Relevant bibliographies by topics / Ketone hydrazones

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  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Ketone hydrazones'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Ketone hydrazones"

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KushalNath Mishra, Shambaditya Goswami, Kumudhavalli M.V, et al. "Hydrazones and their metal complexes: A short review on their biological potentia." International Journal of Research in Pharmaceutical Sciences 11, SPL4 (2020): 1440–47. http://dx.doi.org/10.26452/ijrps.v11ispl4.4319.

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Hydrazones belong to complexes are beneficial in different fields for their essential role in the development of a range of stable complexes in the coordination chemistry. Different researchers have reported the various medicinal properties of hydrazones. Hydrazone and its metal complexes are useful for the detection of some organic components from pharmaceutical formulations. These metallic compounds act as a catalyst for conducting various chemical reactions and help in making different chemical complexes that are effective against bacteria, fungi, and many other microbes. Aromatic hydrazone
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Atici, Oya (Galioǧlu). "Decomposition of cyclohexyl phenyl ketone via their polymeric sulfonyl hydrazones and tosyl hydrazones." Reactive and Functional Polymers 34, no. 2-3 (1997): 175–82. http://dx.doi.org/10.1016/s1381-5148(97)00085-0.

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Fawzy, Ahmed, Saleh A. Ahmed, Ismail I. Althagafi, Moataz H. Morad, and Khalid S. Khairou. "Kinetics and Mechanistic Study of Permanganate Oxidation of Fluorenone Hydrazone in Alkaline Medium." Advances in Physical Chemistry 2016 (July 25, 2016): 1–9. http://dx.doi.org/10.1155/2016/4526578.

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The oxidation kinetics of fluorenone hydrazone (FH) using potassium permanganate in alkaline medium were measured at a constant ionic strength of 0.1 mol dm−3 and at 25°C using UV/VIS spectrophotometer. A first-order kinetics has been monitored in the reaction of FH with respect to [permanganate]. Less-than-unit order dependence of the reaction on [FH] and [OH−] was revealed. No pronounced effect on the reaction rate by increasing ionic strength was recorded. Intervention of free radicals was observed in the reaction. The reaction mechanism describing the kinetic results was illustrated which
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Xiang, Jiahong, Di Wen, Junbo Zhao, Ping Xiang, Yan Shi, and Chunling Ma. "Study of the Metabolic Profiles of “Indazole-3-Carboxamide” and “Isatin Acyl Hydrazone” (OXIZID) Synthetic Cannabinoids in a Human Liver Microsome Model Using UHPLC-QE Orbitrap MS." Metabolites 13, no. 4 (2023): 576. http://dx.doi.org/10.3390/metabo13040576.

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Unregulated core structures, “isatin acyl hydrazones” (OXIZIDs), have quietly appeared on the market since China legislated to ban seven general core scaffolds of synthetic cannabinoids (SCs). The fast evolution of SCs presents clinical and forensic toxicologists with challenges. Due to extensive metabolism, the parent compounds are barely detectable in urine. Therefore, studies on the metabolism of SCs are essential to facilitate their detection in biological matrices. The aim of the present study was to elucidate the metabolism of two cores, “indazole-3-carboxamide” (e.g., ADB-BUTINACA) and
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Okuma, Kentaro, Yuxuan Qu, Aoi Suetome, and Noriyoshi Nagahora. "Reaction of ketone hydrazones with TeCl4: isolation and reactions of novel divinyl telluride." Organic & Biomolecular Chemistry 18, no. 24 (2020): 4583–89. http://dx.doi.org/10.1039/d0ob00782j.

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The reaction of acetophenone hydrazones with TeCl<sub>4</sub> in the presence of DBU gave divinyl tellurides. The reaction of divinyl tellurides with bromine or benzyne afforded the corresponding tellurium dibromides or (E)-2-alkenyl tellurides.
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VIDYA, JOSHI, та K. SHARMA R. "Diazotisation Rearrangement of Tosylhydrazones of ortho- and meta-Substituted-benzophenones and α-Substituted-acetophenones (Synthesis of Anilides)". Journal of Indian Chemical Society Vol. 65, Aug 1988 (1988): 564–66. https://doi.org/10.5281/zenodo.6042085.

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Institute of Science, 15, Madam Cama Road, Bombay-400 032 <em>Manuscript received 25 January 1988, accepted 28 May 2988</em> <em>Ortho</em>- and <em>meta</em>-substituted-benzophenones (1a &mdash;g) and substituted-acetophenones (1h &mdash; i) were converted into tosylhydrazones (2a&mdash; i) by reacting with<em> p</em>-toluenesulphonyl&shy;hydrazide. Conversion of 2a &mdash; i to the anilides (3a &mdash;i) was effected with the reagents H<sub>2</sub>SO<sub>4</sub> and NaNO<sub>2</sub>, and was found to be as facile as In case of the <em>para</em>-substituted&shy;benzophenone hydrazones.
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Nurkenov, O. A., A. Zh Mendibayeva, S. D. Fazylov, et al. "Synthesis of quaternary ammonium saltsisonicotinic and nicotinic hydrazones acids and their anti-inflammatory activity." Chemical Journal of Kazakhstan, no. 1 (March 15, 2024): 154–66. http://dx.doi.org/10.51580/2024-1.2710-1185.15.

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Currently, the number of infections caused by strains of bacteria that are not sensitive to antibiotics and antiseptics is growing worldwide. A similar increase in bacterial resistance is observed for both nosocomial infections and community-acquired human-to-human infections. An important task for chemists and pharmacologists is the synthesis of new compounds and the establishment of a structure-bioactivity relationship. The purpose of this work is to study the effect of the structure of quaternary ammonium derivatives of hydrazones of isonicotinic and nicotinic acids on the manifestation of
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Baccolini, Graziano, and Michele Gianelli. "N-alkenyl-3,5-pyrazolidinediones from ketone hydrazones, PCl3 and malonic acid." Tetrahedron 51, no. 34 (1995): 9487–92. http://dx.doi.org/10.1016/0040-4020(95)00550-r.

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LEE, D. W., Y. S. PARK, and W. K. LEE. "ChemInform Abstract: Oxidation of Aromatic Ketone Hydrazones by Thianthrene Cation Radical." ChemInform 28, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199715056.

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Ienaşcu, Ioana, Alfa Lupea, Iuliana Popescu, Mirabela Pădure, and Alina Zamfir. "The synthesis and characterization of some novel 5-chloro-2-(substituted alkoxy)-N-phenylbenzamide derivatives." Journal of the Serbian Chemical Society 74, no. 8-9 (2009): 847–55. http://dx.doi.org/10.2298/jsc0909847i.

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To obtain biologically active compounds, the synthesis of some new derivatives with an o-hydroxybenzamide structure was performed. The ethyl esters 4-6 were obtained by the reaction of 5-chloro-2-hydroxy-N-phenylbenzamide and chloro-substituted acid ethyl esters 1-3 in ethyl methyl ketone. The obtained ethyl esters were condensed with hydrazine yielding the hydrazides 7-8. The hydrazones 11-14 were obtained by the reaction of the hydrazides and the chloro-substituted benzaldehydes 9-10. All the newly synthesized compounds were characterized by FTIR, 1H-NMR, 13C-NMR, MS and elemental analyses.
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Dissertations / Theses on the topic "Ketone hydrazones"

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Marko, Rodić. "Kompleksi Co(III), Ni(II) i Cu(II) sa hidrazonima nekih 2-piridil-ketona." Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2015. https://www.cris.uns.ac.rs/record.jsf?recordId=95722&source=NDLTD&language=en.

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U disertaciji su opisane sinteze i fizičko-hemijske karakterizacije 32 kompleksa kobalta(III), nikla(II) i bakra(II) sa ligandima S-metilizotiosemikarbazonom 2-acetilpiridina (HL&sup1;), bis(S-metilizotiosemikarbazonom) 2,6-diacetilpiridina (H₂L&sup2;), tiosemikarbazonom-S-metilizotiosemikarbazonom 2,6-diacetilpiridina (HL&sup3;), 1-adamantoilhidrazonom 2-acetilpiridina (HL⁴) i 1-adamantoilhidrazonom di(2-piridil)-ketona (HL⁵).Kako ligandi HL&sup3;, HL⁴ i HL⁵ do sada nisu bili sintetisani, dobijeni rezultati ujedno predstavljaju i prve iz njihove koordinacione hemije. Iako je sa S-metilizotios
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PEREIRA, William. "Estudos cin?ticos de isatina e algumas cetonas arom?ticas frente a novas fosforilidrazonas." Universidade Federal Rural do Rio de Janeiro, 2009. https://tede.ufrrj.br/jspui/handle/jspui/1439.

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Submitted by Jorge Silva (jorgelmsilva@ufrrj.br) on 2017-02-15T17:02:45Z No. of bitstreams: 1 2009 - William Pereira.pdf: 3794972 bytes, checksum: 64fbf9758bbf44329031caf3b369b79a (MD5)<br>Made available in DSpace on 2017-02-15T17:02:45Z (GMT). No. of bitstreams: 1 2009 - William Pereira.pdf: 3794972 bytes, checksum: 64fbf9758bbf44329031caf3b369b79a (MD5) Previous issue date: 2009-10-22<br>CAPES<br>The present study has two specific phases: Early, was studied the isathine irradiation with the presence of diisopropil-phosphoril-dimethylidrazone (diisopfh), in chloroform, at room temperatu
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Book chapters on the topic "Ketone hydrazones"

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Kubik, S. "From Ketone Hydrazones." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00517.

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Döpp, H., and D. Döpp. "Oxidation of 2-(Aminophenyl) Ketone Hydrazones." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00430.

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Okuma, Kentaro, Kento Kubo, and Kosei Shioji. "Synthesis of cis- and trans-1,3,4-Selenadiazolines from Ketone Hydrazones." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50259-8.

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Diaper, C. M. "2,5-Dihydro-1,3,4-oxadiazoles from Ketone Hydrazones by Oxidative Cyclization." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-01426.

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Landais, Y., and J. M. Vincent. "Of Hydrazones." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00610.

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Harrison-Marchand, A., I. Chataigner, and J. Maddaluno. "Hydrolysis of Hydrazones." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-01172.

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Schantl, J. G. "Intramolecular N-Alkylation of Hydrazone by Dehydrohalogenation of (Haloacyl)hydrazones." In Heteroatom Analogues of Aldehydes and Ketones. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00694.

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Desmale, D. "Synthesis from Hydrazone Derivatives." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00228.

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Desmale, D. "Hydrolysis of Hydrazone Derivatives." In Ketones. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-026-00229.

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Kikelj, D. "From 2-(Acylamino)benzamide Oximes, 2-(Acylamino)benzaldehyde Oximes, or Hydrazones and 2-(Acylamino)phenyl Ketone Oximes or -Acylhydrazones." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00836.

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