Relevant bibliographies by topics / Oxime ethers

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Oxime ethers'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Oxime ethers"

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Shan, Z., Y. Chu, D. Liu, and N. Sun. "Spiroborate Ether Mediated Enantioselective Reduction of Oxime Ethers." Synfacts 2006, no. 7 (June 2006): 0691. http://dx.doi.org/10.1055/s-2006-941859.

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Zhang, Jia-Yuan, Jinglin Hu, Xiao-Xuan Li, Wei-Ke Tang, and Yi-Si Feng. "Metal-Free Transformation of Sulfonyl Oxime Ethers with Amines to Oxime Ethers." Journal of Organic Chemistry 86, no. 18 (September 2, 2021): 12676–82. http://dx.doi.org/10.1021/acs.joc.1c01197.

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Mehrez, Asma, Dalila Mtat, and Ridha Touati. "Microwave-Assisted Synthesis of Chiral Oxime Ethers." Letters in Organic Chemistry 16, no. 6 (April 23, 2019): 495–500. http://dx.doi.org/10.2174/1570178615666181106125853.

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An efficient and rapid synthesis of a new class of chiral oxime ethers has been achieved via two-step reaction in which the first step is the reaction of oximes 1a-f with ethyl bromoacetate in the presence of sodium hydride to give oxime ethers 2a-f which are subsequently, in the second step, reacted with different commercially available chiral amines under microwave irradiation conditions to give compounds 3a-l in good to excellent yields. Through this method, we have observed a decrease in reaction time and excellent yields than the previously described conventional method.
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MEIER, H., K. SAUL, R. MENGEL, and H. P. NIEDERMANN. "ChemInform Abstract: Cycloaddition of Benzothiete to Oximes, Oxime Ethers, and Oxime Esters." ChemInform 22, no. 46 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199146227.

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Bartlett, Paul A., Kevin L. McLaren, and Pauline C. Ting. "Radical cyclization of oxime ethers." Journal of the American Chemical Society 110, no. 5 (March 1988): 1633–34. http://dx.doi.org/10.1021/ja00213a052.

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Wimmer, Zdenêk, David Šaman, Jorga Smolíková, and Miroslav Romaňuk. "Oxime ethers as potential juvenoids." Liebigs Annalen der Chemie 1988, no. 11 (November 15, 1988): 1091–94. http://dx.doi.org/10.1002/jlac.198819881114.

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BRAIN, EDWARD G., ANDREW K. FORREST, ERIC HUNT, CHRISTINE SHILLINGFORD, and JENNIFER M. WILSON. "Erythromycin a oxime 11,12-carbonate and its oxime ethers." Journal of Antibiotics 42, no. 12 (1989): 1817–22. http://dx.doi.org/10.7164/antibiotics.42.1817.

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Diaz-Velandia, John, Natalia Durán-Díaz, Jorge Robles-Camargo, and Alix Elena Loaiza. "Síntesis y evaluación “in vitro” de la actividad antifúngica de oximas, éteres de oxima e isoxazoles." Universitas Scientiarum 16, no. 3 (November 1, 2011): 294. http://dx.doi.org/10.11144/javeriana.sc16-3.saiv.

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<p><strong></strong><strong>Objective</strong>. To synthesize and carry out a preliminary evaluation of the <em>in vitro</em> antifungal activity of oximes, oxime ethers and isoxazoles. <strong>Materials and methods</strong>. Oximes were synthesized from aldehydes or ketones with NH<sub>2</sub>OH.HCl and K<sub>2</sub>CO<sub>3</sub>. Oxime ethers were prepared by alkylation of oximes with propargyl bromide or 2-bromobenzyl bromide, using NaOH as base and acetone as solvent. The isoxazoles were obtained by 1,3-dipolar cycloadditions using ceric ammonium nitrate (CAN), chloramine T (CAT) and NaOCl. Products were identified or characterized using nuclear magnetic resonance (NMR) and mass spectrometry (MS). Radial growth inhibition assays against <em>Aspergillus niger</em> and <em>Fusarium roseum</em> were carried out. <strong>Results</strong>. Five oximes, seven oxime ethers, four of them new, and four new isoxazoles were obtained. The assessed substances exhibited antifungal activity in amounts of 1,5 mg and 3,0 mg. <strong>Conclusions</strong>. Although 1,3-dipolar cycloadditions allowed to obtain the desired isoxazoles, this methodology produced a wide variety of side products that reduced yields and made difficult the purification of the target products. Four of the tested compounds showed inhibition percentages greater than 80%.</p> <p><strong>Key words: </strong>oximes, oxime ethers, isoxazoles, antifungal activity.</p> <p> </p><br />
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Ren, Zhi-Hui, Mi-Na Zhao, and Zheng-Hui Guan. "CuI-catalyzed oxidative cross coupling of oximes with tetrahydrofuran: a direct access to O-tetrahydrofuran-2-yl oxime ethers." RSC Advances 6, no. 20 (2016): 16516–19. http://dx.doi.org/10.1039/c5ra27899f.

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Naito, Takeaki. "Heterocycle synthesis via radical reactions." Pure and Applied Chemistry 80, no. 4 (January 1, 2008): 717–26. http://dx.doi.org/10.1351/pac200880040717.

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A novel synthetic method for the preparation of nitrogen-containing heterocycles via the route involving domino-type radical addition/cyclization reaction of oxime ethers is described. Alkyl radical addition/cyclization of oxime ethers carrying an appropriate leaving group proceeded smoothly to form the alkylated nitrogen-containing heterocyclic compounds. Additionally, tin-mediated radical addition/cyclization/elimination (RACE) reaction of oxime ethers is newly found and successfully applied to an asymmetric total synthesis of (-)-martinellic acid.
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Dissertations / Theses on the topic "Oxime ethers"

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Laurent, Pierre. "Asymmetric synthesis using chiral oxime ethers." Thesis, University of Exeter, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248161.

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Hunt, James Charles Atlee. "Chiral oxime ethers in asymmetric synthesis." Thesis, University of Exeter, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302639.

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Lightfoot, Andrew Philip. "Chiral oxime ethers : applications in synthesis." Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/28182.

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Chapter One reviews the literature, discussing the role of nucleophilic additions to oximes and their derivatives. This introduction is primarily concerned with the formation of new carbon–carbon bonds, this is achieved by the addition of organometallic reagents to the carbon–nitrogen double bond functionality of oximes and their derivatives.
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Cooper, Tracey Sara. "Synthesis of amino acids from chiral oxime ethers." Thesis, University of Exeter, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.432786.

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Allcock, Sylvia J. "The Diels-Alder reactions of unsaturated oxime ethers and acyl hydrazones." Thesis, University of Liverpool, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303094.

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Idris, Musa A. "Stereoselective addition reactions of diethylzinc with nitrones, imines and oxime o-ethers." Thesis, University of Sussex, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341803.

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Acord, Douglas A. "The synthesis and study of 5-oxime-2-methoxy-1,3-xylyl-18-crown-5." Muncie, Ind. : Ball State University, 2009. http://cardinalscholar.bsu.edu/634.

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Leutzow, Juliane Linda [Verfasser]. "Rhodium-Catalyzed [2+2+2] Cycloaddition of Oxime Ethers and Diynes and Synthetic Approaches Towards a Novel Benzoquinolinone Alkaloid / Juliane Linda Leutzow." Konstanz : Bibliothek der Universität Konstanz, 2015. http://d-nb.info/1088797350/34.

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Sutherland, Courtney M. "Poly(Arylene) Ethers Prepared From Functionalized 3,5-Difluorotriphenylphosphine Oxide." Wright State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=wright1341862470.

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Bragnier, Nicolas. "Synthèse de C-glycosyl amino-acides par voie radicalaire." Paris 11, 2006. http://www.theses.fr/2006PA112261.

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Books on the topic "Oxime ethers"

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Mendes, M. C. S. Aspects of the chemistry of D-glucopyranosyl oxime ethers. Manchester: UMIST, 1993.

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Horace Wells (1815-1848) et Villiam T.G. Morton (1819-1869): La rencontre improbable de deux précurseurs de l'anesthésie. Paris: L'Harmattan, 2013.

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ZnO bao mo zhi bei ji qi guang, dian xing neng yan jiu. Shanghai Shi: Shanghai da xue chu ban she, 2010.

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Lightfoot, Andrew Philip. Chiral oxime ethers: Applications in synthesis. 1996.

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International Program on Chemical Safety., United Nations Environment Programme, and International Labour Organisation, eds. Propylene oxide health and safety guide. Geneva: World Health Organization, 1988.

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Oxygen plasma resistant phosphine oxide containing imide/arylene ether copolymers. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1993.

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On the use of nitrous oxide and ether as an anesthetic. [Canada: s.n., 1995.

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Center, Langley Research, ed. Summary of GPC/DV results for space exposed poly(arylene ether phosphine oxide)s. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1995.

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McKenzie, Alistair G. The history of anaesthesia. Edited by Philip M. Hopkins. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199642045.003.0031.

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Even though ether was prepared in 1540 and nitrous oxide in 1774, it was not until the 1840s that these agents were used to induce anaesthesia to enable painless surgery. Modern inhalation anaesthesia has evolved from the public demonstration of ether anaesthesia by William Morton at the Massachusetts General Hospital, Boston, United States, on 16 October 1846. In the United Kingdom, from 1847 John Snow applied scientific principles to develop safer anaesthetic practice. Newer and safer agents have replaced ether in most countries. Successful intravenous anaesthesia began with chloral hydrate in 1874; progress was hesitant until the wide acceptance of thiopental from 1934—in turn superseded by propofol from 1985. Regional anaesthesia has evolved from the first use of the local anaesthetic, cocaine, to enable awake eye surgery by Carl Koller in 1884. This progressed to nerve blocks, spinal and epidural anaesthesia with a high degree of sophistication, through provision of better and safer local anaesthetics: lidocaine and bupivacaine. The introduction of neuromuscular blocking agents into anaesthetic practice began with the use of curare by Griffith and Johnson in Montreal in 1942. Muscle relaxation became a component of ‘balanced anaesthesia’—necessitating advances in airway management, including tracheal intubation and safe mechanical ventilation of the lungs. The modern anaesthetic workstation for inhalation anaesthesia has evolved from the early anaesthetic machines over 100 years. Of all the advances in anaesthesia during the past 50 years, developments in monitoring techniques—particularly pulse oximetry and capnography—have probably made the greatest contribution to patient safety. Anaesthetists have embraced enhanced postoperative recovery.
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McKenzie, Alistair G. Historic timeline of obstetric anaesthesia. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198713333.003.0001.

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Foremost in the history of obstetric anaesthesia was the introduction of inhalational analgesia by James Simpson in 1847, first with ether and then chloroform. Nitrous oxide was first used in obstetrics in 1880. Neuraxial anaesthesia in obstetrics began with spinal block by Oskar Kreis in 1900, and within 25 years included pudendal, caudal, and paracervical blocks. From 1902 there was a vogue for ‘twilight sleep’, which remained in use until the 1950s. Spinal anaesthesia only became popular with the advent of procaine in 1905; favour declined in the United Kingdom from 1948 and did not return until 40 years later. In 1930, Aburel described the pain pathways of labour. Continuous caudal analgesia for labour was popularized from 1942; it was superseded by the lumbar epidural approach in the 1960s. The arrival of lidocaine in 1950 was a major advance. Another important event in the 1960s was the elucidation of the supine hypotensive syndrome of late pregnancy. In the 1940s, intravenous barbiturates became popular. Mendelson published on the acid aspiration syndrome in 1946. It took 40 years to establish a reliable system of prevention, including fasting, antacids, and rapid sequence induction. This developed piecemeal, aided by recommendations from the British Confidential Enquiries into Maternal Deaths reports beginning in 1957. Neuraxial anaesthesia advanced: 24-hour epidural services (1960s), bupivacaine (1970s), epidural opioids (1980s), use of low-concentration bupivacaine with fentanyl mixtures, patient-controlled epidural and combined spinal–epidural analgesia (1990s), and pencil-point spinal needles (1990s). From the 1980s obstetric anaesthetists have assumed key roles in management of labour, preeclampsia/eclampsia, major haemorrhage, and perioperative care.
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Book chapters on the topic "Oxime ethers"

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Cullen, Thomas G., Charles J. Manly, Philip A. Cruickshank, and Sandra M. Kellar. "Insecticidal Substituted Biphenylmethyl Oxime Ethers." In ACS Symposium Series, 173–88. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0355.ch016.

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Wohlfarth, Christian. "Refractive index of acetone oxime methyl ether." In Optical Constants, 153. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_142.

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Puri, Anu, Serena Zampino, Mathias Viard, and Bruce A. Shapiro. "Oxime Ether Lipids as Transfection Agents: Assembly and Complexation with siRNA." In RNA Nanostructures, 241–53. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7138-1_16.

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Wohlfarth, Ch. "Liquid-liquid equilibrium data of poly(ethylene oxide-b-propylene fumarate-b-ethylene oxide) dimethyl ether in water." In Polymer Solutions, 2701–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-88057-8_541.

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Wohlfarth, Ch. "Surface tension of the mixture (1) nitric oxide; (2) ethene." In Supplement to IV/16, 264. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_198.

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Wohlfarth, Christian. "Static dielectric constant of the binary liquid mixture of carbon di oxide and dimethyl ether." In Static Dielectric Constants of Pure Liquids and Binary Liquid Mixtures, 220. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-48168-4_219.

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Winkelmann, Jochen. "Diffusion coefficient of toluene into dideuterium oxide, phenyl-methanol and bis-(2-(2-hydroxy-ethoxy)-ethyl)-ether solution." In Diffusion in Gases, Liquids and Electrolytes, 1441. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1211.

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Winkelmann, Jochen. "Diffusion coefficient of phenyl-methanol into dideuterium oxide, toluene and bis-(2-(2-hydroxy-ethoxy)-ethyl)-ether solution." In Diffusion in Gases, Liquids and Electrolytes, 1451. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1221.

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Winkelmann, Jochen. "Diffusion coefficient of bis-(2-(2-hydroxy-ethoxy)-ethyl)-ether into dideuterium oxide, toluene and phenyl-methanol solution." In Diffusion in Gases, Liquids and Electrolytes, 1475. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1245.

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Challenger, S. "Fluorination of Hydrazones, Azines, Oximes, or Oxime Ethers." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00019.

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Conference papers on the topic "Oxime ethers"

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Vágvölgyi, M., A. Martins, Á. Kulmány, I. Zupkó, G. Tóth, and A. Hunyadi. "Preparation and chemo-sensitizing activity of nitrogen-containing ecdysteroid derivatives: 6-oximes, oxime ethers, and a lactam." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608147.

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Ryu, Ilhyong, Sunggak Kim, Hiroki Kuriyama, Hironari Miyazato, Mitsuo Komatsu, and Joo-Yong Yoon. "Novel Synthesis of a,b-Diketoesters from a,a-Dioxo-type Oximes or Oxime Ethers via Zinc-Induced Deoximation." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01829.

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Pélerin, Dominik, Kai Gaukel, Martin Härtl, and Georg Wachtmeister. "Nitrogen Oxide Reduction Potentials Using Dimethyl Ether and Oxymethylene Ether in a Heavy-Duty Diesel Engine." In Automotive Technical Papers. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2020. http://dx.doi.org/10.4271/2020-01-5084.

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Amin, M. A. M., W. L. Chang, M. O. Abdullah, D. N. A. Chee, and N. S. A. Zauzi. "Optimization of Sulphonated Poly(Ether Ether Ketone) (Speek) Multilayer Membrane Incorporated with Calcium Oxide for Fuel Cell." In Proceedings of the International Engineering Conference. Singapore: Research Publishing Services, 2014. http://dx.doi.org/10.3850/978-981-09-4587-9_p32.

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Seetharaman, S., K. Ramya, and K. S. Dhathathreyan. "Electrochemically reduced graphene oxide / sulfonated polyether ether ketone composite membrane for electrochemical applications." In CARBON MATERIALS 2012 (CCM12): Carbon Materials for Energy Harvesting, Environment, Nanoscience and Technology. AIP, 2013. http://dx.doi.org/10.1063/1.4810069.

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Anand, R., G. R. Kannan, and P. Karthikeyan. "Performance Emission and Combustion Characteristics of Diesel Engine Fuelled With Biodiesel–Diesel–Diethyl Ether Blends." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-86712.

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Increasing energy demand and rapid depletion of fossil fuels has accelerated the search for an alternative fuel for diesel engine. Biodiesel produced from waste cooking oil is the most suitable alternative for diesel due to low production cost. Higher viscosity, pour and cloud point of biodiesel causes several engine operating problems such as injector choking, piston ring sticking and unfavorable pumping and spray characteristics. In order to avoid the problem associated with biodiesel various combinations of biodiesel-diesel-diethyl ether were prepared in this present investigation. Based on the stability and fuel properties close to diesel the combination namely B70D20DEE10 (biodiesel 70%, diesel 20% and diethyl ether 10%) was further selected for experimental investigation. Experiments were performed on a single cylinder direct injection water cooled diesel engine under varying load, injection timing and injection pressure while keeping engine speed constant of 1500 rpm. The highest brake thermal efficiency was reported for B70D20DEE10 at an injection timing of 25.5 bTDC and injection pressure of 260 bar at full load condition which is 5.6% higher than diesel. The highest heat release rate (HRR) was observed at above operating condition is 29.4 MJ/°CA, which is 5.3% higher than diesel. Further a slight reduction in unburnt hydrocarbon (UBHC) by 12 ppm, nitric oxide by 116 ppm and smoke opacity by 18% was observed when compared to diesel.
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Das, Susanta K., Salma Rahman, Jianfang Chai, Matthew Quast, Steven E. Keinath, K. Joel Berry, Anja Mueller, and Abhijit Sarkar. "Experimental Performance Evaluation of a Rechargeable Lithium-Air Battery Operating at Room Temperature." In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-39004.

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The effects of electrolyte, catalyst, and the process of preparation of the air-cathode on the performance of Li-air batteries were investigated. An ether based electrolyte was the best choice for Ketjen Black carbon based air cathodes and delivered high specific capacity (1050 mAh/gC) under dry air with cobalt oxide as catalyst. The introduction of an ultrasonication step in the air-cathode fabrication process improved the air-cathode microstructure. BET analyses revealed that the cathode has a higher surface area and mesopore volume when ultrasonication was used compared to those for the cathode fabricated without the ultrasonication step. With the optimized electrolyte and air-cathode, a high capacity of 2620 mAh/gC was obtained for Li-air batteries tested in dry air with a 0.1 mA/cm2 current density.
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Vlahov, Iontcho, Albert Felten, Ning Zou, Kevin Wang, Hari K. Santhapuram, Paul Kleindl, Spencer Hahn, Jeremy Vaughn, and Christopher Leamon. "Abstract 757: Novel warheads for targeted therapies of cancer: The concept and design of oxime-ether-based pro-PBDs." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-757.

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Vedharaj, S., R. Vallinayagam, S. Mani Sarathy, and Robert W. Dibble. "Improving Vegetable Oil Fueled CI Engine Characteristics Through Diethyl Ether Blending." In ASME 2016 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icef2016-9339.

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In this research, the flow and ignition properties of vegetable oil (VO) are improved by blending it with diethyl ether (DEE). DEE, synthesized from ethanol, has lower viscosity than diesel and VO. When DEE is blended with VO, the resultant DEEVO mixtures have favorable properties for compression ignition (CI) engine operation. As such, DEEVO20 (20% DEE + 80% VO) and DEEVO40 (40% DEE + 60% VO) were initially considered in the current study. The viscosity of VO is 32.4*10−6 m2/s; the viscosity is reduced with the increase of DEE in VO. In this study, our blends were limited to a maximum of 40% DEE in VO. The viscosity of DEEVO40 is 2.1*10−6 m2/s, which is comparable to that of diesel (2.3*10−6 m2/s). The lower boiling point and flash point of DEE improves the fuel spray and evaporation for DEEVO mixtures. In addition to the improvement in physical properties, the ignition quality of DEEVO mixtures is also improved, as DEE is a high cetane fuel (DCN = 139). The ignition characteristics of DEEVO mixtures were studied in an ignition quality tester (IQT). There is an evident reduction in ignition delay time (IDT) for DEEVO mixtures compared to VO. The IDT of VO (4.5 ms), DEEVO20 (3.2 ms) and DEEVO40 (2.7 ms) was measured in IQT. Accordingly, the derived cetane number (DCN) of DEEVO mixtures increased with the increase in proportion of DEE. The reported mixtures were also tested in a single cylinder CI engine. The start of combustion (SOC) was advanced for DEEVO20 and DEEVO40 compared to diesel, which is attributed to the high DCN of DEEVO mixtures. On the other hand, the peak heat release rate decreased for DEEVO mixtures compared to diesel. Gaseous emissions such as nitrogen oxide (NOX), total hydrocarbon (THC) and smoke were reduced for DEEVO mixtures compared to diesel. The physical and ignition properties of VO are improved by the addition of DEE, and thus, the need for the trans-esterification process is averted. Furthermore, this blending strategy is simpler and enables operation of straight run oils and fats in CI engine, replacing diesel completely.
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Varanasi, Pushkara R., Kathleen M. Cornett, and Margaret C. Lawson. "Effect of acid labile ether protecting groups on the oxide etch resistance and lithographic performance of 248-nm resists." In Microlithography 2000, edited by Francis M. Houlihan. SPIE, 2000. http://dx.doi.org/10.1117/12.388316.

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