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Journal articles on the topic 'Fluoroketone'

Author: Grafiati

Published: 5 June 2025

Last updated: 8 July 2025

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1

Neufeld, Jessica, Constantin G. Daniliuc, and Ryan Gilmour. "Fluorohydration of alkynes via I(I)/I(III) catalysis." Beilstein Journal of Organic Chemistry 16 (July 10, 2020): 1627–35. http://dx.doi.org/10.3762/bjoc.16.135.

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Substrate specificity is ubiquitous in biological catalysis, but less pervasive in the realm of small-molecule catalysis. Herein, we disclose an intriguing example of substrate specificity that was observed whilst exploring catalysis-based routes to generate α-fluoroketones from terminal and internal alkynes under the auspices of I(I)/I(III) catalysis. Utilising p-TolI as an inexpensive organocatalyst with Selectfluor® and amine/HF mixtures, the formation of protected α-fluoroketones from simple alkynes was realised. Whilst the transient p-TolIF2 species generated in situ productively engaged with pentynyl benzoate scaffolds to generate the desired α-fluoroketone motif, augmentation or contraction of the linker suppressed catalysis. The prerequisite for this substructure was established by molecular editing and was complemented with a physical organic investigation of possible determinants.

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2

Owens, John, Ang Xiao, Jason Bonk, Michael DeLorme, and Agnes Zhang. "Recent Development of Two Alternative Gases to SF6 for High Voltage Electrical Power Applications." Energies 14, no. 16 (2021): 5051. http://dx.doi.org/10.3390/en14165051.

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For many years, SF6 has been the preferred dielectric medium in electrical power applications, particularly in high voltage gas-insulated equipment. However, with the recognition that SF6 has an extremely long atmospheric lifetime and very high global warming potential, governments have pursued emission reductions from gas-filled equipment. The electrical power industry has responded to this environmental challenge applying SF6-free technologies to an expanding range of applications which have traditionally used SF6, including gas-insulated switchgear, gas-insulated circuit breakers and gas-insulated lines or bus bars. Some of these SF6-free solutions include gas mixtures containing fluorinated compounds that have low climate impact, among them, a fluoronitrile and a fluoroketone developed as 3M™ Novec™ 4710 Insulating Gas and 3M™ Novec™ 5110 Insulating Gas, respectively. Both fluoronitrile and fluoroketone mixtures are successfully used in gas-insulated equipment currently operating on the grid where they reduce greenhouse gas emissions by more than 99% versus SF6. This paper reviews these leading components of alternative-gas mixtures with updates on the performance, safety and environmental profiles in electrical power applications.

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3

Legros, Julien, Benoı̂t Crousse, Jack Bourdon, Danièle Bonnet-Delpon, and Jean-Pierre Bégué. "An efficient and robust fluoroketone catalyst epoxidation." Tetrahedron Letters 42, no. 27 (2001): 4463–66. http://dx.doi.org/10.1016/s0040-4039(01)00751-1.

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4

Tarasenko, Karen V., Igor I. Gerus, Valery P. Kukhar та Vitaly V. Polovinko. "Reactions of β-aminovinyl bromodifluoromethyl ketones with alkyl phosphites: Perkow versus Arbuzov". Collection of Czechoslovak Chemical Communications 74, № 2 (2009): 335–46. http://dx.doi.org/10.1135/cccc2008095.

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New bromodifluoromethyl enaminones 1a–1f and γ-bromo-β-morpholinopropenyl fluoromethyl ketones 2a, 2b were synthesized. N-Substituted bromodifluoromethyl enaminones 1a–1d do not react with triethyl or diethyl phosphites, whereas N-acylated enaminones 1e, 1f gave difluorodienyl phosphates 4a, 4b as Perkow rearrangement products. Fluoroketone 2a reacts easily with triethyl phosphite according to the Arbuzov protocol and a perspective building block – trifluoromethyl-containing phosphonate 7a is formed.

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5

Legros, Julien, Benoit Crousse, Jack Bourdon, Daniele Bonnet-Delpon, and Jean-Pierre Begue. "ChemInform Abstract: An Efficient and Robust Fluoroketone Catalyst Epoxidation." ChemInform 32, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.200135112.

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6

Linderman, Russell J., Scott D. Tennyson, and David A. Shultz. "Comparative stability of fluoroketone hemi-thio acetals, ketals and hydrates." Tetrahedron Letters 35, no. 35 (1994): 6437–40. http://dx.doi.org/10.1016/s0040-4039(00)78240-2.

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7

Kokotos, George, Yuan-Hao Hsu, John E. Burke, et al. "Potent and Selective Fluoroketone Inhibitors of Group VIA Calcium-Independent Phospholipase A2." Journal of Medicinal Chemistry 53, no. 9 (2010): 3602–10. http://dx.doi.org/10.1021/jm901872v.

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8

Wang, Feng, Qiaowen Dun, She Chen, Lipeng Zhong, Xiaopeng Fan, and Li Li. "Calculations of total electron impact ionization cross sections for fluoroketone and fluoronitrile." IEEE Transactions on Dielectrics and Electrical Insulation 26, no. 5 (2019): 1693–700. http://dx.doi.org/10.1109/tdei.2019.008255.

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9

LINDERMAN, R. J., S. D. TENNYSON, and D. A. SHULTZ. "ChemInform Abstract: Comparative Stability of Fluoroketone Hemi-thio Acetals, Ketals and Hydrates." ChemInform 26, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199504038.

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10

Subhana, Arik, Nina Sasaki Støa-Aanensen, Marte Gammelsæter, Erik Jonsson Seither, and Frank Mauseth. "Ageing of Technical Air and Technical Air with 7.5% C5-Fluoroketone by Free-Burning Arcs." PLASMA PHYSICS AND TECHNOLOGY 10, no. 2 (2023): 89–93. http://dx.doi.org/10.14311/ppt.2023.2.89.

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This paper reports on the effect of ageing by free-burning arcs in 7.5% C5-fluoroketone (C5-FK) with 92.5% technical air in comparison to that in technical air (80% N2, 20% O2) at 1.3bar absolute pressure. The gases are aged by applying a series of arcs dissipating an accumulated energy of around 315kJ. It is found that the arc voltages in technical air and technical air with C5-FK are in the same range and do not vary significantly as a function of ageing or current amplitude (∼40-900 A). Contact erosion in both mediums is found to be similar if the discharge procedure is same. However, erosion increases significantly if ageing is performed in a short contact gap that needs more arcing operations to achieve similar level of arcing energy accumulation. Furthermore, gas decomposition by-products are analysed using gas chromatography coupled with mass-spectrometry.

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11

Ranjan, N., J. Carstensen, and S. Scheel. "Interruption of Weakly Cooled Arcs in Air and Airplus." PLASMA PHYSICS AND TECHNOLOGY 4, no. 2 (2017): 194–97. http://dx.doi.org/10.14311/ppt.2017.2.194.

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Switching of low current arcs in free burning or weakly cooled conditions is mainly determined by the thermal properties of the gas. Products with such switching conditions are widely found in secondary distribution medium voltage (MV) gas insulated switchgears (GIS). In this study, we compare the current interruption capability of synthetic air and AirPlusTM, i.e. a mixture of synthetic air with C5F10O fluoroketone (C5-FK). We focus on thermal interruption performance of the gases. AirPlus mixture corresponds to -25 °C condensation temperature of C5-FK. An arc is drawn between the contacts and cooled by blowing cold gas from a tank. Blowing pressure required for current interruption is compared. Within the measurement accuracy, the current interruption performance of both gases is similar. Chemical analysis of the AirPlus mixture after 69 shots was performed using Gas Chromatography Mass Spectroscopy (GCMS) and it shows very little decrease in the concentration of C5-FK.

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12

Govardhan, Chandrika P., та Robert H. Abeles. "Structure-activity studies of fluoroketone inhibitors of α-lytic protease and human leukocyte elastase". Archives of Biochemistry and Biophysics 280, № 1 (1990): 137–46. http://dx.doi.org/10.1016/0003-9861(90)90528-7.

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13

Polousova, Yulia E. Polousova, Dmitry I. Pisarev, Oleg O. Novikov, Rimma A. Abramovich, and Karen M. Sakanyan. "The spectrum of pharmacological activity of different groups of natural compounds of laurel leaves and the choice of the optimal extractant for the extraction of essential oil from them." RESEARCH RESULTS IN BIOMEDICINE 7, no. 3 (2021): 281–95. http://dx.doi.org/10.18413/2658-6533-2021-7-3-0-7.

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Laurel noble – Laurus nobilis L., a plant whose leaves are widely used in cooking and are used in folk medicine. L. nobilis L. leaves contain more than 80 volatile components, represented mainly by monocyclic monoterpenes. The identification of more and more new therapeutic properties of the plant testifies to its incompletely undisclosed therapeutic potential. However, despite the impressive therapeutic potential of the plant, it is not used in domestic scientific medicine. The aim of the study: To describe the spectrum of types of pharmacological activity of L. nobilis L. and selection of the optimal extractant for the extraction of essential oil from the leaves of the object under study. Materials and methods: Laurel leaves were used as the test material. The essential oil from the leaves was obtained by extraction with freons, which are methoxynonafluorobutane and fluoroketone. The extractant for comparison was n-hexane. The method of studying essential oils was chromatography- mass spectrometry. Chromatography was performed on a gas chromatograph – mass spectrometer – GCMS-QP2010 Ultra, Shimadzu, Japan. Ionization is carried out in the electronic shock mode, detection by the total ionic current (SCAN) in the programmed temperature mode. Results: According to the literature, the essential oil of L. nobilis L. leaves have a pronounced antibacterial, antioxidant and antiinflammatory effect. Polyphenolic compounds of L. nobilis L. leaves are represented by flavonoids, derivatives of kaempferol and quercetin. It is believed that flavonoids are responsible for hypoglycemic, insular protective, antioxidant effects. The results of chromatography showed that the essential oil is represented mainly by 12 compounds, the dominant of which were 1.8-cineole (eucalyptol), alpha-terpenyl acetate and methyleugenol. During chromatography, it was also found that the optimal extractant is methoxynonafluorobutane, which extracts terpenoids with the highest yield. The prospects of using freons as agents for obtaining essential oil from laurel leaves have been shown. The composition of the essential oil isolated by freons from the leaves of laurel was determined by the method of gas chromatography-mass spectrometry. The results of chromatography showed that in the obtained freon extracts, 1.8-cineole (eucalyptol), alpha-terpenyl acetate and methyleugenol were dominant, which is close in composition to the native essential oil, according to literature data. Conclusion: The prospects of using freons as agents for extracting essential oil from L. nobilis L. leaves were shown. During chromatography, it was found that the optimal extractant is methoxynonafluorobutane, which extracts volatile components with the highest yield compared to fluoroketone and n-hexane; in addition, methoxyfluorobutane is non-toxic compared to n-hexane.

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14

Hsu, Yuan-Hao, Denis Bucher, Jian Cao, et al. "Fluoroketone Inhibition of Ca2+-Independent Phospholipase A2 through Binding Pocket Association Defined by Hydrogen/Deuterium Exchange and Molecular Dynamics." Journal of the American Chemical Society 135, no. 4 (2013): 1330–37. http://dx.doi.org/10.1021/ja306490g.

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15

Xiong, Jiayu, Xingwen Li, Jian Wu, Xiaoxue Guo, and Hu Zhao. "Calculations of total electron-impact ionization cross sections for Fluoroketone C5F10O and Fluoronitrile C4F7N using modified Deutsch–Märk formula." Journal of Physics D: Applied Physics 50, no. 44 (2017): 445206. http://dx.doi.org/10.1088/1361-6463/aa881d.

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16

Chen, Tairan, Biao Huang, Guoyu Wang, Hanzhe Zhang, and Yongkang Wang. "Numerical investigation of thermo-sensitive cavitating flows in a wide range of free-stream temperatures and velocities in fluoroketone." International Journal of Heat and Mass Transfer 112 (September 2017): 125–36. http://dx.doi.org/10.1016/j.ijheatmasstransfer.2017.04.023.

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17

Zhang, Hui, Xiaoyan Ye, Desheng Zhang, Bin Xu, and Xiangxu Kong. "Numerical investigation on the evolution of cavitating dynamics and energy loss around a hydrofoil in fluoroketone under different temperatures." Ocean Engineering 287 (November 2023): 115856. http://dx.doi.org/10.1016/j.oceaneng.2023.115856.

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18

Animesh, Chakravorty. "Contributions of P. C. Rây in organic synthesis." Journal of Indian Chemical Society Vol. 93, Dec 2016 (2016): 1333–36. https://doi.org/10.5281/zenodo.5595838.

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Department of Inorganic Chemistry, Indian Association for the Cultivation of Science, Kolkata-700 032, India <em>E</em>-<em>mail</em> : icac@iacs.res.in <em>Manuscript received 26 September 2016, accepted 18 October 2016</em> During most of his career Rây was busy with his work in the inorganic chemistry area. But he also had a long-standing interest in organic synthesis which finally got expressed only in terminal years of his career. We consider in this work two of his main endeavours in this area. First, synthesis of thioketones in general and thiocamphor and some related species in particular using hydrogen sulfide under acid catalysis as the reagent. Second, his introduction of thallium fluoride as a reagent for organic fluorination. The cases of fluorocarboxylate esters, fluoroketones and some more will be cited.

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19

Hsu, Yuan-Hao, Denis Bucher, Jian Cao, et al. "Correction to “Fluoroketone Inhibition of Ca2+-Independent Phospholipase A2 through Binding Pocket Association Defined by Hydrogen/Deuterium Exchange and Molecular Dynamics”." Journal of the American Chemical Society 135, no. 15 (2013): 5932. http://dx.doi.org/10.1021/ja4023623.

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20

Shibatomi, Kazutaka, Misaki Katada, Kazumasa Kitahara та Seiji Iwasa. "Catalyst-Free Decarboxylative Fluorination of Tertiary β-Keto Carboxylic Acids". Synlett 29, № 18 (2018): 2408–11. http://dx.doi.org/10.1055/s-0037-1611019.

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Decarboxylative fluorination of tertiary β-keto carboxylic acids was performed using an electrophilic fluorinating reagent. The reaction proceeded in the absence of a catalyst or base to yield the corresponding α-fluoroketones with tertiary fluorocarbons in good to high yields. Considering that the α-fluorination of asymmetrical ketones often causes problems with the regioselectivity between the α- and α′-positions, this method could be a good alternative to the α-fluorination of simple ketones for the synthesis of tertiary fluoroketones.

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21

Lu, Yen-Chu, Helen M. Jordan, and Julian G. West. "Rapid and scalable synthesis of fluoroketones via cerium-mediated C–C bond cleavage." Chemical Communications 57, no. 15 (2021): 1871–74. http://dx.doi.org/10.1039/d0cc08183c.

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22

Otevrel, Jan, David Svestka, and Pavel Bobal. "Bianthryl-based organocatalysts for the asymmetric Henry reaction of fluoroketones." Organic & Biomolecular Chemistry 17, no. 21 (2019): 5244–48. http://dx.doi.org/10.1039/c9ob00884e.

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23

Zeifman, Yu V. "Trichloromethylation of fluoroketones." Bulletin of the Russian Academy of Sciences Division of Chemical Science 41, no. 2 (1992): 370–73. http://dx.doi.org/10.1007/bf00869539.

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24

Zhu, Lin, He Chen, Zijia Wang, and Chaozhong Li. "Formal fluorine atom transfer radical addition: silver-catalyzed carbofluorination of unactivated alkenes with ketones in aqueous solution." Org. Chem. Front. 1, no. 11 (2014): 1299–305. http://dx.doi.org/10.1039/c4qo00256c.

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25

Ghazi, Hedieh, Gabriela Mladenova, and Edward Lee-Ruff. "An unusual fluoroketene reaction product." Journal of Fluorine Chemistry 126, no. 11-12 (2005): 1496–501. http://dx.doi.org/10.1016/j.jfluchem.2005.08.008.

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26

Wu, Jingjing, Fanhong Wu, Zhi Li, Mougui Fang, Yunli Liu та Yecheng Liu. "Efficient Monofluoroalkylation of Thiophenols or Phenols with α-Bromo-α-Fluoroketones under Mild Conditions". Synthesis 53, № 13 (2021): 2293–303. http://dx.doi.org/10.1055/a-1395-4788.

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AbstractAn efficient nucleophilic substitution reaction between α-bromo-α-fluoroketones and thiophenols or phenols is reported for the synthesis of α-fluoro-β-ketosulfides or α-fluoro-β-ketone ethers in yields ranging from 78–93%. This method exhibits good functional group tolerance and a broad scope of nucleophilic substrates, including natural phenolic compounds.

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27

Abraham, Shaji, Pravin Patel, Ulhas P. Naik та Steven Edward McKenzie. "iPLA2β Contributes to Activation of Human and Mouse Platelets Via ITAM Receptors Fcγ RIIA and GPVI". Blood 134, Supplement_1 (2019): 2339. http://dx.doi.org/10.1182/blood-2019-128426.

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Platelet activation by ITAM receptors contributes to hemostasis, thrombosis, vascular integrity and host defense. In the course of our studies of FcγRIIA-mediated platelet activation, we became interested in those mechanisms that require neither full Syk activation nor changes in intracellular calcium. Calcium-independent phospholipase family member iPLA2β has been observed to modulate phospholipid remodeling and second messenger generation in human platelets (Beckett, Thromb Res 2007; Duvernay, Biochem 2015), while iPLA2γ has been studied in knockout mouse platelets (Yoda, JTH 2014) with modest effects noted on thrombosis and hemostasis. These enzymes do not require increased cytoplasmic calcium for their activity in cleaving the acyl group from the sn2 position of phospholipids to yield a free fatty acid and a lysophospholipid. However, the precise role of iPLA2β in human and mouse platelet activation has not been elucidated. Neither has the contribution of iPLA2β in the response to FcγRIIA-mediated activation been reported. We identified the presence of iPLA2β protein in western blots of human and FcγRIIA transgenic mouse platelets. Of interest, multiple isoforms arising from proteolytic cleavage were detected. We treated washed human and FcγRIIA transgenic mouse platelets with agonists to FcγRIIA (IV.3 + GAM) and to GPVI (collagen or collagen-related peptide) in the absence and presence of pharmacologic inhibitors of iPLA2β. At a range of agonist doses up to 3X threshold, we observed significant inhibition of aggregation, dense granule secretion and alpha granule secretion (p<0.05 vs. vehicle only, n = 3 to 4 each). Inhibition occurred with either S-BEL (bromo-enolactone) or with FKGK18 (a fluoroketone), two chemically distinct iPLA2β inhibitor molecules with different modes of action. The IC50 for S-BEL was found to be 1.02 uM for human FcγRIIA, 2.04 uM for human GPVI, and 2.76 uM for transgenic mouse FcγRIIA activated platelets. FKGK18 was less potent, with IC50s at 7.88 uM for human FcγRIIA. In contrast, iPLA2γ inhibitor R-BEL was able to inhibit FcγRIIA -mediated activation, but at an IC50 of 2.62 uM. Notably, iPLA2β inhibition could eliminate ATP secretion from dense granules downstream of FcγRIIA and GPVI activation. When we added ADP to FcγRIIA stimulation in the presence of inhibitory doses of S-BEL, we overcame the inhibition. We have identified for the first time that iPLA2β contributes to aggregation and secretion of both human and FcγRIIA transgenic mouse platelets. The platelets were slightly more sensitive to FcγRIIA than to GPVI inhibition. In other activatable secretory cells, iPLA2β plays both a homeostatic and signaling role. The mechanisms of iPLA2β action in platelets merit further study. Studies are in progress with genetic knockdown and knockout of the enzyme, to complement the findings with inhibitors. Disclosures No relevant conflicts of interest to declare.

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28

Zeifman, Yu V., S. A. Postovoi, and L. S. German. "Reductive addition of polychloroalkanes to fluoroketones." Journal of Fluorine Chemistry 58, no. 2-3 (1992): 132. http://dx.doi.org/10.1016/s0022-1139(00)80578-3.

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29

Tarnus, Céline, Michel J. Jung, Jean-Marc Rémy, Sylvie Baltzer, and Daniel G. Schirlin. "New fluoroketones as human renin inhibitors." FEBS Letters 249, no. 1 (1989): 47–50. http://dx.doi.org/10.1016/0014-5793(89)80012-2.

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30

Zeifman, Yu V., S. A. Postovoi, and L. S. German. "Reductive addition of polychloroalkanes to fluoroketones." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 9 (1991): 1916. http://dx.doi.org/10.1007/bf00960433.

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31

Litt, M., and F. W. Bauer. "Copolymerization of fluoroketones with vinyl acetate." Journal of Polymer Science Part C: Polymer Symposia 16, no. 3 (2007): 1551–60. http://dx.doi.org/10.1002/polc.5070160332.

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32

Hynes, John B., Johnny P. Campbell, and John D. Hynes. "Synthesis of 2-aminoquinazolines fromortho-fluoroketones." Journal of Heterocyclic Chemistry 32, no. 4 (1995): 1185–87. http://dx.doi.org/10.1002/jhet.5570320415.

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33

Mohanta, Pramod K., Todd A. Davis, Jeremy R. Gooch та Robert A. Flowers. "Chelation-Controlled Diastereoselective Reduction of α-Fluoroketones". Journal of the American Chemical Society 127, № 34 (2005): 11896–97. http://dx.doi.org/10.1021/ja052546x.

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34

Liang, Junqing, Jie Han, Jingjing Wu та ін. "Nickel-Catalyzed Coupling Reaction of α-Bromo-α-fluoroketones with Arylboronic Acids toward the Synthesis of α-Fluoroketones". Organic Letters 21, № 17 (2019): 6844–49. http://dx.doi.org/10.1021/acs.orglett.9b02474.

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35

Nakamura, M., E. Nakamura, A. Hajra та K. Endo. "Enantioselective Synthesis of Quaternary α-Fluoroketones via Decarboxylation". Synfacts 2006, № 01 (2005): 0050. http://dx.doi.org/10.1055/s-2005-921675.

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36

Jiao, Zhiwei, Jason J. Beiger, Yushu Jin, Shaozhong Ge, Jianrong Steve Zhou та John F. Hartwig. "Palladium-Catalyzed Enantioselective α-Arylation of α-Fluoroketones". Journal of the American Chemical Society 138, № 49 (2016): 15980–86. http://dx.doi.org/10.1021/jacs.6b09580.

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37

Chambers, Richard D., та John Hutchinson. "Elemental fluorine Part 8. Preparation of α-fluoroketones". Journal of Fluorine Chemistry 89, № 2 (1998): 229–32. http://dx.doi.org/10.1016/s0022-1139(98)00132-8.

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38

Pattison, Graham. "Conformational preferences of α-fluoroketones may influence their reactivity". Beilstein Journal of Organic Chemistry 13 (29 грудня 2017): 2915–21. http://dx.doi.org/10.3762/bjoc.13.284.

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Fluorine has been shown in many cases to impart specific and predictable effects on molecular conformation. Here it is shown that these conformational effects may have an influence on reactivity through studying the relative reactivity of various α-halogenated ketones towards borohydride reduction. These results demonstrate that the α-fluoro ketones are in fact a little less reactive than the corresponding α-chloro and α-bromo derivatives. It is suggested, supported by computation, that this effect is due to reactive conformations in which the C–X bond is orthogonal to the carbonyl group for good orbital overlap being disfavoured in the case of fluoro ketones.

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39

Tunge, J., E. Burger та B. Barron. "Catalytic Asymmetric Synthesis of Cyclic α-Allylated α-Fluoroketones". Synlett 2006, № 17 (2006): 2824–26. http://dx.doi.org/10.1055/s-2006-950265.

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40

HYNES, J. B., J. P. CAMPBELL, and J. D. HYNES. "ChemInform Abstract: Synthesis of 2-Aminoquinazolines from ortho-Fluoroketones." ChemInform 26, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199551192.

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41

Nakamura, Masaharu, Alakananda Hajra, Kohei Endo та Eiichi Nakamura. "Synthesis of Chiral α-Fluoroketones through Catalytic Enantioselective Decarboxylation". Angewandte Chemie 117, № 44 (2005): 7414–17. http://dx.doi.org/10.1002/ange.200502703.

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42

Nakamura, Masaharu, Alakananda Hajra, Kohei Endo та Eiichi Nakamura. "Synthesis of Chiral α-Fluoroketones through Catalytic Enantioselective Decarboxylation". Angewandte Chemie International Edition 44, № 44 (2005): 7248–51. http://dx.doi.org/10.1002/anie.200502703.

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43

Purrington, Suzanne T., Nicholas V. Lazaridis та Carl L. Bumgardner. "Preparation of α-fluoroaldehydes and α-fluoroketones using dilute fluorine". Tetrahedron Letters 27, № 24 (1986): 2715–16. http://dx.doi.org/10.1016/s0040-4039(00)84624-9.

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44

Wu, Shu-Wei, та Feng Liu. "Synthesis of α-Fluoroketones from Vinyl Azides and Mechanism Interrogation". Organic Letters 18, № 15 (2016): 3642–45. http://dx.doi.org/10.1021/acs.orglett.6b01691.

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45

Chen, Loomis S., Kent J. Eisentraut, Costandy S. Saba, Mary T. Ryan, and Christ Tamborski. "Fluoro-ketones VIII. Synthesis of some fluoroquinoxaline compounds from fluoroketones." Journal of Fluorine Chemistry 30, no. 4 (1986): 385–98. http://dx.doi.org/10.1016/s0022-1139(00)85094-0.

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46

Deng, Yuanlin, Nabeelah I. Kauser, Shahidul M. Islam та Justin T. Mohr. "AgII -Mediated Synthesis of β-Fluoroketones by Oxidative Cyclopropanol Opening". European Journal of Organic Chemistry 2017, № 39 (2017): 5872–79. http://dx.doi.org/10.1002/ejoc.201700899.

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Brown, R. D., P. D. Godfrey, and B. Kleibömer. "Generation, microwave spectrum, dipole moment and structure of fluoroketene CHFCO." Chemical Physics 105, no. 3 (1986): 301–5. http://dx.doi.org/10.1016/0301-0104(86)80117-3.

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CHAMBERS, R. D., та J. HUTCHINSON. "ChemInform Abstract: Elemental Fluorine. Part 8. Preparation of α-Fluoroketones." ChemInform 29, № 35 (2010): no. http://dx.doi.org/10.1002/chin.199835082.

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He, Yan, Xinying Zhang, Nana Shen та Xuesen Fan. "Synthesis of α-fluoroketones and α-fluoroenones in aqueous media". Journal of Fluorine Chemistry 156 (грудень 2013): 9–14. http://dx.doi.org/10.1016/j.jfluchem.2013.08.006.

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Guo, Yong, Brendan Twamley та Jean'ne M. Shreeve. "Pd-catalyzed arylation of silyl enol ethers of substituted α-fluoroketones". Organic & Biomolecular Chemistry 7, № 8 (2009): 1716. http://dx.doi.org/10.1039/b900311h.

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