Relevant bibliographies by topics / Phenylhydrazones

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Phenylhydrazones'

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

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Journal articles on the topic "Phenylhydrazones"

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Amengor, Cedric Dzidzor Kodjo, Prince Danan Biniyam, Abena Amponsaa Brobbey, et al. "N-Substituted Phenylhydrazones Kill the Ring Stage of Plasmodium falciparum." BioMed Research International 2024 (February 13, 2024): 1–13. http://dx.doi.org/10.1155/2024/6697728.

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Antimalarial resistance has hampered the effective treatment of malaria, a parasitic disease caused by Plasmodium species. As part of our campaign on phenotypic screening of phenylhydrazones, a library of six phenylhydrazones was reconstructed and evaluated for their in vitro antimalarial and in silico receptor binding and pharmacokinetic properties. The structures of the phenylhydrazone hybrids were largely confirmed using nuclear magnetic resonance techniques. We identified two compounds which exhibited significant antimalarial potential against the ring stage (trophozoite) of 3D7 chloroquin
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Liu, Ya-Ping, Sheng-Tao Fang, Zhen-Zhen Shi, Bin-Gui Wang, Xiao-Nian Li, and Nai-Yun Ji. "Phenylhydrazone and Quinazoline Derivatives from the Cold-Seep-Derived Fungus Penicillium oxalicum." Marine Drugs 19, no. 1 (2020): 9. http://dx.doi.org/10.3390/md19010009.

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Three new phenylhydrazones, penoxahydrazones A–C (compounds 1–3), and two new quinazolines, penoxazolones A (compound 4) and B (compound 5), with unique linkages were isolated from the fungus Penicillium oxalicum obtained from the deep sea cold seep. Their structures and relative configurations were assigned by analysis of 1D/2D NMR and mass spectroscopic data, and the absolute configurations of 1, 4, and 5 were established on the basis of X-ray crystallography or ECD calculations. Compound 1 represents the first natural phenylhydrazone-bearing steroid, while compounds 2 and 3 are rarely occur
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Kpoviessi, Bénédicta Kpadonou, Bardieu Atchadé, Basile Goueti, et al. "Synthesis, Spectrometrical Characterization and Pharmacological Properties of Six Substituted Hydrazones with Carbonyl Compounds." Chemical Science International Journal 34, no. 2 (2025): 11–24. https://doi.org/10.9734/csji/2025/v34i2953.

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Hydrazones are molecules that prevent the growth of several microbial and parasitic strains by inhibited the replication of DNA sequences due to their chelating properties of metal ions. They are well recognized for Antiparasitic, Antimicrobial, Antibacterial, Antiviral, Antitumoral, Antimalarial and Anticonvulsive activities. The aim of the current study is to synthesized novel substituted hydrazones of ketones and aromatic aldehydes and to study their antiparasitic activities against Trypanosoma brucei brucei parasite. Synthesized hydrazone derivatives have been confirmed by elemental analys
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Idemudia, Omoruyi G., Anthony I. Okoh, Alexander P. Sadimenko, Eric C. Hosten, and Omobola O. Okoh. "Substituted 4-Acyl-5-methyl-2-phenyl-pyrazol-3-one-phenylhydrazones with Antioxidant Properties: X-Ray Crystal and Spectroscopic Studies." Journal of Chemistry 2017 (2017): 1–10. http://dx.doi.org/10.1155/2017/7943051.

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Phenylhydrazine was reacted with synthesized acylpyrazolone derivatives 4-ethyl-5-methyl-2-phenyl-pyrazol-3-one and 4-propyl-5-methyl-2-phenyl-pyrazol-3-one, to obtain two new azomethine phenylhydrazones, a study in continuation of our probe into the effects of acyl group substitutions on the physicochemical and free radical scavenging properties of acylpyrazolone Schiff bases. The keto imine tautomers of 4-ethyl-5-methyl-2-phenyl-pyrazol-3-one-phenylhydrazone (Empp-Ph) and 4-propyl-5-methyl-2-phenyl-pyrazol-3-one-phenylhydrazone (Prmpp-Ph) according to single X-ray crystallography data which
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Schantl, J. G., P. Hebeisen, and P. Karpellus. "N-Arenesulfonyl-N-phenylhydrazones." Synthetic Communications 19, no. 1-2 (1989): 39–48. http://dx.doi.org/10.1080/00397918908050950.

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Porter, L. C., Ming-Li, F. Cervantes-Lee, and H. H. Murray. "Bonding in phenylhydrazones: X-ray crystal structure and theoretical calculations involving (E)-acetophenone phenylhydrazone." Monatshefte für Chemie / Chemical Monthly 124, no. 6-7 (1993): 775–82. http://dx.doi.org/10.1007/bf00817313.

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Ojala, William H., Jonathan M. Smieja, Jill M. Spude, et al. "Isostructuralism among `bridge-flipped' isomeric benzylideneanilines and phenylhydrazones." Acta Crystallographica Section B Structural Science 63, no. 3 (2007): 485–96. http://dx.doi.org/10.1107/s0108768107018034.

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`Bridge-flipped' isomers may be defined as pairs of molecules related by a reversal of a bridge of atoms connecting two major parts of the individual molecules. This kind of isomerism is commonly found among benzylideneanilines and phenylhydrazones. Isostructural pairs might be suitable for co-crystallization and are thus useful in the preparation of new solid materials. Although most of the examples of bridge-flipped isomeric benzylideneanilines and phenylhydrazones in the crystallographic literature are not isostructural, a small number of isostructural pairs have been reported by previous w
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El Ashry, El Sayed H., Nagwa Rashed, Ahmed Mousaad, and Mahmoud El Habrouk. "Isopropylidenation of aldosulose bis(phenylhydrazones)." Carbohydrate Research 269, no. 2 (1995): 349–57. http://dx.doi.org/10.1016/0008-6215(94)00357-l.

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Afsah, E. M., M. Hammouda, H. Zoorob, M. M. Khalifa, and M. T. Zimaity. "Mannich Reaction with 1 ,3 - Indandione Phenylhydrazones." Zeitschrift für Naturforschung B 45, no. 1 (1990): 80–82. http://dx.doi.org/10.1515/znb-1990-0115.

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Abstract Mannich reaction of 1,3-indandione-1-phenylhydrazone (1) or 1,3-diphenylhydrazone (5) withmorpholine or piperazine gave the Mannich base-phenylhydrazone 2 and 3 or the diphenylhydrazone6 and 7, respectively. Whereas, such reaction with 1 or 5 using primary amines affordedthe indeno[2,1-ƒ]-1,2,4-triazepin-6(2H)-one (4) or its 6-phenylhydrazone (8), respectively.Treatment of 5 with ammonium acetate and formalin afforded 9. The indeno[1,2-ƒ]-1,2,4,5-tetrazepin-10(2H)-one (11) was obtained from the 1,2-diphenylhydrazone 10 and formaldehyde.
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Ojala, William H., Trina M. Arola, Ann M. Brigino, Jeremy D. Leavell, and Charles R. Ojala. "Competing intermolecular interactions in some `bridge-flipped' isomeric phenylhydrazones." Acta Crystallographica Section C Crystal Structure Communications 68, no. 7 (2012): o270—o278. http://dx.doi.org/10.1107/s0108270112026443.

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To examine the roles of competing intermolecular interactions in differentiating the molecular packing arrangements of some isomeric phenylhydrazones from each other, the crystal structures of five nitrile–halogen substituted phenylhydrazones and two nitro–halogen substituted phenylhydrazones have been determined and are described here: (E)-4-cyanobenzaldehyde 4-chlorophenylhydrazone, C14H10ClN3, (Ia); (E)-4-cyanobenzaldehyde 4-bromophenylhydrazone, C14H10BrN3, (Ib); (E)-4-cyanobenzaldehyde 4-iodophenylhydrazone, C14H10IN3, (Ic); (E)-4-bromobenzaldehyde 4-cyanophenylhydrazone, C14H10BrN3, (IIb
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Dissertations / Theses on the topic "Phenylhydrazones"

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GASPARD, SARRA. "Chimie de coordination et topologie du site actif de la prostaglandine h synthetase : reactions avec les hydrazines monosubstituees et avec les phenylhydrazones et caracterisation par spectroscopie de resonance raman." Paris 11, 1994. http://www.theses.fr/1994PA112084.

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La prostaglandine h synthetase (pghs) est une hemoproteine qui intervient dans la biosynthese de mediateurs de l'inflammation, les prostaglandines. Les hydrazines monosubstituees rhnnh#2 sont oxydees par la pghs en diazene rn=nh avec formation de la pghsfe(ii) et du complexe pghsfe#i#i-diazene. L'oxydation de ce complexe conduit a un nouveau complexe a liaison fe-c de l'enzyme: pghsfe#i#i#i-r. La formation de ces complexes montre que la pghs possede un site actif ouvert. Les phenylhydrazones constituent une nouvelle classe de substrats suicide de la fonction dioxygenase de la pghs. Les -azohyd
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Bombard, Sophie. "Mécanisme d'action de la lipoxygènase-1 de soja : étude à l'aide de phénylhydrazones." Paris 5, 1990. http://www.theses.fr/1990PA05P604.

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Lupo, Donald, Werner Prass, Ude Scheunemann, André Laschewsky, Helmut Ringsdorf, and Isabelle Ledoux. "Second-harmonic generation in Langmuir-Blodgett monolayers of stilbazium salt and phenylhydrazone dyes." Universität Potsdam, 1988. http://opus.kobv.de/ubp/volltexte/2009/1740/.

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Contents: 1. INTRODUCTION 2. SYNTHESIS OF THE COMPOUNDS 3. PREPARATION AND CHARACTERIZATION OF MONOLAYERS A. Monolayer Isotherms B. Langmuir-Blodgett Monolayer Films 4. EXPERIMENTAL SETUP FOR NONLINEAR MEASUREMENTS 5. NONLINEAR OPTICAL PROPERTIES 6. DISCUSSION 7. CONCLUSION
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Puntel, Gustavo Orione. "Análise das propriedades antioxidantes das oximas 3-(fenil hidrazona) butano-2-ona e butano-2,3-dionatiosemicarbazona." Universidade Federal de Santa Maria, 2008. http://repositorio.ufsm.br/handle/1/11087.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Oximes are chemical compounds used to reactivate the inhibited acetylcholinesterase (AChE) enzyme by organophosphates (OPs). The OPs, besides classically recognized as AChE irreversible inhibitors, are also involved in the generation of oxidative stress conditions. However, researches focusing on the possible antioxidant properties of oximes are lacking in the literature. The aim of this study was to investigate the potential antioxidant and toxic properties of 3-(phenylhydrazono)butan-2-one oxime and butane-2,3-dionethiosemicarbaz
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Book chapters on the topic "Phenylhydrazones"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_201.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_182.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex of tetraaldehyde phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_248.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chloro complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_495.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) nitrato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_496.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) thiocyanato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_200.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chloro complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_179.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) nitrato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_180.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) thiocyanato complex with benzoin phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_181.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with o-hydroxyacetophenone-phenylhydrazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_176.

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Conference papers on the topic "Phenylhydrazones"

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Azev, Yu A., O. S. Koptyaeva, O. S. Eltsov, Yu A. Yakovleva, T. A. Pospelova, and V. A. Bakulev. "Benzaldehyde phenylhydrazones as c-nucleophiles for functionalization of quinoxaline-2-one. Unusual transformations of indole-3-carbaldehyde phenylhydrazones." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018799.

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Naimi-Jamal, M. R., H. Hamzehali, Mohammad G. Dekamin, and J. Mokhtari. "A Simple and Efficient Method for Quantitative Solvent-Free Synthesis of Phenylhydrazones and 2,4-Dinitrophenylhydrazones." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01315.

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Hou, Zhanjia, Liying Liu, Lei Xu, et al. "Improved optical nonlinearity of poled phenylhydrazone-doped polymer films." In Photonics China '98, edited by Chuangtian Chen. SPIE, 1998. http://dx.doi.org/10.1117/12.318226.

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Ormachea, Carla, and Cristián A. Ferretti. "In Silico Evaluation of Antioxidant Properties of Cinnamaldehyde Phenylhydrazone." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11711.

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Sudheesh, P., and K. Chandrasekharan. "Metal Nanoparticle Induced Enhancement in Third-Order Optical Nonlinearity of Phenylhydrazone/PMMA thin films." In International Conference on Fibre Optics and Photonics. OSA, 2012. http://dx.doi.org/10.1364/photonics.2012.tpo.43.

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Soubhye, Jalal. "Dual Anti-Inflammatory and Anti-Bacterial Effects of Phenylhydrazide and Phenylhydrazone Derivatives." In 3rd International Electronic Conference on Medicinal Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04699.

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Sudheesh, P., D. Mallikharjuna Rao, and K. Chandrasekharan. "Study on metal nanoparticles induced third-order optical nonlinearity in phenylhydrazone derivatives with DFWM technique." In OPTOELECTRONIC MATERIALS AND THIN FILMS: OMTAT 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4862002.

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Bako, Rabiu, Abdullahi Yunusa Idris, Asma’u Nasiru Hamza, Gbonjubola O. Adeshina, and Musa Abdullahi Garba. "Synthesis, Characterization, and In-Silico Studies of Some Novel Phenylhydrazone Derivatives as Potential Agents for Antimicrobial Activities." In International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20254.

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