Relevant bibliographies by topics / 2-aryl-2

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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 '2-aryl-2'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "2-aryl-2"

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Burchardt, Annette, and Detlef Geffken. "N-Substituierte 2-Aryl-2-hydroxycarbohydroxamsäuren N-Substituted 2-Aryl-2-hydroxy-carbohydroxamic Acids." Archiv der Pharmazie 323, no. 3 (1990): 181–83. http://dx.doi.org/10.1002/ardp.19903230310.

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LEHNERT, W. "3-Aryl-2-nitropropansäure-ester aus 3-Aryl-2-nitro-2-propensäure-estern." Synthesis 1976, no. 12 (2002): 827–29. http://dx.doi.org/10.1055/s-1976-24226.

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Feigenbaum, Alexandre, Yves Fort, Jean Pierre Pete, and Denise Scholler. "Photochemical cyclization of 2-alkyl-3-aryl-2-cyclohexenones and 2-alkoxy-3-aryl-2-cyclohexenones." Journal of Organic Chemistry 51, no. 23 (1986): 4424–32. http://dx.doi.org/10.1021/jo00373a015.

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Kashima, Choji, and Hideki Arao. "Synthesis of 2-Aryl- and 5-Alkyl-2-aryloxazoles from 2-Aryl-5-bromooxazoles." Synthesis 1989, no. 11 (1989): 873–74. http://dx.doi.org/10.1055/s-1989-27419.

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Matiichuk, Yuliia, Yuri Gorak, Roman Martyak, et al. "Synthesis and antimicrobial activity of 4-(5-ARYL-2-FUROYL)morpholines and 4-[(5-ARYL-2-FURYL)carbonothioyl] morpholines." Pharmacia 68, no. (1) (2021): 175–79. https://doi.org/10.3897/pharmacia.68.e46942.

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By the reaction of furan-2-carboxylic acids and furfural with diazonium salts 1a-j the arylfuran-2-carboxylic acids 4a-e and 5-arylfuran-2-carbaldehydes 5a-f were synthesized. Acids 4a-e were transformed into appropriated acylchlorides 6a-e and were used for preparation of 4-(5-aryl-2-furoyl)morpholines 7a-e. 4-[(5-Aryl-2-furyl)carbonothioyl]morpholines 8a-f were prepared from aldehydes 5a-f by using Willgerodt-Kindler reaction. The structures of the obtained compounds were confirmed by <sup>1</sup>H NMR spectroscopy and elemental analysis. All these new compounds gave spectroscopic data in ac
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Cativiela, C., M. P. López, and J. A. Mayoral. "Synthesis of 2-Aryl-2-methylglycine Derivatives." Synlett 1992, no. 02 (1992): 121–22. http://dx.doi.org/10.1055/s-1992-21285.

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TODA, Kazuya, Masuo GOTO, Yasuo KIKUCHI, et al. "Synthesis and Herbicidal Activity of N-Aryl-2-methyl-2-aryipropanamides and N-Aryl-2-methyl-2-arylbutanamides." Journal of Pesticide Science 13, no. 1 (1988): 19–27. http://dx.doi.org/10.1584/jpestics.13.19.

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Ciganek, Engelbert. "2-(Methoxymethyl)--3-aryl-2-propenoic Acids and 2-(Bromomethyl)-3-aryl-2-propenoic Acids from Aromatic Aldehydes." Journal of Organic Chemistry 60, no. 14 (1995): 4635–37. http://dx.doi.org/10.1021/jo00119a047.

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Kolyamshin, O. A., and V. A. Danilov. "N-Aryl-2-dialkylaminosuccinimides." Russian Journal of Organic Chemistry 40, no. 7 (2004): 982–85. http://dx.doi.org/10.1023/b:rujo.0000045189.81688.f3.

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Kovalev, Vladimir V., Andrey K. Rozov, and Elvira A. Shokova<. "Stereoselective Isomerisation of 2-Aryl-2-hydroxyadamantanes: A Convenient Method for (Z)-2-Aryl-5-hydroxyadamantanes." Synlett 1990, no. 12 (1990): 739–40. http://dx.doi.org/10.1055/s-1990-21232.

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Dissertations / Theses on the topic "2-aryl-2"

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White, David Charles. "Synthesis of 3-Aryl-2-(2-aryl-2-oxoethyl)pyrido[2,3-d]-4(3H)pyrimidones and 3-Aryl-2-(2-arylethenyl)pyrido[2,3-d]-4(3H)pyrimidones as Potential Antiepileptic Drugs." Thesis, Virginia Tech, 1997. http://hdl.handle.net/10919/46506.

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A series of 2-alkyl-3-arylpyrido[2,3-d]pyrimidones were synthesized for testing as potential antiepileptic drugs. The goal was to achieve better neurological activity and/or lower toxicity than displayed by a series of 2-alkyl-3-aryl-4(3H)-quinazolinones prepared previously in our research group. From the pharmacological testing data of these target compounds, we have found that the additional nitrogen at the C-8 position of the quinazolinone framework increased the anticonvulsant activity. However, the neurological toxicity increased as well. The anticonvulsant and neurotoxic activi
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Fuglseth, Erik. "Synthesis of 1-aryl-2-fluoroethanones and their use in the preparation of enantioenriched 1-aryl-2-fluoroethanols and 1-aryl-2-fluoroethylamines." Doctoral thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for kjemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-11631.

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Tembo, Norbert Olivier. "Synthèse et étude physicochimique des 4-amino-1, 2, 3, 4-tétrahydro-1-isoquinolones et 2-quinolones ; 4-aryl-2, 3-dihydropyrrolizines ; 4-aryl-1-oxo-1, 2, 3, 4-tétrahydro-pyrrolo [1, 2-a] pyrazines ; 4-aryl-2-imidazolidinones." Caen, 1990. http://www.theses.fr/1990CAEN4044.

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Stoddart, Barry. "The structural and spectroscopic characterisation of 2-aryl and 2-heteroaryl isatogens." Thesis, University of Sunderland, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.258718.

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This work reviews the current knowledge of the synthesis , properties , structures and biological activities of isatogens. The unequivocal 2 C NMR assignment of 2-phenylisatogen 1S reported and used to assign the spectra for a range of 2-(4-substituted-phenyl)isatogens. Molecular dynamics of 2-phenylisatogen in chloroform are reported and indicate that there is little if any inter-ring mesomeric resonance in this compound. 1~C , ~N NMR and UV-Visible spectroscopic data are reported for a range of 2-(4-substituted-phenyl)isatogens. Analysis of this data indicates a small but significant degree
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Cui, Xiuhua. "Asymmetric hydrogenations of aryl alkenes using imidazol-2-ylidene iridium complexes." Texas A&M University, 2005. http://hdl.handle.net/1969.1/2456.

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A library of iridium complexes featuring oxazoline and imidazol-2-ylidene ligands were synthesized by reaction of a library of imidazoles with a second library of oxazoline iodides. These complexes were active catalysts for hydrogenations of aryl substituted monoenes. Tri- and 1,1-disubstituted alkenes were hydrogenated quantitatively with ee??s up to 99% at 1 atm hydrogen pressure. Catalyst, substrate, temperature and pressure effects were studied. The iridium complexes were also used for the kinetic study of hydrogenation of 2,3- diphenylbutadiene. This hydrogenation is a stepwise reaction:
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Hassan, Ahmad. "Etude analytique de quelques anti-inflammatoires non stéroi͏̈diens aryl 2 propioniques." Bordeaux 2, 1990. http://www.theses.fr/1990BOR2B001.

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Sheridan, Jared. "Partnership between the aryl hydrocarbon receptor (AHR) and RELB regulates cigarette smoke-induced cyclooxygenase-2 (COX-2) expression." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123307.

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Chronic obstructive pulmonary disease (COPD) is an inflammatory disease of the lungs caused by cigarette smoke exposure; COPD is also now the third leading cause of death worldwide. Controlling lung inflammation is a priority in COPD patients, but currently-available medications offer little relief. Thus, new therapeutic targets represent a major unmet need. Previously, the aryl hydrocarbon receptor (AHR) has been shown to suppress cigarette smoke-induced inflammation. The AHR is a ligand-activated transcription factor, and well-established for its response to xenobiotic ligands. AHR-mediated
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BRINE, NOURDINE. "Etude de la catalyse par des halogenures metalliques supportes sur silica gel, de l'ouverture des 3-aryl-2-cyano-2-methoxycarbonyloxiranes et de l'alkylation par les phenols des 3-aryl-3-hydroxy-2-methylenepropionates de methyle." Rennes 1, 1993. http://www.theses.fr/1993REN10065.

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Ce memoire etudie la modification de la reactivite d'un halogenure metallique (fecl#3, znbr#2, cucl#2, cubr#2, cocl#2) par depot sur le silica gel. Cette reactivite est determinee en utilisant ces halogenures metalliques comme catalyseurs de deux types de reactions: l'ouverture du cycle des 3-aryl-2-cyano-2-methoxycarbonyl oxiranes et l'alkylation des phenols par les 3-aryl-3-hydroxy-2-methylene propionates de methyle. Dans la premiere partie on decrit la transformation des epoxydes en cyanhydrines chlorees par fecl#3/sio#2 et en alpha-ceto esters beta-halogenes par cocl#2/sio#2 ou znbr#2/sio#
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Guan, Zong [Verfasser]. "Eigenschaften und Reaktionen von 2-Alkyl-1-aryl-1H-Indazolcarbenen / Zong Guan." Clausthal-Zellerfeld : Universitätsbibliothek Clausthal, 2015. http://d-nb.info/1078276927/34.

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Soraci, Alejandro L. "Métabolisation stéréosélective comparée des acides aryl-2-propioniques : inversion chirale et glucuronoconjugaison." Lyon 1, 1995. http://www.theses.fr/1995LYO1T073.

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Books on the topic "2-aryl-2"

1

Ikhlef, Fatima. Routes to 4-aryl-1-N-methylanilinobut-3-en-2-ones and reactions of 2-phenylethylamine. University of Salford, 1985.

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2

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. De Montfort University, 1996.

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Schwandt, Samy. Synthese neuer 2-Aryl-1,4-naphthochinone und Formulierung eines Struktur-Wirkungs-Modells zur 5-Lipoxygenase-Inhibition. 1999.

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Jäger, Jürgen. (R)-Oxynitrilase katalysierte Cyanhydrinsynthese mit Hydroxybenzaldehyden: Enantioselektive Synthesen pharmakologisch interessanter 2-Amino-1-aryl-alkohole und Amphetamine. 1996.

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5

Kreher, Mareta. 2,3-Dihydro-pyrrolo[2,1-b]oxazole, 2,3-Dihydro-pyrrolo[2,1-b]thiazole, 2-Aryl-pyrrolo[2,1-b]benzothiazole und 2,3-Dihydro-1H-pyrrolizine: Synthese, Analytik und Testung der antiinflammatorischen Wirksamkeit sowie der modifizierte HET-CAM-Test als Modell zur Bestimmung der antiphlogistichen und antirheumatischen Wirksamkeit von Arzneistoffen. 1995.

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Book chapters on the topic "2-aryl-2"

1

Barnes, K. D., J. A. Furch, M. Rivera, S. Trotto, R. Ward, and D. Wright. "Insecticidal 2-Aryl-3-trifluoromethylsulfonylpyrroles." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch027.

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Konz, M. J., S. J. Cuccia, and S. Sehgel. "2-Aryl-1,2,4-triazin-3-ones and 2-Aryl-1,2,4-triazepin-3-ones." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0355.ch011.

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Guaciaro, Michael A., Marinus Los, Ronald K. Russell, et al. "o-(5-Thiono-2-imidazolin-2-yl)aryl Carboxylates." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0355.ch008.

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Tice, Colin M., Lois M. Bryman, Renee C. Roemmele, et al. "Synthesis of Herbicidal 2-Aryl-4-(3H)-pyrimidinones." In ACS Symposium Series. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0800.ch006.

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Barnes, K. D., Y. Hu, R. E. Diehl, and V. M. Kamhi. "Insecticidal 2-Aryl-5-haloalkylthio-, sulfinyl-and sulfonylpyrroles." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch016.

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Reddy, C. D., K. D. Berlin, M. ElMasri, et al. "Reaction of 2-Amino-4-Substituted Phenols with Aryl Phosphorodichloridates." In ACS Symposium Series. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0486.ch013.

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Karamancheva, Ilyana R., Tzwetanka S. Philipova, Neyko M. Stoyanov, Iwanka S. Losseva, and Boris V. Aleksiev. "FT-IR Spectra of Enol-esters of 2-Aryl-2,3-dihydrophenalene-1,3-diones." In Progress in Fourier Transform Spectroscopy. Springer Vienna, 1997. http://dx.doi.org/10.1007/978-3-7091-6840-0_127.

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Lyga, John W., Blaik P. Halling, Debra A. Witkowski, et al. "Synthesis, Herbicidal Activity, and Action Mechanism of 2-Aryl-1,2,4-triazine-3,5-diones." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch014.

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Cassayre, Jérôme, Ottmar Hüter, Dave Hughes, et al. "Synthesis and Insecticidal Activity of New 2-Aryl-3,5-dihydro-2H-1,4-Benzoxazepine Derivatives." In ACS Symposium Series. American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1204.ch028.

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Shang, Rui. "Construction of C(sp3)–C(sp2) Bonds Via Palladium-Catalyzed Decarboxylative Couplings of 2-(2-Azaaryl)Acetate Salts with Aryl Halides." In Springer Theses. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-3193-9_5.

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Conference papers on the topic "2-aryl-2"

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Eckel, Zak, and Yash Adhia. "New Advances in Corrosion Protection: Powder Coating of PEKK." In CONFERENCE 2024. AMPP, 2024. https://doi.org/10.5006/c2024-20610.

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Abstract Poly Ether Ketone Ketone (PEKK) is part of the Poly Aryl Ether Ketone (PAEK) family of ultra-high-performance polymers. These polymers have an outstanding combination of physical, chemical, and thermal properties making them excellent for anti-corrosive coatings in demanding applications. Through the development of a unique copolymer structure, the ratio of monomer units allows a range of melting points (305 -358 °C) and crystallization rates (t1/2: 2-32 minutes). This capability significantly broadens the processing window of PEKK compared to other PAEKs and thermoplastic powder coat
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Kharche, Ajay, Sandeep Waghulde, Nilesh Gorde, and Mohan Kale. "MICROWAVE ASSISTED SYNTHESIS OF 2-ARYL BENZIMIDAZOLE." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08475.

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Aidhen, Indrapal Singh, and Sivalenka Vijayasaradhi. "A SIMPLE APPROACH TOWARDS 2-DEOXY-C-ARYL PYRANOSIDES." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.573.

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Nunes, Vanessa Lóren, (PG) Ingryd Cristina de Oliveira, and Olga S. do Rêgo Barros. "Copper(I)-Senelenophene-2-carboxylate Catalyzed Cross- Coupling of Aryl or alkyl Thiols And Aryl Halides." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0177-1.

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Radatz, Cátia S., Daniel S. Rampon, Renata A. Balaguez, Diego Alves, and Paulo H. Schneider. "Synthesis of 2-aryl-1,3-benzoselenazoles from bis(2- aminophenyl) diselenides and carboxylic acids using PBu3." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915175028.

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Joubert, Nicolas, Jan Bárta, Milan Urban, and Michal Hocek. "Modular methodology for the syntheses of various aryl C-2'-deoxyribonucleosides." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810173.

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Mayorova, Oksana A., Vyacheslav S. Grinev, and Alevtina Yu Yegorova. "Reaction of 5-aryl-furan-2(3H)-ones with triazolyldiazonium salts." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069329.

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Shipilovskikh, Sergei A., R. R. Makhmudov, S. Yu Balandina, and Aleksandr E. Rubtsov. "Search of antimicrobial activity in a series of substituted 4-aryl-4-oxo-2-tienilaminobut-2-enoic acids." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018494.

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Jampilek, Josef, Jiri Dohnal, Zuzana Kaderavkova, and Jarmila Vinsova. "Synthesis and Hydrophobic Properties of New 2-Aryl-5,7-di-tert-butylbenzoxazoles." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01306.

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Pindjakova, Dominika, Lucia Vrablova, Tomas Strharsky, Jiri Kos, and Josef Jampilek. "Investigation of Interactions of ortho- and para-N-Aryl-Substituted 2-Trifluoromethylcinnamanilides." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11651.

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Reports on the topic "2-aryl-2"

1

Ruangpornvisuti, Vithaya. A Study of conformational equilibrium of semicarbazone derivatives and their complexes with cations : research report. Chulalongkorn University, 2006. https://doi.org/10.58837/chula.res.2006.36.

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The structure optimizations of picolinaldehyde N-oxide thiosemicarbazone (Hpiotsc), 2-benzoylpyridine semicarbazone (H2BzPS), their imino tautomers and their complexes with Ni(II), Cu(II) and Zn(II) were carried out using DFT calculations at the B3LYP/LANL2DZ level of theory. Thermodynamic properties of tautomerizations of Hpiotsc and H2BzPS and complexations of their complexes derived from the frequency calculations at the same level were obtained. The B3LYP/LANL2DZ-optimized geometry parameters for the complexes of [[Ni(Hpiotsc)[subscript 2]][superscript 2+]], [Cu(Hpiotsc).Cl[subscript 2]] a
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