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Статті в журналах з теми "Perfluoroaryl"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Perfluoroaryl.

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 28 січня 2023

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1

Robinson, Stephen D., Arvind Sahajpal, and Derek A. Tocher. "Perfluoroalkyl- and perfluoroaryl-amidato derivatives of ruthenium, osmium and iridium." Journal of the Chemical Society, Dalton Transactions, no. 21 (1995): 3497. http://dx.doi.org/10.1039/dt9950003497.

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2

Diel, Bruce N., Peter J. Deardorff та Catherine M. Zelenski. "Synthesis of new 2,3-perfluoroalkyl- and perfluoroaryl-1,4-diazabutadienes (α-diimines)". Tetrahedron Letters 40, № 49 (грудень 1999): 8523–27. http://dx.doi.org/10.1016/s0040-4039(99)01692-5.

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3

Xie, Sheng, Juan Zhou, Xuan Chen, Na Kong, Yanmiao Fan, Yang Zhang, Gerry Hammer, David G. Castner, Olof Ramström, and Mingdi Yan. "A versatile catalyst-free perfluoroaryl azide–aldehyde–amine conjugation reaction." Materials Chemistry Frontiers 3, no. 2 (2019): 251–56. http://dx.doi.org/10.1039/c8qm00516h.

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4

Bonnier, Catherine, Warren E. Piers, Adeeb Al-Sheikh Ali, Alison Thompson, and Masood Parvez. "Perfluoroaryl-Substituted Boron Dipyrrinato Complexes." Organometallics 28, no. 16 (August 24, 2009): 4845–51. http://dx.doi.org/10.1021/om900402e.

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5

Diel, Bruce N., Peter J. Deardorff та Catherine M. Zelenski. "ChemInform Abstract: Synthesis of New 2,3-Perfluoroalkyl- and Perfluoroaryl-1,4-diazabutadienes (α-Diimines)". ChemInform 31, № 9 (10 червня 2010): no. http://dx.doi.org/10.1002/chin.200009078.

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6

Kato, Hisano, Keiichi Hirano, Daisuke Kurauchi, Naoyuki Toriumi, and Masanobu Uchiyama. "Dialkylzinc-Mediated Cross-Coupling Reactions of Perfluoroalkyl and Perfluoroaryl Halides with Aryl Halides." Chemistry - A European Journal 21, no. 10 (January 28, 2015): 3895–900. http://dx.doi.org/10.1002/chem.201406292.

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7

Gerthoffer, Margaret C., Bohan Xu, Sikai Wu, Jordan Cox, Steven Huss, Shalisa M. Oburn, Steven A. Lopez, Vincent H. Crespi, John V. Badding, and Elizabeth Elacqua. "Mechanistic insights into the pressure-induced polymerization of aryl/perfluoroaryl co-crystals." Polymer Chemistry 13, no. 10 (2022): 1359–68. http://dx.doi.org/10.1039/d1py01387d.

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Анотація:

The pressure-induced polymerization of aryl/perfluoroaryl co-crystals offers a strategic route to obtain sequence-defined polymeric architectures, such as diamond nanothreads, that feature a stiff sp3 hybridized backbone.

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8

Kobayashi, Masafumi, and Kenji Uneyama. "Synthesis of 2-(Perfluoroalkyl)- and 2-(Perfluoroaryl)benzimidazoles by Oxidative Intramolecular Cyclization of Perfluoroalkyl and Aryl Imidamides." Journal of Organic Chemistry 61, no. 11 (January 1996): 3902–5. http://dx.doi.org/10.1021/jo952224j.

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9

McPake, Christopher B., Christopher B. Murray, and Graham Sandford. "Continuous Flow Synthesis of Difluoroamine Systems by Direct Fluorination." Australian Journal of Chemistry 66, no. 2 (2013): 145. http://dx.doi.org/10.1071/ch12381.

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Анотація:

Continuous flow methodology for the synthesis of perfluoroaryl difluoroamine derivatives by reaction of fluorine gas with an appropriate perfluoroaniline substrate is described, further demonstrating the efficient use of flow regimes for reactions involving highly reactive and toxic reagents.

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10

Proietti, Giampiero, Julius Kuzmin, Azamat Z. Temerdashev, and Peter Dinér. "Accessing Perfluoroaryl Sulfonimidamides and Sulfoximines via Photogenerated Perfluoroaryl Nitrenes: Synthesis and Application as a Chiral Auxiliary." Journal of Organic Chemistry 86, no. 23 (November 12, 2021): 17119–28. http://dx.doi.org/10.1021/acs.joc.1c02241.

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11

Xie, Sheng, Sesha Manuguri, Giampiero Proietti, Joakim Romson, Ying Fu, A. Ken Inge, Bin Wu, et al. "Design and synthesis of theranostic antibiotic nanodrugs that display enhanced antibacterial activity and luminescence." Proceedings of the National Academy of Sciences 114, no. 32 (July 25, 2017): 8464–69. http://dx.doi.org/10.1073/pnas.1708556114.

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Анотація:

We report the modular formulation of ciprofloxacin-based pure theranostic nanodrugs that display enhanced antibacterial activities, as well as aggregation-induced emission (AIE) enhancement that was successfully used to image bacteria. The drug derivatives, consisting of ciprofloxacin, a perfluoroaryl ring, and a phenyl ring linked by an amidine bond, were efficiently synthesized by a straightforward protocol from a perfluoroaryl azide, ciprofloxacin, and an aldehyde in acetone at room temperature. These compounds are propeller-shaped, and upon precipitation into water, readily assembled into stable nanoaggregates that transformed ciprofloxacin derivatives into AIE-active luminogens. The nanoaggregates displayed increased luminescence and were successfully used to image bacteria. In addition, these nanodrugs showed enhanced antibacterial activities, lowering the minimum inhibitory concentration (MIC) by more than one order of magnitude against both sensitive and resistant Escherichia coli. The study represents a strategy in the design and development of pure theranostic nanodrugs for combating drug-resistant bacterial infections.

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12

Os’kina, I. A., A. S. Vinogradov, B. A. Selivanov, V. A. Savelyev, V. E. Platonov, and A. Ya Tikhonov. "Synthesis of 4,5-Dialkyl-2-perfluoroaryl-1H-imidazol-1-ols and 4,5-Dimethyl-2-perfluoroaryl-1H-imidazoles." Russian Journal of Organic Chemistry 57, no. 12 (December 2021): 1968–73. http://dx.doi.org/10.1134/s1070428021120101.

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13

Kato, Hisano, Keiichi Hirano, Daisuke Kurauchi, Naoyuki Toriumi, and Masanobu Uchiyama. "ChemInform Abstract: Dialkylzinc-Mediated Cross-Coupling Reactions of Perfluoroalkyl and Perfluoroaryl Halides with Aryl Halides." ChemInform 46, no. 28 (June 25, 2015): no. http://dx.doi.org/10.1002/chin.201528087.

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14

KOBAYASHI, M., and K. UNEYAMA. "ChemInform Abstract: Synthesis of 2-(Perfluoroalkyl)- and 2-(Perfluoroaryl)benzimidazoles by Oxidative Intramolecular Cyclization of Perfluoroalkyl and Aryl Imidamides." ChemInform 27, no. 39 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199639154.

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15

Xie, Sheng, Ryo Fukumoto, Olof Ramström, and Mingdi Yan. "Anilide Formation from Thioacids and Perfluoroaryl Azides." Journal of Organic Chemistry 80, no. 9 (April 13, 2015): 4392–97. http://dx.doi.org/10.1021/acs.joc.5b00240.

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16

Morimoto, Masakazu, Seiya Kobatake, and Masahiro Irie. "Aryl−Perfluoroaryl Interaction in Photochromic Diarylethene Crystals." Crystal Growth & Design 3, no. 5 (September 2003): 847–54. http://dx.doi.org/10.1021/cg034076t.

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17

Bednar, Taylor N., Alissa R. Resnikoff, and Jason Gavenonis. "Microwave-assisted cleavage of cysteine perfluoroaryl thioethers." Amino Acids 52, no. 5 (April 29, 2020): 841–45. http://dx.doi.org/10.1007/s00726-020-02846-z.

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18

Deck, Paul A. "Perfluoroaryl-substituted cyclopentadienyl complexes of transition metals." Coordination Chemistry Reviews 250, no. 9-10 (May 2006): 1032–55. http://dx.doi.org/10.1016/j.ccr.2005.11.001.

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19

Gerhards, Harald, Alexander Krest, Patrick J. Eulgem, Dieter Naumann, Dennis Rokitta, Martin Valldor, and Axel Klein. "Syntheses and coordination chemistry of perfluoroaryl-1H-tetrazoles." Polyhedron 100 (November 2015): 271–81. http://dx.doi.org/10.1016/j.poly.2015.08.006.

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20

Lechel, Tilman, Jyotirmayee Dash, Paul Hommes, Dieter Lentz, and Hans-Ulrich Reissig. "Three-Component Synthesis of Perfluoroalkyl- or Perfluoroaryl-Substituted 4-Hydroxypyridine Derivatives and Their Palladium-Catalyzed Coupling Reactions." Journal of Organic Chemistry 75, no. 3 (February 5, 2010): 726–32. http://dx.doi.org/10.1021/jo9022183.

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21

Pike, Sarah J., Christopher A. Hunter, Lee Brammer, and Robin N. Perutz. "Benchmarking of Halogen Bond Strength in Solution with Nickel Fluorides: Bromine versus Iodine and Perfluoroaryl versus Perfluoroalkyl Donors." Chemistry – A European Journal 25, no. 39 (June 18, 2019): 9237–41. http://dx.doi.org/10.1002/chem.201900924.

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22

Sundhoro, Madanodaya, Seaho Jeon, Jaehyeung Park, Olof Ramström, and Mingdi Yan. "Perfluoroaryl Azide Staudinger Reaction: A Fast and Bioorthogonal Reaction." Angewandte Chemie International Edition 56, no. 40 (September 1, 2017): 12117–21. http://dx.doi.org/10.1002/anie.201705346.

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23

Sundhoro, Madanodaya, Seaho Jeon, Jaehyeung Park, Olof Ramström, and Mingdi Yan. "Perfluoroaryl Azide Staudinger Reaction: A Fast and Bioorthogonal Reaction." Angewandte Chemie 129, no. 40 (September 1, 2017): 12285–89. http://dx.doi.org/10.1002/ange.201705346.

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24

Xie, Sheng, Ryo Fukumoto, Olof Ramstroem, and Mingdi Yan. "ChemInform Abstract: Anilide Formation from Thioacids and Perfluoroaryl Azides." ChemInform 46, no. 36 (August 20, 2015): no. http://dx.doi.org/10.1002/chin.201536088.

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25

Lechel, Tilman, Jyotirmayee Dash, Paul Hommes, Dieter Lentz, and Hans-Ulrich Reissig. "ChemInform Abstract: Three-Component Synthesis of Perfluoroalkyl- or Perfluoroaryl-Substituted 4-Hydroxypyridine Derivatives and Their Palladium-Catalyzed Coupling Reactions." ChemInform 41, no. 22 (June 1, 2010): no. http://dx.doi.org/10.1002/chin.201022124.

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26

Morrison, D. J., J. M. Blackwell, and W. E. Piers. "Mechanistic insights into perfluoroaryl borane-catalyzed allylstannations: Toward asymmetric induction with chiral boranes." Pure and Applied Chemistry 76, no. 3 (January 1, 2004): 615–23. http://dx.doi.org/10.1351/pac200476030615.

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Анотація:

The perfluoroaryl borane B(C6F5)3 is an effective catalyst for a variety of organic transformations. In the hydrosilation of carbonyl functions, it activates the silane rather than the carbonyl substrate. In allylstannation reactions, two competing reaction pathways are observed, one involving tin cation catalysis, the other "true" borane catalysis. For B(C6F5)3, the former mechanism dominates, while for the weaker Lewis acid PhB(C6F5)2, the latter pathway is more prominent. Thus, chiral boranes of similar Lewis acid strength to PhB(C6F5)2 have the potential to mediate asymmetric allylstannation of aldehyde substrates.

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27

Sanji, Takanobu, and Tomokazu Iyoda. "Transition-Metal-Free Controlled Polymerization of 2-Perfluoroaryl-5-trimethylsilylthiophenes." Journal of the American Chemical Society 136, no. 29 (July 10, 2014): 10238–41. http://dx.doi.org/10.1021/ja505282z.

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28

Redshaw, Carl, and Mark R. J. Elsegood. "Synthesis of bis(bora)calix[4]arenes bearing perfluoroaryl substituents." Chemical Communications, no. 40 (2005): 5056. http://dx.doi.org/10.1039/b509556e.

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29

Spokoyny, Alexander M., Yekui Zou, Jingjing J. Ling, Hongtao Yu, Yu-Shan Lin, and Bradley L. Pentelute. "A Perfluoroaryl-Cysteine SNAr Chemistry Approach to Unprotected Peptide Stapling." Journal of the American Chemical Society 135, no. 16 (April 16, 2013): 5946–49. http://dx.doi.org/10.1021/ja400119t.

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30

Xie, Sheng, Giampiero Proietti, Olof Ramström, and Mingdi Yan. "Photoactivatable Fluorogens by Intramolecular C–H Insertion of Perfluoroaryl Azide." Journal of Organic Chemistry 84, no. 22 (October 7, 2019): 14520–28. http://dx.doi.org/10.1021/acs.joc.9b02050.

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31

Morimoto, Masakazu, Seiya Kobatake, and Masahiro Irie. "Crystal Engineering of Photochromic Diarylethene Derivatives by Aryl-perfluoroaryl Interaction." Molecular Crystals and Liquid Crystals 431, no. 1 (June 1, 2005): 529–34. http://dx.doi.org/10.1080/15421400590947324.

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32

Chase, Preston A., Patricio E. Romero, Warren E. Piers, Masood Parvez, and Brian O. Patrick. "Fluorinated 9-borafluorenes vs. conventional perfluoroaryl boranes Comparative Lewis acidity." Canadian Journal of Chemistry 83, no. 12 (December 1, 2005): 2098–105. http://dx.doi.org/10.1139/v05-240.

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Анотація:

Perfluorinated 9-phenyl-9-borafluorene, 1, is an antiaromatic analog of the well-known tris(pentafluorophenyl)borane. Spectroscopic, structural, and electrochemical studies have been performed on 1 and its Lewis base adducts with MeCN, THF, and PMe3 with a view to assessing its comparative Lewis acid strength relative to B(C6F5)3. For the sterically undemanding Lewis base MeCN, 1 and B(C6F5)3 have comparable LA strengths, while for more sterically prominent THF, 1 is clearly the stronger Lewis acid (LA) based on competition experiments. We conclude that steric factors, rather than antiaromaticity, are the most important determinants in the LA strength differences between 1 and B(C6F5)3.Key words: boranes, Lewis acids, fluorinated compounds, heterocycles.

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33

Wolfe, Justin M., Colin M. Fadzen, Rebecca L. Holden, Monica Yao, Gunnar J. Hanson, and Bradley L. Pentelute. "Perfluoroaryl Bicyclic Cell-Penetrating Peptides for Delivery of Antisense Oligonucleotides." Angewandte Chemie 130, no. 17 (March 14, 2018): 4846–49. http://dx.doi.org/10.1002/ange.201801167.

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34

Wolfe, Justin M., Colin M. Fadzen, Rebecca L. Holden, Monica Yao, Gunnar J. Hanson, and Bradley L. Pentelute. "Perfluoroaryl Bicyclic Cell-Penetrating Peptides for Delivery of Antisense Oligonucleotides." Angewandte Chemie International Edition 57, no. 17 (March 14, 2018): 4756–59. http://dx.doi.org/10.1002/anie.201801167.

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35

Xia, Xiongbing, Gary Knerr, and N. R. Natale. "The preparation of perfluoroaryl substituted isoxazolesvianucleophilic aromatic substitution with lithioalkylisoxazoles." Journal of Heterocyclic Chemistry 29, no. 5 (August 1992): 1297–99. http://dx.doi.org/10.1002/jhet.5570290539.

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36

Timoshkin, Alexey Y., and Gernot Frenking. "Gas-Phase Lewis Acidity of Perfluoroaryl Derivatives of Group 13 Elements." Organometallics 27, no. 3 (February 2008): 371–80. http://dx.doi.org/10.1021/om700798t.

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37

Sundhoro, Madanodaya, Jaehyeung Park, Bin Wu, and Mingdi Yan. "Synthesis of Polyphosphazenes by a Fast Perfluoroaryl Azide-Mediated Staudinger Reaction." Macromolecules 51, no. 12 (June 7, 2018): 4532–40. http://dx.doi.org/10.1021/acs.macromol.8b00618.

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38

Chambers, Richard D., and Michael Todd. "A new approach to di(perfluoroaryl)methanes utilising sulphone-stabilised carbanions." Journal of Fluorine Chemistry 27, no. 2 (February 1985): 237–40. http://dx.doi.org/10.1016/s0022-1139(00)84992-1.

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39

Fujii, Kohei, Shigekazu Ito, and Koichi Mikami. "Synthetic Methodologies for Perfluoroaryl-Substituted (Diaryl)methylphosphonates, -Phosphinates via SNAr Reaction." Journal of Organic Chemistry 84, no. 19 (September 4, 2019): 12281–91. http://dx.doi.org/10.1021/acs.joc.9b01402.

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40

Qian, Elaine A., Alex I. Wixtrom, Jonathan C. Axtell, Azin Saebi, Dahee Jung, Pavel Rehak, Yanxiao Han, et al. "Atomically precise organomimetic cluster nanomolecules assembled via perfluoroaryl-thiol SNAr chemistry." Nature Chemistry 9, no. 4 (December 19, 2016): 333–40. http://dx.doi.org/10.1038/nchem.2686.

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41

Goulioukina, Nataliya S., Alexander Y. Mitrofanov та Irina P. Beletskaya. "Convenient synthesis of α-perfluoroaryl and α-perfluorohetaryl substituted α-aminomethanephosphonates". Journal of Fluorine Chemistry 136 (квітень 2012): 26–31. http://dx.doi.org/10.1016/j.jfluchem.2012.01.004.

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42

Reissig, Hans-Ulrich, та Daniel Gladow. "Alkylation and Ring Opening of Perfluoroalkyl- and Perfluoroaryl-Substituted 2-Siloxycyclopropanecarboxylates Yielding Fluorinated γ-Oxo Esters or β,γ-Unsaturated Ketones". Synthesis 45, № 15 (17 червня 2013): 2179–87. http://dx.doi.org/10.1055/s-0033-1338892.

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43

Chase, Preston A., Lee D. Henderson, Warren E. Piers, Masood Parvez, William Clegg, and Mark R. J. Elsegood. "Bifunctional Perfluoroaryl Boranes: Synthesis and Coordination Chemistry with Neutral Lewis Base Donors." Organometallics 25, no. 2 (January 2006): 349–57. http://dx.doi.org/10.1021/om050764t.

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44

Gladow, Daniel, та Hans-Ulrich Reissig. "ChemInform Abstract: Alkylation and Ring Opening of Perfluoroalkyl- and Perfluoroaryl-Substituted 2-Siloxycyclopropanecarboxylates Yielding Fluorinated γ-Oxo Esters or β,γ-Unsaturated Ketones." ChemInform 44, № 51 (2 грудня 2013): no. http://dx.doi.org/10.1002/chin.201351049.

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45

Drover, Marcus W., Laurel L. Schafer та Jennifer A. Love. "Isocyanate deinsertion from κ1-O amidates: facile access to perfluoroaryl rhodium(i) complexes". Dalton Transactions 44, № 45 (2015): 19487–93. http://dx.doi.org/10.1039/c5dt01981h.

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46

Forsyth, Craig M., and Glen B. Deacon. "The First Crystallographically Characterized (Perfluoroaryl)lanthanoid(II) Complex, Eu(C6F5)2(OC4H8)5." Organometallics 19, no. 7 (April 2000): 1205–7. http://dx.doi.org/10.1021/om9909183.

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47

Kultyshev, Roman G., G. K. Surya Prakash, George A. Olah, Jack W. Faller, and Jonathan Parr. "Convenient Syntheses of Aryl and Perfluoroaryl Trichlorogermanes and Germatranes via an Organotin Route." Organometallics 23, no. 13 (June 2004): 3184–88. http://dx.doi.org/10.1021/om0400189.

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48

Buscemi, Silvestre, Andrea Pace, Rosa Calabrese, Nicolò Vivona, and Pierangelo Metrangolo. "Fluorinated heterocyclic compounds. A photochemical synthesis of 3-amino-5-perfluoroaryl-1,2,4-oxadiazoles." Tetrahedron 57, no. 27 (July 2001): 5865–71. http://dx.doi.org/10.1016/s0040-4020(01)00524-5.

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49

Bojan, R. Vilma, Rafal Czerwieniec, Antonio Laguna, Tania Lasanta, José M. López-de-Luzuriaga, Miguel Monge, M. Elena Olmos, and Harmut Yersin. "Luminescent gold–silver complexes derived from neutral bis(perfluoroaryl)diphosphine gold(i) precursors." Dalton Transactions 42, no. 12 (2013): 4267. http://dx.doi.org/10.1039/c2dt32973e.

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50

Verhoork, Sanne J. M., Claire E. Jennings, Neshat Rozatian, Judith Reeks, Jieman Meng, Emily K. Corlett, Fazila Bunglawala, Martin E. M. Noble, Andrew G. Leach, and Christopher R. Coxon. "Tuning the Binding Affinity and Selectivity of Perfluoroaryl‐Stapled Peptides by Cysteine‐Editing." Chemistry – A European Journal 25, no. 1 (November 27, 2018): 177–82. http://dx.doi.org/10.1002/chem.201804163.

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