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Journal articles on the topic 'Fluorinated compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 March 2023

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1

Timperley, Christopher M., Michael Bird, John F. Broderick, Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 104, no. 2 (2000): 215–23. http://dx.doi.org/10.1016/s0022-1139(00)00248-7.

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2

Timperley, Christopher M., John F. Broderick, Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 106, no. 1 (2000): 43–52. http://dx.doi.org/10.1016/s0022-1139(00)00284-0.

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3

Timperley, Christopher M., Ian Holden, Ian J. Morton, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 106, no. 2 (2000): 153–61. http://dx.doi.org/10.1016/s0022-1139(00)00327-4.

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4

Timperley, Christopher M., David J. Sellers, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 107, no. 1 (2001): 155–58. http://dx.doi.org/10.1016/s0022-1139(00)00394-8.

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5

Timperley, Christopher M., and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 109, no. 2 (2001): 103–11. http://dx.doi.org/10.1016/s0022-1139(01)00362-1.

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6

Lowe, K. C., and R. L. Powell. "Fluorinated Bioactive Compounds." Journal of Fluorine Chemistry 109, no. 1 (2001): 1. http://dx.doi.org/10.1016/s0022-1139(01)00371-2.

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7

Timperley, Christopher M., Robert E. Arbon, Sally A. Saunders, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 113, no. 1 (2002): 65–78. http://dx.doi.org/10.1016/s0022-1139(01)00468-7.

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8

Timperley, Christopher M., Stephen N. Marriott, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 113, no. 1 (2002): 111–22. http://dx.doi.org/10.1016/s0022-1139(01)00493-6.

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9

Timperley, Christopher M., Sally A. Saunders, Josef Szpalek, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 119, no. 2 (2003): 161–71. http://dx.doi.org/10.1016/s0022-1139(02)00239-7.

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10

Timperley, Christopher M., Sue Kirkpatrick, Mark Sandford, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 126, no. 6 (2005): 902–6. http://dx.doi.org/10.1016/j.jfluchem.2005.03.026.

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11

Timperley, Christopher M., Michael Bird, and Matthew J. Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 126, no. 6 (2005): 892–901. http://dx.doi.org/10.1016/j.jfluchem.2005.03.027.

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12

Timperley, Christopher M., and Matthew Waters. "Fluorinated phosphorus compounds." Journal of Fluorine Chemistry 126, no. 8 (2005): 1144–49. http://dx.doi.org/10.1016/j.jfluchem.2005.04.016.

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13

Prekupec, Svjetlana, Damjan Makuc, Janez Plavec, et al. "Antiviral and Cytostatic Evaluation of the Novel 6-acyclic Chain Substituted Thymine Derivatives." Antiviral Chemistry and Chemotherapy 16, no. 5 (2005): 327–38. http://dx.doi.org/10.1177/095632020501600505.

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A series of the novel 5-methyl pyrimidine derivatives with an acyclic side chain at the C-6 position were synthesized using lithiation of a 2,4-dimethoxy-5,6-dimethyl pyrimidine and subsequent nucleophilic addition or substitution reactions of the organolithium intermediate thus obtained with acetaldehyde, epichlorhydrine, fluorinated ketones and fluorinated ester. The novel compounds were evaluated for their cytostatic and antiviral activities. Among all the compounds evaluated, two fluorinated acyclic pyrimidine derivatives showed the highest cytostatic activities. The compound containing a

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14

Lacroix-Desmazes, Patrick, Bruno Améduri, and Bernard Boutevin. "Use of Fluorinated Organic Compounds in Living Radical Polymerizations." Collection of Czechoslovak Chemical Communications 67, no. 10 (2002): 1383–415. http://dx.doi.org/10.1135/cccc20021383.

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Controlled/living radical polymerization (LRP) is a field of special interest because it allows tailoring well-defined macromolecular architectures such as telechelic, block, graft or star copolymers. Since the eighties, several techniques have been reported [such as the iniferter method, nitroxide-mediated radical polymerization (NMP), atom transfer radical polymerization (ATRP), iodine transfer polymerization (ITP), and reversible addition-fragmentation chain transfer (RAFT)] giving rise to a huge number of publications and patents. This review aims at illustrating the contribution of fluori

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15

Thomas, George. "Low Temperature Fluorination of Superconducting and Non-superconducting Compounds Using NH4F." Mapana - Journal of Sciences 1, no. 2 (2003): 1–6. http://dx.doi.org/10.12723/mjs.2.1.

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Compounds Y1Ba2Cu3, Pr1Ba2Cu3O7 and La2CuO4 were fluorinated by a low temperature fluorination method using NH4F.The fluorinated samples were analysed by x-ray diffraction and resistivity measurements. The x-ray diffractogram of the fluorinated samples indicated broadening of the peaks. None of the fluorinated samples showed any superconducting behaviour.

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16

Mertens, Lucas, and Rene M. Koenigs. "Fluorinated diazoalkanes – a versatile class of reagents for the synthesis of fluorinated compounds." Organic & Biomolecular Chemistry 14, no. 45 (2016): 10547–56. http://dx.doi.org/10.1039/c6ob01618a.

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Fluorinated diazo compounds were long neglected in organic synthesis. This review discusses the flourishing chemistry of these reagents, ranging from C–H activation to cycloadditions for the synthesis of fluorinated compounds.

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17

Hironaka, Seiichiro, and Akira Sekiya. "Friction Properties of Fluorinated Compounds." Journal of The Japan Petroleum Institute 36, no. 4 (1993): 343–46. http://dx.doi.org/10.1627/jpi1958.36.343.

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18

Cheng, Xinkuan, and Long Ma. "Enzymatic synthesis of fluorinated compounds." Applied Microbiology and Biotechnology 105, no. 21-22 (2021): 8033–58. http://dx.doi.org/10.1007/s00253-021-11608-0.

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19

Boechat, Núbia, and Mônica Bastos. "Fluorinated Compounds Against Mycobacterium tuberculosis." Current Topics in Medicinal Chemistry 13, no. 22 (2013): 2885–904. http://dx.doi.org/10.2174/15680266113136660204.

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20

Burton, Donald J., Zhen-Yu Yang, and Weiming Qiu. "Fluorinated Ylides and Related Compounds†." Chemical Reviews 96, no. 5 (1996): 1641–716. http://dx.doi.org/10.1021/cr941140s.

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21

Sarwar, Ghulam, Nimesh Patel, Robert L. Kirchmeier, and Jean'ne M. Shreeve. "Highly fluorinated high nitrogen compounds." Journal of Fluorine Chemistry 45, no. 1 (1989): 102. http://dx.doi.org/10.1016/s0022-1139(00)84474-7.

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22

Arroyo, Maribel, Sylvain Bernès, Norma Calixto, and Carina Gómez. "Synthesis of fluorinated trithioether compounds." Journal of Fluorine Chemistry 127, no. 1 (2006): 22–28. http://dx.doi.org/10.1016/j.jfluchem.2005.09.017.

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23

Parekh, Kajal, Xin Chen, and Pranesh B. Aswath. "Synthesis of Fluorinated ZDDP Compounds." Tribology Letters 34, no. 2 (2008): 141–53. http://dx.doi.org/10.1007/s11249-008-9373-7.

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24

BURTON, D. J., and L. LU. "ChemInform Abstract: Fluorinated Organometallic Compounds." ChemInform 29, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199813253.

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25

BINOY, NIVYA, SHACHINDRA L. NARGUND, SHRAVAN L. NARGUND, and RAMA NARGUND. "Synthesis of Fluorinated Heterocyclic Compounds for Pharmacological Screening." Journal of Ultra Chemistry 17, no. 3 (2021): 16–24. http://dx.doi.org/10.22147/juc/170301.

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A series of derivatives of (E)-6-chloro-5-fluoro-2-styryl-1H-benzo[d]imidazole, and 5-fluoro-2-methylN-phenyl-1H-benzo[d]imidazol-6-amine was synthesized. Compounds confirmed by melting point, FT-IR, 1HNMR, Mass spectral analytical techniques and predicted for their ADME, Pharmacokinetic properties.Synthesized compounds screened for better antibacterial and antiinflammatory activity. To synthesize a series of novel trisubstituted fluorinated benzimidazole derivatives and evaluate the physicochemical, ADME and pharmacokinetic properties and biological activity. The starting material Flouro-chlo

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26

Li, Ningning, Bingjing Hu, Anming Wang, et al. "Facile Bioinspired Preparation of Fluorinase@Fluoridated Hydroxyapatite Nanoflowers for the Biosynthesis of 5′-Fluorodeoxy Adenosine." Sustainability 12, no. 1 (2020): 431. http://dx.doi.org/10.3390/su12010431.

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To develop an environmentally friendly biocatalyst for the efficient synthesis of organofluorine compounds, we prepared the enzyme@fluoridated hydroxyapatite nanoflowers (FHAp-NFs) using fluorinase expressed in Escherichia coli Rosetta (DE3) as the biomineralization framework. The obtained fluorinase@FHAp-NFs were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), and FT-IR spectrum and used in the enzymatic synthesis of 5′-fluorodeoxy adenosin with S-adenosyl-L-methionine and fluoride as substrate. At an optimum pH of 7.5, fluorinase confined in the hybrid nanoflowe

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27

Boccalon, Mariangela, Silvia Bidoggia, Francesco Romano, et al. "Gold nanoparticles as drug carriers: a contribution to the quest for basic principles for monolayer design." Journal of Materials Chemistry B 3, no. 3 (2015): 432–39. http://dx.doi.org/10.1039/c4tb01536c.

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28

Liu, Jingping, and Hatsuo Ishida. "High Yield Synthesis of Fluorinated Benzoxazine Monomers and Their Molecular Characterization." Polymers and Polymer Composites 10, no. 3 (2002): 191–204. http://dx.doi.org/10.1177/096739110201000301.

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A method for the synthesis of 3,4-dihydro-3-pentafluorophenyl-2H-1,3-benzoxazine in a high yield derived from pentafluoroaniline is described. This fluorinated benzoxazine monomer has been developed as a potential precursor for a polybenzoxazine in electronic applications as well as others taking advantage of the low dielectric constant, low flammability, low refractive index, low coefficient of friction, and high glass transition temperature of fluorinated compounds. The traditional benzoxazine synthesis conditions are inappropriate for the synthesis of fluorinated benzoxazines when the fluor

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29

ISEKI, Katsuhiko, and Yoshiro KOBAYASHI. "Asymmetric Synthesis of Chiral Fluorinated Compounds." Journal of Synthetic Organic Chemistry, Japan 52, no. 1 (1994): 40–48. http://dx.doi.org/10.5059/yukigoseikyokaishi.52.40.

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30

Escorihuela, Jorge, Daniel M. Sedgwick, Alberto Llobat, Mercedes Medio-Simón, Pablo Barrio, and Santos Fustero. "Pauson–Khand reaction of fluorinated compounds." Beilstein Journal of Organic Chemistry 16 (July 14, 2020): 1662–82. http://dx.doi.org/10.3762/bjoc.16.138.

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The Pauson–Khand reaction (PKR) is one of the key methods for the construction of cyclopentenone derivatives, which can in turn undergo diverse chemical transformations to yield more complex biologically active molecules. Despite the increasing availability of fluorinated building blocks and methodologies to incorporate fluorine in compounds with biological interest, there have been few significant advances focused on the fluoro-Pauson–Khand reaction, both in the inter- and intramolecular versions. Furthermore, the use of vinyl fluorides as olefinic counterparts had been completely overlooked.

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31

Whitehead, Heather D., Marta Venier, Yan Wu, et al. "Fluorinated Compounds in North American Cosmetics." Environmental Science & Technology Letters 8, no. 7 (2021): 538–44. http://dx.doi.org/10.1021/acs.estlett.1c00240.

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32

Coleman, William F. "The Chemistry of Highly Fluorinated Compounds." Journal of Chemical Education 83, no. 1 (2006): 92. http://dx.doi.org/10.1021/ed083p92.

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33

Betts, Kellyn S. "Potential explanation for fluorinated compounds' persistence." Environmental Science & Technology 37, no. 17 (2003): 312A—313A. http://dx.doi.org/10.1021/es032554i.

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34

Purrington, Suzanne T., and Sonia C. Weeks. "[3,3]-Sigmatropic rearrangements of fluorinated compounds." Journal of Fluorine Chemistry 56, no. 2 (1992): 165–73. http://dx.doi.org/10.1016/s0022-1139(00)81099-4.

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35

Reichenbächer, Katharina, Antonia Neels, Helen Stoeckli-Evans, et al. "New Fluorinated Channel-type Host Compounds." Crystal Growth & Design 7, no. 8 (2007): 1399–405. http://dx.doi.org/10.1021/cg060682n.

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36

DAGANI, RON. "New route found to fluorinated compounds." Chemical & Engineering News 73, no. 43 (1995): 26–28. http://dx.doi.org/10.1021/cen-v073n043.p026.

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37

Percy, Jonathan M., and Michael E. Prime. "Rearrangement routes to selectively fluorinated compounds." Journal of Fluorine Chemistry 100, no. 1-2 (1999): 147–56. http://dx.doi.org/10.1016/s0022-1139(99)00149-9.

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38

Vargas, C., B. Song, M. Camps, and M. M. Häggblom. "Anaerobic degradation of fluorinated aromatic compounds." Applied Microbiology and Biotechnology 53, no. 3 (2000): 342–47. http://dx.doi.org/10.1007/s002530050032.

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39

Kondo, Shigeo, Youkichi Urano, Kenji Takizawa, Akifumi Takahashi, Kazuaki Tokuhashi, and Akira Sekiya. "Flammability limits of multi-fluorinated compounds." Fire Safety Journal 41, no. 1 (2006): 46–56. http://dx.doi.org/10.1016/j.firesaf.2005.08.002.

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40

LEWANDOWSKI, G., E. MEISSNER, and E. MILCHERT. "Special applications of fluorinated organic compounds." Journal of Hazardous Materials 136, no. 3 (2006): 385–91. http://dx.doi.org/10.1016/j.jhazmat.2006.04.017.

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41

Lahsen, Joaquín, and Jorge Ramos-Grez. "Internal rotation of fluorinated butane compounds." Journal of Fluorine Chemistry 127, no. 3 (2006): 373–76. http://dx.doi.org/10.1016/j.jfluchem.2005.12.030.

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42

Hu, Huawei, Yangen Huang, and Yong Guo. "Henry reaction of fluorinated nitro compounds." Journal of Fluorine Chemistry 133 (January 2012): 108–14. http://dx.doi.org/10.1016/j.jfluchem.2011.09.004.

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43

Biffinger, Justin C., Hong Woo Kim, and Stephen G. DiMagno. "The Polar Hydrophobicity of Fluorinated Compounds." ChemBioChem 5, no. 5 (2004): 622–27. http://dx.doi.org/10.1002/cbic.200300910.

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44

Alves, Anthony V., Marina Tsianou, and Paschalis Alexandridis. "Fluorinated Surfactant Adsorption on Mineral Surfaces: Implications for PFAS Fate and Transport in the Environment." Surfaces 3, no. 4 (2020): 516–66. http://dx.doi.org/10.3390/surfaces3040037.

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Fluorinated surfactants, which fall under the class of per- and polyfluoroalkyl substances (PFAS), are amphiphilic molecules that comprise hydrophobic fluorocarbon chains and hydrophilic head-groups. Fluorinated surfactants have been utilized in many applications, e.g., fire-fighting foams, paints, household/kitchenware items, product packaging, and fabrics. These compounds then made their way into the environment, and have been detected in soil, fresh water, and seawater. From there, they can enter human bodies. Fluorinated surfactants are persistent in water and soil environments, and their

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45

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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46

Sevenard, Dmitri V., Oleg G. Khomutov, Nadezhda S. Boltachova, et al. "Metal and Boron Derivatives of Fluorinated Cyclic 1,3-Dicarbonyl Compounds." Zeitschrift für Naturforschung B 64, no. 5 (2009): 541–50. http://dx.doi.org/10.1515/znb-2009-0510.

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Starting from the corresponding cyclic 1,3-diketones or other precursors (cyclic ketones as well as lactones), several new salts and chelate complexes of fluorinated 1,3-dicarbonyls were obtained. Their preparative significance was demonstrated by straightforward syntheses of fluorinated pyrazoles, benzimidazoles and 1,7-ketoesters. The structure of a boron chelate of 2-(trifluoroacetyl)- cyclohexanone was investigated by X-ray diffraction.

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47

Carvalho, Maria F., and Rui S. Oliveira. "Natural production of fluorinated compounds and biotechnological prospects of the fluorinase enzyme." Critical Reviews in Biotechnology 37, no. 7 (2017): 880–97. http://dx.doi.org/10.1080/07388551.2016.1267109.

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48

Dolbier, William R., Keith W. Palmer, Feng Tian, Piotr Fiedorow, Andrzej Zaganiaczyk, and Henryk Koroniak. "[3,3] Sigmatropic Rearrangement of Some Fluorinated 1,5-Hexadienes." Collection of Czechoslovak Chemical Communications 67, no. 10 (2002): 1517–32. http://dx.doi.org/10.1135/cccc20021517.

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Fluorine atoms incorporated into 1,5-hexadiene molecule should influence the kinetic as well as the thermodynamic parameters of [3,3] sigmatropic rearrangement (Cope rearrangement). Within few decades is has been documented that this transformation proceeds in a concerted manner, rather than stepwise with some radical intermediates involved. Few new terminally fluorinated 1,5-hexadienes (compounds 3, 5A, 7, 9 and 5B) have been synthesized. The activation parameters of rearrangement have been determined and compared with those known for hydrocarbon analogues. While systems developing chair-like

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49

De la Cruz-Claure, María L., Ariel A. Cèspedes-Llave, María T. Ulloa, Miguel Benito-Lama, Enrique Domínguez-Álvarez, and Agatha Bastida. "Inhibition–Disruption of Candida glabrata Biofilms: Symmetrical Selenoesters as Potential Anti-Biofilm Agents." Microorganisms 7, no. 12 (2019): 664. http://dx.doi.org/10.3390/microorganisms7120664.

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Candida glabrata is one of the most prevalent pathogenic Candida species in dental plaque on tooth surfaces. Candida biofilms exhibit an enhanced resistance against most antifungal agents. Thus, the development of alternative more potent and effective antimicrobials is required to overcome this resistance. In this study, three novel fluorinated derivatives and nine selenoester compounds were screened as novel antifungal and antibiofilm agents against C. krusei, C. parapsilosis, and C. glabrata (N = 81 dental isolates). C. glabrata strains were susceptible only to fluorinated compounds while C.

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50

Romanov, Vasily, Evgeny Tretyakov, Galina Selivanova, et al. "Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications." Crystals 10, no. 9 (2020): 786. http://dx.doi.org/10.3390/cryst10090786.

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A simple and general approach to the synthesis (from commercial precursors) of eight out of nine possible (benzo[d]imidazol-2-yl)methanols fluorinated on the benzene ring is reported. Molecular and crystalline structures of most compounds were solved by X-ray diffraction analysis. This made it possible to reveal the influence of the number and arrangement of fluorine atoms in the benzene cycle on the formation of intermolecular hydrogen bonds. It was found that the more fluorine atoms are present in a compound, the higher the dimensionality of the H-bonded structure is. Moreover, the presence

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