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Volumn 14, Issue 7, 2014, Pages 941-951

Trifluoromethyl ethers and -thioethers as tools for medicinal chemistry and drug discovery

Author keywords

Catalysis; Drug discovery; Ethers; Fluorine; Thioethers; Trifluoromethoxylation; Trifluoromethylthiolation

Indexed keywords

ALCOHOL; ALLYLSILANE; ANION; ANISOLE; ANISOLE DERIVATIVE; BORONIC ACID DERIVATIVE; BROMIDE; CARBON; DIMETHYL SULFIDE; DIPHENYLIODONIUM SALT; DISULFIDE; ETHER DERIVATIVE; FLUORINE; FORMIC ACID DERIVATIVE; INDOLE DERIVATIVE; IODINE DERIVATIVE; METHOXYPYRIDINE; NUCLEOPHILE; PALLADIUM; PYRIDINE DERIVATIVE; RADICAL; SILANE DERIVATIVE; SULFIDE; SULFUR; THIOCYANATE; THIOL DERIVATIVE; TRIFLUOROMETHOXYBENZENE; TRIFLUOROMETHYL ETHER; UNCLASSIFIED DRUG; UNINDEXED DRUG; XANTHIC ACID DERIVATIVE;

EID: 84897453921     PISSN: 15680266     EISSN: 18734294     Source Type: Journal    
DOI: 10.2174/1568026614666140202210016     Document Type: Review
Times cited : (285)

References (118)
  • 1
    • 0000362773 scopus 로고    scopus 로고
    • Fluorine-containing natural products
    • David, B.; Harper, D. Fluorine-containing natural products. J. Fluorine Chem., 1999, 100, 127-133.
    • (1999) J. Fluorine Chem , vol.100 , pp. 127-133
    • David, B.1    Harper, D.2
  • 3
    • 33746614663 scopus 로고    scopus 로고
    • Selective fluorination in drug design and development: An overview of biochemical rationales
    • Kirk, K. L. Selective fluorination in drug design and development: an overview of biochemical rationales. Curr. Top. Med. Chem., 2006, 6, 1447-1456.
    • (2006) Curr. Top. Med. Chem , vol.6 , pp. 1447-1456
    • Kirk, K.L.1
  • 4
    • 34848848499 scopus 로고    scopus 로고
    • Fluorine in pharmaceuticals: Looking beyond intuition
    • Muller, K.; Faeh, C.; Diederich, F. Fluorine in pharmaceuticals: looking beyond intuition. Science, 2007, 317, 1881-1886.
    • (2007) Science , vol.317 , pp. 1881-1886
    • Muller, K.1    Faeh, C.2    Diederich, F.3
  • 5
    • 49449097238 scopus 로고    scopus 로고
    • The many roles for fluorine in medicinal chemistry
    • Hagmann, W. K. The many roles for fluorine in medicinal chemistry. J. Med. Chem., 2008, 51, 4359-4369.
    • (2008) J. Med. Chem , vol.51 , pp. 4359-4369
    • Hagmann, W.K.1
  • 6
    • 38149016915 scopus 로고    scopus 로고
    • Understanding organofluorine chemistry. An introduction to the C-F bond
    • O'Hagan, D. Understanding organofluorine chemistry. An introduction to the C-F bond. Chem. Soc. Rev., 2008, 37, 308-319.
    • (2008) Chem. Soc. Rev , vol.37 , pp. 308-319
    • O'Hagan, D.1
  • 8
    • 33746356860 scopus 로고    scopus 로고
    • Recent advances (1995-2005) in fluorinated pharmaceuticals based on natural products
    • Bégué, J.-P.; Bonnet-Delpon, D. Recent advances (1995-2005) in fluorinated pharmaceuticals based on natural products. J. Fluorine Chem., 2006, 127, 992-1012.
    • (2006) J. Fluorine Chem , vol.127 , pp. 992-1012
    • Bégué, J.-P.1    Bonnet-Delpon, D.2
  • 9
    • 0036882589 scopus 로고    scopus 로고
    • Important fluorinated drugs in experimental and clinical use
    • Ismail, F. M. D. Important fluorinated drugs in experimental and clinical use. J. Fluorine Chem., 2002, 118, 27-33.
    • (2002) J. Fluorine Chem , vol.118 , pp. 27-33
    • Ismail, F.M.D.1
  • 10
    • 33645454126 scopus 로고    scopus 로고
    • Fluorine in medicinal chemistry: A review of anti-cancer agents
    • Isanbor, C.; O'Hagan, D. Fluorine in medicinal chemistry: A review of anti-cancer agents. J. Fluorine Chem., 2006, 127, 303-319.
    • (2006) J. Fluorine Chem , vol.127 , pp. 303-319
    • Isanbor, C.1    O'Hagan, D.2
  • 11
    • 35048818924 scopus 로고    scopus 로고
    • β-Fluorinated ethers as "exotic" entity in medicinal chemistry
    • Jeschke, P.; Baston, E.; Leroux, F. R. β-Fluorinated ethers as "exotic" entity in medicinal chemistry. Mini-Rev. Med. Chem., 2007, 7, 1027-1034.
    • (2007) Mini-Rev. Med. Chem , vol.7 , pp. 1027-1034
    • Jeschke, P.1    Baston, E.2    Leroux, F.R.3
  • 17
    • 4544369746 scopus 로고    scopus 로고
    • The unique role of fluorine in the design of active ingredients for modern crop protection
    • Jeschke, P. The unique role of fluorine in the design of active ingredients for modern crop protection. ChemBioChem., 2004, 5, 570-589.
    • (2004) ChemBioChem , vol.5 , pp. 570-589
    • Jeschke, P.1
  • 18
    • 15044342538 scopus 로고    scopus 로고
    • Synthesis and structural characterization of highly fluorinated sulfimides and sulfoximides as functional building blocks for materials science
    • Kirsch, P.; Lenges, M.; Kühne, D.; Wanczek, K. P. Synthesis and structural characterization of highly fluorinated sulfimides and sulfoximides as functional building blocks for materials science. Eur. J. Org. Chem., 2005, 797-802.
    • (2005) Eur. J. Org. Chem , pp. 797-802
    • Kirsch, P.1    Lenges, M.2    Kühne, D.3    Wanczek, K.P.4
  • 19
    • 22544452743 scopus 로고    scopus 로고
    • Liquid crystals based on hypervalent sulfur fluorides: Exploring the steric effects of ortho-fluorine substituents
    • Kirsch, P.; Hahn, A. Liquid crystals based on hypervalent sulfur fluorides: Exploring the steric effects of ortho-fluorine substituents. Eur. J. Org. Chem., 2005, 2005(14), 3095-3100.
    • (2005) Eur. J. Org. Chem , vol.2005 , Issue.14 , pp. 3095-3100
    • Kirsch, P.1    Hahn, A.2
  • 21
    • 0032181872 scopus 로고    scopus 로고
    • Surface-fluorinated coatings
    • Anton, D. Surface-fluorinated coatings. Adv. Mater., 1998, 10, 1197-1205.
    • (1998) Adv. Mater , vol.10 , pp. 1197-1205
    • Anton, D.1
  • 22
    • 84860351735 scopus 로고    scopus 로고
    • Molecular design of photovoltaic materials for polymer solar cells: Toward suitable electronic energy levels and broad absorption
    • Li, Y. Molecular design of photovoltaic materials for polymer solar cells: Toward suitable electronic energy levels and broad absorption. Acc. Chem. Res., 2012, 45, 723-733.
    • (2012) Acc. Chem. Res , vol.45 , pp. 723-733
    • Li, Y.1
  • 25
    • 79959421993 scopus 로고    scopus 로고
    • Organic fluorine compounds: A great opportunity for enhanced materials properties
    • Berger, R.; Resnati, G.; Metrangolo, P.; Weber, E.; Hulliger, J. Organic fluorine compounds: a great opportunity for enhanced materials properties. Chem. Soc. Rev., 2011, 40, 3496-3508.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 3496-3508
    • Berger, R.1    Resnati, G.2    Metrangolo, P.3    Weber, E.4    Hulliger, J.5
  • 26
    • 33847298575 scopus 로고    scopus 로고
    • Fluorinated organic materials for electronic and optoelectronic applications: The role of the fluorine atom
    • DOI: 10. 1039/B611336B
    • Babudri, F.; Farinola, G. M.; Naso, F.; Ragni, R. Fluorinated organic materials for electronic and optoelectronic applications: the role of the fluorine atom. Chem. Commun., 2007, 1003-1022. DOI: 10. 1039/B611336B.
    • (2007) Chem. Commun , pp. 1003-1022
    • Babudri, F.1    Farinola, G.M.2    Naso, F.3    Ragni, R.4
  • 30
    • 84861880589 scopus 로고    scopus 로고
    • Radiosynthesis and preclinical evaluation of 18F-F13714 as a fluorinated 5-HT1A receptor agonist radioligand for PET neuroimaging
    • Lemoine, L.; Becker, G.; Vacher, B.; Billard, T.; Lancelot, S.; Newman-Tancredi, A.; Zimmer, L. Radiosynthesis and preclinical evaluation of 18F-F13714 as a fluorinated 5-HT1A receptor agonist radioligand for PET neuroimaging. J. Nucl. Med., 2012, 53, 969-976.
    • (2012) J. Nucl. Med , vol.53 , pp. 969-976
    • Lemoine, L.1    Becker, G.2    Vacher, B.3    Billard, T.4    Lancelot, S.5    Newman-Tancredi, A.6    Zimmer, L.7
  • 31
    • 80455132099 scopus 로고    scopus 로고
    • Comparison of 4 radiolabeled antagonists for serotonin 5-HT7 receptor neuroimaging: Toward the first PET radiotracer
    • Lemoine, L.; Andries, J.; Le Bars, D.; Billard, T.; Zimmer, L. Comparison of 4 radiolabeled antagonists for serotonin 5-HT7 receptor neuroimaging: Toward the first PET radiotracer. J. Nucl. Med., 2011, 52, 1811-1818.
    • (2011) J. Nucl. Med , vol.52 , pp. 1811-1818
    • Lemoine, L.1    Andries, J.2    Le Bars, D.3    Billard, T.4    Zimmer, L.5
  • 32
    • 79958253126 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of potential 5-HT7 receptor PET radiotracers
    • Andries, J.; Lemoine, L.; Le Bars, D.; Zimmer, L.; Billard, T. Synthesis and biological evaluation of potential 5-HT7 receptor PET radiotracers. Eur. J. Med. Chem., 2011, 46, 3455-3461.
    • (2011) Eur. J. Med. Chem , vol.46 , pp. 3455-3461
    • Andries, J.1    Lemoine, L.2    Le Bars, D.3    Zimmer, L.4    Billard, T.5
  • 36
    • 49849087072 scopus 로고    scopus 로고
    • Chemistry with [18F]fluoride ion
    • Cai, L.; Lu, S.; Pike, V. W. Chemistry with [18F]fluoride ion. Eur. J. Org. Chem., 2008, 2853-2873.
    • (2008) Eur. J. Org. Chem , pp. 2853-2873
    • Cai, L.1    Lu, S.2    Pike, V.W.3
  • 37
    • 56249122581 scopus 로고    scopus 로고
    • Synthesis of 11C, 18F, 15O, and 13N radiolabels for positron emission tomography
    • Miller, P. W.; Long, N. J.; Vilar, R.; Gee, A. D. Synthesis of 11C, 18F, 15O, and 13N radiolabels for positron emission tomography. Angew. Chem. Int. Ed., 2008, 47, 8998-9033.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 8998-9033
    • Miller, P.W.1    Long, N.J.2    Vilar, R.3    Gee, A.D.4
  • 38
    • 84856194256 scopus 로고    scopus 로고
    • Novel strategies for fluorine-18 radiochemistry
    • Littich, R.; Scott, P. J. H. Novel strategies for fluorine-18 radiochemistry. Angew. Chem. Int. Ed., 2012, 51, 1106-1109.
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 1106-1109
    • Littich, R.1    Scott, P.J.H.2
  • 39
    • 74449085744 scopus 로고    scopus 로고
    • New trends in the chemistry of β-Fluorinated ethers, thioethers, amines and phosphines
    • Manteau, B.; Pazenok, S.; Vors, J.-P.; Leroux, F. R. New trends in the chemistry of β-Fluorinated ethers, thioethers, amines and phosphines. J. Fluorine Chem., 2010, 131, 140-158.
    • (2010) J. Fluorine Chem , vol.131 , pp. 140-158
    • Manteau, B.1    Pazenok, S.2    Vors, J.-P.3    Leroux, F.R.4
  • 40
    • 78349255023 scopus 로고    scopus 로고
    • A general approach to (trifluoromethoxy)pyridines: First X-ray structure determinations and quantum chemistry studies
    • Manteau, B.; Genix, P.; Brelot, L.; Vors, J.-P.; Pazenok, S.; Giornal, F.; Leuenberger, C.; Leroux, F. R. A general approach to (trifluoromethoxy)pyridines: First X-ray structure determinations and quantum chemistry studies. Eur. J. Org. Chem., 2010, 2010(31), 6043-6066.
    • (2010) Eur. J. Org. Chem , vol.2010 , Issue.31 , pp. 6043-6066
    • Manteau, B.1    Genix, P.2    Brelot, L.3    Vors, J.-P.4    Pazenok, S.5    Giornal, F.6    Leuenberger, C.7    Leroux, F.R.8
  • 41
    • 70349957073 scopus 로고    scopus 로고
    • Trifluoromethyl ethers--synthesis and properties of an unusual substituent
    • Leroux, F. R.; Manteau, B.; Vors, J. P.; Pazenok, S. Trifluoromethyl ethers--synthesis and properties of an unusual substituent. Beilstein J. Org. Chem., 2008, 4, 13.
    • (2008) Beilstein J. Org. Chem , vol.4 , pp. 13
    • Leroux, F.R.1    Manteau, B.2    Vors, J.P.3    Pazenok, S.4
  • 42
    • 17244371011 scopus 로고    scopus 로고
    • β-Fluorinated ethers, thioethers, and amines: Anomerically biased species
    • Leroux, F.; Jeschke, P.; Schlosser, M. β-Fluorinated ethers, thioethers, and amines: Anomerically biased species. Chem. Rev., 2005, 105, 827-856.
    • (2005) Chem. Rev , vol.105 , pp. 827-856
    • Leroux, F.1    Jeschke, P.2    Schlosser, M.3
  • 43
    • 78349257458 scopus 로고    scopus 로고
    • A new and direct trifluoromethoxylation of aliphatic substrates with 2, 4-dinitro(trifluoromethoxy)benzene
    • Marrec, O.; Billard, T.; Vors, J.-P.; Pazenok, S.; Langlois, B. R. A new and direct trifluoromethoxylation of aliphatic substrates with 2, 4-dinitro(trifluoromethoxy)benzene. Adv. Synth. Catal., 2010, 352, 2831-2837.
    • (2010) Adv. Synth. Catal , vol.352 , pp. 2831-2837
    • Marrec, O.1    Billard, T.2    Vors, J.-P.3    Pazenok, S.4    Langlois, B.R.5
  • 44
    • 74449087837 scopus 로고    scopus 로고
    • A deeper insight into direct trifluoromethoxylation with trifluoromethyl triflate
    • Marrec, O.; Billard, T.; Vors, J.-P.; Pazenok, S.; Langlois, B. R. A deeper insight into direct trifluoromethoxylation with trifluoromethyl triflate. J. Fluorine Chem., 2010, 131, 200-207.
    • (2010) J. Fluorine Chem , vol.131 , pp. 200-207
    • Marrec, O.1    Billard, T.2    Vors, J.-P.3    Pazenok, S.4    Langlois, B.R.5
  • 45
    • 84879363887 scopus 로고    scopus 로고
    • Formation of C-SCF3 bonds through direct trifluoromethylthiolation
    • Tlili, A.; Billard, T. Formation of C-SCF3 bonds through direct trifluoromethylthiolation. Angew. Chem. Int. Ed., 2013, 52, 6818-6819.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 6818-6819
    • Tlili, A.1    Billard, T.2
  • 47
    • 0016721416 scopus 로고
    • Calculation of hydrophobic constant (log P) from and f constants
    • Leo, A.; Jow, P. Y. C.; Silipo, C.; Hansch, C. Calculation of hydrophobic constant (log P) from and f constants. J. Med. Chem., 1975, 18, 865-868.
    • (1975) J. Med. Chem , vol.18 , pp. 865-868
    • Leo, A.1    Jow, P.Y.C.2    Silipo, C.3    Hansch, C.4
  • 48
    • 0015816824 scopus 로고
    • "Aromatic" substituent constants for structure-activity correlations
    • Hansch, C.; Leo, A.; Unger, S. H.; Kim, K. H.; Nikaitani, D.; Lien, E. J. "Aromatic" substituent constants for structure-activity correlations. J. Med. Chem., 1973, 16, 1207-1216.
    • (1973) J. Med. Chem , vol.16 , pp. 1207-1216
    • Hansch, C.1    Leo, A.2    Unger, S.H.3    Kim, K.H.4    Nikaitani, D.5    Lien, E.J.6
  • 49
    • 4544387720 scopus 로고    scopus 로고
    • Atropisomerism, biphenyls, and fluorine: A comparison of rotational barriers and twist angles
    • Leroux, F. Atropisomerism, biphenyls, and fluorine: a comparison of rotational barriers and twist angles. ChemBioChem., 2004, 5, 644-649.
    • (2004) ChemBioChem , vol.5 , pp. 644-649
    • Leroux, F.1
  • 50
    • 0037427752 scopus 로고    scopus 로고
    • On the structure and torsional potential of trifluoromethoxybenzene: An ab initio and density functional study
    • Klocker, J.; Karpfen, A.; Wolschann, P. On the structure and torsional potential of trifluoromethoxybenzene: an ab initio and density functional study. Chem. Phys. Lett., 2003, 367, 566-575.
    • (2003) Chem. Phys. Lett , vol.367 , pp. 566-575
    • Klocker, J.1    Karpfen, A.2    Wolschann, P.3
  • 51
    • 0001753487 scopus 로고
    • Halogen-containing substituents. II. Methoxy system. Reactivity parameters. Charge distribution and conformation of the anisoles
    • Serfaty, I. W.; Hodgins, T.; McBee, E. T. Halogen-containing substituents. II. Methoxy system. Reactivity parameters. Charge distribution and conformation of the anisoles. J. Org. Chem., 1972, 37, 2651-2655.
    • (1972) J. Org. Chem , vol.37 , pp. 2651-2655
    • Serfaty, I.W.1    Hodgins, T.2    McBee, E.T.3
  • 53
    • 17244381924 scopus 로고
    • 1, 4-Dihydropyridine derivatives as antagonists of calcium ions. Pharmacological properties and clinical application
    • Vitolina, R. 1, 4-Dihydropyridine derivatives as antagonists of calcium ions. Pharmacological properties and clinical application. Latv. PSR Zinat. Akad. Vestis., 1987, 75-86.
    • (1987) Latv. PSR Zinat. Akad. Vestis , pp. 75-86
    • Vitolina, R.1
  • 55
    • 0021030188 scopus 로고
    • Qualitative and quantitative effects of fenfluramine and tiflorex on food consumption in trained rats offered dietary choices
    • Curtis-Prior, P. B.; Prouteau, M. Qualitative and quantitative effects of fenfluramine and tiflorex on food consumption in trained rats offered dietary choices. Int. J. Obes., 1983, 7, 575-581.
    • (1983) Int. J. Obes , vol.7 , pp. 575-581
    • Curtis-Prior, P.B.1    Prouteau, M.2
  • 56
    • 0006273775 scopus 로고
    • Synthesis of derivatives of phenyl trifluoromethyl ether
    • Yagupolskii, L. M. Synthesis of derivatives of phenyl trifluoromethyl ether. Dokl. Akad. Nauk S. S. S. R., 1955, 105, 100-102.
    • (1955) Dokl. Akad. Nauk S.S.S. R , vol.105 , pp. 100-102
    • Yagupolskii, L.M.1
  • 57
    • 17244379919 scopus 로고
    • New method of introduction of the trihalomethyl group into organic compounds
    • Yarovenko, N. N.; Vasil'eva, A. S. New method of introduction of the trihalomethyl group into organic compounds. Zh. Obshch. Khim., 1958, 28, 2502-2504.
    • (1958) Zh. Obshch. Khim , vol.28 , pp. 2502-2504
    • Yarovenko, N.N.1    Vasil'eva, A.S.2
  • 58
    • 0006187964 scopus 로고
    • Synthesis of derivatives of phenyl trifluoromethyl ether
    • Yagupol'skii, L. M.; Troitskaya, V. I. Synthesis of derivatives of phenyl trifluoromethyl ether. Zh. Obshch. Khim., 1961, 31, 915-924.
    • (1961) Zh. Obshch. Khim , vol.31 , pp. 915-924
    • Yagupol'skii, L.M.1    Troitskaya, V.I.2
  • 59
    • 17244379088 scopus 로고
    • Selective side-chain chlorination of methoxybenzenes
    • Louw, R.; Franken, P. W. Selective side-chain chlorination of methoxybenzenes. Chem. Ind. 1977, 127-128.
    • (1977) Chem. Ind , pp. 127-128
    • Louw, R.1    Franken, P.W.2
  • 60
    • 0000572301 scopus 로고
    • Chemistry in hydrogen fluoride. 7. A novel synthesis of aryl trifluoromethyl ethers
    • Feiring, A. E. Chemistry in hydrogen fluoride. 7. A novel synthesis of aryl trifluoromethyl ethers. J. Org. Chem., 1979, 44, 2907-2910.
    • (1979) J. Org. Chem , vol.44 , pp. 2907-2910
    • Feiring, A.E.1
  • 61
    • 17244373441 scopus 로고
    • Bis(trifluoromethoxy) and bis(trifluoromethylthio) derivatives of benzene
    • Yagupol'skii, L. M.; Orda, V. V. Bis(trifluoromethoxy) and bis(trifluoromethylthio) derivatives of benzene. Zh. Obshch. Khim., 1964, 34, 1979-1984.
    • (1964) Zh. Obshch. Khim , vol.34 , pp. 1979-1984
    • Yagupol'skii, L.M.1    Orda, V.V.2
  • 62
    • 11444265275 scopus 로고    scopus 로고
    • Synthesis conditions and activity of various Lewis acids for the fluorination of trichloromethoxy-benzene by HF in liquid phase
    • Salomé, J.; Mauger, C.; Brunet, S.; Schanen, V. Synthesis conditions and activity of various Lewis acids for the fluorination of trichloromethoxy-benzene by HF in liquid phase. J. Fluorine Chem., 2004, 125, 1947-1950.
    • (2004) J. Fluorine Chem , vol.125 , pp. 1947-1950
    • Salomé, J.1    Mauger, C.2    Brunet, S.3    Schanen, V.4
  • 63
    • 0008454494 scopus 로고
    • Effect of substituents having a trifluoromethyl group on the reactivity of aromatic compounds
    • Yagupol'skii, L. M.; Bystrov, V. F.; Stepanyants, A. U.; Fialkov, Y. A. Effect of substituents having a trifluoromethyl group on the reactivity of aromatic compounds. Zh. Obshch. Khim., 1964, 34, 3682-3690.
    • (1964) Zh. Obshch. Khim , vol.34 , pp. 3682-3690
    • Yagupol'skii, L.M.1    Bystrov, V.F.2    Stepanyants, A.U.3    Fialkov, Y.A.4
  • 64
    • 0001401275 scopus 로고
    • Reaction de MoF6 avec chlorothioformiates d'aryle. Nouvelle synthese des aryl trifluoromethylethers ArOCF3
    • Mathey, F.; Bensoam, J. Reaction de MoF6 avec chlorothioformiates d'aryle. Nouvelle synthese des aryl trifluoromethylethers ArOCF3. Tetrahedron Lett., 1973, 14, 2253-2256.
    • (1973) Tetrahedron Lett , vol.14 , pp. 2253-2256
    • Mathey, F.1    Bensoam, J.2
  • 65
    • 0002086822 scopus 로고
    • β-Fluorinated ethers. I. Aryl fluoroalkyl ethers
    • Sheppard, W. A. β-Fluorinated ethers. I. Aryl fluoroalkyl ethers. J. Org. Chem., 1964, 29, 1-11.
    • (1964) J. Org. Chem , vol.29 , pp. 1-11
    • Sheppard, W.A.1
  • 66
    • 0001503910 scopus 로고    scopus 로고
    • Oxidative desulfurizationfluorination: A facile entry to a wide variety of organofluorine compounds leading to novel liquid-crystalline materials
    • Kuroboshi, M.; Kanie, K.; Hiyama, T. Oxidative desulfurizationfluorination: a facile entry to a wide variety of organofluorine compounds leading to novel liquid-crystalline materials. Adv. Synth. Catal., 2001, 343, 235-250.
    • (2001) Adv. Synth. Catal , vol.343 , pp. 235-250
    • Kuroboshi, M.1    Kanie, K.2    Hiyama, T.3
  • 67
    • 0034100116 scopus 로고    scopus 로고
    • A convenient synthesis of trifluoromethyl ethers by oxidative desulfurization-fluorination of dithiocarbonates
    • Kanie, K.; Tanaka, Y.; Suzuki, K.; Kuroboshi, M.; Hiyama, T. A convenient synthesis of trifluoromethyl ethers by oxidative desulfurization-fluorination of dithiocarbonates. Bull. Chem. Soc. Jpn., 2000, 73, 471-484.
    • (2000) Bull. Chem. Soc. Jpn , vol.73 , pp. 471-484
    • Kanie, K.1    Tanaka, Y.2    Suzuki, K.3    Kuroboshi, M.4    Hiyama, T.5
  • 68
    • 0026719708 scopus 로고
    • Oxidative desulfurizationfluorination of xanthates. A convenient synthesis of trifluoromethyl ethers and difluoro(methylthio)methyl ethers
    • Kuroboshi, M.; Suzuki, K.; Hiyama, T. Oxidative desulfurizationfluorination of xanthates. A convenient synthesis of trifluoromethyl ethers and difluoro(methylthio)methyl ethers. Tetrahedron Lett., 1992, 33, 4173-4176.
    • (1992) Tetrahedron Lett , vol.33 , pp. 4173-4176
    • Kuroboshi, M.1    Suzuki, K.2    Hiyama, T.3
  • 69
    • 34548763017 scopus 로고    scopus 로고
    • CF3 oxonium salts, O-(trifluoromethyl)dibenzofuranium salts: In situ synthesis, properties, and application as a real CF3+ species reagent
    • Umemoto, T.; Adachi, K.; Ishihara, S. CF3 oxonium salts, O-(trifluoromethyl)dibenzofuranium salts: In situ synthesis, properties, and application as a real CF3+ species reagent. J. Org. Chem., 2007, 72, 6905-6917.
    • (2007) J. Org. Chem , vol.72 , pp. 6905-6917
    • Umemoto, T.1    Adachi, K.2    Ishihara, S.3
  • 70
    • 33644919105 scopus 로고    scopus 로고
    • Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation
    • Eisenberger, P.; Gischig, S.; Togni, A. Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation. Chem. Eur. J., 2006, 12, 2579-2586.
    • (2006) Chem. Eur. J , vol.12 , pp. 2579-2586
    • Eisenberger, P.1    Gischig, S.2    Togni, A.3
  • 71
    • 33846525992 scopus 로고    scopus 로고
    • Mild electrophilic trifluoromethylation of carbon-and sulfur-centered nucleophiles by a hypervalent iodine(III)-CF3 reagent
    • Kieltsch, I.; Eisenberger, P.; Togni, A. Mild electrophilic trifluoromethylation of carbon-and sulfur-centered nucleophiles by a hypervalent iodine(III)-CF3 reagent. Angew. Chem. Int. Ed., 2007, 46, 754-757.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 754-757
    • Kieltsch, I.1    Eisenberger, P.2    Togni, A.3
  • 72
    • 53049110667 scopus 로고    scopus 로고
    • Reactivity of a 10-I-3 hypervalent iodine trifluoromethylation reagent with phenols
    • Stanek, K.; Koller, R.; Togni, A. Reactivity of a 10-I-3 hypervalent iodine trifluoromethylation reagent with phenols. J. Org. Chem., 2008, 73, 7678-7685.
    • (2008) J. Org. Chem , vol.73 , pp. 7678-7685
    • Stanek, K.1    Koller, R.2    Togni, A.3
  • 73
    • 70349961605 scopus 로고    scopus 로고
    • Zinc-mediated formation of trifluoromethyl ethers from alcohols and hypervalent iodine trifluoromethylation reagents
    • Koller, R.; Stanek, K.; Stolz, D.; Aardoom, R.; Niedermann, K.; Togni, A. Zinc-mediated formation of trifluoromethyl ethers from alcohols and hypervalent iodine trifluoromethylation reagents. Angew. Chem. Int. Ed., 2009, 48, 4332-4336.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 4332-4336
    • Koller, R.1    Stanek, K.2    Stolz, D.3    Aardoom, R.4    Niedermann, K.5    Togni, A.6
  • 74
    • 0001462186 scopus 로고
    • Fully fluorinated alkoxides. Part I. Trifluoromethoxides of alkali metals
    • Redwood, M. E.; Willis, C. J. Fully fluorinated alkoxides. Part I. Trifluoromethoxides of alkali metals. Can. J. Chem. 1965, 43, 1893-1898.
    • (1965) Can. J. Chem , vol.43 , pp. 1893-1898
    • Redwood, M.E.1    Willis, C.J.2
  • 75
    • 0001417546 scopus 로고
    • Synthesis of polyfluoro aromatic ethers: A facile route using polyfluoroalkoxides generated from carbonyl and trimethysilyl compounds
    • Nishida, M.; Vij, A.; Kirchmeier, R. L.; Shreeve, J. M. Synthesis of polyfluoro aromatic ethers: A facile route using polyfluoroalkoxides generated from carbonyl and trimethysilyl compounds. Inorg. Chem., 1995, 34, 6085-6092.
    • (1995) Inorg. Chem , vol.34 , pp. 6085-6092
    • Nishida, M.1    Vij, A.2    Kirchmeier, R.L.3    Shreeve, J.M.4
  • 76
    • 33845377652 scopus 로고
    • Crystal and molecular structure of tris(dimethylamino) sulfonium trifluoromethoxide. Evidence for negative fluorine hyperconjugation
    • Farnham, W. B.; Smart, B. E.; Middleton, W. J.; Calabrese, J. C.; Dixon, D. A. Crystal and molecular structure of tris(dimethylamino) sulfonium trifluoromethoxide. Evidence for negative fluorine hyperconjugation. J. Am. Chem. Soc., 1985, 107, 4565-4567.
    • (1985) J. Am. Chem. Soc , vol.107 , pp. 4565-4567
    • Farnham, W.B.1    Smart, B.E.2    Middleton, W.J.3    Calabrese, J.C.4    Dixon, D.A.5
  • 77
    • 0011317329 scopus 로고
    • The preparation of O-trifluoromethyl carbohydrates
    • Trainor, G. L. The preparation of O-trifluoromethyl carbohydrates. J. Carbohydr. Chem., 1985, 4, 545-563.
    • (1985) J. Carbohydr. Chem , vol.4 , pp. 545-563
    • Trainor, G.L.1
  • 78
  • 79
    • 80052093561 scopus 로고    scopus 로고
    • Silvermediated trifluoromethoxylation of aryl stannanes and arylboronic acids
    • Huang, C.; Liang, T.; Harada, S.; Lee, E.; Ritter, T. Silvermediated trifluoromethoxylation of aryl stannanes and arylboronic acids. J. Am. Chem. Soc., 2011, 133, 13308-13310.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 13308-13310
    • Huang, C.1    Liang, T.2    Harada, S.3    Lee, E.4    Ritter, T.5
  • 80
    • 84870007533 scopus 로고    scopus 로고
    • Oxygen-bound trifluoromethoxide complexes of copper and gold
    • Zhang, C.-P.; Vicic, D. A. Oxygen-bound trifluoromethoxide complexes of copper and gold. Organometallics 2012, 31, 7812-7815.
    • (2012) Organometallics , vol.31 , pp. 7812-7815
    • Zhang, C.-P.1    Vicic, D.A.2
  • 82
    • 0001029493 scopus 로고    scopus 로고
    • Selective fluorinations by reagents containing the OF group
    • Rozen, S. Selective fluorinations by reagents containing the OF group. Chem. Rev., 1996, 96, 1717-1736.
    • (1996) Chem. Rev , vol.96 , pp. 1717-1736
    • Rozen, S.1
  • 83
    • 77958605423 scopus 로고    scopus 로고
    • Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation
    • Boiko, V. N. Aromatic and heterocyclic perfluoroalkyl sulfides. Methods of preparation. Beilstein J. Org. Chem., 2010, 6, 880-921.
    • (2010) Beilstein J. Org. Chem , vol.6 , pp. 880-921
    • Boiko, V.N.1
  • 84
    • 4243664295 scopus 로고
    • A survey of Hammett substituent constants and resonance and field parameters
    • Hansch, C.; Leo, A.; Taft, R. W. A survey of Hammett substituent constants and resonance and field parameters. Chem. Rev., 1991, 91, 165-195.
    • (1991) Chem. Rev , vol.91 , pp. 165-195
    • Hansch, C.1    Leo, A.2    Taft, R.W.3
  • 85
    • 0012262822 scopus 로고
    • Power-variable electrophilic trifluoromethylating agents. S-, Se-, and Te-(trifluoromethyl) dibenzothio-,-seleno-, and-tellurophenium salt system
    • Umemoto, T.; Ishihara, S. Power-variable electrophilic trifluoromethylating agents. S-, Se-, and Te-(trifluoromethyl) dibenzothio-,-seleno-, and-tellurophenium salt system. J. Am. Chem. Soc., 1993, 115, 2156-2164.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 2156-2164
    • Umemoto, T.1    Ishihara, S.2
  • 86
    • 57149087723 scopus 로고    scopus 로고
    • Electrophilic S-trifluoromethylation of cysteine side chains in β-and β-peptides: Isolation of trifluoromethylated Sandostatin® (octreotide) derivatives
    • Capone, S.; Kieltsch, I.; Flögel, O.; Lelais, G.; Togni, A.; Seebach, D. Electrophilic S-trifluoromethylation of cysteine side chains in β-and β-peptides: Isolation of trifluoromethylated Sandostatin® (octreotide) derivatives. Helv. Chim. Acta, 2008, 91, 2035-2056.
    • (2008) Helv. Chim. Acta , vol.91 , pp. 2035-2056
    • Capone, S.1    Kieltsch, I.2    Flögel, O.3    Lelais, G.4    Togni, A.5    Seebach, D.6
  • 87
    • 77956037773 scopus 로고    scopus 로고
    • A convenient and efficient synthesis of trifluoromethyl vinyl sulfoxide and its reactivity in addition reactions
    • Sokolenko, L. V.; Maletina, I. I.; Yagupolskii, L. M.; Yagupolskii, Y. L. A convenient and efficient synthesis of trifluoromethyl vinyl sulfoxide and its reactivity in addition reactions. Synlett., 2010, 14, 2075-2078.
    • (2010) Synlett , vol.14 , pp. 2075-2078
    • Sokolenko, L.V.1    Maletina, I.I.2    Yagupolskii, L.M.3    Yagupolskii, Y.L.4
  • 88
    • 80053567092 scopus 로고    scopus 로고
    • Convenient synthesis and isolation of trifluoromethylthiosubstituted building blocks
    • Harsányi, A.; Dorkó, É.; Csapó, Á.; Bakó, T.; Peltz, C.; Rábai, J. Convenient synthesis and isolation of trifluoromethylthiosubstituted building blocks. J. Fluorine Chem., 2011, 132, 1241-1246.
    • (2011) J. Fluorine Chem , vol.132 , pp. 1241-1246
    • Harsányi, A.1    Dorkó, E.2    Csapó, A.3    Bakó, T.4    Peltz, C.5    Rábai, J.6
  • 89
    • 84867043684 scopus 로고    scopus 로고
    • Electrophilic trifluoromethanesulfanylation of organometallic species with trifluoromethanesulfanamides
    • Baert, F.; Colomb, J.; Billard, T. Electrophilic trifluoromethanesulfanylation of organometallic species with trifluoromethanesulfanamides. Angew. Chem. Int. Ed., 2012, 51, 10382-10385.
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 10382-10385
    • Baert, F.1    Colomb, J.2    Billard, T.3
  • 90
    • 84885106676 scopus 로고    scopus 로고
    • Base-catalyzed electrophilic trifluoromethylthiolation of terminal alkynes
    • Alazet, S.; Zimmer, L.; Billard, T. Base-catalyzed electrophilic trifluoromethylthiolation of terminal alkynes. Angew. Chem. Int. Ed., 2013, 52, 10814-10817.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 10814-10817
    • Alazet, S.1    Zimmer, L.2    Billard, T.3
  • 91
    • 70350348244 scopus 로고    scopus 로고
    • Trifluoromethanesulfanylamides as easy-to-handle equivalents of the trifluoromethanesulfanyl cation (CF(3)S(+): Reaction with alkenes and alkynes
    • Ferry, A.; Billard, T.; Langlois, B. R.; Bacque, E. Trifluoromethanesulfanylamides as easy-to-handle equivalents of the trifluoromethanesulfanyl cation (CF(3)S(+): Reaction with alkenes and alkynes. Angew. Chem. Int. Ed., 2009, 48, 8551-8555.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 8551-8555
    • Ferry, A.1    Billard, T.2    Langlois, B.R.3    Bacque, E.4
  • 92
    • 84873967548 scopus 로고    scopus 로고
    • Electrophilic trifluoromethylthiolation of allylsilanes with trifluoromethanesulfanamide
    • Liu, J.; Chu, L.; Qing, F.-L. Electrophilic trifluoromethylthiolation of allylsilanes with trifluoromethanesulfanamide. Org. Lett., 2013, 15, 894-897.
    • (2013) Org. Lett , vol.15 , pp. 894-897
    • Liu, J.1    Chu, L.2    Qing, F.-L.3
  • 93
    • 84856117439 scopus 로고    scopus 로고
    • Electrophilic trifluoromethanesulfanylation of indole derivatives
    • Ferry, A.; Billard, T.; Bacqué, E.; Langlois, B. R. Electrophilic trifluoromethanesulfanylation of indole derivatives. J. Fluorine Chem., 2012, 134, 160-163.
    • (2012) J. Fluorine Chem , vol.134 , pp. 160-163
    • Ferry, A.1    Billard, T.2    Bacqué, E.3    Langlois, B.R.4
  • 94
    • 84866082962 scopus 로고    scopus 로고
    • Sequential electrophilic trifluoromethanesulfanylation-cyclization of tryptamine derivatives: Synthesis of C(3)-trifluoromethanesulfanylated hexahydropyrrolo[2, 3-b]indoles
    • Yang, Y.; Jiang, X.; Qing, F.-L. Sequential electrophilic trifluoromethanesulfanylation-cyclization of tryptamine derivatives: Synthesis of C(3)-trifluoromethanesulfanylated hexahydropyrrolo[2, 3-b]indoles. J. Org. Chem., 2012, 77, 7538-7547.
    • (2012) J. Org. Chem , vol.77 , pp. 7538-7547
    • Yang, Y.1    Jiang, X.2    Qing, F.-L.3
  • 95
    • 0842263583 scopus 로고    scopus 로고
    • A new and efficient method for the synthesis of trifluoromethylthio-and selenoethers
    • Pooput, C.; Medebielle, M.; Dolbier, W. R. A new and efficient method for the synthesis of trifluoromethylthio-and selenoethers. Org. Lett., 2003, 6, 301-303.
    • (2003) Org. Lett , vol.6 , pp. 301-303
    • Pooput, C.1    Medebielle, M.2    Dolbier, W.R.3
  • 96
    • 0034731615 scopus 로고    scopus 로고
    • Nucleophilic trifluoromethylation of carbonyl compounds and disulfides with trifluoromethane and silicon-containing bases
    • Large, S.; Roques, N.; Langlois, B. R. Nucleophilic trifluoromethylation of carbonyl compounds and disulfides with trifluoromethane and silicon-containing bases. J. Org. Chem., 2000, 65, 8848-8856.
    • (2000) J. Org. Chem , vol.65 , pp. 8848-8856
    • Large, S.1    Roques, N.2    Langlois, B.R.3
  • 97
    • 0030577493 scopus 로고    scopus 로고
    • A convenient synthesis of trifluoromethyl aryl sulfides
    • Quiclet-Sire, B.; Saicic, R. N.; Zard, S. Z. A convenient synthesis of trifluoromethyl aryl sulfides. Tetrahedron Lett., 1996, 37, 9057-9058.
    • (1996) Tetrahedron Lett , vol.37 , pp. 9057-9058
    • Quiclet-Sire, B.1    Saicic, R.N.2    Zard, S.Z.3
  • 98
    • 0035953057 scopus 로고    scopus 로고
    • New stable reagents for the nucleophilic trifluoromethylation. Part 4: Trifluoromethylation of disulfides and diselenides with hemiaminals of trifluoroacetaldehyde
    • Blond, G.; Billard, T.; Langlois, B. R. New stable reagents for the nucleophilic trifluoromethylation. Part 4: Trifluoromethylation of disulfides and diselenides with hemiaminals of trifluoroacetaldehyde. Tetrahedron Lett., 2001, 42, 2473-2475.
    • (2001) Tetrahedron Lett , vol.42 , pp. 2473-2475
    • Blond, G.1    Billard, T.2    Langlois, B.R.3
  • 99
    • 0030590504 scopus 로고    scopus 로고
    • A new simple access to trifluoromethyl thioethers or selenoethers from trifluoromethyl trimethylsilane and disulfides or diselenides
    • Billard, T.; Langlois, B. R. A new simple access to trifluoromethyl thioethers or selenoethers from trifluoromethyl trimethylsilane and disulfides or diselenides. Tetrahedron Lett., 1996, 37, 6865-6868.
    • (1996) Tetrahedron Lett , vol.37 , pp. 6865-6868
    • Billard, T.1    Langlois, B.R.2
  • 100
    • 0031013745 scopus 로고    scopus 로고
    • Preparation of trifluoromethyl sulfides or selenides from trifluoromethyl trimethylsilane and thiocyanates or selenocyanates
    • Billard, T.; Large, S.; Langlois, B. R. Preparation of trifluoromethyl sulfides or selenides from trifluoromethyl trimethylsilane and thiocyanates or selenocyanates. Tetrahedron Lett., 1997, 38, 65-68.
    • (1997) Tetrahedron Lett , vol.38 , pp. 65-68
    • Billard, T.1    Large, S.2    Langlois, B.R.3
  • 101
    • 0000130092 scopus 로고
    • Nucleophilic trifluoromethylation of organic substrates using (trifluoromethyl)trimethylsilane in the presence of a fluoride anion II. A convenient route to aryltrifluoromethyl-sulfides,-sulfoxides and-sulfones
    • Movchun, V. N.; Kolomeitsev, A. A.; Yagupolskii, Y. L. Nucleophilic trifluoromethylation of organic substrates using (trifluoromethyl)trimethylsilane in the presence of a fluoride anion II. A convenient route to aryltrifluoromethyl-sulfides,-sulfoxides and-sulfones. J. Fluorine Chem., 1995, 70, 255-257.
    • (1995) J. Fluorine Chem , vol.70 , pp. 255-257
    • Movchun, V.N.1    Kolomeitsev, A.A.2    Yagupolskii, Y.L.3
  • 102
    • 0033612329 scopus 로고    scopus 로고
    • Synthetic uses of thio-and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides
    • Billard, T.; Roques, N.; Langlois, B. R. Synthetic uses of thio-and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides. J. Org. Chem., 1999, 64, 3813-3820.
    • (1999) J. Org. Chem , vol.64 , pp. 3813-3820
    • Billard, T.1    Roques, N.2    Langlois, B.R.3
  • 103
    • 79952442263 scopus 로고    scopus 로고
    • Robust synthesis of trifluoromethionine and its derivatives by reductive trifluoromethylation of amino acid disulfides by CF3I/Na/Liq. NH3 system
    • Yasui, H.; Yamamoto, T.; Tokunaga, E.; Shibata, N. Robust synthesis of trifluoromethionine and its derivatives by reductive trifluoromethylation of amino acid disulfides by CF3I/Na/Liq. NH3 system. J. Fluorine Chem., 2011, 132, 186-189.
    • (2011) J. Fluorine Chem , vol.132 , pp. 186-189
    • Yasui, H.1    Yamamoto, T.2    Tokunaga, E.3    Shibata, N.4
  • 104
    • 84875873164 scopus 로고    scopus 로고
    • A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform
    • Kawai, H.; Yuan, Z.; Tokunaga, E.; Shibata, N. A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform. Org. Biomol. Chem., 2013, 11, 1446-1450.
    • (2013) Org. Biomol. Chem , vol.11 , pp. 1446-1450
    • Kawai, H.1    Yuan, Z.2    Tokunaga, E.3    Shibata, N.4
  • 105
    • 84874077360 scopus 로고    scopus 로고
    • Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate
    • Riofski, M. V.; Hart, A. D.; Colby, D. A. Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate. Org. Lett., 2012, 15, 208-211.
    • (2012) Org. Lett , vol.15 , pp. 208-211
    • Riofski, M.V.1    Hart, A.D.2    Colby, D.A.3
  • 106
    • 84875189703 scopus 로고    scopus 로고
    • An electrophilic hypervalent iodine reagent for trifluoromethylthiolation
    • Shao, X.; Wang, X.; Yang, T.; Lu, L.; Shen, Q. An electrophilic hypervalent iodine reagent for trifluoromethylthiolation. Angew. Chem. Int. Ed., 2013, 52, 3457-3460.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 3457-3460
    • Shao, X.1    Wang, X.2    Yang, T.3    Lu, L.4    Shen, Q.5
  • 107
    • 84888631737 scopus 로고    scopus 로고
    • Enantioselective electrophilic trifluoromethylthiolation of β-Ketoesters: A case of reactivity and selectivity bias for organocatalysis
    • Wang, X.; Yang, T.; Cheng, X.; Shen, Q. Enantioselective electrophilic trifluoromethylthiolation of β-Ketoesters: A case of reactivity and selectivity bias for organocatalysis. Angew. Chem. Int. Ed., 2013, 52, 12860-12864.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 12860-12864
    • Wang, X.1    Yang, T.2    Cheng, X.3    Shen, Q.4
  • 108
    • 84879391847 scopus 로고    scopus 로고
    • Trifluoromethanesulfonyl hypervalent iodonium ylide for copper-catalyzed trifluoromethylthiolation of enamines, indoles, and β-Keto esters
    • Yang, Y. D.; Azuma, A.; Tokunaga, E.; Yamasaki, M.; Shiro, M.; Shibata, N. Trifluoromethanesulfonyl hypervalent iodonium ylide for copper-catalyzed trifluoromethylthiolation of enamines, indoles, and β-Keto esters. J. Am. Chem. Soc., 2013, 135, 8782-8785.
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 8782-8785
    • Yang, Y.D.1    Azuma, A.2    Tokunaga, E.3    Yamasaki, M.4    Shiro, M.5    Shibata, N.6
  • 109
    • 0037207640 scopus 로고    scopus 로고
    • A new synthesis of trifluoromethanethiolates-characterization and properties of tetramethylammonium, cesium and di(benzo-15-crown-5)cesium trifluoromethanethiolates
    • Tyrra, W.; Naumann, D.; Hoge, B.; Yagupolskii, Y. L. A new synthesis of trifluoromethanethiolates-characterization and properties of tetramethylammonium, cesium and di(benzo-15-crown-5)cesium trifluoromethanethiolates. J. Fluorine Chem., 2003, 119, 101-107.
    • (2003) J. Fluorine Chem , vol.119 , pp. 101-107
    • Tyrra, W.1    Naumann, D.2    Hoge, B.3    Yagupolskii, Y.L.4
  • 110
    • 84880015181 scopus 로고    scopus 로고
    • Silver-mediated fluorination, trifluoromethylation, and trifluoromethylthiolation of arynes
    • Wang, K.-P.; Yun, S. Y.; Mamidipalli, P.; Lee, D. Silver-mediated fluorination, trifluoromethylation, and trifluoromethylthiolation of arynes. Chem. Sci., 2013, 4, 3205-3211.
    • (2013) Chem. Sci , vol.4 , pp. 3205-3211
    • Wang, K.-P.1    Yun, S.Y.2    Mamidipalli, P.3    Lee, D.4
  • 111
    • 79960925020 scopus 로고    scopus 로고
    • Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions
    • Teverovskiy, G.; Surry, D. S.; Buchwald, S. L. Pd-catalyzed synthesis of Ar-SCF3 compounds under mild conditions. Angew. Chem. Int. Ed., 2011, 50, 7312-7314.
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 7312-7314
    • Teverovskiy, G.1    Surry, D.S.2    Buchwald, S.L.3
  • 112
    • 84862909182 scopus 로고    scopus 로고
    • Nickel-catalyzed synthesis of aryl trifluoromethyl sulfides at room temperature
    • Zhang, C. P.; Vicic, D. A. Nickel-catalyzed synthesis of aryl trifluoromethyl sulfides at room temperature. J. Am. Chem. Soc., 2012, 134, 183-185.
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 183-185
    • Zhang, C.P.1    Vicic, D.A.2
  • 113
    • 84872845186 scopus 로고    scopus 로고
    • An air-stable copper reagent for nucleophilic trifluoromethylthiolation of aryl halides
    • Weng, Z.; He, W.; Chen, C.; Lee, R.; Tan, D.; Lai, Z.; Kong, D.; Yuan, Y.; Huang, K. W. An air-stable copper reagent for nucleophilic trifluoromethylthiolation of aryl halides. Angew. Chem. Int. Ed., 2013, 52, 1548-1552.
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 1548-1552
    • Weng, Z.1    He, W.2    Chen, C.3    Lee, R.4    Tan, D.5    Lai, Z.6    Kong, D.7    Yuan, Y.8    Huang, K.W.9
  • 114
    • 84878928248 scopus 로고    scopus 로고
    • Room temperature nucleophilic trifluoromethylthiolation of benzyl bromides with (bpy)Cu(SCF3)
    • Kong, D.; Jiang, Z.; Xin, S.; Bai, Z.; Yuan, Y.; Weng, Z. Room temperature nucleophilic trifluoromethylthiolation of benzyl bromides with (bpy)Cu(SCF3). Tetrahedron, 2013, 69, 6046-6050.
    • (2013) Tetrahedron , vol.69 , pp. 6046-6050
    • Kong, D.1    Jiang, Z.2    Xin, S.3    Bai, Z.4    Yuan, Y.5    Weng, Z.6
  • 115
    • 84863229716 scopus 로고    scopus 로고
    • Copper-catalyzed oxidative trifluoromethylthiolation of aryl boronic acids with TMSCF3 and elemental sulfur
    • Chen, C.; Xie, Y.; Chu, L.; Wang, R. W.; Zhang, X.; Qing, F. L. Copper-catalyzed oxidative trifluoromethylthiolation of aryl boronic acids with TMSCF3 and elemental sulfur. Angew. Chem. Int. Ed., 2012, 51, 2492-2495.
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 2492-2495
    • Chen, C.1    Xie, Y.2    Chu, L.3    Wang, R.W.4    Zhang, X.5    Qing, F.L.6
  • 116
    • 84864483240 scopus 로고    scopus 로고
    • Metal-free oxidative trifluoromethylthiolation of terminal alkynes with CF3SiMe3 and elemental sulfur
    • Chen, C.; Chu, L.; Qing, F. L. Metal-free oxidative trifluoromethylthiolation of terminal alkynes with CF3SiMe3 and elemental sulfur. J. Am. Chem. Soc., 2012, 134, 12454-12457.
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 12454-12457
    • Chen, C.1    Chu, L.2    Qing, F.L.3
  • 117
    • 84863824460 scopus 로고    scopus 로고
    • Oxidative trifluoromethylthiolations of aryl boronic acids using a copper/O2-based protocol
    • Zhang, C. P.; Vicic, D. A. Oxidative trifluoromethylthiolations of aryl boronic acids using a copper/O2-based protocol. Chem. Asian J., 2012, 7, 1756-1758.
    • (2012) Chem. Asian J , vol.7 , pp. 1756-1758
    • Zhang, C.P.1    Vicic, D.A.2
  • 118
    • 84868566088 scopus 로고    scopus 로고
    • Copper-Promoted Sulfenylation of sp2 C-H Bonds
    • Tran, L. D.; Popov, I.; Daugulis, O. Copper-Promoted Sulfenylation of sp2 C-H Bonds. J. Am. Chem. Soc., 2012, 134, 18237-18240.
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 18237-18240
    • Tran, L.D.1    Popov, I.2    Daugulis, O.3


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