Relevant bibliographies by topics / Pyrazolones

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

Academic literature on the topic 'Pyrazolones'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 September 2023

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Journal articles on the topic "Pyrazolones"

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Gediz Erturk, Aliye, and Hilal Omerustaoglu. "Synthesis and Cytotoxic Evaluation of Some Substituted 5-Pyrazolones and Their Urea Derivatives." Molecules 25, no. 4 (February 18, 2020): 900. http://dx.doi.org/10.3390/molecules25040900.

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In this paper, a series of new substituted-5-pyrazolones were first synthesized, then formulated by the Vilsmeier–Haack reaction to obtain substituted-4-carbaldehyde-5-pyrazolones. In the final step, when urea was reacted with formulated pyrazolones, we found that, instead of the C=N bond in azomethine form, the compounds tautomerized to form a series of novel pyrazole-4-ylidenemethylurea structures. The structures of these compounds were elucidated by FTIR, 1H, 13C NMR, LC-MS/MS, and elemental analysis methods. The cytotoxic and antioxidant effects of substituted 5-pyrazolones and their pyrazolone-urea derivatives were investigated in metastatic A431 and noncancerous HaCaT human keratinocytes by a mitochondrial activity test. The effects of the compounds on the migration of cancerous and noncancerous cell lines were investigated by using a cell scratch assay. The General Linear Model, Statistical Package for Social Sciences (SPSS v26) was used to determine if there was a statistically significant difference between the control and the treatment groups. Four of the nine compounds showed an antioxidant effect. All 5-pyrazolone-urea compounds showed higher toxicity (p < 0.05) in cancerous A431 cells compared to noncancerous cells at all time points. All compounds also showed a biphasic hormetic effect. Four of the nine compounds inhibited cell migration.
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Sun, Jun-Shu, Ying-Ying Wang, Man Liu, Jing Zhang, Chen-Fei Liu, Yan-Jun Xu, and Lin Dong. "Construction of pyrazolone analogues via rhodium-catalyzed C–H activation from pyrazolones and non-activated free allyl alcohols." Organic Chemistry Frontiers 6, no. 15 (2019): 2713–17. http://dx.doi.org/10.1039/c9qo00504h.

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Yang, Kai, Xiaoze Bao, Ye Yao, Jingping Qu, and Baomin Wang. "Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes." Organic & Biomolecular Chemistry 16, no. 34 (2018): 6275–83. http://dx.doi.org/10.1039/c8ob01645c.

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Zhang, Wande, Shah Nawaz, Yue Huang, Wenjing Gong, Xingfu Wei, Jingping Qu, and Baomin Wang. "C-4 benzofuranylation of pyrazolones by a metal-free catalyzed indirect heteroarylation strategy." Organic & Biomolecular Chemistry 19, no. 46 (2021): 10215–22. http://dx.doi.org/10.1039/d1ob01920a.

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A metal-free catalyzed indirect heteroarylation of pyrazolones with 2-(3-hydroxy-3,3-diarylprop-1-yn-1-yl)phenols has been developed, delivering a wide range of novel 4-benzofuran-substituted pyrazolone derivatives.
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Wei, Shiqiang, Xiaoze Bao, Wenyao Wang, Shah Nawaz, Qimin Dai, Jingping Qu, and Baomin Wang. "Enantioselective construction of dispirotriheterocycles featuring a 4-aminopyrazolone motif through a cascade Michael/cyclization process." Chemical Communications 56, no. 73 (2020): 10690–93. http://dx.doi.org/10.1039/d0cc04215c.

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A highly asymmetric approach to multicyclic dispiro [pyrazolone-pyrrolidinethione-oxindole] core structures bearing three contiguous stereogenic centers through a cascade Michael addition/cyclization reaction of 4-isothiocyanato pyrazolones with 3-ylideneoxindoles was developed.
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Pattan, S. R., P. A. Chavan, R. A. Muluk, S. S. Dengale, S. V. Hiremath, K. D. Pansare, S. S. Vetal, and J. S. Pattan. "SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME HETEROCYCLES CONTAINING OXADIAZOLE AND PYRAZOLE RING FOR ANTI-BACTERIAL, ANTI-FUNGAL AND ANTI-TUBERCULAR ACTIVITIES." INDIAN DRUGS 49, no. 03 (March 28, 2012): 18–24. http://dx.doi.org/10.53879/id.49.03.p0018.

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1, 3, 4-oxadiazoles were synthesized by treating pyrazine-2-carbohydrazide with CS2 and alc. KOH and their derivatives were prepared by using R-Cl compounds. pyrazolones were synthesized by treatingpyrazine-2-carbohydrazide with ethyl acetoacetate. The derivatives of pyrazolone were prepared by refluxing pyrazolone with formaldehyde and different substituted secondary amines. All the synthesized compounds were characterized by IR, 1H-NMR and elemental analysis and evaluated for antibacterial, antifungal and antitubercular activities.
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Kashinath, Dhurke, Kota Sathish, and Sakkani Nagaraju. "Synthesis of Spiro Pyrazolone-Oxindole and Bicyclic Pyrazolone Derivatives via Solvent-Dependent Regioselective Aza-1,4/1,6-Michael and Intramolecular Cycloaddition under Catalyst-Free Conditions." SynOpen 05, no. 02 (April 13, 2021): 123–33. http://dx.doi.org/10.1055/a-1480-9837.

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AbstractA solvent-dependent, highly regioselective [3+2]-cyclo­addition reaction of isoxazole-styrenes and azomethine imines under catalyst-free conditions is reported, furnishing a library of pyrazolone–spirooxindole hybrids. Good regioselectivity for the isomeric structures was achieved by the reaction of isoxazole-styrene and azomethine imine in different solvents and temperatures. The developed method was extended for the synthesis of tri-substituted dinitrogen-fused pyrazolones by using a 1,6-Michael addition reaction. Furthermore, the isoxazole moiety was converted into a carboxylic acid as a model study via ring opening.
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Hassan, Abdalla E. A., Ahmed H. Moustafa, Mervat M. Tolbah, Hussein F. Zohdy, and Abdelfattah Z. Haikal. "Synthesis and Antimicrobial Evaluation of Novel Pyrazolones and Pyrazolone Nucleosides." Nucleosides, Nucleotides and Nucleic Acids 31, no. 11 (November 2012): 783–800. http://dx.doi.org/10.1080/15257770.2012.732250.

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Zhao, Xia, Xiaoyu Lu, Lipeng Zhang, Tianjiao Li, and Kui Lu. "One-pot Synthesis of Pyrazolone Sulfones by Iodine-catalyzed Sulfenylation of Pyrazolones with Aryl Sulfonyl Hydrazides Followed by Oxidation in Water." Current Organic Synthesis 15, no. 3 (April 27, 2018): 380–87. http://dx.doi.org/10.2174/1570179414666171020113745.

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Aim and Objective: Pyrazolone sulfones have been reported to exhibit herbicidal and antibacterial activities. In spite of their good bioactivities, only a few methods have been developed to prepare pyrazolone sulfones. However, the substrate scope of these methods is limited. Moreover, the direct sulfonylation of pyrazolone by aryl sulfonyl chloride failed to give pyrazolone sulfones. Thus, developing a more efficient method to synthesize pyrazolone sulfones is very important. Materials and Method: Pyrazolone, aryl sulphonyl hydrazide, iodine, p-toluenesulphonic acid and water were mixed in a sealed tube, which was heated to 100°C for 12 hours. The mixture was cooled to 0°C and m-CPBA was added in batches. The mixture was allowed to stir for 30 min at room temperature. The crude product was purified by silica gel column chromatography to afford sulfuryl pyrazolone. Results: In all cases, the sulfenylation products were formed smoothly under the optimized reaction conditions, and were then oxidized to the corresponding sulfones in good yields by 3-chloroperoxybenzoic acid (m-CPBA) in water. Single crystal X-ray analysis of pyrazolone sulfone 4aa showed that the major tautomer of pyrazolone sulfones was the amide form instead of the enol form observed for pyrazolone thioethers. Moreover, the C=N double bond isomerized to form an α,β-unsaturated C=C double bond. Conclusion: An efficient method to synthesize pyrazolone thioethers by iodine-catalyzed sulfenylation of pyrazolones with aryl sulfonyl hydrazides in water was developed. Moreover, this method was employed to synthesize pyrazolone sulfones in one-pot by subsequent sulfenylation and oxidation reactions.
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Chu, Ming-Ming, Suo-Suo Qi, Yi-Feng Wang, Biao Wang, Zhen-Hui Jiang, Dan-Qian Xu, and Zhen-Yuan Xu. "Organocatalytic asymmetric [4 + 1] annulation of in situ generated ortho-quinomethanes with 4-halo pyrazolones: straightforward access to chiral spiro-benzofuran pyrazolones." Organic Chemistry Frontiers 6, no. 12 (2019): 1977–82. http://dx.doi.org/10.1039/c9qo00332k.

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Dissertations / Theses on the topic "Pyrazolones"

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Lavergne, Kaitlyn. "Synthesis of Azomethine Imines via Alkene Aminocarbonylation and their Derivatization into Pyrazolones." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32516.

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Nitrogen-containing heterocyclic compounds are very important to the pharmaceutical and agrochemical industries, among others. Over the past few years, the Beauchemin group has been exploring reactivity of N-substituted isocyanates and as part of this has developed a metal-free alkene aminocarbonylation process relying on imino-isocyanates to form azomethine imines. The azomethine imines formed are interesting since they contain a cyclic β-aminocarbonyl motif. Catalysis of this reaction using basic additives allowed milder reaction conditions with electron-rich C=C bonds such as enol ethers. Efforts have also been made towards the derivatization of these azomethine imines into useful products. It was discovered that upon reduction and aromatization of azomethine imines, pyrazolones could be obtained. This is providing a novel modular approach to these compounds, which have relevance in pharmaceuticals and agrochemicals. This reactivity was extended to include imino-isothiocyanates.
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Diantouba, Bertin Aimé. "Effets structuraux des acyl-4-pyrazolones-5 dans l'extraction liquide-liquide des cations metalliques divalents." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13093.

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Etude de l'effet de l'acidite de la lipophilie et effets structuraux des acyl-4 pyrazolones-5 dans l'extraction de cu, co, zu et pb divalents. Extraction de 3 types de complexes metalliques : mononucleaires de type m(l-n-lh)::(2) ou m(l-n-l) et polynucleaires (m(l-n-l))::(j). Meilleures possibilites des bis-acyl-4 pyrazolones-5
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BOUHRIBA, ALI. "Etude de la complexation de divers cations metalliques par des di-(acyl-4- pyrazolones-5)." Université Louis Pasteur (Strasbourg) (1971-2008), 1998. http://www.theses.fr/1998STR13116.

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La premiere partie de ce travail concerne l'etude thermodynamique de la complexation metallique des metaux de transition divalents m#2#+, (m = cu, zn, ni), des ions lanthanides trivalents ln#3#+, (ln = la, pr, sm, eu, ho, yb) et de l'ion uranyle uo#2#+#2 par des pyrazolones. Il s'agit de la mono-(acyl-4 pyrazolone-5), hpmbp et des di-(acyl-4 pyrazolones-5) ligands constitues de deux sites complexants, l, lies par une chaine polymethylene a n motifs -ch#2, ligands symbolises par : hl-n-lh (n = 4, 5, 7, 8). L'etude a ete menee dans l'eau et dans le solvant mixte eau-acetonitrile 40-60% en poids, en presence du sel de fond naclo#4 1 mol. L##1 et a 25c. Les valeurs des constantes de stabilite des complexes formes sont determinees par spectrophotometrie couplee a la ph-metrie et traitement informatise des donnees. Les resultats obtenus montrent la formation de complexes monoligands et biligands de stoechiometrie 1:1 et 1:2 dans le cas de hpmbp et de complexes mononucleaires ou binucleaires de stoechiometrie, (metal:ligand), 1:1 ou 2:1 dans le cas des hl-n-lh. Les resultats sont interpretes en fonction de la longueur de la chaine alkyle du ligand. Les influences du milieu et du rayon ionique des cations metalliques sur la stabilite des complexes sont discutees egalement. Des structures possibles des complexes en solution sont proposees. L'etude cinetique, qui constitue la seconde partie du travail, porte sur la comprehension des cinetiques de formation, de decomposition acide et d'echange metallique des chelates de l'ion ni#2#+ et de l'ion uo#2#+#2 avec les ligands decrits precedemment. L'etude menee par spectrophotometrie a ecoulement bloque, est faite dans les conditions experimentales de la premiere partie. Pour chaque reaction etudiee, une loi de vitesse et un mecanisme sont proposes. Dans le cas des reactions de formation de complexes, les mecanismes font intervenir des etapes rapides de formation d'intermediaires qui seraient des complexes a sphere externe, suivies de reactions d'interchange de ligands controlant la vitesse. Dans le cas de la decomplexation des chelates, nos resultats sont en accord avec le mecanisme generalement admis : l'ouverture de la premiere liaison metal-ligand controle la decomposition.
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LAKKIS, ZAHREDDINE ZEINAB. "Aspects thermodynamiques et cinetiques de l'extraction de metaux divalents par des acyl-4-pyrazolones-5." Strasbourg 1, 1986. http://www.theses.fr/1986STR13001.

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Extraction de cd et zn a partir des milieux aqueux, perchlorate, nitrate et sulfate par des melanges de phenyl-1 methyl-3 benzoyl-4 pyrazolone-5 et de sels d'ammonium lipophiles. Le pyrazolonate de nh::(4) est l'agent reel de synergie. Mecanisme de transport de cuivre par des acyl-4 pyrazolones-5 a travers une membrane liquide epaisse
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Lakkis-Zahreddine, Zeinab. "Aspects thermodynamiques et cinétiques de l'extraction de métaux divalents par des acyl-4-pyrazolones-5." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598930d.

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Diantouba, Bertin Aimé. "Effets structuraux des acyl-4-pyrazolones-5 dans l'extraction liquide-liquide des cations métalliques divalents." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb37613176t.

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Correia, José Tiago Menezes 1986. "Estudos visando a síntese assimétrica da (+)-Napalilactona. Síntese de pirazolidinonas e pirazolonas a partir de adutos de Morita-Baylis-Hillman." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250231.

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Orientador: Fernando Antonio Santos Coelho
Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química
Made available in DSpace on 2018-08-21T05:18:40Z (GMT). No. of bitstreams: 1 Correia_JoseTiagoMenezes_M.pdf: 8686931 bytes, checksum: bcb49e865e00306bf2105e6bcda93583 (MD5) Previous issue date: 2012
Resumo: Esse trabalho é composto de dois capítulos. No primeiro relatamos nossos esforços visando descrever a primeira síntese total da (+)-Napalilactona, um nor-sesquiterpeno clorado extraído do coral Lemnalia africana. Essa substância marinha possui quatro centros estereogênicos consecutivos em sua estrutura, dois deles quaternários, sendo que um destes centros quaternários pertence também a um anel espiro. A estratégia sintética utilizou a (S)-Carvona como material de partida, de modo que foi possível, através do centro pré-existente no monoterpeno de partida, gerar o primeiro centro existente no produto natural. A partir deste centro, utilizando metodologias já bem estabelecidas na literatura, foi possível induzir a formação de dois dos três centros restantes, de modo que 78% do esqueleto carbônico do produto natural foi construído em um total de 10 etapas, com um rendimento global de 3%. Na segunda parte desse trabalho relatamos os resultados obtidos em um estudo metodológico envolvendo a reação entre a aminoguanidinina, um bis-nucleófilo polinitrogenado, e adutos de Morita-Baylis-Hillman (MBH) sililados e acetilados. Frente aos adutos de MBH sililados, as reações com a aminoguanidina conduziram, através de um processo tandem, à formação de uma mistura diastereoisomérica de pirazolidinonas sililadas em excelentes rendimentos, sendo que o diastereoisomero syn é o favorecido em todos os casos. A diastereosseletividade dessa reação variou de 2:1 a 7:1 (syn:anti). Quando investigamos o comportamento da aminoguanidina frente aos adutos de MBH acetilados, utilizando como solvente a acetonitrila, as reações com a aminoguanidina conduziram, também através de um processo tandem, à formação exclusiva de pirazolidinonas benzilidênicas, quando um aduto oriundo de um aldeído alifático ou oriundo de um aldeído aromático substituído com grupos doadores de elétrons foram utilizados. No entanto, frente a adutos oriundos de aldeídos aromáticos com grupos retiradores de elétrons, foi observada uma tendência à formação de pirazolonas, que são regioisomeros das pirazolidinonas previamente obtidas. Estes dados indicaram que, sob estas condições, a natureza do grupo substituinte rege a seletividade destas reações. Mais tarde, observou-se que, ao submetermos as pirazolidinonas a uma solução de 2 equivalentes de K2CO3 em metanol, estas poderiam ser completamente convertidas às respectivas pirazolonas. Mostrando a influência da natureza do solvente nestas transformações químicas
Abstract: This work is composed by two chapters. In the first one we disclosed our efforts towards the first total synthesis of (+)-Napalilactone, a chlorinated nor-sesquiterpene isolated from the coral Lemnalia africana. This marine natural compound has four consecutive stereogenic centers in their structure, two of them quaternaries. One of these quaternary centers belonging to a spiro ring. Our synthetic strategy started from commercially available (S)-carvone. The asymmetric center presented in this monoterpene was used to induce the first stereogenic center exhibited by the natural product. This task was accomplished by employing a sequence of well-established synthetic metodologies. This stereogenic center has induced the formation of two of the remaining three estereogenic centers. So that 78% of the carbon skeleton of the natural product has been built in a total of 10 steps with an overall yield of 3%. In the second part of this work we described the results of a methodological study envolving the reaction between aminoguanidinine, a polynitrogenated bis-nucleophile, and silylated and acetylated Morita-Baylis-Hillman adducts (MBH). The reaction of aminoguanidine with silylated MBH adducts gave, through a tandem process, a diastereoisomeric mixture of silylated pyrazolidinones in excellent yields, in which the syn diastereoisomer is favored in all cases. The diastereoselectivity of theses reactions ranged from 2:1 to 7:1 (syn:anti). When we investigated the reaction of aminoguanidine with acetylated aliphatic and eletron rich aromatic MBH adducts, using acetonitrile as solvent, the reaction afforded exclusively benzylidenic pyrazolidinones. However, when we investigated the reaction with acetylated eletron-poor aromatic MBH adducts, we observed the formation almost exclusively of pyrazolones, which are regioisomers of the previously obtained pyrazolidinones. These data indicated that under these conditions, the nature of the substituent group governed the selectivity of these reactions. Later, it was observed that by subjecting the pyrazolidinones to a solution of 2 equivalents of K2CO3 in methanol, they were completely converted to the corresponding pyrazolones, showing the influence of the nature of the solvent in these chemical transformations
Mestrado
Quimica Inorganica
Mestre em Química
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Metabanzoulou, Jean-Pierre. "Mécanisme de la complexation de l'ion UO²⁺ par des di(acyl-4 pyrazolones-5), des éthers-couronnes, des diazapolyoxamacrocycles et des ligands apparentés." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb376166100.

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Lemire, Philippe. "Hydrolyse d’α-aminoesters et de 1-amino diesters phosphoniques par intramolécularité temporaire organocatalysée & Synthèse de pyrazolones et de triazolium-olates par isomérisation d’azométhine imines N,N’-cycliques." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/38738.

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L’organocatalyse permet l’activation de réactions chimiques diverses et représente une méthode complémentaire à la catalyse métallique ou à la catalyse par les enzymes. Cette stratégie peut être moins toxique et relativement plus accessible, en plus d’être fréquemment économique et écologique. En induisant une intramolécularité temporaire, il est possible de surmonter les pénalités entropiques inhérentes aux réactions intermoléculaires. Les travaux effectués par le groupe de recherche du Pr. Beauchemin ont jusqu’à date permis d’actualiser et d’améliorer des réactions d’hydroamination, d’hydratation d’amino nitriles et d’hydrolyse d’amides organophosphoniques grâce à l’organocatalyse aux aldéhydes simples. Dans cette optique, cette thèse étudie l’application de cette méthodologie dans des réactions d’hydrolyse. Dans un premier temps, les paramètres réactionnels favorisant l’hydrolyse d’α-amino esters furent investigués. Les problèmes de labilité de divers substrats en milieu aqueux furent abordés, de même que les difficultés à effectuer un « turnover » catalytique efficace. Dans un deuxième temps, la mono-hydrolyse de 1-amino diester phosphonique fut étudiée. Les esters d’acide 1-amino phosphoniques suscitent un intérêt en raison de leurs bioactivités diverses, notamment comme analogues d’acides aminés capables d’interactions biologiques avantageuses. Il fut possible d’optimiser plusieurs conditions réactionnelles, de même que d’étendre la portée de cette méthode à la synthèse de dérivés portant des groupements alkyles. Sur un autre ordre d’idées, les hétérocycles azotés font preuve de bioactivités importantes et variées. Conséquemment, leur emploi dans les domaines pharmaceutique et agrochimique est incontournable. Les cycles de type pyrazolone sont particulièrement présents dans des composés pharmaceutiques et dans des insecticides et des herbicides, tandis que les triazolium-olates présentes des activités biologiques intéressantes. Il devient ainsi essentiel de développer des voies polyvalentes, efficaces, peu dispendieuses et plus vertes pour leur synthèse. Des travaux antérieurs du groupe Beauchemin ont élaboré la génération in situ d’isocyanates et d’isothiocyanates N-substitués, des intermédiaires rares dans la littérature. Ils furent utilisés dans des réactions de cycloaddition avec des alcènes et des imines, pour former des azométhine imines. La deuxième partie de cette thèse s’intéresse à la dérivation de ces azométhine imines en dérivés de pyrazolone et en triazolium-olates grâce à une réaction d’isomérisation. Cette approche permet une déconnexion novatrice pour synthétiser directement des hétérocycles riches en azote complexes. L’optimisation de cette réaction fut mise au point et sa portée fut étudiée. Cette méthode s’avère peu dispendieuse, n’emploie aucun catalyseur métallique, ne requière pas de préfonctionnalisation et ne génère pas de sous-produits. Finalement, l’application de cette isomérisation à la résolution cinétique des azométhines imines fut tentée.
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Metabanzoulou, Jean-Pierre. "Mecanisme de la complexation de l'ion uo : :(2)**(2+) par des di(acyl-4 pyrazolones-5), des ethers-couronnes, des diazapolyoxamacrocycles et des ligands apparentes." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13146.

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Etude spectrophotometrique de la stabilite des complexes de l'ion uo::(2)**(2+) et de l'ion cu**(2+), dans l'eau et eau-acetonitrile. Structures possibles des complexes 1:1, 1:2 et 2:1. Mecanismes de formation des complexes
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Books on the topic "Pyrazolones"

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Wiley, Richard H., and Paul F. Wiley. Pyrazolones, Pyrazolidones, and Derivatives. Wiley & Sons, Incorporated, John, 2009.

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Wiley, Richard H., and Paul F. Wiley. Pyrazolones, Pyrazolidones, and Derivatives. Wiley & Sons, Limited, John, 2007.

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Wiley, Richard H., and Paul F. Wiley. Chemistry of Heterocyclic Compounds, Pyrazolones, Pyrazolidones, and Derivatives. Wiley & Sons, Incorporated, John, 2008.

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100 Years of Pyrazolone Drugs. Birkhauser, 1986.

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100 years of pyrazolone drugs: An update. Basel: Birkhäuser, 1986.

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Book chapters on the topic "Pyrazolones"

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Bien, E., and M. Witt. "Influence of Pyrazolones on Hepatic Glutathione in Rats." In Archives of Toxicology, 366–69. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-69928-3_75.

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Campi, Paolo, Mariangela Manfredi, and Maurizio Severino. "IgE-Mediated Allergy to Pyrazolones, Quinolones and Other Non- &Bg;; -Lactam Antibiotics." In Drug Hypersensitivity, 216–32. Basel: KARGER, 2007. http://dx.doi.org/10.1159/000104202.

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Gooch, Jan W. "Pyrazolone Red." In Encyclopedic Dictionary of Polymers, 598. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9654.

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Bährle-Rapp, Marina. "Phenyl Methyl Pyrazolone." In Springer Lexikon Kosmetik und Körperpflege, 424. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7912.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex of 4-(sulfonylazido)phenylazo-pyrazolone." In Magnetic Properties of Paramagnetic Compounds, 943–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_502.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex of 4-(sulfonylazido)phenylazo-pyrazolone." In Magnetic Properties of Paramagnetic Compounds, 945–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_503.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chloro complex with pyrazolone-hydrazide Schiff-base." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 1139–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_468.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) bromo complex with pyrazolone-hydrazide Schiff-base." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 1141–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_469.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of polymeric chain assemblies of cobalt(II) with bis-pyrazolone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7, 531–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_197.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of polymeric chain assemblies of copper(II) with bis-pyrazolone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7, 976–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_360.

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Conference papers on the topic "Pyrazolones"

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Zeoly, Lucas A., Rosimeire C. Barcelos, Manoel T. Rodrigues Jr., Lucimara J. Martins, and Fernando Coelho. "Synthesis of Substituted Pyrazolones from Morita-Baylis-Hillman Adducts." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391521329.

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Khan, Mohd Shahnawaz. "An expedient synthesis of some new Pyrazole, Pyrazolone, Hydrazone and Thiosemicarbazide." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a026.

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Abubaker, Mariam, Che Wan Zanariah Che Wan Ngah, Musa Ahmad, and Bambang Kuswandi. "Colorimetric determination of Al(III) based on the aggregation of gold nanoparticles functionalized with novel 4-benzoyl pyrazolone derivative." In RECENT ADVANCEMENT ON APPLIED PHYSICS, INDUSTRIAL CHEMISTRY AND CHEMICAL TECHNOLOGY: Proceedings of the International Conference on Recent Advancements in Science and Technology 2017 (ICoRAST2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5041233.

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Pratiwi, S., and A. H. Cahyana. "Synthesis of pyrazolone derivatives compound using nanomagnetic Fe3O4 catalyst from waste cooking oil and iron rust and antioxidant activity test." In PROCEEDINGS OF THE 6TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2020 (ISCPMS 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0059243.

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You might also be interested in the extended bibliographies on the topic 'Pyrazolones' for particular source types:
Journal articles Dissertations / Theses
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