메뉴 건너뛰기




Volumn 112, Issue 1, 2010, Pages 31-50

The refinement of renewable resources: New important derivatives of fatty acids and glycerol

Author keywords

Catalysis; Fats; Glycerol; Oils; Transition metals

Indexed keywords

BRASSICA NAPUS; ELAEIS; HELIANTHUS;

EID: 77049108689     PISSN: 14387697     EISSN: 14389312     Source Type: Journal    
DOI: 10.1002/ejlt.200900091     Document Type: Review
Times cited : (107)

References (130)
  • 2
    • 10444273957 scopus 로고    scopus 로고
    • Products and processes for a sustainable chemical industry: A review of achievements and prospects
    • J.F. Jenck, F. Agterberg, M.J. Droescher: Products and processes for a sustainable chemical industry: A review of achievements and prospects. Green Chem. 2004, 6, 544-556.
    • (2004) Green Chem , vol.6 , pp. 544-556
    • Jenck, J.F.1    Agterberg, F.2    Droescher, M.J.3
  • 3
    • 20344372708 scopus 로고    scopus 로고
    • Production of liquid alkanes by aqueous-phase processing of biomass-derived carbohydrates
    • G.W. Huber, J.N. Chheda, C.J. Barrett, J.A. Dumesic: Production of liquid alkanes by aqueous-phase processing of biomass-derived carbohydrates. Science. 2005, 308, 1446-1450.
    • (2005) Science , vol.308 , pp. 1446-1450
    • Huber, G.W.1    Chheda, J.N.2    Barrett, C.J.3    Dumesic, J.A.4
  • 5
    • 34249113083 scopus 로고    scopus 로고
    • Non-food use of oils and fats
    • F.D. Gunstone: Non-food use of oils and fats. Lipid Technol. 2006, 18, 216.
    • (2006) Lipid Technol , vol.18 , pp. 216
    • Gunstone, F.D.1
  • 7
    • 44049103461 scopus 로고    scopus 로고
    • Catalytic processes for the technical use of natural fats and oils
    • A. Behr, A. Westfechtel, J. Pérez Gomes: Catalytic processes for the technical use of natural fats and oils. Chem Eng Technol. 2008, 31, 700-714.
    • (2008) Chem Eng Technol , vol.31 , pp. 700-714
    • Behr, A.1    Westfechtel, A.2    Pérez Gomes, J.3
  • 10
    • 0035110268 scopus 로고    scopus 로고
    • Polymers and surfactants on the basis of renewable resources
    • S. Warwel, F. Bruse, C. Demes, M. Kunz, M.R.G. Klaas: Polymers and surfactants on the basis of renewable resources. Chemosphere. 2001, 43, 39-48.
    • (2001) Chemosphere , vol.43 , pp. 39-48
    • Warwel, S.1    Bruse, F.2    Demes, C.3    Kunz, M.4    Klaas, M.R.G.5
  • 11
    • 0015372606 scopus 로고
    • Role of fats and oils in pharmaceuticals
    • J.B. Jerome: Role of fats and oils in pharmaceuticals. J Am Oil Chem Soc. 1972, 49, 405-408.
    • (1972) J Am Oil Chem Soc , vol.49 , pp. 405-408
    • Jerome, J.B.1
  • 12
    • 77049102817 scopus 로고
    • Glycerol in pharmaceuticals and cosmetics
    • F.J. Steele: Glycerol in pharmaceuticals and cosmetics. Am Prof Pharm. 1957, 23, 959-963.
    • (1957) Am Prof Pharm , vol.23 , pp. 959-963
    • Steele, F.J.1
  • 15
    • 0344305526 scopus 로고    scopus 로고
    • Chromatographic reactors: Esterification of glycerol with acetic acid using acidic polymeric resins
    • D. Gelosa, M. Ramaioli, G.Valente, M. Morbidelli: Chromatographic reactors: Esterification of glycerol with acetic acid using acidic polymeric resins. Ind Eng Chem Res. 2003, 42, 6536-6544.
    • (2003) Ind Eng Chem Res , vol.42 , pp. 6536-6544
    • Gelosa, D.1    Ramaioli, M.2    Valente, G.3    Morbidelli, M.4
  • 16
    • 0001168269 scopus 로고
    • Homogeneous transition-metal catalysis in oleochemistry
    • A. Behr: Homogeneous transition-metal catalysis in oleochemistry. Fat Sci Technol. 1990, 92, 376-388.
    • (1990) Fat Sci Technol , vol.92 , pp. 376-388
    • Behr, A.1
  • 18
    • 84982066730 scopus 로고
    • Homogeneous selective catalytic hydrogenation of soybean oil
    • E. Fedeli, G. Jacini: Homogeneous selective catalytic hydrogenation of soybean oil. Fette Seifen Anstrichm. 1976, 78, 30-34.
    • (1976) Fette Seifen Anstrichm , vol.78 , pp. 30-34
    • Fedeli, E.1    Jacini, G.2
  • 19
    • 0022027032 scopus 로고
    • Homogeneous catalytic hydrogenation of soybean oil: Palladium acetylacetonate
    • S. Koritala: Homogeneous catalytic hydrogenation of soybean oil: Palladium acetylacetonate. J Am Oil Chem Soc. 1985, 62, 517-520.
    • (1985) J Am Oil Chem Soc , vol.62 , pp. 517-520
    • Koritala, S.1
  • 20
    • 77049101147 scopus 로고
    • Correlation effect between fatty acids and nickel catalyst during hydrogenation
    • V. Filip, J. Zajic: Correlation effect between fatty acids and nickel catalyst during hydrogenation. Fat Sci Technol. 1987, 89, 220-224.
    • (1987) Fat Sci Technol , vol.89 , pp. 220-224
    • Filip, V.1    Zajic, J.2
  • 21
    • 0021428387 scopus 로고
    • Homogeneously catalyzed hydrogenation and gas-liquid chromatography analysis of the methyl esters of cyclopropene fatty acids
    • W.J. Bland, T.C. Dine, R.N. Jobanputra, G.G. Shone: Homogeneously catalyzed hydrogenation and gas-liquid chromatography analysis of the methyl esters of cyclopropene fatty acids. J Am Oil Chem Soc. 1984, 61, 924-928.
    • (1984) J Am Oil Chem Soc , vol.61 , pp. 924-928
    • Bland, W.J.1    Dine, T.C.2    Jobanputra, R.N.3    Shone, G.G.4
  • 26
    • 0347898718 scopus 로고    scopus 로고
    • Platinum-catalysed hydrosilylation of unsaturated fatty acid esters
    • A. Behr, F. Naendrup, D. Obst: Platinum-catalysed hydrosilylation of unsaturated fatty acid esters. Adv Synth Catal. 2002, 344, 1142-1145.
    • (2002) Adv Synth Catal , vol.344 , pp. 1142-1145
    • Behr, A.1    Naendrup, F.2    Obst, D.3
  • 27
    • 77049092227 scopus 로고    scopus 로고
    • Catalytic hydrosilylation of fatty compounds
    • V. Eds. N. Auner, J. Weis, Wiley-VCH, Weinheim (Germany)
    • A. Behr, F. Naendrup, D. Obst: Catalytic hydrosilylation of fatty compounds. In: Organosilicon Chemistry V. Eds. N. Auner, J. Weis, Wiley-VCH, Weinheim (Germany) 2003.
    • (2003) Organosilicon Chemistry
    • Behr, A.1    Naendrup, F.2    Obst, D.3
  • 28
    • 0036005351 scopus 로고    scopus 로고
    • The synthesis of silicon oleochemicals by hydrosilylation of unsaturated fatty acid derivatives
    • A. Behr, F. Naendrup, D. Obst: The synthesis of silicon oleochemicals by hydrosilylation of unsaturated fatty acid derivatives. Eur J Lipid Sci Technol. 2002, 104, 161-166.
    • (2002) Eur J Lipid Sci Technol , vol.104 , pp. 161-166
    • Behr, A.1    Naendrup, F.2    Obst, D.3
  • 29
    • 34249078792 scopus 로고
    • Etude préliminaire de l'hydroformylation de l'oléate de méthyle
    • R. Lai, M. Naudet, E. Ucciani: Étude préliminaire de l'hydroformylation de l'oléate de méthyle. Rev Fr Corps Gras. 1966, 13, 737-745.
    • (1966) Rev Fr Corps Gras , vol.13 , pp. 737-745
    • Lai, R.1    Naudet, M.2    Ucciani, E.3
  • 30
    • 34249044744 scopus 로고
    • Etude complémentaire de l'hydroformylation de l'oléate de méthyle
    • R. Lai, M. Naudet, E. Ucciani: Étude complémentaire de l'hydroformylation de l'oléate de méthyle. Rev Fr Corps Gras. 1968, 15, 15-21.
    • (1968) Rev Fr Corps Gras , vol.15 , pp. 15-21
    • Lai, R.1    Naudet, M.2    Ucciani, E.3
  • 32
    • 0000553796 scopus 로고    scopus 로고
    • Recent developments of hydroformylation of olefins of higher molecular weight into oxo-alcohols
    • B. Fell: Recent developments of hydroformylation of olefins of higher molecular weight into oxo-alcohols. Tens Surf Deterg. 1998, 35, 326-337.
    • (1998) Tens Surf Deterg , vol.35 , pp. 326-337
    • Fell, B.1
  • 33
    • 0037124245 scopus 로고    scopus 로고
    • The hydroformylation of vegetable oils and model compounds by ligand modified rhodium catalysis
    • P. Kandanarachchi, A. Guo, Z. Petrovic: The hydroformylation of vegetable oils and model compounds by ligand modified rhodium catalysis. J Mol Catal A Chem. 2002, 184, 65-71.
    • (2002) J Mol Catal A Chem , vol.184 , pp. 65-71
    • Kandanarachchi, P.1    Guo, A.2    Petrovic, Z.3
  • 34
    • 18244409360 scopus 로고    scopus 로고
    • Isomerising hydroformylation of fatty acids esters: Formation of omega-aldehydes
    • A. Behr, D. Obst, A. Westfechtel: Isomerising hydroformylation of fatty acids esters: Formation of omega-aldehydes. Eur J Lipid Sci Technol. 2005, 107, 213-219.
    • (2005) Eur J Lipid Sci Technol , vol.107 , pp. 213-219
    • Behr, A.1    Obst, D.2    Westfechtel, A.3
  • 35
    • 24944448712 scopus 로고    scopus 로고
    • Dicarboxylic acid esters from the carbonylation of unsaturated esters under mild conditions
    • C. Jiménez-Rodriguez, G.R. Eastham, D.J. Cole-Hamilton: Dicarboxylic acid esters from the carbonylation of unsaturated esters under mild conditions. Inorg Chem Commun. 2005, 8, 878-881.
    • (2005) Inorg Chem Commun , vol.8 , pp. 878-881
    • Jiménez-Rodriguez, C.1    Eastham, G.R.2    Cole-Hamilton, D.J.3
  • 37
    • 77049101930 scopus 로고    scopus 로고
    • Hydroaminomethylation of alkenes
    • A. Boerner, M. Beller, B. Wünsch: Hydroaminomethylation of alkenes. Sci Synth. 2009, 40a, 111-117.
    • (2009) Sci Synth , vol.40 a , pp. 111-117
    • Boerner, A.1    Beller, M.2    Wünsch, B.3
  • 38
    • 34247890085 scopus 로고    scopus 로고
    • Catalytic hydroaminomethylation for highly selective synthesis of linear fatty amines
    • C. Buch, R. Jackstell, D. Bühring, M. Beller: Catalytic hydroaminomethylation for highly selective synthesis of linear fatty amines. Chem Ing Tech. 2007, 79, 434-441.
    • (2007) Chem Ing Tech , vol.79 , pp. 434-441
    • Buch, C.1    Jackstell, R.2    Bühring, D.3    Beller, M.4
  • 39
    • 23444436410 scopus 로고    scopus 로고
    • Hydroaminomethylation in thermomorphic solvent systems
    • A. Behr, R. Roll: Hydroaminomethylation in thermomorphic solvent systems. J Mol Catal A Chem. 2005, 239, 180-184.
    • (2005) J Mol Catal A Chem , vol.239 , pp. 180-184
    • Behr, A.1    Roll, R.2
  • 40
    • 0034391858 scopus 로고    scopus 로고
    • Hydroaminomethylation of fatty acids with primary and secondary amines - A new route to interesting surfactant substrates
    • A. Behr, M. Fiene, C. Buß, P. Eilbracht: Hydroaminomethylation of fatty acids with primary and secondary amines - A new route to interesting surfactant substrates. Eur J Lipid Sci Technol. 2000, 102, 467-471.
    • (2000) Eur J Lipid Sci Technol , vol.102 , pp. 467-471
    • Behr, A.1    Fiene, M.2    Buß, C.3    Eilbracht, P.4
  • 41
    • 34347372676 scopus 로고    scopus 로고
    • New environmentally acceptable process for manufacture of primary amines by hydroaminomethylation of olefins in supercritical ammonia
    • A. Martin, M. Kant, R. Jackstell, H. Klein, M. Beller: New environmentally acceptable process for manufacture of primary amines by hydroaminomethylation of olefins in supercritical ammonia. Chem Ing Tech. 2007, 79, 891-900.
    • (2007) Chem Ing Tech , vol.79 , pp. 891-900
    • Martin, A.1    Kant, M.2    Jackstell, R.3    Klein, H.4    Beller, M.5
  • 42
    • 55449136490 scopus 로고    scopus 로고
    • Synthesis of alkyl-branched fatty acids
    • U. Biermanm, J.O. Metzger: Synthesis of alkyl-branched fatty acids. Eur J Lipid Sci Technol. 2008, 110, 805-811.
    • (2008) Eur J Lipid Sci Technol , vol.110 , pp. 805-811
    • Biermanm, U.1    Metzger, J.O.2
  • 43
    • 0346388976 scopus 로고    scopus 로고
    • Einsatz ionischer Flüssigkeiten bei der Diels-Alder-Reaktion mit Oleochemikalien
    • A. Behr, F. Naendrup, S. Nave: Einsatz ionischer Flüssigkeiten bei der Diels-Alder-Reaktion mit Oleochemikalien. Chem Ing Tech. 2002, 74, 1174-1177.
    • (2002) Chem Ing Tech , vol.74 , pp. 1174-1177
    • Behr, A.1    Naendrup, F.2    Nave, S.3
  • 44
    • 0001169494 scopus 로고    scopus 로고
    • Addition of glyoxylic acid ethyl ester to unsaturated acid derivatives
    • A. Behr, M. Fiene: Addition of glyoxylic acid ethyl ester to unsaturated acid derivatives. Fett/Lipid. 1999, 101, 199-202.
    • (1999) Fett/Lipid , vol.101 , pp. 199-202
    • Behr, A.1    Fiene, M.2
  • 45
    • 0034340776 scopus 로고    scopus 로고
    • Lewis-acid catalysed ene reaction of electron-deficient aldehydes and ketones at unsaturated fatty acid derivatives
    • A. Behr, M. Fiene: Lewis-acid catalysed ene reaction of electron-deficient aldehydes and ketones at unsaturated fatty acid derivatives. Eur J Lipid Sci Technol. 2000, 102, 212-217.
    • (2000) Eur J Lipid Sci Technol , vol.102 , pp. 212-217
    • Behr, A.1    Fiene, M.2
  • 46
    • 0034343051 scopus 로고    scopus 로고
    • Transitionmetal trifluoromethane-sulphonates - recyclable catalysts for the synthesis of branched fatty derivatives by Diels-Alder reactions at unsaturated fatty esters
    • A. Behr, M. Fiene, F. Naendrup, K. Schürmann: Transitionmetal trifluoromethane-sulphonates - recyclable catalysts for the synthesis of branched fatty derivatives by Diels-Alder reactions at unsaturated fatty esters. Eur J Lipid Sci Technol. 2000, 102, 342-350.
    • (2000) Eur J Lipid Sci Technol , vol.102 , pp. 342-350
    • Behr, A.1    Fiene, M.2    Naendrup, F.3    Schürmann, K.4
  • 47
    • 34249001277 scopus 로고
    • Katalytische Oligomerisierung von Fettsäuren
    • A. Behr, S. Bellmann, H.-P. Handwerk: Katalytische Oligomerisierung von Fettsäuren. Fat Sci Technol. 1992, 93, 340-345.
    • (1992) Fat Sci Technol , vol.93 , pp. 340-345
    • Behr, A.1    Bellmann, S.2    Handwerk, H.-P.3
  • 48
    • 0001552264 scopus 로고
    • Ubergangsmetallkatalysierte Addition von Maleinsäureanhydrid an Fettstoffe
    • A. Behr, H.-P. Handwerk: Übergangsmetallkatalysierte Addition von Maleinsäureanhydrid an Fettstoffe. Fat Sci Technol. 1992, 94, 204-208.
    • (1992) Fat Sci Technol , vol.94 , pp. 204-208
    • Behr, A.1    Handwerk, H.-P.2
  • 49
    • 0000723023 scopus 로고
    • Katalytische Verknüpfung ungesättigter Fettstoffe mit Formaldehyd
    • A. Behr, H.-P. Handwerk: Katalytische Verknüpfung ungesättigter Fettstoffe mit Formaldehyd. Fat Sci Technol. 1992, 94, 443-447.
    • (1992) Fat Sci Technol , vol.94 , pp. 443-447
    • Behr, A.1    Handwerk, H.-P.2
  • 50
    • 34249029859 scopus 로고
    • Katalytische Addition von Acrylund Vinylverbindungen an ungesättigten Fettstoffen
    • A. Behr, H.-P. Handwerk: Katalytische Addition von Acrylund Vinylverbindungen an ungesättigten Fettstoffen. Chem Ing Tech. 1993, 65, 1377-1379.
    • (1993) Chem Ing Tech , vol.65 , pp. 1377-1379
    • Behr, A.1    Handwerk, H.-P.2
  • 53
    • 77049101146 scopus 로고    scopus 로고
    • Utilisations et application des matières premières renouvables
    • D. Proriol: Utilisations et application des matières premières renouvables. Oléagineux Corps Gras Lipides. 2003, 10, 370-372.
    • (2003) Oléagineux Corps Gras Lipides , vol.10 , pp. 370-372
    • Proriol, D.1
  • 54
    • 77049125472 scopus 로고
    • (Henkel KGaA): German Patent 4002008
    • A. Behr, A. Laufenberg (Henkel KGaA): German Patent 4002008 (1990).
    • (1990)
    • Behr, A.1    Laufenberg, A.2
  • 55
    • 77049127749 scopus 로고
    • (Henkel KGaA): German Patent 4002009
    • A. Behr, A. Laufenberg (Henkel KGaA): German Patent 4002009 (1990).
    • (1990)
    • Behr, A.1    Laufenberg, A.2
  • 56
    • 77049095116 scopus 로고
    • (Henkel KGaA): German Patent 4002012
    • A. Behr, A. Laufenberg (Henkel KGaA): German Patent 4002012 (1990).
    • (1990)
    • Behr, A.1    Laufenberg, A.2
  • 57
    • 77049106550 scopus 로고
    • (Henkel KGaA): German Patent 4002011
    • A. Behr, A. Laufenberg (Henkel KGaA): German Patent 4002011 (1990).
    • (1990)
    • Behr, A.1    Laufenberg, A.2
  • 58
    • 0002608883 scopus 로고
    • Synthese neuer verzweigter Fettsäureester durch homogene Rhodiumkatalyse
    • A. Behr, A. Laufenberg: Synthese neuer verzweigter Fettsäureester durch homogene Rhodiumkatalyse. Fat Sci Technol. 1991, 93, 20-24.
    • (1991) Fat Sci Technol , vol.93 , pp. 20-24
    • Behr, A.1    Laufenberg, A.2
  • 59
    • 0037453186 scopus 로고    scopus 로고
    • Rhodium-catalyzed synthesis of branched fatty compounds in temperature-dependent solvent systems
    • A. Behr, C. Fängewisch: Rhodium-catalyzed synthesis of branched fatty compounds in temperature-dependent solvent systems. J Mol Catal A Chem. 2003, 197, 115-126.
    • (2003) J Mol Catal A Chem , vol.197 , pp. 115-126
    • Behr, A.1    Fängewisch, C.2
  • 60
    • 5144228359 scopus 로고    scopus 로고
    • A new temperature-dependent solvent system based on polyethylene glycol 1000 and its use in rhodium catalysed cooligomerisation
    • A. Behr, Q. Miao: A new temperature-dependent solvent system based on polyethylene glycol 1000 and its use in rhodium catalysed cooligomerisation. J Mol Catal A Chem. 2004, 222, 127-132.
    • (2004) J Mol Catal A Chem , vol.222 , pp. 127-132
    • Behr, A.1    Miao, Q.2
  • 61
    • 77049106054 scopus 로고    scopus 로고
    • http://nobelprize.org/nobel_prizes/chemistry/laureates/2005/index.html.
  • 62
    • 0038362094 scopus 로고
    • Metathesis of functionalized olefins
    • J.C. Mol: Metathesis of functionalized olefins. Chemtech. 1983, 13, 250-255.
    • (1983) Chemtech , vol.13 , pp. 250-255
    • Mol, J.C.1
  • 63
    • 0020709619 scopus 로고
    • Metathesis of fatty-acid esters
    • C. Boelhouwer, J.C. Mol: Metathesis of fatty-acid esters. JAm Oil Chem Soc. 1984, 61, 425-430.
    • (1984) JAm Oil Chem Soc , vol.61 , pp. 425-430
    • Boelhouwer, C.1    Mol, J.C.2
  • 64
    • 0022025072 scopus 로고
    • Metathesis of methyl oleate with a homogeneous and a heterogeneous catalyst
    • H. Kohashi, T.A. Foglia: Metathesis of methyl oleate with a homogeneous and a heterogeneous catalyst. J Am Oil Chem Soc. 1985, 62, 549-554.
    • (1985) J Am Oil Chem Soc , vol.62 , pp. 549-554
    • Kohashi, H.1    Foglia, T.A.2
  • 65
    • 37049112160 scopus 로고
    • 4,a highly-active catalyst for the metathesis of functionalized alkenes
    • 4,a highly-active catalyst for the metathesis of functionalized alkenes. Chem Commun. 1985, 631-633.
    • (1985) Chem Commun , pp. 631-633
    • Xiaoding, X.1    Mol, J.C.2
  • 68
    • 34248995471 scopus 로고
    • Olefin-Metathese ungesättigter C18Fettstoffe
    • S. Warwel, A. Deckers: Olefin-Metathese ungesättigter C18Fettstoffe. Tenside Deterg. 1989, 26, 252-259.
    • (1989) Tenside Deterg , vol.26 , pp. 252-259
    • Warwel, S.1    Deckers, A.2
  • 69
    • 0026414952 scopus 로고
    • Activity of supported Re2O7 catalysts for the metathesis of methyl oleate
    • M. Sibeijn, J.C. Mol: Activity of supported Re2O7 catalysts for the metathesis of methyl oleate. Appl Catal. 1991, 67, 279-295.
    • (1991) Appl Catal , vol.67 , pp. 279-295
    • Sibeijn, M.1    Mol, J.C.2
  • 71
    • 34249079960 scopus 로고
    • Fatty-acids as chemical raw-materials
    • S. Warwel: Fatty-acids as chemical raw-materials. Fat Sci Technol. 1992, 94, 512-523.
    • (1992) Fat Sci Technol , vol.94 , pp. 512-523
    • Warwel, S.1
  • 72
    • 0000789392 scopus 로고
    • Metathesis of unsaturated fatty acid esters - a simple approach to long-chained dicarboxylic-acids
    • S. Warwel, H.-G. Jägers, S. Thomas: Metathesis of unsaturated fatty acid esters - a simple approach to long-chained dicarboxylic-acids. Fat Sci Technol. 1992, 94, 323-328.
    • (1992) Fat Sci Technol , vol.94 , pp. 323-328
    • Warwel, S.1    Jägers, H.-G.2    Thomas, S.3
  • 73
    • 0028429898 scopus 로고
    • Metathesis of unsaturated fatty-acid esters and fatty oils
    • J.C. Mol: Metathesis of unsaturated fatty-acid esters and fatty oils. J Mol Catal. 1994, 90, 185-199.
    • (1994) J Mol Catal , vol.90 , pp. 185-199
    • Mol, J.C.1
  • 74
    • 57249113641 scopus 로고    scopus 로고
    • Application of olefin metathesis in oleochemistry: An example of green chemistry
    • J.C. Mol: Application of olefin metathesis in oleochemistry: An example of green chemistry. Green Chem. 2002, 4, 5-13.
    • (2002) Green Chem , vol.4 , pp. 5-13
    • Mol, J.C.1
  • 75
    • 3543136004 scopus 로고    scopus 로고
    • Catalytic metathesis of unsaturated fatty acid esters and oils
    • J.C. Mol: Catalytic metathesis of unsaturated fatty acid esters and oils. Topics Catal. 2004, 27, 97-104.
    • (2004) Topics Catal , vol.27 , pp. 97-104
    • Mol, J.C.1
  • 76
    • 33746917204 scopus 로고    scopus 로고
    • Metathesis of unsaturated fatty acids: Synthesis of long-chain unsaturated - alpha, omega - dicarboxylic acids
    • H.L. Ngo, K. Jones, T.A. Foglia: Metathesis of unsaturated fatty acids: Synthesis of long-chain unsaturated - alpha, omega - dicarboxylic acids. J Am Oil Chem Soc. 2006, 83, 629-634.
    • (2006) J Am Oil Chem Soc , vol.83 , pp. 629-634
    • Ngo, H.L.1    Jones, K.2    Foglia, T.A.3
  • 77
    • 0001855961 scopus 로고    scopus 로고
    • 2. Influence of the alkylidene moiety on the metathesis activity
    • 2. Influence of the alkylidene moiety on the metathesis activity. J Am Chem Soc. 1996, 118, 100-110.
    • (1996) J Am Chem Soc. , vol.118 , pp. 100-110
    • Schwab, P.1    Grubbs, R.H.2    Ziller, J.W.3
  • 78
    • 0034746687 scopus 로고    scopus 로고
    • 2Ru=CHR olefin metathesis catalysts: An organometallic success story
    • 2Ru=CHR olefin metathesis catalysts: An organometallic success story. Acc Chem Res. 2001, 34, 18-29.
    • (2001) Acc Chem Res , vol.34 , pp. 18-29
    • Trnka, T.M.1    Grubbs, R.H.2
  • 79
    • 0000713963 scopus 로고    scopus 로고
    • Indenylidene-imidazolylidene complexes of ruthenium as ringclosing metathesis catalysts
    • L. Jafarpour, H.-J. Schanz, E.D. Stevens, S.P. Nolan: Indenylidene-imidazolylidene complexes of ruthenium as ringclosing metathesis catalysts. Organometallics. 1999, 18, 5416-5419.
    • (1999) Organometallics , vol.18 , pp. 5416-5419
    • Jafarpour, L.1    Schanz, H.-J.2    Stevens, E.D.3    Nolan, S.P.4
  • 80
    • 35048885561 scopus 로고    scopus 로고
    • N-Heterocyclic carbene and phosphine ruthenium indenylidene precatalysts: A comparative study in olefin metathesis
    • H. Clavier, S. Nolan: N-Heterocyclic carbene and phosphine ruthenium indenylidene precatalysts: A comparative study in olefin metathesis. Chem Eur J. 2007, 13, 8029-8036.
    • (2007) Chem Eur J , vol.13 , pp. 8029-8036
    • Clavier, H.1    Nolan, S.2
  • 82
    • 3342982883 scopus 로고    scopus 로고
    • Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation
    • A. Michrowska, R. Bujok, S. Harutyunyan, V. Sashuk, G. Dolognus, K. Grela: Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation. J Am Chem Soc. 2004, 126, 9318-9325.
    • (2004) J Am Chem Soc , vol.126 , pp. 9318-9325
    • Michrowska, A.1    Bujok, R.2    Harutyunyan, S.3    Sashuk, V.4    Dolognus, G.5    Grela, K.6
  • 83
    • 43049140817 scopus 로고    scopus 로고
    • Ruthenium carbene mediated metathesis of oleate-type fatty compounds
    • B.B. Marvey, C.K. Segakweng, M.H. Vosloo: Ruthenium carbene mediated metathesis of oleate-type fatty compounds. Int Mol Sci. 2008, 9, 615-625.
    • (2008) Int Mol Sci , vol.9 , pp. 615-625
    • Marvey, B.B.1    Segakweng, C.K.2    Vosloo, M.H.3
  • 84
    • 2442625578 scopus 로고    scopus 로고
    • Renewable monomer feedstocks via olefin metathesis: Fundamental mechanistic studies of methyl oleate ethenolysis with the firstgeneration Grubbs catalyst
    • K.A. Burdett, L.D. Harris, P. Margl, B.R. Maughon, T. Mokhtar-Zadeh, P.C. Saucier, E.P. Wasserman: Renewable monomer feedstocks via olefin metathesis: Fundamental mechanistic studies of methyl oleate ethenolysis with the firstgeneration Grubbs catalyst. Organometallics. 2004, 23, 2027-2047.
    • (2004) Organometallics , vol.23 , pp. 2027-2047
    • Burdett, K.A.1    Harris, L.D.2    Margl, P.3    Maughon, B.R.4    Mokhtar-Zadeh, T.5    Saucier, P.C.6    Wasserman, E.P.7
  • 85
    • 33751378204 scopus 로고    scopus 로고
    • Metathesis of renewable unsaturated fatty acid esters catalysed by a phoban-indenylidene ruthenium catalyst
    • G.S. Forman, R.M. Bellabarba, R.P. Tooze, A.M.Z. Slawin, R. Karch, R. Winde: Metathesis of renewable unsaturated fatty acid esters catalysed by a phoban-indenylidene ruthenium catalyst. J Organomet Chem. 2006, 691, 5513-5516.
    • (2006) J Organomet Chem , vol.691 , pp. 5513-5516
    • Forman, G.S.1    Bellabarba, R.M.2    Tooze, R.P.3    Slawin, A.M.Z.4    Karch, R.5    Winde, R.6
  • 87
    • 0000789392 scopus 로고
    • Metathesis of unsaturated fatty acid esters-A simple approach to long-chained dicarboxylic acids
    • S. Warwel, H.G. Jaegers, S. Thomas: Metathesis of unsaturated fatty acid esters. A simple approach to long-chained dicarboxylic acids. Fett Wiss Technol. 1992, 94, 323-328.
    • (1992) Fett Wiss Technol. , vol.94 , pp. 323-328
    • Warwel, S.1    Jaegers, H.G.2    Thomas, S.3
  • 88
    • 0038307825 scopus 로고    scopus 로고
    • New polymers from plant oils as raw material
    • S. Warwel, F. Bruese, M. Kunz: New polymers from plant oils as raw material. Fresenius Environ Bull. 2003, 12, 534-539.
    • (2003) Fresenius Environ Bull , vol.12 , pp. 534-539
    • Warwel, S.1    Bruese, F.2    Kunz, M.3
  • 89
    • 33646561851 scopus 로고    scopus 로고
    • High conversion and productive catalyst turnovers in cross-metathesis reactions of natural oils with 2butene
    • J. Patel, S. Mujcinovic, W.R. Jackson, A.J. Robinson, A.K. Serelis, C. Such: High conversion and productive catalyst turnovers in cross-metathesis reactions of natural oils with 2butene. Green Chem. 2006, 8, 450-454.
    • (2006) Green Chem , vol.8 , pp. 450-454
    • Patel, J.1    Mujcinovic, S.2    Jackson, W.R.3    Robinson, A.J.4    Serelis, A.K.5    Such, C.6
  • 91
    • 52949149348 scopus 로고    scopus 로고
    • Cross-metathesis of oleyl alcohol with methyl acrylate: Optimization of reaction conditions and comparison of their environmental impact
    • A. Rybak, M.A.R. Meier: Cross-metathesis of oleyl alcohol with methyl acrylate: Optimization of reaction conditions and comparison of their environmental impact. Green Chem. 2008, 10, 1099-1104.
    • (2008) Green Chem , vol.10 , pp. 1099-1104
    • Rybak, A.1    Meier, M.A.R.2
  • 92
    • 57649217307 scopus 로고    scopus 로고
    • Cross-metathesis reactions of allyl chloride with fatty acid methyl esters: Efficient synthesis of a,o-difunctional chemical intermediates from renewable raw materials
    • T. Jacobs, A. Rybak, M.A.R. Meier: Cross-metathesis reactions of allyl chloride with fatty acid methyl esters: Efficient synthesis of a,o-difunctional chemical intermediates from renewable raw materials. Appl Catal A Gen. 2009, 353, 32-35.
    • (2009) Appl Catal A Gen , vol.353 , pp. 32-35
    • Jacobs, T.1    Rybak, A.2    Meier, M.A.R.3
  • 93
    • 70149112400 scopus 로고    scopus 로고
    • A direct route to bifunctional aldehyde derivatives via selfand crossmetathesis of unsaturated aldehydes
    • X. Miao, C. Fischmeister, C. Bruneau, P.H. Dixneuf: A direct route to bifunctional aldehyde derivatives via selfand crossmetathesis of unsaturated aldehydes. ChemSusChem. 2009, 2, 542-545.
    • (2009) ChemSusChem , vol.2 , pp. 542-545
    • Miao, X.1    Fischmeister, C.2    Bruneau, C.3    Dixneuf, P.H.4
  • 94
    • 66149123451 scopus 로고    scopus 로고
    • Renewable materials as precursors of linear nitrile-acid derivatives via cross-metathesis of fatty esters and acids with acrylonitrile and fumaronitrile
    • R. Malacea, C. Fischmeister, C. Bruneau, J.-L. Dubois, J.-L. Couturier, P.H. Dixneuf: Renewable materials as precursors of linear nitrile-acid derivatives via cross-metathesis of fatty esters and acids with acrylonitrile and fumaronitrile. Green Chem. 2009, 11, 152-155.
    • (2009) Green Chem , vol.11 , pp. 152-155
    • Malacea, R.1    Fischmeister, C.2    Bruneau, C.3    Dubois, J.-L.4    Couturier, J.-L.5    Dixneuf, P.H.6
  • 95
    • 37049124316 scopus 로고
    • Metathesis of unsaturated fatty acid esters by a homogeneous tungsten hexachloride-tetramethyltin catalyst
    • P.B. Van Dam, M.C. Mittelmeijer, C. Boelhouwer: Metathesis of unsaturated fatty acid esters by a homogeneous tungsten hexachloride-tetramethyltin catalyst. Chem Commun. 1972, 1221-1222.
    • (1972) Chem Commun , pp. 1221-1222
    • Van Dam, P.B.1    Mittelmeijer, M.C.2    Boelhouwer, C.3
  • 96
    • 0036737289 scopus 로고    scopus 로고
    • Structure and properties of triolein-based polyurethane networks
    • A. Zlatanić, Z.S. Petrović, K. Dušek: Structure and properties of triolein-based polyurethane networks. Biomacromolecules. 2002, 3, 1048-1056.
    • (2002) Biomacromolecules , vol.3 , pp. 1048-1056
    • Zlatanić, A.1    Petrović, Z.S.2    Dušek, K.3
  • 97
    • 55449118988 scopus 로고    scopus 로고
    • Oxidation of unsaturated fatty acid derivatives and vegetable oils
    • A. Köckritz, A. Martin: Oxidation of unsaturated fatty acid derivatives and vegetable oils. Eur J Lipid Sci Technol. 2009, 110, 812-824.
    • (2009) Eur J Lipid Sci Technol , vol.110 , pp. 812-824
    • Köckritz, A.1    Martin, A.2
  • 98
    • 77049085689 scopus 로고    scopus 로고
    • http://nobelprize.org/nobel_prizes/chemistry/laureates/2001/index.html.
  • 99
    • 0343341049 scopus 로고
    • Enantioselective epoxidation of unfunctionalized olefins catalyzed by salen manganese complexes
    • W. Zhang, J.L. Loebach, S.R. Wilson, E.N. Jacobsen: Enantioselective epoxidation of unfunctionalized olefins catalyzed by salen manganese complexes. J Am Chem Soc. 1990, 112, 2801-2813.
    • (1990) J Am Chem Soc , vol.112 , pp. 2801-2813
    • Zhang, W.1    Loebach, J.L.2    Wilson, S.R.3    Jacobsen, E.N.4
  • 100
    • 0042628218 scopus 로고    scopus 로고
    • Molybdenum complex-catalysed epoxidation of unsaturated fatty acids by organic hydroperoxides
    • J.M. Sobczak, J.J. Ziolkowski: Molybdenum complex-catalysed epoxidation of unsaturated fatty acids by organic hydroperoxides. Appl Catal A Gen. 2003, 248, 261-268.
    • (2003) Appl Catal A Gen , vol.248 , pp. 261-268
    • Sobczak, J.M.1    Ziolkowski, J.J.2
  • 101
    • 37049049512 scopus 로고
    • Fatty acids. Part VIII. The partial oxidation of unsaturated acids with performic acid, and a new method of determining the structure of non-conjugated polyethenoid acids
    • F.D. Gunstone, P.J. Sykes: Fatty acids. Part VIII. The partial oxidation of unsaturated acids with performic acid, and a new method of determining the structure of non-conjugated polyethenoid acids. J Chem Soc. 1962, 3058-3063.
    • (1962) J Chem Soc , pp. 3058-3063
    • Gunstone, F.D.1    Sykes, P.J.2
  • 102
    • 84858686443 scopus 로고
    • Direct hydroxylation of fats and derivatives with a hydrogen peroxide tungstic acid system
    • T.M. Luong, H. Schriftman, D. Swern: Direct hydroxylation of fats and derivatives with a hydrogen peroxide tungstic acid system. J Am Oil Chem Soc. 1967, 44, 316-319.
    • (1967) J Am Oil Chem Soc , vol.44 , pp. 316-319
    • Luong, T.M.1    Schriftman, H.2    Swern, D.3
  • 103
    • 77049086531 scopus 로고
    • Essays on organometallic chemistry 5. Rhenium chemistry in catalysis - present and future
    • W.A. Herrmann: Essays on organometallic chemistry. 5. Rhenium chemistry in catalysis - present and future. J Organomet Chem. 1990, 382, 1-18.
    • (1990) J Organomet Chem , vol.382 , pp. 1-18
    • Herrmann, W.A.1
  • 104
    • 0034254044 scopus 로고    scopus 로고
    • Oxidative cleavage of the double bond of monoenic fatty chains in two steps: A new promising route to azelaic acid and other industrial products
    • E. Santacesaria, A. Sorrentino, F. Rainone, M. Di Serio, F. Speranza: Oxidative cleavage of the double bond of monoenic fatty chains in two steps: A new promising route to azelaic acid and other industrial products. Ind Eng Chem Res. 2000, 39, 2766-2771.
    • (2000) Ind Eng Chem Res , vol.39 , pp. 2766-2771
    • Santacesaria, E.1    Sorrentino, A.2    Rainone, F.3    Di Serio, M.4    Speranza, F.5
  • 106
    • 33747226065 scopus 로고    scopus 로고
    • Ruthenium nanoparticles supported on hydroxyapatite as an efficient and recyclable catalyst for cis-dihydroxylation and oxidative cleavage of alkenes
    • C.-M. Ho, W.-Y. Yu, C.-M. Che: Ruthenium nanoparticles supported on hydroxyapatite as an efficient and recyclable catalyst for cis-dihydroxylation and oxidative cleavage of alkenes. Angew Chem. 2004, 116, 3365-3369.
    • (2004) Angew Chem , vol.116 , pp. 3365-3369
    • Ho, C.-M.1    Yu, W.-Y.2    Che, C.-M.3
  • 107
    • 17044413629 scopus 로고    scopus 로고
    • Ruthenium-catalysed oxidation without CCl4 of oleic acid, other monoenic fatty acids and alkenes
    • F. Zimmermann, E. Meux, J.-L. Mieloszynski, J.-M. Lecuire, N. Oget: Ruthenium-catalysed oxidation without CCl4 of oleic acid, other monoenic fatty acids and alkenes. Tetrahedron Lett. 2005, 46, 3201-3203.
    • (2005) Tetrahedron Lett , vol.46 , pp. 3201-3203
    • Zimmermann, F.1    Meux, E.2    Mieloszynski, J.-L.3    Lecuire, J.-M.4    Oget, N.5
  • 109
    • 38549149213 scopus 로고    scopus 로고
    • Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals
    • Z. C.-H. C. Zhou, J.N. Beltramini, Y.-X. Fan, G.Q.M. Lu: Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals. Chem Soc Rev. 2008, 37, 527-549.
    • (2008) Chem Soc Rev , vol.37 , pp. 527-549
    • Zhou, Z.-H.1    Beltramini, J.N.2    Fan, Y.-X.3    Lu, G.Q.M.4
  • 110
    • 37849012760 scopus 로고    scopus 로고
    • Improved utilisation of renewable resources: New important derivatives of glycerol
    • A. Behr, J. Eilting, K. Irawadi, J. Leschinski, F. Lindner: Improved utilisation of renewable resources: New important derivatives of glycerol. Green Chem. 2008, 10, 13-30.
    • (2008) Green Chem , vol.10 , pp. 13-30
    • Behr, A.1    Eilting, J.2    Irawadi, K.3    Leschinski, J.4    Lindner, F.5
  • 113
    • 77049125725 scopus 로고    scopus 로고
    • American Patent 20070919383
    • D. Bradin, G.L. Grune: American Patent 20070919383 (2007).
    • (2007)
    • Bradin, D.1    Grune, G.L.2
  • 115
    • 53849112680 scopus 로고    scopus 로고
    • Glycerol etherification over highly active CaO-based materials: New mechanistic aspects and related colloidal particle formation
    • A.M. Ruppert, J.D. Meeldijk, B.W.M. Kuipers, B.H. Erne, B.M. Weckhuysen: Glycerol etherification over highly active CaO-based materials: New mechanistic aspects and related colloidal particle formation. Eur J Chem. 2008, 14, 2016-2024.
    • (2008) Eur J Chem , vol.14 , pp. 2016-2024
    • Ruppert, A.M.1    Meeldijk, J.D.2    Kuipers, B.W.M.3    Erne, B.H.4    Weckhuysen, B.M.5
  • 116
    • 33846682385 scopus 로고    scopus 로고
    • Development of a process for the acid-catalyzed etherification of glycerine and isobutene forming glycerine tertiary butyl ethers
    • A. Behr, L. Obendorf: Development of a process for the acid-catalyzed etherification of glycerine and isobutene forming glycerine tertiary butyl ethers. Eng Life Sci. 2003, 2, 185-189.
    • (2003) Eng Life Sci , vol.2 , pp. 185-189
    • Behr, A.1    Obendorf, L.2
  • 117
    • 0442282121 scopus 로고    scopus 로고
    • Verfahrensentwicklung der säurekatalysierten Veretherung von Glycerin mit Isobuten zu Glycerintertiärbutylethern
    • A. Behr, L. Obendorf: Verfahrensentwicklung der säurekatalysierten Veretherung von Glycerin mit Isobuten zu Glycerintertiärbutylethern. Chem Ing Tech. 2001, 73, 1463-1467.
    • (2001) Chem Ing Tech , vol.73 , pp. 1463-1467
    • Behr, A.1    Obendorf, L.2
  • 118
    • 0037040317 scopus 로고    scopus 로고
    • Selective etherification of glycerol to polyglycerols over impregnated basic MCM-41 type mesoporous catalysts
    • J.-M. Clacens, Y. Pouilloux, J. Barrault: Selective etherification of glycerol to polyglycerols over impregnated basic MCM-41 type mesoporous catalysts. Appl Catal A Gen. 2002, 227, 181-190.
    • (2002) Appl Catal A Gen , vol.227 , pp. 181-190
    • Clacens, J.-M.1    Pouilloux, Y.2    Barrault, J.3
  • 119
    • 19844380153 scopus 로고    scopus 로고
    • Selective oligomerization of glycerol over mesoporous catalysts
    • J. Barrault, J.-M. Clacens, Y. Pouilloux: Selective oligomerization of glycerol over mesoporous catalysts. Topics Catal. 2004, 27, 137-142.
    • (2004) Topics Catal , vol.27 , pp. 137-142
    • Barrault, J.1    Clacens, J.-M.2    Pouilloux, Y.3
  • 122
    • 77049092717 scopus 로고
    • American Patent 3080288
    • T. Gorge, J.M. Smith Jr.: American Patent 3080288 (1963).
    • (1963)
    • Gorge, T.1    Smith J.M., Jr.2
  • 123
    • 65849289675 scopus 로고    scopus 로고
    • Oxidation of glycerol with oxygen in a base-free aqueous solution over Pt/ AC and Pt/MWNTs catalysts
    • J. Gao, D. Liang, P. Chen, Z. Hou, X. Zheng: Oxidation of glycerol with oxygen in a base-free aqueous solution over Pt/ AC and Pt/MWNTs catalysts. Catal Lett. 2009, 130, 185-191.
    • (2009) Catal Lett , vol.130 , pp. 185-191
    • Gao, J.1    Liang, D.2    Chen, P.3    Hou, Z.4    Zheng, X.5
  • 124
    • 2342513324 scopus 로고    scopus 로고
    • Selective oxidation of glycerol to sodium glycerate with gold-on-carbon catalyst: An insight into reaction selectivity
    • F. Porta, L. Prati: Selective oxidation of glycerol to sodium glycerate with gold-on-carbon catalyst: An insight into reaction selectivity. J Catal. 2004, 224, 397-403.
    • (2004) J Catal , vol.224 , pp. 397-403
    • Porta, F.1    Prati, L.2
  • 125
    • 0000162785 scopus 로고    scopus 로고
    • Gold on carbon as a new catalyst for selective liquid phase oxidation of diols
    • L. Prati, M. Rossi: Gold on carbon as a new catalyst for selective liquid phase oxidation of diols. J Catal. 1998, 176, 552-560.
    • (1998) J Catal , vol.176 , pp. 552-560
    • Prati, L.1    Rossi, M.2
  • 126
    • 18844456254 scopus 로고    scopus 로고
    • Selective oxidation of glycerol with oxygen using mono and bimetallic catalysts based on Au Pd and Pt metals
    • C.L. Bianchi, P. Canton, N. Dimitratos, F. Porta, L. Prati: Selective oxidation of glycerol with oxygen using mono and bimetallic catalysts based on Au, Pd and Pt metals. Catal Today. 2005, 102/103, 203-212.
    • (2005) Catal Today , vol.102-103 , pp. 203-212
    • Bianchi, C.L.1    Canton, P.2    Dimitratos, N.3    Porta, F.4    Prati, L.5
  • 128
    • 48849085813 scopus 로고    scopus 로고
    • Highly active catalysts for the telomerization of crude glycerol with 1,3-butadiene
    • R. Palkovits, I. Nieddu, J.M.K. Gebbink Robertus, B.M. Weckhuysen: Highly active catalysts for the telomerization of crude glycerol with 1,3-butadiene. ChemSusChem. 2008, 1, 193-196.
    • (2008) ChemSusChem. , vol.1 , pp. 193-196
    • Palkovits, R.1    Nieddu, I.2    Gebbink Robertus, J.M.K.3    Weckhuysen, B.M.4
  • 129
    • 60549095494 scopus 로고    scopus 로고
    • Telomerization of butadiene with glycerol: Reaction control through process engineering, solvents, and additives
    • A. Behr, J. Leschinski, C. Awungacha, S. Simic, T. Knoth: Telomerization of butadiene with glycerol: Reaction control through process engineering, solvents, and additives. ChemSusChem. 2009, 2, 71-76.
    • (2009) ChemSusChem , vol.2 , pp. 71-76
    • Behr, A.1    Leschinski, J.2    Awungacha, C.3    Simic, S.4    Knoth, T.5
  • 130
    • 66849089917 scopus 로고    scopus 로고
    • Continuous reactive extraction for selective telomerisation of butadiene
    • A. Behr, J. Leschinski, A. Prinz, M. Stoffers: Continuous reactive extraction for selective telomerisation of butadiene. Chem Eng Proc. 2009, 48, 1140-1145.
    • (2009) Chem Eng Proc , vol.48 , pp. 1140-1145
    • Behr, A.1    Leschinski, J.2    Prinz, A.3    Stoffers, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.