Academic literature on the topic '-(benzylideneamino)- 2'

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Journal articles on the topic "-(benzylideneamino)- 2"

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Shrivastava, Shobhit, and Dharmendra Ahuja. "Synthesis, Characterization and Antimicrobial Activity of Some Novel Mannich Bases of Indole-2,3-dione." Asian Journal of Chemistry 35, no. 5 (2023): 1183–88. http://dx.doi.org/10.14233/ajchem.2023.27738.

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Indole-2,3-dione (isatin) and its 5-substituted derivatives have been reacted with N2-benzylidenepyridine-2,6-diamine to form Schiff bases and the Mannich bases of these compounds were synthesized by reacting them with some secondary amines in presence of formaldehyde. Their chemical structures have been confirmed by mean of their IR and 1H NMR. Antimicrobial screening of synthesized compounds was done by well diffusion method against 4 pathogenic bacteria and 2 pathogenic fungi. Amongst the tested compounds 3-{[6-(benzylideneamino)pyridin-2-yl]imino}-1- (piperazin-1-ylmethyl)-5-fluoro-indolin
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Wang, Yong, Shanshan Shi, Yanhua Han, and Guo-Dong Wei. "Bis[2-(benzylideneamino)phenyl] disulfide." Acta Crystallographica Section E Structure Reports Online 67, no. 12 (2011): o3364. http://dx.doi.org/10.1107/s1600536811048239.

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Khan, Muhammad Naeem, Misbahul Ain Khan, Noreen Aslam, Pir Bakhsh Khan, and Ehsan ul Haq. "Tetracyclic Heteroaromatic Systems-Synthesis of Ethoxycarbonylphenylpyrido[3',2':5,6] Thiopyranoquinolines." Pakistan Journal of Scientific & Industrial Research Series A: Physical Sciences 64, no. 3 (2021): 191–94. http://dx.doi.org/10.52763/pjsir.phys.sci.64.3.2021.191.194.

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7-benzylideneamino-5H-thiochromeno[2,3-b]pyridin-5-ones and 9-benzylideneamino-5H-thio- chromeno[2,3-b]pyridin-5-ones, on reaction with ethyl pyruvate to afford 1-ethoxycarbonyl-3-phenyl-12H- pyrido[3',2':5,6]thiopyrano[3,2-f]quinoline-12-ones and 4-ethoxycarbonyl-2-phenyl-7H- pyrido[3',2':5,6]thiopyrano[3,2-h]quinoline-7-ones respectively by the two different methods. These products were precipitated by addition of ethanol, water (1:1), were purified by recrystalizing from appropriate solvents and were characterized from their IR, 1H-NMR, mass spectra and elemental analysis data.
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Varsha, G., V. Arun, Manju Sebastian, P. Leeju, Digna Varghese, and K. K. M. Yusuff. "(Z)-2-Amino-3-[(E)-benzylideneamino]but-2-enedinitrile." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o919. http://dx.doi.org/10.1107/s1600536809010873.

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Karadağ, Aslı Tosyalı, Şehriman Atalay, and Hasan Genç. "2-[(E)-2-Hydroxy-5-(trifluoromethoxy)benzylideneamino]-4-methylphenol." Acta Crystallographica Section E Structure Reports Online 67, no. 1 (2010): o95. http://dx.doi.org/10.1107/s1600536810050579.

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Khlebnikov, A. F., E. I. Kostik, and R. R. Kostikov. "Reaction of dihalocarbenes with 2-(benzylideneamino)pyridines. Cyclization of 2-(benzylideneamino)pyridinium dihalomethylids to give 2-aryl-3-haloimidazo[1,2-?]pyridines." Chemistry of Heterocyclic Compounds 27, no. 6 (1991): 636–42. http://dx.doi.org/10.1007/bf00472515.

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Vennila, M., G. Manikandan, V. Thanikachalam, and J. Jayabharathi. "Non-Isothermal Decomposition of 2-(2-Hydroxybenzylideneamino)-3-phenylpropanoic Acid in Nitrogen Atmosphere." E-Journal of Chemistry 8, no. 2 (2011): 819–29. http://dx.doi.org/10.1155/2011/235090.

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The non-isothermal decomposition properties of 2-(2-hydroxy- benzylideneamino)-3-phenylpropanoic acid [HBAPPA] have been studied using microanalysis, FT-IR, UV, DTA, DTG and TG techniques. The TG studies were carried out at different heating rates of 10, 15 and 20 K/min. The Schiff base decomposed in three stages. The kinetic parameters were deduced for each stage. A probable mechanism has been proposed for the decomposition process.
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Deohate, Pradip P., and Roshani S. Mulani. "Microwave Irradiative Synthesis of Triazine Substituted Pyrazoles and Study of Antitubercular and Antimicrobial Activities." Asian Journal of Chemistry 31, no. 5 (2019): 1087–90. http://dx.doi.org/10.14233/ajchem.2019.21826.

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Microwave irradiative synthesis of triazine substituted pyrazoles i.e. (4-benzylideneamino-6-methyl-[1,3,5]-triazin-2-yl)-(5-methyl-2-substituted benzoyl/isonicotinoyl/cinnamoyl-pyrazol-3-yl)-amines have been achieved by the cyclocondensation of N-(4-benzylideneamino-6-methyl-[1,3,5]-triazin-2-yl)-3-oxo butyramide with substituted acid hydrazides. Synthesis of required butyramide was done by reacting 2,4-diamino-6-methyl-[1,3,5]-triazine with benzaldehyde and then condensing the product with ethyl acetoacetate. Structural investigation of synthesized compounds has been done by chemical transfo
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Akerman, Matthew P., and Sarah J. Maher. "(E)-2,3-Bis[(E)-benzylideneamino]but-2-enedinitrile." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (2012): o688. http://dx.doi.org/10.1107/s1600536812005363.

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Balcázar, J. L., F. Florencio та S. García-Blanco. "Structure of 2-[α-(methylthio)benzylideneamino]-2-phenyl-1,1-ethylenedicarbonitrile". Acta Crystallographica Section C Crystal Structure Communications 41, № 12 (1985): 1795–97. http://dx.doi.org/10.1107/s0108270185009490.

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Book chapters on the topic "-(benzylideneamino)- 2"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chelate of 3-(2-hydroxy-5-chloro-benzylideneamino)-5-methylisoxazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_519.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chelate of 3-(2-hydroxy-5-bromo-benzylideneamino)-5-methylisoxazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_520.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chelate of 3-(2-hydroxy-5-chloro-benzylideneamino)-5-methylisoxazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_212.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chelate of 3-(2-hydroxy-5-bromo-benzylideneamino)-5-methylisoxazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_213.

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Conference papers on the topic "-(benzylideneamino)- 2"

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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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