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Relevant bibliographies by topics / Oxime Chemistry

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Academic literature on the topic 'Oxime Chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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Journal articles on the topic "Oxime Chemistry"

1

Dhuguru, Jyothi, Eugene Zviagin, and Rachid Skouta. "FDA-Approved Oximes and Their Significance in Medicinal Chemistry." Pharmaceuticals 15, no. 1 (2022): 66. http://dx.doi.org/10.3390/ph15010066.

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Despite the scientific advancements, organophosphate (OP) poisoning continues to be a major threat to humans, accounting for nearly one million poisoning cases every year leading to at least 20,000 deaths worldwide. Oximes represent the most important class in medicinal chemistry, renowned for their widespread applications as OP antidotes, drugs and intermediates for the synthesis of several pharmacological derivatives. Common oxime based reactivators or nerve antidotes include pralidoxime, obidoxime, HI-6, trimedoxime and methoxime, among which pralidoxime is the only FDA-approved drug. Cepha

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2

Ahmed, Sarbast M., Faiq H. S. Hussain, and Paolo Quadrelli. "9-Anthraldehyde oxime: a synthetic tool for variable applications." Monatshefte für Chemie - Chemical Monthly 151, no. 11 (2020): 1643–58. http://dx.doi.org/10.1007/s00706-020-02695-2.

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Abstract Oximes are one of the most important and prolific functional groups in organic chemistry; among them, 9-anthraldehyde oxime represents a valuable example both from the preparative side and the synthetic applications. There are many strategies to prepare 9-anthraldehyde oxime from different functional groups that were summarized in the present review, focusing on the most recent and innovative. The main synthetic applications of 9-anthraldehyde oxime are presented and thoroughly discussed, focusing on the most recent and innovative synthetic strategies. Graphic abstract

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3

Diedrichs, Nicole, Ralf Krelaus, Ina Gedrath, and Bernhard Westermann. "Kinetic resolution of oxime esters with lipases synthesis of enantiomerically enriched building blocks with quaternary carbon centers and formal total synthesis of perhydro histrionicotoxin." Canadian Journal of Chemistry 80, no. 6 (2002): 686–91. http://dx.doi.org/10.1139/v02-097.

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Enantiomerically enriched oximes bearing stereogenic quaternary carbon centers can be obtained by lipase-catalyzed kinetic resolution of oxime esters. Substrate specificity, solvent effects, and the use of different lipases are discussed. Kinetic resolution of butyrylated oximes by lipase PS in the presence of n-butanol gave the best ee-values of both the saponified oxime and the residual oxime ester. Subsequent stereospecific Beckmann rearrangement of an enantiomerically enriched oxime provided lactams, which could be employed for the synthesis of optically active perhydro histrionicotoxin.Ke

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4

Low, John Nicolson, James Lewis Wardell, Cristiane Franca Da Costa, Marcus Vicinius Nora Souza, and Ligia Rebelo Gomes. "Structural study of three heteroaryl oximes, heteroaryl-N=OH: Compounds forming strong C3 molecular chains." European Journal of Chemistry 9, no. 3 (2018): 151–60. http://dx.doi.org/10.5155/eurjchem.9.3.151-160.1734.

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In order to further investigate the structural chemistry of oximes and to further establish the main structural arrangements adopted, we have determined the crystal structure of and carried out Hirshfeld surface calculations on three heteroaryl oximes, namely (Z)-thiophene-2-carbaldehyde oxime (1), (Z)-1H-pyrrole-2 carbaldehyde oxime (2) and (Z)-5-nitrofuran-2-carbaldehyde oxime (3). As confirmed by both techniques, the major intermolecular interactions in each compound are classical N—H···O hydrogen bonds, which link the molecules into C3 chains. Such an arrangement has been previous reported

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5

Kubicki, Maciej, Teresa Borowiak, and Wiesław Z. Antkowiak. "Hydrogen Bonds in "Carboxyoximes": the Case of Bomane Derivatives." Zeitschrift für Naturforschung B 55, no. 8 (2000): 677–84. http://dx.doi.org/10.1515/znb-2000-0802.

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Abstract The tendency of forming mixed carboxyl-to-oxime hydrogen bonds was tested on the series of bornane derivatives: one with the acid function only (bornane-2-endo-carboxylic acid), one with the oxime function (2,2′-diethylthiobomane-3-oxime), and one with both oxime and carboxylic functions (bornane-2-oxime-3-endo-carboxylic acid). The crystal structures of these compounds were determined by means of X-ray diffraction. In bornane-2-endo-carboxylic acid and 2,2′-diethylthiobornane-3-oxime 'homogenic' hydrogen bonds were found, and these hydrogen bonds close eight-and six-membered rings, r

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6

Gulla, Mahendra, Lars Bierer, Stefan Schmidt, Leo Redcliffe, and Volker Jäger. "Bromocyclization of Unsaturated Oximes. Synthesis of Five-Membered Cyclic Nitrones (Pyrroline N-Oxides)." Zeitschrift für Naturforschung B 61, no. 4 (2006): 471–85. http://dx.doi.org/10.1515/znb-2006-0414.

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The cyclization of a ribose-derived pentenose oxime with various halogen electrophiles showed bromine to be the most effective reagent, leading to 80% of L-lyxo/D-ribo-pyrroline N-oxides in an 84:16 diastereomeric ratio. In order to explore the scope of this facile process, several other γ,δ - unsaturated oximes were submitted to this reaction. Depending on the substitution pattern, 23 - 87%, yields of pyrroline N-oxides of were registered. With α-allyl-β -ketoester oximes the alkoxycarbonyl group proved a similar (ethoxy) or even better (t-butoxy) trapping nucleophile, leading preferentially

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7

Yamamoto, Hitoshi, Toshikage Asakura, Yuichi Nishimae, et al. "Oxime Sulfonate Chemistry for Advanced Microlithography." Journal of Photopolymer Science and Technology 20, no. 5 (2007): 637–42. http://dx.doi.org/10.2494/photopolymer.20.637.

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8

Grover, Gregory N., Jonathan Lam, Thi H. Nguyen, Tatiana Segura, and Heather D. Maynard. "Biocompatible Hydrogels by Oxime Click Chemistry." Biomacromolecules 13, no. 10 (2012): 3013–17. http://dx.doi.org/10.1021/bm301346e.

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9

Canário, Catarina, Mariana Matias, Vanessa Brito, et al. "New Estrone Oxime Derivatives: Synthesis, Cytotoxic Evaluation and Docking Studies." Molecules 26, no. 9 (2021): 2687. http://dx.doi.org/10.3390/molecules26092687.

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The interest in the introduction of the oxime group in molecules aiming to improve their biological effects is increasing. This work aimed to develop new steroidal oximes of the estrane series with potential antitumor interest. For this, several oximes were synthesized by reaction of hydroxylamine with the 17-ketone of estrone derivatives. Then, their cytotoxicity was evaluated in six cell lines. An estrogenicity assay, a cell cycle distribution analysis and a fluorescence microscopy study with Hoechst 3358 staining were performed with the most promising compound. In addition, molecular dockin

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10

Plater, M. John, William TA Harrison, and Ross Killah. "Potential photoacid generators based on oxime sulfonates." Journal of Chemical Research 43, no. 1-2 (2019): 26–33. http://dx.doi.org/10.1177/1747519819831829.

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The bis-oxime of acenaphthenequinone and the mono-oxime of benzil have been sulfonated by reaction with 4-methylbenzenesulfonyl chloride and propylsulfonyl chloride. The four sulfonated oximes were characterised by X-ray single-crystal structure determinations. Some photochemical decompositions were studied using a 6-W 254-nm immersion well lamp in dichloromethane. The 4-methylbenzenesulfonate bis-oxime of acenaphthenequinone and the 4-methylbenzenesulfonate mono-oxime of benzil both give 4-methylbenzenesulfonic acid upon irradiation but not 4-methylbenzenesulfinic acid. Fragmentation pathways

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Dissertations / Theses on the topic "Oxime Chemistry"

1

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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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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3

王淑儀 and Shuk-yee Janet Wong. "The chemistry of osmium carbonyl clusters containing oxime and oxo ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2003. http://hub.hku.hk/bib/B31244932.

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4

劉曉霞 and Xiaoxia Liu. "Coordination Chemistry of 1,2-naphthoquinone-mono-oxime withruthenium, rhodium and palladium." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2000. http://hub.hku.hk/bib/B3124063X.

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Liu, Xiaoxia. "Coordination Chemistry of 1,2-naphthoquinone-mono-oxime with ruthenium, rhodium and palladium /." Hong Kong : University of Hong Kong, 2000. http://sunzi.lib.hku.hk/hkuto/record.jsp?B2168781X.

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6

Portela-Cubillo, Fernando. "Oxime derivatives : versatile reagents for radical-mediated syntheses of heterocycles." Thesis, St Andrews, 2009. http://hdl.handle.net/10023/856.

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7

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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8

Yasapala, Sumana Nilahthi. "Reactivation of Organophosphorus agent inhibited-human acetylcholinesterase." Diss., University of Iowa, 2016. https://ir.uiowa.edu/etd/2169.

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Organophosphorus compounds (OPs) are used as pesticides, e.g. parathion, which is converted in the body to paraoxon, and chemical warfare nerve agents, such as sarin, soman, cyclosarin, VX, and tabun. Even small amounts of OP exposure can be fatal, depending on the toxicity of the compound. Great stocks of highly toxic chemical warfare nerve agents exit around the world and are considered a serious threat to national security and international stability. OPs exert their toxicity by covalent irreversible inhibition of acetylcholinester

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9

Barjesteh, Hengameh. "Studies of complexes derived from 5-acetylamino-1,2-benzoquinone 2-oxime and related ligands." Thesis, London Metropolitan University, 1991. http://repository.londonmet.ac.uk/3334/.

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5-Acatylamino-l,2-benzoquinone 2-oxine [5-AcqoH] results from the direct nitrosation of 3-acatylaminophenol together with its isomer 3-acetylamino-l,4-benzoquinone 4-oxine [3-AcqoH]. The quinone oximic structure of the former has been indicated by i.r. and n.m.r. studies. In the case of 3-AcqoH this type of structure has been established by X-ray crystallography. Following a brief review of quinone oxinic complexes, a study of the synthesis, properties and structure of Cu(II), Ni(II), Co(III), and Mn(III) complexes of 5-AcqoH is presented. The complexes Ni(5-Acqo)2.nH2O (n = 2-6), Cu(5-Acqo)2,

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10

Guven, Sinem. "Construction Of Pyrrolo[1,2-a]pyrazine Structure By Metal Catalyzed Cyclization Of N-propargyl Substituted Pyrroles." Master's thesis, METU, 2013. http://etd.lib.metu.edu.tr/upload/12615582/index.pdf.

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Pyrrolo[1,2-a]pyrazine is one of the isomers of pyrolodiazine family. Pyrrolo[1,2-a]pyrazine possesses a bicyclic heteroaromatic structure that have 10 electrons. It has various biological importances in synthetic chemistry<br>therefore, many different approaches to generate this skeleton have been developed so far. In this study, our prior aim was to develop a new synthetic methodology for the formation of pyrrolo[1,2-a]pyrazine moiety. In the first part of this focus, the starting compound, methyl 2-(2-methoxy-2-oxoethyl)-1-(prop-2-yn-1-yl)-1H-pyrrole-3-carboxylate was successfully synthesiz

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Books on the topic "Oxime Chemistry"

1

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

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2

Rao, C. N. R. 1934- and International Union of Pure and Applied Chemistry., eds. Chemistry of oxide superconductors. Blackwell Scientific Publications, 1988.

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3

Metal oxide chemistry and synthesis: From solution to oxide. John Wiley, 2000.

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4

1944-, Woodruff D. P., ed. Oxide surfaces. Elsevier, 2001.

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A, Wingrave James, ed. Oxide surfaces. Marcel Dekker, 2001.

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6

Kapustin, Vladimir, and Illarion Li. Theory, electronic structure and physical chemistry of materials cathodes for microwave devices. INFRA-M Academic Publishing LLC., 2020. http://dx.doi.org/10.12737/1041298.

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In the monograph the kinetic theory of cathode materials based on metal and oxide phases, analytical methods of research of the cathodes, methods of study of their emission properties. Details the authors discuss the theory and physico-chemistry of oxide-Nickel, metalloplastic, and metal alloyed oxide-yttrium cathodes, including a cathode for magnetrons with cold start. Designed for scientific and engineering-technical workers, specializing in electronic materials and electronic devices.

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7

Martin, Jansen, ed. High performance non-oxide ceramics. Springer, 2002.

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8

Ryshkewitch, Eugene. Oxide ceramics: Physical chemistry and technology. 2nd ed. General Ceramics, 1985.

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9

Noguera, Claudine. Physics and chemistry at oxide surfaces. Cambridge University Press, 1996.

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Eugene, Ryshkewitch. Oxide ceramics: Physical chemistry and technology. 2nd ed. General Ceramics, 1985.

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Book chapters on the topic "Oxime Chemistry"

1

Kubler-Kielb, Joanna. "Conjugation of LPS-Derived Oligosaccharides to Proteins Using Oxime Chemistry." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-151-2_20.

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2

Gao, Wei. "The Chemistry of Graphene Oxide." In Graphene Oxide. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15500-5_3.

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3

Waychunas, Glenn A. "Chapter 2.CRYSTAL CHEMISTRY OF OXIDES AND OXYHYDROXIDES." In Oxide Minerals, edited by Donald H. Lindsley. De Gruyter, 1991. http://dx.doi.org/10.1515/9781501508684-005.

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4

Sleight, A. W. "Chemistry of Oxide Superconductors." In High Temperature Superconductivity. CRC Press, 2021. http://dx.doi.org/10.1201/9781003209621-4.

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5

Hogg, Neil, and Owen W. Griffith. "The Biological Chemistry of NO." In Nitric Oxide and the Kidney. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6039-5_1.

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6

Seshadri, R. "Oxide Nanoparticles." In The Chemistry of Nanomaterials. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/352760247x.ch5.

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7

Fueki, K., K. Kitazawa, K. Kishio, and T. Hasegawa. "Defect Chemistry of Oxide Superconductors." In High-T c Superconductors. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-0846-9_4.

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8

Asthagiri, Aravind, David A. Dixon, Zdenek Dohnálek, et al. "Catalytic Chemistry on Oxide Nanostructures." In Oxide Materials at the Two-Dimensional Limit. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28332-6_9.

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9

Garrel, C., and M. Fontecave. "Nitric oxide: Chemistry and biology." In Analysis of Free Radicals in Biological Systems. Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9074-8_3.

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10

Ueda, Wataru. "Catalysis Chemistry of Crystalline Complex Metal Oxide Catalysts." In Crystalline Metal Oxide Catalysts. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-5013-1_2.

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Conference papers on the topic "Oxime Chemistry"

1

Ajduković, Jovana, Marija Filipović, Milana Perković, Elizabeta Stanić, and Dimitar Jakimov. "Antiproliferative activity of steroidal oxime and its O-alkylated derivatives." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05569.

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2

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. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01829.

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3

Rodríguez-Borges, José, Carlos Sousa, M. Luísa Vale, and Xerardo García-Mera. "Aza-Diels-Alder versus 1,3-Dipolar Cycloadditions of Methyl Glyoxylate Oxime with Cyclopentadiene." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01218.

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Katagi, Manjunath, Girish Bolakatti, Sujatha ML, Suchitra M, and Shivlingrao Mamledesai. "<em>In vitro</em> reactivation of chlorpyrifos-inhibited rat brain acetylcholinesterase from pyrazole-oxime derivatives." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07376.

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5

Dekamin, Mohammad, and Neda Nazary. "Synthesis of Acetaminophen by Liquid Phase Beckmann Rearrangement of 4-Hydroxyacetophenone Oxime over Nano-Ordered Zn-MCM-41." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00446.

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MacNaughton, S., D. F. DeMeo, S. Sonkusale, and T. E. Vandervelde. "Wet chemistry based copper oxide and zinc oxide nanowire photovoltaic cells." In 2009 International Semiconductor Device Research Symposium (ISDRS 2009). IEEE, 2009. http://dx.doi.org/10.1109/isdrs.2009.5378097.

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Wypych, A., A. Opasinska, I. Bobowska, and P. Wojciechowski. "Synthesis and dielectric investigations of BaTiO3 obtained by soft chemistry route." In 2012 IEEE International Conference on Oxide Materials for Electronic Engineering (OMEE). IEEE, 2012. http://dx.doi.org/10.1109/omee.2012.6464859.

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Abdul Allah, K. A., and U. A. Al-Rawi. "Preparation and characterization of aluminum oxide/iron oxide/graphene oxide nanocomposite by co-precipitation method." In International Conference of Chemistry and Petrochemical Techniques (ICCPT). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0095331.

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Arisman, Chris, Craig T. Johansen, Wagner Galuppo, and Allison McPhail. "Nitric Oxide Chemistry Effects in Hypersonic Boundary Layers." In 43rd AIAA Fluid Dynamics Conference. American Institute of Aeronautics and Astronautics, 2013. http://dx.doi.org/10.2514/6.2013-3104.

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Wuenschell, Jeffrey K., Youngseok Jee, Paul R. Ohodnicki, Michael P. Buric, and Benjamin T. Chorpening. "The role of oxide defect chemistry in the drude and plasmonic response of optical fiber-based sensing layers for high-temperature gas sensing." In Oxide-based Materials and Devices XII, edited by Ferechteh H. Teherani, David C. Look, and David J. Rogers. SPIE, 2021. http://dx.doi.org/10.1117/12.2578459.

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Reports on the topic "Oxime Chemistry"

1

Hernandez, Rigoberto. Open Chemistry Collaborative in Diversity Equity (OXIDE). Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1504746.

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Deininger. PR-443-13605-R01 Sensors for Gas Quality Monitoring. Pipeline Research Council International, Inc. (PRCI), 2014. http://dx.doi.org/10.55274/r0010127.

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The purpose of this project was to determine the suitability of low cost environmental air quality sensors, for detection of pipeline gas quality. In particular, this project examined options for detection and quantification of hydrogen sulfide (H2S), water (H2O), and oxygen (O2). All of the sensors used were based on Synkeras existing anodic aluminum oxide (AAO) platform and detection chemistry. The key challenge of this effort was laboratory based demonstration of the feasibility of detecting these three components in natural gas at pressures exceeding 1 atmosphere

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RODRIGUEZ, J. A. CHEMISTRY OF SO2 AND DESOX PROCESSES ON OXIDE NANOPARTICLES. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/893860.

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Green, Patrick. The chemistry of chromium (VI) and chromium (V) oxide fluorides. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.5923.

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Brown, J. R. Surface chemistry and reduction behaviour of y-alumina supported molybdenum oxide. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/304349.

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Klabunde, Kenneth J. Nanoscale Metal and Metal Oxide Particles Chemistry. Reagents for Decontamination and Remediation. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada391675.

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Nicollet, Clement, and Harry Tuller. Self-regulating surface chemistry for more robust highly durable solid oxide fuel cell cathodes. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1569264.

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Tuller, Harry, and Clement Nicollet. Self-regulating surface chemistry for more robust highly durable solid oxide fuel cell cathodes. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1644391.

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Gopalan, Srikanth. Solid Oxide Fuel Cell Cathodes. Unraveling the Relationship Between Structure, Surface Chemistry and Oxygen Reduction. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1214271.

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Seo, Han Gil, and Harry Tuller. Robust highly durable solid oxide fuel cell cathodes – Improved materials compatibility & self-regulating surface chemistry. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1960547.

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