Relevant bibliographies by topics / Aryl Compounds

Academic literature on the topic 'Aryl Compounds'

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Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "Aryl Compounds"

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Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang, and Zheng Li. "An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water." Journal of Chemical Research 2005, no. 11 (November 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.

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Treatment 1-aryl-3-aroyl/benzofuroyl thioureas with α-bromo substituted carbonyl compounds in water affording 1-aroyl/benzofuroyl-3-aryl-4-substituted imidazole-2-thiones in excellent yields within short time.
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Krutošíková, Alžbeta, Miloslava Dandárová, and Juraj Alföldi. "5-Aryl-2-furancarbaldehyde Hydrazones and Related Compounds." Collection of Czechoslovak Chemical Communications 58, no. 8 (1993): 1905–13. http://dx.doi.org/10.1135/cccc19931905.

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A series of 5-aryl-2-furancarbaldehyde 2,6-dialkylphenylhydrazones (Ia - Iv) and dimethylhydrazones (IIa - IIf) as well as related compound benzo[b]furan-2-carbaldehyde dimethylhydrazone (III) were prepared. Compounds Ia - Iv were synthesized by condensing 5-aryl-2-furancarbaldehydes with 2,6-dialkylphenylhydrazines, compounds IIa - IIf were obtained from the same starting compounds and N,N-dimethylhydrazine. The intermediate 5-aryl-2-furancarbaldehydes were prepared by reaction of aryldiazonium chlorides with 2-furancarbaldehyde. The structure of the compounds were proven by 1H, 13C and 15N NMR spectra.
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Soni, Love Kumar, Tamanna Narsinghani, and Rica Jain. "Synthesis and Antibacterial Screening of Some 1-Aroyl-3-aryl Thiourea Derivatives." ISRN Medicinal Chemistry 2014 (January 29, 2014): 1–6. http://dx.doi.org/10.1155/2014/393102.

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A series of 1-aroyl-3-aryl thioureas derivatives were synthesized and evaluated for antibacterial activity. The results indicated that the compounds possessed higher activity against gram-negative bacteria than gram-positive bacteria. Amongst all these compounds, C18 (89.4%) exhibited the greatest antibacterial activity against gram-negative bacteria while C5 (85.6%) displayed maximum antibacterial activity against gram-positive bacteria. Preliminary study of the structure-activity relationship revealed that an electronic factor on aryl rings had a great effect on the antibacterial activity of these compounds.
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Kalam, Sirisha, Rajyalaxmi I, and Olivia S. "Synthesis and In vitro P-Glycoprotein Inhibitory Activity of Novel 1,4-Dihydropyridine Derivatives." International Journal of Pharmaceutical Sciences and Nanotechnology 7, no. 3 (August 31, 2014): 2544–52. http://dx.doi.org/10.37285/ijpsn.2014.7.3.6.

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Two series of new symmetrical 4-aryl-2,6-dimethyl-3,5-bis-N-(aryl/heteroaryl)-carbamoyl-1,4-dihydropyridines (4a-f) and asymmetrical 4-aryl-2,6-dimethyl-3-N-(aryl/hetero-aryl)-carbamoyl-5-ethyl carboxylate-1,4-dihydro-pyridines (5a-f) have been synthesized by simple, economical and eco-friendly, modified Hantzsch reaction using N-aryl/heteroarylacetoacetamides (3a-c), ethylaceto-acetate (for asymmetric), arylaldehydes and urea in presence of catalytic amounts of LiBr/Iodine and by microwave irradiation methods. The newly synthesized compounds were characterized by physical and spectral data, and evaluated for their possible in vitro MDR reversal activity by everted sac method using verapamil as standard P-gp inhibitor and domperidone as the standard P-gp substrate. Amongst the compounds tested, compound 4f exhibited the highest in vitro P-gp inhibitory activity. It was found to be more potent than the standard verapamil.
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Raval, J. P., and K. R. Desai. "Synthesis of 3-Phenyl-4[4-(m-nitrophenyl)-N-2-(2’-arylureido / arylthioureido-4’-N-morpholino-s-triazin)-benzo-[6,7]-coumarins and their Applicatiions." E-Journal of Chemistry 1, no. 5 (2004): 211–15. http://dx.doi.org/10.1155/2004/873425.

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Several 3 – phenyl – 4 [4-(m– nitrophenyl) –N– 2 - (2’-arylureido /arylthioureido - 4’-N-morpholino-s-triazin)-benzo-(6,7)-coumarins were prepared using 2-(m–nitrophenyl)-3-hydroxy naphthalene, cyanuric chloride, morpholine and various aryl – ureas / aryl – thioureas derivatives to give desired compound. The structures of the compounds were confirmed by elemental analysis and spectral analysis. The antibacterial activities of these compounds have been screened and were also applied as Flourescent Brighteners on Polyester fabrics.
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Kudalkar, Gaurav P., Virendra K. Tiwari, Joshua D. Lee, and David B. Berkowitz. "A Hammett Study of Clostridium acetobutylicum Alcohol Dehydrogenase (CaADH): An Enzyme with Remarkable Substrate Promiscuity and Utility for Organic Synthesis." Synlett 31, no. 03 (January 16, 2020): 237–47. http://dx.doi.org/10.1055/s-0039-1691576.

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Described is a physical organic study of the reduction of three sets of carbonyl compounds by the NADPH-dependent enzyme Clostridium acetobutylicum alcohol dehydrogenase (CaADH). Previous studies in our group have shown this enzyme to display broad substrate promiscuity, yet remarkable stereochemical fidelity, in the reduction of carbonyl compounds, including α-, β- and γ-keto esters (d-stereochemistry), as well as α,α-difluorinated-β-keto phosphonate esters (l-stereochemistry). To better mechanistically characterize this promising dehydrogenase enzyme, we report here the results of a Hammett linear free-energy relationship (LFER) study across three distinct classes of carbonyl substrates; namely aryl aldehydes, aryl β-keto esters and aryl trifluoromethyl ketones. Rates are measured by monitoring the decrease in NADPH fluorescence at 460 nm with time across a range of substrate concentrations for each member of each carbonyl compound class. The resulting v 0 versus [S] data are subjected to least-squares hyperbolic fitting to the Michaelis–Menton equation. Hammett plots of log(V max) versus σX yield the following Hammett parameters: (i) for p-substituted aldehydes, ρ = 0.99 ± 0.10, ρ = 0.40 ± 0.09; two domains observed, (ii) for p-substituted β-keto esters ρ = 1.02 ± 0.31, and (iii) for p-substituted aryl trifluoromethyl ketones ρ = –0.97 ± 0.12. The positive sign of ρ indicated for the first two compound classes suggests that the hydride transfer from the nicotinamide cofactor is at least partially rate-limiting, whereas the negative sign of ρ for the aryl trifluoromethyl ketone class suggests that dehydration of the ketone hydrate may be rate-limiting for this compound class. Consistent with this notion, examination of the 13C NMR spectra for the set of p-substituted aryl trifluo­romethyl ketones in 2% aqueous DMSO reveals significant formation of the hydrate (gem-diol) for this compound family, with compounds bearing the more electron-withdrawing groups showing greater degrees of hydration. This work also presents the first examples of the CaADH-mediated reduction of aryl trifluoromethyl ketones, and chiral HPLC analysis indicates that the parent compound α,α,α-trifluoroacetophenone is enzymatically reduced in 99% ee and 95% yield, providing the (S)-stereoisomer, suggesting yet another compound class for which this enzyme displays high enantioselectivity.
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Chandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.

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Introduction: In the present study a novel series of twelve 1-(aryl)-2-(1H-imidazol-1-yl)methanones 3(a-l) were synthesized and characterised by physicochemical and spectral analysis,viz. elemental analysis, IR spectroscopy, NMR spectroscopy. The antibacterial property of the compounds were examined, in order to develop new broad spectrum antibiotics. Methods: The compounds 3(a-l) were synthesised by reacting the corresponding 2-(aryl)-1H-imidazoles 2 with substituted benzoyl chlorides. Binding mode analysis of the most active compound was carried out. Predictive ADME studies were carried out for all the compounds. Results and Discussions: Among the synthesized compounds, (2-(3-nitrophenyl) (2,4-dichlorophenyl) -1Himidazol-1-yl)methanone 3i exhibited highest antibacterial activity. Binding mode analysis of the highest active compound was carried out in the active site of glucosamine-6-phosphate synthase (2VF5).
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Chandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.

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Introduction: In the present study a novel series of twelve 1-(aryl)-2-(1H-imidazol-1-yl)methanones 3(a-l) were synthesized and characterised by physicochemical and spectral analysis,viz. elemental analysis, IR spectroscopy, NMR spectroscopy. The antibacterial property of the compounds were examined, in order to develop new broad spectrum antibiotics. Methods: The compounds 3(a-l) were synthesised by reacting the corresponding 2-(aryl)-1H-imidazoles 2 with substituted benzoyl chlorides. Binding mode analysis of the most active compound was carried out. Predictive ADME studies were carried out for all the compounds. Results and Discussions: Among the synthesized compounds, (2-(3-nitrophenyl) (2,4-dichlorophenyl) -1Himidazol-1-yl)methanone 3i exhibited highest antibacterial activity. Binding mode analysis of the highest active compound was carried out in the active site of glucosamine-6-phosphate synthase (2VF5).
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Wang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye, and Cunde Wang. "Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates." Journal of Chemical Research 41, no. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.

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2,3-Disubstituted cyclopropane-1-carbonitriles were efficiently formed via a selective decarboxylation reaction of substituted 2-aroyl-3-aryl-1-cyano-cyclopropane-1-carboxylates in up to 92% yield. The structures of three typical compounds were confirmed by X-ray crystallography.
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Utri, Gerhard, Karl-Eberhard Schwarzhans, and Günter M. Allmaier. "Ferrocenyl-aryl-plumbane / Ferrocenyl-aryl-plumbanes." Zeitschrift für Naturforschung B 45, no. 6 (June 1, 1990): 755–62. http://dx.doi.org/10.1515/znb-1990-0606.

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The first example of a diplumba[1.1]ferrocenophane[cpPb(ø2)cp]2Fe2 has been prepared from ø2PbCl2 and 1,1′-dilithioferrocene 2 TMEDA. The preparation of further four ferrocenyl-phenyl-plumbanes, including the hitherto unknown compounds (ø3Pbcp)2Fe, Fc2Pb2ø2 and [(ø3Pb)cpFecp]FcPbø2 has been achieved by reaction of a mixture of monolithioferrocene · TMEDA and 1,1′-dilithioferrocene 2 TMEDA with ø 2PbCl2 and ø3PbCl, respectively.These compounds have been investigated by 1H, 13C and 207Pb NMR spectroscopy as well as by half-wave potential measurements, EI, FD and PD mass spectrometry.The results were discussed in terms of the possibility of Pb/Fe metal orbital overlap.There is evidence from the VT 1H NMR spectra for conformational flexibility of the diplumba[ 1.1 ]ferrocenophane.
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Dissertations / Theses on the topic "Aryl Compounds"

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Leyva-Ramos, Elisa. "The temperature dependent photochemistry of aryl azides and aryl diazo compounds /." The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487267024997622.

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Leary, Edmund. "Single Molecule Conductance of Dithiahexyl-Aryl Compounds." Thesis, University of Liverpool, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507724.

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Ross, Jennifer Nicola. "Alkoxy- substituted aryl- and benzyl- organotin compounds." Thesis, University of Aberdeen, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324880.

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New organotin compounds containing alkoxy- functionalities have been prepared. The methods of preparation of the tetraorganotin species have involved three routes. Hydrostannation reactions using triphenyltin hydride have resulted in the synthesis of triphenyltin derivatives of a series of alkoxy- substituted allyl ethers. The addition of tin IV chloride, diphenyltin dichloride and phenyltin trichloride to alkoxy- substituted aryl- and benzyl- Grignard reagents have also been successful. Alkoxy- substituted benzyltin compounds have been prepared by following an alternative preparation of benzylmagnesium halides from that commonly used to prepare Grignard reagents. Nucleophilic substitution of (iodomethyl)triphenyltin by a novel ligand has been effective. The structures of the products have been investigated by 1H, 13C and 119Sn nmr. Single crystal X-ray diffraction studies have led to the determination of the crystal structures of tetra-2-anisyltin, tetrakis-(2-methoxybenzyl)tin and N,N'-bis(5-triphenylstannoxymethyl-2-phenyl-1,3-dioxan-5-yl)ethanediamide. Selective tin-carbon bond cleavage has been effected by the use of iodine and bromine to give rise to mono- and dihalo- organotin compounds and the crystal structures of tri-2-anisyltin iodide and di-2-anisyltin dibromide have been elucidated by X-ray crystallography. Chloro(3-ethoxypropyl)diphenyltin has been synthesised directly from diphenyltin dichloride and has been found to contain a penta-co-ordinate tin centre with a four membered chelate ring as a result of intramolecular tin-oxygen co-ordination. Other tin-carbon bond cleavage reactions by halogens have been studied by 1H and 119Sn nmr and GLC and the results discussed.
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Khashoqji, Moayad. "Structural characterisation of novel poly-aryl compounds." Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/structural-characterisation-of-novel-polyaryl-compounds(3fb1fac6-548a-4afc-8ac2-5a14885b0ba4).html.

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Poly-aryl, also known as polyphenylene compounds are a class of dendrimer, which contain a large number of aromatic rings. They are of interest because they display restricted rotation of their stearically congested aromatic rings. These extended structures have the potential to act as precursors for even larger aromatic systems and have many applications including electronic devices, drug delivery and catalysis. A total of 23 novel poly-aryl compounds have been examined using single crystal X-ray diffraction and a number of structural patterns have emerged. Six of the compounds contain alkynes and it has been observed that their conformation is governed by a combination of conjugation between the alkyne and aryl groups and inter-molecular interactions. In the more extended poly-aryl compounds steric congestion rules out any possibility of conjugation between the rings and their conformation is governed by intra-molecular non-bonded interactions in the core of the molecules and by inter-molecular interactions in their periphery. Where possible, solution NMR measurements were carried out on the poly-aryl compounds and confirmed that the solution structures are in agreement with those obtained from individual crystal.
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Rowland, Keith E. (Keith Edward). "An NMR Investigation of Aryl Mercury Compounds." Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc500453/.

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A variable temperature ^13 C and ^199 Hg NMR study has been conducted for diphenyl-, bis(o-tolyl)-, bis(m-tolyl)-, and bis(2, 6-xylyl)mercury in dimethyl sulfoxide and 1,1,2,2 tetrachloroethane; ^13 C T1 relaxation times are reported as a function of temperature. Barriers to rotation of the aryl rings are obtained. Chemical shifts and couplings in CDCl_3 are given for bis(p-tolyl)-, bis(2, 5-xylyl)-, bis(mesityl)-,phenyl(o-tolyl)-, phenyl(m-tolyl)mercury, and the compounds listed above. The steric interactions of these aryl mercury compounds are discussed.
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Guena, Thierry. "Electrochemistry of aryl carbonyl compounds in flow cells." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243180.

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Heaton, Julie N. "Generation and reactions of aryl and alkyl thionitroso compounds." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/6129/.

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Transient thionitrosoarenes (102) with para substituents have been generated from N-(arylaminothio)-phthalimide derivatives (101) and intercepted with chloroprene and piperylene to give regioisomeric Diels- Alder adducts. Reaction of thionitrosoarenes (102) with 1-methylcyclohexene, a-pinene and β-pinene gave sulphenamides. Sulphenamides (110) and(123) have been reacted with 2,6-difluorobenzoylisocyanate. Heteroaryl thionitroso compounds have been prepared. Thionitrosoarenes with an ortho substituent have been generated via two different routes and trapped with 2,3-dimethyl-l,3-butadiene to give mixtures of Diels-Alder and ene adducts; the ene adduct was the major isomer for each system. Thionitrosoarene (159b) was generated from 3- aminobenzisothiazole (157b) using lead tetraacetate and was intercepted with 2,3-dimethyl-l,3-butadiene to give Diels-Alder (160) and ene (161) adducts. Thionitrosoalkanes have been generated using two different routes and trapped with 2,3-dimethyl-l,3-butadiene to give Diels-Alder and ene adducts.
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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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Al-Harthy, Farida. "Separation of aryl nitro-compounds by HPLC on monolithic columns." Thesis, Loughborough University, 2009. https://dspace.lboro.ac.uk/2134/8683.

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The project has demonstrated the use of both poly(styrene-divinylbenzene) PS-DVB and silica monolithic columns for the separation of nitro-compounds. Methods were developed with PS-DVB and ODS silica packed columns for the separation of these compounds. The first part of the project was the preparation of the monolithic stationary phases prepared from PS-DVB of (250 μm I.D. × 70 mm) functionalized with methacrylate by in-situ polymerisation. The alkylated PS-DVB then was used successfully for the first time in the separation of three aryl nitro-compounds (2-NA, 1,4-DNB and 4-NT) on micro-HPLC. However, the efficiency of this column was poor N = 318 (4675/m).The second part of the thesis used a commercial column (Chromolith Performance from Merck), with different diameters for the separation of nitro-compounds. Nitrocompounds were analysed on both Chromolith Performance 3 mm I.D. column and Chromolith Performance 4 mm I.D. column by HPLC/UV. Van Deemter plots showed that the 3 mm I.D. column gave higher efficiencies at higher flow rates than the 4.6 mm I.D. column. The plate number was 8216 (H = 0.0121 mm) at a flow rate of 0.4 ml/min (1.0206 mm/sec) and for Chromolith 4.6 mm I.D. it was 9436 (H = 0.0105 mm) at a flow rate of 0.8 ml/min (0.8577 mm/sec). The nitro-compounds analysed in this study were nitroaromatic, nitramines and nitrate esters which are used in the manufacture of explosives. These compounds were analysed for the first time using a Chromolith Performance 3 mm I.D. column on LCMS using both ESI and APCI in negative ionization modes. The sensitivity was higher in the APCI than the ESI mode in terms of higher intensity and lower background noise especially for nitroaromatic compounds. The LC-ESI-MS method was evaluated by injection of samples of pentaerythritol tetranitrate (PETN) in different concentrations. Calibration curves were constructed over the range of 1-1000 pg/μl with a correlation coefficient of (R2 = 0.9986) and with a concentration range between 1-200 ng/μl with a correlation coefficient of (R2 = 0.9971) and were found to be linear. The limit of detection (LOT) for pentaerythritol tetranitrate (PETN) was 5 pg/μl at a signal-to-noise ratio (S/N) of 3:1 and the limit of quantification (LOQ) was 10 pg/μl at a signal-to-noise ratio of 10:1. The applicability of the monolithic column for the LC-ESI-MS method was evaluated by injection of samples of the commercial explosives, P9 and Semtex 1H. The results showed that Semtex 1H contains 35% PETN using calibration curve 1-200 ng/μl and was much higher than in P9 0.0082% using calibration curve 1-1000 pg/μl.
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Ng, Fei-yeung, and 吳飛洋. "Structure and properties of self-assembled coordination compounds: homoleptic d10-metal aryl/alkylacetylides, ruthenium n-heterocyclesand picolinates." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37878566.

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Books on the topic "Aryl Compounds"

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Chehimi, Mohamed M., Jean Pinson, and Fatima Mousli, eds. Aryl Diazonium Salts and Related Compounds. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7.

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Elings, Jacob Antonius. Solid-acid catalysed reactions with epoxides and allyl aryl ethers. Delft, Netherlands: Delft University Press, 1997.

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R, Williams John. Development and preliminary evaluation of aryl ester boundary additives for perfluoropolyethers. Cleveland, Ohio: National Aeronautics and Space Administration, Lewis Research Center, 1994.

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International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds (3rd 1987 Dearborn, Mich.). Carcinogenic and mutagenic responses to aromatic amines and nitroarenes: Proceedings of the Third International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds, held April 25-28, 1987, in Dearborn Michigan. Edited by King Charles M. 1932-, Romano Louis James 1950-, and Schuetzle Dennis 1942-. New York: Elsevier, 1988.

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Perry, Philip J. Synthesis and biological evaluation of novel cytotoxic heterocyclic compounds: Furo (2,3-b) naphthoquinones and 2-aryl-4H-3,1-benzoxazin-4-ones. Leicester: De Montfort University, 1996.

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Baltrušis, Romualdas. Sintez, prevrashchenii︠a︡ i svoĭstva N-aril (geterot︠s︡iklil)-[beta]-alaninov: Monografii︠a︡. Kaunas: Tekhnologii︠a︡, 1999.

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Pohjanvirta, Raimo. The AH receptor in biology and toxicology. Hoboken, N.J: Wiley, 2011.

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Carcinogenic and mutagenic N-substituted aryl compounds. [Research Triangle Park, NC]: National Institutes of Health, National Institute of Environmental Health Sciences, 1994.

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Mousli, Fatima, Mohamed Mehdi Chehimi, and Jean Pinson. Aryl Diazonium Salts and Related Compounds: Surface Chemistry and Applications. Springer International Publishing AG, 2022.

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Incorporated, John, 2012.

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Book chapters on the topic "Aryl Compounds"

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McCreery, Richard, and Adam Johan Bergren. "Diazonium Compounds in Molecular Electronics." In Aryl Diazonium Salts, 219–39. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch10.

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Rappich, Jörg, Xin Zhang, and Karsten Hinrichs. "Electronic Properties of Si Surfaces Modified by Aryl Diazonium Compounds." In Aryl Diazonium Salts, 241–53. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch11.

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Saad, Ahmed, and Marta Cerruti. "Diazonium Salts and Related Compounds for Biomedical Applications." In Aryl Diazonium Salts and Related Compounds, 263–85. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_14.

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Bélanger, Daniel. "Diazonium Salts and Related Compounds in Electrochemical Energy Storage and Conversion." In Aryl Diazonium Salts and Related Compounds, 427–51. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_22.

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Vieillard, Julien, Franck Le Derf, Charlène Gadroy, and Brahim Samir. "Modification and Uses of Synthetic and Biobased Polymeric Materials." In Aryl Diazonium Salts and Related Compounds, 195–209. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_10.

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Guselnikova, Olga, Natalia S. Soldatova, and Pavel S. Postnikov. "Iodonium Salts as Reagents for Surface Modification: From Preparation to Reactivity in Surface-Assisted Transformations." In Aryl Diazonium Salts and Related Compounds, 79–96. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_4.

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Yagci, Yusuf, and Mohamed M. Chehimi. "Aryldiazonium Salts as Photoinitiators for Cationic and Free Radical Polymerizations." In Aryl Diazonium Salts and Related Compounds, 309–15. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_16.

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Rodríguez González, Miriam C., Kunal S. Mali, and Steven De Feyter. "Covalent Modification of Graphite and Graphene Using Diazonium Chemistry." In Aryl Diazonium Salts and Related Compounds, 157–81. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_8.

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Mousli, Fatima, Youssef Snoussi, Mohamed M. Chehimi, and Robert Wojcieszak. "On the Use of Diazonium Salts in the Design of Catalytic Hybrid Materials and Coatings." In Aryl Diazonium Salts and Related Compounds, 287–308. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_15.

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Vautrin-Ul, Christine. "Modification of sp2 Carbon Allotropes with Diazonium Salts—Focus on Carbon Nanotubes Functionalization." In Aryl Diazonium Salts and Related Compounds, 137–56. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7_7.

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Conference papers on the topic "Aryl Compounds"

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Forostyanko, Anna, Elena Vasileva, and Irina Proskurina. "SYNTHESIS OF 5-(4’-NITROPHENYL)-3-ARYL-1,2,4-OXADIAZOLES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m758.aks-2019/222-226.

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Andrić, Deana B., Slađana Dukić-Stefanovic, Jelena Z. Penjišević, Ivana I. Jevtić, Vladimir B. Šukalović, Relja Suručić, and Slađana Kostić-Rajačić. "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 pharmacological evaluation of the synthesized compounds revealed three compounds (5b, 6b and 6c) with high 5HT1A binding affinity, comparable with aripiprazole (Ki 12.0, 4.8, 12.8, 5.6 nM, respectively). Compounds from b series, 5b and 6b, possess 2-methoxyphenyl substituents, while 6c possess 2,3-dichlorophenyl substituent in the arylpiperazine part of the molecule. The pharmacological results are therefore in accordance with the molecular docking simulations thus proving the rational design. Compounds 5c, 6b and 6c can be considered as the candidates for further evaluation as new, potential antidepressants.
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Anichina, K. "SYNTHESIS AND ANTINEMATODAL ACTIVITY STUDIES OF SOME FUSED TRIAZINOBENZIMIDAZOLES." In International Trends in Science and Technology. RS Global Sp. z O.O., 2020. http://dx.doi.org/10.31435/rsglobal_conf/30122020/7351.

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4-Aryl-3,4-dihydro[1,3,5]triazino[1,2-a]benzimidazole-2-amines 3a-f were synthesized in the reaction of cyclocondensation between 2-guanidinobenzimidazole and versatilebenzaldehydes. Structures of all prepared compounds were confirmed by IR, 1H NMR spectroscopyand elemental analysis.Antinematodal activity in vitro of the substances was investigated using isolated Trichinella spiralis muscle larvae. The tested triazonobenzimidazoles showed different activity depending on the substituent R in their moleculeas the derivatives substituted with a hydroxyl group demonstrated the best anti-Trichinella spiralis activity in the series.
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Vasilenko, Dmitry, Kirill Sadovnikov, Arina Tukhbatullina, and Elena Averina. "NOVEL REACTION OF HETEROCYCLIZATION OF β-ARYL SUBSTITUTED α,β-UNSATURATED KETONES. SYNTHESIS OF 4-NITROISOXAZOLES AND π-CONJUGATED ISOXAZOLE-BASED SYSTEMS WITH VALUABLE PHOTOPHYSICAL PROPARTIESE PHOTOPHYSICAL PROPARTIES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m731.aks-2019/102-104.

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D., Chavan M., Karamthoti M. B., and Kurra S. B. "Screening of Antiseizure Activity of Aryl Acetic Acid Compounds in Wistar Albino Rats by using PTZ and MES Tests." In 20th Joint Annual Conference of Indian Epilepsy Society and Indian Epilepsy Association. Thieme Medical and Scientific Publishers Private Ltd., 2018. http://dx.doi.org/10.1055/s-0039-1694877.

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Aparicio, Carmen Blanco, Julen Oyarzabal, Oliver Renner, Rosa Maria Alvarez, Sandra Peregrina, Ana Corrionero, Carl Gustaf Saluste, et al. "Abstract B227: Discovery of 3-aryl-3H-[1,2,3]triazolo[4,5-b]pyridin-5-ylamine compounds as potent, selective and orally bioavailable inhibitors of PIM kinases." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b227.

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Aparicio, Carmen Blanco, Sonia Martinez, Beatriz Garcia-Serelde, Ana Maria Garcia-Collazo, Nuria Ajenjo, Beatriz Noya, Ana Corrionero, et al. "Abstract B228: Discovery of 6-Methyl-3-aryl-7,8-dihydro-6H-9-oxa-1,2,3a,4,6-pentaaza-cyclopenta[a]naphthalen-5-ylamine compounds as Pim kinase inhibitors with potent activity in tumoral cell lines and special binding mode." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b228.

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Cline, Kjetil, Andrew LaFlam, Logan Smith, Margaret Nowicki, and Nicholas Ku. "Additive Manufacturing With Ceramics." In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23253.

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Abstract The purpose of this project is to design a device that improves the performance of a ceramic additive manufacturing (AM) 3D printer constructed by Army Research Labs (ARL). ARL modified a standard LulzBot Taz 6 3D printer to print a ceramic slurry mixture of Boron Carbide (B4C) and Silicon Carbide (SiC) instead of plastic filament. Since these compounds are often used in body armor, ARL has been observing the effects on properties when these components are 3D printed. The current printer utilizes an auger in the print head to receive and mix the B4C and SiC slurries and extrude the combined slurry out of the print nozzle. The current design is limited in its ability to thoroughly mix the slurries during the printing process. Therefore, team Concept Creators has designed an improved auger that will increase the mixedness of the slurries, thus increasing the print quality of the composite specimen.
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Reports on the topic "Aryl Compounds"

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Jayatissa, Kuruppu. A Metal-Free Approach to Biaryl Compounds: Carbon-Carbon Bond Formation from Diaryliodonium Salts and Aryl Triolborates. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2226.

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