메뉴 건너뛰기




Volumn , Issue , 2012, Pages 35-59

Synthesis Methods for Exotic Inorganic Fluorides with Varied Applications

Author keywords

Copper fluoride preparation; inorganic fluoride synthesis methods, and applications; K2NiF6, LiPF6 preparation; Metal triflates, subject of academic industrial research; Superacid systems, mixing Lewis and Bronsted acids

Indexed keywords


EID: 84886357739     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118409466.ch9     Document Type: Chapter
Times cited : (1)

References (99)
  • 7
    • 33947206081 scopus 로고    scopus 로고
    • Rare earth triflate catalysts in the synthesis of vitamin E and its derivatives
    • Bonrath W, Dittel C, Giraudi L, Netscher T, Pabst T. Rare earth triflate catalysts in the synthesis of vitamin E and its derivatives. Catal Today 2007;121:65-70.
    • (2007) Catal Today , vol.121 , pp. 65-70
    • Bonrath, W.1    Dittel, C.2    Giraudi, L.3    Netscher, T.4    Pabst, T.5
  • 10
    • 0004060819 scopus 로고
    • A.C.S Monograph 187 American Chemical Society: Washington D.C
    • Meshri D. Chemistry of Organic Fluorine Compounds II. ACS Monograph 187; American Chemical Society: Washington, DC, 1995; p 23-40.
    • (1995) Chemistry of Organic Fluorine Compounds I.I , pp. 23-40
    • Meshri, D.1
  • 11
    • 0038780804 scopus 로고    scopus 로고
    • Reversible formation decomposition of LiF clusters using transition metal fluorides as precursors and their application in rechargeable Li batteries
    • Li H, Richter G, Maier J. Reversible formation and decomposition of LiF clusters using transition metal fluorides as precursors and their application in rechargeable Li batteries. Adv Mater 2003;15:736.
    • (2003) Adv Mater , vol.15 , pp. 736
    • Li, H.1    Richter, G.2    Maier, J.3
  • 12
    • 10944228053 scopus 로고    scopus 로고
    • Li-storage via heterogeneous reaction in selected binary metal fluorides and oxides
    • H. Li, Balaya P, Maier J. Li-storage via heterogeneous reaction in selected binary metal fluorides and oxides. J Electrochem Soc 2004;151:A1878.
    • (2004) J Electrochem Soc , vol.151
    • Li, H.1    Balaya, P.2    Maier, J.3
  • 13
    • 79551535587 scopus 로고    scopus 로고
    • The investigation on electrochemical reaction mechanism of CuF2 thin film with lithium
    • Cui Y, Xue M, Zhou Y, Peng S, Wang X, Fu Z. The investigation on electrochemical reaction mechanism of CuF2 thin film with lithium. Electrochim Acta 2011;56:2328.
    • (2011) Electrochim Acta , vol.56 , pp. 2328
    • Cui, Y.1    Xue, M.2    Zhou, Y.3    Peng, S.4    Wang, X.5    Fu, Z.6
  • 14
    • 0000509897 scopus 로고
    • The preparation of very pure fluorine gas
    • Asprey LB. The preparation of very pure fluorine gas. J Fluorine Chem 1976;7:359-361.
    • (1976) J Fluorine Chem , vol.7 , pp. 359-361
    • Asprey, L.B.1
  • 16
    • 0038329197 scopus 로고    scopus 로고
    • Isolation and characterisation of both the first fluoroxyfluorofullerene C60F17O.F and oxahomofluorofullerenol C60F17O.O.H
    • Darwish AD, Abdul-Sada AK, Avent AG, Street JM, Taylor R. Isolation and characterisation of both the first fluoroxyfluorofullerene C60F17OF and oxahomofluorofullerenol C60F17O.OH. J Fluorine Chem 2003;121:185-192.
    • (2003) J Fluorine Chem , vol.121 , pp. 185-192
    • Darwish, A.D.1    Abdul-Sada, A.K.2    Avent, A.G.3    Street, J.M.4    Taylor, R.5
  • 17
    • 0033876885 scopus 로고    scopus 로고
    • Electrochemical behavior of graphite highly fluorinated by high oxidation state complex fluorides and elemental fluorine
    • Nakajima T, Koh M, Gupta V, Zemva B, Lutar K. Electrochemical behavior of graphite highly fluorinated by high oxidation state complex fluorides and elemental fluorine. Electrochim Acta 2000;45:1655-1661.
    • (2000) Electrochim Acta , vol.45 , pp. 1655-1661
    • Nakajima, T.1    Koh, M.2    Gupta, V.3    Zemva, B.4    Lutar, K.5
  • 18
    • 33947465895 scopus 로고
    • Solubility of fluorides of metals in liquid hydrogen fluoride
    • Jache AW, Cady GH. Solubility of fluorides of metals in liquid hydrogen fluoride. J Phys Chem 1952;56:1106-1109.
    • (1952) J Phys Chem , vol.56 , pp. 1106-1109
    • Jache, A.W.1    Cady, G.H.2
  • 19
    • 49049135720 scopus 로고
    • Preparation of some new pentafluorosulfur fluoroethanes and the vibrational spectrum of 1-hydro-1-pentafluorosulfur-F-ethane its deuterium isotopomer
    • Efner HF, Kirk R, Noftle RE, Uhrig M. Preparation of some new pentafluorosulfur fluoroethanes; the vibrational spectrum of 1-hydro-1-pentafluorosulfur-F-ethane and its deuterium isotopomer. Polyhedron 1982;1:723-734.
    • (1982) Polyhedron , vol.1 , pp. 723-734
    • Efner, H.F.1    Kirk, R.2    Noftle, R.E.3    Uhrig, M.4
  • 23
    • 49549159320 scopus 로고
    • The fluorination of benzene tetrahydrofuran and cyclohexanone with silver difluoride and potassium tetrafluoroargentate(I.I.I). J Fluorine Chem
    • Plevey RG, Steward MP, Tatlow JC. Fluorination with complex metal fluorides Part II. The fluorination of benzene, tetrahydrofuran and cyclohexanone with silver difluoride and potassium tetrafluoroargentate(III). J Fluorine Chem 1973/74;3:259-266.
    • (1973) Fluorination with complex metal fluorides Part I.I , vol.3 , Issue.74 , pp. 259-266
    • Plevey, R.G.1    Steward, M.P.2    Tatlow, J.C.3
  • 24
    • 0343695015 scopus 로고
    • The addition of fluorine to halogenated olefins by means of metal fluorides
    • Rausch DA, Davis RA, Osborne DW. The addition of fluorine to halogenated olefins by means of metal fluorides. J Org Chem 1963;28:494-497.
    • (1963) J Org Chem , vol.28 , pp. 494-497
    • Rausch, D.A.1    Davis, R.A.2    Osborne, D.W.3
  • 27
    • 0000983514 scopus 로고
    • Ueber trishydrofluoride tertiaerer amine und ihren einsatz als fluorierungsmittel
    • Franz R. Ueber trishydrofluoride tertiaerer amine und ihren einsatz als fluorierungsmittel. J Fluorine Chem 1980;15:423-434.
    • (1980) J Fluorine Chem , vol.15 , pp. 423-434
    • Franz, R.1
  • 28
    • 0000232292 scopus 로고
    • Different selectivities in bromofluorination reactions using N-bromosuccinimide/triethylamine tris hydrofluoride or Olah's reagent
    • Haufe G, Alvernhe G, Laurent A. Different selectivities in bromofluorination reactions using N-bromosuccinimide/triethylamine tris hydrofluoride or Olah's reagent. Tetrahedron Lett 1986;27:4449-4452.
    • (1986) Tetrahedron Lett , vol.27 , pp. 4449-4452
    • Haufe, G.1    Alvernhe, G.2    Laurent, A.3
  • 29
    • 85082689727 scopus 로고
    • Triethylamine tris-hydrofluoride [(C2H5)3Ṅ3H.F]: a highly versatile source of fluoride ion for the halofluorination of alkenes synthesis
    • Alvernhe G, Laurent A, Haufe G. Triethylamine tris-hydrofluoride [(C2H5)3Ṅ3HF]: a highly versatile source of fluoride ion for the halofluorination of alkenes synthesis. Synthesis 1987;6:562.
    • (1987) Synthesis , vol.6 , pp. 562
    • Alvernhe, G.1    Laurent, A.2    Haufe, G.3
  • 30
    • 11844281277 scopus 로고
    • Formal addition of methanesulfenyl fluoride to unsaturated substrates
    • Haufe G, Alvernhe G, Anker D, Laurent A, Saluzzo C. Formal addition of methanesulfenyl fluoride to unsaturated substrates. Tetrahedron Lett 1988;29:2311-2314.
    • (1988) Tetrahedron Lett , vol.29 , pp. 2311-2314
    • Haufe, G.1    Alvernhe, G.2    Anker, D.3    Laurent, A.4    Saluzzo, C.5
  • 31
    • 0012245409 scopus 로고
    • Utilisation du complexe triethylamine acide fluorhydrique pour la synthese de d'esoxyfluoropyranosides et la scission de groupes silyles substitues
    • Picq D, Anker D. Utilisation du complexe triethylamineacide fluorhydrique pour la synthese de d'esoxyfluoropyranosides et la scission de groupes silyles substitues. Carbohydr Res 1987;166:309.
    • (1987) Carbohydr Res , vol.166 , pp. 309
    • Picq, D.1    Anker, D.2
  • 32
    • 0000496674 scopus 로고
    • Trimethylsilyl cyanide-a reagent for umpolungX.I.I.I. Furfural a convenient precursor for intramolecular Diels-Alder reactions via umpolung with trimethylsilyl cyanide
    • Fischer K, Huenig S. Trimethylsilyl cyanide-a reagent for umpolung. XIII. Furfural, a convenient precursor for intramolecular Diels-Alder reactions via umpolung with trimethylsilyl cyanide. J Org Chem 1987;52:564-569.
    • (1987) J Org Chem , vol.52 , pp. 564-569
    • Fischer, K.1    Huenig, S.2
  • 33
    • 0028277664 scopus 로고
    • A convenient procedure for the deprotection of silylated nucleosides and nucleotides using triethylamine trihydrofluoride
    • Pirrung MC, Shuey SW, Lever DC, Fallon L. A convenient procedure for the deprotection of silylated nucleosides and nucleotides using triethylamine trihydrofluoride. Bioorg Med Chem Lett 1994;4:1345.
    • (1994) Bioorg Med Chem Lett , vol.4 , pp. 1345
    • Pirrung, M.C.1    Shuey, S.W.2    Lever, D.C.3    Fallon, L.4
  • 35
    • 0002096709 scopus 로고    scopus 로고
    • Triethylamine Trishydrofluoride in synthesis
    • Haufe G. Triethylamine Trishydrofluoride in synthesis. J Prakt Chem/Chem Ztg 1996;338:99.
    • (1996) J Prakt Chem/Chem Ztg , vol.338 , pp. 99
    • Haufe, G.1
  • 36
    • 0036573204 scopus 로고    scopus 로고
    • Study of LiB.F4 as an electrolyte salt for a Li-ion battery
    • Zhang SS, Xu K, Jow TR. Study of LiBF4 as an electrolyte salt for a Li-ion battery. J Electrochem Soc 2002;149:A586-A590.
    • (2002) J Electrochem Soc , vol.149
    • Zhang, S.S.1    Xu, K.2    Jow, T.R.3
  • 37
    • 0025979634 scopus 로고
    • LiB.F4: a mild lewis acid for intramolecular Diels-Alder reactions
    • Smith DA, Houk KN. LiBF4: a mild lewis acid for intramolecular Diels-Alder reactions. Tetrahedron Lett 1991;32:1549-1552.
    • (1991) Tetrahedron Lett , vol.32 , pp. 1549-1552
    • Smith, D.A.1    Houk, K.N.2
  • 40
    • 0345811005 scopus 로고
    • Recent aspects of nitration: new preparative methods mechanistic studies (a review)
    • Olah GA, Narang SC, Olah JA, Lammertsma K. Recent aspects of nitration: new preparative methods and mechanistic studies (a review). Proc Natl Acad Sci USA 1982;79:4487.
    • (1982) Proc Natl Acad Sci U.S.A , vol.79 , pp. 4487
    • Olah, G.A.1    Narang, S.C.2    Olah, J.A.3    Lammertsma, K.4
  • 41
    • 77953399155 scopus 로고    scopus 로고
    • Efficient nitration of meso-tetraphenylporphyrin with nitronium tetrafluoroborate
    • Smith NW, Dzyuba SV. Efficient nitration of meso-tetraphenylporphyrin with nitronium tetrafluoroborate. Arkivoc 2010;7:10-18.
    • (2010) Arkivoc , vol.7 , pp. 10-18
    • Smith, N.W.1    Dzyuba, S.V.2
  • 45
    • 0001068045 scopus 로고
    • A mild convenient halogen-exchange route to gem-difluorides and trifluorides
    • Bloodworth AJ, Bowyer KJ, Mitchell JC. A mild, convenient, halogen-exchange route to gem-difluorides and trifluorides. Tetrahedron Lett 1987;28:5347-5350.
    • (1987) Tetrahedron Lett , vol.28 , pp. 5347-5350
    • Bloodworth, A.J.1    Bowyer, K.J.2    Mitchell, J.C.3
  • 46
    • 38649098142 scopus 로고    scopus 로고
    • Silver(I) tetrafluoroborate as a potent promoter for chemical glycosylation
    • Kaeothip S, Pornsuriyasak P, Demchenko AV. Silver(I) tetrafluoroborate as a potent promoter for chemical glycosylation. Tetrahedron Lett 2008;49:1542-1545.
    • (2008) Tetrahedron Lett , vol.49 , pp. 1542-1545
    • Kaeothip, S.1    Pornsuriyasak, P.2    Demchenko, A.V.3
  • 47
    • 0001235576 scopus 로고
    • The use of hexafluorophosphoric acid in the schiemann reaction
    • Rutherford KG, Redmond W, Rigamonti J. The use of hexafluorophosphoric acid in the schiemann reaction. J Org Chem 1961;26:5149-5152.
    • (1961) J Org Chem , vol.26 , pp. 5149-5152
    • Rutherford, K.G.1    Redmond, W.2    Rigamonti, J.3
  • 51
    • 76249131385 scopus 로고    scopus 로고
    • Challenges for rechargeable Li batteries
    • Goodenough JB, Kim Y. Challenges for rechargeable Li batteries. Chem Mater 2010;22:587-603.
    • (2010) Chem Mater , vol.22 , pp. 587-603
    • Goodenough, J.B.1    Kim, Y.2
  • 52
    • 4143105737 scopus 로고    scopus 로고
    • Lithium hexafluorophosphate-catalyzed efficient tetrahydropyranylation of tertiary alcohols under mild reaction conditions
    • Hamada N, Tsuneo S. Lithium hexafluorophosphate-catalyzed efficient tetrahydropyranylation of tertiary alcohols under mild reaction conditions. Synlett 2004;10:1802.
    • (2004) Synlett , vol.10 , pp. 1802
    • Hamada, N.1    Tsuneo, S.2
  • 53
    • 0007063684 scopus 로고
    • Potassium hexafluorophosphate-an associated electrolyte
    • Robinson RA, Stokes JM, Stokes RH. Potassium hexafluorophosphate-an associated electrolyte. J Phys Chem 1961;65:542-546.
    • (1961) J Phys Chem , vol.65 , pp. 542-546
    • Robinson, R.A.1    Stokes, J.M.2    Stokes, R.H.3
  • 55
    • 84886323828 scopus 로고    scopus 로고
    • inventor; Cellular Technology International, Inc. and Chemfoan International, Inc., assignee. U.S patent 5,955,526. Sept 21
    • Spicher DR, inventor; Cellular Technology International, Inc. and Chemfoan International, Inc., assignee. Antistatic additive for organic polymer compositions. US patent 5,955,526. 1999 Sept 21.
    • (1999) Antistatic additive for organic polymer compositions
    • Spicher, D.R.1
  • 56
    • 33846490499 scopus 로고    scopus 로고
    • Preparation of 1-butyl-3-methyl imidazolium-based room temperature ionic liquids
    • 2002;79:236
    • Dupont J, Consorti CS, Suarez PAZ, deSouza RF. Preparation of 1-butyl-3-methyl imidazolium-based room temperature ionic liquids. Org Synth, Coll 2004;10:184; 2002;79:236.
    • (2004) Org Synth Coll , vol.10 , pp. 184
    • Dupont, J.1    Consorti, C.S.2    Suarez, P.A.Z.3    deSouza, R.F.4
  • 57
    • 84886330965 scopus 로고    scopus 로고
    • Preparation of bis(2,4,6-Trimethylpyridine)iodine(I) hexafluorophosphate bis(2,4,6-trimethylpyridine) bromine(I) hexafluorophosphate
    • 2000;77:206
    • Homsi F, Robin S, Rousseau G. Preparation of bis(2,4,6-Trimethylpyridine)iodine(I) hexafluorophosphate and bis(2,4,6-trimethylpyridine) bromine(I) hexafluorophosphate. Org Synth, Coll 2004;10:122; 2000;77:206.
    • (2004) Org Synth Coll , vol.10 , pp. 122
    • Homsi, F.1    Robin, S.2    Rousseau, G.3
  • 58
    • 26444553613 scopus 로고    scopus 로고
    • Aluminium triflate: a remarkable Lewis acid catalyst for the ring opening of epoxides by alcohols
    • Williams DBG, Lawton M. Aluminium triflate: a remarkable Lewis acid catalyst for the ring opening of epoxides by alcohols. Org Biomol Chem 2005;3:3269.
    • (2005) Org Biomol Chem , vol.3 , pp. 3269
    • Williams, D.B.G.1    Lawton, M.2
  • 59
    • 29244483910 scopus 로고    scopus 로고
    • Aluminium triflate as catalyst for epoxide ring-opening and esterification reactions-Mechanistic aspects
    • Terblans YM, Huyser JJ, Huyser M, Green MJ, Young DA, Sibiya MS. Aluminium triflate as catalyst for epoxide ring-opening and esterification reactions-Mechanistic aspects. Can J Chem 2005;83:854.
    • (2005) Can J Chem , vol.83 , pp. 854
    • Terblans, Y.M.1    Huyser, J.J.2    Huyser, M.3    Green, M.J.4    Young, D.A.5    Sibiya, M.S.6
  • 60
    • 33746820989 scopus 로고    scopus 로고
    • Aluminium triflate: an efficient recyclable Lewis acid catalyst for the aminolysis of epoxides
    • Williams DBG, Lawton M. Aluminium triflate: an efficient recyclable Lewis acid catalyst for the aminolysis of epoxides. Tetrahedron Lett 2006;47:6557-6560.
    • (2006) Tetrahedron Lett , vol.47 , pp. 6557-6560
    • Williams D.B.G Lawton, M.1
  • 61
    • 0037273188 scopus 로고    scopus 로고
    • Highly efficient and chemoselective thioacetalization of carbonyl compounds catalyzed with aluminum trifluromethanesulfonate [Al(O.Tf)3]
    • Firouzabadi H, Iranpoor N, Kohmareh G. Highly efficient and chemoselective thioacetalization of carbonyl compounds catalyzed with aluminum trifluromethanesulfonate [Al(OTf)3]. Synth Commun 2003;33:167.
    • (2003) Synth Commun , vol.33 , pp. 167
    • Firouzabadi, H.1    Iranpoor, N.2    Kohmareh, G.3
  • 62
    • 15444379396 scopus 로고    scopus 로고
    • Aluminium triflate [Al(O.Tf)3] as a recyclable catalyst for the conversion of -hydroxyphosphonates alcohols and phenols to their corresponding O-silylated products with hexamethyldisilazane (H.M.D.S)
    • Firouzabadi H, Iranpoor N, Sobhani S, Ghassamipour S. Aluminium triflate [Al(OTf)3] as a recyclable catalyst for the conversion of -hydroxyphosphonates, alcohols and phenols to their corresponding O-silylated products with hexamethyldisilazane (HMDS). Synthesis 2005;4: 595.
    • (2005) Synthesis , vol.4 , pp. 595
    • Firouzabadi, H.1    Iranpoor, N.2    Sobhani, S.3    Ghassamipour, S.4
  • 63
    • 34247582284 scopus 로고    scopus 로고
    • Al(O.Tf)3 as a highly efficient catalyst for the rapid acetylation of alcohols phenols and thiophenols under solvent-free conditions
    • Kamal A, KhanMNA, Reddy KS, Srikant YVV, Krishnaji T. Al(OTf)3 as a highly efficient catalyst for the rapid acetylation of alcohols, phenols and thiophenols under solvent-free conditions. Tetrahedron Lett 2007;48:3813-3818.
    • (2007) Tetrahedron Lett , vol.48 , pp. 3813-3818
    • Kamal, A.1    Khan, M.N.A.2    Reddy, K.S.3    Srikant, Y.V.V.4    Krishnaji, T.5
  • 64
    • 57049100943 scopus 로고    scopus 로고
    • Al(O.Tf)3-a highly efficient catalyst for the tetrahydropyranylation of alcohols under solvent-free conditions
    • Kamal A, Khan MNA, Srikant YVV, Reddy KS. Al(OTf)3-a highly efficient catalyst for the tetrahydropyranylation of alcohols under solvent-free conditions. Can J Chem 2008;86:1099.
    • (2008) Can J Chem , vol.86 , pp. 1099
    • Kamal, A.1    Khan, M.N.A.2    Srikant, Y.V.V.3    Reddy, K.S.4
  • 67
    • 0000158989 scopus 로고
    • Copper(I.I) triflate a new reagent for mild dehydration of alcohols: synthetic usefulness and mechanistic insight
    • Laali K, Gerzina RJ, Flajnik CM, Geric CM, Dombroski AM. Copper(II) triflate, a new reagent for mild dehydration of alcohols: synthetic usefulness and mechanistic insight. Helv Chim Acta 1987;70:607-611.
    • (1987) Helv Chim Acta , vol.70 , pp. 607-611
    • Laali, K.1    Gerzina, R.J.2    Flajnik, C.M.3    Geric, C.M.4    Dombroski, A.M.5
  • 68
    • 0033534609 scopus 로고    scopus 로고
    • An efficient method for cleavage of epoxides with aromatic amines
    • Sekar G, Singh VK. An efficient method for cleavage of epoxides with aromatic amines. J Org Chem 1999;64:287-289.
    • (1999) J Org Chem , vol.64 , pp. 287-289
    • Sekar, G.1    Singh, V.K.2
  • 69
    • 0034835354 scopus 로고    scopus 로고
    • Highly enantioselective Hetero-Diels-Alder reactions catalyzed by a C2-symmetric bis(sulfoximine) copper(I.I) complex
    • Bolm C, Simic O. Highly enantioselective Hetero-Diels-Alder reactions catalyzed by a C2-symmetric bis(sulfoximine) copper(II) complex. J Am Chem Soc 2001;123:3830-3831.
    • (2001) J Am Chem Soc , vol.123 , pp. 3830-3831
    • Bolm, C.1    Simic, O.2
  • 70
    • 35348944869 scopus 로고    scopus 로고
    • Catalytic asymmetric Michael reactions with enamides as nucleophiles
    • Berthiol F, Matsubara R, Kawai N, Kobayashi S. Catalytic asymmetric Michael reactions with enamides as nucleophiles. Angew. Chem, Int Ed 2007;46:7803-7805.
    • (2007) Angew. Chem Int Ed , vol.46 , pp. 7803-7805
    • Berthiol, F.1    Matsubara, R.2    Kawai, N.3    Kobayashi, S.4
  • 71
    • 33646034636 scopus 로고    scopus 로고
    • Catalytic enantioselective O-H insertion reactions
    • Maier TC, Fu GC. Catalytic enantioselective O-H insertion reactions. J Am Chem Soc 2006;128:4594-4595.
    • (2006) J Am Chem Soc , vol.128 , pp. 4594-4595
    • Maier, T.C.1    Fu, G.C.2
  • 72
    • 0034343051 scopus 로고    scopus 로고
    • Transition-metal trifluoromethanesulphonates- recyclable catalysts for the synthesis of branched fatty derivatives by Diels- Alder reactions at unsaturated fatty esters
    • Behr A, Fiene M, Naendrup F, Schurmann K. Transition-metal trifluoromethanesulphonates- recyclable catalysts for the synthesis of branched fatty derivatives by Diels- Alder reactions at unsaturated fatty esters. Eur J Lipid Sci Technol 2000;102:342.
    • (2000) Eur J Lipid Sci Technol , vol.102 , pp. 342
    • Behr, A.1    Fiene, M.2    Naendrup, F.3    Schurmann, K.4
  • 73
    • 0034583413 scopus 로고    scopus 로고
    • Green Lewis acid catalysis in organic synthesis
    • Kobayashi S, Manabe K. Green Lewis acid catalysis in organic synthesis. Pure Appl Chem 2000;72:1373.
    • (2000) Pure Appl Chem , vol.72 , pp. 1373
    • Kobayashi, S.1    Manabe, K.2
  • 74
    • 0001641894 scopus 로고    scopus 로고
    • Lanthanide(I.I.I) triflates as recyclable catalysts for atom economic aromatic nitration
    • Waller FJ, Barrett AGM, Braddock DC, Ramprasad D. Lanthanide(III) triflates as recyclable catalysts for atom economic aromatic nitration. Chem Commun 1997;6:613-614.
    • (1997) Chem Commun , vol.6 , pp. 613-614
    • Waller, F.J.1    Barrett, A.G.M.2    Braddock, D.C.3    Ramprasad, D.4
  • 75
    • 0000516236 scopus 로고    scopus 로고
    • Metal- and ligand-accelerated catalysis of the Baylis-Hillman reaction
    • Aggarwal VK, Mereu A, Tarver GJ, McCague R. Metal- and ligand-accelerated catalysis of the Baylis-Hillman reaction. J Org Chem 1998;63:7183-7189.
    • (1998) J Org Chem , vol.63 , pp. 7183-7189
    • Aggarwal, V.K.1    Mereu, A.2    Tarver, G.J.3    McCague, R.4
  • 76
    • 31144441931 scopus 로고    scopus 로고
    • Expanding the scope of Lewis acid catalysis in water: remarkable ligand acceleration of aqueous ytterbium triflate catalyzed Michael addition reactions
    • Ding R, Katebzadeh K, Roman L, Bergquist K-E, Lindstr̈om UM. Expanding the scope of Lewis acid catalysis in water: remarkable ligand acceleration of aqueous ytterbium triflate catalyzed Michael addition reactions. J Org Chem 2006;71:352-355.
    • (2006) J Org Chem , vol.71 , pp. 352-355
    • Ding, R.1    Katebzadeh, K.2    Roman, L.3    Bergquist, K.-E.4    Lindstr̈om, U.M.5
  • 77
    • 0037033222 scopus 로고    scopus 로고
    • Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid
    • Aspinall HC, Bissett JS, Greeves N, Levin D. Lanthanum triflate-catalysed allylation of aldehydes: crucial activation by benzoic acid. Tetrahedron Lett 2002;43:319-321.
    • (2002) Tetrahedron Lett , vol.43 , pp. 319-321
    • Aspinall, H.C.1    Bissett, J.S.2    Greeves, N.3    Levin, D.4
  • 79
    • 0037430569 scopus 로고    scopus 로고
    • An efficient method for para-methoxybenzyl ether formation with lanthanum triflate
    • Rai AN, Basu A. An efficient method for para-methoxybenzyl ether formation with lanthanum triflate. Tetrahedron Lett 2003;44:2267-2269.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2267-2269
    • Rai, A.N.1    Basu, A.2
  • 80
    • 84886359418 scopus 로고    scopus 로고
    • inventors and Medtronic Inc. Electrolyte for L.I/S.V.O batteries. U.S patent 5,766,797. 1998 June 16
    • Crespi AM, Chen K, inventors; Medtronic, Inc. assignee. Electrolyte for LI/SVO batteries. US patent 5,766,797. 1998 June 16.
    • assignee
    • Crespi, A.M.1    Chen, K.2
  • 82
    • 54249085343 scopus 로고    scopus 로고
    • Solid polymer electrolytes based on polyethylene oxide and lithium trifluoro- methane sulfonate (P.E.O-LiC.F3S.O3): ionic conductivity and dielectric relaxation
    • Karan NK, Pradhan DK, Thomas R, Natesan B, Katiyar RS. Solid polymer electrolytes based on polyethylene oxide and lithium trifluoro- methane sulfonate (PEO-LiCF3SO3): ionic conductivity and dielectric relaxation. Solid State Ionics 2008;179:689.
    • (2008) Solid State Ionics , vol.179 , pp. 689
    • Karan, N.K.1    Pradhan, D.K.2    Thomas, R.3    Natesan, B.4    Katiyar, R.S.5
  • 83
    • 0033591185 scopus 로고    scopus 로고
    • Lithium trifluoromethanesulfonate (LiO.Tf) as a highly efficient catalyst for chemoselective dithioacetalization of carbonyl compounds under neutral and solvent-free conditions
    • Firouzabadi H, Karimi B, Eslami S. Lithium trifluoromethanesulfonate (LiOTf) as a highly efficient catalyst for chemoselective dithioacetalization of carbonyl compounds under neutral and solvent-free conditions. Tetrahedron Lett 1999;40:4055-4058.
    • (1999) Tetrahedron Lett , vol.40 , pp. 4055-4058
    • Firouzabadi, H.1    Karimi, B.2    Eslami, S.3
  • 84
    • 0030597092 scopus 로고    scopus 로고
    • Lithium trifluoromethanesulfonate-catalysed aminolysis of oxiranes
    • Auge J, Leroy F. Lithium trifluoromethanesulfonate-catalysed aminolysis of oxiranes. Tetrahedron Lett 1996;37:7715-7716.
    • (1996) Tetrahedron Lett , vol.37 , pp. 7715-7716
    • Auge, J.1    Leroy, F.2
  • 85
    • 0031498704 scopus 로고    scopus 로고
    • Lithium triflate as a new promoter of glycosylation under neutral conditions
    • Lubineau A, Drouillat B. Lithium triflate as a new promoter of glycosylation under neutral conditions. J Carbohydr Chem 1997;16:1179.
    • (1997) J Carbohydr Chem , vol.16 , pp. 1179
    • Lubineau, A.1    Drouillat, B.2
  • 86
    • 0037940236 scopus 로고    scopus 로고
    • Lithium trifluoromethanesulfonate (LiO.Tf) as a recyclable catalyst for highly efficient acetylation of alcohols and diacetylation of aldehydes under mild and neutral reaction conditions
    • Karimi B, Maleki J. Lithium trifluoromethanesulfonate (LiOTf) as a recyclable catalyst for highly efficient acetylation of alcohols and diacetylation of aldehydes under mild and neutral reaction conditions. J Org Chem 2003;68:4951-4954.
    • (2003) J Org Chem , vol.68 , pp. 4951-4954
    • Karimi, B.1    Maleki, J.2
  • 87
    • 85007950754 scopus 로고
    • Perfluoroalkanesulfonic esters: methods of preparation and applications in organic chemistry
    • Stang PJ, Hanack M, Subramanian LR. Perfluoroalkanesulfonic esters: methods of preparation and applications in organic chemistry. Synthesis 1982;2:85.
    • (1982) Synthesis , vol.2 , pp. 85
    • Stang, P.J.1    Hanack, M.2    Subramanian, L.R.3
  • 89
    • 0028876781 scopus 로고
    • New synthetic methods for olefins from secondary phosphates thiophosphates
    • Shimagaki M, Fujieda Y, Kimura T, Nakata T. New synthetic methods for olefins from secondary phosphates and thiophosphates. Tetrahedron Lett 1995;36:719-722.
    • (1995) Tetrahedron Lett , vol.36 , pp. 719-722
    • Shimagaki, M.1    Fujieda, Y.2    Kimura, T.3    Nakata, T.4
  • 90
    • 0028104478 scopus 로고
    • A mild procedure for etherification of alcohols with primary alkyl halides in the presence of silver triflate
    • Burk RM, Gac TS, Roof MB. A mild procedure for etherification of alcohols with primary alkyl halides in the presence of silver triflate. Tetrahedron Lett 1994;35:8111-8112.
    • (1994) Tetrahedron Lett , vol.35 , pp. 8111-8112
    • Burk, R.M.1    Gac, T.S.2    Roof, M.B.3
  • 91
    • 0037190848 scopus 로고    scopus 로고
    • Koch carbonylation using silver trifluoromethanesulfonate
    • Mori H, Mori A, Xu Q, Souma Y. Koch carbonylation using silver trifluoromethanesulfonate. Tetrahedron Lett 2002;43:7871-7874.
    • (2002) Tetrahedron Lett , vol.43 , pp. 7871-7874
    • Mori, H.1    Mori, A.2    Xu, Q.3    Souma, Y.4
  • 92
    • 0035932570 scopus 로고    scopus 로고
    • Iodine monochloride/silver trifluoromethanesulfonate (I.Cl/AgO.Tf) as a convenient promoter system for O-glycoside synthesis
    • Ercegovic T, Meijer A, Magnusson G, Ellervik U. Iodine monochloride/silver trifluoromethanesulfonate (ICl/AgOTf) as a convenient promoter system for O-glycoside synthesis. Org Lett 2001;3:913-915.
    • (2001) Org Lett , vol.3 , pp. 913-915
    • Ercegovic, T.1    Meijer, A.2    Magnusson, G.3    Ellervik, U.4
  • 93
    • 0025359156 scopus 로고
    • A galvanic gas sensor using poly (ethylene oxide) complex of silver trifluoromethane sulphonate electrolyte
    • Nagashima K, Meguro K, Hobo T. A galvanic gas sensor using poly (ethylene oxide) complex of silver trifluoromethane sulphonate electrolyte. Fresenius J Anal Chem 1990;336:571-574.
    • (1990) Fresenius J Anal Chem , vol.336 , pp. 571-574
    • Nagashima, K.1    Meguro, K.2    Hobo, T.3
  • 94
    • 17144417199 scopus 로고    scopus 로고
    • Crossing conventional boundaries in half a century of research
    • Olah GA. Crossing conventional boundaries in half a century of research. J Org Chem 2005;70:2413-2429.
    • (2005) J Org Chem , vol.70 , pp. 2413-2429
    • Olah, G.A.1
  • 95
    • 0008522331 scopus 로고
    • Oxyfunctionalization of hydrocarbons 1. Protolytic cleavage-rearrangement reactions of tertiary alkyl hydroperoxides with magic acid.
    • Olah GA, Parker DG, Yoneda Y, Pelizza F. Oxyfunctionalization of hydrocarbons. 1. Protolytic cleavage-rearrangement reactions of tertiary alkyl hydroperoxides with magic acid. J Am Chem Soc 1976;98:2245-2250.
    • (1976) J Am Chem Soc , vol.98 , pp. 2245-2250
    • Olah, G.A.1    Parker, D.G.2    Yoneda, Y.3    Pelizza, F.4
  • 96
    • 0000173062 scopus 로고
    • Oxyfunctionalization of hydrocarbons 8. Electrophilic hydroxylation of benzene alkylbenzenes and halobenzenes with hydrogen peroxide in superacids.
    • Olah GA, Ohnishi R. Oxyfunctionalization of hydrocarbons. 8. Electrophilic hydroxylation of benzene, alkylbenzenes, and halobenzenes with hydrogen peroxide in superacids. J Org Chem 1978;43:865-867.
    • (1978) J Org Chem , vol.43 , pp. 865-867
    • Olah, G.A.1    Ohnishi, R.2
  • 97
    • 37049136687 scopus 로고
    • Chemistry and spectroscopy in strongly acidic solutions: reversible reaction between aliphatic carbonium ions hydrogen
    • Bickel AF, Gaasbeek CJ, Hogeveen H, Oelderik JM, Platteeuw JC. Chemistry and spectroscopy in strongly acidic solutions: reversible reaction between aliphatic carbonium ions and hydrogen. Chem Commun 1967;13:634-635.
    • (1967) Chem Commun , vol.13 , pp. 634-635
    • Bickel, A.F.1    Gaasbeek, C.J.2    Hogeveen, H.3    Oelderik, J.M.4    Platteeuw, J.C.5
  • 98
    • 37049125102 scopus 로고
    • Chemistry and spectroscopy in strongly acidic solutions: electrophilic substitution at alkane-carbon by protons
    • Hogeveen H, Bickel AF. Chemistry and spectroscopy in strongly acidic solutions: electrophilic substitution at alkane-carbon by protons. Chem Commun 1967;13:635-636.
    • (1967) Chem Commun , vol.13 , pp. 635-636
    • Hogeveen, H.1    Bickel, A.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.