-
1
-
-
84886360874
-
-
15th European Symposium on Fluorine Chemistry; July 15-20; Prague Czech Republic
-
Meshri DT, Meshri SD, Sridhar CN, Adams RL, Mathur NC. Exciting role of inorganic fluorides in 21st century. 15th European Symposium on Fluorine Chemistry; 2007 July 15-20; Prague, Czech Republic.
-
(2007)
Exciting role of inorganic fluorides in 21st century
-
-
Meshri, D.T.1
Meshri, S.D.2
Sridhar, C.N.3
Adams, R.L.4
Mathur, N.C.5
-
2
-
-
84886352019
-
-
A.C.S 19th International Symposium on Fluorine Chemistry; Aug 23-28; Jackson Hole W.Y
-
Meshri DT, Meshri S, Adams R, Jain R, Mathur NC, Pinnapareddy D. Inorganic fluorides: opportunities and challenges in energy sector. ACS 19th International Symposium on Fluorine Chemistry; 2009 Aug 23-28; Jackson Hole, WY.
-
(2009)
Inorganic fluorides: opportunities challenges in energy sector
-
-
Meshri, D.T.1
Meshri, S.2
Adams, R.3
Jain, R.4
Mathur, N.C.5
Pinnapareddy, D.6
-
3
-
-
84886318830
-
-
Fluorinated Materials and Energy Conversion Workshop Apr 12-13 Bordeaux France
-
Meshri DT, Shembel E, Meshri S, Mathur NC, Adams R, Bhagat S, Pinnapareddy D, Jain. R. Fluorine: the backbone of electrochemical conversion and storage. Fluorinated Materials & Energy Conversion Workshop; 2010 Apr 12-13; Bordeaux, France.
-
(2010)
Fluorine: the backbone of electrochemical conversion and storage.
-
-
Meshri, D.T.1
Shembel, E.2
Meshri, S.3
Mathur, N.C.4
Adams, R.5
Bhagat, S.6
Pinnapareddy, D.7
Jain, R.8
-
4
-
-
84886347911
-
-
The 16th European Symposium on Fluorine Chemistry (16th E.S.F.C) July 18-23 Ljubljana Slovenia
-
Meshri DT, Mathur NC, Meshri S, Adams R, Jain R, Pinnapareddy D, Shembel E. Applications of fluorine based materials in electrochemical conversion and storage devices. The 16th European Symposium on Fluorine Chemistry (16th ESFC); 2010 July 18-23; Ljubljana, Slovenia.
-
(2010)
Applications of fluorine based materials in electrochemical conversion and storage devices
-
-
Meshri, D.T.1
Mathur, N.C.2
Meshri, S.3
Adams, R.4
Jain, R.5
Pinnapareddy, D.6
Shembel, E.7
-
5
-
-
84886318588
-
-
inventors E.P 1 687 264 B1
-
Finmans P, Hoell D, Vossler H-J, Heppner M, Green M, Roggenbuck R, inventors. Process for the production of metal salts of trifluoromethane sulphonic acid. EP 1 687 264 B1. 2010.
-
(2010)
Process for the production of metal salts of trifluoromethane sulphonic acid
-
-
Finmans, P.1
Hoell, D.2
Vossler, H.-J.3
Heppner, M.4
Green, M.5
Roggenbuck, R.6
-
7
-
-
33947206081
-
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
-
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
20
-
-
0010732087
-
Sonoda N
-
Ryu I, Suzuki H, Ogawa A, Kambe M. Sonoda N. Allylative ring opening of siloxycyclopropanes by silver fluoride and allylic chlorides affording, e-unsaturated ketones. Tetrahedron Lett 1988;29:6137-6140.
-
(1988)
Allylative ring opening of siloxycyclopropanes by silver fluoride allylic chlorides affording e-unsaturated ketones. Tetrahedron Lett
, vol.29
, pp. 6137-6140
-
-
Ryu, I.1
Suzuki, H.2
Ogawa, A.3
Kambe, M.4
-
22
-
-
84886336353
-
-
1983 and Chem Abstr 99 175351m
-
Fisher RG, Jr, Zweig A. US patent 4,394,527. 1983; Chem Abstr 99, 175351m, 1983.
-
(1983)
U.S patent 4,394,527
-
-
Fisher, R.G.J.1
Zweig, A.2
-
23
-
-
49549159320
-
-
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
-
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
-
25
-
-
0035966030
-
Reaction of silver(I) and (I.I) fluorides with C60: thermodynamic control over fluorination level
-
Goryunkov AA, Markov VY, BoltalinaOV, ZemvaB, Abdul-Sada AK, Taylor, R. Reaction of silver(I) and (II) fluorides with C60: thermodynamic control over fluorination level. J Fluorine Chem 2001;112:191-196.
-
(2001)
J Fluorine Chem
, vol.112
, pp. 191-196
-
-
Goryunkov, A.A.1
Markov, V.Y.2
Boltalina, O.V.3
Zemva, B.4
Abdul-Sada, A.K.5
Taylor, R.6
-
27
-
-
0000983514
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
39
-
-
0035801853
-
LiB.F4-catalyzed formation of fused pyrano- and furanobenzopyrans
-
Yadav JS, Reddy BV, Madhuri CH, Sabitha G, Jagannadh B, Kumar SK, Kunwar AC. LiBF4-catalyzed formation of fused pyrano- and furanobenzopyrans. Tetrahedron Lett 2001;42:6381-6384.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 6381-6384
-
-
Yadav, J.S.1
Reddy, B.V.2
Madhuri, C.H.3
Sabitha, G.4
Jagannadh, B.5
Kumar, S.K.6
Kunwar, A.C.7
-
41
-
-
77953399155
-
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
-
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
-
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
-
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
-
49
-
-
0004699579
-
-
inventors; Merck & Co., Inc., assignee. U.S patent 6,040,319. Mar 21
-
Corley EG, Davis IW, Larsen RD, Pye PJ, Rossen K, inventors; Merck & Co., Inc., assignee. Process for synthesizing COX-2 inhibitors. US patent 6,040,319. 2000 Mar 21.
-
(2000)
Process for synthesizing C.O.X-2 inhibitors
-
-
Corley, E.G.1
Davis, I.W.2
Larsen, R.D.3
Pye, P.J.4
Rossen, K.5
-
51
-
-
76249131385
-
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
-
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
-
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
-
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
65
-
-
84886321026
-
-
inventors;M̈uller Schupfner Partner assignee. E.P 2 113 499 A1. Nov 4
-
Finmans P, Hoell D, Vossler H-J, Heppner M, Roggenbuck R, Green M, inventors;M̈uller Schupfner & Partner, assignee. Use of metal salts of trifuoromethane sulphonic acid as esterification catalyst and/or transesterification catalyst. EP 2 113 499 A1. 2009 Nov 4.
-
(2009)
Use of metal salts of trifuoromethane sulphonic acid as esterification catalyst and/or transesterification catalyst
-
-
Finmans, P.1
Hoell, D.2
Vossler, H.-J.3
Heppner, M.4
Roggenbuck, R.5
Green, M.6
-
67
-
-
0000158989
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
99
-
-
0344125255
-
Halogenated carboxonium salts: preparation structural analysis
-
Minkwitz R, Reinemann S, Blecher O, Hartl H, Br̈udgam I. Halogenated carboxonium salts: preparation and structural analysis. Inorg Chem 1999;38:844-847.
-
(1999)
Inorg Chem
, vol.38
, pp. 844-847
-
-
Minkwitz, R.1
Reinemann, S.2
Blecher, O.3
Hartl, H.4
Br̈udgam, I.5
|