Novel methodologies for the improved extraction of bioactive carbohydrates that fulfill the principles of green chemistry have been reviewed in this manuscript. As an alternative to conventional water extraction methods, advantages of the use of new green solvents such as ionic liquids and deep eutectic solvents have been discussed. Recent applications of advanced techniques such as ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), pressurized liquid extraction (PLE), supercritical fluid extraction (SFE) and enzyme-assisted extraction (EAE) have also been revised. Special attention has been paid to those procedures based on the combination of several of these techniques which provide a better performance [e.g. ultrasound-microwave-assisted extraction (UMAE)] or show an improved selectivity [e.g. microwave-assisted aqueous two-phase extraction (MAATPE), microwave-assisted enzymatic extraction or enzymolysis-ultrasound-assisted extraction (MAEE or EUAE), etc.]. Finally, future perspectives regarding the possible application of these new eco-friendly methodologies at industrial scale together with the advances required to that aim are presented. © 2019 Elsevier B.V.

Dicationic ionic liquids are promising solvents for safe high performance Li-ion battery applications. In this work, we report on the synthesis and characterization of new electrolytes based on geminal dicationic pyrrolidinium and piperidinium bis(trifluoromethane)sulfonimide ionic liquids, where the two cations are linked by variable length oxyethylene chain spacers. All 1 M LiTFSI doped synthesized electrolytes are thermally stable up to 300 °C, and they exhibited remarkable electrochemical stability window up to 6.0 V vs. Li/Li+. Electrolytes were assembled with LiMn2O4 (LMO) spinel in lithium half-cells. Electrochemical cell performance in terms of cyclic voltammetry, rate capability and galvanostatic cycling studies have been studied at 60 °C. Results obtained indicate that both the cationic structure and the length of the oxyethylene chain spacer has a significant influence on the electrochemical performance of LMO-cells. The cell based on the pyrrolidinium electrolyte with the two cationic structures linked by two oxyethylene units exhibit the faster rate capability, with a capacity retention of 45\% at 5C, and the highest reversible capacity (ca. 80 mAhg-1). © 2019 Elsevier B.V.

Herein, we report the synthesis of adamantyl-BINOL-based chiral porous aromatic polymers (Ad-BINOL-PAFs) for heterogeneous catalysis. Ad-BINOL-OH-PAF (365 m2·g−1 SABET) was built through the covalent bonds among of 4,4′-dibromo-O-ethyl-protected adamantyl-BINOL with 1,3,5-Triphenylbenzene-4′,4″,4′″-triboronic acid and in the presence of [Ti(OiPr)4] results an effective recyclable catalyst in the asymmetric addition of diethylzinc to aromatic aldehydes (ee up to 88\%). The corresponding heterogenized phosphoric acid (Ad-BINOL-PO2H-PAF) was applied as heterogeneous recyclable organocatalyst for the cascade condensation/amine addition of anthranilamide with aldehydes and transfer hydrogenation reactions obtaining high yields but low enantioselectivity. On the other hand, heterogeneous phosphoric acid (Ad-BINOLs-PO2H-PAF) was also used as effective phosphate ligands for synthesis of rhodium(II) complexes which were effective catalysts in cyclopropanation of styrene affording chiral cyclopropanes in good yield and high diastereoselectivity (>99\%) and moderate enantioselectivity (ee < 50\%). © 2019 Elsevier Inc.

In this study, we evaluate the main factors driving the exposure of Southern Ocean seabirds to perfluoroalkyl substances (PFASs) across a wide geographic range. Five perfluoroalkane sulfonates (PFSAs, C4-12), 10 perfluoroalkyl carboxylic acids (PFCAs, C4-13), and perfluorooctane sulfonamide (FOSA) were analyzed in plasma (n = 128) from eight species, including penguins, giant petrels, skuas, albatrosses, and shearwaters, breeding at four sites in the Antarctic, sub-Antarctic, and adjacent cool-temperate regions. Mean σPFAS concentrations ranged from 0.53 to 53 ng/g wet weight from black-browed albatross to giant petrels, respectively. As expected due to biomagnification, greater concentrations of most PFASs were found in species near the top of marine food webs such as giant petrels. However, our results suggest that other factors, i.e., metabolic capabilities and spatial movements, can mask interspecies differences in PFASs, especially PFCAs, expected from trophic structure. For instance, trans-equatorial migratory seabirds exhibited PFAS levels and profiles that are consistent with northern hemisphere exposure, reflecting their potential biovector role in the global transport of these pollutants. Among resident species, greater concentrations of PFASs, especially long-chain PFCAs, were found in seabirds breeding or foraging north of the Antarctic Circumpolar Current (ACC) than in those restricted to Antarctic/sub-Antarctic distributions. Moreover, composition profiles of PFAS in Antarctic seabirds agree well with those expected from long-range transport. Our results confirm the importance of the ACC in protecting Antarctic food webs from water-phase-transported PFASs. © 2019 American Chemical Society.

1,2,3-Triazole-derived mesoionic carbenes (MICs) having a chiral sulfur functional group at the C5 position are easily available through a CuAAC between chiral alkynyl sulfoxides and different azides. The MICs form complexes with several metals (Au, Ag, Ir, Rh, and Ru) that are enantiomerically pure. Moreover, enantiomerically pure MIC sulfinilimines are obtained from the corresponding sulfoxide retaining the chirality. Through this article, the participation of sulfoxide moieties in different catalytic and chirality transfer processes, as well as in discovering mechanistically new processes will be shown. The role of the sulfur chiral moiety in catalytic cycloisomerization and cycloisomerization-dimerization processes using Au-MIC catalysts is dual. The sulfur functional group either stabilizes intermediates in the catalytic cycle, allowing for the reaction to occur or significantly increases the selectivity of the cyclization processes. 1,2,3-Triazole MICs having chiral sulfoxides at C5 are extremely efficient in preparing chiral at the metal complexes by C-H insertion processes. The chiral at the metal half-sandwich complexes, having the enantiopure sulfur chiral group unaltered, experiences different reactions with complete retention of the configuration. Finally, mechanistically new processes, like the desulfinilation of 1,2,3-triazolium salts in Ag-MIC complexes have been uncovered. These still-nascent classes of compounds will offer opportunities for the discovery of novel catalytic applications and to study new mechanistically sound processes. © 2019 American Chemical Society.

In this work we describe the synthesis, Ca+2 channel blockade capacity and antioxidant power of N3,N5-bis(2-(5-methoxy-1H-indol-3-yl)ethyl)-2,6-dimethyl-4-aryl-1,4-dihydropyridine-3,5-dicarboxamides 1–9, a number of multi-target small 1,4-dihydropyridines (DHP), designed by juxtaposition of melatonin and nimodipine. As a result, we have identified antioxidant DHP 7 (Ca2+ channel blockade: 55\%, and 8.78 Trolox/Equivalents), the most balanced DHP analyzed here, for potential Alzheimer's disease therapy. © 2019 Elsevier Inc.

This study reports on the potential of comprehensive two-dimensional gas chromatography combined with time-of-flight mass spectrometry (GC×GC−ToF MS) for the exhaustive untargeted characterization of the volatile and semi-volatile analytes migrating from four commercial polypropylene food containers into four simulants (water, 3\% acetic acid, 10\% ethanol, and isooctane) according to European Regulation 10/2011. Collected extracts were concentrated and directly subjected to GC×GC−ToF MS analysis without any further treatment to preserve migrants integrity. As expected, the nature and total number of compounds detected in the migrates depended on both the brand (i.e., manufacture and/or sterilization procedure) and the simulant applied. In total, 107 analytes, including some less volatile compounds, were either positively or tentatively identified in the investigated simulants, a number of these compounds being reported for the first time as migrants from this type of material. A database containing chromatographic, mass spectral and partition information concerning these compounds, plus 23 remaining unidentified, is provided. © 2018 Elsevier B.V.

A novel protocol has been established to prepare the kanamycin ring II/III fragment, which has been validated as a minimum structural motif for the development of new aminoglycosides on the basis of its bactericidal activity even against resistant strains. Furthermore, its ability to act as a AAC-(6′) and APH-(3′) binder, and as a poor substrate for the ravenous ANT-(4′), makes it an excellent candidate for the design of inhibitors of these aminoglycoside modifying enzymes. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.

Many legacy and emerging persistent organic pollutants (POPs) have been reported in polar regions, and act as sentinels of global pollution. Maritime Antarctica is recipient of abundant snow precipitation. Snow scavenges air pollutants, and after snow melting, it can induce an unquantified and poorly understood amplification of concentrations of POPs. Air, snow, the fugacity in soils and snow, seawater and plankton were sampled concurrently from late spring to late summer at Livingston Island (Antarctica). Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) concentrations in snow and air were close to equilibrium. POPs in soils showed concentrations close to soil-air equilibrium or net volatilization depending on chemical volatility. Seawater-air fugacity ratios were highly correlated with the product of the snow-air partition coefficient and the Henry's law constant (KSA H'), a measure of snow amplification of fugacity. Therefore, coastal seawater mirrored the PCB congener profile and increased concentrations in snowmelt due to snowpack releasing POPs to seawater. The influence of snowpack and glacier inputs was further evidenced by the correlation between net volatilization fluxes of PCBs and seawater salinity. A meta-analysis of KSA, estimated as the ratio of POP concentrations in snow and air from previously reported simultaneous field measurements, showed that snow amplification is relevant for diverse families of POPs, independent of their volatility. We claim that the potential impact of atmospheric pollution on aquatic ecosystems has been under-predicted by only considering air-water partitioning, as snow amplification influences, and may even control, the POP occurrence in cold environments. © 2019 American Chemical Society.

A series of 33 novel (thio)urea-containing compounds were initially designed and synthesized as potential ligands for the histamine H4 receptor (H4R). However, only 3 compounds showed a statistically significant affinity towards H4R (Ki<10 μM). Considering the structural analogy of these thioureas to previously described seleno/thiourea compounds with anticancer and/or reversal multidrug resistance action in cancer cells, selected thioureas were evaluated in in vitro cytotoxicity- and cancer multidrug resistance assays. The thiourea derivatives showed a good cytotoxic activity, being the compound 13 d (4-methyl-N-(p-phenylphenyl)-piperazine-1-carbothiamide) the most active (IC50= 11.9 μM). They also enhanced the cytotoxicity of the topoisomerase inhibitors topotecan and doxorubicin in a checkerboard combination assay. Compound 13 d showed the strongest synergistic effect on topotecan activity, whereas 13 c (4-methyl-N-(p-tolyl)-piperazine-1-carbothiamide) was the best in combination with doxorubicin. These results can be a good starting point to design more potent and effective (thio)urea derivatives with anticancer activity. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Background/Aim: Selenium-containing compounds are becoming new alternatives in experimental chemotherapy in order to overcome multidrug resistance in cancer. The main goal of this study was to determine whether combined treatment with new Se-compounds would increase the effect of conventional doxorubicin chemotherapy in breast cancer cell lines. Materials and Methods: Se-compounds were evaluated regarding their cytotoxic and apoptosis-inducing effect on MCF-7 and ATP-binding cassette subfamily B member 1 (ABCB1)-overexpressing KCR breast cancer cell lines. Moreover, the interaction of Se-compounds with doxorubicin was assessed using the MTT assay. Results: Selenoanhydride exerted a selective activity towards the doxorubicin-resistant KCR cell line overexpressing ABCB1. Among the selenoesters, only ketone-containing selenoesters exerted significant cytotoxic activity against MCF-7 and KCR cell lines and the Se-compounds acted synergistically with doxorubicin on the KCR cell line. Conclusion: The importance of the COSeCH2COCH3 and COSeCH2CO(CH3)3 moieties for the cytotoxic and adjuvant role of Se-compounds was highlighted. © 2019 International Institute of Anticancer Research. All rights reserved.

Chamaemelum fuscatum (Brot.) Vasc. is a south west Iberian chamomile that has been traditionally used as folk medicine in its natural distribution area but currently it is underestimated regarding its biological activities. For this reason, it is proposed in this paper to get insight into the scientific validation of the traditional knowledge of this plant with the aim of taking advantage of its anti-inflammatory, gastroprotective and antinociceptive activities, among others. To this aim, the chemical composition of the essential oil from the whole plant, the flowers and the green parts of this plant has been evaluated by gas chromatography-mass spectrometry (GC-MS). Plant materials were collected in Badajoz (Spain). A total of 61 components including monoterpenoids, sesquiterpenoids and aliphatic esters were identified. (E)-2-Methyl-2-butenyl methacrylate (27.57\%-18.53\%) and 2-methylallyl isobutyrate (9.79\%-7.51\%) were the most abundant compounds in the essential oils of flowers and of the whole plant, whereas α-curcumene, trans-pinocarveol, α-bergamotene and pinocarvone were the major terpenoids irrespective of the plant part considered. Certain compounds showing a relative high abundance as isobutyl methacrylate, isoamyl butyrate, α-bergamotene and pinocarvone were identified for the first time in this species. Finally, we have reviewed the bioactivity of several compounds to relate the ethnobotanical use of this plant in Spain with its volatile profile. This work is a preliminary contribution to reinforce the use to this Mediterranean endemic plant as a natural source of bioactives. © 2019 by the authors.

Background: Transglycosylation represents one of the most promising approaches for obtaining novel glycosides, and plant phenols and polyphenols are emerging as one of the best targets for creating new molecules with enhanced capacities. These compounds can be found in diet and exhibit a wide range of bioactivities, such as antioxidant, antihypertensive, antitumor, neuroprotective and anti-inflammatory, and the eco-friendly synthesis of glycosides from these molecules can be a suitable alternative for increasing their health benefits. Results: Transglycosylation experiments were carried out using different GH3 β-glucosidases from the fungus Talaromyces amestolkiae. After a first screening with a wide variety of potential transglycosylation acceptors, mono-glucosylated derivatives of hydroxytyrosol, vanillin alcohol, 4-hydroxybenzyl alcohol, and hydroquinone were detected. The reaction products were analyzed by thin-layer chromatography, high-pressure liquid chromatography, and mass spectrometry. Hydroxytyrosol and vanillyl alcohol were selected as the best options for transglycosylation optimization, with a final conversion yield of 13.8 and 19\% of hydroxytyrosol and vanillin glucosides, respectively. NMR analysis confirmed the structures of these compounds. The evaluation of the biological effect of these glucosides using models of breast cancer cells, showed an enhancement in the anti-proliferative capacity of the vanillin derivative, and an improved safety profile of both glucosides. Conclusions: GH3 β-glucosidases from T. amestolkiae expressed in P. pastoris were able to transglycosylate a wide variety of acceptors. Between them, phenolic molecules like hydroxytyrosol, vanillin alcohol, 4-hydroxybenzyl alcohol, and hydroquinone were the most suitable for its interesting biological properties. The glycosides of hydroxytyrosol and vanillin were tested, and they improved the biological activities of the original aglycons on breast cancer cells. © 2019 The Author(s).

While testing the ability of cyclodextrin glucanotransferases (CGTases) to glucosylate a series of flavonoids in the presence of organic cosolvents, we found out that this enzyme was able to glycosylate a tertiary alcohol (tert-butyl alcohol). In particular, CGTases from Thermoanaerobacter sp. and Thermoanaerobacterium thermosulfurigenes EM1 gave rise to the appearance of at least two glycosylation products, which were characterized by mass spectrometry (MS) and nuclear magnetic resonance (NMR) as tert-butyl-α-D-glucoside (major product) and tert-butyl-α-D-maltoside (minor product). Using partially hydrolyzed starch as glucose donor, the yield of transglucosylation was approximately 44\% (13 g/L of tert-butyl-α-D-glucoside and 4 g/L of tert-butyl-α-D-maltoside). The synthesized tert-butyl-α-D-glucoside exhibited the typical surfactant behavior (critical micellar concentration, 4.0–4.5 mM) and its properties compared well with those of the related octyl-α-D-glucoside. To the best of our knowledge, this is the first description of an enzymatic α-glucosylation of a tertiary alcohol. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.

Carbohydrate/aromatic stacking represents a recurring key motif for the molecular recognition of glycosides, either by protein binding domains, enzymes, or synthetic receptors. Interestingly, it has been proposed that aromatic residues might also assist in the formation/cleavage of glycosidic bonds by stabilizing positively charged oxocarbenium-like intermediates/transition states through cation/πinteractions. While the significance of aromatic stacking on glycoside recognition is well stablished, its impact on the reactivity of glycosyl donors is yet to be explored. Herein, we report the first experimental study on this relevant topic. Our strategy is based on the design, synthesis, and reactivity evaluation of a large number of model systems, comprising a wide range of glycosidic donor/aromatic complexes. Different stacking geometries and dynamic features, anomeric leaving groups, sugar configurations, and reaction conditions have been explicitly considered. The obtained results underline the opposing influence exerted by van der Waals and Coulombic forces on the reactivity of the carbohydrate/aromatic complex: depending on the outcome of this balance, aromatic platforms can indeed exert a variety of effects, stretching from reaction inhibition all the way to rate enhancements. Although aromatic/glycosyl cation contacts are highly dynamic, the conclusions of our study suggest that aromatic assistance to glycosylation processes must indeed be feasible, with far reaching implications for enzyme engineering and organocatalysis. © 2019 American Chemical Society.

The development of efficient and stable red and near-IR emitting materials under hard radiation doses and/or prolonged times is a sought-after task due to their widespread applications in optoelectronics and biophotonics. To this aim, novel symmetric all-BODIPY-triads, -pentads, and -hexads have been designed and synthesized as light-harvesting arrays. These photonic materials are spectrally active in the 655–730 nm region and display high molar absorption across UV–visible region. Furthermore, they provide, to the best of our knowledge, the highest lasing efficiency (up to 68 \%) and the highest photostability (tolerance >1300 GJ mol−1) in the near-IR spectral region ever recorded under drastic pumping conditions. Additionally, the modular synthetic strategy to access the cassettes allows the systematic study of their photonic behavior related to structural factors. Collectively, the outstanding behavior of these multichromophoric photonic materials provides the keystone for engineering multifunctional systems to expedite the next generation of effective red optical materials. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

A recent review from Prof. Garrett on the causes and cures of Alzheimer's disease prompts the author to insist in that beyond the AβTau praxis other alternate, more open therapeutic strategic approaches are possible, and chemistry, medicinal chemistry, should be the starting point, where all the inspiring contributions should find their place to play the match of our health. Copyright © 2019 American Chemical Society.

Enantiopure bimetallic systems containing three different elements of chirality, namely a main-group-based chiral center (sulfur), a transition-metal chiral center (rhodium or iridium), and a planar chiral element (ferrocene or ruthenocene), have been prepared by a sequence of diastereoselective reactions. The chirality of the chiral sulfur center attached to C-5 of a 1,2,3-triazolylidene mesoionic carbene (MIC) ligand coordinated to a metal (Ir, Rh) was transferred through the formation of bimetallic complexes having a chiral-at-metal center and a planar chiral metallocene by C−H activation of the sandwich moiety (M=Fe, Ru). The sense of the planar chirality formed in this sequence of reactions depended on the nature of the ligands at the metal center of the starting complex. The configurations of these species were assigned on the basis of a combination of X-ray diffraction and CD measurements. An electrochemical study of these bimetallic complexes in coordinating solvents showed an equilibrium between the cationic complexes and the neutral species. The effect of the half-sandwich moiety on the oxidation potentials of the system is remarkable, producing notable cathodic displacements. DFT calculations support these findings. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

We report herein a new method for the synthesis of 4-aryl-3,4-dihydro-2H-benzo[g]chromene-2,5,10-triones 4 that proceeds in good yields (74–86\%) and mild reaction conditions between readily available 2-amino-4-aryl-5,10-dioxo-5,10-dihydro-4H-benzo[g]chromene-3-carbonitriles 1, and formic acid (88\%), at reflux for 6 h. In addition, we have also studied the antioxidant activities using DPPH and total TAC methods. © 2019, © 2019 Taylor & Francis Group, LLC.

Five commercial ionic liquid (IL) columns have been evaluated for the first time for the gas chromatography-mass spectrometry (GC-MS) analysis of low molecular weight carbohydrate (LMWC) standards (mono-, di-, and trisaccharides, inositols, and iminosugars). A previous derivatization step was necessary to convert the LMWCs into their volatile and stable derivatives. Compared with conventional GC stationary phases, such as HP-1 and Supelcowax® 10, IL columns have shown a different selectivity in the separation of target compounds. Among the IL columns, only SLB™-IL82 allowed the elution of all the LMWCs studied. Its performance in terms of peak width and asymmetry, evaluated under different oven temperature conditions, was shown to be dependent on the carbohydrate class considered. As an example of application, a SLB™-IL82 column was successfully used to separate the complex mixtures of LMWCs in hyacinth and mulberry extracts. This column is an interesting alternative to the conventional stationary phases used in the GC analysis of LMWCs in real-world samples. [Figure not available: see fulltext.]. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.