The Recent Impact of Natural Deep Eutectic Solvents on Asymmetric Organocatalysis

Abstract

Over the last 20 years, Deep-Eutectic Solvents (DES) have been making a significant impact in the field of chemistry, with applications in nanotechnology, biomass transformation, electrochemistry pharmaceuticals and a host of other applications that includes catalysis. Considering the importance of chiral organocatalysis for the selective synthesis of drugs, pharmaceuticals and fragrances, etc. DESs were quickly harnessed as the media for carrying out organocatalytic transformations. In this review, we discuss some of the most important examples from the literature that have made an impact in the field over the last 5 years. A more recent development has been the incorporation of DESs in structured and self-organized gel-like assemblies that are known as EutectoGels. These soft structures offer a more defined and compact environment that can influence stereoselectivity by pre-organizing the reactants in three-dimensional space, and potential control the types of transition states that can be formed.

1. Introduction

The pharmaceutical synthesis sector faces exponential growth to adopt more sustainable methodologies, driven by environmental and economic considerations. The search for alternatives to volatile and toxic organic solvents (VOTS) has been one of the most dynamic areas of research. In this context, deep eutectic solvents (DES) emerged as a promising class of green solvents, characterized by their negligible vapor pressure, low toxicity, and excellent biodegradability.

These remarkable substances known as DESs were developed by Andrew Abbott and coworkers in 2003; the first example was reline, which is a 1:2 mixture of choline chloride and urea. A DES is a mixture of two or more solid components that, when combined in a specific ratio, results in a liquid with a melting point significantly lower than that of each of the individual components [1]. This remarkable melting point depression is attributed to the formation of an intense network of intermolecular interactions, predominantly hydrogen bonds, between the components of the mixture. DESs can be tailored for specific applications by varying their composition or by diluting them with a limited amount of water.

In addition to their environmental advantages, DESs also present significant economic potential, particularly when composed of inexpensive and widely available components such as choline chloride, urea, glycerol, or organic acids. Their preparation is generally straightforward and does not require complex purification steps; as noted, DESs are typically obtained by simple mixing and heating of the components, which contributes to their attractiveness for both laboratory and industrial applications. Furthermore, their negligible vapor pressure minimizes losses due to volatilization and facilitates solvent reuse, providing an additional factor that can contribute to cost reduction in sustainable processes [1].

Due to the high boiling points and negligible vapor pressures of DESs, products cannot be isolated by simple evaporation of the solvents, unlike many conventional organic solvents. However, recovery is possible using conventional methods such as liquid–liquid extraction, solubilization and deconstruction of the DES by solubilization in water, precipitation by addition of water, or cooling of the reaction mixture, followed by purification through chromatography or recrystallization. These methods are widely employed and compatible with established laboratory and industrial practices.

Another important feature of DESs is their potential recyclability. In many catalytic systems, after product separation by extraction or filtration, the DES-containing phase can be directly reused in subsequent reaction cycles (see the examples in Section 2.1.1—Michael addition and Section 2.1.4—Multi-component reactions). In several examples reported in the literature (including the examples in Section 2.1.1 and Section 2.1.4), catalytic performance, including yield and selectivity, remains relatively stable over multiple cycles, although gradual decreases in activity may occur due to impurity accumulation, changes in water content, or partial component degradation. Thus, reusability constitutes one of the advantages often associated with DESs, especially in the context of sustainable processes.

Despite these promising properties, it is important to acknowledge that DESs also present certain limitations that must be considered when developing practical applications. Major challenges include the relatively high viscosity of many systems, which can limit mass transfer and slow reaction rates, as well as sensitivity to water content, which can significantly alter physicochemical properties and catalytic performance. Moreover, in some cases, efficient product isolation may require additional optimization, and scale-up implementation demands careful assessment of process stability and economic feasibility.

Within this class, Natural DESs (NADES), composed of primary metabolites such as sugars, amino acids, and organic acids, are of particular interest due to their biological origin and inherent biocompatibility. Current research has shown that the unique properties of DESs allow them to act not only as a simple reaction medium, but also as an active participant in catalytic processes, opening new avenues for the synthesis of drugs in a more efficient and sustainable way. In fact, other key developments include (a) reactive DESs (RDESs, see below) in which one or more of the components is a reactant in the actual reaction and (b) EutectoGels (see below), in which the DES forms part of a highly structured self-organized system that can support various types of reactions.

Although there have been reviews on the application of DESs in catalytic reactions over the last 5 years [2,3,4,5], including a list of named reactions performed in DESs published in 2025 [6,7], there has been no recent specific review uniquely focused on asymmetric organocatalysis in DESs in the last 5 years, since that of Alonso, Fanjul-Mosteirín and Amo, in 2021 [8,9].

2. Asymmetric Organocatalysis in Deep-Eutectic-Solvents

2.1. In DESs and NADES

For more than 10 years, DESs (and NADES) have been used to support all types of organic reaction, ranging from metal-based catalysis [7], to biocatalysis [1,8] and organocatalysis [5]. DESs have excellent attributes for this challenge, particularly as their physicochemical properties, like polarity, polarizability, viscosity and refractive index can be tailored to the necessities of the reactions at hand. In fact, there have been some computational studies carried out to try and match these properties with those required for efficient reactivity [10].

Organocatalysis uses small organic molecules, without the presence of transition metals, to accelerate and control reactions, with a remarkable ability to induce stereoselectivity. The operating mechanisms, involve to the larger extent, the formation of enamines and imines, or key structured and oriented hydrogen-bonding networks to operate and are essential for the high selectivity observed. In fact, the former operating mode is the key to why DESs can be so useful as replacements to normal organocatalysts.

The types of DESs that have been successfully used so far in asymmetric organic catalysis are indicated in

Table 1. Survey of the DES that have already been used in Asymmetric Organocatalysis.

Entry	Hydrogen-Bond Donor	Hydrogen-Bond Acceptor	Organocatalyst	Reaction Type	Reference
1	Glycerol	ChCl	I	Cross-Aldol Reaction	[11]
2	Fructose	ChCl	II	Michael Reaction	[12]
3	Urea	Ch Cl	III	Aldol Reaction	[13]
4	D-Glucose	(D/L)-malic acid	III	Aldol Reaction	[14]
5	Ethylene glycol	ChCl	IV	Aldol Reaction	[15]
6	Glycine	Ph3MePBr	V	Michael Reaction	[16]
7	Glycine	ChCl	VI	Michael Reaction	[17]
8	Glycerol	ChCl	VI	α-amination	[18]
9	(+)-camphor-sulfonic acid	(S) or (R)-N,N,N-trimethyl-(1-phenylethyl)ammonium methanesulfonate	-	Michael-type Friedel-Crafts reaction	[19]
10	L-proline	Glycolic acid	-	Michael Reaction	[20]
11	Ethylene Glycol	ChCl	VII	Conjugate additions	[21]

and the best performing chiral organocatalysts, are shown in Figure 1.

Current knowledge shows that DESs do not function as mere inert solvents in this type of catalysis, and research shows that they can be active participants in the reaction. A notable example was the observation that a Betaine/Sorbitol/Water DES, a NADES, was able to catalyze a Michael addition reaction with 99% yield, even in the absence of an organic catalyst [22]. This phenomenon suggests that the acid-base properties or hydrogen bonding interactions of the DES itself are sufficient to activate the substrate. This dual function, acting both as a solvent and a catalyst, is a unique feature of DESs.

2.1.1. The Michael Addition and Other Conjugate Additions

In 2023, our group published a study on the application of betaine-derived DESs in organocatalytic Michael addition reactions, simultaneously evaluating catalytic efficiency, system recyclability, and the potential of the DESs themselves to induce asymmetry [22]. Three chiral deep eutectic solvent systems (CDESs) were investigated: betaine/D-sorbitol/water, betaine/D-xylitol/water, and betaine/D-mannitol/water, in a 1:1:3 molar ratio. It should be noted that xylitol (sold as D-xylitol) is a meso compound, but was included as a bench-mark in this study. The Rawal organocatalyst, previously recognized for its high efficiency in this type of transformation, was employed. In reactions between acetylacetone or methyl 2-oxocyclopentane-1-carboxylate and trans-β-nitrostyrene, all three DESs afforded outstanding yields and enantioselectivities, reaching values of up to 99% for both parameters (Scheme 1). The reactions were carried out at 40 °C for 24 h, a temperature required to maintain the eutectic systems in the liquid state with suitable viscosity. These results show that the extensive hydrogen-bonding network characteristic of DESs does not compromise the activity of the organocatalyst; on the contrary, it may even play a beneficial role by stabilizing the transition state through hydrogen-bonding interactions with the catalyst.

One of the most relevant aspects of this work was the high recyclability of the system. In the case of the betaine/D-sorbitol/water DES, up to 10 consecutive cycles could be performed in the reaction with methyl 2-oxocyclopentane-1-carboxylate while maintaining high yields and enantioselectivities (97% yield and 93% ee in the 10th cycle) [22]. These results demonstrate that the DES acts simultaneously as the reaction medium and as a non-covalent immobilization matrix for the organocatalyst, clearly contributing to the sustainability of the process.

Particularly interesting was the study carried out in the absence of catalyst, aimed at evaluating the intrinsic contribution of the DES chirality to asymmetric induction. Remarkably, the betaine/D-sorbitol/water system promoted the reaction with 81% yield and 75% ee, demonstrating that the CDES itself can act as a direct source of asymmetry (Scheme 2). In contrast, the DES containing D-mannitol afforded an ee value of 3%, suggesting that small structural differences in the saccharide component have a decisive impact on the organization of the hydrogen-bonding network and on the differential stabilization of the transition state [22]. D-xylitol (the achiral benchmark) gave an ee of 3%, which was undoubtedly due to experimental error.

DFT-based computational studies corroborated this interpretation, showing that the presence of D-sorbitol leads to a lowering of the transition-state energy, most likely due to hydrogen-bonding interactions with the reaction transition-state complex. Taken together, these results support the idea that DESs can exert a cooperative catalytic effect, not only as green solvents or immobilization matrices, but also as structurally organized entities capable of energetically modulating the transition state [22].

Overall, this work demonstrates that betaine-derived CDESs can play a multifunctional role in asymmetric organocatalysis, acting simultaneously as a sustainable reaction medium, a reusable catalyst immobilization system, and a potential direct inducer of enantioselectivity.

In a more recent study, Alonso and co-workers developed a new class of CDESs based on L-prolinol and (ammonium-methyl)pyrrolidine salts derived from L-proline, designed to integrate, within a single platform, both the eutectic medium and the chiral organocatalyst [23,24]. The formation of the CDESs was confirmed by comparing theoretical and experimental solid-liquid equilibrium curves, as well as by Differential Scanning Calorimetry (DSC) and NMR studies, which revealed the non-ideal behavior of the mixtures and the presence of extensive intermolecular hydrogen-bonding interactions. These systems were applied as reaction media in the asymmetric conjugate addition between cyclohexanone and trans-β-nitrostyrene at 30 °C.

Regarding the CDESs composed of L-prolinol-based chiral liquids, they were evaluated both as solvent media and as chiral organocatalysts in the asymmetric conjugate addition of cyclohexanone to trans-β-nitrostyrene at 30 °C over 3 days (Scheme 3) [23]. The CDESs that showed the best performance, higher conversions, diastereoselectivities and enantioselectivies, were L-prolinol/glycolic acid (1:1) (CDES A) and L-prolinol/TBAB (2:1) (CDES B), with CDES A exhibiting slightly higher enantioselectivity values (Scheme CDES). The authors also compared the results obtained with the chiral liquid L-prolinol/GA (1:1) to reactions performed with L-prolinol in VOCs or under neat conditions, which proved to be similar or superior.

Another important aspect of these CDESs is their recyclability. The system was recycled and reused for five cycles under the same reaction conditions. Both conversion and diastereoselectivity remained practically constant throughout the five cycles. However, enantioselectivity remained nearly constant during the first four cycles, but a marked decrease was observed in the fifth cycle, particularly for the syn-diastereoisomer. The authors also investigated the reaction scope for the best-performing CDES system. A modest range of substrates was tested, showing very good activity and moderate to good diastereo- and enantioselectivities in the organocatalyzed conjugate addition of ketones to β-nitrostyrenes. Furthermore, a gram-scale protocol for the conjugate addition was developed.

Among the CDESs evaluated, the mixtures (S)-2-hydroxy-N,N-dimethyl-N-(pyrrolidin-2-ylmethyl)ethan-1-ammonium bromide/ethylene glycol (1:3) and (S)-(1-pyrrolidin-2-ylmethyl)quinuclidinium bromide/urea (1:2) afforded quantitative conversions (>99%) within 24 h (Scheme 4). In the case of the (S)-2-hydroxy-N,N-dimethyl-N-(pyrrolidin-2-ylmethyl)ethan-1-ammonium bromide/ethylene glycol system, moderate diastereoselectivities (dr 60:40) and very high enantioselectivity for the minor diastereomer (ee > 99% for the anti isomer) were observed, whereas the major diastereomer displayed 61% ee. Similar results were obtained with the (S)-(1-pyrrolidin-2-ylmethyl)quinuclidinium bromide/urea system, albeit with lower enantioselectivity for the predominant isomer (34% ee) [24]. It is particularly noteworthy that the isolated chiral salts showed virtually no catalytic activity (<5% conversion) [24]. This finding demonstrates that the supramolecular structure of the CDES is crucial for reaction activation, likely by promoting the iminium–enamine equilibrium and stabilizing the nitronate intermediate.

Recyclability studies further showed that the (S)-2-hydroxy-N,N-dimethyl-N-(pyrrolidin-2-ylmethyl)ethan-1-ammonium bromide/ethylene glycol system can be reused for up to four cycles while maintaining the dr and ee values, although a progressive decrease in conversion is observed after the second cycle. This decline is attributed to the strengthening of intermolecular interactions within the CDES, which progressively makes the catalytic center less accessible over successive cycles [24].

These results once again reinforce the concept of CDESs as multifunctional catalytic systems, in which the supramolecular organization of the reaction medium directly influences not only the reactivity but also the stereochemical control of the transformation.

2.1.2. The Aldol Condensation

Another particularly illustrative example of the role of DESs in modulating selectivity in asymmetric organocatalysis was reported by Hassan Al Beiruty et al. in 2024, in a study of the competitive reaction between cyclohexanone and 4-nitrobenzaldehyde in the presence of acetylacetone [25]. In ChCl/Urea (1:2), using 30 mol% of chiral organocatalyst 1 and magnetic stirring, high conversion was achieved (92% in 36 h), but only modest diastereoselectivity (1.7:1) and low enantiomeric excess (32% ee) were obtained. Replacing magnetic stirring with ball milling significantly reduced the reaction time to 7 h and led to clear improvements in both diastereoselectivity and enantioselectivity [25]. An even more pronounced effect was observed upon controlled addition of water, forming the ternary ChCl/urea/water system (1:2:5.7). Under these conditions, a marked increase in chemoselectivity (aldol/Knoevenagel ratio = 15:1), diastereoselectivity (8:1), and enantioselectivity (96% ee for the anti-product) was observed, while maintaining high conversion (93%) (Scheme 5). In addition, the catalyst loading could be reduced to 5 mol% without significant loss of performance. Screening of other DES compositions further showed that both conversion and selectivity depend critically on the nature of the eutectic solvent and, in particular, on the controlled presence of water. The study of the scope further revealed that different ketones, especially cyclic ones, afforded enantiomeric excesses between 53% and 99% ee for the anti-product, highlighting the robustness and versatility of the system [25].

In 2026, Benrzeil et al. reported the synthesis of a new chiral organocatalyst, 14-(4-(pyrrolidine-2-carboxamido)phenyl)-14H-dibenzo[a,j]xanthene, and evaluated its catalytic performance in the enantioselective aldol reaction between cyclohexanone and p-nitrobenzaldehyde [26]. The catalyst displayed very good activity, affording high yields and excellent enantioselectivities under optimized conditions. Notably, the DES, choline chloride/ethylene glycol (1:2) led to an enhancement in reaction rate, allowing efficient product formation under relatively mild conditions (Scheme 6). However, water was identified as the optimal medium, furnishing the product in 5.5 h with 99% yield, 72% de, and 89% ee, thus providing the most favorable balance between reactivity and stereocontrol. In comparison, organic solvents generally resulted in lower diastereoselectivities, with the exception of DMSO, which maintained comparatively high de values, however reaction times of up to 48 h were required.

Unfortunately, the authors did not evaluate the recyclability of the organocatalyst. The use of a DES medium facilitated more efficient catalyst recycling, owing to the inherent properties of these.

Overall, these results confirm that DESs can act as structured reaction media in this type of transformation, simultaneously modulating reactivity, chemoselectivity, and chiral induction—an effect that is not observed under purely aqueous conditions or in conventional organic solvents.

Another representative example of the use of CDESs in aldol reactions was reported by Zárate-Roldán and co-workers, who developed chiral DESs based on L-proline (as the HBA) combined with different hydrogen-bond donors (EG, DEG, TEG, glycerol and xylitol) (Scheme 7) [27]. These systems were explored as “2-in-1” platforms for the asymmetric aldol reaction between cyclohexanone and 3-nitrobenzaldehyde, carried out at room temperature over 18–74 h (Scheme 6). In these CDESs, the incorporated L-proline (LP) acts simultaneously as the organocatalyst, via enamine formation, and as part of the DES [27].

Among the systems evaluated, the L-Proline (LP)/DEG (Diethyleneglycol) (1:130) DES showed the best performance, allowing the effective L-proline loading to be reduced to only 10 mol% while achieving near-quantitative yields, an anti/syn diastereomeric ratio of 10:1, and enantiomeric excesses of up to 96% for the anti-isomer. Other DESs also displayed high selectivity: LP/EG (Ethyleneglycol) reached up to 93% ee, LP/TEG (Triethyleneglycol) up to 84% ee, and LP/Gly (Glycerol) and LP/Xy (Xylitol) up to 92% ee [27]. These results highlight that the nature of the glycol directly shapes the supramolecular microenvironment, contributing to stereochemical control and selective stabilization of the transition state.

It was further observed that, in several cases, reducing the fraction of L-proline in the DES led to simultaneous improvements in both diastereoselectivity and enantioselectivity, suggesting that the hydrogen-bonding network established by the glycol plays a crucial role in the selective stabilization of the transition state. Compared with conventional methodologies, which typically require about 30 mol% of L-proline in solvents such as DMSO, this system enables a significant reduction in catalyst loading while maintaining or even surpassing enantioselectivity levels. The absolute configuration of the products was confirmed by X-ray crystallography, supporting the proposed stereochemical model [27].

Overall, these results demonstrate that amino acid-based CDESs can also operate as multifunctional catalytic systems, in which the supramolecular organization of the reaction medium directly influences both reactivity and enantioinduction. Moreover, this approach represents a sustainable and highly efficient alternative to conventional asymmetric organocatalysis.

2.1.3. Carbonyl α-Aminations

The study by Guillena and coworkers in 2018 provides a representative example of enantioselective α-amination of 1,3-dicarbonyl compounds efficiently carried out in sustainable reaction medium [18]. The authors demonstrated that DESs, particularly ChCl/Gly and ChCl/Urea (molar ratio 1:2), can serve as effective reaction media when combined with chiral organocatalysts derived from 2-aminobenzimidazole [18].

Under mild conditions (0 °C or 25 °C under ultrasound irradiation at 360 W), high conversions of up to 95% and ees of up to 84% in ChCl/Urea and 82% in ChCl/Gly were achieved (Scheme 8). The catalyst bearing nitro substituents on the benzimidazole ring exhibited the highest selectivity. These results highlight that cooperative interactions between the catalyst and the supramolecular DES network, mediated by hydrogen bonding, organize the reaction environment in a way that favors the formation of the R enantiomer [18].

The catalytic system also showed good recyclability, allowing recovery and reuse of both the catalyst and the reaction medium for at least five cycles while maintaining high ee values, although some loss of activity was observed depending on the extraction conditions. Studies on the reaction scope revealed that various β-ketoesters and 1,3-diketones are compatible with the system, whereas bulkier or more structurally rigid substrates led to more modest enantioselectivities (13–36% ee). Among the electrophiles evaluated, di-tert-butyl azodicarboxylate (DBAB) delivered the best results, underscoring the importance of this electrophile’s nature on the stereoselective performance of the reaction [18].

The robustness and synthetic applicability of the method were further demonstrated by its implementation on gram scale, maintaining high yields and enantioselectivity (95% and 85% ee, respectively). In addition, the methodology was applied to the functionalization of oxindoles and indolinones, as well as to conjugate addition reactions, affording products with high diastereoselectivity and enantiomeric excesses of up to 57% [18].

Overall, these results confirm that the integration of asymmetric organocatalysis with DESs constitutes a green, efficient, and scalable strategy for the enantioselective functionalization of 1,3-dicarbonyl compounds, reinforcing the key role of the solvent’s supramolecular microenvironment in stereochemical control.

2.1.4. Multi-Component Reactions

A relevant example of the potential of DESs in asymmetric multicomponent reactions is one from the Burke group, that focused on the first Bucherer-Bergs reaction in DESs, using N-benzylisatins giving spiro-oxindole hydantoins [28] (Scheme 9). Different eutectic systems in a molar ratio of 1:1:3—betaine/D-sorbitol/water (DES A), a reactive DES based on ammonium carbonate/D-sorbitol/water (DES B), and an isotopic variant containing deuterium oxide (DES C)—were evaluated as sustainable alternatives to the conventional MeOH/H₂O system. Although the yields obtained in DESs did not, overall, surpass those achieved in the conventional medium, the reactions could be performed at significantly lower temperatures (60 °C vs. 95 °C). This suggests that the microstructure of the DES may favorably influence the energetic profile of the transformation, despite limitations associated with high viscosity and mass transfer.

Comparison between DES A and its isotopic variant (DES C) highlighted the structural role of water in organizing the solvent hydrogen-bonding network, with a direct impact on reaction yield.

Strategies for asymmetric induction were explored using the chiral DESs based on D-sorbitol and by adding chiral organocatalysts (Rawal’s catalyst and L-proline). However, under all conditions tested, only racemic products were obtained. This suggests that, in complex multicomponent reactions such as the Bucherer-Bergs reaction, the creation of chiral microenvironments in the solvent or the addition of certain organocatalysts alone is insufficient to impose stereochemical control. This limitation likely arises from the multistep nature of the process, the conformational flexibility of the intermediates, and the relatively demanding thermal conditions. In this context, the development of alternative CDESs and more active catalysts capable of operating at lower temperatures emerges as a promising strategy to promote enantioselectivity in this type of transformation [28]. Besides, the planning can be assisted by computational tools that can match the chiral organocatalyst with the DES environment.

2.2. In Eutectogels

Another innovation is the use of eutectogels, which are a combination of DESs with low molecular weight gelling agents (LMWGs). These “soft” and organized materials help to create a structured environment that can influence stereoselectivity by pre-organizing the reactants in three-dimensional space, a level of control that is not possible in liquid solvents. This approach to reaction environment engineering demonstrates that the application of DES in organic catalysis goes far beyond the simple replacement of solvents, representing a breakthrough in the design of new catalytic systems. Eutectogels present promising physicochemical properties and have been successfully applied in a wide range of applications [29], including wastewater treatment [30], underwater applications [31], CO₂ separation [32], lubricants [33], energy-related applications [34], packaging [35], drug delivery systems [36,37], biocatalysis [38] and chiral applications [39].

To the best of our knowledge, despite their enormous potential, eutectogels remain largely unexplored in asymmetric organocatalysis, with only two reported examples describing their application in Aldol and Michael reactions.

2.2.1. The Aldol Reaction

In 2021, D’Anna and coworkers reported the first example of the application of natural eutectogels in enantioselective Aldol and Michael reactions [40]. They prepared and characterized several eutectogels using natural amino acids as gelators, namely L-proline, L-serine, L-cysteine, L-isoleucine, L-asparagine, and L-tryptophan, as well as L-proline derivatives such as L-prolinamide and trans-4-hydroxy-L-proline. Several hydrogen-bond donors (HBDs) and hydrogen-bond acceptors (HBAs) were tested; however, only choline chloride:urea (1:2) formed a gel.

After full characterization, the eutectogels with the best physicochemical properties were evaluated in the benchmark Aldol reaction. Reaction conditions were optimized using acetone and p-nitrobenzaldehyde in different ChCl/urea-based eutectogels, achieving a yield of 87% and an enantiomeric excess (ee) of 62% at 20 °C for 24 h using 5 wt% of L-proline (Scheme 10). Furthermore, the L-proline/ChCl/urea eutectogel was recycled over five cycles while maintaining the ee; however, the yield gradually decreased, reaching approximately half of its initial value by the fifth cycle. This eutectogel was successfully used to study the reaction scope. Various aromatic aldehydes bearing different electronic substituents at the ortho, meta, or para positions were investigated. In general, aldehydes containing electron-withdrawing groups favored the reaction outcome. The best results were obtained with cyano and nitro substituents, affording yields and enantioselectivities of up to 95% and 72% ee, respectively. The scope of ketone substrates was also evaluated, including cyclohexanone, cyclopentanone, and propanone derivatives (Scheme 10).

Among the four ketones studied, methoxypropanone provided the best results, likely due to its greater structural flexibility. The authors concluded that, considering the rigidity of the eutectogel network, more flexible substrates are better at supporting the formation of the enamine intermediate, which is an essential step for achieving efficient stereocontrol.

Overall, this work shows that DES-based natural eutectogels constitute a promising platform for sustainable organocatalysis, combining controlled stereochemical induction, high catalytic efficiency, and reusability, in clear alignment with the principles of Green Chemistry.

2.2.2. The Michael Reaction

D’Anna and coworkers. also applied the eutectogel, L-proline (5 wt%)/ChCl/urea (1:2) to asymmetric Michael reactions between nitrostyrene or maleimide derivatives (as electrophiles) and isobutyraldehyde (as nucleophile), in the presence of various additives (acids or organic bases) [40]. Excellent yields (>99%) were obtained for trans-β-styrene in the presence of 4-dimethylaminopyridine (DMAP), 1,4-diazabicyclo[2.2.2]octane (DABCO), imidazole, or 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU); however, the enantioselectivities were moderate (up to 23% ee) (Scheme 11A).

In the case of maleimide-based substrates, which possess more rigid structures, the combined rigidity of both the substrate and the eutectogel likely hindered access to the catalytic site, thereby limiting the reaction. Only trace amounts of products were obtained, and no conclusions regarding enantioselectivity could be drawn, as the ee values were not determined.

The same research group developed another series of eutectogels based on 1,3:2,4-dibenzylidene-D-sorbitol (DBS), in which DBS was used as the gelator in cholinium chloride-based DESs [41]. The systems varied according to the nature of the HBD, which included ethylene glycol, diethylene glycol, triethylene glycol, glycerol, and urea.

After full characterization, both the gels and the corresponding DESs were evaluated as solvent media for the asymmetric Michael addition between malononitrile and trans-chalcone, using L-proline (20 mol%) as a chiral organocatalyst at 25 °C for 24 h (Scheme 11B). In general, the gels provided similar or higher conversions and yields compared to the corresponding DESs; however, no enantioselectivity was observed in either medium. The best-performing system was DBS/ChCl/urea (1:2), which afforded a yield of 99%.

Several substrates were tested under the same reaction conditions, but no enantioselectivity was detected in the obtained products. In fact, the eutectogel network is more organized and may generate stronger intermolecular interactions, which could favor reactions involving substrates with greater structural flexibility, as previously observed for L-proline/ChCl/urea eutectogels.

Comparing these two types of gels, it can be noted that when L-proline acts both as gelator and organocatalyst, high yields can be achieved, depending on the nature of the substrates and additives, along with low enantioselectivities (below 27% ee). In contrast, when L-proline is used solely as an organocatalyst in the DBS-based eutectogels, no enantioselectivity is observed.

3. Conclusions

Deep eutectic solvents represent a paradigm shift in organic synthesis, transcending their role as simple green substitutes to become intrinsic and functional components of catalytic systems. Detailed analysis of their applications in biocatalysis, metal catalysis, and organic catalysis demonstrates their vast potential.

In organocatalysis DESs have proven to be more than inert solvents; they function as co-catalysts or even as autonomous catalysts, opening new avenues for the design of simpler and more efficient reactions. Their excellent recyclability and the possibility of creating structured materials such as eutectogels reinforce their role as a versatile platform for stereochemical control.

At the current time, the democratization of chemical sciences is an important issue, various useful chemical tools have been introduced during the last 2 decades in this context, notable examples include Click chemistry and catalysis, where due to the operational simplicity of these methods, specialist pre-training is not required. Along, with these “plug-and-play” type methods, one can certainly include DESs. These systems can really become bone-fide “plug-and-play” systems, due to their modular nature, and for their potential for harnessing with computational and AI methods [10].

With respect to costs, DESs are cheaper than ILs ($50–150/kilo), and also cheaper than most conventional solvents, whose price depends on various factors that include, purity, quantity and, petrochemical supply chains which is a critical issue at the current time [42].

Nevertheless, there are still important challenges to be addressed for applications in asymmetric organocatalysis: gaining a deeper understanding of the mechanistic role of the DES components in stereoselectivity (we are only scratching the surface at the moment), reducing the viscosity of the systems to optimize mass transfer, establishing standardized protocols for solvent recycling and reuse, and evaluating scalability and economic feasibility for industrial applications. Overcoming these issues will be essential to fully realize the potential of DESs as sustainable and efficient tools in drug synthesis, thereby consolidating their role in the future of green chemistry.

From an industrial point of view, although DESs are used in the cosmetic, nutraceutical sectors and biotech (biocatalysis), quite frequently, as well as in pharma R&D and process development, they still have not been applied for GMP API manufacturing.

In conclusion, intensive research on DESs is justified by the potential benefits in terms of efficiency, safety, and sustainability. The future of this area lies in the development of “tailor-made” DESs for specific reactions and in exploring their role as a structural and active matrix, beyond a simple solvation medium. This class of solvents is a pillar of green chemistry and an indispensable tool for the next generation of drug synthesis processes.