Relevant bibliographies by topics / Oxime Chemistry

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

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"

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Dhuguru, Jyothi, Eugene Zviagin, and Rachid Skouta. "FDA-Approved Oximes and Their Significance in Medicinal Chemistry." Pharmaceuticals 15, no. 1 (January 4, 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. Cephalosporins are β-lactam based antibiotics and serve as widely acclaimed tools in fighting bacterial infections. Oxime based cephalosporins have emerged as an important class of drugs with improved efficacy and a broad spectrum of anti-microbial activity against Gram-positive and Gram-negative pathogens. Among the several oxime based derivatives, cefuroxime, ceftizoxime, cefpodoxime and cefmenoxime are the FDA approved oxime-based antibiotics. Given the pharmacological significance of oximes, in the present paper, we put together all the FDA-approved oximes and discuss their mechanism of action, pharmacokinetics and synthesis.
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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 (November 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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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 (June 1, 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.Key words: oxime, lipase, kinetic resolution, Beckmann rearrangement, perhydro histrionicotoxin.
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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 (September 30, 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 as an important aggregation mode for oximes. Secondary interactions, C—H···π and C—H···O interactions, in compounds 1 and 2, and interactions involving the nitro group oxygen atoms in compound 3 link the chains into three dimensional arrays.
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Kubicki, Maciej, Teresa Borowiak, and Wiesław Z. Antkowiak. "Hydrogen Bonds in "Carboxyoximes": the Case of Bomane Derivatives." Zeitschrift für Naturforschung B 55, no. 8 (August 1, 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, respectively. By contrast, in bornane-2-oxime-3-endo-carboxylic acid 'heterogenic' hydrogen bonds between carboxylic and oxime bonds were found. This carboxylic-oxime, or 'carboxyoxime' system is almost always present in compounds which have both oxime and carboxylic groups; therefore it can be regarded as an element of supramolecular structures (synthon). The presence of such synthons can break the tendency of carboxylic acids and oximes towards crystallizing in centrosymmetric structures.
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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 (April 1, 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 to the corresponding bromolactone oxime. - With 2,2-dimethyl-3-butene aldoxime, the corresponding 3-bromopyrroline N-oxide was formed, due to a formal, unusual N-endo cyclization to the chain terminus. This was exploited for a new access to six-membered nitrones from a γ,δ -pentene aldoxime, with addition of Br/OH to the C=C of the 4-pentenal first, and oximation/cyclization following then
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Yamamoto, Hitoshi, Toshikage Asakura, Yuichi Nishimae, Akira Matsumoto, Junichi Tanabe, Jean-Luc Birbaum, Peter Murer, Tobias Hinterman, and Masaki Ohwa. "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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Grover, Gregory N., Jonathan Lam, Thi H. Nguyen, Tatiana Segura, and Heather D. Maynard. "Biocompatible Hydrogels by Oxime Click Chemistry." Biomacromolecules 13, no. 10 (September 12, 2012): 3013–17. http://dx.doi.org/10.1021/bm301346e.

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Canário, Catarina, Mariana Matias, Vanessa Brito, Adriana O. Santos, Amílcar Falcão, Samuel Silvestre, and Gilberto Alves. "New Estrone Oxime Derivatives: Synthesis, Cytotoxic Evaluation and Docking Studies." Molecules 26, no. 9 (May 4, 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 docking studies against estrogen receptor α, steroid sulfatase, 17β-hydroxysteroid dehydrogenase type 1 and β-tubulin were also accomplished. The 2-nitroestrone oxime showed higher cytotoxicity than the parent compound on MCF-7 cancer cells. Furthermore, the oximes bearing halogen groups in A-ring evidenced selectivity for HepaRG cells. Remarkably, the Δ9,11-estrone oxime was the most cytotoxic and arrested LNCaP cells in the G2/M phase. Fluorescence microscopy studies showed the presence of condensed DNA typical of prophase and condensed and fragmented nuclei characteristic of apoptosis. However, this oxime promoted the proliferation of T47-D cells. Interestingly, molecular docking studies estimated a strong interaction between Δ9,11-estrone oxime and estrogen receptor α and β-tubulin, which may account for the described effects.
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Plater, M. John, William TA Harrison, and Ross Killah. "Potential photoacid generators based on oxime sulfonates." Journal of Chemical Research 43, no. 1-2 (January 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 are discussed. The possible use of these compounds as photoacid generators in polymer resists and the role of secondary reactions to liberate acid is discussed.
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Dissertations / Theses on the topic "Oxime Chemistry"

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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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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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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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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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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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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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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 acetylcholinesterase (AChE) that prevents the enzyme from hydrolyzing acetylcholine (ACh), a neurotransmitter in the central and peripheral nervous systems (CNS and PNS). Therefore, ACh accumulates in the cholinergic synapses throughout the body, which results in overstimulation of the ACh receptors. Removal of the phosphyl moiety from the OP-bound AChE active site has been a promising method to restore AChE’s catalytic activity. However, a secondary process called aging also occurs in the OP-AChE complex. Once aging occurs, currently available oximes are ineffective in removing the phosphyl moiety from the enzyme’s active site, and hence are ineffective as antidotes against the aged enzyme. Several families of alkylating and acylating agents including several classes of agents that combine alkylating moieties with known active site or peripheral cite (PAS) binding motifs were synthesized and evaluated. The general aim of the research was that successful alkylation or acylation of the phosphonate monoanion of aged AChE would produce neutral phosphyl complexes that would either spontaneously reactivate or would be reactivatable in the presence of oxime antidotes. Methoxylamine analogs of the oxime antidote 2-PAM were synthesized with the aim that methyl transfer to the aged AChE adduct would produce a neutral phosphyl AChE adduct simultaneously with 2-PAM in situ, and subsequent 2-PAM nucleophilic attack would reactivate the newly formed neutral phosphyl-AChE adduct. However, none of these 2-PAM analogs resurrected the activity of aged AChE. Another strategy for resurrecting the activity of aged AChE utilizes N-methylpyridiniums that are substituted at the 2-position with a beta-lactam moiety. For these compounds, opening of the electrophilic beta-lactam unmasks a nucleophilic amidine function which could putatively attack at phosphorus to expel the free enzyme. For this class of agents, only the active site directed compound that possessed the 5-CF₃ substituent showed possible resurrection of the activity of aged AChE, though activities in both the control and treated samples were low. Methyl transfers are common in Nature, and the natural transfer agent is S-adenosylmethionine, a sulfonium methyl donor. Consequently, the array of sulfonium compounds were evaluated on the expectation that they would bind to the AChE active site and transfer a methyl group to the phosphonate monoanion of the aged enzyme. Though high-affinity binding was noted for these compounds, none of these resurrected the activity of the aged AChE complex. Finally, several selected agents were evaluated on reactivating the initial OP-AChE complex before aging has occurred. It was observed that degraded samples of selected inhibitors are capable of reactivating initial complexes of sarin and soman inhibited AChE at low concentration that is an important character of efficient reactivators. However, the structure of reactivator is still unknown. Two major challenges still face researchers in the quest to design effective medicinal agents for counteracting poisoning by AChE-inhibiting nerve agents. The first is that there is no universal oxime antidote. Oximes that are effective against certain nerve agents are ineffective against others. The second is that, despite extensive efforts that span two generations, aged phosphyl-AChE adducts have never been reactivated. However, given the powerful tools of modern structural biology, medicinal chemistry and molecular biology, there is still hope that these considerable challenges can be met.
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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, Co(5-Acqo)3, and Mn(5-Acqo)2, .H2O were prepared by the direct reaction of 5-AcqoH with the appropriate metal(II) chloride or by the nitrosation of 3-acetylaminophenol in the presence of the metal salt. Co(5-Acqo)3 was also prepared by the reaction of the ligand with Na3[Co(NO2)6]. The complex Na(Co(5-Acqo)2 (NO2)2 ], resulted from the nitrosation of Na3(Co(NO2)6] in the presence of 3-acetylaminophenol. Pyrolysis of Ni(5-Acqo)2.6H2O gave Ni(5-Acqo)2. The complexes Cu(5-Acqo)2 and Ni(5-Acqo)2.nH2O (n = 0, 2-6) reacted with pyridine and 2,2-dipyridyl to give adducts whereas the complexes of M(5-Acqo)3 (M = Co, Mn) showed no reaction with pyridine. Magnetochemical measurements, indicated that all complexes, [except Ni(5-Acqo)2], are magnetically dilute and hence monomeric. Ni(5-Acqo)2 complex has a subnormal magnetic moment due to association. The diamagnetism of Co(5-Acqo)3 and the low spin configuration of Mn(5-Acqo)3.H2O are indicative of the strong field character of the ligand. COSY, H- and C n.m.r. studies have shown that Co(5-Acqo)3 is a mixture of facial and meridial isomers. For all complexes i.r. studies indicate the involvement of the ring CO in bonding. Their electronic spectra show strong absorption in the u.v. region which tails into the visible but d - d transitions have been clearly Identified for Ni(5-Acqo)2.6H20 and Mn(5-Acqo)3 .H20. Reexamination of the reaction of several complexes of type M(Rqo)2 [M = Ni or Cu) with dimethyl acetylenedicarboxylate has confirmed the occurence of cycloaddition and the formation of oxazine. A metal-containing product, M(II)(butynedioate), and in some cases an additional organic product, l,4-benoxazin-2-one, have been isolated. Mechanistic appraisals for the 1,4-benoxazinone formation are presented and the structure of one has been elucidated by X-ray crystallography. The reaction of the new complex Cu(5-Acqo)2 with DMAD leads to analogous products. The reaction of the complexes M(l-nqo)2 [M = Cu, Ni) with methyl propiolate give the hydrated M(II)(propynoate)2 and oxazine.
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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
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 synthesized, then the conversion of the ester group at the lower arm to the amine group was carried out. Heteroatom cyclization catalyzed by CuI afforded the desired substituted pyrrolo[1,2-a]pyrazine structure. In the second part, it was aimed to synthesize new compounds with unusual structures which are not described in the literature
namely, as pyrrolo[1,2-a]pyrazine N-oxide. In this direction, first pyrrole was submitted to Vilsmeier-Haack reaction to attach a formyl group at C-2. Substitution reaction then effectively gave 1-(prop-2-yn-1-yl)-1H-pyrrole-2-carbaldehyde, which was a key molecule to synthesize the aldoxime. AuCl3 catalyzed cyclization of the corresponding oxime afforded pyrrolo[1,2-a]pyrazine N-oxide. In the next step, Sonogashira coupling reactions were carried out to obtain terminal alkynes (RC&equiv
CR'
) starting from 1-(prop-2-yn-1-yl)-1H-pyrrole-2-carbaldehyde. The aim of this part was to study the effect of aryl groups to the activated alkyl functional group by a metal catalyst. In this case, unexpected oxime-oxime transformation was observed, which is unprecedented in the literature
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Books on the topic "Oxime Chemistry"

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

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

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

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

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A, Wingrave James, ed. Oxide surfaces. New York: Marcel Dekker, 2001.

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Kapustin, Vladimir, and Illarion Li. Theory, electronic structure and physical chemistry of materials cathodes for microwave devices. ru: 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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Martin, Jansen, ed. High performance non-oxide ceramics. Berlin: Springer, 2002.

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

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Noguera, Claudine. Physics and chemistry at oxide surfaces. Cambridge [England]: Cambridge University Press, 1996.

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

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Book chapters on the topic "Oxime Chemistry"

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Kubler-Kielb, Joanna. "Conjugation of LPS-Derived Oligosaccharides to Proteins Using Oxime Chemistry." In Methods in Molecular Biology, 317–27. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-151-2_20.

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Gao, Wei. "The Chemistry of Graphene Oxide." In Graphene Oxide, 61–95. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15500-5_3.

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Waychunas, Glenn A. "Chapter 2.CRYSTAL CHEMISTRY OF OXIDES AND OXYHYDROXIDES." In Oxide Minerals, edited by Donald H. Lindsley, 11–68. Berlin, Boston: De Gruyter, 1991. http://dx.doi.org/10.1515/9781501508684-005.

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Sleight, A. W. "Chemistry of Oxide Superconductors." In High Temperature Superconductivity, 97–143. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003209621-4.

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Hogg, Neil, and Owen W. Griffith. "The Biological Chemistry of NO." In Nitric Oxide and the Kidney, 3–21. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6039-5_1.

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Seshadri, R. "Oxide Nanoparticles." In The Chemistry of Nanomaterials, 94–112. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/352760247x.ch5.

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Fueki, K., K. Kitazawa, K. Kishio, and T. Hasegawa. "Defect Chemistry of Oxide Superconductors." In High-T c Superconductors, 41–52. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-0846-9_4.

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Asthagiri, Aravind, David A. Dixon, Zdenek Dohnálek, Bruce D. Kay, José A. Rodriguez, Roger Rousseau, Darío J. Stacchiola, and Jason F. Weaver. "Catalytic Chemistry on Oxide Nanostructures." In Oxide Materials at the Two-Dimensional Limit, 251–80. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28332-6_9.

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Garrel, C., and M. Fontecave. "Nitric oxide: Chemistry and biology." In Analysis of Free Radicals in Biological Systems, 21–35. Basel: Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9074-8_3.

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Ueda, Wataru. "Catalysis Chemistry of Crystalline Complex Metal Oxide Catalysts." In Crystalline Metal Oxide Catalysts, 53–81. Singapore: 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"

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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. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05569.

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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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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. Basel, Switzerland: 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. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07376.

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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. Basel, Switzerland: 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. Reston, Virginia: 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"

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

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

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Abstract:
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), June 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, January 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. Fort Belvoir, VA: Defense Technical Information Center, June 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), October 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), October 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), March 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), March 2023. http://dx.doi.org/10.2172/1960547.

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