Relevant bibliographies by topics / Nitrochalcone

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Nitrochalcone'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Nitrochalcone"

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D., R. GUPTA, KAMALUDDIN, and NAITHANI SHOBHA. "Epoxidation of Chalcones with t-Butylhydroperoxide in Presence of a Cobalt(II) Schiff Base Complex." Journal of Indian Chemical Society Vol. 66, Mar 1989 (1989): 160–63. https://doi.org/10.5281/zenodo.5939979.

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Department of Chemistry, University of Roorkee, Roorkee-217 667 <em>Manuscript received 8 June 1988, revised 15 November 1988, accepted 14 December 1988</em> The epoxidation of some chalcones, i.e. 3-nitrochalcone, 4&#39;-methoxy-3- nitrochalcone, 4&#39;-hydroxy-4-methoxychalcone, 3&#39;-aminochalcone, 3&#39;-amino3-nitrochalcone, 2-methoxychalcone and 2-hydroxy-chalcone has been carried out with t-butylhydroperoxide using cobalt(II) Schiff&#39; base complex as a catalyst. The effects of solvent, temperature, different substituents and quantity of catalyst on the yield of the epoxides have als
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Hall, Charlie L., Victoria Hamilton, Jason Potticary, et al. "Crystal structures of three functionalized chalcones: 4′-dimethylamino-3-nitrochalcone, 3-dimethylamino-3′-nitrochalcone and 3′-nitrochalcone." Acta Crystallographica Section E Crystallographic Communications 76, no. 10 (2020): 1599–604. http://dx.doi.org/10.1107/s2056989020011858.

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The structure of three functionalized chalcones (1,3-diarylprop-2-en-1-ones), containing combinations of nitro and dimethylamino functional groups, are presented, namely, 1-[4-(dimethylamino)phenyl]-3-(3-nitrophenyl)prop-2-en-1-one, C17H16N2O3, Gp8m, 3-[3-(dimethylamino)phenyl]-1-(3-nitrophenyl)prop-2-en-1-one, C17H16N2O3, Hm7m and 1-(3-nitrophenyl)-3-phenylprop-2-en-1-one, C15H11NO3, Hm1-. Each of the molecules contains bonding motifs seen in previously solved crystal structures of functionalized chalcones, adding to the large dataset available for these small organic molecules. The structure
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3

Orlov, V. D., N. V. Getmanskii, O. V. Shishkin, E. E. Lakin, and V. P. Kuznetsov. "Pyrazolines ? Derivatives of 2-nitrochalcone." Chemistry of Heterocyclic Compounds 29, no. 3 (1993): 301–6. http://dx.doi.org/10.1007/bf00531506.

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ORLOV, V. D., N. V. GETMANSKII, O. V. SHISHKIN, E. E. LAKIN, and V. P. KUZNETSOV. "ChemInform Abstract: Pyrazoline Derivatives of 2-Nitrochalcone." ChemInform 25, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199405157.

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PRAVIN, B. RAGHUWANSHI, G. DOSHI A., and L. NARWADE M. "Studies on Interaction between Cobalt-, Nickel- and Copper(II) Metal Ions and Substituted Chalcones and Isoxazolines at 0.1M Ionic Strength Potentiometrically and Spectrophotometrically." Journal of Indian Chemical Society Vol. 73, Jan 1996 (1996): 21–24. https://doi.org/10.5281/zenodo.5883464.

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Chemistry Department. Vidya Bharti Science College, Vidya Bharti Mahavidyalaya, Karanja (Lad), Akola-444 105 Government V. M. V.&nbsp;Amravati <em>Manuscript received 16 November 1993. revised 11 April 1994. accepted 17 June 1994</em> The interaction of Co<sup>II</sup>, Ni<sup>ll</sup> and Cu<sup>ll</sup> with 2&#39;-hydroxy-5&#39;-methyl-3-nitrochalcone (1), 2&#39;-hydroxy-3&#39;-nitro-5&#39;- methyl-3-nitrochalcone (2), 3-(2-hydroxy-5-methylphenyl)-5-(3-nitrophenyl)isoxazoline (3) and 3-(2-hydroxy&shy;3-niro-5-methylpheny1)-5-(3-nitrophenyl)isoxazoline (4) have been investigated potentiometr
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6

Assolini, João Paulo, Thais Peron da Silva, Bruna Taciane da Silva Bortoleti, et al. "4-nitrochalcone exerts leishmanicidal effect on L. amazonensis promastigotes and intracellular amastigotes, and the 4-nitrochalcone encapsulation in beeswax copaiba oil nanoparticles reduces macrophages cytotoxicity." European Journal of Pharmacology 884 (October 2020): 173392. http://dx.doi.org/10.1016/j.ejphar.2020.173392.

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Quinalia, Mariana Beatriz, and Maria Helena Andrade Santana. "Elasticity of Liposomes Sized by Shearing and Incorporation of CH8 Nitrochalcone." Advanced Science, Engineering and Medicine 6, no. 5 (2014): 618–24. http://dx.doi.org/10.1166/asem.2014.1536.

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8

Hidayah, Nurul, Bambang Purwono, and Ika Dyah Kumalasari. "A Novel Synthesis Route of Phenyl Quinoline from Nitrochalcone with Hydrazine Hydrate in the Presence of Pd/C." Key Engineering Materials 989 (October 28, 2024): 79–86. http://dx.doi.org/10.4028/p-17rfom.

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Quinoline is widely known to have many biological activities. Therefore, the development of the synthesis method of a quinoline derivative framework is a priority. A phenyl quinoline derivative, 6,7-dimethoxy-2-phenylquinoline Q1, has been successfully synthesized via a novel one-pot reaction that involves reduction, cyclization, and followed by dehydration of nitrochalcone derivate, 3-(4,5-dimethoxy-2-nitrophenyl)-1-phenylprop-2-en-1-one C1. The reaction was carried out using 80 % hydrazine hydrate in the presence of 10% Pd/C as a catalyst in an ethanol medium. Target compound Q1 was afforded
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Maegawa, Tomohiro, Akira Nakamura, Reo Takane, Junki Tanaka, and Junya Morimoto. "Construction of Azaisoflavone Derivatives by Hypervalent Iodine Reagent-Mediated Oxidative Rearrangement of 2’-Nitrochalcone." HETEROCYCLES 97, no. 2 (2018): 785. http://dx.doi.org/10.3987/com-18-s(t)51.

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Bombarda, Gabriela F., Pedro L. Rosalen, Eder R. Paganini, et al. "Bioactive molecule optimized for biofilm reduction related to childhood caries." Future Microbiology 14, no. 14 (2019): 1207–20. http://dx.doi.org/10.2217/fmb-2019-0144.

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Aim: To evaluate antimicrobial activity of a new nitrochalcone (NC-E08) against Candida albicans and Streptococcus mutans, and its toxicity. Materials &amp; methods: Minimum inhibitory concentration (MIC) and minimum bactericidal concentration/minimum fungicidal concentration (MFC) were determined against C. albicans and S. mutans, as well as antibiofilm potential and toxicity (human gingival fibroblast and Galleria mellonella). Infection and treatment were performed in G. mellonella. Results &amp; conclusion: NC-E08 showed antimicrobial activity in C. albicans (MIC: 0.054 mM) and S. mutans (M
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Dissertations / Theses on the topic "Nitrochalcone"

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Paganini, Éder Ramos. "Síntese e atividade anti-HCV, anti-Candida e antibacteriana de nitrochalconas /." São José do Rio Preto, 2016. http://hdl.handle.net/11449/137815.

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Orientador: Luis Octavio Regasini<br>Coorientador: Ana Carolina Gomes Jardim<br>Banca: Diogo Paschoalini Volanti<br>Banca: Margarete Teresa Gottardo de Almeida<br>Resumo: Chalconas são flavonoides de cadeia aberta com uma cetona α,β-insaturada, a qual separa duas subunidades fenílicas (anéis A e B). Estas substâncias podem ser sintetizadas pela condensação de Claisen-Schmidt e apresentam inúmeras atividades biológicas, tais como; antioxidante, anti-inflamatória, antimicrobiana e antitumoral. O presente trabalho objetivou a síntese de uma série de 21 chalconas contendo o grupo nitro em diferent
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Conference papers on the topic "Nitrochalcone"

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Hidalgo, Alam Yair, Quirino Torres-Sauret, Carlos Ernesto Lobato-García, et al. "Efficient Synthesis of Substituted 2-Nitrochalcone Derivatives." In ECSOC 2024. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20109.

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