ArticleBeilstein journal of organic chemistry2016
Towards the development of continuous, organocatalytic, and stereoselective reactions in deep eutectic solvents.
Article in Beilstein journal of organic chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Chiral Bicomponent Melamine/Amino Acid Eutectogels: Efficient Catalysts for the Aldol Reaction.ChemSusChem · 2026Article
- Organic Named Reactions in Green Deep Eutectic Solvents (DESs).Topics in current chemistry (Cham) · 2025Review
- Selective Aerobic Oxidation of Alcohols in Low Melting Mixtures and Water and Use for Telescoped One-Pot Hybrid Reactions.ChemistryOpen · 2022Article
- Deep Eutectic Solvents in Solar Energy Technologies.Molecules (Basel, Switzerland) · 2022Review
- Nitroalkene reduction in deep eutectic solvents promoted by BHBeilstein journal of organic chemistry · 2021Article
- Deep Eutectic Solvents as Effective Reaction Media for the Synthesis of 2-Hydroxyphenylbenzimidazole-based Scaffolds en Route to Donepezil-Like Compounds.Molecules (Basel, Switzerland) · 2020Article
- Organocatalytic Asymmetric Conjugate Addition of Aldehydes to Maleimides and Nitroalkenes in Deep Eutectic Solvents.Molecules (Basel, Switzerland) · 2019Article
- Increased Selectivity of Novozym 435 in the Asymmetric Hydrolysis of a Substrate with High Hydrophobicity Through the Use of Deep Eutectic Solvents and High Substrate Concentrations.Molecules (Basel, Switzerland) · 2019Article
- Deep Eutectic Solvents as Novel and Effective Extraction Media for Quantitative Determination of Ochratoxin A in Wheat and Derived Products.Molecules (Basel, Switzerland) · 2017Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Different deep eutectic solvent (DES) mixtures were studied as reaction media for the continuous synthesis of enantiomerically enriched products by testing different experimental set-ups. L-Proline-catalysed cross-aldol reactions were efficiently performed in continuo, with high yield (99%),
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Registered trials
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