Cinnamaldehyde Derivatives Research Articles

Antifungal activity of Cinnamaldehyde derivatives against fluconazole-resistant Candida albicans

BackgroundCandida albicans is an opportunistic pathogen commonly found in human mucous membranes. In light of the escalating challenge posed by antibiotic resistance of C. albicans strains worldwide, it is an urgently necessary to explore alternative therapeutic options. ObjectiveThis study aims to assess the efficacy of two Cinnamaldehyde derivatives, 2-Cl Cinnamaldehyde (2-Cl CA) and 4-Cl Cinnamaldehyde (4-Cl CA), against C. albicans through both in vitro experiments and in vivo murine models and to evaluate their potential as new drug candidates for treating C. albicans. Methods and resultsThe minimum inhibitory concentrations (MICs) of Cinnamaldehyde 2-Cl and 4-Cl benzene ring derivatives against C. albicans were 25 μg/mL. Time-killing experiments revealed that both Cinnamaldehyde derivatives exhibited fungicidal activity against C. albicans at concentrations of 5 MIC and 10 MIC. In the checkerboard experiment, 4-Cl CA did not show any antagonistic effect when combined with first-line antifungal drugs. Instead, it exhibited additive effects in combination with nystatin. Both 2-Cl and 4-Cl CA demonstrated inhibitory activity against C. albicans biofilm formation, especially at 8 MIC and 16 MIC concentrations. In C. albicans biofilm eradication experiments, although high drug concentrations of 2-Cl and 4-Cl CA were unable to eradicate the biofilm completely, they were still effective in killing C. albicans cells within the biofilm. Moreover, sub-inhibitory concentrations of 4-Cl CA (ranging from 5 to 20 μg/mL) significantly inhibited cell aggregation and hyphal formation. Furthermore, 4-Cl CA effectively inhibited intracellular C. albicans infection in macrophages. Lastly, the effectiveness of 4-Cl CA was evaluated in a mouse model of hematogenous disseminated candidiasis caused by C. albicans, which revealed that 4-Cl CA significantly reduced fungal burden and improved mouse survival compared to the untreated controls. ConclusionThe 4-Cl CA exhibited inhibitory effects against C. albicans through both in vivo and in vitro models, demonstrating its therapeutic potential as a promising new drug candidate for treating drug-resistant candidiasis albicans.

Use of p-methoxy cinnamaldehyde in label-assisted laser desorption/ionization mass spectrometry (LALDI-MS) for detection of different classes of primary amines, amino acids and neurotransmitters

Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS), useful for the detection of macromolecules, is generally not suitable for recording the mass spectrum of small molecules, especially within the range of m/z 500, because of the appearance of matrix cluster peaks in the small molecular weight range. To circumvent this problem, a matrix-free variant of MALDI-MS, namely Label-assisted laser desorption/ionization mass spectrometry (LALDI-MS) has been developed in recent years where analytes get covalently attached to a laser absorbing label which induces the desorption/ionization process thus facilitating the recording the mass spectra and avoiding the problem of formation of cluster peaks. In general, the probes used for such detections are all pyrene-based scaffolds which despite being a good laser-active chromophore have both reactivity and solubility problems. Inspired by the right chromophoric nature, we have undertaken a systematic study to design and optimize cinnamaldehyde derivatives and have found that p-methoxy cinnamaldehyde (PMC) as a simpler, cost-effective, less hydrophobic laser-active label, which can detect a series of primary amines, including the neurotransmitters and amino acids. The label PMC can also discriminate between aliphatic and aromatic primary amines.

Anti-inflammatory and antioxidant mechanisms of coniferaldehyde in lipopolysaccharide-induced neuroinflammation: Involvement of AMPK/Nrf2 and TAK1/MAPK/NF-κB signaling pathways

Microglia are primarily involved in inflammatory reactions and oxidative stress in the brain; as such reducing microglial activation has been proposed as a potential therapeutic strategy for neurodegenerative disorders. Herein, we investigated the anti-inflammatory and antioxidant activities of coniferaldehyde (CFA), a naturally occurring cinnamaldehyde derivative, on activated microglia to evaluate its therapeutic potential. CFA inhibited the production of nitric oxide (NO) and proinflammatory cytokines, such as tumor necrosis factor-α, interleukin (IL)-1β, and IL-6, in lipopolysaccharide (LPS)-stimulated BV2 microglial cells. CFA also inhibited intracellular reactive oxygen species levels and oxidative stress markers such as 4-HNE and 8-OHdG. Detailed mechanistic studies showed that CFA exerted anti-inflammatory effects by inhibiting TAK1-mediated MAP kinase/NF-κB activation and upregulating AMPK signaling pathways. In addition, CFA exerted antioxidant effects by inhibiting the NADPH oxidase subunits and by increasing the expression of antioxidant enzymes such as HO-1, NQO1, and catalase by upregulating Nrf2 signaling. Finally, we confirmed the effects of CFA on the brains of the LPS-injected mice. CFA inhibited microglial activation and the expression of proinflammatory markers and increased Nrf2-driven antioxidant enzymes. Furthermore, CFA inhibited the production of 4-HNE and 8-OHdG in the brains of LPS-injected mice. As a result, CFA's significant anti-inflammatory and antioxidant properties may have therapeutic applications in neuroinflammatory disorders related with oxidative stress and microglial activation.

Effects of Cinnamon on Cancer Prevention and Progression

Cinnamon has been used medicinally for centuries, but recently research has suggested it may have a role in cancer prevention and potentially treatment. The search for alternative and subjunctive therapies is essential due to the public demand and the increasing cost of healthcare. Here we review the biologically active components of cinnamon and discuss the methods of potential cinnamon activity against cancer including: transcription factor regulation and kinase activity. Nuclear Factor kappa B (NF-\(𝜿\)B) is a stress sensitive transcription factor that regulates transcription of genes involved in tumor progression and is inhibited by cinnamon components. Another way that cinnamon inhibits tumor growth is by suppression of transcription factor activator protein -1 (AP-1) which interacts with genes responsible for apoptosis, metastasis and inflammation. Hypoxia-inducible transcription factor-1 (HIF-1) and vascular endothelial growth factor (VEGF) are involved in angiogenesis, especially in the tumor microenvironment. The HIF-1-VEGF pathway are targeted by cinnamaldehyde, a compound found in cinnamon. Nuclear factor erythroid related factor 2 (Nrf2) is also examined and has been indicated to both potentially prevent cancer as well as induce it; various cinnamon derivatives target Nrf2. A cinnamaldehyde derivative has been implicated in a reduction of the mitogen-activated protein kinases (MAPKs), which are a group of kinases that regulate proliferation. Additionally, cinnamon components have been tied to cancer prevention by positively affecting the gut microbiome and inhibiting inflammation. The review concludes with a discussion of the future research needed and potential risk associated with cinnamon intake.

Advancing flame retardancy, mechanical properties, and hydrophobicity of epoxy resins through bio-based cinnamaldehyde derivative

Developing flame retardants based on biomass materials to improve the flame retardancy and multifunctionality of epoxy resin (EP) is crucial. Herein, we synthesized a novel derivative, PPABCA, combining cinnamaldehyde and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide to serve as flame retardants for EP. Incorporating 5 wt% PPABCA into EP (EP/PPABCA-5) demonstrated remarkable flame retardancy, with a limiting oxygen index of 33.7% and a V-0 rating in UL-94 test. It also reduced the peak heat release rate, total heat release, and peak CO2 production by 32.9%, 29.9%, and 42.8%, respectively. The enhanced flame retardancy was facilitated by the capture of phosphorus-containing free radicals coupled with dilution of combustible gas characterized by the blow-out phenomenon and formation of a dense char layer enriched with triazine and phosphorus. Furthermore, EP/PPABCA-5 exhibited enhanced flexural and tensile strengths by 20.5% and 16.5% compared to EP, attributed to the increased cross-linking density and π-π conjugation from the high rigidity of PPABCA, along with its good compatibility with EP. Additionally, the improved hydrophobic properties of PPABCA, confirmed by electrostatic potential analysis, further enhanced the hydrophobicity of EP composites. Overall, this work underscored a strategic development of multifunctional, bio-based flame retardant, showcasing efficient flame retardancy, enhanced mechanical properties, and boosted hydrophobicity in EP.

Tuning the linear optical properties and two-photon absorption on the cinnamylideneacetophenone derivatives: The effect of methoxy group by a experimental and theoretical point of view

The present work studied the effect of the methoxy group position in two cinnamylideneacetophenone (CA) derivatives on both one-photon (1PA) and two-photon absorption (2PA) processes. Our outcomes exhibit a dependence on the methoxy group position spectrally and in magnitude for both. A decrease in the lower energy 1PA band of 0.23eV was observed when the methoxy group was moved to the more conjugated part of the cinnamaldehyde molecule. The opposite was also observed for the next higher absorption band. The Quantum Chemical Calculations (QCCs), besides a good agreement between the experimental and simulated 1PA spectra, except for the magnitude of the high energy absorption band, showed that the effect behind the observed experimental red-shift of the lower absorption band is caused by the higher charge transfer when the methoxy group is bounded to the longer conjugated part of the cinnamaldehyde derivative. For experimental 2PA spectra, the higher energy band is strongly affected by the presence of the methoxy group, pointing out an increase of about 56 % in the values of the two-photon absorption cross-section (2PACS). Furthermore, the phenomenological Sum-Over-Essential States (SOS) approach and QCCs were performed for further clarification in the 2PACS experimental results. Hence, our findings demonstrate that changing the methoxy position on opposite sides of the CA may open up a novel insight for designing new organic molecules, particularly when seeking to enhance the values of 2PACS significantly of CA derivatives.

Ether, sulfide and sulfone derivatives of cinnamaldehyde: Insights into synthesis, structural elucidation and solvatochromism

Symmetric ether, sulfide and sulfone derivatives based on Schiff base functionalized group (3a-c) were synthesized via classical condensation of 4,4′-diaminodiphenyl precursors (1a-c) and cinnamaldehyde (2) in methanol at ambient reaction settings. The compounds were characterized using CHN, UV–Vis, FTIR, and 1H- and 13CNMR . The origin of absorption spectra was chased using Time-Dependent Density-Functional Theory (TD-DFT) in order to figure out the electronic transitions. The compounds exhibited almost a similar electronic potential as displayed by the molecular electrostatic potential. The energy gap of these materials was extracted from the computational approaches, showing ΔE of 3.778, 3.724, and 4.014 eV respectively for 3a, 3b, and 3c. These values were further harnessed to estimate the global reactivity parameters. Moreover, the electrophilic and nucleophilic points were examined through surface analysis of the optimized structures via DFT simulations. Such investigations support the compounds’ molecular structures via common noncovalent interaction, like hydrogen bonding and non-classical CH…π forces. Experimental and computational findings were in a respectable agreement to display that only compound 3c possesses the ability of altering its maximum absorption under different solvent conditions. A substantial shifting of the maximum absorption was noticed with ethyl alcohol at λmax = 321 nm, referring to a 32 nm of blue shift in respect to acetic acid, which could be responsible for the partial protonation of the sulfone group.

Tsuji-Trost Based Cascades: From Passerini Adducts of Cinnamaldehyde to Allylated Oxazolones.

The Passerini coupling of cinnamaldehyde derivatives affords allylic esters that may behave as both electrophiles and nucleophiles in Tsuji-Trost reactions. We present herein the interaction of the latter with methylallylcarbonate, leading to the formation of oxazolidine-diones. The efficiency of the process relies on the building up of a CO2 overpressure in the medium. A reaction mechanism highlighting the reversibility of the Tsuji-Trost reaction is proposed for the process.

Catalyst-Controlled Regiodivergent Oxidative Annulation of 2-Arylimidazo[1,2-a]pyridines with Cinnamaldehyde Derivatives for Construction of Fused N-Heterocyclic Frameworks.

Catalyst-dependent regioselective oxidative annulation of 2-arylimidazo[1,2-a]pyridines with cinnamaldehyde derivatives to construct fused N-heterocyclic frameworks has been described. The annulation reaction afforded 5-arylnaphtho[1',2':4,5]imidazo[1,2-a]pyridine-6-carbaldehydes in the presence of [RhCp*Cl2]2 as catalyst while 1,7-diarylimidazo[5,1,2-cd]indolizine-6-carbaldehydes were obtained using Pd(OAc)2 as catalyst. The reaction produced annulated products in good yields and exhibited broad substrate scope and excellent functional group tolerance. The method provides two different isomeric annulated products bearing an aldehyde functionality which can be elaborated into an array of functionalities leading to valuable compounds.

Design, Synthesis, and Biological Activity of Coniferyl Aldehyde Derivatives as Potential Anticancer and Antioxidant Agents

Natural products are known to exhibit antimicrobial, anticancer, and antioxidant activities. Among these natural products is cinnamon which contains cinnamaldehyde. Cinnamaldehyde and its derivatives have been reported to have anticancer and antioxidant activities. Coniferyl aldehyde, a non-cytotoxic compound and a cinnamaldehyde derivative, has also been shown to have anticancer activity. In this study, several derivatives of coniferyl aldehyde were synthesized and evaluated for their anticancer and antioxidant activities. Compounds 1, 2, 4, and 8-11 showed cytotoxic activity against H1299 cell line, a non-small cell lung cancer cells, with 4 being the most potent with IC50 value of 6.7 μM. The antioxidant assay experiment showed that compounds 1, 2, and 4 resulted in half the scavenging activity of vitamin C at all tested concentrations. The coniferyl aldehyde itself showed dose-dependent antioxidant activity, with a proposed free radical stabilization mechanism. Thus, our study showed that the synthesized coniferyl aldehyde derivatives exhibit anticancer and antioxidant activities, which might act as potential therapeutic agents.

Evaluation of cinnamaldehyde derivatives as potential protective agents against oxidative-stress induced myotube atrophy using chemical, biological and computational analysis

Skeletal muscle atrophy, associated with increased morbidity, mortality and poor quality of life, is a metabolic disorder with no FDA approved drug. Oxidative stress is one of the key mediators of atrophy that influences various cell signaling molecules. The goal of this study is to identify potential antioxidant agents that could be used to treat atrophy. In this study in vitro and in situ screening of different cinnamaldehyde (CNA) derivatives for their antioxidant effects was done along with computational analysis to understand the relationship between their chemical structure and biological activity.Data show that 2-hydroxycinnamaldehyde (2HCNA) worked better than other CNA analogues at physiological pH, while 4-Fluoro-2-methoxycinnamaldehyde (4FoCNA) showed the maximum antioxidant activity under acidic conditions. However, these derivatives (2HCNA and 4FoCNA) were found to be toxic to the cultured myotubes (mature myofiber) under both physiological and pathophysiological conditions. Immunofluorescence, bright-field microscopic and biochemical studies conducted using live C2C12 cells showed that pre-incubation with other CNA analogues i.e. 2-methoxycinnamaldehyde (2MeCNA) and 2-benzyloxycinnamaldehyde (2BzCNA) not only maintained the normal morphology of myotubes but also protected them from H2O2-induced atrophy. These compounds (2MeCNA and 2BzCNA) showed higher stability and antioxidant potential, as indicated by computer simulation data analyzed by Density Functional Theory (DFT) based molecular modeling. Overall, the chemical, biological, and computational studies reveal the therapeutic potential of CNA analogues (BzCNA and MeCNA) against oxidative-stress induced muscle atrophy in C2C12 cells.

Observation of the two-photon transition enhanced first hyperpolarizability spectra in cinnamaldehyde derivatives: A femtosecond regime study.

The application of nonlinear optical effects in optoelectronic devices is still scarce because the irradiance threshold necessary to induce a specific effect is very high. In this context, knowing the frequency-resolved first order molecular hyperpolarizability (β) is essential to identifying regions where this response is intense enough to allow for applications in commercial devices. Thus, herein, we have determined the β spectral dependence of five new push-pull cinnamylidene acetophenone derivatives using femtosecond laser-induced Hyper-Rayleigh Scattering (HRS). A considerable increase in β values was observed in molecules. We found remarkable β values in regions near the two-photon resonance, which are mediated by electron withdrawing and donating groups. This effect was mapped using wavelength-tunable femtosecond Z-scan technique. Furthermore, it was modeled in light of the sum-over-states approach for the second- and third-order nonlinearities. Finally, our outcomes suggest a strategy to obtain large β values mediated by the 2PA transition.

Triphenylamine-Modified Cinnamaldehyde Derivate as a Molecular Sensor for Viscosity Detection in Liquids.

Liquid safety is considered a serious public health problem; a convenient and effective viscosity determination method has been regarded as one of the powerful means to detect liquid safety. Herein, one kind of triphenylamine-modified cinnamaldehyde-based fluorescent sensor (3-(4'-(diphenylamino)-[1,1'-biphenyl]-4-yl)acrylaldehyde (DPABA)) has been developed for sensing viscosity fluctuations in a liquid system, where a cinnamaldehyde derivative was extracted from one kind of natural plant cinnamon and acted as an acceptor, which has been combined with a triphenylamine derivate via the Suzuki coupling reaction within one facile step. Twisted intramolecular charge transfer (TICT) was observed, and the rotation could be restricted in the high-viscosity microenvironment; thus, the fluorescent signal was released at 548 nm. Featured with a larger Stokes shift (223.8 nm in water, 145.0 nm in glycerol), high adaptability, sensitivity, selectivity, and good photostability, the capability of high signal-to-noise ratio sensing was achieved. Importantly, this sensor DPABA has achieved noninvasively identifying thickening efficiency investigation, and viscosity fluctuations during the liquid deterioration program have been screened as well. We believed that this unique strategy can accelerate intelligent molecular platforms toward liquid quality and safety inspection.

Highly regioselective and diastereoselective synthesis of novel pyrazinoindolones via a base-mediated Ugi-N-alkylation sequence.

An efficient base-mediated/metal-free approach has been developed for the synthesis of 1-oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indole-3-carboxamide derivatives via intramolecular indole N-H alkylation of novel bis-amide Ugi-adducts. In this protocol the Ugi reaction of (E)-cinnamaldehyde derivatives, 2-chloroaniline, indole-2-carboxylic acid and different isocyanides was designed for the preparation of bis-amides. The main highlight of this study is the practical and highly regioselective preparation of new polycyclic functionalized pyrazino derivatives. This system is facilitated by Na2CO3 mediation in DMSO and 100 °C conditions.

Derivatized photosensitizer for an improved performance of the dye-sensitized solar cell

In recent years, Dye-Sensitized Solar Cell (DSSC) has drawn enormous attention due to its advantages over conventional silicon solar cells in terms of technological, financial, and environmental sustainability. In this work, experimental and computational methods were employed to investigate the effect of derivatization of dyes—cyanoacetic acid derivatives of cinnamaldehyde (HB1) photosensitizers on the performance of the TiO2-based DSSCs. The optical properties and the functional groups of the two dyes were determined by using UV–vis spectrophotometer and FT-IR spectroscopy, respectively. The J-V characterization and power-conversion efficiency of dyes in TiO2-based DSSCs containing I-/I3- electrolyte, and Graphite-carbon based FTO-glass (counter electrode) were examined. The study revealed that the HB1 (derivatized dye) was shown to improve the DSSC performance compared to cinnamic acid (underivatized dye). The HOMO-LUMO energy bandgap was estimated using the density functional theory density (DFT) tool as implemented in Gaussian09 software with a basis set of B3LYP/6-31G (d, p) level of theory. The bandgap of dyes before and after derivatization were found to be 4.93 and 3.73 eV, respectively, higher than the bandgap of TiO2 (3.2 eV). HB1 offers the highest VOC, JSC, fill factor (%FF), and power-conversion efficiency of 0.48 V, 0.19 mA/cm2, 0.61, and 0.50 %, respectively. The study found that the derivatization technique greatly improved the conversion efficiency of the DSSCs by about 22 % in comparison to the cinnamic acid dye (0.39 %).

Antioxidant and Antibacterial Activity of Cinnamaldehyde Derivative

Abstract: This study reports the antibacterial and antioxidant properties of cinnamaldehyde derivatives. DPPH, Superoxide Anion Radical, Hydroxy Radical, and Nitric Oxide Radical Scavenging Activities were used to assess the test compound's antioxidant capacity. The well diffusion method was used to examine the antibacterial efficiency against both Gram positive and Gram-negative microorganisms. Both Gram positive and Gram-negative bacterial strains responded favourably to the antibacterial effects of cinnamaldehyde derivatives. The study revealed the test substance possesses strong antibacterial and radical scavenging abilities.

NHC-Pd(II) full pincer catalyzed Mizoroki-Heck Type Cross-Coupling of Vinyl Chloride and Alkenes: Synthesis of Novel Ferrocenylated Conjugated Dienes

This manuscript strives to establish a methodology for synthesizing new ferrocenylated conjugated dienes via a solvent-free Heck reaction of (2-formyl-1chlorovinyl) ferrocene/phenyl with vinyl arenes and acrylates by selanated NHC-Pd(II) full pincer complex. The complex was found to be highly efficient and robustly stable at high temperature and bring the desired coupling in quite instant time of 3 h under the solvent and inert-free condition. Apart from ferrocene derivatives, the reaction was found to be equally active for the β‑chloro cinnamaldehyde derivatives. Moreover, reaction shows high tolerance for all the functional groups and yields significant results with all variants of styrene, acrylate, while some unusual coupling with internal alkenes were also obtained.

Inhibition of growth, biofilm formation, virulence, and surface attachment of Agrobacterium tumefaciens by cinnamaldehyde derivatives.

Agrobacterium tumefaciens, a soil-borne, saprophytic plant pathogen that colonizes plant surfaces and induces tumors in a wide range of dicotyledonous plants by transferring and expressing its T-DNA genes. The limited availabilities and efficacies of current treatments necessitate the exploration of new anti-Agrobacterium agents. We examined the effects of trans-cinnamaldehyde (t-CNMA) and its derivatives on the cell surface hydrophobicity, exopolysaccharide and exo-protease production, swimming motility on agar, and biofilm forming ability of A. tumefaciens. Based on initial biofilm inhibition results and minimum inhibitory concentration (MIC) data, 4-nitro, 4-chloro, and 4-fluoro CNMAs were further tested. 4-Nitro, 4-chloro, and 4-fluoro CNMA at ≥150 μg/ml significantly inhibited biofilm formation by 94–99%. Similarly, biofilm formation on polystyrene or nylon was substantially reduced by 4-nitro and 4-chloro CNMAs as determined by optical microscopy and scanning electron microscopy (SEM) and 3-D spectrum plots. 4-Nitro and 4-chloro CNMAs induced cell shortening and concentration- and time-dependently reduced cell growth. Virulence factors were significantly and dose-dependently suppressed by 4-nitro and 4-chloro CNMAs (P ≤ 0.05). Gene expressional changes were greater after 4-nitro CNMA than t-CNMA treatment, as determined by qRT-PCR. Furthermore, some genes essential for biofilm formation, motility, and virulence genes significantly downregulated by 4-nitro CNMA. Seed germination of Raphanus sativus was not hindered by 4-nitro or 4-fluoro CNMA at concentrations ≤200 μg/ml, but root surface biofilm formation was severely inhibited. This study is the first to report the anti-Agrobacterium biofilm and anti-virulence effects of 4-nitro, 4-chloro, and 4-fluoro CNMAs and t-CNMA and indicates that they should be considered starting points for the development of anti-Agrobacterium agents.

Novel Cinnamaldehyde Derivatives Inhibit Peripheral Nerve Degeneration by Targeting Schwann Cells.

Peripheral nerve degeneration (PND) is a preparative process for peripheral nerve regeneration and is regulated by Schwann cells, a unique glial cell in the peripheral nervous system. Dysregulated PND induces irreversible peripheral neurodegenerative diseases (e.g., diabetic peripheral neuropathy). To develop novel synthetic drugs for these diseases, we synthesized a set of new cinnamaldehyde (CAH) derivatives and evaluated their activities in vitro, ex vivo, and in vivo. The 12 CAH derivatives had phenyl or naphthyl groups with different substitution patterns on either side of the α,β-unsaturated ketone. Among them, 3f, which had a naphthaldehyde group, was the most potent at inhibiting PND in vitro, ex vivo, and in vivo. To assess their interactions with transient receptor potential cation channel subfamily A member 1 (TRPA1) as a target of CAH, molecular docking studies were performed. Hydrophobic interactions had the highest binding affinity. To evaluate the underlying pharmacological mechanism, we performed bioinformatics analysis of the effect of 3f on PND based on coding genes and miRNAs regulated by CAH, suggesting that 3f affects oxidative stress in Schwann cells. The results show 3f to be a potential lead compound for the development of novel synthetic drugs for the treatment of peripheral neurodegenerative diseases.

N-Heterocyclic Carbene Catalyzed Cross Dehydrogenative Coupling of Aldehydes with Methanol: Combined Use of Eosin Y and Hexachloroethane

AbstractCross dehydrogenative coupling of aldehydes with methanol was investigated under organocatalytic conditions based on the cooperation­ between N-heterocyclic carbene and eosin Y·Na as an organophotocatalys­t. The combined use of eosin Y·Na and hexachloro­ethane (C2Cl6) was the effective method for the oxidative esterification of various aldehydes, because the oxidation steps are promoted by two pathways associated with the activated photocatalyst and C2Cl6. In contrast, the combined use of eosin Y·Na and bromotrichloromethane (BrCCl3) was effective only for the oxidative esterification of simple cinnamaldehyde derivatives, in which BrCCl3 promotes the oxidation as a brominating reagent toward radical intermediates.