Relevant bibliographies by topics / Arylidenes

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

Academic literature on the topic 'Arylidenes'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Arylidenes"

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El-Sayed Ebead, Eman, Asmaa Aboelnaga, Ekhlass Nassar, Mohamed M. Naguib, and Mahmoud F. Ismail. "Ultrasonic-induced synthesis of novel diverse arylidenes via Knoevenagel condensation reaction. Antitumor, QSAR, docking and DFT assessment." RSC Advances 13, no. 42 (2023): 29749–67. http://dx.doi.org/10.1039/d3ra05799b.

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Ibrahim, Hamada Mohamed, Wael Abdelgayed Ahmed Arafa, and Haider Behbehani. "l-Proline catalyzed one-pot synthesis of polysubstituted pyridine system incorporating benzothiazole moietyviasustainable sonochemical approach." RSC Advances 8, no. 66 (2018): 37606–17. http://dx.doi.org/10.1039/c8ra07013j.

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Thel-proline catalyzed ultrasonic-mediated synthesis of polysubstituted pyridone derivatives through the reaction ofN-(benzothiazol-2-yl)-2-cyanoacetamides with an assortment of arylidenes has demonstrated as an efficient protocol.
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Apoorva, Upadhyay, K. Srivastava S., D. Srivastava S., and Upadhyay Navneeta. "Microwave assisted synthesis of 4-thiazolidinones and its 5-arylidene derivatives : Screening of antimicrobial activity with various microorganisms." Journal of Indian Chemical Society Vol. 88, Jul 2011 (2011): 1025–31. https://doi.org/10.5281/zenodo.5785163.

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Synthetic Organic Chemistry Laboratory, Department of Chemistry, Dr. H. S. Gour University (A Central University), Sagar-470 003, Madhya Pradesh, India <em>E-mail</em> : upadhyay .apoorva@gmail.com Department of Chemistry, Chameli Devi Institute of Technology, Indore, Madhya Pradesh, India <em>Manuscript received 06 April 2010, revised 29 December 2010, accepted 30 December 2010</em> Several new ethyl(isonicotinamid-4-yl)acetate (1), 2-(isonicotinamid-4-yl)acetohydrazide (2), 2-(isonicotinamid- 4-yl)acetylhydrazino arylidenes (3a-j), 2-aryl-3-[(isonicotinamid-4-yl)acetamido]-4-oxo-1,3-thiazoli
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George, S., R. Chakraborty, F. Saleshier, and T. K. Ravi. "SYNTHESIS OF NOVEL BENZOTRIAZOLYL FORMAZANS AND THEIR ANTIMICROBIAL AND ANTIOXIDANT ACTIVITY." INDIAN DRUGS 50, no. 11 (2013): 29–33. http://dx.doi.org/10.53879/id.50.11.p0029.

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Benzotriazolyl hydrazide (2) has been obtained from the ester ethyl benzotriazolyl acetate (1). The hydrazide with various aromatic aldehydes in presence of glacial acetic acid gave corresponding arylidenes 3(a-h). The arylidenes were made to react with fluoro substituted diazonium salt whereby, benzotriazolyl formazans 4(a-h) were obtained. The structures of the compounds were confirmed by FTIR, 1 H-NMR, mass spectral data and elemental analysis. All the synthesized compounds were screened for their in-vitro antimicrobial activity against the bacterial strains Bacillus subtilis and Escherichi
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Khattab, Ahmed F., and Farag A. El-Essawy. "Formation of Novel Pyrido[3′,2′:4,5]Thieno [2,3-e][1,2,4]Triazolo[4,3-c] Pyrimidines and their Acyclic C-Nucleosides Analogues: Synthesis of 3-(Alditol-1-yl)Pyridothienotriazolopyrimidines." Journal of Chemical Research 2005, no. 11 (2005): 736–40. http://dx.doi.org/10.3184/030823405774909298.

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A series of the hydrazones were prepared by the reaction of 4-hydrazino-7,9-dimethylpyrido[3′,2′:4,5]thieno [2,3-d]pyrimidine (1) with monosaccharides, and their acetylation was studied. The oxidative cyclisation of the hydrazones 3a–c gave 3-(Alditol-1-yl)-pyridothienotriazolopyrimidenes 5a–c, whose acetylation was carried out. Also, oxidative cyclisation of arylidenes 7a,b gave the pyridothienotriazolopyrimidines 8a,b.
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Gouda, Moustafa. "LiOH.H2O as a catalyst for Knoevenagel and Gewald reactions." Polish Journal of Chemical Technology 12, no. 4 (2010): 31–35. http://dx.doi.org/10.2478/v10026-010-0046-6.

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LiOH.H2O as a catalyst for Knoevenagel and Gewald reactions Commercial available lithium hydroxide monohydrate LiOH.H2O was found to be a novel ‘dual activation’ catalyst for tandem cross Knoevenagel condensation between malononitrile or ethylcyanoacetate and aromatic aldehydes leading to an efficient and easy synthesis of the corresponding arylidenes at room temperature in a short reaction time. In the case of salicyaldehyde the reaction lead to the formation of 3-substituted coumarins. The high efficacy, cheapness and easy availability of LiOH.H2O prompted us to investigate its validity as a
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Sonia, George, Knolin K. Thachil, Manoj Kumar Parameswaran, and Ravi Thengungal Kochupappy. "Synthesis of some benzoxazinyl pyrazolone arylidenes as potent antimicrobials and antioxidants." Medicinal Chemistry Research 23, no. 3 (2013): 1320–26. http://dx.doi.org/10.1007/s00044-013-0719-9.

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Kohli, P., S. D. Srivastava, and S. K. Srivastava. "Synthesis and Biological Activity of Mercaptobenzoxazole Based Thiazolidinones and Their Arylidenes." Journal of the Chinese Chemical Society 54, no. 4 (2007): 1003–10. http://dx.doi.org/10.1002/jccs.200700144.

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El-Haty, M. T., A. E. Mohamed, F. A. Adam, and A. A. Gabr. "Spectral behaviour and acidity constants of some arylidenes—2-amino-1,3-pyrimidine." Spectrochimica Acta Part A: Molecular Spectroscopy 46, no. 12 (1990): 1743–49. http://dx.doi.org/10.1016/0584-8539(90)80246-u.

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El-Haty, MohamedT, AdilaE Mohamed, FaroukA Adam, and AzzaA Gabr. "Spectral behaviour and acidity constants of some arylidenes—2-amino-1,3-pyrimidine." Spectrochimica Acta Part A: Molecular Spectroscopy 47, no. 1 (1991): 149. http://dx.doi.org/10.1016/0584-8539(91)80187-n.

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Dissertations / Theses on the topic "Arylidenes"

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Repasky, Paul J. "Novel Trisubstituted Arylidene Oxindoles with Potent Anti-Apoptotic Properties." Wright State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=wright1310326721.

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Cersosimo, Ulma. "Synthesis and Pro-apoptotic activity of Arylidene-Cyclo-Alkanones." Doctoral thesis, Università degli studi di Trieste, 2010. http://hdl.handle.net/10077/3519.

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2008/2009<br>Screening of a small chemical library (the Developmental Therapeutics Program-National Cancer Institute "challenge set") on cells expressing mutated caspase-9, allowed the identification of two compounds, named G5 (3,5-bis(4-nitro-benzyliden)-tetrahydrothiapyran-4-one-1,1-dioxide) and F6 (3,5-bis(4-methyl-benzyliden)-4-piperidone hydrochloride) (Fig. 1), capable of activating caspases and to induce cell death with an apoptosome-independent apoptotic pathway. G5 and F6 are typified by a cross-conjugated α,β-unsatured dienone with two sterically accessible electrophilic β-carbons ,
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Knisley, Kyle James. "Libraries from Libraries Approach to the Synthesis of Arylidene Oxindoles." Wright State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=wright1388766101.

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Zoto, Christopher A. "Structural and Photophysical Properties of Internal Charge Transfer 2-Arylidene and 2,5-Diarylidene Cyclopentanones." Digital WPI, 2012. https://digitalcommons.wpi.edu/etd-dissertations/330.

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" A series of symmetric and asymmetric 2-arylidene and 2,5-diarylidene cyclopentanone dyes have been synthesized. Their electronic absorption and fluorescence spectra have been measured in a wide variety of nonpolar and polar, aprotic and protic solvents. Absorption and fluorescence spectral maxima have been correlated with the ET(30) empirical solvent polarity scale. Lippert-Mataga analysis (in aprotic solvents) demonstrates the increase in the electronic dipole moment from the ground singlet to excited singlet states, consistent with the internal charge transfer (ICT) nature of the S0 --
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Almassan, Maha. "Etude cinétique, spectrométrique et radiocristallographique des produits de condensation entre des esters thioglycoliques et des 3-arylidene-chromanones." Besançon, 1991. http://www.theses.fr/1991BESA2003.

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Zhang, Saisai. "Ιnnovative [C-Χ/C-Η]-type palladium-catalyzed dοmino reactions on 4,4'-arylidene imidazolones : new access to rigidified GFΡ-analogs fluorophores". Electronic Thesis or Diss., Normandie, 2025. http://www.theses.fr/2025NORMIR11.

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L'imidazolone, un composé hétérocyclique important, a attiré une grande attention en raison de ses propriétés optiques uniques, et sa synthèse a toujours été un point d’intérêt en recherche. Depuis plusieurs décennies, la réaction C-X/C-H catalysée par le palladium a été largement étudiée. Cependant, aucun cas de stratégie de rigidification par cyclisation d'imidazolone [C(Ar)X-C(4)] via un couplage domino C-X/C-H catalysé par le palladium n'a été rapporté, en tant que création tardive de contrainte structurelle. Cette nouvelle stratégie représente une opportunité précieuse et une nouvelle dir
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Jadhav, V. H. "New 2-arylidene tetralone, 5-hydroxycyclopentenone derivatives with potential anticancer activity; furanone and azole derivatives as antifungal agents and some organic transformations." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2007. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2611.

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Ambeu, N'ta Christelle. "Synthèse d'analogues de la pentamidine porteurs de plateformes hétérocycliques (rhodanine, benzimidazole, pyrazole et imidazole) et leurs évaluations biologiques." Thesis, Rennes 1, 2015. http://www.theses.fr/2015REN1S137/document.

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Ce manuscrit de thèse concerne le développement d'une stratégie de synthèse multi-étapes de nouveaux composés comportant plusieurs plateformes hétérocycliques (rhodanine, benzimidazole, pyrazole et imidazole) à visée thérapeutique multiple contre la malaria, la leishmaniose, le cancer et les maladies neurodégénératives. Les pharmacomodulations de ces composés ont été élaborées sur la base du modèle de la pentamidine 35 comportant 2 motifs benzamidines (parties « Ouest » et « Est »). En effet, la substitution de sa partie « Ouest » par une plateforme rhodanine ou benzimidazole et de sa partie «
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Kerbal, Abdelali. "Cycloaddition de diarylnitrilimines et d'azides sur diverses énones et énamines dérivées d'indadones et de tétralones : Regiochimie, diasteréochimie et transformation des cycloadduits." Besançon, 1988. http://www.theses.fr/1988BESA2038.

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La cycloaddition dipolaire-1,3 des diarylnitrilimines sur diverses enones a double-liaison dipolarophile juxtacyclique est regiospecifique. Lorsque le dipolarophile présente deux faces diastereotopiques, l'approche dipole-dipolarographie se fait du côté le moins encombré : - de façon diastereospecifique sur les enones dérivées de l'indanone-1 substituée ou de la tetralone-1 substituée lorsque ces dernières portent en -3 ou -4 un substituant occupant une position axiale - de facon diastereoselective sur les enones dérivées de la tetralone-1 portant un substituant en -4 qui peut adopter une disp
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陳允中. "螢光蛋白質吸收基團類似物 4-Arylidene-5-imidazolinones 的簡易合成". Thesis, 2011. http://ndltd.ncl.edu.tw/handle/58394697021635601108.

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Book chapters on the topic "Arylidenes"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cerium(III) complex with arylidene Schiff-base." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_331.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cerium(III) complex with arylidene Schiff-base." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_330.

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Larsen, R. D., and D. Cai. "From Arylidene -Arylamines." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00737.

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Lindsley, C. W., and M. E. Layton. "Cyclization of Bis(arylidene)- or Bis(alkylidene)acetone Diaminomethylenehydrazones." 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-017-00568.

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Levai, Albert, Erzsebet Patonay-Peli, Tamas Patonay, and Gabor Tóth. "Substrate-specific reactions of dibromides of α-arylidene-benzocyclanones with azide nucleophile." In Advances in Organobromine Chemistry II. Elsevier, 1995. http://dx.doi.org/10.1016/s0926-9614(05)80019-x.

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Aravind, S., T. Somasekhar, T. Kiran Kumar, et al. "Preparation and Antimicrobial Evaluation of N'-arylidene-3-(4-phenyloxazol-2 yl)propanehydrazides." In Recent Developments in Chemistry and Biochemistry Research Vol. 5. B P International, 2024. http://dx.doi.org/10.9734/bpi/rdcbr/v5/1418.

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S., Christos, Dimitris Matiadis, John Markopoulos, and Olga Igglessi-Markopoulou. "Homogeneous Chemoselective Hydrogenation of Heterocyclic Compounds – The Case of 1,4 Addition on Conjugated C-C and C-O Double Bonds of Arylidene Tetramic Acids." In Hydrogenation. InTech, 2012. http://dx.doi.org/10.5772/48739.

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Conference papers on the topic "Arylidenes"

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Stanić, Petar B., Biljana Šmit, Jovana Muškinja, et al. "Normal and Reversed Phases Thin-Layer Chromatography of Arylidene 2- Thiohydantoin Derivatives." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.531s.

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In this paper, the retention behavior of thirteen newly synthesized arylidene derivatives of 2-hydamthione was investigated by normal and reversed phases thin-layer chromatography. In normal phase chromatography, thin layers of silica gel and cyano-propyl (CN) silica gel with fluorescent indicator F254 were used as the stationary phase. As the mobile phase, binary systems of non-aqueous solvents benzene-ethyl acetate and hexane-ethyl acetate were used, 8:2 (v/v). Reversed phase chromatography was performed using a thin layer of octadecyl (C-18) silica gel with fluorescent indicator F254 as the
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Bezsonova, E., M. Dubar, D. Melekhina, К. Evdokimov, V. Klochkov, and E. Sokolova. "3-ARYLIDENE-2-OXINDOLES AS QUINONE REDUCTASE II INHIBITORS." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-392.

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Kotlovanov, A. A., K. L. Obydennov, and T. V. Glukhareva. "The synthesis of new 5-arylidene-4-oxothiazolidin-2-ylideneethanethioamides." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087362.

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Krivoshey, Alexander I., Lidiya A. Kutulya, Natalia I. Shkolnikova, and Nikolay S. Pivnenko. "Arylidene derivatives of 3R-methylcyclohexanone as chiral dopants for induced cholesterics." In SPIE Proceedings, edited by Galyna O. Puchkovska, Tatiana A. Gavrilko, and Olexandr I. Lizengevich. SPIE, 2004. http://dx.doi.org/10.1117/12.569830.

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Chepeleva, L. V., A. O. Doroshenko, Lidiya A. Kutulya, T. G. Drushlyak, N. S. Pivnenko, and Valery V. Vashchenko. "Photochemical transformations of 2-arylidene-menthanones: chiral dopants for liquid crystalline systems." In SPIE Proceedings, edited by Gertruda V. Klimusheva, Andrey G. Iljin, and Sergey A. Kostyukevych. SPIE, 2003. http://dx.doi.org/10.1117/12.545805.

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Zou, Qianli, Hongyou Zhao, Yuxia Zhao, Ying Wang, Ying Gu, and Feipeng Wu. "Polyethylene glycol-functionalized bis(arylidene)cycloalkanone photosensitizers for two-photon excited photodynamic therapy." In Photonics Asia, edited by Qingming Luo, Ying Gu, and Xingde D. Li. SPIE, 2012. http://dx.doi.org/10.1117/12.999874.

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Barcelos, R. C., L. C. A. Barbosa, C. R. A. Maltha, A. J. Demuner, A. Donà, and G. Forlani. "Synthesis of 4-Aryl-5-arylidene-3-bromofuran-2(5H)-one Rubrolides Analogues." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0343-1.

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Marques, M. Matilde, Mohamed Mahgoub, Awatef Elmaghraby, et al. "Synthesis and characterization of 2-arylidene derivatives of thiazolopyrimidines with potential biological activity." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-b008.

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Stanić, Petar, Darko Ašanin, Marijana Vasić, Tanja Soldatović, and Biljana Šmit. "KINETICS OF THE REACTION OF AN ARYLIDENE 2-THIOHYDANTOIN DERIVATIVE WITH SOME Pd(II) COMPLEXES." In 1st INTERNATIONAL SYMPOSIUM ON BIOTECHNOLOGY. University of Kragujevac, Faculty of Agronomy, 2023. http://dx.doi.org/10.46793/sbt28.497s.

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Reactions of 3-(benzylideneamino)-2-thioxoimidazolidin-4-one with some palladium complexes (PdCl2, Pd(DMSO)2Cl2 and K2PdCl4) were monitored with NMR spectroscopy, which is used as a convenient and practical tool for determining the kinetic parameters of the reactions. Rate constants of the reactions were determined and reactivity of the complexes towards the 2-thiohydantoin derivative was compared.
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Pivnenko, Nikolay S., Alexander I. Krivoshey, Lidiya A. Kutulya, and V. I. Musatov. "Smectogenic C* 2,6-bis-arylidene derivatives of 3(R)-ethylcyclohexanone exhibiting inversion of spontaneous polarization sign." In SPIE Proceedings, edited by Galyna O. Puchkovska, Tatiana A. Gavrilko, and Olexandr I. Lizengevich. SPIE, 2004. http://dx.doi.org/10.1117/12.569834.

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