Relevant bibliographies by topics / Arylidene compounds

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

Academic literature on the topic 'Arylidene compounds'

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

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Journal articles on the topic "Arylidene compounds"

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Shah, Shalini K., and Anju Goyal. "Synthesis and Biological Evaluation of Some Novel Arylidene Hydrazides Derivatives." Asian Pacific Journal of Health Sciences 9, no. 4 (2022): 203–9. http://dx.doi.org/10.21276/apjhs.2022.9.4s.39.

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There has been considerable interest in the development of novel compounds with anticonvulsant, antioxidant, antibacterial, and antifungal activities. The present study explores the antimicrobial activity of some new arylidene hydrazide derivatives and correlates the effect on the antimicrobial potency by varying the substituents on hydrazide part of the arylidine hydrazide. Hydrazones possessing an azomethine–NHN=CH- proton constitute an important class of compounds for new drug developments; therefore, a series of arylidene hydrazides were synthesized with various aromatic aldehydes/ketones.
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Kouzi, Olympia, Eleni Pontiki, and Dimitra Hadjipavlou-Litina. "2-Arylidene-1-indandiones as Pleiotropic Agents with Antioxidant and Inhibitory Enzymes Activities." Molecules 24, no. 23 (2019): 4411. http://dx.doi.org/10.3390/molecules24234411.

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Indandiones are a relatively new group of compounds presenting a wide range of biological activities. The synthesis of these compounds was performed via a Knoevenagel reaction between an aldehyde and 1,3-indandione and were obtained with a yield up to 54%. IR, 1H-Nucleic Magnetic Resonance (NMR), 13C-NMR, LC/MS ESI+ and elemental analysis were used for the confirmation of the structures of the novel derivatives. Lipophilicity values of compounds were calculated theoretically and experimentally by reversed chromatography method as values RM. The novel derivatives were studied through in vitro a
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Guarda, V. L. M., C. Bosso, S. L. Galdino, et al. "Mass spectrometry of some arylidene thioxobenzyl or thioxobiphenyloxoethyl thiazolidinone compounds." Spectroscopy 18, no. 4 (2004): 613–19. http://dx.doi.org/10.1155/2004/175870.

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This paper reports the results of a comparative study of the electron impact mass spectrometry data for a series of previously synthetized 5-arylidene-3-(4-chloro-benzyl)-4-thioxo-thiazolidin-2-one, and 5-arylidene-3-(2-biphenyl-4-yl-2-oxo-ethyl)-4-thioxo-thiazolidin-2-one derivatives. Theoretical calculations of molecular mechanics, MOPAC‒AM1, were used to explain the fragmentations observed.
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Husain, Asif, Mumtaz Alam, and Nadeem Siddiqui. "Synthesis, reactions and biological activity of 3-arylidene-5-(4-methylphenyl)-2(3H)-furanones?" Journal of the Serbian Chemical Society 74, no. 2 (2009): 103–15. http://dx.doi.org/10.2298/jsc0902103h.

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3-Arylidene-5-(4-methylphenyl)-2(3H)-furanones 2a-m were prepared from 3-(4-methyl-benzoyl)propanoic acid 1 and several aromatic aldehydes. Some of the selected furanones were reacted with ammonia gas and benzylamine to give corresponding 3-arylidene-1,3-dihydro-5-(4-methylphenyl)-2H-pyrrol- 2-ones 3a-h and 3-arylidene-1-benzyl-1,3-dihydro-5-(4-methylphenyl)-2H- -pyrrol-2-ones 4a-f, respectively, which were characterized on the basis of IR, 1H-NMR, mass spectral data and elemental analysis results. These compounds were tested for their anti-inflammatory and antibacterial activities. The compou
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Basavaiah, Deevi, and Daggula Mallikarjuna Reddy. "The Baylis–Hillman acetates in organic synthesis: Unprecedented sodium nitrite induced intramolecular Friedel–Crafts cyclization of secondary nitro compounds." RSC Adv. 4, no. 46 (2014): 23966–70. http://dx.doi.org/10.1039/c4ra03573a.

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Unprecedented sodium nitrite mediated intramolecular Friedel–Crafts cyclization of alkyl (E)-2-arylidene-4-nitroalkanoates and (E)-3-arylidene-5-nitroalkan-2-ones derived from Baylis–Hillman acetates has been described.
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N. R., Mohame, El-Saidi M. M. T., Abdel Aziz S . A., and Zayed M. F. "The Behaviour of Arylidene Barbituric Acid and Cyclohexadione Derivatives Towards Tris(dimethy1amino)phosphin." Scientia Pharmaceutica 70, no. 2 (2002): 147–63. http://dx.doi.org/10.3797/scipharm.aut-02-17.

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Tris(dimethy1amino)phosphine 1 reacted with phenylarylidene barbituric acids 4 to yield the triaminophosphonium dipolar ion adduct 7. 2-Arylidene-1,3- cyclohexanedione 5 and 2-Arylidene-5,5-dimethylcyclohaxane1-,3 -diones 6 reacted with phosphine 1 to produce the dioxyxanthenes 10 and 12, respectively. Structural assignments are based on analytical, chemical, and spectroscopic evidences. A mechanism is proposed to explain the formation of these compounds. The biological acitivity of the new synthesized compounds against Aphis Craccivora, a serious pest infecting many crops in Egypt, was studie
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Brito, Vanessa, Gilberto Alves, Paulo Almeida, and Samuel Silvestre. "Highlights on Steroidal Arylidene Derivatives as a Source of Pharmacologically Active Compounds: A Review." Molecules 26, no. 7 (2021): 2032. http://dx.doi.org/10.3390/molecules26072032.

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Steroids constitute a unique class of chemical compounds, playing an important role in physiopathological processes, and have high pharmacological interest. Additionally, steroids have been associated with a relatively low toxicity and high bioavailability. Nowadays, multiple steroidal derivatives are clinically available for the treatment of numerous diseases. Moreover, different structural modifications on their skeleton have been explored, aiming to develop compounds with new and improved pharmacological properties. Thus, steroidal arylidene derivatives emerged as a relevant example of thes
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8

Özdemir, Ahmet, Sevtem Gökbulut, Belgin Sever, Gülşen A. Çiftçi, and Mehlika D. Altıntop. "Synthesis and Evaluation of a New Series of Arylidene Indanones as Potential Anticancer Agents." Anti-Cancer Agents in Medicinal Chemistry 18, no. 10 (2019): 1394–404. http://dx.doi.org/10.2174/1871520618666171206111923.

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Background: Arylidene indanones have attracted a great deal of interest due to their outstanding therapeutic applications. In particular, considerable research has pointed out the importance of arylidene indanones in the field of cancer research. Objective: The aim of the current work was to design and synthesize arylidene indanone-based anticancer agents. Method: New arylidene indanones were obtained via the Claisen-Schmidt condensation of 5-chloro-6-methoxy- 2,3-dihydro-1H-inden-1-one with p-substituted benzaldehyde derivatives. MTT assay was performed to evaluate their cytotoxic effects on
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Allahyani, Mamdouh, Mazen Almehmadi, Osama Abdulaziz, et al. "Synthesis and in vitro antimicrobial screening of some 5-methyl-2-substituted phenyl-3- (phenylsulfonyl)thiazolidin-4-ones." INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 34, no. 04 (2024): 499. https://doi.org/10.59467/ijhc.2024.34.499.

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The synthesis of some new thiazolidine-sulfonamide derivatives was achieved in two steps. In the first step, appropriate aryl aldehyde reacted with benzene sulfonamide to yield N-arylidene benzene sulfonamide derivatives (1a-h). In the second step, compounds (1a-h) reacted with thiolactic acid to give the 5-methyl-2-substituted phenyl-3-(phenylsulfonyl) thiazolidin-4-one derivatives (2a-h). The compounds 2a-h were screened for their in vitro antimicrobial activity by agar disc diffusion method. The results showed that compounds 2b, 2c, and 2d exhibited anti-microbial activity against the teste
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Dabholkar, Vijay, and Faisal Ansari. "Synthesis and characterization of selected fused isoxazole and pyrazole derivatives and their antimicrobial activity." Journal of the Serbian Chemical Society 74, no. 11 (2009): 1219–28. http://dx.doi.org/10.2298/jsc0911219d.

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New potent antibacterials, fused isoxazole and pyrazole derivatives, were synthesized using 5,5-dimethylcyclohexane-1,3-dione (1) and 3-[(4-chlorobenzylidene) amino]-2-thioxoimidazolidin-4-one (2) as synthons. Aromatic aldehydes on condensation with 1 and 2 gave 2-arylidene-5,5-dimethylcyclohexane- 1,3-dione (3) and 5-arylidene-3-[(4-chlorobenzylidene)amino]-2-thioxoimidazolidin-4-one (4), respectively. Compounds 3 and 4 were forced to undergo heterocyclization reaction with nucleophilic reagents to give the title compounds. The newly synthesized heterocyles (5-8) were characterized based on t
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Dissertations / Theses on the topic "Arylidene compounds"

1

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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Book chapters on the topic "Arylidene compounds"

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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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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 "Arylidene compounds"

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"Synthesis and Characterization of a New Series of Arylidene Compounds from 2-Iminothiazolidine-4-one derivatives." In 5th International Conference on Applied Science Energy and Environment. Ishik University, 2018. http://dx.doi.org/10.23918/icasee2018.18.

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Popova, E. V., Lidiya A. Kutulya, V. V. Vashchenko, Mikhail N. Pivnenko, A. I. Krivoshey, and A. P. Fedoryako. "Ferroelectric liquid crystal mixtures containing chiral ether and ester compounds with the 2-arylidene-p-menthan-3-one skeleton." In XIV Conference on Liquid Crystals, Chemistry, Physics, and Applications, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, and Jerzy Zielinski. SPIE, 2002. http://dx.doi.org/10.1117/12.472142.

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