, 84, 131967. doi:10.1016/j.tet.2021.131967
• Płotka-Wasylka, J.; Rutkowska, M.; de la Guardia, M. Are deep eutectic solvents useful in chromatography? A short review. Journal of chromatography. A 2021, 1639, 461918. doi:10.1016/j.chroma.2021.461918
• Cicco, L.; Dilauro, G.; Perna, F. M.; Vitale, P.; Capriati, V. Advances in deep eutectic solvents and water: applications in metal- and biocatalyzed processes, in the synthesis of APIs, and other biologically active compounds. Organic & biomolecular chemistry 2021, 19, 2558–2577. doi:10.1039/d0ob02491k
• Bjelić, A.; Hočevar, B.; Grilc, M.; Novak, U.; Likozar, B. A review of sustainable lignocellulose biorefining applying (natural) deep eutectic solvents (DESs) for separations, catalysis and enzymatic biotransformation processes. Reviews in Chemical Engineering 2020, -1.
• Bjelić, A.; Hočevar, B.; Grilc, M.; Novak, U.; Likozar, B. A review of sustainable lignocellulose biorefining applying (natural) deep eutectic solvents (DESs) for separations, catalysis and enzymatic biotransformation processes. Reviews in Chemical Engineering 2020, 38, 243–272. doi:10.1515/revce-2019-0077
• Pelliccioli, V.; Dilauro, G.; Grecchi, S.; Arnaboldi, S.; Graiff, C.; Perna, F. M.; Vitale, P.; Licandro, E.; Aliprandi, A.; Cauteruccio, S.; Capriati, V. Ligand-Free Suzuki–Miyaura Cross-Coupling Reactions in Deep Eutectic Solvents : Synthesis of Benzodithiophene Derivatives and Study of their Optical and Electrochemical Performance. European Journal of Organic Chemistry 2020, 2020, 6981–6988. doi:10.1002/ejoc.202000889
• Emma, M. G.; Tamburrini, A.; Martinelli, A.; Lombardo, M.; Quintavalla, A.; Trombini, C. A Simple and Efficient Protocol for Proline-Catalysed Asymmetric Aldol Reaction. Catalysts 2020, 10, 649. doi:10.3390/catal10060649
• Krištofíková, D.; Modrocká, V.; Mečiarová, M.; Šebesta, R. Green Asymmetric Organocatalysis. ChemSusChem 2020, 13, 2828–2858. doi:10.1002/cssc.202000137
• Piemontese, L.; Sergio, R.; Rinaldo, F.; Brunetti, L.; Perna, F. M.; Santos, M. A.; Capriati, V. Deep Eutectic Solvents as Effective Reaction Media for the Synthesis of 2-Hydroxyphenylbenzimidazole-based Scaffolds en Route to Donepezil-Like Compounds. Molecules (Basel, Switzerland) 2020, 25, 574. doi:10.3390/molecules25030574
• Marset, X.; Ramón, D. J.; Guillena, G. Catalyst Immobilization; Wiley, 2019; pp 187–216. doi:10.1002/9783527817290.ch6
• Perna, F. M.; Vitale, P.; Capriati, V. Deep Eutectic Solvents; Wiley, 2019; pp 111–134. doi:10.1002/9783527818488.ch7

Explore citations to this article at