418 research outputs found

    The Contribution of Air Logistics to the Development of Sicilian Economy

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    The role, played by globalization and the “just in time” supplying logic in present world economic scenario, implies that the opportunity of frequent, quick, safe and low-priced freight deliveries can be considered a key element for competitiveness. For these reasons, transportation systems, in the last years, have been characterized by the diffusion of intermodality and the “hub and spoke” distribution pattern. The phenomenon of organizing freight transport services according to a network and modal integration logic, has involved also the air transport field: to meet the new requirements of freight transportation market, in many cases, airline companies have become “global players”, expanding their network, in order to develop links among the main economic centres in the world. The goods moving by air can be defined as “top range products”; which means that only high value products (“market value” and “need value”) and the perishable ones (from a physical and economic point of view) demand air transport. The research described in this abstract aims at determining the contribution that can derive from air logistics to face a challenging problem: overcoming the peripheral role, in international trade, played by Sicily, which can boast high quality outputs in the agroindustrial sector and in the high technology one. The research consists of the following stages: 1. Analysing the sicilian freight transport system, with regard to the demand-supply relationship, paying particular attention to the commodity typologies mentioned above. 2. Identifying key actions for the air cargo services, in order to make Sicily improve in competitiveness, also taking into account the possibility of connecting Sicily with hub airports. 3. Determining the economic and social impact of the proposed solutions, considering different evolutionary scenarios and using also input-output analysis techniques.

    Synthesis of the isoquinoline alkaloid, crispine C

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    The first total synthesis of the isoquinoline alkaloid, crispine C is described in seven steps using a Henry reaction and the Pictet–Gams variant of the Bischler–Napieralski reaction to effect the key transformations

    Early Versus Delayed Treatment With Glatiramer Acetate: Analysis of up to 27 Years of Continuous Follow-up in a US Open-Label Extension Study

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    BACKGROUND: Glatiramer acetate (GA) is US-approved for relapsing multiple sclerosis. OBJECTIVES: To describe GA long-term clinical profile. To compare effectiveness of early start (ES) versus delayed start (DS; up to 3 years) with GA. METHODS: Phase 3 trial participants entered a randomized placebo-controlled period then an open-label extension (OLE) with GA. RESULTS: Overall, 208 out of 251 (82.9%) randomized participants entered the OLE; 24 out of 101 (23.8%, ES) and 28 out of 107 (26.2%, DS) participants completed the OLE. Median GA treatment was 9.8 (0.1-26.3) years. Annualized change in Expanded Disability Status Scale (EDSS) score was lower with ES versus DS ( CONCLUSION: GA long-term treatment maintained clinical benefit with a similar safety profile to phase 3 results; a key limitation was that only 25% of participants completed the OLE. Early initiation of GA had sustained benefits versus delayed treatment

    Design, synthesis and biological assessment of novel N-substituted 3-(phthalimidin-2-yl)-2,6-dioxopiperidines and 3-substituted 2,6-dioxopiperidines for TNF-α inhibitory activity

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    Eight novel 2-(2,6-dioxopiperidin-3-yl)phthalimidine EM-12 dithiocarbamates 9 and 10, N-substituted 3-(phthalimidin-2-yl)-2,6-dioxopiperidines 11-14 and 3-substituted 2,6-dioxopiperidines 16 and 18 were synthesized as tumor necrosis factor-α (TNF-α) synthesis inhibitors. Synthesis involved utilization of a novel condensation approach, a one-pot reaction involving addition, iminium rearrangement and elimination, to generate the phthalimidine ring required for the creation of compounds 9-14. Agents were, thereafter, quantitatively assessed for their ability to suppress the synthesis on TNF-α in a lipopolysaccharide (LPS)-challenged mouse macrophage-like cellular screen, utilizing cultured RAW 264.7 cells. Whereas compounds 9, 14 and 16 exhibited potent TNF-α lowering activity, reducing TNF-α by up to 48% at 30 ΌM, compounds 12, 17 and 18 presented moderate TNF-α inhibitory action. The TNF-α lowering properties of these analogs proved more potent than that of revlimid (3) and thalidomide (1). In particular, N-dithiophthalimidomethyl-3-(phthalimidin-2-yl)-2,6-dioxopiperidine 14 not only possessed the greatest potency of the analogs to reduce TNF-α synthesis, but achieved this with minor cellular toxicity at 30 ΌM. The pharmacological focus of the presented compounds is towards the development of well-tolerated agents to ameliorate the neuroinflammation, that is, commonly associated with neurodegenerative disorders, epitomized by Alzheimer's disease and Parkinson's disease

    Bimetallic Oriented (Au/Cu2O) vs. Monometallic 1.1.1 Au (0) or 2.0.0 Cu2O Graphene-Supported Nanoplatelets as Very Efficient Catalysts for Michael and Henry Additions

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    "This is the peer reviewed version of the following article: Simion, Andrada, Natalia Candu, Simona M. Coman, Ana Primo, Ivan Esteve-Adell, VĂ©ronique Michelet, Vasile I. Parvulescu, and Hermenegildo Garcia. 2018. Bimetallic Oriented (Au /Cu2 O) vs. Monometallic 1.1.1 Au (0) or 2.0.0 Cu2 O Graphene-Supported Nanoplatelets as Very Efficient Catalysts for Michael and Henry Additions. European Journal of Organic Chemistry 2018 (44). Wiley: 6185 90. doi:10.1002/ejoc.201801443, which has been published in final form at https://doi.org/10.1002/ejoc.201801443. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving."[EN] Michael and Henry addition reactions have been investigated using mono (Au and Cu2O) and bimetallic nanoplatelets (Au/Cu2O) grafted onto few-layers graphene (fl-G) films as heterogeneous catalysts by comparison with homogeneous NaOH and K2CO3 ones. In the presence of the heterogeneous catalysts, these reactions occurred in the absence of any extrinsic (NaOH and K2CO3) base with turnover numbers (TONs) at least four orders of magnitude higher. While the homogeneous catalysts provided TONs close to the unity for Au/Cu2O/fl-G this was of the order of 10(7). These reactions also occurred with a very good selectivity to the targeted products. These performances are in line with the basicity of these catalysts demonstrated from CO2 chemisorption measurements. The effect of the nanosize and the interaction of the nanoparticles with the graphene are also important to achieve this high activity.This work was supported by the Ministere de l' Education, de la Recherche et des Affaires Etrangeres (Brancusi Program) of France (PN-III-CEI-BIM-PM, nr. 80BM/2017), UEFISCDI (PN-III-P4-ID-PCE-2016-0146, nr. 121/2017) and COST Action CA15106 (CHAOS)Simion, A.; Candu, N.; Coman, SM.; Primo Arnau, AM.; Esteve-Adell, I.; Michelet, V.; Parvulescu, VI.... (2018). Bimetallic Oriented (Au/Cu2O) vs. Monometallic 1.1.1 Au (0) or 2.0.0 Cu2O Graphene-Supported Nanoplatelets as Very Efficient Catalysts for Michael and Henry Additions. European Journal of Organic Chemistry. 2018(44):6185-6190. https://doi.org/10.1002/ejoc.201801443S61856190201844Michael, A. (1887). Ueber die Addition von Natriumacetessig- und NatriummalonsĂ€ureĂ€thern zu den Aethern ungesĂ€ttigter SĂ€uren. Journal fĂŒr Praktische Chemie, 35(1), 349-356. doi:10.1002/prac.18870350136Michael, A. (1894). Ueber die Addition von Natriumacetessig- und NatriummalonsĂ€ureĂ€ther zu den Aethern ungesĂ€ttigter SĂ€uren. Journal fĂŒr Praktische Chemie, 49(1), 20-25. doi:10.1002/prac.18940490103Tokoroyama, T. (2010). Discovery of the Michael Reaction. European Journal of Organic Chemistry, 2010(10), 2009-2016. doi:10.1002/ejoc.200901130Huebner, C. F., Sullivan, W. R., Stahmann, M. A., & Link, K. P. (1943). Studies on 4-Hydroxycoumarin. III. Dehydration of the Aldehyde Condensation Products1. Journal of the American Chemical Society, 65(12), 2292-2296. doi:10.1021/ja01252a009Mukaiyama, T. (1977). Titanium Tetrachloride in Organic Synthesis[New synthetic methods(21)]. Angewandte Chemie International Edition in English, 16(12), 817-826. doi:10.1002/anie.197708171Mukaiyama, T. (1977). Titantetrachlorid in der organischen Synthese. Angewandte Chemie, 89(12), 858-866. doi:10.1002/ange.19770891205Pansare, S. V., & Pandya, K. (2006). Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes. Journal of the American Chemical Society, 128(30), 9624-9625. doi:10.1021/ja062701nIkawa, M., Stahmann, M. A., & Link, K. P. (1944). Studies on 4-Hydroxycoumarins. V. The Condensation of α,ÎČ-Unsaturated Ketones with 4-Hydroxycoumarin1. Journal of the American Chemical Society, 66(6), 902-906. doi:10.1021/ja01234a019Iwamura, M., Gotoh, Y., Hashimoto, T., & Sakurai, R. (2005). Michael addition reactions of acetoacetates and malonates with acrylates in water under strongly alkaline conditions. Tetrahedron Letters, 46(37), 6275-6277. doi:10.1016/j.tetlet.2005.07.045Xu, X., Hu, W.-H., & Doyle, M. P. (2011). Highly Enantioselective Catalytic Synthesis of Functionalized Chiral Diazoacetoacetates. Angewandte Chemie International Edition, 50(28), 6392-6395. doi:10.1002/anie.201102405Xu, X., Hu, W.-H., & Doyle, M. P. (2011). Highly Enantioselective Catalytic Synthesis of Functionalized Chiral Diazoacetoacetates. Angewandte Chemie, 123(28), 6516-6519. doi:10.1002/ange.201102405Martinez, R., Simon, M.-O., Chevalier, R., Pautigny, C., Genet, J.-P., & Darses, S. (2009). C−C Bond Formation via C−H Bond Activation Using an in Situ-Generated Ruthenium Catalyst. Journal of the American Chemical Society, 131(22), 7887-7895. doi:10.1021/ja9017489Halland, N., Hansen, T., & JĂžrgensen, K. A. (2003). Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,ÎČ-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant. Angewandte Chemie International Edition, 42(40), 4955-4957. doi:10.1002/anie.200352136Halland, N., Hansen, T., & JĂžrgensen, K. A. (2003). Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,ÎČ-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant. Angewandte Chemie, 115(40), 5105-5107. doi:10.1002/ange.200352136Izquierdo, J., & PericĂ s, M. A. (2015). A Recyclable, Immobilized Analogue of Benzotetramisole for Catalytic Enantioselective Domino Michael Addition/Cyclization Reactions in Batch and Flow. ACS Catalysis, 6(1), 348-356. doi:10.1021/acscatal.5b02121Nicolaou, K. C., Rhoades, D., & Kumar, S. M. (2018). Total Syntheses of Thailanstatins A–C, Spliceostatin D, and Analogues Thereof. Stereodivergent Synthesis of Tetrasubstituted Dihydro- and Tetrahydropyrans and Design, Synthesis, Biological Evaluation, and Discovery of Potent Antitumor Agents. Journal of the American Chemical Society, 140(26), 8303-8320. doi:10.1021/jacs.8b04634Ye, R., Faucher, F. F., & Somorjai, G. A. (2018). Supported iron catalysts for Michael addition reactions. Molecular Catalysis, 447, 65-71. doi:10.1016/j.mcat.2017.12.029Morita, N., Yasuda, A., Shibata, M., Ban, S., Hashimoto, Y., Okamoto, I., & Tamura, O. (2015). Gold(I)/(III)-Catalyzed Synthesis of Cyclic Ethers; Valency-Controlled Cyclization Modes. Organic Letters, 17(11), 2668-2671. doi:10.1021/acs.orglett.5b01046Li, Z., Song, L., Van Meervelt, L., Tian, G., & Van der Eycken, E. V. (2018). Cationic Gold(I)-Catalyzed Cascade Bicyclizations for Divergent Synthesis of (Spiro)polyheterocycles. ACS Catalysis, 8(7), 6388-6393. doi:10.1021/acscatal.8b01789Pagadala, R., Maddila, S., Moodley, V., van Zyl, W. E., & Jonnalagadda, S. B. (2014). An efficient method for the multicomponent synthesis of multisubstituted pyridines, a rapid procedure using Au/MgO as the catalyst. Tetrahedron Letters, 55(29), 4006-4010. doi:10.1016/j.tetlet.2014.05.089Oliver-Meseguer, J., Boronat, M., Vidal-Moya, A., ConcepciĂłn, P., Rivero-Crespo, M. Á., Leyva-PĂ©rez, A., & Corma, A. (2018). Generation and Reactivity of Electron-Rich Carbenes on the Surface of Catalytic Gold Nanoparticles. Journal of the American Chemical Society, 140(9), 3215-3218. doi:10.1021/jacs.7b13696Leyva-PĂ©rez, A., Oliver-Meseguer, J., Cabrero-Antonino, J. R., Rubio-MarquĂ©s, P., Serna, P., Al-Resayes, S. I., & Corma, A. (2013). Reactivity of Electron-Deficient Alkynes on Gold Nanoparticles. ACS Catalysis, 3(8), 1865-1873. doi:10.1021/cs400362cMegia-Fernandez, A., Ortega-Muñoz, M., Lopez-Jaramillo, J., Hernandez-Mateo, F., & Santoyo-Gonzalez, F. (2010). Non-Magnetic and Magnetic Supported Copper(I) Chelating Adsorbents as Efficient Heterogeneous Catalysts and Copper Scavengers for Click Chemistry. Advanced Synthesis & Catalysis, 352(18), 3306-3320. doi:10.1002/adsc.201000530Kawabata, T., Kato, M., Mizugaki, T., Ebitani, K., & Kaneda, K. (2005). Monomeric Metal Aqua Complexes in the Interlayer Space of Montmorillonites as Strong Lewis Acid Catalysts for Heterogeneous Carbon-Carbon Bond-Forming Reactions. Chemistry - A European Journal, 11(1), 288-297. doi:10.1002/chem.200400672Palomo, C., Oiarbide, M., & Laso, A. (2005). Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands. Angewandte Chemie International Edition, 44(25), 3881-3884. doi:10.1002/anie.200463075Palomo, C., Oiarbide, M., & Laso, A. (2005). Enantioselective Henry Reactions under Dual Lewis Acid/Amine Catalysis Using Chiral Amino Alcohol Ligands. Angewandte Chemie, 117(25), 3949-3952. doi:10.1002/ange.200463075Ganesan, S., Ganesan, A., & Kothandapani, J. (2014). Hyperbranched Polyamines: Tunable Catalysts for the Henry Reaction. Synlett, 25(13), 1847-1850. doi:10.1055/s-0034-1378534Li, H., Wang, B., & Deng, L. (2006). Enantioselective Nitroaldol Reaction of α-Ketoesters Catalyzed by Cinchona Alkaloids. Journal of the American Chemical Society, 128(3), 732-733. doi:10.1021/ja057237lGurbanov, A. V., Hazra, S., Maharramov, A. M., Zubkov, F. I., Guseinov, F. I., & Pombeiro, A. J. L. (2018). The Henry reaction catalyzed by NiII and CuII complexes bearing arylhydrazones of acetoacetanilide. Journal of Organometallic Chemistry, 869, 48-53. doi:10.1016/j.jorganchem.2018.05.025Sels, B. F., De Vos, D. E., & Jacobs, P. A. (2001). Hydrotalcite-like anionic clays in catalytic organic reactions. Catalysis Reviews, 43(4), 443-488. doi:10.1081/cr-120001809Choudary, B. M., Kantam, M. L., & Kavita, B. (2001). Synthesis of 2-nitroalkanols by MgAlO-t-Bu hydrotalcite. Journal of Molecular Catalysis A: Chemical, 169(1-2), 193-197. doi:10.1016/s1381-1169(00)00558-6Cwik, A., Fuchs, A., Hell, Z., & Clacens, J.-M. (2005). Nitroaldol-reaction of aldehydes in the presence of non-activated Mg:Al 2:1 hydrotalcite; a possible new mechanism for the formation of 2-aryl-1,3-dinitropropanes. Tetrahedron, 61(16), 4015-4021. doi:10.1016/j.tet.2005.02.055Evans, D. A., Seidel, D., Rueping, M., Lam, H. W., Shaw, J. T., & Downey, C. W. (2003). A New Copper Acetate-Bis(oxazoline)-Catalyzed, Enantioselective Henry Reaction. Journal of the American Chemical Society, 125(42), 12692-12693. doi:10.1021/ja0373871Risgaard, T., Gothelf, K. V., & JĂžrgensen, K. A. (2003). Catalytic asymmetric Henry reactions of silyl nitronates with aldehydes. Org. Biomol. Chem., 1(1), 153-156. doi:10.1039/b208859mArai, T., Watanabe, M., & Yanagisawa, A. (2007). Practical Asymmetric Henry Reaction Catalyzed by a Chiral Diamine-Cu(OAc)2Complex. Organic Letters, 9(18), 3595-3597. doi:10.1021/ol7014362Jin, W., Li, X., & Wan, B. (2011). A Highly Diastereo- and Enantioselective Copper(I)-Catalyzed Henry Reaction Using a Bis(sulfonamide)−Diamine Ligand. The Journal of Organic Chemistry, 76(2), 484-491. doi:10.1021/jo101932aWhite, J. D., & Shaw, S. (2012). A New Catalyst for the Asymmetric Henry Reaction: Synthesis of ÎČ-Nitroethanols in High Enantiomeric Excess. Organic Letters, 14(24), 6270-6273. doi:10.1021/ol3030023Jones, M. D., Cooper, C. J., Mahon, M. F., Raithby, P. R., Apperley, D., Wolowska, J., & Collison, D. (2010). Cu(II) homogeneous and heterogeneous catalysts for the asymmetric Henry reaction. Journal of Molecular Catalysis A: Chemical, 325(1-2), 8-14. doi:10.1016/j.molcata.2010.03.013Gupta, A. K., De, D., & Bharadwaj, P. K. (2017). A NbO type Cu(ii) metal–organic framework showing efficient catalytic activity in the FriedlĂ€nder and Henry reactions. Dalton Transactions, 46(24), 7782-7790. doi:10.1039/c7dt01595jGupta, M., De, D., Pal, S., Pal, T. K., & Tomar, K. (2017). A porous two-dimensional Zn(ii)-coordination polymer exhibiting SC–SC transmetalation with Cu(ii): efficient heterogeneous catalysis for the Henry reaction and detection of nitro explosives. Dalton Transactions, 46(23), 7619-7627. doi:10.1039/c7dt01074ePark, S., & Ruoff, R. S. (2009). Chemical methods for the production of graphenes. Nature Nanotechnology, 4(4), 217-224. doi:10.1038/nnano.2009.58Bottari, G., Herranz, M. Á., Wibmer, L., Volland, M., RodrĂ­guez-PĂ©rez, L., Guldi, D. M., 
 Torres, T. (2017). Chemical functionalization and characterization of graphene-based materials. Chemical Society Reviews, 46(15), 4464-4500. doi:10.1039/c7cs00229gBostwick, A., Speck, F., Seyller, T., Horn, K., Polini, M., Asgari, R., 
 Rotenberg, E. (2010). Observation of Plasmarons in Quasi-Freestanding Doped Graphene. Science, 328(5981), 999-1002. doi:10.1126/science.1186489Esrafili, M. D., Nematollahi, P., & Nurazar, R. (2016). Pd-embedded graphene: An efficient and highly active catalyst for oxidation of CO. Superlattices and Microstructures, 92, 60-67. doi:10.1016/j.spmi.2016.02.006Woo, H., Kim, J. W., Kim, M., Park, S., & Park, K. H. (2015). Au nanoparticles supported on magnetically separable Fe2O3–graphene oxide hybrid nanosheets for the catalytic reduction of 4-nitrophenol. RSC Advances, 5(10), 7554-7558. doi:10.1039/c4ra13989ePourjavadi, A., Doroudian, M., Abedin-Moghanaki, A., & Bennett, C. (2017). Magnetic GO-PANI decorated with Au NPs: A highly efficient and reusable catalyst for reduction of dyes and nitro aromatic compounds. Applied Organometallic Chemistry, 31(12), e3881. doi:10.1002/aoc.3881Sarvestani, M., & Azadi, R. (2016). Palladium nanoparticles deposited on a graphene-benzimidazole support as an efficient and recyclable catalyst for aqueous-phase Suzuki-Miyaura coupling reaction. Applied Organometallic Chemistry, 31(8), e3667. doi:10.1002/aoc.3667Primo, A., Esteve-Adell, I., Coman, S. N., Candu, N., Parvulescu, V. I., & Garcia, H. (2015). One-Step Pyrolysis Preparation of 1.1.1 Oriented Gold Nanoplatelets Supported on Graphene and Six Orders of Magnitude Enhancement of the Resulting Catalytic Activity. Angewandte Chemie International Edition, 55(2), 607-612. doi:10.1002/anie.201508908Primo, A., Esteve-Adell, I., Coman, S. N., Candu, N., Parvulescu, V. I., & Garcia, H. (2015). One-Step Pyrolysis Preparation of 1.1.1 Oriented Gold Nanoplatelets Supported on Graphene and Six Orders of Magnitude Enhancement of the Resulting Catalytic Activity. Angewandte Chemie, 128(2), 617-622. doi:10.1002/ange.201508908Mahdavi, H., & Rahmani, O. (2016). Polyacrylamide-g-Reduced Graphene Oxide Supported Pd Nanoparticles as a Highly Efficient Catalyst for Suzuki–Miyaura Reactions in Water. Catalysis Letters, 146(11), 2292-2305. doi:10.1007/s10562-016-1851-1Primo, A., Esteve-Adell, I., Blandez, J. F., Dhakshinamoorthy, A., Álvaro, M., Candu, N., 
 GarcĂ­a, H. (2015). High catalytic activity of oriented 2.0.0 copper(I) oxide grown on graphene film. Nature Communications, 6(1). doi:10.1038/ncomms9561Primo, A., Atienzar, P., Sanchez, E., Delgado, J. M., & GarcĂ­a, H. (2012). From biomass wastes to large-area, high-quality, N-doped graphene: catalyst-free carbonization of chitosan coatings on arbitrary substrates. Chemical Communications, 48(74), 9254. doi:10.1039/c2cc34978gPrimo, A., SĂĄnchez, E., Delgado, J. M., & GarcĂ­a, H. (2014). High-yield production of N-doped graphitic platelets by aqueous exfoliation of pyrolyzed chitosan. Carbon, 68, 777-783. doi:10.1016/j.carbon.2013.11.068Boruwa, J., Gogoi, N., Saikia, P. P., & Barua, N. C. (2006). Catalytic asymmetric Henry reaction. Tetrahedron: Asymmetry, 17(24), 3315-3326. doi:10.1016/j.tetasy.2006.12.005Palomo, C., Oiarbide, M., & Laso, A. (2007). Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction. European Journal of Organic Chemistry, 2007(16), 2561-2574. doi:10.1002/ejoc.200700021Akutu, K., Kabashima, H., Seki, T., & Hattori, H. (2003). Nitroaldol reaction over solid base catalysts. Applied Catalysis A: General, 247(1), 65-74. doi:10.1016/s0926-860x(03)00124-8Ballini, R., Bosica, G., Fiorini, D., Palmieri, A., & Petrini, M. (2005). Conjugate Additions of Nitroalkanes to Electron-Poor Alkenes:  Recent Results. Chemical Reviews, 105(3), 933-972. doi:10.1021/cr040602rChoudary, B. M., Rajasekhar, C. V., Gopi Krishna, G., & Rajender Reddy, K. (2007). L‐Proline‐Catalyzed Michael Addition of Aldehydes and Unmodified Ketones to Nitro Olefins Accelerated by Et3N. Synthetic Communications, 37(1), 91-98. doi:10.1080/00397910600978218Ding, R., Katebzadeh, K., Roman, L., Bergquist, K.-E., & Lindström, U. M. (2006). Expanding the Scope of Lewis Acid Catalysis in Water:  Remarkable Ligand Acceleration of Aqueous Ytterbium Triflate Catalyzed Michael Addition Reactions. The Journal of Organic Chemistry, 71(1), 352-355. doi:10.1021/jo051540nPrimo, A., Neatu, F., Florea, M., Parvulescu, V., & Garcia, H. (2014). Graphenes in the absence of metals as carbocatalysts for selective acetylene hydrogenation and alkene hydrogenation. Nature Communications, 5(1). doi:10.1038/ncomms6291Milner, S. E., Moody, T. S., & Maguire, A. R. (2012). Biocatalytic Approaches to the Henry (Nitroaldol) Reaction. European Journal of Organic Chemistry, 2012(16), 3059-3067. doi:10.1002/ejoc.201101840Ballini, R., & Palmieri, A. (2006). Synthetic Applications of Nitroalkanes Promoted by Solid Catalysis: Recent Results. Current Organic Chemistry, 10(17), 2145-2169. doi:10.2174/138527206778742632Luzzio, F. A. (2001). The Henry reaction: recent examples. Tetrahedron, 57(6), 915-945. doi:10.1016/s0040-4020(00)00965-02011 http://www.skb.se/upload/publications/pdf/TR-11-08Glorius, M., Markovits, M. A. C., & Breitkopf, C. (2018). Design of Specific Acid-Base-Properties in CeO2-ZrO2-Mixed Oxides via Templating and Au Modification. Catalysts, 8(9), 358. doi:10.3390/catal809035

    Epidemiology and cost of herpes zoster and postherpetic neuralgia among patients treated in primary care centres in the valencian community of Spain

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    <p>Abstract</p> <p>Background</p> <p>Data on the epidemiology and costs related to herpes zoster (HZ) and postherpetic neuralgia (PHN) in Spain are scarce; therefore, studies are needed to evaluate the epidemiological and economic impact of HZ and its most common complication, PHN. The present study aimed to estimate the clinical and economic burden of HZ and PHN in Valencia (Spain).</p> <p>Methods</p> <p>We prospectively analyzed the burden of HZ and PHN and their attributable costs in patients from 25 general practices in the Autonomous Community of Valencia serving 36,030 persons aged > 14 years. All patients with a clinical diagnosis of HZ who attended these centers between December 1<sup>st </sup>2006 and November 30<sup>th </sup>2007 were asked to participate. Patients included were followed for 1 year.</p> <p>Results</p> <p>Of the 130 cases of HZ followed up, continued pain was experienced by 47.6% (95% confidence interval (CI) = 35.6-56.7%) at 1 month after rash onset, by 14.5% (95% CI = 7.8-1.2%) at 3 months, by 9.0% (95% CI = 3.7-14.3%) at 6 months, and by 5.9% (95% CI = 1.5-10.3%) at 12 months. The percentage of patients with PHN increased with age, from 21.4% (95% CI = 8.3-40) in patients < 50 years to 59.2% (95% CI = 44.4-74) in patients ≄ 70 years. The estimated total cost for the 130 HZ cases during the follow-up period was €49,160 (67,349).Meancostperpatientwas€378(range53−2,830)(67,349). Mean cost per patient was €378 (range 53-2,830) (517, range 73-3,877).</p> <p>Conclusions</p> <p>This study shows that PHN is a relatively common complication of HZ and that both conditions combined give rise to a significant clinical and economic burden for patients and providers.</p
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