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Relevant bibliographies by topics / Fluoro compounds

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Academic literature on the topic 'Fluoro compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Fluoro compounds"

1

Protiva, Miroslav, Jiří Jílek, Miroslav Rajšner, et al. "Fluorinated tricyclic neuroleptics with prolonged action: derivatives and analogues of 2-(4-(7-fluoro-2-isopropyl-10,11-dihydrodibenzo[b,f]thiepin-11-yl)-piperazine-1-yl)ethanol." Collection of Czechoslovak Chemical Communications 52, no. 7 (1987): 1811–33. http://dx.doi.org/10.1135/cccc19871811.

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The preparation of 4-fluoro-2-nitrobenzonitrile (V), an intermediate in the synthesis of the title compound I, from 4-fluoro-2-nitroaniline via 5-fluoro-2-iodonitrobenzene (VII) was elaborated. Syntheses of 1,1,1,3,3,3-hexadeutero-2-propyl (XX) and 1,3,4-trideutero (XXVIII) analogues of compound I from hexadeuteroacetone, and pentadeuterobromobenzene, respectively, were carried out. Compound I was esterified with acetic anhydride, decanoic acid and 3,4,5-trimethoxybenzoyl chloride to give the esters II-IV. Acylation of compound XXX with acetyl chloride, 4-fluorophenoxyacetyl chloride and (4-fl

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2

Sathe, B. S., E. Jaychandran, G. M. Sreenivasa, and V. A. Jagtap. "Antimycobacterial Activity of Some Synthesized Fluorinated Benzothiazolo Imidazole Compounds." E-Journal of Chemistry 8, no. 2 (2011): 830–34. http://dx.doi.org/10.1155/2011/581429.

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4-Fluoro-3-chloroanilline treated with potassium thiocyanate in presence of glacial acetic acid and bromine was converted into 2-amino-6-fluoro-7-chlorobenzothiazole, resulting into 2-amino benzothiazole. The synthesized compound in presence of 2-phenyl-4-benzylidine-5-oxazolinone refluxed in pyridine to obtain 2-(2-phenyl-4-benzylidenyl-5-oxo-imidazolin-1-yl amino)-6-fluoro-7-substituted(1,3)benzothiazoles. The above said compound was treated withortho, metaandpara nitroanillines, ortho, meta, parachloroanillines, morpholino, piperazine, diphenylamine in the presence of DMF to obtain differen

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3

Sudlow, Kevin, and Alfred A. Woolf. "Destabilization of fluoro imino and fluoro oxy compounds." Journal of Fluorine Chemistry 73, no. 1 (1995): 47–50. http://dx.doi.org/10.1016/0022-1139(94)03196-7.

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4

Makki, Mohammed S. I., Reda M. Abdel-Rahman, and Khalid A. Khan. "Fluorine Substituted 1,2,4-Triazinones as Potential Anti-HIV-1 and CDK2 Inhibitors." Journal of Chemistry 2014 (2014): 1–14. http://dx.doi.org/10.1155/2014/430573.

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Fluorine substituted 1,2,4-triazinones have been synthesized via alkylation, amination, and/or oxidation of 6-(2-amino-5-fluorophenyl)-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one1and 4-fluoro-N-(4-fluoro-2-(5-oxo-3-thioxo-2,3,4,5-tetrahydro-1,2,4-triazin-6-yl)phenyl)benzamide5as possible anti-HIV-1 and CDK2 inhibitors. Alkylation on positions 2 and 4 in 1,2,4-triazinone gave compounds6–8. Further modification was performed by selective alkylation and amination on position 3 to form compounds9–15. However oxidation of5yielded compounds16–18. Structures of the target compounds have been establi

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5

Hiebl, J., E. Zbiral, M. von Janta-Lipinski, J. Balzarini, and E. De Clercq. "Side-Chain Derivatives of Biologically Active Nucleosides. Part 2: Synthesis and anti-HIV Activity of 5′-C-Methyl Derivatives of 3′-Fluoro-3′-Deoxythymidine." Antiviral Chemistry and Chemotherapy 7, no. 3 (1996): 173–77. http://dx.doi.org/10.1177/095632029600700308.

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1-(3′-Fluoro-2′,3′,6′-trideoxy-β-D-allofuranosyl)thymine [7] and 1-(3′-fluoro-2′,3′,6′-trideoxy-α-L-talofuranosyl) thymine [8] were synthesized starting from the corresponding 2,3′-anhydro nucleoside derivatives. The fluorine was introduced stereoselectively by opening of the anhydro bridge in the presence of HF/AIF3. The 5′-C-methyl derivatives, [7] and [8], of 3′-fluoro-3′-deoxythymidine (FLT) were evaluated for their inhibitory effect against human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2). The compounds [7] and [8] had antiviral activity which was three orders of magnitude l

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6

Wang, Xin, Jia Lei, Guofeng Li, et al. "Synthetic methods for compounds containing fluoro-lactam units." Organic & Biomolecular Chemistry 18, no. 48 (2020): 9762–74. http://dx.doi.org/10.1039/d0ob02168g.

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This review highlights recent progress in the construction of fluorinated lactams, including fluoro-β-lactams, fluoro-γ-lactams, and fluoro-δ-lactams, with an emphasis on the scopes, limitations and mechanisms of these different reactions.

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7

Ramachandran, P. Veeraraghavan, M. Venkat Ram Reddy, Michael T. Rudd, and Javier Read de Alaniz. "Vinylalumination of fluoro-carbonyl compounds." Tetrahedron Letters 39, no. 48 (1998): 8791–94. http://dx.doi.org/10.1016/s0040-4039(98)01974-1.

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8

Abeles, R. H., and T. A. Alston. "Enzyme inhibition by fluoro compounds." Journal of Biological Chemistry 265, no. 28 (1990): 16705–8. http://dx.doi.org/10.1016/s0021-9258(17)44813-7.

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9

CASSIDAY, LAURA. "FLUORO COMPOUNDS MAY DELAY PUBERTY." Chemical & Engineering News Archive 89, no. 20 (2011): 8. http://dx.doi.org/10.1021/cen-v089n020.p008a.

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Mistry, Bhavnaben D., Kishor R. Desai, and Nigam J. Desai. "SYNTHESIS, IN VITRO ANTIMICROBIAL ACTIVITY OF SCHIFF’S BASE, AZETIDINONES AND THIAZOLIDINONES." International Journal of Current Pharmaceutical Research 9, no. 1 (2016): 126. http://dx.doi.org/10.22159/ijcpr.2017v9i1.16634.

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Objective: The objective of the present study is to synthesize 3-Chloro-4-[3-(2,4-dichloro-5-fluoro phenyl)-1H-pyrazol-4-yl]-1-(substituted) azetidin-2-one [4a-n] and 2-[3-(2,4-Dichloro-5-fluoro phenyl)-1H-pyraol-4-yl]-3-(substituted phenyl)-1,3-thiazolidin-4-one [5a-n]. The structure of all synthesized compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral studies. Methods: The titled compounds 3-Chloro-4-[3-(2,4-dichloro-5-fluoro phenyl)-1H-pyrazol-4-yl]-1-(substituted) azetidin-2-one [4a-n] and 2-[3-(2,4-Dichloro-5-fluoro phenyl)-1H-pyraol-4-yl]-3-(substituted phenyl)-1,3-thi

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Dissertations / Theses on the topic "Fluoro compounds"

1

Chambers, Eric James. "Conformational studies of fluoro- and hydroxy- compounds in solution." Thesis, University of Liverpool, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316776.

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Andrella, Nicholas Orlando. "Synthesis of Organo-fluorine Compounds by Metal Complex-mediated and -Catalyzed Transformations of Fluoro-alkenes and Fluoro-arenes." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/39509.

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The prevalence of fluorine in natural products is scarce. There are but a handful of compounds that have been discovered to date. This could be largely attributable to the occurrence of fluorine in nature as fluoride (F-). — One might recognize such nomenclature from the ingredients list on a toothpaste tube — In fact, naturally occurring fluoride is most commonly found as fluorite (CaF2) or cryolite (Na3AlF6). As such, the introduction of fluorine via biological pathways has been limited to use of aqueous F- (a very poor nucleophile). This fact — coupled with its naturally low concentration i

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Sutivisedsak, Nongnuch. "Synthesis of [alpha]-hydroxy and fluoro phosphonates and cyclic ether-containing natural products." Diss., St. Louis, Mo. : University of Missouri--St. Louis, 2008. http://etd.umsl.edu/r3246.

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Greedy, Benjamin. "The application of electrophilic fluorodesilylation to the preparation of fluoro-organic compounds." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400574.

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Gooseman, Natalie. "The influence of the C-N⁺------F-C charge dipole interaction in fluoro organic chemistry /." St Andrews, 2008. http://hdl.handle.net/10023/695.

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Moraux, Thomas. "Synthesis and evaluation of α-fluoro analogues of capsaicin and 2-(aminomethyl)piperidine derivatives". Thesis, University of St Andrews, 2011. http://hdl.handle.net/10023/2094.

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Chapter 1 gives an overview of the fluorine chemistry field, from its early developments to recent applications in medicinal chemistry. The development of asymmetric electrophilic or nucleophilic installation of fluorine in organic molecules is highlighten. Chapter 2 of this thesis discusses the enantioselective synthesis of α-fluoroamides. The study is applied to the synthesis of fluoroenantiomers of the bioactive molecule capsaicin and short-chain analogues. The biological activity of these compounds is assayed with the TRPV1 receptor. Results show that enantioselective α-fluoroamides (R)-97

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De, Kavita. "Applications of fluoro-alcohols as reaction media for the synthesis of heterocyclic compounds and perspectives in the design of hybrid materials." Paris 11, 2010. http://www.theses.fr/2010PA114821.

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Fluoro-alcohols like hexafluoroisopropanol (HFIP) and trifluoroethanol (TFE) display unique properties like high hydrogen bond donating ability, poor nucleophilicity, high ionizing power and low pKa’s compared to their non fluorinated counterparts. Owing to these properties HFIP/TFE are known to promote different reactions. HFIP was explored as an effective solvent system for the synthesis of 2,3-unsaturated glycosides via Ferrier rearrangement of 3,4,6 tri-O-acetyl glucal. Aza-Michael addition of anilines onto Michael acceptors was found to proceed easily in polar protic solvents like HFIP,TF

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Tellier, Frédérique. "Synthese et reactivite de dienes, enynes et styrenes fluores." Paris 6, 1986. http://www.theses.fr/1986PA066521.

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9

Åkerblom, Denize, and Erik Göranzon. "Greener Water Repellency? Feasible alternatives to fluoro chemicals for DWOR treatments on textiles." Thesis, Högskolan i Borås, Institutionen Textilhögskolan, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:hb:diva-17695.

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BACKGROUND: Perfluorinated compounds (PFCs) have been used as durable water and oil repellent treatments in clothing for more than 50 years. The reason for its popularity is related to the chemical structure, which also makes these compounds persistent in the environment. Numerous studies have shown negative environmental and health effects related to high concentrations of perfluorinated compounds in blood serum. Due to these studies, this paper aimed to find out if perfluorinated compounds could be replaced by non-perfluorinated without compromising performance related to water and oil repel

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Rayala, Ramanjaneyulu. "Design and Synthesis of Novel Nucleoside Analogues: Oxidative and Reductive Approaches toward Synthesis of 2'-Fluoro Pyrimidine Nucleosides." FIU Digital Commons, 2015. http://digitalcommons.fiu.edu/etd/2172.

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Fluorinated nucleosides, especially the analogues with fluorine atom(s) in the ribose ring, have been known to exert potent biological activities. The first part of this dissertation was aimed at developing oxidative desulfurization-fluorination and reductive desulfonylation-fluorination methodologies toward the synthesis of 2'-mono and/or 2',2'-difluoro pyrimidine nucleosides from the corresponding 2'-arylthiopyrimidine precursors. Novel oxidative desulfurization-difluorination methodology was developed for the synthesis of α,α-difluorinted esters from the corresponding α-arylthio esters, whe

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Books on the topic "Fluoro compounds"

1

Hösler, Klaus. Neue Fluoro- und Chlorokomplexe von Molybdän und Wolfram mit stickstoffhaltigen Liganden. A.S. Intemann und C.C. Intemann, 1989.

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2

Morris, Michelle L. Evaluation of alternatives for trichlorotrifluoroethane (CFC-113) to clean and verify liquid oxygen system. National Aeronautics and Space Administration, Langley Research Center, 1996.

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3

Horváth, István T., and J. L. Aceña. Fluorous chemistry. Springer, 2012.

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Curran, Dennis P., István T. Horváth, and John A. Gladysz. Handbook of fluorous chemistry. Wiley-VCH, 2004.

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Bégué, Jean-Pierre. Chimie bioorganique et médicinale du fluor. EDP Science, 2005.

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6

Motov, David Lazarevich. FLUORIC, SULFATIC and FLUOROSULFATIC COMPOUNDS of GROUP IV ELEMENTS: FORMING & PROPERTIES. Nauka, 2009.

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7

Kirsch, Peer. Modern fluoroorganic chemistry: Synthesis, reactivity, applications. Wiley-VCH, 2004.

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8

A, Soloshonok V., ed. Enantiocontrolled synthesis of fluoro-organic compounds: Stereochemical challenges and biomedical targets. Wiley, 1999.

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Soloshonok, V. A. Enantiocontrolled Synthesis of Fluoro-Organic Compounds: Stereochemical Challenges and Biomedical Targets. Wiley, 1999.

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Horváth, István T. Fluorous Chemistry. Springer, 2011.

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Book chapters on the topic "Fluoro compounds"

1

Julien, Christian, Alain Mauger, Ashok Vijh, and Karim Zaghib. "Fluoro-polyanionic Compounds." In Lithium Batteries. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-19108-9_8.

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2

Walkowiak, Justyna, and Henryk Koroniak. "Preparation of α-Fluoro Amino and α-Fluoro Enamino Reagents." In Efficient Preparations of Fluorine Compounds. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch58.

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3

Zhang, Xiao-Jian, Ting-Bong Lai, and Richard Yuen-Chong Kong. "Biology of Fluoro-Organic Compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_270.

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4

Fuchigami, Toshio. "Electrochemical reactions of fluoro organic compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/3-540-57729-7_1.

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Kolditz, Lothar. "Fluoro and Fluorohydroxy Complexes of As, Sb, and Sn." In Efficient Preparations of Fluorine Compounds. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118409466.ch20.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with fluoro and imidazole ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_169.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with fluoro and imidazole ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_170.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with fluoro and imidazole ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_171.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with fluoro and imidazole ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_172.

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Gál, E. Martin. "Effect of Fluoro Compounds on Metabolic Control in Brain Mitochondria." In Novartis Foundation Symposia. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719855.ch5.

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Conference papers on the topic "Fluoro compounds"

1

Gorelik, Vladimir S., Anatolii V. Chervyakov, Ludmila I. Zlobina, and Olga N. Sharts. "Raman and fluorescence spectra of fluoro-organic compounds." In Photonics East '99, edited by Joseph Leonelli and Mark L. Althouse. SPIE, 1999. http://dx.doi.org/10.1117/12.371274.

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Palanisamy, Kumar, Abhirami Kumar, Santhakumar Kannappan, Paik-Kyun Shin, and Shizuyasu Ochiai. "High performance PEDOT:PSS films prepared through a treatment with fluoro compounds and their application in polymer solar cells." In SPIE Organic Photonics + Electronics, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2013. http://dx.doi.org/10.1117/12.2023460.

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Kim, Yong B., and Il K. Huh. "High-speed response time of LC mixtures containing fluoro-isothiocyanato liquid crystal compounds for LCD monitor and TV applications." In Electronic Imaging 2002, edited by Liang-Chy Chien. SPIE, 2002. http://dx.doi.org/10.1117/12.467446.

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Nakano, Mitsuyuki, Haruko Sasaki, and Harumi Ono. "Radiation Resistance of Rubber Compound for Gasket." In ASME 2011 Small Modular Reactors Symposium. ASMEDC, 2011. http://dx.doi.org/10.1115/smr2011-6567.

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Seals of small and medium modular reactors are considered as not important components compared with seals for the large modular reactors which are current-generation plants. Leakage of seals has been a safety concern, however seal maintenance and replacement are costly and time consuming for the current-generation plants. Therefore, integral designs of small and medium modular reactors eliminate the need for seals. However it is impossible to eliminate seals completely from the detail design and equipments. Seals consisting of organic materials are estimated as serious damaged components at de

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Lee, Young Bok, Deog Joong Kim, Gina Chun Kost, Julie Frank, Chang-Ho Ahn, and Zhi-Ren Liu. "Abstract 5507: Mechanistic study of a new 4-(3, 5-dimethoxyphenyl)-N-(7-fluoro-3-methoxyquinoxalin-2-yl)piperazine-1-carboxamide compound (RX-5902)." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-5507.

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Lloyd, E. R., L. C. Zinsli, M. B. Lackey, and J. M. Stevens. "Open-Air Demolition of Facilities Highly Contaminated With Plutonium." In The 11th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2007. http://dx.doi.org/10.1115/icem2007-7318.

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The demolition of highly contaminated plutonium buildings usually is a long and expensive process that involves decontaminating the building to near free-release standards and then using conventional methods to remove the structure. It doesn’t, however, have to be that way. Fluor has torn down buildings highly contaminated with plutonium without excessive decontamination. By removing the select source term and fixing the remaining contamination on the walls, ceilings, floors, and equipment surfaces; open-air demolition is not only feasible, but it can be done cheaper, better (safer), and faste

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