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Relevant bibliographies by topics / Arylamino compounds

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Academic literature on the topic 'Arylamino compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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Journal articles on the topic "Arylamino compounds"

1

M. Daher AI-.libory, Abed, and Halla ldrees. "Synthesis of some aromatic chloro acetamide from aromatic amines compounds, and (Z) -5- (4-dimctlryl amino benzelidcn) -2- amino - thiazalidin -4- one derivatives." Tikrit Journal of Pharmaceutical Sciences 11, no. 1 (2023): 55–66. http://dx.doi.org/10.25130/tjphs.2013.11.1.6.55.66.

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Arylamine compounds were reacted with chloro acetyl chloride to convert the amino group to amide (compounds -1, 4, 7) these later compounds allowed to reacts with arylamino to produce the new (compounds -3, 6, 9), and the above compounds allowed to react with potassium thiocynate to prepare the new compounds which containing thiazolidinone (five membered rings) the (compounds -2, 5, 8), the later compounds allowed to react with aryl aldehydes to prepare the (compounds -10, 11, 12). The prepared compounds were identified using melting point apparatus, Infrared spectroscopy, and (H1-NMR).

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2

Ivakhnenko, Eugeny, Vasily Malay, Pavel Knyazev, et al. "Facile approach to N,O,S-heteropentacycles via condensation of sterically crowded 3H-phenoxazin-3-one with ortho-substituted anilines." Beilstein Journal of Organic Chemistry 20 (February 21, 2024): 336–45. http://dx.doi.org/10.3762/bjoc.20.34.

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A convenient method for the synthesis of a series of 2-(arylamino)-3H-phenoxazin-3-ones based on the nucleophilic substitution reaction between sterically crowded 3H-phenoxazin-3-one and arylamines performed by short-term heating of the melted reactants at 220–250 °C is described, and the compounds were characterized by means of single-crystal X-ray crystallography, NMR, UV–vis, and IR spectroscopy, as well as cyclic voltammetry. The reaction with o-amino-, o-hydroxy-, and o-mercapto-substituted arylamines widened the scope and provided an access to derivatives of N,O- and N,S-heteropentacycli

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V., Madhura, Hrishikesh M. Revankar, and Manohar V. Kulkarni. "A new route for the synthesis of 4-arylacetamido-2-aminothiazoles and their biological evaluation." Zeitschrift für Naturforschung B 70, no. 7 (2015): 483–89. http://dx.doi.org/10.1515/znb-2015-0013.

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AbstractA series of 4-arylacetamido-2-amino- and 2-arylamino-1,3-thiazoles (4a–o) were synthesized in a single step in high yields from ω-bromoacetoacetanilides and thiourea/phenyl thioureas and were characterized by spectral and analytical methods. The compounds were evaluated for their in vitro antibacterial antifungal and antioxidant activities. In vitro antimicrobial evaluation of these compounds indicated their specificity towards Gram-positive species. p-Tolyl and m-chlorophenyl substituents on the arylamino moiety (compounds 4b and 4g) exhibited the lowest minimum inhibitory concentrati

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Edrees, Mastoura M. "Synthesis of 4-hydrazinopyrazolo[3,4-d]pyrimidines and their Reactions with Carbonyl Compounds." Journal of Chemical Research 37, no. 1 (2013): 6–10. http://dx.doi.org/10.3184/174751912x13543818811749.

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Synthesis of a new 4-hydrazinopyrazolo[3,4- d]pyrimidine was achieved via heating (4,6-dithioxo-1 H-pyrazolo[3,4- d] pyrimidin-3-yl)acetonitrile with hydrazine hydrate. Reactions of the latter product with thiophene-2-carbaldehyde and ethyl hydrazonoacetoacetate analogues afforded the corresponding hydrazone and pyrazole derivatives, respectively. Similarly, condensation of 2-[6-(benzylsulfanyl)-4-hydrazino-1 H-pyrazolo[3,4- d]pyrimidin-3-yl]acetonitrile with thiophene-2-carbaldehyde and ethyl hydrazonoacetoacetate analogues gave the respective hydrazone and pyrazolone derivatives. Alkylation

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Crossley, MJ, S. Gorjian, S. Sternhell, and KM Tansey. "The Synthesis of Some Lipophilic Tetradentate Ligands for Use in the Formation of Metal-Linked Polymers." Australian Journal of Chemistry 47, no. 4 (1994): 723. http://dx.doi.org/10.1071/ch9940723.

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Two lipophilic tetradentate ligands, 5,5′-di-t-butyl- and 5,5′-dihexyl-2,2′-bipyrimidine, were prepared via either Ullmann or nickel(0)-promoted reactions in low but useful yields. Approaches towards the synthesis of lipophilic ligands based on 2,2′-biimidazole, namely 4,4′,5,5′-tetrabutyl-2,2′-biimidazole (from decane-4,5-dione) and various 4,4′,5,5′-tetra( arylamino )- 2,2′-biimidazoles (from 4,4′,5,5′-tetrabromo-2,2′-biimidazole and arylamines), and a 2,2′- bibenzimidazole , 5,5′,6,6?-tetra( octyloxy )-2,2′-bibenzimidazole (from N,N′- bis [4,5-di( octyloxy )-2-nitrophenyl] oxamide ), were u

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Sakamoto, Ryota, Suzaliza Mustafar, and Hiroshi Nishihara. "Meso-N-arylamino- and N, N-diarylaminoporphyrinoids: Syntheses, properties and applications." Journal of Porphyrins and Phthalocyanines 19, no. 01-03 (2015): 21–31. http://dx.doi.org/10.1142/s1088424615500091.

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This review is devoted to porphyrinoids with N-arylamino groups tethered directly to their meso positions, the study of which has significantly progressed in the past two decades. After a brief introductory description, various synthetic procedures for these compounds are described. The third section focuses on their photochemical and electrochemical properties, and reviews the synergetic effects that arise between the porphyrinoids and the N-arylamino groups. Potential applications are then discussed, focusing on dye-sensitized solar cells (DSSCs).

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Tisovský, Pavol, Klaudia Csicsai, Jana Donovalová, Róbert Šandrik, Róbert Sokolík, and Anton Gáplovský. "Effect of a =X-NH-Fragment, (X = C, N), on Z/E Isomerization and ON/OFF Functionality of Isatin Arylhydrazones, ((Arylamino)Methylene)Indolin-2-Ones and Their Anions." Molecules 25, no. 13 (2020): 3082. http://dx.doi.org/10.3390/molecules25133082.

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The subject of this work was the study of thermally and photochemically stimulated Z ↔ E isomerization and hydrazo ↔ azo tautomerism of Z- and E-isomers of isatin arylhydrazones and ((arylamino)methylene)indolin-2-ones and their anions. Using NMR, UV-Vis spectroscopy, kinetic measurements, and HPLC, we studied the relationship of structure, (Z- and E-isomers), of these compounds and hydrazo=azo tautomerism. The ON/OFF functionality of these compounds and their anions using light to stimulate switching between ON and OFF states was investigated. We pointed out the characterization of the effect

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El Ashry, El Sayed H., Laila Fathy Awad, Mohamed Nabil Abd Al Moaty, and Omayma Kh Bdeewy. "A novel trans-amination process in 3-arylamino- 5,5-dimethylcyclohex-2-en-1-one with nucleophiles and antimicrobial activity of selected products." Mediterranean Journal of Chemistry 7, no. 6 (2019): 452–62. http://dx.doi.org/10.13171/mjc7619019140eshea.

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Reaction of dimedone with arylamines afforded the respective enaminones. Some N-acetyl derivatives were prepared. The reaction of enaminones with hydroxylamine was found to be dependent on the nature of the arylamine moiety and the molar ratio of hydroxylamine to give the mono-, di- or tri-oximes. Cyclization of the trioxime by acetic anhydride gave dihydrobenzo[c][1,2,5]oxadiazol-4(5H)-one-5-O-acetyloxime. Coupling of the synthesized enaminones with benzene diazonium chloride gave 2,4-bis-phenylhydrazones or a mixture of 2-mono hydrazones and bis-hydrazones depending on the nature of the aryl

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9

Gornostaev, Leonid M. "Synthesis of 5-hydroxy-10-R-benzo[a]phenazine-12-oxides by cyclization of 2-arylamino-1,4-naphthoquinone-1-oximes under the action of nitrating mixture." Butlerov Communications 61, no. 2 (2020): 12–23. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-12.

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The synthesis of рolycyclic quinoid compounds, which exhibit a wide range of biological activity is one of the most promising and actively developing areas of the fine organic synthesis. Heterocyclic compounds including those that can be donors of nitrogen oxide NO occupy a special place among biologically active structures. These substances include a number of N-oxides, e.g., 1,2-diazet-1,2-dioxides, furoxanes and their benzo analogs, and N,N′-pyrazole dioxides. The reason for the high biological activity of N-oxides of nitrogenous heterocycles, which cannot easily generate nitrogen oxide NO

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Jebalenet, J., J. Jenisha, and Reji T. F. Abbs Fen. "Synthesis, computational and anti-oxidant studies of 2-[2-(4-arylamino)-4-phenylaminothiazol-5-oyl]naphthalene." Research Journal of Chemistry and Environment 27, no. 9 (2023): 8–16. http://dx.doi.org/10.25303/2709rjce08016.

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The compound 2-[2-(4-arylamino)-4-phenylamino thiazol-5-oyl]naphthalene was synthesized and characterized by different physico-chemical techniques such as IR, electronic parameters, antioxidant studies etc. The geometrical and electronic characteristics of 2-[2-(4-arylamino)-4-phenylaminothiazol-5-oyl]napht halene were calculated theoretically using the Gaussian 09W software at the B3LYP/6-31G level of theory. The predicted geometrical characteristics are close to those published for 2-[2-(4-arylamino)-4-phenylaminothiazol-5-oyl]naphthalene with similar structures. Geometrical parameters are d

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Dissertations / Theses on the topic "Arylamino compounds"

1

Moore, Adam L. "N-heterocyclic carbenes with pendant arylamine donor substituents as supports for metal-metal interactions of closed shell metal ions." abstract, 2008. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3326620.

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Haelters, Jean-Pierre. "Synthèse de dérivés phosphono-indoliques-benzofuranniques et -pyrroliques à partir d'hydrazones phosphonates." Brest, 1987. http://www.theses.fr/1987BRES2002.

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Des derives phosphonoindoliques sont prepares par cyclisation d'arylhydrazones d'oxoalkylphosphonates selon fisher et par cyclodeshydratation d'arylamino-1 et arylamino-3 oxo-2 propylphosphonates selon bischler. Des indolyl-2 et indolyl-3 phosphonates, des indolylmethyl-2 et des indolylmethyl-3 phosphonates diversement substitues et leurs acides phosphoniques correspondants sont decrits. Toutes structures sont analysees par rmn **(1)h, **(31)p et 1**(3)c. L'analogue phosphore de l'intermediaire a aussi ete prepare. L'extention de la reaction de bischler aux aryloxycetones permet d'atteindre de

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3

"Synthesis, structure and oxygenation reactivity of copper complexes supported by monodentate arylamido ligands." 2013. http://library.cuhk.edu.hk/record=b5549320.

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本研究主要集中在苯胺基配體及全氟苯胺基配體　[N(R')(2,6-R₂C₆H₃)]⁻ [R = Me, Pr{U+2071} ; R' = SiMe₃, SiBu{U+1D57}Me₂, C₆F₅]　衍生出來的一價銅的配位化學，包括其絡合物的合成、結構及氧化反應的研究。<br>第一章概括地介紹了金屬胺他物及銅配合物氧化反應的研究背景。<br>第二章敘述了由苯胺基配體所衍生的一價銅絡合物的裝備及結構。透過苯胺基鹼金屬絡合物 [(M)N(R')(2,6-R₂C₆H₃)] (M = Li, K) 與銅鹵化物CuX (X = Cl, I) 反應，成功合成一系列一價銅絡合物 [Cu₂(L¹)₂(tmeda)] (L¹= [N(SiMe₃)(2,6-Me₂C₆H₃)]⁻)⁻ 及[{Cu(tmeda)₂}{Cu(L{U+207F})₂}] (L{U+207F} = [N(R')(2,6-R₂C₆H₃)]⁻: n = 2, R = Pr{U+2071}, R' = SiMe₃; n = 3, R = Me, R' = SiBu{U+1D57}Me₂; n = 4, R = Pr{U+2071}, R' = SiBu{U+1D57}Me₂; n = 5, R = Me, R' = C₆F₅; n = 6, R = Pri, R' = C₆F₅)。另外，銅碘化物與兩倍的苯胺基鉀絡合物反應[KN(R'

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Book chapters on the topic "Arylamino compounds"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of titanium(III) silylated arylamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_28.

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2

Cordero, F. M., and S. Cicchi. "Reaction of Nitroso Compounds with (Aryl)(arylamino)acetonitrile." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00403.

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3

Neumann, Hans-Günter, Gerhard Birner, and Gabriele Sabbioni. "Haemoglobin adducts of aromatic amines as a dosimeter for exposure control and risk assessment." In Human Carcinogen Exposure. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780199631858.003.0028.

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Abstract N-substituted aryl compounds comprise a large family of industrial and environmental chemicals. This includes not only arylamines as such but also those chemicals which are convertible into arylamines (or reactive Noxidation products) such as nitroso-arenes and azo-compounds. Many of them are established or suspected carcinogens and their uptake increases the risk of developing tumours in humans. Exposure, therefore, should be controlled in order to identify major sources of hazard and to take preventive measures. Biochemical effect monitoring represents an improved procedure of expos

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4

Jung, N., and S. Bräse. "Diazotization of Arylamines and Reaction with Secondary Amines." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00580.

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Tracey, M. R., R. P. Hsung, J. Antoline, et al. "Generation of Solid-Supported -Arylalkanamides by Three-Component Coupling of -Arylamines, Carbon Dioxide, and Merrifield's Resin." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00335.

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Conference papers on the topic "Arylamino compounds"

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Choi, W. H., and S. K. So. "Charge injection and transport in spiro-linked arylamine compounds." In SPIE Photonic Devices + Applications, edited by Franky So and Chihaya Adachi. SPIE, 2009. http://dx.doi.org/10.1117/12.825555.

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Julianto, Tatang Shabur, Jumina Jumina, Hardjono Sastrohamidjojo, and Mustofa Mustofa. "Synthesis and heme polymerization inhibitory assay of a new arylamino alcohol derivative compound from methyl eugenol and aniline." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5065064.

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Reports on the topic "Arylamino compounds"

1

Rimdusit, Sarawut, Nitinat Suppakarn, and Chanchira Jubsilp. Effect of triphenylphosphate flame retardant on properties of polybenzoxazines : Research Report. Chulalongkorn University, 2011. https://doi.org/10.58837/chula.res.2011.97.

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To enhance flame retardancy of polybenzoxazines, non-halogenated phosphorus compound has been evaluated for its potential flame retardant. In this research, the resulting flame retardanted polybenzoxazines were prepared by mixing phosphorus flame retardant with three types of arylamine-based benzoxazine resins. Their fire resistance, thermal, and mechanical properties were investigated. The weight ratios of benzoxazine resins/TPP were varied to different phosphorus content. DSC results indicated that, in the presence of TPP, the onset and maximum temperature of the exothermic peak due to the r

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