-
2
-
-
84889840383
-
-
John Wiley & Sons, Inc.: Hoboken, NJ, USA
-
Ohno, H. Electrochemical Aspects of Ionic Liquids, John Wiley & Sons, Inc.: Hoboken, NJ, USA, 2005.
-
(2005)
Electrochemical Aspects of Ionic Liquids
-
-
Ohno, H.1
-
4
-
-
4444303269
-
Industrial applications of ionic liquids
-
June
-
Holbrey, J.D. Industrial applications of ionic liquids. Chem. Today 2004, June, 35-37.
-
(2004)
Chem. Today
, pp. 35-37
-
-
Holbrey, J.D.1
-
5
-
-
0008716626
-
Lewis acid-catalysed sequential reaction in ionic liquids
-
Zulfigar, F.; Kitazume, T. Lewis acid-catalysed sequential reaction in ionic liquids. Green Chem. 2000, 2, 296-298.
-
(2000)
Green Chem.
, vol.2
, pp. 296-298
-
-
Zulfigar, F.1
Kitazume, T.2
-
6
-
-
80052324492
-
Fluorolactonization of unsaturated carboxylic acids with f-teda-bf4 in ionic liquids
-
Serguchev, Y.S.; Lourie, L.F.; Ponomarenko, M.V.; Rusanov, E.B.; Ignat'ev, N.V. Fluorolactonization of unsaturated carboxylic acids with F-TEDA-BF4 in ionic liquids. Tetrahedron Lett. 2011, 52, 5166-5169.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 5166-5169
-
-
Serguchev, Y.S.1
Lourie, L.F.2
Ponomarenko, M.V.3
Rusanov, E.B.4
Ignat'ev, N.V.5
-
7
-
-
78649621023
-
The first example of the schmidt reaction in ionic liquids
-
Epishina, M.A.; Kulikov, A.S.; Ignat'ev, N.V.; Schulte, M.; Makhova, N.N. The first example of the Schmidt reaction in ionic liquids. Mendeleev Commun. 2010, 20, 335-336.
-
(2010)
Mendeleev Commun.
, vol.20
, pp. 335-336
-
-
Epishina, M.A.1
Kulikov, A.S.2
Ignat'ev, N.V.3
Schulte, M.4
Makhova, N.N.5
-
8
-
-
33846697660
-
The influence of ionic liquid's nature on free radical polymerization of vinyl monomers and ionic conductivity of the obtained polymeric materials
-
Vygodskii, Y.S.; Mel'nik, O.A.; Lozinskaya, E.I.; Shaplov, A.S.; Malyshkina, I.A.; Gavrilova, N.D.; Lyssenko, K.A.; Antipin, M.Y.; Golovanov, D.G.; Korlyukov, A.A.; et al. The influence of ionic liquid's nature on free radical polymerization of vinyl monomers and ionic conductivity of the obtained polymeric materials. Polym. Adv. Technol. 2007, 18, 50-63.
-
(2007)
Polym. Adv. Technol.
, vol.18
, pp. 50-63
-
-
Vygodskii, Y.S.1
Mel'nik, O.A.2
Lozinskaya, E.I.3
Shaplov, A.S.4
Malyshkina, I.A.5
Gavrilova, N.D.6
Lyssenko, K.A.7
Antipin, M.Y.8
Golovanov, D.G.9
Korlyukov, A.A.10
-
9
-
-
56349103336
-
-
WO2004/080974
-
Choi, D.S.; Choi, D.W.; Park, E.J.; Chang, S.K.; Byun, I.S.; Kim, W.J. A Purification Method of Ionic Liquids to Obtain Their High Purity. WO2004/080974, 2004.
-
(2004)
A Purification Method of Ionic Liquids to Obtain Their High Purity.
-
-
Choi, D.S.1
Choi, D.W.2
Park, E.J.3
Chang, S.K.4
Byun, I.S.5
Kim, W.J.6
-
10
-
-
0035669246
-
Molecular states of water in room temperature ionic liquids
-
Cammarata, L.; Kazarian, S.; Salter, P.; Welton, T. Molecular states of water in room temperature ionic liquids. Phys. Chem. Chem. Phys. 2001, 3, 5192-5200.
-
(2001)
Phys. Chem. Chem. Phys.
, vol.3
, pp. 5192-5200
-
-
Cammarata, L.1
Kazarian, S.2
Salter, P.3
Welton, T.4
-
12
-
-
84861509995
-
-
WO2006/104305
-
Kim, H.G.; Lee, S.D.; Ahn, B.S.; Lee, J.S.; Kim, U.S.; Cho, B.W.; Kim, H.S. The Lithium Salts of Pyrrolidinium Type Zwitterion and the Preparation Method of the Same. WO2006/104305, 2006.
-
(2006)
The Lithium Salts of Pyrrolidinium Type Zwitterion and the Preparation Method of the Same.
-
-
Kim, H.G.1
Lee, S.D.2
Ahn, B.S.3
Lee, J.S.4
Kim, U.S.5
Cho, B.W.6
Kim, H.S.7
-
13
-
-
84861512041
-
-
US5994345
-
Cama, L.D.; Wilkening, R.R.; Ratcliffe, R.W.; Wildonger, K.J.; Sun, W. Carbapenem Antibacterial Compounds, Compositions Containing such Compounds and Method of Treatment. US5994345, 1999.
-
(1999)
Carbapenem Antibacterial Compounds Compositions Containing such Compounds and Method of Treatment
-
-
Cama, L.D.1
Wilkening, R.R.2
Ratcliffe, R.W.3
Wildonger, K.J.4
Sun, W.5
-
14
-
-
0012290163
-
Facile preparation of tetrafluoroborate and trifluoromethanesulfonate room-temperature ionic liquids. In
-
Fuller, J.; Carlin, R.T. Facile Preparation of Tetrafluoroborate and Trifluoromethanesulfonate Room-Temperature Ionic Liquids. In Proceedings of the 11th International Symposium on Molten Salts XI; Truvol, P.C., De Long, H.C., Stafford, C.R., Deki, S., Eds.; The Electrochemical Society, Inc.: Pennington, NJ, USA, 1998; Volume 98-11, pp. 227-230.
-
(1998)
Proceedings of the 11th International Symposium on Molten Salts XI; Truvol, P.C., De Long, H.C., Stafford, C.R., Deki, S., Eds.; The Electrochemical Society, Inc.: Pennington, NJ, USA
, vol.98
, Issue.11
, pp. 227-230
-
-
Fuller, J.1
Carlin, R.T.2
-
15
-
-
84861513769
-
-
EP1642894, EP1837333
-
Tetsuo, N.; Yasutaka, T.; Megumi, T.; Masashi, Y.; Kazutaka, H.; Akihiro, N.; Hiroaki, T.; Kenji, S.; Takashi, H. Quaternary Ammonium Salt, Electrolyte, and Electrochemical Device. EP1642894, 2006; EP1837333, 2007.
-
(2006)
Quaternary Ammonium Salt Electrolyte and Electrochemical Device.
, pp. 2007
-
-
Tetsuo, N.1
Yasutaka, T.2
Megumi, T.3
Masashi, Y.4
Kazutaka, H.5
Akihiro, N.6
Hiroaki, T.7
Kenji, S.8
Takashi, H.9
-
16
-
-
84861512046
-
-
Presented at the First Congress on Ionic Liquids, Salzburg, Austria, 19-23 June
-
Ignatiev, N.; Welz-Biermann, U. New Technologies for Ionic Liquids Production. Presented at the First Congress on Ionic Liquids, Salzburg, Austria, 19-23 June 2005.
-
(2005)
New Technologies for Ionic Liquids Production
-
-
Ignatiev, N.1
Welz-Biermann, U.2
-
18
-
-
38949210336
-
Preparation of second generation ionic liquids by efficient solvent-free alkylation of n-heterocycles with chloroalkanes
-
Cravotto, G.; Gaudino, E.C.; Boffa, L.; Lévêque, J.-M.; Estager, J.; Bonrath, W. Preparation of second generation ionic liquids by efficient solvent-free alkylation of N-heterocycles with chloroalkanes. Molecules 2008, 13, 149-156.
-
(2008)
Molecules
, vol.13
, pp. 149-156
-
-
Cravotto, G.1
Gaudino, E.C.2
Boffa, L.3
Lévêque, J.-M.4
Estager, J.5
Bonrath, W.6
-
19
-
-
34548147300
-
One-pot and solventless synthesis of ionic liquids under ultrasonic irradiation
-
Estager, J.; Lévêque, J.-M.; Cravotto, G.; Boffa, L.; Bonrath, W.; Draye, M. One-pot and solventless synthesis of ionic liquids under ultrasonic irradiation. Synlett 2007, 13, 2065-2068.
-
(2007)
Synlett
, vol.13
, pp. 2065-2068
-
-
Estager, J.1
Lévêque, J.-M.2
Cravotto, G.3
Boffa, L.4
Bonrath, W.5
Draye, M.6
-
20
-
-
77149142893
-
Assessing the greenness of some typical laboratory ionic liquid preparations
-
Deetlefs, M.; Seddon, K.J. Assessing the greenness of some typical laboratory ionic liquid preparations. Green Chem. 2010, 12, 17-30.
-
(2010)
Green Chem.
, vol.12
, pp. 17-30
-
-
Deetlefs, M.1
Seddon, K.J.2
-
21
-
-
65749085454
-
-
2nd ed.; John Wiley & Sons, Inc.: Hoboken, NJ, USA
-
Olah, G.A.; Prakash, G.K.S.; Molnar, A.; Sommer, J. Superacid Chemistry, 2nd ed.; John Wiley & Sons, Inc.: Hoboken, NJ, USA, 2009; p. 38.
-
(2009)
Superacid Chemistry
, pp. 38
-
-
Olah, G.A.1
Prakash, G.K.S.2
Molnar, A.3
Sommer, J.4
-
22
-
-
2942709502
-
Triflic acid and its derivatives. A family of useful reagents for synthesis
-
March/April
-
Rakita, P.H. Triflic acid and its derivatives. A family of useful reagents for synthesis. Chem. Today 2004, March/April, 48-50.
-
(2004)
Chem. Today
, pp. 48-50
-
-
Rakita, P.H.1
-
23
-
-
0002780248
-
Perfluoroalkyl derivatives of sulphur. Part vii. Alkyl trifluoromethunesulphonates as alkylating agents, trifluoromethanesulphonic anhydride as a promoter for esterification, and some reactions of trifluoromethanesulphonic acid
-
Gramstadt, T.; Haszeldine, R.N. Perfluoroalkyl derivatives of sulphur. Part VII. Alkyl trifluoromethunesulphonates as alkylating agents, trifluoromethanesulphonic anhydride as a promoter for esterification, and some reactions of trifluoromethanesulphonic acid. J. Chem. Soc. 1956, 173-180.
-
(1956)
J. Chem. Soc.
, pp. 173-180
-
-
Gramstadt, T.1
Haszeldine, R.N.2
-
24
-
-
37049102530
-
Alkyltrifluoromethanesulphonates as alkylating reagents for aromatic compounds
-
Booth, B.L.; Haszeldine, R.N.; Laali, K. Alkyltrifluoromethanesulphonates as alkylating reagents for aromatic compounds. J. Chem. Soc. Perkin Trans. I 1980, 2887-2894.
-
(1980)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 2887-2894
-
-
Booth, B.L.1
Haszeldine, R.N.2
Laali, K.3
-
25
-
-
0002130947
-
Trifluoromfthanesulphonate esters and their alkylating properties
-
Burdon, J.; McLoughlin, V.C.R. Trifluoromfthanesulphonate esters and their alkylating properties. Tetrahedron 1965, 21, 1-4.
-
(1965)
Tetrahedron
, vol.21
, pp. 1-4
-
-
Burdon, J.1
McLoughlin, V.C.R.2
-
26
-
-
0030820689
-
The generation and cyclisation of pyridinium radicals as a potential route to indolizidine alkaloids
-
Dobbs, A.P.; Jones, K.; Veal, K.T. The generation and cyclisation of pyridinium radicals as a potential route to indolizidine alkaloids. Tetrahedron Lett. 1997, 38, 5383-5386.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 5383-5386
-
-
Dobbs, A.P.1
Jones, K.2
Veal, K.T.3
-
27
-
-
0006678730
-
Synthesis of some novel trifluoromethanesulfonates and their reactions with alcohols
-
Beard, C.D.; Baum, K.; Grakauskas, V. Synthesis of some novel trifluoromethanesulfonates and their reactions with alcohols. J. Org. Chem. 1973, 38, 3673-3677.
-
(1973)
J. Org. Chem.
, vol.38
, pp. 3673-3677
-
-
Beard, C.D.1
Baum, K.2
Grakauskas, V.3
-
28
-
-
84861518142
-
-
WO2002/098844, EP1399 417 B1, 2002, Merck Patent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Schmidt, M.; Heider, U.; Sartori, P.; Kucheryna, A. Method for Producing Perfluoroalkanesulfonic Acid Esters. WO 2002/098844, EP 1 399 417 B1, 2002, Merck Patent GmbH, Darmstadt, Germany.
-
Method for Producing Perfluoroalkanesulfonic Acid Esters
-
-
Ignatyev, N.1
Schmidt, M.2
Heider, U.3
Sartori, P.4
Kucheryna, A.5
-
29
-
-
84861518142
-
-
WO2003/053918, EP1472 217 B1, 2003, Merck Patent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Schmidt, M.; Heider, U.; Sartori, P.; Kucheryna, A. Method for Producing Perfluoroalkane Sulfonic Acid Esters and the Salts Thereof. WO 2003/053918, EP 1 472 217 B1, 2003, Merck Patent GmbH, Darmstadt, Germany.
-
Method for Producing Perfluoroalkane Sulfonic Acid Esters and the Salts Thereof
-
-
Ignatyev, N.1
Schmidt, M.2
Heider, U.3
Sartori, P.4
Kucheryna, A.5
-
30
-
-
0242626227
-
Hydrophobic highly conductive ambient-temperature molten salts
-
Bonhöte, P.; Dias, A.; Papageorgiou, N.; Kalyanasundaram, K.; Grätzel, M. Hydrophobic, highly conductive ambient-temperature molten salts. Inorg. Chem. 1996, 35, 1168-1178.
-
(1996)
Inorg. Chem.
, vol.35
, pp. 1168-1178
-
-
Bonhöte, P.1
Dias, A.2
Papageorgiou, N.3
Kalyanasundaram, K.4
Grätzel, M.5
-
31
-
-
0000225906
-
Catalytic epoxidation of alkenes with oxone
-
Denmark, S.E.; Forbes, D.C.; Hays, D.S.; DePue, J.S.; Wilde, R.G. Catalytic epoxidation of alkenes with oxone. J. Org. Chem. 1995, 60, 1391-1407.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1391-1407
-
-
Denmark, S.E.1
Forbes, D.C.2
Hays, D.S.3
DePue, J.S.4
Wilde, R.G.5
-
32
-
-
0345306294
-
Prototypal dithiazolodithiazolyl radicals: Synthesis, structures, and transport properties
-
Beer, L.; Britten, J.F.; Brusso, J.L.; Cordes, A.W.; Haddon, R.C.; Itkis, M.E.; MacGregor, D.S.; Oakley, R.T.; Reed, R.W.; Robertson, C.M. Prototypal dithiazolodithiazolyl radicals: Synthesis, structures, and transport properties. J. Am. Chem. Soc. 2003, 125, 14394-14403.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 14394-14403
-
-
Beer, L.1
Britten, J.F.2
Brusso, J.L.3
Cordes, A.W.4
Haddon, R.C.5
Itkis, M.E.6
MacGregor, D.S.7
Oakley, R.T.8
Reed, R.W.9
Robertson, C.M.10
-
33
-
-
53549129796
-
A diaminocarbene-phosphonium ylide: Direct access to c,c chelating ligands
-
Canac, Y.; Duhayon, C.; Chauvin, R. A diaminocarbene-phosphonium ylide: Direct access to C,C chelating ligands. Angew. Chem. 2007, 119, 6429-6431.
-
(2007)
Angew. Chem.
, vol.119
, pp. 6429-6431
-
-
Canac, Y.1
Duhayon, C.2
Chauvin, R.3
-
34
-
-
46349100846
-
Reaction of aromatic nitroso compounds with chemical models of 'thiamine active aldehyde'
-
Ferreira, L.M.; Marques, M.M.B.; Glória, P.M.C.; Chaves, H.T.; Franco, J.-P.P.; Mourato, I.; Antunes, J.-R.T.; Rzepa, H.S.; Lobo, A.M.; Prabhakar, S. Reaction of aromatic nitroso compounds with chemical models of 'thiamine active aldehyde'. Tetrahedron 2008, 64, 7759-7770.
-
(2008)
Tetrahedron
, vol.64
, pp. 7759-7770
-
-
Ferreira, L.M.1
Marques, M.M.B.2
Glória, P.M.C.3
Chaves, H.T.4
Franco, J.-P.P.5
Mourato, I.6
Antunes, J.-R.T.7
Rzepa, H.S.8
Lobo, A.M.9
Prabhakar, S.10
-
35
-
-
35948972820
-
Synthesis and characterization of elusive cyclo-di-and-tri-phosphino-13- diphosphonium salts: Fundamental frameworks in catenaorganophosphorus chemistry
-
Riegel, S.D.; Burford, N.; Lumsdenb, M.D.; Decken, A. Synthesis and characterization of elusive cyclo-di-and-tri-phosphino-1,3-diphosphonium salts: Fundamental frameworks in catenaorganophosphorus chemistry. Chem. Commun. 2007, 4668-4670.
-
(2007)
Chem. Commun.
, pp. 4668-4670
-
-
Riegel, S.D.1
Burford, N.2
Lumsdenb, M.D.3
Decken, A.4
-
36
-
-
36048945418
-
Preparation and characterization of a ligandstabilized trimethylphosphane dication
-
Weigand, J.J.; Burford, N.; Decken, A.; Schulz, A. Preparation and characterization of a ligandstabilized trimethylphosphane dication. Eur. J. Inorg. Chem. 2007, 2007, 4868-4872.
-
(2007)
Eur. J. Inorg. Chem.
, vol.2007
, pp. 4868-4872
-
-
Weigand, J.J.1
Burford, N.2
Decken, A.3
Schulz, A.4
-
37
-
-
41849101366
-
Nucleophilic fluoroalkylation of iminium salts
-
Levin, V.V.; Kozlov, M.A.; Song, Y.-H.; Dilman, A.D.; Belyakov, P.A.; Struchkova, M.I.; Tartakovsky, V.A. Nucleophilic fluoroalkylation of iminium salts. Tetrahedron Lett. 2008, 49, 3108-3111.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 3108-3111
-
-
Levin, V.V.1
Kozlov, M.A.2
Song, Y.-H.3
Dilman, A.D.4
Belyakov, P.A.5
Struchkova, M.I.6
Tartakovsky, V.A.7
-
38
-
-
0009488928
-
Methylaluminum bis(4-bromo-26-di-tert-butylphenoxide) as a key reagent for effecting primary a-alkylation of carbonyl compounds
-
Maruoka, K.; Sato, J.; Yamamoto, H. Methylaluminum bis(4-bromo-2,6-di- tert-butylphenoxide) as a key reagent for effecting primary a-alkylation of carbonyl compounds. J. Am. Chem. Soc. 1992, 114, 4422-4423.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4422-4423
-
-
Maruoka, K.1
Sato, J.2
Yamamoto, H.3
-
39
-
-
0001527718
-
The cheletropic fragmentation of hypervalent three-membered thiaheterocyclic intermediates
-
Zoller, U. The cheletropic fragmentation of hypervalent three-membered thiaheterocyclic intermediates. Tetrahedron 1988, 44, 7413-7426.
-
(1988)
Tetrahedron
, vol.44
, pp. 7413-7426
-
-
Zoller, U.1
-
40
-
-
0242626227
-
Hydrophobic highly conductive ambient-temperature molten salts
-
Bonhöte, P.; Dias, A.; Papageorgiou, N.; Kalyanasundaram, K.; Grätzel, M. Hydrophobic, highly conductive ambient-temperature molten salts. Inorg. Chem. 1996, 35, 1168-1178.
-
(1996)
Inorg. Chem.
, vol.35
, pp. 1168-1178
-
-
Bonhöte, P.1
Dias, A.2
Papageorgiou, N.3
Kalyanasundaram, K.4
Grätzel, M.5
-
41
-
-
0343410923
-
A comparison of leaving-group abilities in reactions of powerful methylating agents
-
Kevill, D.N.; Lin, G.M.L. A comparison of leaving-group abilities in reactions of powerful methylating agents. Tetrahedron Lett. 1978, 11, 949-952.
-
(1978)
Tetrahedron Lett.
, vol.11
, pp. 949-952
-
-
Kevill, D.N.1
Lin, G.M.L.2
-
42
-
-
84861512048
-
-
231st ACS National Meeting Atlanta GA USA March 26-30, Abstract I&EC 126
-
Ignat'ev, N.V.; Welz-Biermann, U.; Kucheryna, A.I.; Willner, H. Close the Gap: Synthesis of Highly Unsymmetrical Ionic Liquids; 231st ACS National Meeting, Atlanta, GA, USA, March 26-30, 2006; Abstract I&EC 126.
-
(2006)
Close the Gap: Synthesis of Highly Unsymmetrical Ionic Liquids
-
-
Ignat'ev, N.V.1
Welz-Biermann, U.2
Kucheryna, A.I.3
Willner, H.4
-
43
-
-
84861510008
-
-
WO2006/063656 A1,2006, Merck Patent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Welz-Biermann, U.; Kucheryna, A.; Willner, H. Method for Producing Onium Salts Comprising Alkyl- or Aryl-Sulfonate Anions or Alkyl-Aryl-Carboxylate Anions Having a Low Halide Content. WO 2006/063656 A1, 2006, Merck Patent GmbH, Darmstadt, Germany.
-
Method for Producing Onium Salts Comprising Alkyl- or Aryl-Sulfonate Anions or Alkyl-Aryl-Carboxylate Anions Having a Low Halide Content
-
-
Ignatyev, N.1
Welz-Biermann, U.2
Kucheryna, A.3
Willner, H.4
-
44
-
-
84861516877
-
How to make ionic liquids more liquid
-
Brennecke, J.F., Rogers, R.D., Seddon, K.R., Eds.; American Chemical Society, Washington, DC, USA, ACS Symposium Series 975, Chapter 22
-
Ignat'ev, N.V.; Kucheryna, A.; Bissky, G.; Willner, H. How to Make Ionic Liquids More Liquid. In Ionic Liquids: Not Just Solvents Anymore; Brennecke, J.F., Rogers, R.D., Seddon, K.R., Eds.; American Chemical Society, Washington, DC, USA, 2007; ACS Symposium Series 975, Chapter 22.
-
(2007)
Ionic Liquids: Not Just Solvents Anymore
-
-
Ignat'ev, N.V.1
Kucheryna, A.2
Bissky, G.3
Willner, H.4
-
45
-
-
23044444096
-
New ionic liquids with tris(perfluoroalkyl)trifluorophosphate (fap) anions
-
Ignat'ev, N.V.; Welz-Biermann, U.; Kucheryna, A.; Bissky, G.; Willner, H. New ionic liquids with tris(perfluoroalkyl)trifluorophosphate (FAP) anions. J. Fluorine Chem. 2005, 126, 1150-1159.
-
(2005)
J. Fluorine Chem.
, vol.126
, pp. 1150-1159
-
-
Ignat'ev, N.V.1
Welz-Biermann, U.2
Kucheryna, A.3
Bissky, G.4
Willner, H.5
-
46
-
-
84861518147
-
-
WO 2007/014613,2007, MerckPatent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Welz-Biermann, U.; Koppe, K.; Barthen, P.; Frohn, H.-J. Dehydration of Alcohols to Form Alkenes or Ethers. WO 2007/014613, 2007, Merck Patent GmbH, Darmstadt, Germany.
-
Dehydration of Alcohols to Form Alkenes or Ethers
-
-
Ignatyev, N.1
Welz-Biermann, U.2
Koppe, K.3
Barthen, P.4
Frohn, H.-J.5
-
47
-
-
84861510011
-
-
WO2007/104380,2007, Merck Patent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Koppe, K.; Frohn, H.-J.; Barthen, P. Splitting of Dialkoxyalkanes in Ionic Liquids. WO 2007/104380, 2007, Merck Patent GmbH, Darmstadt, Germany.
-
Splitting of Dialkoxyalkanes in Ionic Liquids
-
-
Ignatyev, N.1
Koppe, K.2
Frohn, H.-J.3
Barthen, P.4
-
48
-
-
84861512052
-
-
WO 2008/086847 A2,2008, MerckPatent GmbH, Darmstadt, Germany
-
Ignatyev, N.; Koppe, K.; Barthen, P.; Frohn, H.-J. Synthesis of Chromane Derivatives. WO 2008/086847 A2, 2008, Merck Patent GmbH, Darmstadt, Germany.
-
Synthesis of Chromane Derivatives
-
-
Ignatyev, N.1
Koppe, K.2
Barthen, P.3
Frohn, H.-J.4
|