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Relevant bibliographies by topics / Oximes (Organic Chemistry)

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Academic literature on the topic 'Oximes (Organic Chemistry)'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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Journal articles on the topic "Oximes (Organic Chemistry)"

1

Abele, Edgars, and Ramona Abele. "Oximes of Nucleosides and Related Compounds: Synthesis, Reactions and Biological Activity." Current Organic Synthesis 15, no. 5 (2018): 650–65. http://dx.doi.org/10.2174/1570179415666180524112811.

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Background: Literature data on the synthesis and structure of oximes of nucleosides and related nitrogenous bases from pyrimidine and purine were reviewed. Synthesis of novel heterocyclic systems from nucleoside oximes related pyrimidine oximes was described. The biological activity of derivatives of nucleoside and nitrogenous base oximes was also reviewed. <p> Objective: The review focuses on the recent progress in the area of nucleoside oxime synthesis, reactions and biological activity. Conclusion: In summary, literature data on the synthesis and structure of oximes of nucleosides and

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2

Zeng, Qingle, Nutao Li, Yiding Wang, Hongqin Yang, and Ze He. "I2-Catalyzed Oxidative Coupling of Ketone Oximes and Dialkyl/Diarylphosphine Oxides." Synlett 32, no. 01 (2020): 75–80. http://dx.doi.org/10.1055/s-0040-1707306.

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AbstractA new protocol for the oxidative coupling of ketone oximes with dialkyl/diarylphosphine oxides to synthesize O-(dialkylphosphinyl)ketone oximes has been developed. Hydrogen peroxide is used as a green oxidizing agent, and molecular iodine is used as a nonmetal catalyst. The reaction has a high atom economy, with water as the only byproduct. O-(Dialkylphosphinyl)ketone oximes with 26 examples have been obtained with high yields. Furthermore, the product may be transformed into other molecules, i.e., by reduction.

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de Lijser, HJ Peter, Jason S. Kim, Suzanne M. McGrorty, and Erin M. Ulloa. "Substituent effects in oxime radical cations. 1. Photosensitized reactions of acetophenone oximes." Canadian Journal of Chemistry 81, no. 6 (2003): 575–85. http://dx.doi.org/10.1139/v03-052.

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A variety of ortho-, meta-, and para-substituted (-H, -F, -Cl, -CF3, -CN (meta and para only), -CH3, -OCH3, and -NO2) acetophenone oximes were synthesized and studied using laser flash photolysis (LFP) and steady-state photolysis experiments in acetonitrile with chloranil as the photosensitizer. In addition, semi-empirical (AM1) calculations were performed on the neutral species, the radical cations, and the corresponding iminoxyl radicals. The data was analyzed in terms of the electrochemical peak potentials of the oximes, the quenching rates of triplet chloranil (LFP), the calculated ionizat

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4

Vaidya, Vipraja V., Karuna S. Wankhede, Manikrao M. Salunkhe, and Girish K. Trivedi. "Synthesis of isoxazole conjugates of sugars via 1,3-dipolar cycloaddition." Canadian Journal of Chemistry 86, no. 2 (2008): 138–41. http://dx.doi.org/10.1139/v07-145.

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Isoxazole conjugates of sugar have been synthesized by the aid of 1,3-dipolar cycloaddition in a click chemistry approach. The sugar-derived propargyl ethers underwent 1,3-dipolar cycloadditions smoothly with in situ generated nitrile oxides from aromatic oximes in good yields. The reaction exhibited a high degree of regioselectivity.Key words: isoxazole conjugates, 1,3-dipolar cycloadditions, nitrile oxides.

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Lorke, Dietrich E., and Georg A. Petroianu. "Treatment of Organophosphate Poisoning with Experimental Oximes: A Review." Current Organic Chemistry 23, no. 5 (2019): 628–39. http://dx.doi.org/10.2174/1385272823666190408114001.

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Standard therapy of Organophosphorus Compound (OPC) poisoning with oxime-type acetylcholinesterase (AChE) reactivators is unsatisfactory. New bispyridinium oximes have therefore been synthesized. This review summarizes in vitro characteristics of established (pralidoxime, obidoxime, trimedoxime, HI-6) and experimental (K-)oximes, and compares their protective efficacy in vivo, when administered shortly after exposure to Diisopropylfluorophosphate (DFP) and three OPC pesticides (ethyl-paraoxon, methylparaoxon, azinphos-methyl) in the same experimental setting. In addition to reactivating cholin

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6

Foretić, Blaženka, Vladimir Damjanović, Robert Vianello, and Igor Picek. "Novel Insights into the Thioesterolytic Activity of N-Substituted Pyridinium-4-oximes." Molecules 25, no. 10 (2020): 2385. http://dx.doi.org/10.3390/molecules25102385.

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The pyridinium oximes are known esterolytic agents, usually classified in the literature as catalysts, which mimic the catalytic mode of hydrolases. Herein, we combined kinetic and computational studies of the pyridinium-4-oxime-mediated acetylthiocholine (AcSCh+) hydrolysis to provide novel insights into their potential catalytic activity. The N-methyl- and N-benzylpyridinium-4-oximes have been tested as oximolytic agents toward the AcSCh+, while the newly synthesized O-acetyl-N-methylpyridinium-4-oxime iodide was employed for studying the consecutive hydrolytic reaction. The relevance of the

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7

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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8

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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9

Musaev, Yurii I., Eleonora B. Musaeva, Svetlana Yu Khashirova, Marina O. Sanakoeva, and Artur E. Baykaziev. "Synthesis of Aromatic Diketoximes and their Complexes with Nickel Salts." Key Engineering Materials 869 (October 2020): 571–76. http://dx.doi.org/10.4028/www.scientific.net/kem.869.571.

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The diketoximes of 4,4'-diacetyldiphenyl oxide and 4,4'-diacetyldiphenyl sulfide were synthesized, the possibility of their use for the synthesis of simple and complex polyesters and polypyrroles, as well as the ability to complex with nickel salts. Organic chemistry used oximes in the 19th century, afterward, as an analytical reagent in the 20th century. Currently, oximes are superior to carbonyl compounds and alcohols in the variety of reactions and the widespread use in synthetic chemistry. Oximes easily turn into other classes of organic compounds – amines, cyano and nitro compounds, carbo

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Sun, Baozhen, Shuang Liu, Mengru Zhang, Jinbo Zhao та Qian Zhang. "Pd-Catalyzed carboannulation of γ,δ-alkenyl oximes: efficient access to 5-membered cyclic nitrones and dihydroazines". Organic Chemistry Frontiers 6, № 3 (2019): 388–92. http://dx.doi.org/10.1039/c8qo01076e.

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Dissertations / Theses on the topic "Oximes (Organic Chemistry)"

1

Markandu, Jasothara. "Oximes as precursors of 1,3-dipoles." Thesis, Queen's University Belfast, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334568.

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Heaney, Mary Frances Teresa. "Cycloaddition reactions of oximes and imines." Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335415.

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3

Warnock, William James. "1,3-dipolar cycloaddition reactions of imines and oximes." Thesis, Queen's University Belfast, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356974.

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Ekcan, Ismail. "Metal complexes of selected 5-alkylamino-1,2-benzoquinone-2-oximes and their applicability in solvent extraction." Thesis, London Metropolitan University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341731.

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5

Altinel, Ertan. "Manganese(iii) Acetate Mediated Regeneration Of Carbonyl Compounds From Oximes." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/12607333/index.pdf.

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A facile method for the direct conversion of oximes into carbonyl compounds by treatment with manganese triacetate is described. Manganese triacetate can be used for an effective and mild oxidizing agent for the regeneration of carbonyl compounds in good yield. Many functional groups are tolerated under reaction conditions.

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Slaughter, Kimari. "Synthesis and Development of Potential CB1 Receptor Neutral Antagonists." ScholarWorks@UNO, 2012. http://scholarworks.uno.edu/td/1483.

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Cannabis and its derivatives have been used for both medicinal and recreational purposes. The study of this plant led to the discovery of over 60 cannabinoids, found exclusively in cannabis, that contribute to the behavioral effects of cannabis use, the most common is delta-9-tetrahydrocannabinol. Cannabinoid receptors function to increase activity in the mesolimbic dopamine reward system. Dopamine is a neurotransmitter that plays a major role in addition and its regulation plays a crucial role in mental and physical well-being. There is evidence that CB1 receptors are important to the reinfor

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Ribeiro, Douglas da Silva. "Estudo conformacional e estereoeletrônico de oximas de cicloexanonas α-heterossubstituídas e de seus éteres metílicos." Universidade de São Paulo, 1999. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-25022015-180231/.

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As populações axial/equatorial em oximas e O-metiI oximas de 2-X-cicloexanonas (X= F, CI, Br, OCH3, SCH3 e N(CH3)2) foram efetivamente determinadas pela análise dos deslocamentos químicos dos prótons 6, utilizando-se os derivados da 4-tércio-butil-cicloexanona como modelos das conformações equatorial e axial. As populações dos confôrmeros axiais também foram determinadas pela análise dos deslocamentos químicos do carbono 4. Este carbono está em uma posição gama gauche em relação ao heteroátomo e sofre assim uma blindagem quando a conformação é axial. Usando-se os deslocamentos químicos observa

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8

Thorpe, Heidi Ruth. "Chemistry of allene oxides." Thesis, Loughborough University, 1997. https://dspace.lboro.ac.uk/2134/13751.

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Chapter One reviews aspects of the chemistry of allene oxides reported in the chemical literature. The review is organised into three sections describing the available methods for the preparation of allene oxides, the reactions of allene oxides and allene oxides in biological systems. Chapter Two discusses attempts to develop new methods for the generation and trapping of allene oxides. Firstly, an unsuccessful attempt to employ a selenoxide elimination to generate an allene oxide is described. This is followed by a section detailing an improved method for the generation and in situ capmre of

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9

Makgae, Mosidi Elizabeth. "Environmental electrochemistry of organic compounds at metal oxide electrodes." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/49947.

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Dissertation (PhD)--Stellenbosch University, 2004.<br>ENGLISH ABSTRACT: This study investigates the electrochemical oxidation of phenol. Phenol is a major toxin and water pollutant. In addition, during water treatment it reacts with chlorine to produce carcinogenic chlorophenols. lts treatment down to trace levels is therefore of increasing concern. For this purpose, dynamically stable anodes for the breakdown of phenols to carbon dioxide or other less harmful substances were developed and characterized. The anodes were prepared from mixed oxides of tin (Sn) and the precious metals ruthe

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10

McCluskey, Adam. "Carbonyl oxides." Thesis, University of Strathclyde, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303277.

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Books on the topic "Oximes (Organic Chemistry)"

1

Petrus Adrianus Johannes Marinus Angevaare. Surface chemistry of oxygen containing organic compounds on oxides. Pasmans Offsetdrukkerij BV, 1991.

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2

Schlenker, Claire. Low-Dimensional Electronic Properties of Molybdenum Bronzes and Oxides. Springer Netherlands, 1990.

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3

Maekawa, Sadamichi. Physics of Transition Metal Oxides. Springer Berlin Heidelberg, 2004.

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

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5

Gusev, Alexandr I. Disorder and Order in Strongly Nonstoichiometric Compounds: Transition Metal Carbides, Nitrides and Oxides. Springer Berlin Heidelberg, 2001.

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6

Carpenter, Michael A. Metal Oxide Nanomaterials for Chemical Sensors. Springer New York, 2013.

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Silvio, Pietra, ed. Heterocyclic N-oxides. CRC Press, 1990.

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8

International Meeting on the Biology of Nitric Oxide (2nd 1991 London, England). The biology of nitric oxide: Proceedings of the 2nd International Meeting on the Biology of Nitric Oxide, London. Edited by Moncada S. portland Press, 1992.

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9

Iye, Y. The Physics and Chemistry of Oxide Superconductors: Proceedings of the Second ISSP International Symposium, Tokyo, Japan, January 16-18, 1991. Springer Berlin Heidelberg, 1992.

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10

Fabrichnaya, Olga B. Thermodynamic Data, Models, and Phase Diagrams in Multicomponent Oxide Systems: An Assessment for Materials and Planetary Scientists Based on Calorimetric, Volumetric and Phase Equilibrium Data. Springer Berlin Heidelberg, 2004.

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Book chapters on the topic "Oximes (Organic Chemistry)"

1

Parhi, Pankaj K., Snehasish Mishra, Ranjan K. Mohapatra, et al. "Arsenic Contamination: Sources, Chemistry and Remediation Strategies." In Metal, Metal-Oxides and Metal-Organic Frameworks for Environmental Remediation. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68976-6_8.

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2

Petit, Marc, and Julien Monot. "Functionalization of Zirconium Oxide Surfaces." In Chemistry of Organo-Hybrids. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118870068.ch5.

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3

Day, Victor W., Walter G. Klemperer, Curtis Schwartz, and Ren-Chain Wang. "Molecular Models of Early Transition Metal Oxides: Polyoxoanions as Organic Functional Groups." In Surface Organometallic Chemistry: Molecular Approaches to Surface Catalysis. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-2971-5_9.

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Schoedel, Alexander, and Sahar Rajeh. "Why design matters: From decorated metal-oxide clusters to functional metal-organic frameworks." In Topics in Current Chemistry Collections. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47340-2_1.

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Nagarajan, S., J. Nimita Jebaranjitham, B. Ganesh Kumar, and Devaraj Manoj. "Emerging Nano-Structured Metal Oxides for Detoxification of Organic Pollutants Towards Environmental Remediation: Overview and Future Aspects." In Environmental Chemistry for a Sustainable World. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-79899-4_7.

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Plata, José J., Veronica Collico, Antonio M. Márquez, and Javier Fdez Sanz. "Analysis of the origin of lateral interactions in the adsorption of small organic molecules on oxide surfaces." In Highlights in Theoretical Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-41272-1_20.

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Hazarika, Kumar Kashyap, Chiranjita Goswami, and Pankaj Bharali. "Removal of Persistent Organic Pollutants Using Redox Active Metal Oxide Nanocatalysts via Advanced Oxidation Process." In Environmental Chemistry for a Sustainable World. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-79899-4_9.

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Adams, D. R., M. Brochwicz-Lewinski, and A. R. Butler. "Nitric Oxide: Physiological Roles, Biosynthesis and Medical Uses." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1999. http://dx.doi.org/10.1007/978-3-7091-6351-1_1.

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Schoedel, Alexander, and Omar M. Yaghi. "Reticular Chemistry of Metal-Organic Frameworks Composed of Copper and Zinc Metal Oxide Secondary Building Units as Nodes." In The Chemistry of Metal-Organic Frameworks: Synthesis, Characterization, and Applications. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527693078.ch3.

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DeRosa, Thomas F. "Oximes." In Advances in Synthetic Organic Chemistry and Methods Reported in US Patents. Elsevier, 2006. http://dx.doi.org/10.1016/b978-008044474-1/50067-0.

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Conference papers on the topic "Oximes (Organic Chemistry)"

1

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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Naimi-Jamal, M., H. Hamzehali, and J. Mokhtari. "Quantitative Regeneration of Carbonyl Compounds from Oximes and hydrazones by Gaseous Nitrogen Dioxide." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01300.

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Gharib, Ali, Manouchehr Jahangir, and Mina Roshani. "Effective Catalytic Conversion of Carbonyl groups to Oximes using H14[NaP5W30O110]/SiO2 in Green conditions." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01215.

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Thiemann, Thies, Mariam Al Azani, and John Graham. "Preparation and Photochemistry of 3-O-Methylestra-1,3,5(10)-Triene-17beta-yl Cinnamates and 3-O-Methylestra-1,3,5(10)-Trien-17-one O-Cinnamoyl-17-Oximes." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a039.

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Tyumkina, Tatyana V., Denis N. Islamov, Alevtina L. Makhamatkhanova, and Marina I. Mallyabaeva. "Cyclic 1H-Phospolane Oxides as a Potential Candidate for Cancer Therapy." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13713.

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Bulavka, Vladimir, Alexandr Gekhman, and Konstantin Koshelev. "Triarylamine-N-oxides. I. The First Attempt of (4,4´,4´´- Trimethyl)triphenylamine-n-oxide Synthesis and direct Proof of its Formation." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01864.

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Sander, W., K. Schroeder, K. Block, and W. Kappert. "Stable Carbonyl O-oxides and Dioxiranes." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01868.

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Thiemann, Thies, Kazuya Arima, Daisuke Ohira, Kazuja Kumazoe, and Shuntaro Mataka. "Preparation and Photochemistry of Thiophene-S-oxides." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01871.

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Brandi, Alberto, Stefano Cicchi, Franca Cordero, and Andrea Goti. "Imino-sugars by Stereoselective Processes Employing Pyrroline N-oxides." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01843.

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Rossi-Fernández, Lucía, Rodrigo Gette, Gabriel Radivoy, and Viviana Dorn. "DFT Studies on the Allylation of Styrene Oxide Catalyzed by Indium Nanoparticles (InNPs)." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13545.

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