Log in

Relevant bibliographies by topics / Acetophenone oxime / Journal articles

To see the other types of publications on this topic, follow the link: Acetophenone oxime.

Journal articles on the topic 'Acetophenone oxime'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Acetophenone oxime.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

Ali Bawa, Ramadan, and Hana Mansoure Elmajdoub. "Synthesis of Some Bridged Unsymmetrical Terphthaloyl Oxime Esters." Academic Journal of Chemistry, no. 56 (June 10, 2020): 55–57. http://dx.doi.org/10.32861/ajc.56.55.57.

Full text

Abstract:

Three unsymmetrical bridged terphthaloyl acetophenone oxime esters have been synthesized throughout an esterification process between three acetophenone oximes and the terphthaloyl chloride under mild basic conditions. Spectroscopic techniques, such as IR, HNMR and mass spectrometer, were used to confirm the structures of the desired oxime esters. The yields of the resulting oxime esters ranged from 50% to 73%.

APA, Harvard, Vancouver, ISO, and other styles

3

Ali Bawa, Ramadan, and Hana Mansoure Elmajdoub. "Synthesis of a Number of Unsymmetrical Bridged Terphthaloyl Acetophenone Oxime Esters." Academic Journal of Chemistry, no. 57 (August 8, 2020): 98–100. http://dx.doi.org/10.32861/ajc.57.98.100.

Full text

Abstract:

A number of unsymmetrical bridged terphthaloyl acetophenone oxime esters has been synthesized throughout an esterification reaction between four different acetophenone oximes and the terphthaloyl chloride in a molar ratio of (2:1) under mild basic conditions. Spectroscopic techniques, such as IR, HNMR and mass spectrometer, were used to confirm the structures of the targeted oxime esters. The yields of the obtained oxime esters ranged from 80% to 95%.

APA, Harvard, Vancouver, ISO, and other styles

4

Ali Bawa, Ramadan, and Mona Mohammed Friwan. "Synthesis of Some Acetophenone Oximes and Their Corresponding Bridged Terphthaloyl Oxime Esters." Academic Journal of Life Sciences, no. 511 (November 2, 2019): 87–92. http://dx.doi.org/10.32861/ajls.511.87.92.

Full text

Abstract:

The objective of this study is to synthesize a number of oximes along with their terphthaloyl oxime esters derived from acetophenone, 4-methylacetophenone, 4-hydroxyacetophenone, 4-aminoacetophenone and 4-nitroacetophenone as a part of ongoing research. Five acetophenone oximes have been synthesized by refluxing the acetophenone derivative with a solution of hydroxylamine hydrochloride in the presence of potassium hydroxide. The corresponding acetophenone oximes were obtained as solid materials in moderate to good yields. The structures of the resulting oximes were confirmed using IR, NMR and

APA, Harvard, Vancouver, ISO, and other styles

5

Song, J. H., S. M. Bae, E. J. Lee, J. H. Cho, and D. I. Jung. "Formation of Benzodiazepines and Pyrazinylquinoxalines from Aromatic and Heteroaromatic Ketones via Deoximation." Asian Journal of Chemistry 32, no. 7 (2020): 1676–80. http://dx.doi.org/10.14233/ajchem.2020.22639.

Full text

Abstract:

The report stated that the treatment of o-phenylenediamine with acetone dicarboxylic acid, acetone and acetophenone afforded 2,4,4-trimethyl-3H-5-hydro-1,5-benzodiazepine. However, direct reactions of o-phenylenediamine with oximes (acetone oxime, acetophenone oxime, and benzophenone oxime) as ketone equivalents did not occur. In the course of present investigations, it is found that dichloroamine-T can be an efficient reagent for the conversion of oximes into the corresponding carbonyl compounds. As a part of a research program related to the synthetic study of pharmacologically interesting b

APA, Harvard, Vancouver, ISO, and other styles

6

Beirakhov, A. G., I. M. Orlova, E. G. Il’in, Yu E. Gorbunova, and Yu N. Mikhailov. "Uranyl complexes with acetophenone oxime." Russian Journal of Inorganic Chemistry 52, no. 1 (2007): 34–41. http://dx.doi.org/10.1134/s003602360701007x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Ali Bawa, Ramadan, and Mona Mohammed Friwan. "Synthesis and Antifungal Study of Some Acetophenone Oximes and Their Terphthaloyl Oxime Esters." Academic Journal of Chemistry, no. 410 (October 25, 2018): 96–101. http://dx.doi.org/10.32861/ajc.510.96.101.

Full text

Abstract:

Acetophenone oximes 1 – 5 along with their terphthaloyl oxime esters 6 – 10 have been synthesized in moderate to good yields. Only one oxime was formed in as E/Z two isomers in a ratio of (8:1). These resulting oxime derivatives were involved in an antifungal screening against the Aspergillus niger at concentration of 30 ppm. Two commercially available antifungal agents, clorotimazole and daktarin, were employed as references at the same concentration, 30 ppm. The antifungal results for the oxime derivatives 1 – 10 showed inhibitory levels ranging from 38% to 100%, whereas the antifungal poten

APA, Harvard, Vancouver, ISO, and other styles

8

Pham, Phuc H., Khang X. Nguyen, Hoai T. B. Pham, Thien T. Tran, Tung T. Nguyen, and Nam T. S. Phan. "Functionalization of C–H bonds in acetophenone oximes with arylacetic acids and elemental sulfur." RSC Advances 10, no. 19 (2020): 11024–32. http://dx.doi.org/10.1039/d0ra00808g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

10

Perekalin, Dmitry S., Evgeniya A. Trifonova, Alina A. Komarova, and Denis Chusov. "Variability of Rhodium(III)-Catalyzed Reactions of Aromatic Oximes with Alkenes." Synlett 31, no. 11 (2020): 1117–20. http://dx.doi.org/10.1055/s-0040-1707961.

Full text

Abstract:

Acetophenone oxime reacts with various alkenes in the presence of the rhodium catalyst [Cp*RhCl2]2 (2.5 mol%; Cp* = pentamethylcyclopentadienyl) and 1,1,1,3,3,3-hexafluoropropan-2-ol as an important cosolvent. Styrene, aliphatic terminal alkenes, and strained cyclic alkenes gave the corresponding substituted dihydroisoquinolines in yields of 50–99%. On the other hand, alkenes containing functional groups close to the double bond gave a variety of different products. The reactions of acetophenone oxime with styrene or dec-1-ene in the presence of the chiral catalyst [(C5H2 t Bu2CH2 t Bu)RhI2]2

APA, Harvard, Vancouver, ISO, and other styles

11

Luo, Beibei, and Zhiqiang Weng. "Elemental tellurium mediated synthesis of 2-(trifluoromethyl)oxazoles using trifluoroacetic anhydride as reagent." Chemical Communications 54, no. 76 (2018): 10750–53. http://dx.doi.org/10.1039/c8cc05670f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Zhang, Yong, Hong-Jun Zang, Bo-Wen Cheng, and Jun Song. "Bis(acetophenone oxime)O,O′-methylene ether." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (2008): o2452. http://dx.doi.org/10.1107/s160053680803897x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Palacios, Javier, Adrián Paredes, Marcelo A. Catalán, Chukwuemeka R. Nwokocha, and Fredi Cifuentes. "Novel Oxime Synthesized from a Natural Product of Senecio nutans SCh. Bip. (Asteraceae) Enhances Vascular Relaxation in Rats by an Endothelium-Independent Mechanism." Molecules 27, no. 10 (2022): 3333. http://dx.doi.org/10.3390/molecules27103333.

Full text

Abstract:

Senecio nutans Sch. Bip. and its constituents are reported to have antihypertensive effects. We isolated metabolite–1, a natural compound from S. nutans (4-hydroxy-3-(isopenten-2-yl)-acetophenone), and synthesized novel oxime – 1 (4-hydroxy-3-(isopenten-2-yl)-acetophenoxime) to evaluate their effect on vascular reactivity. Compounds were purified (metabolite–1) or synthetized (oxime–1) and characterized using IR and NMR spectroscopy and Heteronuclear Multiple Quantum Coherence (HMQC). Using pharmacological agents such as phenylephrine (PE) and KCl (enhancing contraction), acetylcholine (ACh),

APA, Harvard, Vancouver, ISO, and other styles

14

Kosmalski, Tomasz, Anna Hetmann, Renata Studzińska, Szymon Baumgart, Daria Kupczyk, and Katarzyna Roszek. "The Oxime Ethers with Heterocyclic, Alicyclic and Aromatic Moiety as Potential Anti-Cancer Agents." Molecules 27, no. 4 (2022): 1374. http://dx.doi.org/10.3390/molecules27041374.

Full text

Abstract:

Chemotherapy is one of the most commonly used methods of cancer disease treatment. Due to the acquisition of drug resistance and the possibility of cancer recurrence, there is an urgent need to search for new molecules that would be more effective in destroying cancer cells. In this study, 1-(benzofuran-2-yl)ethan-1-one oxime and 26 oxime ethers containing heterocyclic, alicyclic or aromatic moiety were screened for their cytotoxicity against HeLa cancer cell line. The most promising derivatives with potential antitumor activity were 2-(cyclohexylideneaminoxy)acetic acid (18) and (E)-acetophen

APA, Harvard, Vancouver, ISO, and other styles

15

K., Lakshmi Devi, and Chandraiah Chowdary M. "Oxidation kinetics of acetophenone oximes with vanadium(V)." Journal of Indian Chemical Society Vol. 76, Apr 1999 (1999): 195–97. https://doi.org/10.5281/zenodo.5848195.

Full text

Abstract:

Department of Biochemistry, Department of Chemistry, Sri Krishnadevaraya University, Anantapur-515 003, India <em>Manuscript received 18 February 1998, revised 10 November 1998, accepted 23 December 1998</em> Oxidation kinetics of acetophenone oxime (<strong>APO</strong>) and <em>p</em>-hydroxyacetophenone oxime (<strong>HAPO</strong>) by vanadium(<strong>V</strong>) in aqueous acetic acid medium is reported. The reactions are totally second order, first order with respect to each reactant under second order conditions and negative order with respect to substrate under pseudo-first order condi

APA, Harvard, Vancouver, ISO, and other styles

16

Möhrle, Hans, and Michael Gehlen. "Reaktionsbeteiligung Von Oximfunktionen Bei Der Dehydrierung Von 2-Phenylpiperidin-Derivaten." Zeitschrift für Naturforschung B 62, no. 6 (2007): 841–53. http://dx.doi.org/10.1515/znb-2007-0614.

Full text

Abstract:

Mercury(II)-induced dehydrogenation of α-(2-phenylpiperidin-1-yl)-acetophenone oximes 7 gives rise to two different iminium compounds which subsequently react with the neighbouring oxime group. With the mercury(II)-EDTA reagent, (E)-7 forms the cyclic nitrones 9 and 11a, b, whereas (Z)-7 is transformed into oxadiazines 12 and 13a, b. The pairs of diastereomers 11a, b and 13a, b result from the equilibrium involving an iminium oximate species. The introduction of electron donor or acceptor groups into the phenyl substituent in (E)-15 and (E)-16 does not influence significantly the direction of

APA, Harvard, Vancouver, ISO, and other styles

17

Jílek, Jiří, Karel Šindelář, Jaroslava Grimová, et al. "Potential antidepressant and anti-inflammatory agents: 4-(2-Propylthio)acetophenone oximes and 4-(2-propylthio)phenylalkanoic acids." Collection of Czechoslovak Chemical Communications 55, no. 5 (1990): 1266–77. http://dx.doi.org/10.1135/cccc19901266.

Full text

Abstract:

4-(2-Propylthio)acetophenone oxime (IV) was reacted with 2-aminoethyl chloride and 3-dimethylaminopropyl chloride to give the O-(aminoalkyl)oximes V and VI which are analogues of the antidepressant agent fluvoxamine (I). Kindler-Willgerodt reaction of 4-(2-propylthio)acetophenone (III) gave the thiomorpholide VII which was hydrolyzed to the acid IX. Friedel-Crafts reaction of (2-propylthio)benzene with ethoxalyl chloride afforded ethyl 4-(2-propylthio)benzoylformate (X) which was transformed by reaction with methylmagnesium iodide, by the following hydrolysis and reduction with hydroiodic acid

APA, Harvard, Vancouver, ISO, and other styles

18

Banks, R. E., W. J. Jondi, R. G. Pritchard, and A. E. Tipping. "(E)-Acetophenone O-(3,4,5,6-Tetrafluoro-2-pyridyl)oxime, Formed by 2-Substitution of Pentafluoropyridine by (E)-Acetophenone Oximate." Acta Crystallographica Section C Crystal Structure Communications 51, no. 2 (1995): 293–95. http://dx.doi.org/10.1107/s0108270194009133.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Lalevée, J., X. Allonas, and J. P. Fouassier. "Computational study of ground and triplet states of acetophenone oxime derivatives." Journal of Molecular Structure: THEOCHEM 588, no. 1-3 (2002): 233–38. http://dx.doi.org/10.1016/s0166-1280(02)00139-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Ito, Ken-ichi, Yoshitaka Shigeru, Yu-uichi Kawata, Katsuhiko Ito, and Masahiro Tsunooka. "Photo-initiated and thermal curing of epoxides by the use of photo-base generators bearing acyloxyimino groups." Canadian Journal of Chemistry 73, no. 11 (1995): 1924–32. http://dx.doi.org/10.1139/v95-237.

Full text

Abstract:

The formation of amines by the photolysis of O-acyloximes derived from acetophenone oxime, benzophenone oxime, fluorenone oxime, and 2-acetonaphthone oxime and the curing of epoxides by the resulting amines were investigated. The quantum yields of their photolysis at 366 nm in polystyrene films depend on their structures, and those for bifunctional ones bearing phenyl or naphthyl moieties were found to be very high, at 0.88 and 0.76, respectively. The yields of the resulting amines in polymer matrices were higher than those in solution. The yields for O-acyloximes bearing a naphthyl moiety wer

APA, Harvard, Vancouver, ISO, and other styles

21

Cistrone, Philip A., Anouk Dirksen, Sampat Ingale, and Philip E. Dawson. "Scandium(III) Triflate as a Lewis Acid Catalyst of Oxime Ligation." Australian Journal of Chemistry 73, no. 4 (2020): 377. http://dx.doi.org/10.1071/ch20042.

Full text

Abstract:

Imine-forming reactions are widely applicable in bioconjugation owing to their high chemoselectivity. The ligation of a ketone or aldehyde with an aminooxy functional group to form a physiologically stable oxime bond is often used to link complex and precious biomolecules. Although the reaction proceeds modestly in acidic solution, the abundance of protonated carbonyl species at pH 7 limits its utility in many biological applications. The use of nucleophilic aryl amines, such as aniline or a phenylenediamine, allows a high population of protonated Schiff base to undergo transimination to the o

APA, Harvard, Vancouver, ISO, and other styles

22

Wasylishen, Roderick E., Glenn H. Penner, William P. Power, and Ronald D. Curtis. "Dipolar NMR spectra of the oxime moiety in (E)-acetophenone oxime. Carbon and nitrogen chemical shielding anisotropies." Journal of the American Chemical Society 111, no. 16 (1989): 6082–86. http://dx.doi.org/10.1021/ja00198a016.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Chipps, Elizabeth S., Renuka Jayini, Shoko Ando, et al. "Cytotoxicity Analysis of Active Components in Bitter Melon (Momordica charantia) Seed Extracts Using Human Embryonic Kidney and Colon Tumor Cells." Natural Product Communications 7, no. 9 (2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700926.

Full text

Abstract:

Bitter melon (Momordica charantia) seed extracts (BMSE) have been used as traditional medicine for treating various ailments, although in many cases, the active component(s) are unidentified. In this study, bitter melon seeds were extracted in water, ethanol, or ethanol: water (1:1). The aqueous seed extracts (BMSE-W) exhibited marked cytotoxicity towards human embryonic kidney 293T (HEK293T) and human colon tumor 116 (HCT116) cells. The activity in BMSE-W was unaffected by heat and proteinases treatments, and eluted in the total volume of size-exclusion HPLC, suggesting the small, organic nat

APA, Harvard, Vancouver, ISO, and other styles

24

Itsuno, Shinichi, Kazuo Tanaka, and Koichi Ito. "Asymmetric Reduction of Chiral Acetophenone Oxime Ethers to Optically Active Primary Amines." Chemistry Letters 15, no. 7 (1986): 1133–36. http://dx.doi.org/10.1246/cl.1986.1133.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Xu, Xiangjian, Xinhong Cai, Bin Wang, et al. "Synthesis and Herbicidal Activities of Novel Substituted Acetophenone Oxime Esters of Pyrithiobac." ChemistrySelect 5, no. 1 (2020): 69–74. http://dx.doi.org/10.1002/slct.201903927.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

L., V. S. PRASADA RAO, and BRAHMAJl RAO S. "Kinetics of Oxidation of Acetophenone Oximes by Chromium(VI)." Journal of Indian Chemical Society Vol. 65, Jun 1988 (1988): 404–6. https://doi.org/10.5281/zenodo.6298884.

Full text

Abstract:

Department of Chemistry, S. V. U. Autonomous Post-Graduate Centre, Anantapur-515 008 <em>Manuscript received 28 May 1981,  accepted 12 August 1986</em> Kinetics of the oxidation of acetophenone oxime and its <em>\({para}\)</em>-substituted derivatives by chromium (VI) has been studied at 30˚. The product analysis indicates that the reaction is oxidative hydrolysis. The rate increases with the increase in concentration of  hydrogen ions. The first order rate dependence on the substrate concentration and inverse dependence on chromium(VI) concentration are observed. The effect of DMF o

APA, Harvard, Vancouver, ISO, and other styles

27

O'Ferrall, RA More, D. M. O'Brien, and D. G. Murphy. "Rate and equilibrium constants for formation and hydrolysis of 9-formylfluorene oxime: diffusion-controlled trapping of a protonated aldehyde by hydroxylamine." Canadian Journal of Chemistry 78, no. 12 (2000): 1594–612. http://dx.doi.org/10.1139/v00-129.

Full text

Abstract:

Equilibrium constants Kadd = 440 and Kox = 3.0 × 108 for formation of a carbinolamine adduct and oxime, respectively from 9-formylfluorene and hydroxylamine, and pKa = 1.62 for protonation of the oxime, have been evaluated at 25°C in aqueous solution, based on measurements in hydroxylamine buffers, acetic acid buffers, and dilute HCl. Rate constants for hydrolysis of the oxime have been measured in the acidity range pH 412 M HClO4. At the highest acidities, a reaction pathway via protonated carbinolamine has been identified: evidence is presented that the reverse of this reaction involves ra

APA, Harvard, Vancouver, ISO, and other styles

28

de Souza, Ronan F. F., Gislaine A. da Cunha, José C. M. Pereira, et al. "Orthopalladated acetophenone oxime compounds bearing thioamides as ligands: Synthesis, structure and cytotoxic evaluation." Inorganica Chimica Acta 486 (February 2019): 617–24. http://dx.doi.org/10.1016/j.ica.2018.11.022.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

REHMAN, F., and SAMYA MAIRAJ. "Spectrophotometric Determination of Manganese by Biologically Active 2-Hydroxy-4-methoxy Acetophenone Oxime." Oriental Journal Of Chemistry 28, no. 2 (2012): 881–85. http://dx.doi.org/10.13005/ojc/280230.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Wiesenthal, Karina, Alexander Jehlar, and Shane S. Que Hee. "Synthesis of the O-(2,3,4,5,6-Pentafluorobenzyl)Hydroxylamine Oximes of Selected Carbonyl Compounds and Their Determination by Liquid Chromatography with Ultraviolet Detection." Journal of AOAC INTERNATIONAL 83, no. 4 (2000): 859–70. http://dx.doi.org/10.1093/jaoac/83.4.859.

Full text

Abstract:

Abstract The aims were to develop a liquid chromatographic (LC) method with ultraviolet detection (UVD) for O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine hydrochloride (PFBHA) O-oximes of common aldehydes and ketones, and to define the steric limits of the synthetic reaction used to make the PFBHA O-oxime standards for gas chromatographic (GC) and LC methods. Ten new O-oximes were synthesized with the new optimized method, and their purities were demonstrated by GC/electron-capture detection (ECD), GC/mass spectrometry (MS), ultraviolet spectroscopy, infrared spectroscopy, and proton and 13C-nu

APA, Harvard, Vancouver, ISO, and other styles

31

Reddy, Daggula Mallikarjuna, Shao-Chien Wang, Kai Du, and Chin-Fa Lee. "Palladium-Catalyzed ortho–C-H Arylation of Acetophenone Oxime Ethers with Aryl Pinacol Boronic Esters." Journal of Organic Chemistry 82, no. 19 (2017): 10070–76. http://dx.doi.org/10.1021/acs.joc.7b01524.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Mikhaleva, A. I., O. V. Petrova, and L. N. Sobenina. "2-Phenylpyrrole: one-pot selective synthesis from acetophenone oxime and acetylene by a Trofimov reaction*." Chemistry of Heterocyclic Compounds 47, no. 11 (2012): 1367–71. http://dx.doi.org/10.1007/s10593-012-0922-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Maurin, J. K., M. Winnicka-Maurin, I. C. Paul, and D. Y. Curtin. "Hydrogen-bonded complex formation of oximes with carboxylic acids and with amides. (E)-Acetophenone oxime–benzoic acid (1/1) and (E)-benzaldehyde oxime–benzamide (1/1)." Acta Crystallographica Section B Structural Science 49, no. 1 (1993): 90–96. http://dx.doi.org/10.1107/s0108768192006190.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Didier, Eric, Bernard Loubinoux, Gerardo H. Ramos Tombo, and Grety Rihs. "Chemo-enzymatic synthesis of 1,2- and 1,3- amino-alcohols and their use in the enantioselective reduction of acetophenone and anti-acetophenone oxime methyl ether with borane." Tetrahedron 47, no. 27 (1991): 4941–58. http://dx.doi.org/10.1016/s0040-4020(01)80959-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Chauhan, Narendra P. S., and Suresh C. Ameta. "Preparation and thermal studies of self-crosslinked terpolymer derived from 4-acetylpyridine oxime, formaldehyde and acetophenone." Polymer Degradation and Stability 96, no. 8 (2011): 1420–29. http://dx.doi.org/10.1016/j.polymdegradstab.2011.05.014.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Katagi, Manjunatha S., Jennifer Fernandes, Shivalingrao Mamledesai, Sujatha M.L., Rekha A., and Girish Bolakatti. "Schiff Base Oxime Derivatives Reactivate Chlorpyrifos-induced Acetylcholinesterase Inhibition." INNOSC Theranostics and Pharmacological Sciences 2, no. 1 (2019): 12–16. http://dx.doi.org/10.26689/itps.v2i1.499.

Full text

Abstract:

Background: The biological effects of organophosphorus (OP) compounds are connected with the irreversible inhibition of acetylcholinesterase (AChE), an important neuromediator acetylcholine (ACh) splitting enzyme in the human body at the synaptic clefts. Due to this inhibition, AChE is unable to fulfil its physiological function resulting in the accumulation of ACh, which, in turn over stimulates the parasympathetic nerve receptors, and causes fatal cholinergic crisis. Objective: The objective of the study was to synthesize a series of Schiff base oximes and to assess their evaluating fo

APA, Harvard, Vancouver, ISO, and other styles

37

DIDIER, E., B. LOUBINOUX, G. M. RAMOS TOMBO, and G. RIHS. "ChemInform Abstract: Chemoenzymatic Synthesis of 1,2- and 1,3-Amino Alcohols and Their Use in the Enantioselective Reduction of Acetophenone and anti-Acetophenone Oxime Methyl Ether with Borane." ChemInform 22, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199141057.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Petrova, O. V., A. I. Mikhaleva, L. N. Sobenina, and B. A. Trofimov. "p-Terphenyl as unexpected by-product in the synthesis of 2,5-diphenylpyrrole from acetophenone oxime and phenylacetylene." Russian Journal of Organic Chemistry 46, no. 3 (2010): 452–54. http://dx.doi.org/10.1134/s1070428010030279.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Shmidt, E. Yu, N. V. Zorina, A. I. Mikhaleva, I. A. Ushakov, E. V. Skital’tseva, and B. A. Trofimov. "1,3,5-triphenylbenzene as unexpected by-product in the synthesis of 2,5-diphenylpyrrole from acetophenone oxime and phenylacetylene." Russian Journal of Organic Chemistry 46, no. 3 (2010): 457–58. http://dx.doi.org/10.1134/s1070428010030292.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Schmidt, E. Yu, N. V. Zorina, I. A. Ushakov, E. V. Skital’tseva, A. I. Mikhaleva, and B. A. Trofimov. "Unexpected formation of 2,4,6-triphenylpyridine in the synthesis of 2,5-diphenyl-pyrrole from acetophenone oxime and phenylacetylene." Chemistry of Heterocyclic Compounds 45, no. 7 (2009): 868–70. http://dx.doi.org/10.1007/s10593-009-0345-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Li, Chunbao, Hang Zhang, Yi Cui, et al. "One-Pot Synthesis of Oxime Ethers from Benzaldehyde or Acetophenone, Hydroxylamine Salt, Potassium Hydroxide, and Alkyl Halides." Synthetic Communications 33, no. 4 (2003): 543–46. http://dx.doi.org/10.1081/scc-120015807.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Suyama, Kanji, Katsuhiko Ito, and Masahiro Tsunooka. "Photo-induced polarity alteration and photodegradation behavior of O-acryloyl acetophenone oxime and phenyl vinyl ketone copolymers." Journal of Polymer Science Part A: Polymer Chemistry 34, no. 11 (1996): 2181–87. http://dx.doi.org/10.1002/(sici)1099-0518(199608)34:11<2181::aid-pola11>3.0.co;2-b.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Mikhaleva, A. I., O. V. Petrova, and L. N. Sobenina. "ChemInform Abstract: 2-Phenylpyrrole: One-Pot Selective Synthesis from Acetophenone Oxime and Acetylene by a Trofimov Reaction." ChemInform 43, no. 32 (2012): no. http://dx.doi.org/10.1002/chin.201232113.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Fernandez, Ana Belen, Ines Lezcano-Gonzalez, Mercedes Boronat, Teresa Blasco, and Avelino Corma. "Study of the Beckmann rearrangement of acetophenone oxime over porous solids by means of solid state NMR spectroscopy." Physical Chemistry Chemical Physics 11, no. 25 (2009): 5134. http://dx.doi.org/10.1039/b816276j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Prakash, Om, Kamaljeet Pannu, Rajesh Naithani, and Harpreet Kaur. "One‐Pot Synthesis of Oxime Derivatives of 1,3‐Diphenylpyrazole‐4‐carboxaldehydes from Acetophenone Phenylhydrazones Using Vilsmeier–Haack Reagent." Synthetic Communications 36, no. 23 (2006): 3479–85. http://dx.doi.org/10.1080/00397910600942941.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Petrova, O. V., A. I. Mikhaleva, L. N. Sobenina, and B. A. Trofimov. "ChemInform Abstract: p-Terphenyl as Unexpected By-Product in the Synthesis of 2,5-Diphenylpyrrole from Acetophenone Oxime and Phenylacetylene." ChemInform 41, no. 37 (2010): no. http://dx.doi.org/10.1002/chin.201037076.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Shmidt, E. Yu, N. V. Zorina, A. I. Mikhaleva, I. A. Ushakov, E. V. Skital'tseva, and B. A. Trofimov. "ChemInform Abstract: 1,3,5-Triphenylbenzene as Unexpected By-Product in the Synthesis of 2,5-Diphenylpyrrole from Acetophenone Oxime and Phenylacetylene." ChemInform 41, no. 37 (2010): no. http://dx.doi.org/10.1002/chin.201037077.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Saran, Anil, та R. P. Ojha. "Molecular orbital studies on β-blockers: conformation of acetophenone-o-(tert- butylamino-3-hydroxy-2-propyl) oxime and (tert- butylamino". Journal of Molecular Structure: THEOCHEM 233 (вересень 1991): 301–14. http://dx.doi.org/10.1016/0166-1280(91)85070-n.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Li, Sun-Yong, Xu Zhang, Fan Teng, Yang Li, and Jin-Heng Li. "Rh(iii)-Catalyzed [3 + 2]/[4 + 2] annulation of acetophenone oxime ethers with 3-acetoxy-1,4-enynes involving C–H activation." Organic Chemistry Frontiers 8, no. 12 (2021): 2955–62. http://dx.doi.org/10.1039/d1qo00090j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Hassan, Ali Zamani, Mazloum Soghra, and Feizyzadeh Babak. "Synthesis of 1,2-bis(4-chloro)acetophenone oxime ethyl ether as a carrier and its application for construction of a new ytterbium(III)-PVC membrane sensor." Journal of Indian Chemical Society Vol. 91, Apr 2014 (2014): 613–18. https://doi.org/10.5281/zenodo.5717854.

Full text

Abstract:

Department of Applied Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran <em>E-mail</em> : haszamani@yahoo.com Department of Applied Chemistry, Quchan Branch, Islamic Azad University, Quchan, Iran Manuscript received online 20 July 2013, accepted 08 August 2013 The new ytterbium(III)-PVC membrane, containing 1,2-bis(4-chloro)acetophenone oxime ethyl ether (AOEE) as an ion carrier, showed a Nernstian response for the Yb<sup>3+</sup> ions over a wide dynamic linear range between 1.0 × 10<sup>–6</sup> and 1 × 10<sup>–2</sup> <em>M</em>. The detection limit i

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!