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1

Gormen, Meral. "Synthesis Of Ferrocenyl Substituted Pyrazoles." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12606358/index.pdf.

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Pyrazoles have been studied for over a century as an important class of heterocyclic compounds and continue to attract considerable interest due to the broad range of biological activities they possess. The incorporation of the essential structural features of pyrazoles with a ferrocene moiety could provide new derivatives with unexpected and/or enhanced biological activities since several ferrocene derivatives have already been shown to be active against a number of tumors. For this reason, we investigated the synthesis of ferrocenyl-substituted pyrazoles, such as 1-alkyl/aryl-5-ferrocenylpyr
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2

ERVITHAYASUPORN, VUTHICHAI. "Synthesis and Photochemistry of Pyrano[2,3-c]pyrazoles." Digital WPI, 2006. https://digitalcommons.wpi.edu/etd-theses/228.

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Two different synthetic approaches to the synthesis of pyrano[2,3-c]pyrazoles have been investigated. In one approach, dehydroacetic acid derivatives were treated with phenylhydrazine and methylhydrazine led to the formation of the phenylhydrazones and methylhydrazones, which undergo rearrangement in refluxing acetic acid to diketo-phenylpyrazoles and diketo-methylpyrazoles. Upon treatment with a mixture of acetic and sulfuric acid these compounds isomerize to the phenylpyrano[2,3-c]pyrazol-4-one and methylpyrano[2,3-c]pyrazol-4-one derivatives. In a second approach, phenylhydrazine and methyl
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3

Ervithayasuporn, Vuthichai. "Synthesis and photochemistry of pyrano[2,3-c]pyrazoles." Link to electronic thesis, 2006. http://www.wpi.edu/Pubs/ETD/Available/etd-042006-160619/.

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4

Demirci, Deniz. "Synthesis Of 4-phenylselenyl-1h-pyrazoles By Electrophilic Cyclization." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613910/index.pdf.

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In this study, the synthesis of 5-ferrocenyl/aryl-4-(phenylselenyl)-1H-pyrazole derivatives was investigated since the integration of ferrocenyl and selenium moieties into pyrazole derivatives may increase their current biological activities. Initially, the starting propargyl aldehydes were synthesized from corresponding acetylenes. Subsequently, propargyl aldehydes were reacted with hydrazines to yield corresponding hydrazones. Then the in situ synthesized hydrazones were subjected to electrophilic cyclization with phenylselenyl chloride, which afforded 5-ferrocenyl/aryl-4-(phenylselenyl)-1H-
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5

Cooper, David Arthur. "The synthesis and characterization of some molybdenum, rhenium and rhodium complexes incorporating pyrazolylgallate ligands." Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/24597.

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Several uninegative ligands based on a gallium core and incorporating pyrazolyl groups have been synthesized and their metathesis reactions with molybdenum, rhenium and rhodium halides have been studied. The bidentate pyrazolylgallate ligand [formula omitted] has been incorporated in the complexes [formula omitted]. The unsymmetric tridentate pyrazolylgallate ligands [formula omitted] display a variable reactivity towards molybdenum, rhenium and rhodium precursors. Although no complexes incorporating L⁴ were isolated, L₂ and L₃ were shown to co-ordinate facially in the octahedral complexes
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6

Dunham, Jason C. "Synthesis of 4-alkyl-3,5-diamino-1-phenylpyrazoles." Virtual Press, 2006. http://liblink.bsu.edu/uhtbin/catkey/1339144.

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The goal of this project is to synthesize and purify a library of novel 4-alkyl-3,5-diamino-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazoles. These molecules are similar to other fiproles, which have been shown by Sammelson et al. to have pesticidal activities at the GABA receptor.' Fiproles are analogues of Fipronil, a very important pesticide. Replacing the cyano group normally located at the 3-position of the pyrazole ring with an amino group will change the binding potency of the phenylpyrazoles. Changes in binding produced by the changes introduced in molecular structure can create more
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7

Oleksik, Laurence. "Methodology for the synthesis of 4 or 5-substituted-3-perfluoroalkyl pyrazoles." Thesis, University of Leicester, 2004. http://hdl.handle.net/2381/30087.

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Initially the perfluoroacylation of a range of commercially available vinyl ethers and conversion of the resulting perfluoroacylated enol ethers to 1-H-pyrazoles via reaction with hydrazine is reported. The selective synthesis of a range of alpha-aryl vinyl ethers using Heck chemistry is then reported. Subsequent perfluoroacylations of the vinyl ethers followed by reaction of the resulting perfluoroacyl enol ethers with hydrazine affords a range of 5-aryl-3-perfluoroalkyl pyrazoles in good yields.;Alternative methodology for the synthesis of 5-aryl-3-perfluoroalkyl pyrazoles is then described
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8

Poulsen, Sally-Ann, and n/a. "Pyrazolo(3,4-d)pyrimidines: Synthesis and Structure-Activity Relationships for Binding to Adenosine Receptors." Griffith University. School of Science, 1996. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20050901.161632.

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Chapter 1 of thesis is a literature review of adenosine research. The central importance of the contributions of both classical pharmacology and, more recently, molecular biology to adenosine research is demonstrated. These disciplines have enabled the classification and characterisation of adenosine receptors and as well an understanding of the physiological significance of endogenous adenosine. The significant benefits of developing therapeutics for regulation of the diverse physiological functions of adenosine, by regulation of adenosine receptors, is outlined. For this therapeutic potentia
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9

Poulsen, Sally-Ann. "Pyrazolo(3,4-d)pyrimidines: Synthesis and Structure-Activity Relationships for Binding to Adenosine Receptors." Thesis, Griffith University, 1996. http://hdl.handle.net/10072/365893.

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Chapter 1 of thesis is a literature review of adenosine research. The central importance of the contributions of both classical pharmacology and, more recently, molecular biology to adenosine research is demonstrated. These disciplines have enabled the classification and characterisation of adenosine receptors and as well an understanding of the physiological significance of endogenous adenosine. The significant benefits of developing therapeutics for regulation of the diverse physiological functions of adenosine, by regulation of adenosine receptors, is outlined. For this therapeutic potentia
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10

Karabiyikoglu, Sedef. "Synthesis Of Ferrocenyl Substituted Pyrazoles By Sonogashira And Suzuki-miyaura Cross-coupling Reactions." Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/3/12612139/index.pdf.

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Pyrazoles constitute one of the most important classes of heterocyclic compounds due to their interesting chemical and biochemical features. Researchers have studied many pyrazole containing structures for almost over a century in order to investigate the various biological activities possessed by these molecules. A new and important trend in these studies is to produce ferrocenyl substituted pyrazoles since ferrocene attracts considerable interest in the research field of organometallic and bioorganometallic chemistry because of its valuable chemical characteristics like high stability, low t
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11

Karahan, Dag Fulya. "Synthesis Of 5-ferrocenyl-4-((4-nitrophenyl)sulfenyl)-1h-pyrazoles By Electrophilic Cyclization." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613443/index.pdf.

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Pyrazoles have been intensely studied in the design and synthesis of biologically active agents because they display considerable medicinal activities. Recent studies have shown that integration of a ferrocenyl unit with structural features of pyrazoles can result in the formation of the new products with enhanced or/and unexpected biological activity since several ferrocene derivatives have already been illustrated to be active against a number of tumors. Therefore, we have investigated the electrophilic cyclizations of the hydrazones to afford 5-ferrocenyl-4-((4-nitrophenyl)sulfenyl)-substit
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12

Pinar, Ayse Nur. "Reaction Of Propargyl Aldehydes With Hydrazinium Salts: Synthesis Of Ferrocenyl And Phenyl Substituted Pyrazoles." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609769/index.pdf.

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Pyrazoles have been focus of a large number of investigations in the design and synthesis of novel biologically active agents that show remarkable medicinal activities. Although pyrazoles have been studied for over a century as an important class of heterocyclic compounds, they still continue to attract considerable attention due to the wide range of medicinal activities they possess. Recent studies have shown that combination of a ferrocenyl unit with structural features of pyrazoles can lead to products with enhanced or/and unexpected biological activity since several ferrocene derivatives h
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13

Santos, Nádia Alexandra Esteves. "Synthesis and evaluation of new pyrazoles, glycosylpyrazoles and rutheniumpyrazoles for antioxidant and antitumoral activity." Master's thesis, Universidade de Aveiro, 2017. http://hdl.handle.net/10773/22521.

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Mestrado em Biotecnologia - Biotecnologia Molecular<br>O cancro é a segunda maior razão de morte em Portugal, a seguir às doenças cardiovasculares. A quimioterapia continua a ser o tratamento mais utilizado e eficaz, no entanto o intervalo onde a dose é eficiente e ao mesmo tempo segura ainda é muito pequeno, podendo ser tóxico para o organismo do paciente. Dessa forma, a procura de novos agentes antitumorais eficientes e seguros tem sido crucial, tendo os pirazóis e os complexos de ruténio (II) um papel muito importante. Vários compostos contendo o anel de pirazol nas suas estruturas já demon
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14

Kivrak, Arif. "Development Of New Methods For The Synthesis Of Pyrazoles, 4-iodopyrazoles, Isoxazoles And 1,2,4-oxadiazoles." Phd thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12612945/index.pdf.

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Synthesis of five-membered heteroaromatic compounds such as pyrazoles, isoxazoles and 1,2,4-oxadiazoles are important for pharmaceutical industry and material science due to their applications. Although there are many methods to prepare such compounds, new variants continue to appear since they exhibit a wide range of biological and medicinal activities. In this thesis, new methods were developed for the synthesis of 4-iodopyrazoles, pyrazoles, isoxazoles, 1,2,4-oxadiazoles and/or 1,2,4-oxadiazepines. In the first part of the study, electrophilic cyclization of &alpha<br>,&beta<br>-alkynic hy
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15

Prado, Guilherme Cervi. "Study of reaction parameters in ball mill in the Synthesis of aryl(heteroaryl)-1h-pyrazoles." Universidade Federal de Santa Maria, 2012. http://repositorio.ufsm.br/handle/1/10505.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>In order to eliminate the problems related to deficient intake of vitamins folate class, many food products are being subjected to the enrichment process. Among them, all types of wheat flour must be enriched with folic acid. Therefore, it is evident the need of analytical methods for routine able to effectively determine the levels of folic acid in enriched matrix. The objective of this work was the development and validation of a rapid method for determination of folic acid added to wheat flour, using the technique of high perf
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16

Dengiz, Cagatay. "Acyl Azides: Application To The Synthesis Of Various Heterocycles." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613892/index.pdf.

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Pyrazoles, isoindolinones, benzodizepinones and dihydroquinolinones are very important heterocycles for their biological properties. Many pharmaceutical agents include these units as core structures. Reactive molecules such as acyl azides, free radicals and formyl groups are used as key step reactants in these studies. Regiospesific hydrolysis and esterifications are used to reach target starting materials. Two different methodology are used for critical ring closure steps. Benzodiazepinones, and isoindolinones are obtained by base mediated ring closure reactions whereas thionyl chloride media
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17

Chi, Li-Jen. "Synthesis and computer-aided structural investigation of potentially photochromic spirooxazines." Thesis, Heriot-Watt University, 2000. http://hdl.handle.net/10399/564.

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18

Acquah, Chris. "Syntheses and Characterization of a New Cyano-Substituted Bis(pyrazolyl)borate and its Thallium (I) Complex." Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etd/3141.

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Scorpionates are versatile and flexible ligands with a wide range of applications including catalysis, C-H bond activation, formation of new class of materials, and mimicking enzymatic reactions. This is as a result of its steric and electronic properties, and due to the relative ease with which the 3, and 5-positions of the pyrazole ring can be functionalized. In this work, we report the synthesis of a new class of scorpionate ligands known as cyanoscorpionates which can crosslink various metal centers. Thus, bis (4-cyano-3,5-diphenylpyrazolyl)borate BpPh2,4CN was synthesized and fully charac
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19

Keter, Frankline Kiplangat. "Pyrazole and pyrazolyl palladium(II) and platinum(II) complexes: synthesis and in vitro evaluation as anticancer agents." Thesis, University of the Western Cape, 2004. http://etd.uwc.ac.za/index.php?module=etd&amp.

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The use of metallo-pharmaceuticals, such as the platinum drugs, for cancer treatment illustrates the utility of metal complexes as therapeutic agents. Platinum group metal complexes therefore offer potential as anti-tumour agents to fight cancer. This study was aimed at synthesizing and evaluating the effects of palladium(II) and platinum(II) complexes as anticancer agents.
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20

Comas-Barceló, Júlia. "Lewis acid-promoted synthesis of pyrazole building blocks." Thesis, University of Sheffield, 2016. http://etheses.whiterose.ac.uk/15943/.

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The present work investigated copper(II)-promoted regioselective synthesis of disubstituted pyrazole scaffolds via cycloaddition reactions between sydnones and alkynes. Cu(OTf)2 has been found to mediate the formation of 1,3-pyrazoles, while Cu(OAc)2·H2O promotes the exclusive formation of the 1,4-regioisomer. Both transformations have been optimised and the scope has been explored for both reactions. A mechanistic proposal is also reported herein that has been derived from both experimental and theoretical investigations, the latter performed in collaboration with colleagues at Universidad de
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21

Schmitt, Étienne. "Towards the synthesis of novel heterocyclic agrophores bearing emergent fluorinated substituents." Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF056.

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Durant ce doctorat en collaboration avec Bayer CropScience, une famille de réactifs appelés Réactifs de type Fluoroalkyl Amines (ou FARs) a été étudiée (spécialement le TFEDMA) pour réaliser ’introduction de groupes fluorés émergents (EFSs). Après une activation à l’aide d’un acide de Lewis, les sels de fluoro-iminium obtenus ont été utilisés pour la difluoroacylation d’arenes et hétéroarènes riches en électrons, ou la synthèse efficace et régiosélective de pyrazoles et d’isoxazoles possédant un groupe -CHF2 à partir d’éthers vinyliques et apparentés, d’éthers d’énol silylés ou de composés CH-
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22

Nakhai, Azadeh. "Synthetic studies of nitrogen containing heterocycles, particularly pyrazole and benzotriazine derivatives." Stockholm, 2009. http://diss.kib.ki.se/2009/978-91-7409-687-3/.

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23

McFadden, Helen Georgina, and n/a. "Synthesis and herbicidal properties of some pyrazole and pyrimidine heteocycles." University of Canberra. Biomedical Sciences, 1992. http://erl.canberra.edu.au./public/adt-AUC20060918.160845.

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Four main series of novel heterocyclic compounds were successfully syniliesised. Two of these series were found to be post-emergence herbicides with the activities of each being based on a different mode of action. The (pyrazole-4-yl)alkanones are inhibitors of protoporphyrinogen oxidase, an enzyme in chlorophyll biosynthesis, whereas alkyl 3-arylsulfonylamino- 3-methyllhio-2-(pyrimidin-2-ylcarbamoyl)acrylates and pyrimidin-2-yl 3-(2- chlorophenyl)sulfonyl-amino-3-methylthio-2-cyanoacrylamides (collectively termed "vinylogous sulfonylureas") are inhibitors of acetohydroxy acid synthase (AHAS).
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24

Kerr, G. "The synthesis of pyrazole C-nucleosides as potential antitumour agents." Thesis, Heriot-Watt University, 1992. http://hdl.handle.net/10399/1454.

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25

Joshi, V. S. "Synthesis and structure of new organomolybdenum complexes containing pyrazole-derived ligands." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1993. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3069.

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26

Ozcan, Sevil. "Development Of New Synthetic Methodologies For The Synthesis Of Unusual Isocoumarin And Indole Derivatives:the Chemistry Of Homophthalic Acid." Phd thesis, METU, 2007. http://etd.lib.metu.edu.tr/upload/3/12608197/index.pdf.

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Many heterocyclic compounds containing nitrogen, oxygen and sulfur show wide range of physiological activities and their synthesis has always been attracted the interest of chemists. The aim of this research is to develop new synthetic methodologies leading to the synthesis of new derivatives of isocoumarines, indoles, isoquinolines, benzodiazepinones and quinazolines, which have been found to show important biological activities. Starting from homophthalic acid and bishomophthalic acid the corresponding acyl azides were proposed to be synthesized, which then would be used for the synthesis of
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27

Smith, Duncan. "The synthesis of pyrazole C-nucleosides containing D-arabinose and D-xylose." Thesis, Heriot-Watt University, 1985. http://hdl.handle.net/10399/1617.

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28

Panasenko, N. V. "Synthesis and fluorescence spectrum of 9-(4-pyrazolyl)decahydroacridindiones-1,8." Thesis, БДМУ, 2022. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/19545.

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29

DuMez, Darin David. "Synthesis and selective oxidations of rhenium hydrotris(1-pyrazolyl) borate compounds /." Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/8674.

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30

Blackburn, J. B. "The synthesis and properties of pyrazolo[4,3-B]pyridines and their evaluation as anti-inflammatory agents." Thesis, University of Sunderland, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.382813.

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31

Bertuzzi, Giulio. "Synthesis and functionalization of a lactam-pyrazole molecular scaffold as a promising anticancer compound." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2015. http://amslaurea.unibo.it/9035/.

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The importance of pyrazole and lactam-based molecules in medical and pharmaceutical fields is underlined by the multitude of active ingredients on trade, such as Sildenafil or Apixaban, by Pfizer. In this work, a synthesis of an organic molecule with promising anticancer activity has been developed. This molecular scaffold is characterized by a δ-lactam-fused pyrazolic core, with a well-known biological activity and amenable of further functionalization. The synthetic strategy adopted for the obtainment of the core was based on a 1,3-dipolar cycloaddition of a nitrilimine with an α,β-unsaturat
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32

Mavel, Sylvie. "Synthèses et approche pharmacologique en série Pyrazolo 1,5-D 1,2,4 triazinique." Clermont-Ferrand 1, 1992. http://www.theses.fr/1992CLF1P001.

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33

Yazici, Ceyda. "Synthesis Of 4-iodopyrazole Derivatives." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609750/index.pdf.

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Pyrazoles have been studied for over a century as an important class of heterocyclic compounds and continue to attract considerable interest due to the broad range of biological activities they possess. The electrophilic cyclization of the acetylenic hydrazones initiated by molecular iodine could provide new ways of synthesizing biologically active 4-iodopyrazole derivatives, which are important precursors for the synthesis of highly substituted pyrazole derivatives. For this reason, we investigated the synthesis of 4-iodopyrazole derivatives, such as 1-aryl- 5-alkyl/aryl-4-iodopyrazoles, star
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34

Ojwach, Stephen Otieno. "Heterocycle carbonyl pyrazolyl palladium(II) complexes :synthesis, ethylene oligomerisation and polymerisation catalysis." Thesis, University of the Western Cape, 2004. http://etd.uwc.ac.za/index.php?module=etd&amp.

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35

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. E
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36

Heider, Silvio. "Synthese neuer tri- und hexadentater Stickstoffbasen für Eisen(II) Spin Crossover Komplexe." Doctoral thesis, Universitätsbibliothek Chemnitz, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-120783.

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Die vorliegende Arbeit thematisiert Eisen(II)-Komplexe mit Spinübergangseigenschaften. Dafür wurden neue hexadentate Liganden auf Basis von N,N'-Bis(2,2'-bipyridin-6-ylmethyl)-2,2'-biphenylendiamin entwickelt. Die in Kapitel 3.1 vorgestellten Systeme variieren dabei in den jeweiligen Substituenten der 6,6‘-Positionen der Biphenyleinheit. Es wird der Einfluss dieser Gruppen auf die magnetischen Eigenschaften der resultierenden Komplexe gezeigt. Im darauffolgenden Kapitel 3.2 wird ein variiertes Ligandensystem vorgestellt, in welchem anstelle einfacher Substituenten Donorfunktionen eingeführt wu
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Salazar, Garza Gustavo Adolfo. "Microwave-Assisted Synthesis, Characterization, and Photophysical Properties of New Rhenium(I) Pyrazolyl-Triazine Complexes." Thesis, University of North Texas, 2010. https://digital.library.unt.edu/ark:/67531/metadc28473/.

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The reaction of the chelating ligand 4-[4,6-bis(3,5-dimethyl-1H-pyrazol-1-yl)-1,3,5-triazin-2-yl]-N,N-diethyl-benzenamine, L, with pentacarbonylchlororhenium by conventional heating method produces the complexes fac-[ReL(CO)3Cl2] and fac-[Re2L(CO)6Cl2] in a period of 48 hours. The use of microwaves as the source of heat and the increase in the equivalents of one of the reactants leads to a more selective reaction and also decreases the reaction time to 1 hour. After proper purification, the photophysical properties of fac-[ReL(CO)3Cl] were analyzed. The solid-state photoluminescence analysis s
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38

Chandanshive, Jay Zumbar <1983&gt. "Regiocontrolled Synthesis of Pyrazole Derivatives Through 1,3-Dipolar Cycloaddition Reaction And Synthesis of Helicene-Thiourea based and Polymer Supported Soos's Catalyst for Asymmetric Synthesis." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5826/1/Chandanshive_JAY_ZUMBAR_Thesis.pdf.

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In first part we have developed a simple regiocontrolled protocol of 1,3-DC to get ring fused pyrazole derivatives. These pyrazole derivatives were synthesized using 1,3-DC between nitrile imine and various dipolarophiles such as alkynes, cyclic α,β-ketones, lactones, thiocatones and lactums. The reactions were found to be highly regiospecific. In second part we have discussed about helicene, its properties, synthesis and applications as asymmetric catalyst.Due to inherent chirality, herein we have made an attempt to synthesize the helicene-thiourea based catalyst for asymmetric catalysi
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Chandanshive, Jay Zumbar <1983&gt. "Regiocontrolled Synthesis of Pyrazole Derivatives Through 1,3-Dipolar Cycloaddition Reaction And Synthesis of Helicene-Thiourea based and Polymer Supported Soos's Catalyst for Asymmetric Synthesis." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5826/.

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In first part we have developed a simple regiocontrolled protocol of 1,3-DC to get ring fused pyrazole derivatives. These pyrazole derivatives were synthesized using 1,3-DC between nitrile imine and various dipolarophiles such as alkynes, cyclic α,β-ketones, lactones, thiocatones and lactums. The reactions were found to be highly regiospecific. In second part we have discussed about helicene, its properties, synthesis and applications as asymmetric catalyst.Due to inherent chirality, herein we have made an attempt to synthesize the helicene-thiourea based catalyst for asymmetric catalysi
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40

Davies, Emyr D. "Novel bis (pyrazol-3-yl) ligands : their synthesis and coordination chemistry." Thesis, Cardiff University, 2007. http://orca.cf.ac.uk/54683/.

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This thesis describes studies into the development of new bis(pyrazol-3-yl) ligands including our studies into their coordination chemistry. Chapter 1 is a brief introduction to chelating ligands based on heterocycles and outlines specifically looks at poly(pyrazole-l-yl) ligands as well as the few bis(pyrazole-3-yl) ligands publishes to date. Chapter 2 looks at the traditional synthetic routes to bis(pyrazol-3-yl) ligands and describes how we have manipulated these techniques to synthesise some novel ligands of our own. Chapter 3 includes a study of the transition metal coordination chemistry
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41

Bhambri, Sameer. "Ruthenium arene poly(pyrazolyl)borates and methanes : synthesis, reactivity and molecular orbital calculations." Thesis, University College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300010.

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42

Panasenko, N. V., and М. K. Bratenko. "Synthesis of 3-(3-aryl-1-phenyl-1H-4-pyrazolil)-chromen-2-ones." Thesis, БДМУ, 2017. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/16864.

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43

Evans, Wynne. "The synthesis and properties of selected transition metal-pyrazole complexes and their application towards homogeneous catalysis." Thesis, Open University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280668.

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Şahin, Engin Sözüer Topaloğlu Işıl. "Synthesis And Characterization Oxo-İmido [Tris (3,5-Dimethyl-Pyrazol) Borate] Molybdenum Complexes/." [s.l.]: [s.n.], 2004. http://library.iyte.edu.tr/tezler/master/kimya/T000444.rar.

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Couchman, Samantha M. "Syntheses and structural studies of complexes of mixed donor pyridine/phenol and pyridine/pyrazole ligands." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299312.

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Psillakis, Eleftheria. "The synthesis and study of metal complexes of poly(pyrazolyl)borate and related ligands." Thesis, University of Bristol, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387968.

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Hama, Salih Mariwan Abdulla. "Synthesis of azetidines, γ-lactams, fused furan bispyrrolidines and 2-pyrazolines : towards medical application". Thesis, University of Birmingham, 2016. http://etheses.bham.ac.uk//id/eprint/6838/.

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Azetidines are important class of heterocyclic organic compounds in drug discovery and natural product synthesis. Several natural products and pharmaceuticals are containing azetidine precursors such as, penaresidin and Azelnidipine. Iodine mediated cyclisation of homoallylamines were found to furnish iodoazetidines at 20 °C and further reaction with amine nucelophiles afforded aminoazetidines in high yields. The cyclisation of various homoallylamines which different substitution patterns using molecular iodine to furnish new classes of compounds with interesting biological applications were s
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WILLISON, STUART ALAN. "Synthesis and Investigation of Pyrazole-Containing Platinum Complexes for the Design of Macrocyclic Molecules and Potential Two-electron Reagents." University of Cincinnati / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1202480145.

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Shen, Tzu-Hsuan, and 沈子玄. "Synthesis of a series of pyrazolines and pyrazoles from chalcone." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/k9xxyb.

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碩士<br>淡江大學<br>化學學系碩士班<br>106<br>Flavonols are naturally occurring molecules. They are recognized as good antioxidants. Many Flavonols are used for reactive oxygen species scavengers, oxidase, inhibitors and anticancer drugs. Pyrazole are discovered in natural plants and considered as pain relieving and muscle relaxation. A number of pyrazole derivates are famous for their efficacy and these drugs display different mechanisms of actions. For example, Celecoxib demonstrates anti-inflammatory; Rimonabant is used to treat obesity; Sildenafil is used to treat erectile dysfunction and pulmonary arte
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Huang, Hon-Cha, and 黃浤珈. "Synthesis and Cytotoxic Activities of 4,5-Disubstituted isoxazoles and pyrazoles." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/30026283384892445645.

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碩士<br>中國文化大學<br>應用化學研究所<br>98<br>Abstract Combretastatin A-4 (CA-4), a naturally occurring stilbene, was isolated from Combretum caffrum (African bush willow). CA-4 strongly inhibited the polymerization of tubulin by binding to the colchicine site and showed potent cytotoxicity against a variety of human cancer cell lines including multiple drug resistant cancer cell lines. CA-4 also showed strong anti-vascular activity. In the previously comparative studies of the combretastatins it appears that the cis orientation of the two aromatic rings plays an important role of cytotoxicity. Therefore,
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