Relevant bibliographies by topics / 2-aminobenzonitrile

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

Academic literature on the topic '2-aminobenzonitrile'

Author: Grafiati
Published: 27 February 2024

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Journal articles on the topic "2-aminobenzonitrile"

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Ru, Zong-Ling, and Guo-Xi Wang. "Bis(2-aminobenzonitrile)tetraaquacobalt(II) dichloride." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (November 28, 2009): m1688. http://dx.doi.org/10.1107/s1600536809050272.

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Marinho, Elina, and M. Proença. "The Reaction of 2-(Acylamino)benzonitriles with Primary Aromatic Amines: A Convenient Synthesis of 2-Substituted 4-(Arylamino)quinazolines." Synthesis 47, no. 11 (March 17, 2015): 1623–32. http://dx.doi.org/10.1055/s-0034-1380322.

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2-Substituted 4-(arylamino)quinazolines were prepared from 2-(acylamino)benzonitriles and primary arylamines by refluxing in either ethanol using trifluoroacetic acid as a catalyst or acetic acid. The 2-aminobenzonitrile was acylated by reaction with anhydrides, isocyanates, or ethyl chloroformate at room temperature.
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Sheng, Zhi-Zheng, Min-Min Huang, Teng Xue, Fei Xia, and Hai-Hong Wu. "Alcohol amine-catalyzed CO2 conversion for the synthesis of quinazoline-2,4-(1H,3H)-dione in water." RSC Advances 10, no. 57 (2020): 34910–15. http://dx.doi.org/10.1039/d0ra06439d.

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Commercial DEA is proposed for efficiently promoting the cyclization of CO2 and 2-aminobenzonitrile to quinazoline-2,4(1H,3H)-dione (up to 94% yield) while water acts as the solvent and co-catalyst.
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Fuster, Marta G., Imane Moulefera, Mercedes G. Montalbán, José Pérez, Gloria Víllora, and Gabriel García. "Synthesis and Characterization of New Ruthenium (II) Complexes of Stoichiometry [Ru(p-Cymene)Cl2L] and Their Cytotoxicity against HeLa-Type Cancer Cells." Molecules 27, no. 21 (October 26, 2022): 7264. http://dx.doi.org/10.3390/molecules27217264.

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When the [Ru(p-cymene)(μ-Cl)Cl]2 complex is made to react, in dichloromethane, with the following ligands: 2-aminobenzonitrile (2abn), 4-aminobenzonitrile (4abn), 2-aminopyridine (2ampy) and 4-aminopyridine (4ampy), after addition of hexane, the following compounds are obtained: [Ru(p-cymene)Cl2(2abn)] (I), [Ru(p-cymene)Cl2(4abn)] (II), [Ru(p-cymene)Cl2(2ampy] (III) and [Ru(p-cymene)Cl2(μ-(4ampy)] (IV). All the compounds are characterized by elemental analysis of carbon, hydrogen and nitrogen, proton nuclear magnetic resonance, COSY 1H-1H, high-resolution mass spectrometry (ESI), thermogravimetry and single-crystal X-ray diffraction (the crystal structure of III is reported and compared with the closely related literature of II). The cytotoxicity effects of complexes were described for cervical cancer HeLa cells via 3-(4.5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide (MTT) assay. The results demonstrate a low in vitro anticancer potential of the complexes.
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Boukthir, Mona, Fathi Zribi, Mohamed Belhouchet, and Fakher Chabchoub. "A Facile Synthesis of Pyrimidoquinazoline Derivatives." JOURNAL OF ADVANCES IN CHEMISTRY 7, no. 3 (December 17, 2011): 1434–39. http://dx.doi.org/10.24297/jac.v7i3.2379.

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A series of pyrimidoquinazoline are prepared via the reaction of ethyl 2,2-dicyano-1-arylvinylcarbamate derivatives 1a-b with methyl 2-aminobenzoate, 1-(2-aminophenyl)ethanone and 2-aminobenzonitrile. The reactivity of compounds 1a-b toward 3-amino-4,6-diphénylnicotinonitrile are studied. The structures of the synthesized compounds are elucidated by X-ray diffraction, IR spectroscopy and nuclear magnetic resonance.
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Ahuja, I. S., and Shailendra Tripathi. "X-ray diffraction studies on dichloro-(2-aminobenzonitrile)copper(II)." Crystal Research and Technology 25, no. 6 (June 1990): K130—K132. http://dx.doi.org/10.1002/crat.2170250623.

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Lang, Xian-Dong, Shuai Zhang, Qing-Wen Song, and Liang-Nian He. "Tetra-butylphosphonium arginine-based ionic liquid-promoted cyclization of 2-aminobenzonitrile with carbon dioxide." RSC Advances 5, no. 20 (2015): 15668–73. http://dx.doi.org/10.1039/c4ra16057f.

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Tetra-butylphosphonium arginine-based IL able to activate both amino-groups and CO2 proved to be an efficient and recyclable catalyst for the synthesis of quinazoline-2,4(1H,3H)-diones from 2-aminobenzonitriles and CO2 under solvent-free conditions.
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Brodersen, Klaus, and Jürgen Hofmann. "Synthese und Kristallstruktur von Bis(o-aminobenzonitril)-diquecksilber(I)-dinitrat / Synthesis and Crystal Structure of Bis(o-aminobenzonitrile)dimercury(I)-dinitrate." Zeitschrift für Naturforschung B 46, no. 12 (December 1, 1991): 1684–88. http://dx.doi.org/10.1515/znb-1991-1217.

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[Hg2(o-NH2C6H4CN)2](NO3)2 is formed by the reaction of o-aminobenzonitrile with dimercury(I)-dinitrate in methanol. It crystallizes in the monoclinic space group P 2/c with a = 8.6819(5)Å, b = 5.3696(6)Å, c = 19.7645(8)Å, β = 95.138(12)° and Ζ = 2. The crystal structure has been determined by single crystal X-ray diffraction with applied gaussian absorption correction and refined to an Rw-value of 0.027.The Hg22+-ion is coordinated to both amino nitrogen atoms. Strong hydrogen bonds and bridging nitrate ions lead to chain structure.
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Jonathan Fray, M., Paul Allen, Paul R. Bradley, Clare E. Challenger, Michael Closier, Tim J. Evans, Mark L. Lewis, et al. "Synthesis of 5-Heterocyclic Substituted Quinazolin-4-ones via 2-Aminobenzonitrile Derivatives." HETEROCYCLES 67, no. 2 (2006): 489. http://dx.doi.org/10.3987/com-05-s(t)17.

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Moitsheki, Lesego J., Susan A. Bourne, and Luigi R. Nassimbeni. "catena-Poly[[bis(thiocyanato-κN)cobalt(II)]-di-μ-2-aminobenzonitrile-κ2N,N′]." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (November 16, 2005): m2580—m2581. http://dx.doi.org/10.1107/s1600536805036846.

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Dissertations / Theses on the topic "2-aminobenzonitrile"

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El, Haj Brahim Ichrak. "Préparation stéréosélective de 2-alcynyldiols-1,3 ou 2-alcynylaminoalcools-1,3 : synthèse des hétérocycles condensés issus du 2- aminobenzonitrile." Electronic Thesis or Diss., Sorbonne université, 2023. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2023SORUS495.pdf.

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Cette thèse s'est orientée autour de deux axes de recherche distincts. En premier lieu, nous avons exploré la synthèse des 4-hydroxy-1-boryl-1-allenylsilanes, en adoptant une approche innovante à partir d'époxydes acétyléniques et du (triéthylsilyl)pinacolborane. Cette méthode a permis une préparation stéréosélective et stéréospécifique d'allénylboranes, suivant un mécanisme SNi anti. De plus, l'utilisation de ces 4-hydroxy-1-boryl-1-allenylsilanes pour la propargylation des aldéhydes a conduit, de manière stéréosélective, aux 2-alcynyldiols-1,3. Un état de transition impliquant une structure à six chaînons fermés a été proposé pour cette transformation, suggérant un mécanisme SE2’. L'ampleur et les limitations de ces deux processus ont été rigoureusement examinées. Ensuite, le second aspect de cette thèse a concerné la synthèse de composés hétérocycliques à partir du 2-aminobenzonitrile, en mettant l'accent sur le 1,2,4-triazole. Nous avons par la suite élaboré des dimères et étudié leur réactivité envers des électrophiles, tels que le hexaméthylphosphoramide, avec l'objectif de créer des dérivés de diazaphorine. À l'heure actuelle, une analyse est en cours pour évaluer les propriétés antioxydantes des molécules récemment synthétisées, en particulier des dimères iminiques et phosphoazotés
This thesis revolved around two distinct research avenues. Firstly, we delved into the synthesis of 4-hydroxy-1-boryl-1-allenylsilanes, adopting an innovative approach using acetylenic epoxide and silylborane. This method enabled a stereoselective and stereospecific preparation of allenylboranes, following an SNi anti mechanism. Moreover, we employed these allenes for the propargylation of aldehydes, which led to the stereoselective formation of the corresponding 2-alkynyl-1,3-diols. A transition state involving a closed six-membered ring structure was proposed for this transformation, suggesting an SE2' mechanism. The scope and limitations of these processes were meticulously assessed. Subsequently, the second focus of the thesis pertained to the synthesis of heterocyclic compounds starting from 2-aminobenzonitrile, with a particular emphasis on the 1,2,4-triazole. Following this, we synthesized dimers and investigated their reactivity towards electrophiles, such as hexamethylphosphoramide, aiming to generate diazaphorine derivatives. As of now, an evaluation is underway to gauge the antioxidant properties of the newly synthesized molecules, especially the iminic and phosphoazo dimers
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Book chapters on the topic "2-aminobenzonitrile"

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Döpp, H., and D. Döpp. "Diazotization of 2-Aminobenzonitrile or Aminohetarenecarbonitrile/Cyclization with Primary Amines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00424.

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Larsen, R. D. "From Anthranilates or 2-Aminobenzonitriles." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00930.

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Kikelj, D. "From 2-Aminobenzonitriles and Nitriles." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00766.

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Kikelj, D. "From 2-Aminobenzonitriles and Formic Acid." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00790.

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Kikelj, D. "From 2-Aminobenzonitriles and Guanidines, Imidates, or Formimidamides." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00765.

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Kikelj, D. "From 2-Aminobenzonitriles and Formamide or 1,3,5-Triazine." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00767.

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Kikelj, D. "From 2-Aminobenzonitriles and Thioamides or Thioacetic Acid." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00791.

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Kikelj, D. "From 2-Aminobenzonitriles and Chlorosulfonyl Isocyanate, Urea, or Thiourea." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00764.

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Döpp, H., and D. Döpp. "Cyclization of 2-Aminobenzonitriles and Related Compounds with Nitric Acid." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00417.

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Kikelj, D. "From 2-Aminobenzonitriles, Grignard Reagents, and Carbonyl Compounds or Phosgene Iminium Chlorides." In Six-Membered Hetarenes with Two Identical Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00792.

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Conference papers on the topic "2-aminobenzonitrile"

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Molis, Steven E., and Robert J. Twieg. "Fourier-transform IR characterization of molecular orientation in poled polymer glasses." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.the2.

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The electro-optical activity of organic, nonlinear optical (NLO) systems in part depends on the extent of molecular orientation of the NLO moiety. In this investigation, the technique of using infrared absorption spectroscopy to characterize molecular orientation is introduced as a means of characterizing orientational order in poled polymer glasses. A quantitative understanding of this orientation can be used in modeling the field-induced orientation of a dipole as well as for determining the polarizabilities of new NLO substituents. In this initial investigation the orientation of organic guest molecules in corona-poled guest/host systems is investigated with FTIR spectroscopy. The guest molecules include 2-methyl-4-nitroanaline and 4-aminobenzonitrile. For compatibility, we usually used polymethylmethacrylate (PMMA) as the matrix polymer, and it is interesting that some of the PMMA substituent groups also exhibit field-induced orientation. Molecular orientation parameters and relaxation behavior of these systems will be presented.
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