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

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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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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3

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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5

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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10

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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11

Baláž, Matej, Zuzana Kudličková, Mária Vilková, Ján Imrich, Ľudmila Balážová, and Nina Daneu. "Mechanochemical Synthesis and Isomerization of N-Substituted Indole-3-carboxaldehyde Oximes †." Molecules 24, no. 18 (2019): 3347. http://dx.doi.org/10.3390/molecules24183347.

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Performing solution-phase oximation reactions with hydroxylamine hydrochloride (NH2OH·HCl) carries significant risk, especially in aqueous solutions. In the present study, four N-substituted indole-3-carboxaldehyde oximes were prepared from the corresponding aldehydes by solvent-free reaction with NH2OH·HCl and a base (NaOH or Na2CO3) using a mechanochemical approach, thus minimizing the possible risk. In all cases, the conversion to oximes was almost complete. The focus of this work is on 1-methoxyindole-3-carboxaldehyde oxime, a key intermediate in the production of indole phytoalexins with

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12

Ãbele, Edgars, and Edmunds Lukevics. "RECENT ADVANCES IN THE CHEMISTRY OF OXIMES." Organic Preparations and Procedures International 32, no. 3 (2000): 235–64. http://dx.doi.org/10.1080/00304940009355921.

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13

Yashunsky, D. V., Yu V. Morozova, and G. V. Ponomarev. "Chemistry ofmeso-formylporphyrin oximes. Isomerization to isophlorins." Chemistry of Heterocyclic Compounds 36, no. 4 (2000): 489–90. http://dx.doi.org/10.1007/bf02269556.

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14

Bhattacharyya, Aditya, Subhomoy Das, Navya Chauhan, Pronay K. Biswas, and Manas K. Ghorai. "Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed SN2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes." Synlett 31, no. 07 (2020): 708–12. http://dx.doi.org/10.1055/s-0039-1691596.

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A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed SN2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.

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15

Adarve-Cardona, Laura, David Ezenarro-Salcedo, Mario A. Macías, and Diego Gamba-Sánchez. "One-Pot Synthesis of Dioxime Oxalates." Molbank 2022, no. 4 (2022): M1473. http://dx.doi.org/10.3390/m1473.

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Dioxime oxalates, a type of carbonyl oximes, are well-known as clean sources of iminyl radicals that undergo key organic chemistry transformations. A series of dioxime oxalates is reported in this manuscript, obtained by the reaction of the corresponding oximes with oxalyl chloride and Et3N at room temperature. This one-pot method afforded three novel dioxime oxalates and the crystal structure of cyclopentanone dioxime oxalate analysis is also presented.

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16

Kayouka, Maya, Pascal Houzé, Marc Lejay, Frédéric J. Baud, and Kamil Kuca. "Safety and Efficacy of New Oximes to Reverse Low Dose Diethyl-Paraoxon-Induced Ventilatory Effects in Rats." Molecules 25, no. 13 (2020): 3056. http://dx.doi.org/10.3390/molecules25133056.

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Background: Oximes are used in addition to atropine to treat organophosphate poisoning. However, the efficiency of oximes is still a matter of debate. In vitro experiments suggested than new oximes are more potent than the commercial oximes. However, the antidotal activity of new oximes has not been assessed in vivo. Methods: The aim of this work was to assess the safety and efficiency of new oximes compared to pralidoxime in a rat model of diethyl paraoxon-induced non-lethal respiratory toxicity. Results: Safety study of oximes showed no adverse effects on ventilation in rats. KO-33, KO-48, K

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17

Sahyoun, Tanya, Axelle Arrault, and Raphaël Schneider. "Amidoximes and Oximes: Synthesis, Structure, and Their Key Role as NO Donors." Molecules 24, no. 13 (2019): 2470. http://dx.doi.org/10.3390/molecules24132470.

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Nitric oxide (NO) is naturally synthesized in the human body and presents many beneficial biological effects; in particular on the cardiovascular system. Recently; many researchers tried to develop external sources to increase the NO level in the body; for example by using amidoximes and oximes which can be oxidized in vivo and release NO. In this review; the classical methods and most recent advances for the synthesis of both amidoximes and oximes are presented first. The isomers of amidoximes and oximes and their stabilities will also be described; (Z)-amidoximes and (Z)-oximes being usually

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18

El Kaïm, Laurent, Mansour Dolé Kerim, Pakoupati Boyode, and Julian Garrec. "Metal-Free Addition of Boronic Acids to Silylnitronates." Synlett 31, no. 09 (2020): 856–60. http://dx.doi.org/10.1055/s-0039-1690845.

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We report for the first time a metal-free addition of boronic acids to silylnitronates to afford oxime derivatives through aryl transfer on the carbon nitrogen double bond. A reaction mechanism has been proposed in relation with a DFT study on the key aryl transfer. This arylation process is effective for cycloalkenyl nitro derivatives leading to oximes that may be oxidatively converted into 3-arylisoxazole derivatives.

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19

Ferwanah, Abdel-Rahman, and Adel Awadallah. "Reaction of Nitrilimines and Nitrile Oxides with Hydrazines, Hydrazones and Oximes." Molecules 10, no. 2 (2005): 492–507. http://dx.doi.org/10.3390/10020492.

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20

Gomes, Ana R., Ana S. Pires, Fernanda M. F. Roleira, and Elisiário J. Tavares-da-Silva. "The Structural Diversity and Biological Activity of Steroid Oximes." Molecules 28, no. 4 (2023): 1690. http://dx.doi.org/10.3390/molecules28041690.

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Steroids and their derivatives have been the subject of extensive research among investigators due to their wide range of pharmacological properties, in which steroidal oximes are included. Oximes are a chemical group with the general formula R1R2C=N−OH and they exist as colorless crystals and are poorly soluble in water. Oximes can be easily obtained through the condensation of aldehydes or ketones with various amine derivatives, making them a very interesting chemical group in medicinal chemistry for the design of drugs as potential treatments for several diseases. In this review, we will fo

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21

Adams, Joseph P. "Imines, enamines and oximes." Contemporary Organic Synthesis 4, no. 6 (1997): 517. http://dx.doi.org/10.1039/co9970400517.

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22

Sumino, Shuhei, Takahide Fukuyama, Mika Sasano, et al. "Vicinal difunctionalization of alkenes by four-component radical cascade reaction of xanthogenates, alkenes, CO, and sulfonyl oxime ethers." Beilstein Journal of Organic Chemistry 15 (July 31, 2019): 1822–28. http://dx.doi.org/10.3762/bjoc.15.176.

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Four-component coupling reactions between xanthogenates, alkenes, CO, and sulfonyl oxime ethers were studied. In the presence of hexabutylditin, working as a propagating radical reagent, the chain reaction proceeds, as expected, taking into account reagents polarities, affording the corresponding functionalized α-keto oximes. Although yields are modest, this rare one-pot four-component process is easy to carry out and the resulting compounds, bearing multiple functionalities, have the potential for further elaboration.

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23

Ntsimango, Songeziwe, Kennedy J. Ngwira, Moira L. Bode, and Charles B. de Koning. "Synthesis of phenanthridines via a novel photochemically-mediated cyclization and application to the synthesis of triphaeridine." Beilstein Journal of Organic Chemistry 17 (September 8, 2021): 2340–47. http://dx.doi.org/10.3762/bjoc.17.152.

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Readily synthesized biphenyl-2-carbaldehyde O-acetyl oximes were exposed to UV radiation affording phenanthridines. The scope and limitations of this novel reaction were explored. For example, exposure of 2',3'-dimethoxy-[1,1'-biphenyl]-2-carbaldehyde O-acetyl oxime to UV radiation afforded 4-methoxyphenanthridine in 54% yield. This methodology was applied to the synthesis of trisphaeridine to afford the product in four linear steps in an overall yield of 6.5% from 1-bromo-2,4,5-trimethoxybenzene.

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24

Polanc, Slovenko, Biserka Mlakar, Bogdan Stefane, and Marijan Kocevar. "An Approach to Pyrimidine N-Oxides: Carboxamide Oximes as Precursors." HETEROCYCLES 48, no. 5 (1998): 961. http://dx.doi.org/10.3987/com-98-8132.

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25

Jen, Tim, Brian A. Mendelsohn та Marco A. Ciufolini. "Oxidation of α-Oxo-Oximes to Nitrile Oxides with Hypervalent Iodine Reagents". Journal of Organic Chemistry 76, № 2 (2011): 728–31. http://dx.doi.org/10.1021/jo102241s.

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26

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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27

Sun, Jingjing, Yanyan He, Xiao-De An, Xu Zhang, Lei Yu, and Shouyun Yu. "Visible-light-induced iminyl radical formation via electron-donor–acceptor complexes: a photocatalyst-free approach to phenanthridines and quinolines." Organic Chemistry Frontiers 5, no. 6 (2018): 977–81. http://dx.doi.org/10.1039/c7qo00992e.

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A visible light-induced synthesis of nitrogen-containing arenes from O-2,4-dinitrophenyl oximes has been reported. This photochemical strategy is photocatalyst-free and enabled by electron-donor–acceptor (EDA) complexes of O-2,4-dinitrophenyl oximes and Et3N.

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28

Yashunsky, D. V., Yu V. Morozova, and G. V. Ponomarev. "Chemistry ofmeso-formly-porphyrin oximes. An elegant synthesis ofmeso-cyanoporphyrins." Chemistry of Heterocyclic Compounds 36, no. 4 (2000): 485–86. http://dx.doi.org/10.1007/bf02269554.

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29

Mehrez, Asma, Dalila Mtat, and Ridha Touati. "Microwave-Assisted Synthesis of Chiral Oxime Ethers." Letters in Organic Chemistry 16, no. 6 (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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30

Hajipour, A. R., I. Mohammadpoor-baltork, K. Nikbaghat, and G. Imanzadeh. "Solid-Phase Synthesis of Oximes." Synthetic Communications 29, no. 10 (1999): 1697–701. http://dx.doi.org/10.1080/00397919908086156.

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31

Toda, Fumio, and Hiroshi Akai. "Isolation of optically active oximes." Journal of Organic Chemistry 55, no. 16 (1990): 4973–74. http://dx.doi.org/10.1021/jo00303a047.

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32

Kerdesky, Francis A. J., and Bruce W. Horrom. "Reduction of Aryl Trifluoromethyl Oximes." Synthetic Communications 21, no. 21 (1991): 2203–5. http://dx.doi.org/10.1080/00397919108055454.

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33

Izumi, Taeko, and Kouji Suenaga. "Enzymatic resolution of flavanone oximes." Journal of Heterocyclic Chemistry 34, no. 5 (1997): 1535–38. http://dx.doi.org/10.1002/jhet.5570340524.

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34

Narasaka, Koichi, and Mitsuru Kitamura. "Amination with Oximes." European Journal of Organic Chemistry 2005, no. 21 (2005): 4505–19. http://dx.doi.org/10.1002/ejoc.200500389.

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35

Wang, Guangwei, Lianxin Wang, Hongtai Chen та Wentao Zhao. "Copper-Catalyzed Oxydifluoroalkylation of β,γ-Unsaturated Oximes for the Construction of Isoxazolines with a Difluoroalkyl Side Chain". Synlett 32, № 10 (2021): 1029–33. http://dx.doi.org/10.1055/a-1495-7966.

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AbstractA copper-catalyzed oxydifluoroalkylation of β,γ-unsaturated oximes has been developed. This reaction proceeded through a cascade of difluoroalkylation of alkene followed by a nucleophilic attack of the hydroxyl group of oximes. This protocol features mild reaction conditions, low-cost catalyst, and broad substrate scope, which provides a facile method to synthesize isoxazolines with a fluorinated side chain

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36

Takemoto, Yoshiji, Hideto Miyabe, Akira Matsumura, Kazumasa Yoshida, and Masashige Yamauchi. "Novel Synthesis of O-Allylated Oxime Ethers Based on Allylic Substitution with Oximes." Synlett, no. 12 (2004): 2123–26. http://dx.doi.org/10.1055/s-2004-831327.

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37

Singh, Surinderjit, M. PS Ishar, Gajendra Singh, and Rajinder Singh. "Efficient, microwave-assisted intramolecular 1,3-dipolar cycloadditions of oximes and N-methylnitrones derived from o-alkenylmethoxy-acetophenones." Canadian Journal of Chemistry 83, no. 3 (2005): 260–65. http://dx.doi.org/10.1139/v05-049.

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Contrary to literature reports, the o-allyloxy- and crotyloxy-acetophenone-oximes (2a, 2b) are transformed to nitrones, which undergo regio- and stereoselective intramolecular 1,3-dipolar cycloadditions, both on microwave heating under solvent free conditions and refluxing in toluene, to afford novel cycloadducts (5a, 5b); the oxazepine-N-oxide (3a) reported to be formed in 98% yield was obtained only as a minor product (~10%). However, o-cinnamyloxy-acetophenone-oxime (2c) under similar conditions undergoes intramolecular N-alkylation to afford nitrone (3c). The reactions carried out under mi

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38

Mosher, Michael D., and Scott Meisenbach. "Syn and Anti Isomer Preference in Oximes: An Undergraduate Organic Chemistry Experiment." Chemical Educator 7, no. 6 (2002): 356–58. http://dx.doi.org/10.1007/s00897020623a.

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39

Krylov, Igor B., Stanislav A. Paveliev, Alexander S. Budnikov, and Alexander O. Terent’ev. "Oxime radicals: generation, properties and application in organic synthesis." Beilstein Journal of Organic Chemistry 16 (June 5, 2020): 1234–76. http://dx.doi.org/10.3762/bjoc.16.107.

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N-Oxyl radicals (compounds with an N–O• fragment) represent one of the richest families of stable and persistent organic radicals with applications ranging from catalysis of selective oxidation processes and mechanistic studies to production of polymers, energy storage, magnetic materials design and spectroscopic studies of biological objects. Compared to other N-oxyl radicals, oxime radicals (or iminoxyl radicals) have been underestimated for a long time as useful intermediates for organic synthesis, despite the fact that their precursors, oximes, are extremely widespread and easily available

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40

Nakamura, Itaru, Keigo Shiga, Mao Suzuki, and Masahiro Terada. "Efficient Synthesis of O-tert-Propargylic Oximes via Nicholas Reaction." Synthesis 52, no. 22 (2020): 3461–65. http://dx.doi.org/10.1055/s-0040-1707191.

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A synthetic protocol to access O-tert-propargylic oximes derived from tertiary propargylic alcohols was established via Nicholas reaction. Thus, BF3·OEt2-mediated reaction between the dicobalt hexacarbonyl complex of tert-propargylic alcohols and p-nitrobenzaldoxime followed by decomplexation with cerium(IV) ammonium nitrate afforded the corresponding O-tert-propargylic oximes in good to high yields. The obtained O-tert-propargylic oximes were effectively converted into heterocycles, such as four-membered cyclic nitrones, oxazepines, and isoxazolines, by using π-Lewis acidic catalysts.

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41

Boyle, Peter H., Haslin Dato Paduka Ali, and Thomas J. Mc Donald. "Sigmatropic rearrangements of 2,4-dinitrophenyl oximes." Arkivoc 2003, no. 7 (2003): 67–79. http://dx.doi.org/10.3998/ark.5550190.0004.708.

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42

Ding, Yixuan, and Yonggui Zhou. "Nickel-Catalyzed Asymmetric Hydrogenation of Oximes." Chinese Journal of Organic Chemistry 42, no. 9 (2022): 2994. http://dx.doi.org/10.6023/cjoc202200045.

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43

Geneste, Florence, Nadia Racelma, and Alec Moradpour. "Mo(Co)6Induced Cleavage of Oximes." Synthetic Communications 27, no. 6 (1997): 957–60. http://dx.doi.org/10.1080/00397919708003039.

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44

Schnur, Dora M., and David R. Dalton. "MM2 force field parameters for oximes." Journal of Organic Chemistry 53, no. 14 (1988): 3313–16. http://dx.doi.org/10.1021/jo00249a033.

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45

Mantrov, S. N., Yu M. Lapina, and E. A. Shukhtina. "New Synthesis of 2-Oxoalkanamide Oximes." Russian Journal of Organic Chemistry 55, no. 4 (2019): 540–45. http://dx.doi.org/10.1134/s1070428019040201.

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46

Terent'ev, P. B., L. I. Mazhilis, A. G. Kalandarishvili, and A. P. Stankyavichus. "Mass-spectrometric behavior of isatin oximes." Chemistry of Heterocyclic Compounds 22, no. 8 (1986): 848–51. http://dx.doi.org/10.1007/bf01175057.

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47

Tordeux, Marc, Khalid Boumizane, and Claude Wakselman. "Preparation of gem-dichloroalkanes from oximes." Journal of Organic Chemistry 58, no. 7 (1993): 1939–40. http://dx.doi.org/10.1021/jo00059a057.

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48

Lowe, James D., and Kenneth Turnbull. "Synthesis and reactions of sydnone oximes." Journal of Heterocyclic Chemistry 23, no. 1 (1986): 125–28. http://dx.doi.org/10.1002/jhet.5570230125.

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49

Meadows, Mikala, Lei Yang, Cody Turner, Mikhail Berezin, Sergiy Tyukhtenko, and Nikolay Gerasimchuk. "Synthesis and Characterization of Pt(II) and Pd(II) Complexes with Planar Aromatic Oximes." Inorganics 11, no. 3 (2023): 116. http://dx.doi.org/10.3390/inorganics11030116.

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Abstract:

A series of four Werner-type complexes of Pd(II) and Pt(II) with planar, isomeric conjugated aromatic naphtoquinone oximes were synthesized for the first time. These ligands were 1-oxime-2-naphtoquinone (HL1) and 2-oxime-1-napthoquinone (HL2). Compounds were characterized using thermal analysis, spectroscopic methods, and X-ray analysis. TG/DSC data were collected for pure starting organic ligands, their complexes, and indicated vigorous exothermic decomposition with at ~155 °C for starting HL and ~350 °C for transition metal complexes. Crystal structures for two Pt compounds with 2-oxime-1-qu

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50

Thakur, Ashima, Pooja Patil, Abha Sharma, and S. J. S. Flora. "Advances in the Development of Reactivators for the Treatment of Organophosphorus Inhibited Cholinesterase." Current Organic Chemistry 24, no. 24 (2020): 2845–64. http://dx.doi.org/10.2174/1385272824999201020203544.

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Abstract:: Organophosphorus Compounds (OPCs) are used as pesticides to control pest, as chemical weapons in military conflict and unfortunately in the terrorist attack. These compounds are irreversible inhibitors of acetylcholinesterase, resulting in the accumulation of acetylcholine that leads to severe health complications which may be ended with the death of the victim. Current antidotes used for reactivation of organophosphorus inhibited acetylcholinesterase (OP-AChE) are not able to cross the blood-brain barrier efficiently, therefore being incapable to reactivate OP-AChE of the central n

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