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Journal articles on the topic '2-trifluoroethyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Fu, Xian-Shu, Xiao-Ping Yu, Wei-Min Wang, and Fang Lin. "2-(2,2,2-Trifluoroethyl)isoindoline-1,3-dione." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1745. http://dx.doi.org/10.1107/s1600536810020222.

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2

Liška, František, Jiří Fikar, and Petr Kuzmič. "Radical Reduction of C-Cl Bonds in Chlorofluoro Ethers." Collection of Czechoslovak Chemical Communications 58, no. 3 (1993): 565–74. http://dx.doi.org/10.1135/cccc19930565.

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Reduction of C-Cl bonds in 2,2-dichloro-1,1,2-trifluoroethyl trichloromethyl ether (I), 2-chloro-1,1,2-trifluoroethyl trichloromethyl ether (II), and 2,2-dichloro-1,1,2-trifluoroethyl dichloromethyl ether (III) with 2-propanol, 2-butanol, cyclohexanol, tetrahydrofurane, diethyl ether, and 1,3-dioxolane initiated photochemically and by radiation has been investigated. Beside the main reduction products - 2-chloro-1,1,2-difluoroethyl trichloromethyl ether (IV) and 2-chloro-1,1,2-difluoroethyl chloromethyl ether (V) - it was also possible to prove the formation of 1,2-dichloro-1,2-bis(2-chloro-1,

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3

Fu, Weijun, Mei Zhu, Chen Xu, Guanglong Zou, Zhiqiang Wang, and Baoming Ji. "Visible-light-mediated trifluoroethylation of 2-isocyanobiaryl with trifluoroethyl iodide: Synthesis of 6-trifluoroethyl-phenanthridines." Journal of Fluorine Chemistry 168 (December 2014): 50–54. http://dx.doi.org/10.1016/j.jfluchem.2014.08.022.

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4

Li, Man, Fu-Sheng He, Long-Shan Ji, et al. "Synthesis and biological evaluation of fluorinated 3,4-dihydroquinolin-2(1H)-ones and 2-oxindoles for anti-hepatic fibrosis." RSC Advances 11, no. 11 (2021): 5923–27. http://dx.doi.org/10.1039/d0ra09430g.

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5

Langler, Richard Francis, and Nancy Ann Morrison. "Chemoselective reaction of a sulfonate ester with methoxide ions in preference to benzyl mercaptide anions." Canadian Journal of Chemistry 65, no. 10 (1987): 2385–89. http://dx.doi.org/10.1139/v87-398.

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Trifluoroethyl benzyl sulfide was prepared (in 2-propanol) and subsequently chlorinated as a further test of substituent electronegativity based regiochemical predictions. The initial attempt to prepare that sulfide by reaction of 2,2,2-trifluoroethyl methanesulfonate and benzyl mercaptide anions (in methanol) furnished benzyl methyl sulfide. Mechanistic possibilities are discussed in detail and some synthetic consequences of this novel reaction are presented.

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6

Fu, Xian-Shu, Xiao-Ping Yu, Wei-Min Wang, and Fang Lin. "4,5,6,7-Tetrachloro-2-(2,2,2-trifluoroethyl)isoindoline-1,3-dione." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1743. http://dx.doi.org/10.1107/s1600536810023019.

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7

Zhu, Wen-Run, Zhen-Wei Zhang, Wei-Hua Huang, et al. "Asymmetric Synthesis of Vicinally Bis(trifluoromethyl)-Substituted 3,3′-Pyrrolidinyl Spirooxindoles via Organocatalytic 1,3-Dipolar Cycloaddition Reactions." Synthesis 51, no. 09 (2019): 1969–79. http://dx.doi.org/10.1055/s-0037-1612089.

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Under bifunctional squaramide and thiourea organocatalysis, a series of vicinally bis(trifluoromethyl)-substituted 3,3′-pyrrolidinyl spirooxindoles were successfully synthesized via 1,3-dipolar cycloaddition reactions of 3-(trifluoroethylidene)oxindoles with diethyl 2-((2,2,2-trifluoroethyl)imino)malonate and N-(2,2,2-trifluoroethyl)isatin ketimines. The highlight of this protocol is the efficient construction of the vicinally bis(trifluoromethyl)-substituted pyrrolidine unit of spirooxindoles, including multiple contiguous stereogenic centres, in excellent yields and stereoselectivities.

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8

Wu, Wei, Beibei Luo, Yi You, and Zhiqiang Weng. "Copper-catalyzed one-pot synthesis of 2-(2,2,2-trifluoroethyl)-substituted benzofused heterocycles." Organic Chemistry Frontiers 8, no. 9 (2021): 1997–2001. http://dx.doi.org/10.1039/d1qo00157d.

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A method for copper-catalyzed synthesis of 2-trifluoroethyl-substituted benzofurans and indoles from the reaction of salicylaldehyde/2-aminobenzaldehyde p-tosylhydrazones with 2-bromo-3,3,3-trifluoropropene has been developed.

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9

Li, Zhengyu, Jingnan Dong, Junwen Wang, Ding-Yah Yang, and Zhiqiang Weng. "Elemental sulfur-promoted one-pot synthesis of 2-(2,2,2-trifluoroethyl)benzoxazoles and their derivatives." Chemical Communications 55, no. 87 (2019): 13132–35. http://dx.doi.org/10.1039/c9cc06822h.

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An elemental sulfur promoted one-pot synthesis of 2-(2,2,2-trifluoroethyl)benzoxazole derivatives from the reaction of o-aminophenols, thiols, and anilines with 2-bromo-3,3,3-trifluoropropene is reported.

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10

Fu, Weijun, Mei Zhu, Chen Xu, Guanglong Zou, Zhiqiang Wang, and Baoming Ji. "ChemInform Abstract: Visible-Light-Mediated Trifluoroethylation of 2-Isocyanobiaryl with Trifluoroethyl Iodide: Synthesis of 6-Trifluoroethyl-phenanthridines." ChemInform 46, no. 17 (2015): no. http://dx.doi.org/10.1002/chin.201517215.

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11

Pošta, A., I. Hemer, M. Bárta, and V. Dědek. "Some properties of alkyl 2-chloro-1,1,2-trifluoroethyl ethers." Journal of Fluorine Chemistry 45, no. 1 (1989): 128. http://dx.doi.org/10.1016/s0022-1139(00)84500-5.

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12

Perpétuo, G. J., J. Buschmann, P. Luger, D. Lentz, and D. Dreissig. "Low-temperature crystallization and structure determination of N-(trifluoromethyl)formamide, N-(2,2,2-trifluoroethyl)formamide and 2,2,2-trifluoroethyl isocyanide." Acta Crystallographica Section B Structural Science 55, no. 1 (1999): 70–77. http://dx.doi.org/10.1107/s0108768198006570.

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Crystals of N-(trifluoromethyl)formamide, C2H2F3NO, (I), N-(2,2,2-trifluoroethyl)formamide, C3H4F3NO, (II), and 2,2,2-trifluoroethyl isocyanide, C3H2F3N, (III), were grown in situ on an X-ray diffractometer and analysed by single-crystal X-ray diffraction methods at low temperatures. Crystal data: (I) orthorhombic, P212121, a = 4.547 (2) Å, b = 5.947 (3) Å, c = 14.731 (9) Å, V = 398.3 (4) Å3, Z = 4, M r = 113.05, T = 143 K, D x = 1.885 Mg m−3; (II) monoclinic, P21/n, a = 4.807 (1) Å, b = 16.707 (3) Å, c = 6.708 (1) Å, β = 109.90 (1)°, V = 506.6 (2) Å3, Z = 4, M r = 127.07, T = 141 K, D x = 1.6

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13

Dvořák, David, Eva Neugebauerová, František Liška, and Jiří Ludvík. "Electroreductive Additions of Aromatic Dichalcogenides to Fluorinated Ethenes." Collection of Czechoslovak Chemical Communications 63, no. 3 (1998): 378–86. http://dx.doi.org/10.1135/cccc19980378.

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Intermediates and products formed during the electrochemical reduction of diphenyl disulfide (1) add to chlorotrifluoroethene (3) under the formation of 2-chloro-1,1,2-trifluoroethyl phenyl sulfide (5) and the E/Z isomers of 2-chloro-1,2-difluoroethenyl phenyl sulfide (6). The analogous reaction with 1,2-dichlorodifluoroethene (4) led to a mixture of E/Z isomers of 6. Electrochemically reduced diphenyl diselenide (2) reacted with 3 giving rise to 2-chloro-1,1,2-trifluoroethyl phenyl selenide (7) whereas the reaction with 4 does not proceed. Addition of disulfide 1 to 4 gives evidence of the pa

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14

Schoth, Ralph-Matthias, Enno Lork, and Gerd-Volker Röschenthaler. "Syntheses and molecular structures of 2- [1′-N-(alkyl)imino-2′,2′,2′-trifluoroethyl] phenols." Journal of Fluorine Chemistry 78, no. 2 (1996): 187–91. http://dx.doi.org/10.1016/0022-1139(96)03441-0.

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15

Chen, Hao, Li Cai, Chaochao Yu, and Hongqi Li. "3-{1-[2-(2-Chlorophenyl)hydrazinylidene]-2,2,2-trifluoroethyl}-7-diethylamino-2H-chromen-2-one." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2344. http://dx.doi.org/10.1107/s1600536811031916.

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16

Dědek, Václav, and Ivan Hemer. "Photochemical chlorotrifluoroethylation of 1,2-, 1,3-, and 1,4-diols." Collection of Czechoslovak Chemical Communications 50, no. 12 (1985): 2743–52. http://dx.doi.org/10.1135/cccc19852743.

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The UV light-initiated reaction of chlorotrifluoroethylene with 1,2-ethanediol (I) proceeds only in the presence of acetone and affords 2-(2-chloro-1,1,2-trifluoroethyl)-2-methyl-1,3-dioxolane (VI). It has been proved that I is first photolyzed to acetaldehyde. Its acetalization in the reaction mixture gives 2-methyl-1,3-dioxolane (V) which then undergoes chlorotrifluoroethylation. The chlorotrifluoro derivative of 1,2-ethanediol XII was prepared by hydrolysis of 4-(2-chloro-1,1,2-trifluoroethyl)-2,2-dimethyl-1,3-dioxolane (XIII). 1,3-Propanediol (II) reacted to give 5-chloro-4,4,5-trifluoro-1

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17

Lei, Lei, Qi Zhang, Shuxian Shi, and Shiping Zhu. "Oxygen-switchable thermo-responsive random copolymers." Polymer Chemistry 7, no. 34 (2016): 5456–62. http://dx.doi.org/10.1039/c6py01145d.

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In this paper, we report the synthesis of oxygen (O<sub>2</sub>)-switchable thermo-responsive random copolymers based on fluorinated acrylamide monomer homologues: N-(2-fluoroethyl)acrylamide (F1EA), N-(2,2-difluoroethyl)acrylamide (F2EA), and N-(2,2,2-trifluoroethyl)acrylamide (F3EA).

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18

A.M. Nalibayeva, G.K. Bishimbayeva, S.A. Saidullayeva, S.I. Verhoturova, S.N. Arbuzova, and N.K. Gusarova. "BIS(2,2,2-TRIFLUOROETHYL)(2-CYANOETHYL) PHOSPHATE – A NEW URANIUM EXTRAGENT." SERIES CHEMISTRY AND TECHNOLOGY 1, no. 439 (2020): 109–15. http://dx.doi.org/10.32014/2020.2518-1491.14.

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19

Wang, Wei, Shi Xiong Wang, Yun Bo He, Xiang Jun Yang, and Hong Guo. "Tris (2, 2, 2-Trifluoroethyl) Phosphate (TFP) as Flame-Retarded Additives for Li-Ion Batteries." Advanced Materials Research 787 (September 2013): 40–45. http://dx.doi.org/10.4028/www.scientific.net/amr.787.40.

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With high energy density, long cycle life and high voltage Lithium-ion batteries are one of very promising pollution-free power supply. The electrolytes for these batteries consist of flammable organic solvents which are serious hazard under abusive conditions especially for large-scale lithium batteries. To reduce flammability of electrolyte of lithium-ion batteries and resolve safety problem, Tris (2, 2, 2-trifluoroethyl) phosphate (TFP) was synthesized and added into electrolytes as additive. It was found that the SET decreased significantly with the increase of the concentration of TFP. Wh

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20

Banerjee, Sanjib, Bhausaheb V. Tawade, and Bruno Améduri. "Functional fluorinated polymer materials and preliminary self-healing behavior." Polymer Chemistry 10, no. 16 (2019): 1993–97. http://dx.doi.org/10.1039/c9py00122k.

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Effective use of Diels–Alder chemistry led to the development of thermally amendable and self-healing polymeric materials based on a copolymer of cyclopenta-1,3-dien-1-ylmethyl 2-(trifluoromethyl)acrylate (MAF-Furan) and 2,2,2-trifluoroethyl α-fluoroacrylate (FATRIFE).

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21

SCHOTH, R. M., E. LORK, and G. V. ROESCHENTHALER. "ChemInform Abstract: Syntheses and Molecular Structures of 2-(1′-N-(Alkyl)imino-2′,2′,2′- trifluoroethyl)phenols." ChemInform 27, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.199649109.

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22

Luo, Y., R. J. Barton, B. E. Robertson, C. C. Lee, and D. Wanigasekera. "Structure of (Z)-1,2-diphenyl-2-p-tolylvinyl 2,2,2-trifluoroethyl ether." Acta Crystallographica Section C Crystal Structure Communications 42, no. 9 (1986): 1220–22. http://dx.doi.org/10.1107/s010827018609282x.

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23

Melnik, Yu, M. Vorona, G. Veinberg, J. Popelis, L. Ignatovich, and E. Lukevics. "Synthesis and Stereoisomerization of 2-(1-Alkoxyimino-2,2,2-trifluoroethyl)-5-trimethylsilylfurans." Chemistry of Heterocyclic Compounds 41, no. 6 (2005): 718–21. http://dx.doi.org/10.1007/s10593-005-0211-7.

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24

Ng, Raymond A., Jihua Guan, Vernon C. Alford, et al. "2-(2,2,2-Trifluoroethyl)-5,6-dichlorobenzimidazole derivatives as potent androgen receptor antagonists." Bioorganic & Medicinal Chemistry Letters 17, no. 4 (2007): 955–58. http://dx.doi.org/10.1016/j.bmcl.2006.11.047.

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25

Kamiya, Naohiro, Atsushi Kubota, Yumiko Iwase, Kouichi Sekiya, Masaru Ubasawa, and Satoshi Yuasa. "Antiviral Activities of MCC-478, a Novel and Specific Inhibitor of Hepatitis B Virus." Antimicrobial Agents and Chemotherapy 46, no. 9 (2002): 2872–77. http://dx.doi.org/10.1128/aac.46.9.2872-2877.2002.

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ABSTRACT MCC-478 is a newly synthesized 2-amino-6-arylthio-9-phosphonomethoxyethylpurine bis(2,2,2-trifluoroethyl) ester derivative. MCC-478 showed a substantially higher (ca. 80-fold) anti-hepatitis B virus (HBV) activity than that of lamivudine, despite no significant anti-human immunodeficiency virus activity. Since the bis(2,2,2-trifluoroethyl) ester group was used to improve the oral bioavailability of the phosphonomethoxyethylpurine derivatives, two monoester derivatives and one phosphonic acid derivative were also evaluated. It was suggested that these hydrolyzed derivatives, which appe

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26

Saktura, Maciej, Anna Skrzyńska, Sebastian Frankowski, Sylwia Wódka, and Łukasz Albrecht. "Asymmetric Dearomative (3+2)-Cycloaddition Involving Nitro-Substituted Benzoheteroarenes under H-Bonding Catalysis." Molecules 26, no. 16 (2021): 4992. http://dx.doi.org/10.3390/molecules26164992.

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In our studies, the organocatalytic 1,3-dipolar cycloaddition between 2-nitrobenzofurans or 2-nitrobenzothiophene and N-2,2,2-trifluoroethyl-substituted isatin imines has been developed. The reaction has been realized by employing bifunctional organocatalysis, with the use of squaramide derivative being crucial for the stereochemical efficiency of the process. The usefulness of the cycloadducts obtained has been confirmed in selected transformations, including aromative and non-aromative removal of the nitro group.

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27

Yang, Qizhi, Marc Guerre, Vincent Ladmiral та Bruno Ameduri. "Thermal and photo-RAFT polymerization of 2,2,2-trifluoroethyl α-fluoroacrylate". Polymer Chemistry 9, № 24 (2018): 3388–97. http://dx.doi.org/10.1039/c8py00571k.

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RAFT polymerization of 2,2,2-trifluoroethyl α-fluoroacrylate (FATRIFE) was studied under thermal conditions and light irradiation in the presence of four chain transfer agents. Polymers with narrow dispersities were obtained in the presence of trithiocarbonate CTA<sub>2</sub>, and this further led to fluorinated block copolymers.

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28

Kwong-Chip, Jean-Marc, and Thomas T. Tidwell. "Solvolytic reactivity of 1-(1-methyl-2-pyrrolyl)-2,2,2-trifluoroethyl p-nitrobenzoate." Tetrahedron Letters 30, no. 11 (1989): 1319–22. http://dx.doi.org/10.1016/s0040-4039(00)99454-1.

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29

Molnár, Katalin, László Takács, Mihály Kádár, Zsuzsanna Kardos, and Ferenc Faigl. "A Practical Route for the Preparation of Bis(2,2,2-trifluoroethyl) 2-Oxoalkylphosphonates." Synthesis 47, no. 08 (2015): 1085–90. http://dx.doi.org/10.1055/s-0034-1380162.

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30

Molnár, Katalin, Julien Behra, László Takács, Mihály Kádár, Zsuzsanna Kardos, and Ferenc Faigl. "A Convenient Procedure for the Synthesis of 2,2,2-Trifluoroethyl Methyl 2-Oxoalkylphosphonates." Phosphorus, Sulfur, and Silicon and the Related Elements 190, no. 5-6 (2015): 677–80. http://dx.doi.org/10.1080/10426507.2014.978326.

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31

Bárta, Milan, František Hampl, František Liška, and Václav Dědek. "Radical Additions of Tertiary Amines to Chlorotrifluoroethylene." Collection of Czechoslovak Chemical Communications 59, no. 8 (1994): 1820–32. http://dx.doi.org/10.1135/cccc19941820.

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Radical addition of ethyldimethylamine, cyclohexyldimethylamine, 1-methylpyrrolidine, 1-methylpiperidine, 1-methylperhydroazepine and 1-methylmorpholine to chlorotrifluoroethylene afforded 1 : 1 and 1 : 2 adducts containing 2-chloro-1,1,2-trifluoroethyl groups in the α- or α,α'-positions. Further reaction products were 1 : 2 telomers and secondary products arising by reduction of the chlorine atom in CHFCl groups by tertiary amines. The reaction course and mass and NMR spectra of the products are discussed.

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32

Lee, Choi Chuck, and Dave Wanigasekera. "Solvolytic rearrangement studies with (E)- and (Z)-2-anisyl-1,2-ditolyl[2-13C]vinyl bromides." Canadian Journal of Chemistry 65, no. 5 (1987): 933–40. http://dx.doi.org/10.1139/v87-158.

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Reaction of (E,Z)-or (E)-2-anisyl-1,2-ditolyl[2-13C]vinyl bromides ((E,Z)- or (E)-6-Br-2-13C) with HOAc–AgOAc gave a 1:1 mixture of (E)- and (Z)-2-anisyl-1,2-ditolyl[1,2-13C]vinyl acetates ((E,Z)-6-OAc-1,2-13C), with about 37.4% scrambling of the label from C-2 to C-1 arising from degenerate 1,2-anisyl shifts in the 2-anisyl-1,2-ditolyl[2-13C]vinyl cation (6-2-13C). No detectable amount of 1-anisyl-2,2-ditolylvinyl acetate was formed, indicating no nondegenerate 1,2-tolyl shift in cation 6 to give the more stable 1 -anisyl-2,2-ditolylvinyl cation (10) in the reaction with HOAc–AgOAc. Reaction

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33

Allen, Annette D., Jean-Marc Kwong-Chip, Wing Cheung Lin, Paul Nguyen, and Thomas T. Tidwell. "Formation and reactivity of 1-pyrrolyl-2,2,2-trifluoroethyl cations." Canadian Journal of Chemistry 68, no. 10 (1990): 1709–13. http://dx.doi.org/10.1139/v90-265.

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1-(1-Methyl-2-pyrrolyl)-2,2,2-trifluoroethyl p-nitrobenzoate (3) reacts by carbocation formation with an m value for the dependence of rate on the solvent polarity parameter YOTs of 0.56, and a rate 41 times slower than (1-methyl-2-pyrrolyl)methyl p-nitrobenzoate. The products from 3 include significant amounts of material derived from solvent attack at the 5-position of the pyrrole ring. The results indicate a high degree of charge delocalization by the strongly donating pyrrolyl group, resulting in a low k(H)/k(CF3) rate ratio and nucleophilic attack on the ring. 1,1, l-Trifluoro-2-(1-methyl

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34

Sano, Shigeki, Tomoya Matsumoto, Munehisa Toguchi, and Michiyasu Nakao. "Facile Two-Step Synthesis of Methyl Bis(2,2,2-trifluoroethyl)phosphonoacetate by Exploiting Garegg–Samuelsson Reaction Conditions." Synlett 29, no. 11 (2018): 1461–64. http://dx.doi.org/10.1055/s-0036-1591566.

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A facile two-step synthesis of methyl bis(2,2,2-trifluoroethyl)phosphonoacetate (Still–Gennari reagent) has been developed by exploiting Garegg–Samuelsson reaction conditions. Starting from trimethyl phosphonoacetate, Still–Gennari reagent was prepared in 94% yield via methyl 2-{bis[(trimethylsilyl)oxy]phosphoryl}acetate intermediate. This synthetic procedure was also used to prepare some kinds of Horner–Wadsworth–Emmons reagents and related compounds.

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35

Banki, Katalin, Adnan A. Elfarra, Lawrence H. Lash, and M. W. Anders. "Metabolism of S-(2-chloro-1,1,2-trifluoroethyl)-L-cysteine to hydrogen sulfide and the role of hydrogen sulfide in S-(2-chloro-1,1,2-trifluoroethyl)-L-cysteine-induced mitochondrial toxicity." Biochemical and Biophysical Research Communications 138, no. 2 (1986): 707–13. http://dx.doi.org/10.1016/s0006-291x(86)80554-x.

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36

Ambrose, D., and N. B. Ghiassee. "Vapour pressures, critical temperatures, and critical pressures of 2-chloro-1,1,2-trifluoroethyl difluoromethyl ether (enflurane) and of 1-chloro-2,2,2-trifluoroethyl difluoromethyl ether (isoflurane)." Journal of Chemical Thermodynamics 20, no. 6 (1988): 765–66. http://dx.doi.org/10.1016/0021-9614(88)90029-8.

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37

Moorcroft, Matthew J., César Prado, Richard G. Compton, Hanne B. McPeak, and Clive E. W. Hahn. "Electrochemical reduction of the anaesthetic gas enflurane (2-chloro-1,1,2-trifluoroethyl difluoromethyl ether)." Journal of Electroanalytical Chemistry 528, no. 1-2 (2002): 127–34. http://dx.doi.org/10.1016/s0022-0728(02)00903-8.

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38

Li, Weizuo, Jingya Li, Hongfeng Li, Pengfei Yan, Guangfeng Hou, and Guangming Li. "NIR luminescence of 2-(2,2,2-trifluoroethyl)-1-indone (TFI) neodymium and ytterbium complexes." Journal of Luminescence 146 (February 2014): 205–10. http://dx.doi.org/10.1016/j.jlumin.2013.09.009.

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39

Dong, Yanping, Weizuo Li, Xiaoyan Zou, Guangfeng Hou, and Guangming Li. "Electron-donating effect dominated 5,6-dimethoxy-2-(2,2,2-trifluoroethyl)-1-indone dysprosium SMM." Inorganica Chimica Acta 466 (September 2017): 599–603. http://dx.doi.org/10.1016/j.ica.2017.06.019.

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40

Hassen, Zied, Azaïez Ben Akacha, and Bechir Hajjem. "1-(2′,2′,2′-Trifluoroethyl)-4-phosphopyrazoles: Synthese et Etude Spectroscopique ir et RMN 1H, 13C, 19F, et 31P." Phosphorus, Sulfur, and Silicon and the Related Elements 178, no. 11 (2003): 2349–56. http://dx.doi.org/10.1080/714040948.

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41

Li, Jingya, Hongfeng Li, Pengfei Yan, Peng Chen, Guangfeng Hou, and Guangming Li. "Synthesis, Crystal Structure, and Luminescent Properties of 2-(2,2,2-Trifluoroethyl)-1-indone Lanthanide Complexes." Inorganic Chemistry 51, no. 9 (2012): 5050–57. http://dx.doi.org/10.1021/ic202473b.

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42

Kim, Won D., Garry E. Kiefer, Jurriaan Huskens, and A. Dean Sherry. "NMR Studies of the Lanthanide(III) Complexes of 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetrakis(methanephosphonic acid mono(2‘,2‘,2‘-trifluoroethyl) ester)." Inorganic Chemistry 36, no. 18 (1997): 4128–34. http://dx.doi.org/10.1021/ic970169m.

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Bouillon, J. P., C. Ates, Z. Janousek, H. G. Viehe, B. Tinant та J. P. Declercq. "New Trifluoromethylated Imidazolidines, Oxazolidines and Thiazolidines Starting from 3-(1,1-Dihydroxy-2,2,2-Trifluoroethyl)-1-Methyl-Tetrahy-Droazepin-2-one and α-(1,1-Dihydroxy-2,2,2-Trifluoroethyl)-γ-Butyrolactone". Bulletin des Sociétés Chimiques Belges 104, № 12 (2010): 707–16. http://dx.doi.org/10.1002/bscb.19951041207.

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BOUILLON, J. P., C. ATES, Z. JANOUSEK, H. G. VIEHE, B. TINANT та J. P. DECLERCQ. "ChemInform Abstract: New Trifluoromethylated Imidazolidines, Oxazolidines and Thiazolidines Starting from 3-(1,1-Dihydroxy-2,2,2-trifluoroethyl)-1-methyl- tetrahydroazepin-2-one and α-(1,1-Dihydroxy-2,2,2-trifluoroethyl) -γ-butyrolactone." ChemInform 27, № 17 (2010): no. http://dx.doi.org/10.1002/chin.199617049.

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Ichikawa, Junji, Satoshi Yonemaru, and Toru Minami. "A Novel Synthesis of 2,2-Difluorovinyl- and 2-Fluorovinylphosphorus Compounds from 2,2,2-Trifluoroethyl p-Toluenesulfonate." Synlett 1992, no. 10 (2002): 833–34. http://dx.doi.org/10.1055/s-1992-21509.

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Balsells, Jaume, Marjorie Waters, Karl Hansen, Gerard Kieczykowski, and Zhiguo Song. "A Short and Efficient Synthesis of 3-[2,2,2-Trifluoroethyl]hexahydro-2H-1,4-diazepin-2-one." Synthesis 2007, no. 18 (2007): 2779–81. http://dx.doi.org/10.1055/s-2007-983876.

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Ng, Raymond A., James C. Lanter, Vernon C. Alford, et al. "Synthesis of potent and tissue-selective androgen receptor modulators (SARMs): 2-(2,2,2)-Trifluoroethyl-benzimidazole scaffold." Bioorganic & Medicinal Chemistry Letters 17, no. 6 (2007): 1784–87. http://dx.doi.org/10.1016/j.bmcl.2006.12.045.

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Sekiya, Kouichi, Hideaki Takashima, Naoko Ueda, et al. "2-Amino-6-arylthio-9-[2-(phosphonomethoxy)ethyl]purine Bis(2,2,2-trifluoroethyl) Esters as Novel HBV-Specific Antiviral Reagents." Journal of Medicinal Chemistry 45, no. 14 (2002): 3138–42. http://dx.doi.org/10.1021/jm020036x.

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Harris, James W., Michael E. Fitzsimmons, and M. W. Anders. "Synthesis of [2-3H-ethyl]S-(2-chloro-1,1,2-trifluoroethyl)-l-cysteine and its use in covalent-binding studies." Analytical Biochemistry 204, no. 2 (1992): 300–304. http://dx.doi.org/10.1016/0003-2697(92)90242-y.

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Sehgal, Raj K., and Joseph G. Turcotte. "The Reaction of 2′-Deoxynucleosides with N-(2-Chloro-1,1,2-trifluoroethyl)diethylamine: Mechanisms of O2,3′-Anhydro-2′-deoxynucleoside and By-product Formation." Journal of Chemical Research, no. 1 (1998): 24–25. http://dx.doi.org/10.1039/a705686i.

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