Academic literature on the topic 'Imidazoles – Derivatives'

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Journal articles on the topic "Imidazoles – Derivatives"

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Aly, Ashraf A. "Base Catalyzed Synthesis of Novel Fused-Imidazoles from N-Vinyl-1H-imidazole." Zeitschrift für Naturforschung B 60, no. 1 (2005): 106–12. http://dx.doi.org/10.1515/znb-2005-0116.

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Syntheses of various classes of fused-imidazoles are reported. The key to their successful synthesis depends on the reaction of N-vinyl-1H-imidazole with the π-deficient compounds under basic conditions. Reaction of the target imidazole with 1,1,2,2-tetracyanoethylene and dimethyl acetylenedicarboxylate afforded pyrrolo[1,2-a]imidazoles. On the other site, reaction of the target imidazole with 2-dicyanomethyleneindane-1,3-dione, 2,3-dicyano-1,4-naphthoquinone gave indanylimidazolo- [1,2-a]azepine and imidazolo[2,1-a]phenanthridine derivatives, respectively. Under basic reaction condition, vari
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Beckert, Rainer, Catharina Hippius, Tillmann Gebauer, et al. "Syntheses and Properties of Cycloamidines Based on 4H-Imidazoles." Zeitschrift für Naturforschung B 61, no. 4 (2006): 437–47. http://dx.doi.org/10.1515/znb-2006-0411.

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Employing three different syntheses a broad spectrum of 4H-imidazoles 3a - 3s has been synthesized. In the course of the two-fold aminolysis reaction leading to derivatives 3q - 3s, deeply colored byproducts could be isolated and structural characterized.These novel donor-acceptor derivatives of type 7 consist of an 1H- and 4H-imidazole which are connected by a nitrogen bridge and rearrange via rapid 1,3-/1,5-hydride shifts. Using 1H NMR experiments the aminolysis product 3p shows prototropic isomers which could be detected in equilibrium for the first time. Cyclovoltammetric measurements of a
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Matschke, Martin, Jorg Blumhoff, Rainer Beckert, and Wolfgang Imhof. "The Synthesis of Carboxy- and Cyano-substituted 4H-Imidazoles: Redoxactive Ligands as Starting Materials for Metal-Metal Multiply Bonded Compounds and Heterobimetallic Complexes." Zeitschrift für Naturforschung B 64, no. 6 (2009): 624–28. http://dx.doi.org/10.1515/znb-2009-0606.

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Cyanobenzoic acids proved to be suitable starting materials for the transformation into multifunctional products of the 4H-imidazole type. Employing two different pathways, the new derivatives 1b-d which possess carboxy/cyano groups were synthesized. In addition, derivative 1d formed the basis for the construction of novel bis-4H-imidazoles with two different complexation spheres. The structures of all new derivatives were confirmed by NMR spectroscopy, mass spectrometry, elemental analysis, UV/Vis-/fluorescence spectroscopy, and electrochemical measurements.
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Singh, Praveen, Ranjeet Kumar, and Ashish Kumar Tewari. "Hydrogen bonding framework in imidazole derivatives: Crystal structure and Hirshfeld surface analysis." European Journal of Chemistry 11, no. 1 (2020): 50–59. http://dx.doi.org/10.5155/eurjchem.11.1.50-59.1945.

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A series of imidazole derivatives (1-3) were synthesized with three component reaction among benzil, ammonium acetate and formaldehyde/aromatic aldehyde at 110 °C without a catalyst and solvent. These synthesized imidazole derivatives have shown intermolecular hydrogen bonding such as N-H···N and O-H···N. The imidazole 1 and 2 exhibited N-H···N intermolecular hydrogen bonding while imidazole 3 exhibited O-H···N intermolecular hydrogen bonding. The hydrogen bonds in imidazoles were studied by X-ray crystallography and Hirshfeld Surface Analysis at dnorm surface which show the visible red spots,
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Yakovychuk, N. D., S. Y. Deyneka, A. M. Grozav, A. V. Humenna, V. B. Popovych та V. S. Djuiriak. "Аntifungal activity of 5-(2-nitrovinyl) imidazoles and their derivatives against the causative agents of vulvovaginal candidiasis". Regulatory Mechanisms in Biosystems 9, № 3 (2018): 369–73. http://dx.doi.org/10.15421/021854.

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Development of resistance of yeast-like fungi belonging to the Candida genus to the existing antifungal medicines as well as the high toxicity and low tolerance of these medicines in many cases stipulate the acute need for new antibiotic compounds. In this context, an extremely promising group of chemical substances is imidazole derivatives. Therefore, the search for more active and less toxic medical preparations based on imidazole is a relevant and important issue for medical practice. Considering the urgent demand for new antifungal preparations, four new nitro containing imidazole derivati
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Knölker, Hans-Joachim, and Abdel-Aziz El-Ahl. "Imidazole Derivatives, Part VIII. Stereoselective Formation of 1-[(E) 3-(1-Imidazolyl)-2-alkenoyl]imidazoles." HETEROCYCLES 36, no. 6 (1993): 1381. http://dx.doi.org/10.3987/com-93-6335.

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Aggarwal, Mayank, Bhargav Kondeti, Chingkuang Tu, C. Mark Maupin, David N. Silverman, and Robert McKenna. "Structural insight into activity enhancement and inhibition of H64A carbonic anhydrase II by imidazoles." IUCrJ 1, no. 2 (2014): 129–35. http://dx.doi.org/10.1107/s2052252514004096.

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Human carbonic anhydrases (CAs) are zinc metalloenzymes that catalyze the hydration and dehydration of CO2and HCO3−, respectively. The reaction follows a ping-pong mechanism, in which the rate-limiting step is the transfer of a proton from the zinc-bound solvent (OH−/H2O) in/out of the active siteviaHis64, which is widely believed to be the proton-shuttling residue. The decreased catalytic activity (∼20-fold lower with respect to the wild type) of a variant of CA II in which His64 is replaced with Ala (H64A CA II) can be enhanced by exogenous proton donors/acceptors, usually derivatives of imi
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Skonieczny, Kamil, Jarosław Jaźwiński, and Daniel Gryko. "The Synthesis of Imidazo[1,2-f]phenanthridines, Phenanthro-[9,10-d]imidazoles, and Phenanthro[9′,10′:4,5]imidazo[1,2-f]-phenanthridines via Intramolecular Oxidative Aromatic Coupling." Synthesis 49, no. 20 (2017): 4651–62. http://dx.doi.org/10.1055/s-0036-1589053.

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A short and efficient access to phenanthro[9,10-d]imidazoles, imidazo[1,2-f]phenanthridines, and phenanthro[9′,10′:4,5]imidazo[1,2-f]phenanthridines was achieved by the action of [bis(trifluoroacetoxy)iodo]benzene (PIFA) on properly substituted tetraaryl­-imidazoles. By pre-installing suitable electron-donating groups, it is possible to control the site of intramolecular oxidative aromatic coupling. In particular, by placing 3,4-dimethoxyphenyl and 3-methoxyphenyl moieties in close proximity, it was possible to direct the reaction into forming two biaryl linkages leading eventually to the form
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Aggarwal, Mayank, Chingkuang Tu, David Silverman, and Robert McKenna. "Insights into Activity Enhancement of H64A Carbonic Anhydrase by Imidazoles." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C803. http://dx.doi.org/10.1107/s2053273314091967.

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Human carbonic anhydrases (CAs) are zinc metalloenzymes that catalyze the hydration and dehydration of CO2 and HCO3-, respectively. The reaction follows a ping-pong mechanism, where the rate limiting step is the transfer of a proton from the zinc-bound solvent out of the active site, via His64 which is widely believed to be the proton shuttling residue. Being involved in a number of physiological processes such as respiration, pH regulation, ureagenesis etc., CAs are therapeutic targets for inhibition to treat various diseases. However, the physiologically dominant isoform is CA II, which is c
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Al-Soud, Yaseen A., Ala’a H. Al-Ahmad, Luay Abu-Qatouseh, et al. "Nitroimidazoles Part 9. Synthesis, molecular docking, and anticancer evaluations of piperazine-tagged imidazole derivatives." Zeitschrift für Naturforschung B 76, no. 5 (2021): 293–302. http://dx.doi.org/10.1515/znb-2020-0200.

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Abstract New piperazine-tagged imidazole derivatives were synthesized via reaction of 1-alkyl/aryl-5-bromo-2-alkyl-4-nitro-1H-imidazoles 1–3 with piperazine nucleophiles. Nine selected compounds were assessed for their antiproliferative inhibition potency against five human cancer cell lines (MCF-7, PC3, Du145, HepG2 and Dermal/Fibroblast). Compounds 7 and 10 are the most potent anticancer agents on HepG2 cell line with IC50 values of (5.6 ± 0.5 µm) and (29.6 ± 7.6 µm) respectively, and on MCF-7 with IC50 values of (32.1 ± 5.6 µm) and (46.2 ± 8.2 µm) respectively. The molecular docking of comp
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Dissertations / Theses on the topic "Imidazoles – Derivatives"

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Björk, Malin. "Synthesis of sulfur and seleniumn heterocycles, including derivatives of imidazopyridine and benzimidazole /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-597-6/.

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Ierno, Hélène. "Modélisation chimique de protéines fer-soufre : synthèses et caractérisations physico-chimiques de nouveaux agrégats à ligands imidazoles." Université Joseph Fourier (Grenoble ; 1971-2015), 1995. http://www.theses.fr/1995GRE10151.

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Durant ces dernieres annees, de nombreuses proteines fer-soufre ont ete decouvertes dont le site actif est relie a l'apoproteine par des ligands non-cysteinyles ; elles presentent des proprietes spectroscopiques et electrochimiques particulieres, liees a la nature des acides amines impliques dans la coordination du cur fer-soufre. Pour modeliser la coordination d'histidines sur les centres fer-soufre, nous avons prepare des agregats a ligands imidazoles neutres. Notre demarche synthetique fait intervenir des centres fer-soufre deja formes, a ligands halogenures, sur lesquels nous realisons une
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Moody, David John. "Studies of some fused imidazole derivatives." Thesis, University of St Andrews, 1986. http://hdl.handle.net/10023/11011.

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The main synthetic routes to benzimidazole N-oxides are outlined and some indication is given as to the current and potential pharmacological usefulness of such materials. A claim that 4-methyl-2-nitrophenylglycine is cyclised in acetic anhydride to give either 5-methylbenzimidazole 3-oxide or the isomeric 5 methylbenzimidazolone was investigated. This work was found to be impossible to duplicate. It is established that, by employing flash vacuum pyrolysis, the claimed products can be obtained thermolytically from the starting glycine. This is the first recorded example of the formation of an
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Wells, Doran K. "Synthesis of imidazole derivatives related to pinacidil." Thesis, Heriot-Watt University, 1993. http://hdl.handle.net/10399/1413.

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Sweidan, Kamal. "Derivate des Imidazols und der Barbitursäure heterozyklische Carben-Fragmente mit p-Donor- und Akzeptor-Funktion = Imidazol and barbituric acid derivatives /." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=979465427.

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Lothian, Aileen Patricia. "The synthesis and properties of novel imidazole derivatives." Thesis, Keele University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296074.

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Galgano, Paula Decot. "Líquidos iônicos tensoativos: correlação entre estrutura molecular e propriedades micelares de cloretos de 1,3-dialquilimidazólio." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-02052013-111536/.

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Este trabalho tem como objetivo a síntese e a determinação de propriedades micelares de líquidos iônicos tensoativos (LITs) catiônicos. Dentre as características importantes desses compostos destacamos: alta deslocalização da carga e caráter ácido no hidrogênio H2 do anel heterocíclico e a grande flexibilidade estrutural, estas são relevantes para as propriedades de soluções desses tensoativos, e, consequentemente, para suas aplicações. A influência da variação estrutural nas suas propriedades é importante para modular as propriedades micelares e, por consequência suas aplicações. A síntese de
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Jandu, Baljeet Kaur. "The synthesis of imidazole derivatives for the inhibition of steroid-mediated prostrate tumour growth." Thesis, Kingston University, 2013. http://eprints.kingston.ac.uk/28187/.

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The majority of prostate cancer cases are shown to be androgen-dependant for growth as the blocking of androgen production has shown to reduce the size of prostate metastasis. The biosynthesis of the androgens is catalysed by the cytochrome P450 enzyme 17a-hydroxylase/17,20-lyase (P45017a) by converting the C21 steroids (pregnenolone and progesterone) to the androgens (dehydroepiandrosterone and androstenedione, respectively). Inhibition of P45017a would therefore bring about a decrease in the level of androgen production and furthermore prevent an increase in the stimulation of androgen-depen
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Albuquerque, Cristina Northfleet de. "Synthèses et études physico-chimiques d'analogues du MEGAZOL, anti-parasitaire du type nitro-imidazole : étude de leur mode d'action." Toulouse 3, 1995. http://www.theses.fr/1995TOU30039.

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Le travail presente relevant d'une collaboration entre plusieurs equipes bresiliennes et celles de l'ups, porte sur l'etude de derives nitro-imidazoles susceptibles d'interagir par voie radicalaire pour produire diverses especes oxygenees. Ces composes sont utilises comme modeles pour definir les caracteristiques de nouvelles generations de molecules pouvant agir sur le metabolisme de l'oxygene de differents organismes. Cette strategie est plus particulierement appliquee au trypanosoma cruzi (responsable de la maladie de chagas, trypanosomiase de l'amerique du sud) parasite tres sensible aux m
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Sweidan, Kamal. "Imidazol and barbituric acid derivatives heterocyclic carbene fragments with pi-donor and acceptor properties /." [S.l. : s.n.], 2006.

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Books on the topic "Imidazoles – Derivatives"

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International Symposium on Agmatine and Imidazoline Systems (4th 2003 San Diego, Calif.). Agmatine and imidazolines: Their novel receptors and enzymes. New York Academy of Sciences, 2003.

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(Editor), John E. Piletz, Soundar Regunathan (Editor), and Paul Ernsberger (Editor), eds. Agmatine and Imidazolines: Their Novel Receptors and Enzymes (Annals of the New York Academy of Sciences). New York Academy of Sciences, 2004.

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Imidazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2009.

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The Treatment of Mycosis with Imidazole Derivatives. Springer, 2012.

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Arpe, H. J. High-Performance Fibers to Imidazole and Derivatives, Volume A13, Ullmann's Encyclopedia of Industrial Chemistry. 5th ed. Wiley-VCH, 1996.

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M, Göthert, Molderings Gerhard J, and Reis Donald J, eds. Imidazoline receptors and their endogenous ligands: Current concepts and therapeutic potential. New York Academy of Sciences, 1999.

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(Editor), M. Gothert, Gerhard J. Molderings (Editor), and Donald J. Reis (Editor), eds. Imidazoline Receptors and Their Endogenous Ligands: Current Concepts and Therapeutic Potential (Annals of the New York Academy of Sciences). New York Academy of Sciences, 1999.

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Imidazoline Receptors and Their Endogenous Ligands: Current Concepts and Therapeutic Potential (Annals of the New York Academy of Sciences, V. 881). New York Academy of Sciences, 1999.

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J, Reis Donald, Bousquet Pascal, Parini Angelo, and International Symposium on Imidazoline Receptors (2nd : 1994 : New York, N.Y.), eds. The imidazoline receptor: Pharmacology, functions, ligands, and relevance to biology and medicine. New York Academy of Sciences, 1995.

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The Imidazoline Receptor: Pharmacology, Functions, Ligands, and Relevance to Biology and Medicine (Annals of the New York Academy of Sciences, V. 763). New York Academy of Sciences, 1995.

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Book chapters on the topic "Imidazoles – Derivatives"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with imidazole derivative." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_470.

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Marzilli, Luigi G., and Patricia A. Marzilli. "FT-Raman Spectroscopy of Methyl-B12and of Imidazole and Imidazolate Methylcobinamide Derivatives." In Vitamin B12and B12-Proteins. Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612192.ch24.

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van Doorne, H., E. H. Bosch, and C. F. Lerk. "Interactions between Cyclodextrins and Some Antimycotic Imidazole Derivatives: Studies on Solubility and Antimicrobial Activity." In Proceedings of the Fourth International Symposium on Cyclodextrins. Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-2637-0_42.

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Alaoui, Khaoula, Nadia Dkhireche, Mohamed Ebn Touhami, and Younes El Kacimi. "Review of Application of Imidazole and Imidazole Derivatives as Corrosion Inhibitors of Metals." In New Challenges and Industrial Applications for Corrosion Prevention and Control. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-2775-7.ch005.

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Imidazole is part of the theophylline molecule, found in tea leaves and coffee beans, which stimulates the central nervous system. Imidazole and its derivatives are an important class of heterocyclic compounds that exhibit a wide range of biological and pharmacological activities. Furthermore, synthetic Imidazole are present in many fungicides, analgesic, anti-inflammatory, antibacterial, antitumor activities, antiprotozoal, and antihypertensive medications. Apart of its use for biological and pharmaceutical purpose, it also has varying applications in industries: the imidazole has been used extensively as a corrosion inhibitor on metals such as iron, copper, zinc, carbon steel, and their alloys. Imidazole and its derivatives have been reported as effective corrosion inhibitors due to their excellent excited state intra-molecular proton transfer, which elevates the performances of their adsorption into the metallic surface. In this chapter, the authors have reported a review of some works that investigated the effects of some Imidazole molecule on corrosion inhibition properties.
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McKenna, C. E., B. A. Kashemirov, and K. M. Błażewska. "Fluorination of P—N Imidazole Derivatives." In Organophosphorus Compounds (incl. RO-P and RN-P). Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00962.

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Ouakki, Moussa, M. Galai, Z. Aribou, M. Rbaa, B. Lakhrissi, and M. Cherkaoui. "Novel Compounds of Imidazole Derivatives as Effective Corrosion Inhibitors for Mild Steel in Hydrochloric Acid Solution." In New Challenges and Industrial Applications for Corrosion Prevention and Control. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-2775-7.ch006.

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The inhibition performance of two imidazole derivatives, IM-Cl and IM-CH3, on the corrosion behavior of MS in 1M HCl acid solution was studied through weight loss method and electrochemical tests. The results obtained from the electrochemical methods show that inhibition efficiency increases with the increase of inhibitors concentration. The adsorption of inhibitors on the mild steel surface obeys Langmuir adsorption isotherm. The corrosion protection was once also investigated with the aid of UV–Vis spectrophotometry. SEM-EDX was performed and discussed for surface study of uninhibited and inhibited mild steel samples.
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Schmidt, A. "Using 1-Imidazole-1-carbonitrile." In Three Carbon-Heteroatom Bonds: Nitriles, Isocyanides, and Derivatives. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-019-00105.

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Singh, Sundaram, and Shivam Bajpai. "Eco-Friendly and Facile Synthesis of Substituted Imidazoles via Nano Zirconia Catalyzed One-Pot Multicomponent Reaction of Isatin Derivatives with Ammonium Acetate and Substituted Aromatic Aldehydes under Solvent Free Conditions." In Nanocatalysts. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.82720.

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Fackler, J. P., and C. W. Liu. "Silver–Carbene Homoleptic Complexes from Imidazol-2-ylidene Derivatives." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au). Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-003-00423.

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Wicha, J. "Deoxygenation of Alcohols via Their 1-Imidazol-1-ylcarbonothioyl Derivatives." In Alkanes. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-048-00099.

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Conference papers on the topic "Imidazoles – Derivatives"

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Трофимов, Б., B. Trofimov, Н. Гусарова, and N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives." In Topical issues of translational medicine: a collection of articles dedicated to the 5th anniversary of the day The creation of a department for biomedical research and technology of the Irkutsk Scientific Center Siberian Branch of RAS. INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/conferencearticle_58be81ec92d17.

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New reactions, which have been discovered and continue to be developed in A.E. Favorsky Irkutsk institute of chemistry SB RAS on the basis of acetylene, a product of oil, gas and coal processing and multi-faceted building block for organic synthesis, have been considered. These reactions provide for the shortest routes to construction of fundamental heterocyclic scaffolds (pyrroles, imidazoles, pyrazoles, indoles, pyridines, dihydropyridines, etc.) with desirable and optimum combination of functional pharmacophoric groups and fragments, which are responsible for antiviral (HIV, flu), antitumor
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Dhilna, C. R., S. M. Gopinath, B. Savitha, D. Parthasarathi, M. Surya, and Muthipeedika Nibin Joy. "Molecular docking studies of some urea derivatives linked with imidazolyl benzamides." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018040.

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Lajci, Nushe. "CORROSION�INHIBITION�OF�ARMCO�IRON�IN�HYDROCHLORIC�ACID�SOLUTION�BY�NEW�IMIDAZOLE�DERIVATIVES�." In SGEM2012 12th International Multidisciplinary Scientific GeoConference and EXPO. Stef92 Technology, 2012. http://dx.doi.org/10.5593/sgem2012/s20.v5029.

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Omar, Abdel-Sattar M., Eman M. El-labbad, and Ahmed M. Al-Abd. "Abstract 287: Design and synthesis of imidazole derivatives as augmented prooxidant anticancer agents." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-287.

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Santos, Marilia S., Manoel T. Rodrigues Jr., and Fernando Coelho. "A simple access to ionic liquids using N-substituted imidazole derivatives from Morita-Baylis-Hillman adducts." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201310110101.

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Hanoon, Haitham Dalol, Sajid Maksad Radhi, and Sawsan Khudhair Abbas. "Simple and efficient synthesis of 2,4,5-triarylsubstituted imidazole derivatives via a multicomponent reaction using microwave irradiation." In THE 7TH INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY (ICAST 2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5123062.

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Cahyana, A. H., B. Ardiansah, and A. Mubardiani. "CoFe2O4 magnetic catalyst assisted a facile one-pot multicomponent construction of 2,4,5-trisubstituted-1H-imidazole derivatives." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064054.

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Mei, Wenjie, Li Li, Hao Zhang, Yong-Chang Zeng, and Xicheng Wang. "Microwave-assisted Synthesis of Imidazole[4,5f][1,10]phenanthroline Derivatives as Potential Inhibitor in Chemotherapy." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-c004.

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Hanoon, Haitham Dalol, Elaheh Kowsari, Mohammad Hadi Ghasemi, and Hassan Zandi. "The effects of substituent type and position on the aromaticity of certain derivatives of imidazole and benzimidazole." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0027541.

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Veeraragavan, Vijayakumar, Radhakrishnan Narayanaswamy, and Rameshkumar Chidambaram. "Molecular docking analysis of imidazole derivatives and polybenzimidazole analogs as inhibitors of superoxide dismutase (SOD) and xanthine oxidase (XO)." In 2017 IEEE International Conference on Smart Technologies and Management for Computing, Communication, Controls, Energy and Materials (ICSTM). IEEE, 2017. http://dx.doi.org/10.1109/icstm.2017.8089213.

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Reports on the topic "Imidazoles – Derivatives"

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Ramakrishnan, V. T., M. Vedachalam, and J. H. Boyer. Dense Compounds of C, H, N, and O Atoms. 2. Nitramine and Nitrosamine Derivatives of 2-Oxo- and 2-Iminooctahydroimidazo(4,5-d)Imidazole. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada238856.

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