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Volumn 110, Issue 9, 2008, Pages 805-811

Synthesis of alkyl-branched fatty acids

Author keywords

Alkyl branched fatty compounds; Lewis acid induced hydro alkylation; Radical addition; Renewable raw materials; Zeolite and clay catalyzed isomerization

Indexed keywords


EID: 55449136490     PISSN: 14387697     EISSN: 14389312     Source Type: Journal    
DOI: 10.1002/ejlt.200800033     Document Type: Conference Paper
Times cited : (46)

References (41)
  • 2
    • 3042829399 scopus 로고    scopus 로고
    • Catalytic C,C-bond forming additions to unsaturated fatty compounds
    • U. Biermann, J. O. Metzger: Catalytic C,C-bond forming additions to unsaturated fatty compounds. Topics Catal. 2004, 27, 119-130.
    • (2004) Topics Catal , vol.27 , pp. 119-130
    • Biermann, U.1    Metzger, J.O.2
  • 7
    • 0012733884 scopus 로고    scopus 로고
    • New chemistry of oils and fats
    • Eds. F. D. Gunstone, R. J. Hamilton, Sheffield Academic Press, Sheffield UK
    • U. Biermann, S. Fürmeier, J. O. Metzger: New chemistry of oils and fats. In: Oleochemical Manufacture and Applications. Eds. F. D. Gunstone, R. J. Hamilton, Sheffield Academic Press, Sheffield (UK) 2001, pp. 266-299.
    • (2001) Oleochemical Manufacture and Applications , pp. 266-299
    • Biermann, U.1    Fürmeier, S.2    Metzger, J.O.3
  • 9
    • 0001744739 scopus 로고
    • Branched-chain fatty acids
    • Eds. R. W. Johnson, E. Fritz, Marcel Dekker, New York, NY USA
    • D. V. Kinsman: Branched-chain fatty acids. In: Fatty Acids in Industry. Eds. R. W. Johnson, E. Fritz, Marcel Dekker, New York, NY (USA) 1989, pp. 233-276.
    • (1989) Fatty Acids in Industry , pp. 233-276
    • Kinsman, D.V.1
  • 11
    • 0011302313 scopus 로고
    • Mixed- and plug-flow performances of an anaerobic biofilter treating 2-ethylhexanoic acid
    • H. Chua, M. G. S. Yap, W. J. Ng: Mixed- and plug-flow performances of an anaerobic biofilter treating 2-ethylhexanoic acid. Appl Biochem Biotechnol. 1992, 34/35, 789-800.
    • (1992) Appl Biochem Biotechnol , vol.34-35 , pp. 789-800
    • Chua, H.1    Yap, M.G.S.2    Ng, W.J.3
  • 12
    • 0026511859 scopus 로고
    • Performance of an anaerobic biofilter for 2-ethylhexanoic acid degradation
    • M. G. S. Yap, W. J. Ng, H. Chua: Performance of an anaerobic biofilter for 2-ethylhexanoic acid degradation. Biores Technol. 1992, 41, 45-51.
    • (1992) Biores Technol , vol.41 , pp. 45-51
    • Yap, M.G.S.1    Ng, W.J.2    Chua, H.3
  • 13
    • 0034053067 scopus 로고    scopus 로고
    • Degradation pathway of persistent branched fatty acids in natural anaerobic ecosystem
    • S. N. Sin, H. Chua: Degradation pathway of persistent branched fatty acids in natural anaerobic ecosystem. Chemosphere. 2000, 41, 149-153.
    • (2000) Chemosphere , vol.41 , pp. 149-153
    • Sin, S.N.1    Chua, H.2
  • 14
    • 14844294800 scopus 로고    scopus 로고
    • New process for the production of branched-chain fatty acids
    • Z. C. Zhang, M. Dery, S. Zhang, D. Steichen: New process for the production of branched-chain fatty acids. J Surfac. Deterg. 2004, 7, 211-215.
    • (2004) J Surfac. Deterg , vol.7 , pp. 211-215
    • Zhang, Z.C.1    Dery, M.2    Zhang, S.3    Steichen, D.4
  • 15
    • 55449116896 scopus 로고    scopus 로고
    • Technical Data Sheet: Emersol 874 Isostearic Acid. Henkel Corporation (USA) 1999.
    • Technical Data Sheet: Emersol 874 Isostearic Acid. Henkel Corporation (USA) 1999.
  • 16
    • 0343722123 scopus 로고
    • The dimerization of oleic acid with a montmorillonite catalyst. I. Important process parameters; some main reactions
    • M. J. A. M. den Otter: The dimerization of oleic acid with a montmorillonite catalyst. I. Important process parameters; some main reactions. Fette Seifen Anstrichm. 1970, 72, 667-673.
    • (1970) Fette Seifen Anstrichm , vol.72 , pp. 667-673
    • den Otter, M.J.A.M.1
  • 17
    • 84985412416 scopus 로고
    • The dimerization of oleic acid with a montmorillonite catalyst. II. GLC analysis of the monomer; the structure of the dimer; a reaction model
    • M. J. A. M. den Otter: The dimerization of oleic acid with a montmorillonite catalyst. II. GLC analysis of the monomer; the structure of the dimer; a reaction model. Fette Seifen Anstrichm. 1970, 72, 875-883.
    • (1970) Fette Seifen Anstrichm , vol.72 , pp. 875-883
    • den Otter, M.J.A.M.1
  • 18
    • 0002704660 scopus 로고
    • Produkte der Dimerisierung ungesättigter Fettsäuren. I. Die Monomerfraktion der Dimerisierung reiner Ölsäure.
    • W. Link, G. Spiteller: Produkte der Dimerisierung ungesättigter Fettsäuren. I. Die Monomerfraktion der Dimerisierung reiner Ölsäure. Fat Sci Technol. 1990, 92, 19-25.
    • (1990) Fat Sci Technol , vol.92 , pp. 19-25
    • Link, W.1    Spiteller, G.2
  • 19
    • 55449093646 scopus 로고
    • Produkte der Dimerisierung ungesättigter Fettsäuren. II. Die Monomerfraktion der Dimerisierung reiner Linolsäure, 1. Aromatenfraktion.
    • H. Möhring, G. Spitteller: Produkte der Dimerisierung ungesättigter Fettsäuren. II. Die Monomerfraktion der Dimerisierung reiner Linolsäure, 1. Aromatenfraktion. Fat Sci Technol. 1990, 92, 126-131.
    • (1990) Fat Sci Technol , vol.92 , pp. 126-131
    • Möhring, H.1    Spitteller, G.2
  • 20
    • 55449122370 scopus 로고
    • Produkte der Dimerisierung ungesättigter Fettsäuren. IV. Fettsäuren mit längerkettigen Alkylverzweigungen in der Monomerfraktion der Fettsäuredimerisierung aus Öl-/Linolsäure.
    • H. Möhring, G. Spitteller: Produkte der Dimerisierung ungesättigter Fettsäuren. IV. Fettsäuren mit längerkettigen Alkylverzweigungen in der Monomerfraktion der Fettsäuredimerisierung aus Öl-/Linolsäure. Fat Sci Technol. 1990, 92, 255-259.
    • (1990) Fat Sci Technol , vol.92 , pp. 255-259
    • Möhring, H.1    Spitteller, G.2
  • 21
    • 0022056567 scopus 로고
    • Thermal alteration of oleic acid in the presence of clay catalysts with co-catalysts
    • Y. Nakano, T. A. Foglia, H. Kohashi, T. Perlstein, U. Serota: Thermal alteration of oleic acid in the presence of clay catalysts with co-catalysts. J Am Oil Chem Soc. 1985, 62, 888-891.
    • (1985) J Am Oil Chem Soc , vol.62 , pp. 888-891
    • Nakano, Y.1    Foglia, T.A.2    Kohashi, H.3    Perlstein, T.4    Serota, U.5
  • 22
    • 34047185808 scopus 로고
    • Process for the preparation of branched chain fatty acids and esters
    • US Patent 4,371,469
    • T. A. Foglia, L. Hill, T. Perlstein, Y. Nakano, G. Maerker: Process for the preparation of branched chain fatty acids and esters. US Patent 4,371,469 (1983).
    • (1983)
    • Foglia, T.A.1    Hill, L.2    Perlstein, T.3    Nakano, Y.4    Maerker, G.5
  • 23
    • 34047133222 scopus 로고
    • Process for the production of branched fatty acids and esters thereof
    • US Patent 5,364,949
    • M. Neuss, H. Eierdanz: Process for the production of branched fatty acids and esters thereof. US Patent 5,364,949 (1994).
    • (1994)
    • Neuss, M.1    Eierdanz, H.2
  • 24
    • 34047126440 scopus 로고    scopus 로고
    • Zeolite-catalyzed isomerization of oleic acid to branched-chain isomers
    • H. L. Ngo, A. Nunez, W. Lin, T. A. Foglia: Zeolite-catalyzed isomerization of oleic acid to branched-chain isomers. Eur J Lipid Sci Technol. 2007, 108, 214-224.
    • (2007) Eur J Lipid Sci Technol , vol.108 , pp. 214-224
    • Ngo, H.L.1    Nunez, A.2    Lin, W.3    Foglia, T.A.4
  • 25
    • 34047138379 scopus 로고    scopus 로고
    • Process for the preparation of branched chain fatty acids and alkyl esters
    • US Patent 5,677,473
    • T. Tomifuji, H. Abe, Y. Matsumura, Y. Sakuma: Process for the preparation of branched chain fatty acids and alkyl esters. US Patent 5,677,473 (1997).
    • (1997)
    • Tomifuji, T.1    Abe, H.2    Matsumura, Y.3    Sakuma, Y.4
  • 26
    • 55449134267 scopus 로고    scopus 로고
    • Process for the branching of saturated and/or unsaturated fatty acids and/or alkyl esters thereof
    • US Patent 6,455,716 B2 2001
    • C. J. Kenneally, D. S. Connor: Process for the branching of saturated and/or unsaturated fatty acids and/or alkyl esters thereof. US Patent 6,455,716 B2 (2001).
    • Kenneally, C.J.1    Connor, D.S.2
  • 27
    • 34047155022 scopus 로고    scopus 로고
    • Skeletal isomerization of alkyl esters and derivates prepared therefrom
    • US Patent 6,946,567 B2 2005
    • S. Zhang, Z. Zhang, D. Steichen: Skeletal isomerization of alkyl esters and derivates prepared therefrom. US Patent 6,946,567 B2 (2005).
    • Zhang, S.1    Zhang, Z.2    Steichen, D.3
  • 28
    • 0002982981 scopus 로고
    • Radikalische Additionen an ungesättigte Fettstoffe.
    • J. O. Metzger, U. Riedner: Radikalische Additionen an ungesättigte Fettstoffe. Fat Sci Technol. 1989, 91, 18-23.
    • (1989) Fat Sci Technol , vol.91 , pp. 18-23
    • Metzger, J.O.1    Riedner, U.2
  • 29
    • 0039354066 scopus 로고
    • Ane additions to unsaturated fatty compounds: Thermally initiated additions of alkanes to methyl 10-undecenoate
    • J. O. Metzger, F. Bangert: Ane additions to unsaturated fatty compounds: Thermally initiated additions of alkanes to methyl 10-undecenoate. Fat Sci Technol. 1995, 97, 7-9.
    • (1995) Fat Sci Technol , vol.97 , pp. 7-9
    • Metzger, J.O.1    Bangert, F.2
  • 30
    • 0002455067 scopus 로고    scopus 로고
    • Biosynthesis of omega-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius: The stereochemistry of the initial 1,4-conjugate elimination
    • S. Handa, H. G. Floss: Biosynthesis of omega-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius: The stereochemistry of the initial 1,4-conjugate elimination. Chem Commun. 1997, 153-154.
    • (1997) Chem Commun , pp. 153-154
    • Handa, S.1    Floss, H.G.2
  • 31
    • 0000712414 scopus 로고
    • New results on free radical additions to unsaturated fatty compounds
    • J. O. Metzger, U. Linker: New results on free radical additions to unsaturated fatty compounds. Fat Sci Technol. 1991, 93, 244-249.
    • (1991) Fat Sci Technol , vol.93 , pp. 244-249
    • Metzger, J.O.1    Linker, U.2
  • 32
    • 84986637953 scopus 로고
    • Synthese linearer und verzweigter perfluoralkylierter Carbonsäuren durch radikalische Addition von Perfluoralkyliodiden an ungesättigte Fettsäuren.
    • J. O. Metzger, U. Linker: Synthese linearer und verzweigter perfluoralkylierter Carbonsäuren durch radikalische Addition von Perfluoralkyliodiden an ungesättigte Fettsäuren. Liebigs Ann Chem. 1992, 209-216.
    • (1992) Liebigs Ann Chem , pp. 209-216
    • Metzger, J.O.1    Linker, U.2
  • 33
    • 33748732143 scopus 로고    scopus 로고
    • Electron transfer initiated free radical additions of perfluoroalkyl iodides and diiodides to alkenes
    • J. O. Metzger, R. Mahler, A. Schmidt: Electron transfer initiated free radical additions of perfluoroalkyl iodides and diiodides to alkenes. Liebigs 1996, 693-696.
    • (1996) Liebigs , pp. 693-696
    • Metzger, J.O.1    Mahler, R.2    Schmidt, A.3
  • 35
    • 0033576710 scopus 로고    scopus 로고
    • Friedel-Crafts-alkylation of alkenes: Ethylaluminium-sesquichloride induced alkylations with alkyl chloroformates
    • U. Biermann, J. O. Metzger: Friedel-Crafts-alkylation of alkenes: Ethylaluminium-sesquichloride induced alkylations with alkyl chloroformates. Angew Chem Int Ed. 1999, 38, 3675-3677.
    • (1999) Angew Chem Int Ed , vol.38 , pp. 3675-3677
    • Biermann, U.1    Metzger, J.O.2
  • 36
    • 4143102504 scopus 로고    scopus 로고
    • Alkylation of alkenes: Ethylaluminum sesquichloride mediated hydro-alkyladditions with alkyl chloroformates and di-tert-butylpyrocarbonate
    • U. Biermann, J. O. Metzger: Alkylation of alkenes: Ethylaluminum sesquichloride mediated hydro-alkyladditions with alkyl chloroformates and di-tert-butylpyrocarbonate. J Am Chem Soc. 2004, 126, 10319-10330.
    • (2004) J Am Chem Soc , vol.126 , pp. 10319-10330
    • Biermann, U.1    Metzger, J.O.2
  • 37
    • 27644521902 scopus 로고    scopus 로고
    • Branched-chain fatty acids as activators of peroxisome proliferator-activated receptors
    • T. Hanhoff, S. Benjamin, T. Börchers, F. Spener: Branched-chain fatty acids as activators of peroxisome proliferator-activated receptors. Eur J Lipid Sci Technol. 2005, 107, 716-729.
    • (2005) Eur J Lipid Sci Technol , vol.107 , pp. 716-729
    • Hanhoff, T.1    Benjamin, S.2    Börchers, T.3    Spener, F.4
  • 39
    • 33746216403 scopus 로고    scopus 로고
    • Intramolecular concerted insertion of vinyl cations into C-H bonds: Hydroalkylating cyclization of alkynes with alkyl chloroformates to give cyclopentanes
    • U. Biermann, R. Koch, J. O. Metzger: Intramolecular concerted insertion of vinyl cations into C-H bonds: Hydroalkylating cyclization of alkynes with alkyl chloroformates to give cyclopentanes. Angew Chem Int Ed. 2006, 45, 3076-3079.
    • (2006) Angew Chem Int Ed , vol.45 , pp. 3076-3079
    • Biermann, U.1    Koch, R.2    Metzger, J.O.3
  • 40
    • 0037453186 scopus 로고    scopus 로고
    • Rhodium-catalysed synthesis of branched fatty compounds in temperature dependent solvent systems
    • A. Behr, C. Fangewisch: Rhodium-catalysed 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    Fangewisch, C.2


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