Relevant bibliographies by topics / Phenyl compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Phenyl compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 July 2024

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Journal articles on the topic "Phenyl compounds"

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Hussain, Sabir, Jyoti Sharma, and Mohd Amir. "Synthesis and Antimicrobial Activities of 1,2,4-Triazole and 1,3,4-Thiadiazole Derivatives of 5-Amino-2-Hydroxybenzoic Acid." E-Journal of Chemistry 5, no. 4 (2008): 963–68. http://dx.doi.org/10.1155/2008/924734.

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Various 4-amino-2-[4-(4-substituted phenyl)-5-sulfanyl-4H-1,2,4-triazol-3-yl] phenol (4a-c), 4-amino-2-{4-amino-5-[(4-substituted phenyl)amino]-4H-1,2,4-triazol-3-yl} phenol (5a-c) and 4-amino-2-{5-[(4-substituted phenyl)amino]-1,3,4-thiadiazole-2-yl} phenol (6a-g) were synthesized and evaluated for their antibacterial and antifungal activity. The compounds showed significant antibacterial activity againstS. aureus(gram-positive) andE.coli(gram-negative) bacteria and antifungal activity againstA. nigerfungi using cup plate technique
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Deli, József, Tamás Lóránd, Dezsö Szabó, András Földesi, and Adolf Zschunke. "Synthesis of 2-amino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydro- and -5,6,7,8-tetrahydroquinazoline derivatives." Collection of Czechoslovak Chemical Communications 50, no. 7 (1985): 1602–10. http://dx.doi.org/10.1135/cccc19851602.

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Base-catalyzed reaction of 2,6-dibenzylidenecyclohexanone and alkylguanidines gave 2-alkylamino-8-benzylidene-4-phenyl-3,4,5,6,7,8-hexahydroquinazolines IVa-c, which were oxidized to 2-alkylamino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazolines Va-c. The acylamino (VIa-c, VIIa-d, IXa,b) and diacylamino derivatives (VIIIa,b) of the 2-amino-8-benzylidene-4-pheny]-3,4,5,6,7,8-hexahydroquinazoline (II), 2-amino-8-benzylidene-4-phenyl-5,6,7,8-tetrahydroquinazoline (III) and compounds Va-c have also been prepared. These compounds having the E-configuration were converted into the Z isomers XIIa
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Ho, Boon Kui, Zainab Ngaini, Paul Matthew Neilsen, et al. "Synthesis and Anticancer Activities of 4-[(Halophenyl)diazenyl]phenol and 4-[(Halophenyl)diazenyl]phenyl Aspirinate Derivatives against Nasopharyngeal Cancer Cell Lines." Journal of Chemistry 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/6760413.

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Aspirin and azo derivatives have been widely studied and have drawn considerable attention due to diverse biological activities. In this study, a series of 4-[(halophenyl)diazenyl]phenyl aspirinate derivatives were synthesized from the reaction of aspirin with 4-[(halophenyl)diazenyl]phenol via esterification, in the presence of DCC/DMAP in DCM with overall yield of 45–54%. 4-[(Halophenyl)diazenyl]phenol was prepared prior to esterification from coupling reaction of aniline derivatives and phenol in basic solution. All compounds were characterized using elemental analysis, FTIR, and 1H and 13C
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Journal, Baghdad Science. "Preparation of some azo compounds by diazotization and coupling of 2- amino -5 – thiol -1,3,4- thiadizaole." Baghdad Science Journal 4, no. 2 (2015): 271–75. http://dx.doi.org/10.21123/bsj.4.2.271-275.

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2- amino -5- thiol-1,3,4- thiadiazole (S1) was prepared by cyclic locking of thiosemicarbazide in the presence of anhydrous sodium carbonate and CS2. diazotization of (S1) compound gave diazonium salt (S2) that reacts with different activated aromatic compounds to get the following azo compounds ,2 [(4- aminophenyl) diazenyl ] 1,3,4- thiazdiazole-5- thiol (S3) ,2-[4-amino- 1-naphthyl diazenyl] -1,3,4 – thiazdiazole-5-thiol (S4) , 3-amino-4-[(5- mercapto -1,3,4- thiadiazole -2-yl) diazenyl ] phenol(S5) ,1-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] -2-naphthol (S6) , 5-{[4-(dimethylamino) ph
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Saleh, Mohammad M., and Suhair S. Dauood. "Preparation of some azo compounds by diazotization and coupling of 2- amino -5 – thiol -1,3,4- thiadizaole." Baghdad Science Journal 4, no. 2 (2021): 271–75. http://dx.doi.org/10.21123/bsj.2007.4.2.271-275.

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2- amino -5- thiol-1,3,4- thiadiazole (S1) was prepared by cyclic locking of thiosemicarbazide in the presence of anhydrous sodium carbonate and CS2. diazotization of (S1) compound gave diazonium salt (S2) that reacts with different activated aromatic compounds to get the following azo compounds ,2 [(4- aminophenyl) diazenyl ] 1,3,4- thiazdiazole-5- thiol (S3) ,2-[4-amino- 1-naphthyl diazenyl] -1,3,4 – thiazdiazole-5-thiol (S4) , 3-amino-4-[(5- mercapto -1,3,4- thiadiazole -2-yl) diazenyl ] phenol(S5) ,1-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] -2-naphthol (S6) , 5-{[4-(dimethylamino) ph
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Janam Singh, Ram, and Dharmendra Kumar Singh. "Syntheses of Some 3,5-Diaryl-4H-1,2,4-triazole Derivatives and their Antifungal Activity." E-Journal of Chemistry 6, s1 (2009): S219—S224. http://dx.doi.org/10.1155/2009/925964.

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Syntheses of a series of 3, 5-diaryl-4H-1, 2, 4-triazole derivatives are described. In this present work, 4-amino-3-phenyl-5-p-tolyl-4H-1,2,4-triazole(1) was converted toN,N’-bis[3-phenyl-5-p-tolyl-4H-1,2,4-triazolyl]-1,4-xylenediimine(2) and 3-Phenyl-5-p-tolyl-4-[4-methyl benzylidenamino]-4H-1,2,4-triazole (3) in good yields by treatment with aldehydes OHC-C6H4-CHO and Ar-CHO respectively. The compoundsN,N’-bis[3-phenyl-5-p-tolyl-4H-1,2,4-triazolyl]-1,4-xylenediimine (2) and 3-phenyl-5-p-tolyl-4-[4-methyl benzylidenamino]-4H-1,2,4-triazole (3) were reduced with NaBH4to afford the correspondin
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Ozer, Erdem Kamil, Miyase Gozde Gunduz, Ahmed El-Khouly, et al. "Synthesis of fused 1,4-dihydropyridines as potential calcium channel blockers." Turkish Journal of Biochemistry 43, no. 6 (2017): 578–86. http://dx.doi.org/10.1515/tjb-2016-0247.

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AbstractObjectiveThe aim of this study was to synthesize ten 1,4-dihydropyridine (DHP) derivatives in which substituted cyclohexane rings were fused to the DHP ring and to determine how different ester groups and the benzoyl substituent introduced in 4-phenyl ring affected their calcium channel blocking activity.MethodsA microwave-assisted one-pot method was applied for the synthesis of compound1–5according to a modified Hantzsch reaction. The benzoyl moiety was introduced in the 4-phenyl ring of these dihydropyridines by refluxing with benzoyl chloride in acetone in the presence of anhydrous
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Rajput, Chatrasal Singh, and Shiwani Singhal. "Synthesis, Characterization, and Anti-Inflammatory Activity of Newer Quinazolinone Analogs." Journal of Pharmaceutics 2013 (January 17, 2013): 1–7. http://dx.doi.org/10.1155/2013/907525.

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A series of 3-[2′-(Substitutedbenzylideneamino)phenyl]-2-methyl-6-substituted quinazolin-4-ones (5–10), 3-[2′-(3″-chloro-2″-oxo-4″-substitutedphenylazetidin-1″-yl)phenyl]-2-methyl-6-substitutedquinazolin-4-ones (11–16), and 3-[2′-(2″-substitutedphenyl-4″-oxo-1″,3″-thiazolidin-3″-yl)phentl]-2-methyl-6-substitutedquinazolin-4-ones (17–22) have been synthesized in the present study. The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, H1 NMR, and mass spectral data. All the newly synthesized compounds were screened for anti-inflammatory and analgesic a
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Journal, Baghdad Science. "Synthesized azodyes of 2-amino-1, 3, 4- thiadiazole - 5 - thiol." Baghdad Science Journal 8, no. 2 (2011): 269–73. http://dx.doi.org/10.21123/bsj.8.2.269-273.

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Several azo dyes were synthesized through coupling reaetion of some substituted phenols and B.naphthol with diazonium salt of 2- amino-1,3-4- thiadiazol -5- thiol. All the synthesized compounds during this work were characterized using some speetral data (F.TIRand UV)andM.P . 2-[4 --Hydroxy napthyl-azo ] -1,3,4-Thiadiazol -5-Thiol • 2- [2-- hydroxy –4- NO2 – phenyl- azo]- 1,3,4 - Thiadiazol –5-Thiol. • 2- [3--Amino-4-Hydroxy phenyl –azo]-1,3,4 - Thiadiazol –5-Thiol. . • 2-[2--Amino-4-Hydroxy phenyl -azo]-1,3,4 - Thiadiazol –5-Thiol . • 2- [3--Amino-6- Hydroxy phenyl -azo]-1,3,4 - Thiadiazol –5
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Vaghasiya, Yogesh, Rathish Nair, Mayur Soni, Shipra Baluja, and Sumitra Shanda. "Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine." Journal of the Serbian Chemical Society 69, no. 12 (2004): 991–98. http://dx.doi.org/10.2298/jsc0412991v.

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Schiff bases derived from 4-aminoantipyrine and vanillin were evaluated for their potential as antibacterial agents against some Gram positive and Gram negative bacterial strains. The antibacterial activity was studied against P. pseudoalcaligenes ATCC 17440, P. vulgaris NCTC 8313, C. freundii ATCC 10787 E. aerogenes ATCC 13048, S. subfava NCIM 2178 and B. megaterium ATCC 9885. The determination of the antibacterial activity was done using the Agar Ditsh method. The Schiff bases produced were: (1) 4-(4-hydroxy 3-methoxybenzylideneamino) -1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one [VV1]; (
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Dissertations / Theses on the topic "Phenyl compounds"

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Faleni, Nobathembu. "Inclusion behaviour of related organic host compounds." Thesis, Cape Peninsula University of Technology, 2007. http://hdl.handle.net/20.500.11838/739.

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Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2007<br>The inclusion behaviour of the two host compounds, 9-(4-methoxyphenyl)-9Hxanthen- 9-o1 (A1)• and 9-(4-methylphenyl)-9H-xanthen-9-o1 (A10) were investigated. These host compounds are large, bulky, rigid and they contain functionalities that allow them to selectively interact with other molecules, such as the guests in this work. The host molecules form inclusion complexes with small organic guest molecules. The host•••guest interactions are the interesting focus of this study. The host A1 included the guests
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Hopman, Martyn. "Organometallic compounds with bulky, phenyl-substituted, or derived donor-substituted ligands." Thesis, University of Sussex, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285105.

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Aprahamian, Steve Lawrence. "Rearrangement-displacement of aryl(chloromethyl)diphenylsilanes with nucleophiles /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487265555439529.

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Mizori, Farhad G. "Transmetallation from zirconium to boron : the synthesis and conjugate addition of mixed unsymmetrical tricoordinate organoboranes containing phenyl and methyl groups /." Diss., Connect to a 24 p. preview or request complete full text in PDF formate. Access restricted to UC campuses, 2004. http://wwwlib.umi.com/cr/ucsd/fullcit?p3138868.

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Tsay, Fuh-Rong. "Synthesis and 2-D NMR Analysis of a New Phenyl-Substituted Polycyclic Compound." Thesis, University of North Texas, 1991. https://digital.library.unt.edu/ark:/67531/metadc504049/.

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Diels-Alder [4+2] cycloaddition of a mixture of 1- and 2 methylcyclopentadiene to 2-phenyl-g.-benzoquinone affords a mixture of four nd cycloadducts. A single, isomerically pure cycloadduct was isolated by careful column chromatography. Stereospecific reduction of this material with sodium borohydride and cerium(III) chloride 'affords a single, isomerically pure tricyclic diol. The structures of the cycloadduct and this tricyclic diol, established via analysis of their one- and two-dimensionial NMR spectra, were shown to be (1-methyl-5-phenyltricyclo[6.2.1.02,7]undec a-4,9 diene-3,6-dione and
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Martin, Patricia. "Investigation of the synthesis and thermal rearrangements of 1,2,3,4,5-Pentaphenyl-2,4,-Cyclopentadiene Alkyl Ethers." Diss., Virginia Polytechnic Institute and State University, 1987. http://hdl.handle.net/10919/49858.

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A comparative synthetic study of a series of six 1,2,3,4,5-pentaphenyl-2,4-cyclopentadiene alkyl ethers was investigated. It was determined that the most efficient route to these ethers was not the most generally accepted route to ethers - the Williamson Reaction - but rather a solvolysis reaction between 1-bromo-1,2,3,4,5-pentaphenyl-2,4-cyclopentadiene and the appropriate alcohol. Thermal rearrangement of the ethers had been expected to rearrange by a [1,5]-sigmatropic shift of the phenyl group in the 1-position to yield the corresponding enol ether. However, this appeared to occur only as
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Wait, Simon Timothy. "The synthesis of poly(sulphur nitride) and some novel 4-phenyl-1,2,3,5-dithiadiazolium compounds." Thesis, Durham University, 1989. http://etheses.dur.ac.uk/6481/.

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[S(-5)N(_5)]Cl has been reacted with a wide variety of reducing agents leading to a new non-explosive route to high quality powdered (SN)x. Data collected from these reductions has led to a new mechanistic proposal for the formation of the powdered polymer. The vacuum thermolysis of [S(_5)N(_5)Cl with Li(_3)N produced S(_2)N(_2) in low yield. The new supporting electrolyte, [Bu(_4)N]AsF(_6), was prepared, and has a greater scanning window in SO(_2) compared with any others previously reported. S(_5)N(_5)ASF(_6) has been produced in high purity and is much less moisture and oxygen sensitive tha
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Eagan, Robert Lee. "Investigation of the steric and/or electronic effects associated with the (1,5)-sigmatropic rearrangement of 1-substituted-2,3,4,5-tetraphenyl- 2,4-cyclopentadien-1-ols." Diss., Virginia Polytechnic Institute and State University, 1986. http://hdl.handle.net/10919/74730.

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A series of eight l-substituted-2,3,4,5-tetraphenyl-2,4-cyclopentadien-l-ols were efficiently synthesized by the addition of the appropriate organometallic reagent to tetracyclone. It was determined that the steric and electronic nature of the migrating groups played a predictable role in the [l,5]-sigmatropic rearrangement of these compounds. Electron donating groups increased the rate of migration whereas electron withdrawing substituents were responsible for slowing the migration. Likewise, smaller groups accelerated the rate while bulky groups deterred the migration. Consequently, the expe
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Dunham, Jason C. "Synthesis of 4-alkyl-3,5-diamino-1-phenylpyrazoles." Virtual Press, 2006. http://liblink.bsu.edu/uhtbin/catkey/1339144.

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The goal of this project is to synthesize and purify a library of novel 4-alkyl-3,5-diamino-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoles. These molecules are similar to other fiproles, which have been shown by Sammelson et al. to have pesticidal activities at the GABA receptor.' Fiproles are analogues of Fipronil, a very important pesticide. Replacing the cyano group normally located at the 3-position of the pyrazole ring with an amino group will change the binding potency of the phenylpyrazoles. Changes in binding produced by the changes introduced in molecular structure can create more
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Al-Zubail, Saleh Abdullah. "An evaluation of efficiency of phenylenediamines as corrosion inhibitors for ASTM-A-179 steel in 1.0 N hydrochloric acid at room temperature." Ohio : Ohio University, 1986. http://www.ohiolink.edu/etd/view.cgi?ohiou1183039807.

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Books on the topic "Phenyl compounds"

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Molinarolo, William E. The high temperature alkaline degradation of phenyl B-D-glucopyranoside. Institute of Paper Chemistry, 1989.

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J, Sekizawa, World Health Organization, International Program on Chemical Safety., and Inter-Organization Programme for the Sound Management of Chemicals., eds. Triphenyltin compounds. World Health Organization, 1999.

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Wąsicki, Jan Wojciech. Dynamika molekularna kryształów rodziny polifenyli. Wydawn. Nauk. Uniwersytetu im. Adama Mickiewicza w Poznaniu, 1991.

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Wilfred, Vermerris. Phenolic compound biochemistry. Springer, 2006.

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Wilfred, Vermerris. Phenolic compound biochemistry. Springer, 2006.

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Wilfred, Vermerris. Phenolic compound biochemistry. Springer, 2006.

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Nicholas, David Henry. Complexation of borates by phenol-formaldehyde resins and related compounds. University of Birmingham, 1990.

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Juha, Kallas, and Lappeenrannan teknillinen korkeakoulu, eds. Treatment technology of wastewater containing phenols and phenolic compounds. Lappeenranta University of Technology, 1992.

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Corporation, Syracuse Research, Clement International Corporation, and United States. Agency for Toxic Substances and Disease Registry, eds. Toxicological profile for nitrophenols: 2-nitrophenol, 4-nitrophenol. The Agency, 1992.

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1951-, Shahidi Fereidoon, Ho Chi-Tang 1944-, and American Chemical Society. Division of Agricultural and Food Chemistry, eds. Phenolic compounds in foods and natural health products. American Chemical Society, 2005.

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Book chapters on the topic "Phenyl compounds"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of binuclear copper(II) chelate with 1-(2-hydroxy-phenyl)-3-phenyl-1,3-propanedione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_502.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of chromium bis{trimethylsilyl(phenyl)amidinate} complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_132.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with 6-(phenyl)thymine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_592.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 6-(phenyl)thymine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_304.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with l-3-phenyl-2-(3-phenyl-ureido)propionic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_57.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of titanium(III) phenyl supported by di(isopropyl) amide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_22.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) chloro complex with phenyl- diphenylphosphinate ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_372.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) bromo complex with phenyl- diphenylphosphinate ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_373.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) iodo complex with phenyl- diphenylphosphinate ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_374.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) thiocyanato complex with phenyl- diphenylphosphinate ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_375.

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Conference papers on the topic "Phenyl compounds"

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Kusumaningrum, Vivi Ambar, Ahmad Hanapi, Rachmawati Ningsih, Sri Ani Nafiah, and Ainun Nadhiroh. "Synthesis, Characterization, and Antioxidant Activity of 2-methoxy-4 - ((4-methoxy phenyl imino) -methyl) phenol compounds." In International Conference on Engineering, Technology and Social Science (ICONETOS 2020). Atlantis Press, 2021. http://dx.doi.org/10.2991/assehr.k.210421.042.

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Popusoi, Ana, Nicanor Barba, and Aurelian Gulea. "Synthesis of 1,3-Phenyl(Pyridyl)propenones with thiosemicarbazidic groups." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab03.

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The bibliographic study of chalcones of the type 1,3-aryl(heteryl)propen-2-one with thiosemicarbazidic 4- and 1,4-disubstituted and thisemicarbazonic groups respectively gives us the information that they have a wide spectrum of biological activity, but methods of their synthesis are less described in the literature, and they became our object of study. 4,5-Dihydro-1-H-(pyrazol-3-yl)phenylhydrazinecarbothioamides 3a and 3b were obtained according to the following scheme:Reagents and reaction conditions: i, ii) 2-Py, 25oC – 24h, 90-95oC – 3h, 77-82%; iii) DMF, CH3COOH, 70-80oC, 2-3h, 60-63%. Fi
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Simijonović, Dušica, Marko Antonijević, Edina Avdović, Zorica Petrović, and Zoran Marković. "INHIBITORY EFFECT OF COUMARIN BENZOYLHYDRAZONES ON MCL-1 PROTEIN." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.442s.

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The protein that controls cell differentiation in acute myeloid leukemia is MCL-1. High-level of this protein causes the carcinogenesis. In this paper inhibitory effect of two coumarin benzoylhydrazones,(E)-2-hydroxy-N’-(1-(2-oxo-2H-chromen-3-yl)ethylidene)benzohydrazide (A) and (E)-4-hydroxy-N’-(1-(2-oxo-2H-chromen-3-yl)ethylidene)benzohydrazide (B) against MCL-1 protein was investigated. For this purpose, a molecular docking simulations were used. The obtained results showed that compound A showed better activity than compound B. Also, the docking simulations against MCL-1 protein were perfo
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Komarova, Ol’ga, Ruslan Baichurin, and Nataliya Aboskalova. "GEMINALLY ACTIVATED 4-PHENYL-1-NITRO-1,3-BUTADIENES IN CYCLOADDITION REACTIONS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m791.aks-2019/352-355.

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Radovanović, Marko, Ignjat Filipović, Maja Đukić, Marija Ristić, Ivan Jakovljević, and Zoran D. Matović. "Molecular docking study of ruthenium-p-cymene complexes with isothiazole derivatives as SARS-CoV-2 main protease inhibitors." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.387r.

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Since proper treatment for COVID-19 still has not been developed, exploration of novel options is required. Activities of different metal complexes, promising results gained from examining different thiazole derivatives, and research in the field of natural products like p-cymene, produced an idea to test piano stool ruthenium p-cymene complexes with isothiazole derivatives as ligands. In silico methods are often used as the first step in a series of experiments during the development of new drugs, and docking simulations are a quick way to determine the feasibility of novel compounds as poten
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Andrić, Deana B., Slađana Dukić-Stefanovic, Jelena Z. Penjišević, et al. "DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NOVEL N- {4-[2-(4-ARYL-PIPERAZIN-1-YL)-ETHYL]-PHENYL}-ARYLAMIDES." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.355a.

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5HT1A receptor targeting drugs have been used as the treatment for the many neuropsychiatric disorders, such as schizophrenia and depression. As a part of ongoing research, we designed series of new compounds that share arylpiperazine common structural motif with the 5HT1A receptor ligand aripiprazole. Receptor-ligand interactions were determined by the molecular docking simulations, revealing the positive impact of the phenyl substitution in the arylpiperazine part of the molecules. Nine selected compounds were synthesized in four reaction steps in high overall yields (59-73%). In vitro pharm
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Zelenskaya, Veronika, Ruslan Baichurin, Vladislav Sergeev, and Sergey Makarenko. "FEATURES OF THE INTERACTION OF 1-ACETYL-1-NITRO-4-PHENYL-1,3-BUTADIENE WITH 4-METHYL(CHLORO)THIOPHENOLS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m785.aks-2019/322-324.

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Lazić, Anita, Luka Matović, Jelena Lađarević, Aleksandra Mašulović, Kristina Gak Simić, and Nataša Valentić. "In vitro antioxidant activity evaluation of ferrocenyl chalcones." In 36th International Congress on process engineering. SMEITS, 2023. http://dx.doi.org/10.24094/ptk.023.207.

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Ferrocene derivatives are known as antioxidants, antiparasitic, antitumor, antiviral, antibacterial and antifungal agents. In addition to applications in medicinal chemistry and drug design, ferrocene derivatives are of exceptional importance in synthetic organic chemistry, especially in catalytic asymmetric transformations. They are also used in electrochemistry and polymer chemistry, as additives in fuels, as chemosensors in agrochemistry and biosensors of glucose and active components in molecular electronics. To design new antioxidant agents, five ferrocenyl chalcones were synthesized, and
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Baichurin, Ruslan, Vladislav Sergeev, and Sergey Makarenko. "SYNTHESIS OF 4-METHYL-3-NITRO-2-STYRYL-2,3-DIHYDROBENZO[b][1,4]THIAZEPINE BASED ON THE REACTION OF 1-ACETYL1-NITRO-4-PHENYL-1,3-BUTADIENE WITH 2-AMINOTHIOPHENOL." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m756.aks-2019/218-219.

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Mašulović, Aleksandra, Anita Lazić, Ivana Đorđević, et al. "Assessing the pharmacological potential of synthetic colorants with pyridone core." In 37th International Congress on Process Industry. SMEITS, 2024. http://dx.doi.org/10.24094/ptk.024.299.

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Azo dyes are known as structurally diverse class of organic compounds bearing one or more azo groups (–N=N–) as a bridge between organic residues of which at least one is an aromatic moiety. This group of synthetic dyes is obtained easily by the reaction of diazo coupling with high yield. The importance of azo dyes is reflected in the fact that they account for 60 % of the total number of the dye structures known to be manufactured and used in the coloration of textiles, leather, plastics and cosmetics. Aside from their traditional usage, azo dyes are known for their therapeutic properties and
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Reports on the topic "Phenyl compounds"

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Naim, Michael, Gary R. Takeoka, Haim D. Rabinowitch, and Ron G. Buttery. Identification of Impact Aroma Compounds in Tomato: Implications to New Hybrids with Improved Acceptance through Sensory, Chemical, Breeding and Agrotechnical Techniques. United States Department of Agriculture, 2002. http://dx.doi.org/10.32747/2002.7585204.bard.

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The tomato, a profitable vegetable crop in both the USA and Israel, has benefited significantly from intensive breeding efforts in both countries, and elsewhere (esp. Holland). : Modem hybrids are highly prolific and resistant to a variety of major pests. They produce attractive, firm fruit for both processing and fresh-marketing. In all cases, however, reduction in flavor and aroma have occurred concomitantly with the increase in yield. Sugars-acids ratio dominate fruit taste, whereas aroma volatiles (potent at minute ppb and ppt levels) contribute to the total characteristic tomato flavor. A
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