메뉴 건너뛰기




Volumn 100, Issue 6, 2005, Pages 662-666

Enzymatic chemoselective synthesis of secondary-amide surfactant from N-methylethanol amine

Author keywords

Chirazyme L 2; methyl laurate; N methyl lauroylethanolamide; N methylethanol amine; secondary amide surfactant

Indexed keywords

AMINES; CHEMOSTATS; ENZYME KINETICS; ESTERS; ETHANOL; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 33645524515     PISSN: 13891723     EISSN: None     Source Type: Journal    
DOI: 10.1263/jbb.100.662     Document Type: Article
Times cited : (16)

References (22)
  • 1
    • 0020709645 scopus 로고
    • Fatty acid derivatives; important surfactants for household, cosmetic and industrial purposes
    • Maag H. Fatty acid derivatives; important surfactants for household, cosmetic and industrial purposes. J. Am. Oil Chem. Soc. 61 (1984) 259-267
    • (1984) J. Am. Oil Chem. Soc. , vol.61 , pp. 259-267
    • Maag, H.1
  • 2
    • 0002728748 scopus 로고
    • Synthesis of N-lauryloleyamide by Mucor miehei lipase in organic medium
    • Montet D., Pina M., Graille J., Renard G., and Grimaud J. Synthesis of N-lauryloleyamide by Mucor miehei lipase in organic medium. Fat Sci. Technol. 91 (1989) 14-18
    • (1989) Fat Sci. Technol. , vol.91 , pp. 14-18
    • Montet, D.1    Pina, M.2    Graille, J.3    Renard, G.4    Grimaud, J.5
  • 6
    • 0031186602 scopus 로고    scopus 로고
    • Enzymatic synthesis of N-lauroyl-β-alanine homologs in organic media
    • Izumi T., Yaginuma Y., and Haga M. Enzymatic synthesis of N-lauroyl-β-alanine homologs in organic media. J. Am. Oil Chem. Soc. 74 (1997) 875-878
    • (1997) J. Am. Oil Chem. Soc. , vol.74 , pp. 875-878
    • Izumi, T.1    Yaginuma, Y.2    Haga, M.3
  • 7
    • 8644256800 scopus 로고    scopus 로고
    • A novel process for enzymatic synthesis of N-lauroyl-β-amino propionitrile using packed bed reactor coupled with online separation
    • Xia Y., Fang Y., Xu, Shen Y., and Brown J. A novel process for enzymatic synthesis of N-lauroyl-β-amino propionitrile using packed bed reactor coupled with online separation. J. Mol. Catal. B: Enzym. 31 (2004) 111-115
    • (2004) J. Mol. Catal. B: Enzym. , vol.31 , pp. 111-115
    • Xia, Y.1    Fang, Y.2    Xu, Shen, Y.3    Brown, J.4
  • 8
    • 0030897974 scopus 로고    scopus 로고
    • Enzymatic synthesis of glycamide surfactants by amidation reaction
    • Maugard T., Remaud-Simeon M., Petre D., and Manson P. Enzymatic synthesis of glycamide surfactants by amidation reaction. Tetrahedron 53 (1997) 5185-5194
    • (1997) Tetrahedron , vol.53 , pp. 5185-5194
    • Maugard, T.1    Remaud-Simeon, M.2    Petre, D.3    Manson, P.4
  • 9
    • 0030981562 scopus 로고    scopus 로고
    • Lipase-catalyzed chemoselective N-acylation of amino-sugar derivatives in hydrophobic solvent: acid-amine ion-pair effects
    • Maugard T., Remaud-Simeon M., Petre D., and Manson P. Lipase-catalyzed chemoselective N-acylation of amino-sugar derivatives in hydrophobic solvent: acid-amine ion-pair effects. Tetrahedron 53 (1997) 7587-7594
    • (1997) Tetrahedron , vol.53 , pp. 7587-7594
    • Maugard, T.1    Remaud-Simeon, M.2    Petre, D.3    Manson, P.4
  • 10
    • 0035810270 scopus 로고    scopus 로고
    • Enzymatic synthesis of amide surfactants from diethanolamine
    • Fernandez-Perez M., and Otero C. Enzymatic synthesis of amide surfactants from diethanolamine. Enzyme Microb. Technol. 28 (2001) 527-536
    • (2001) Enzyme Microb. Technol. , vol.28 , pp. 527-536
    • Fernandez-Perez, M.1    Otero, C.2
  • 11
    • 0001635545 scopus 로고
    • First stereoselective synthesis of D-amino acid amide catalyzed by a novel aminopeptidase
    • Kato Y., Asano Y., Nakazawa A., and Kondo K. First stereoselective synthesis of D-amino acid amide catalyzed by a novel aminopeptidase. Tetrahedron 45 (1989) 5743-5754
    • (1989) Tetrahedron , vol.45 , pp. 5743-5754
    • Kato, Y.1    Asano, Y.2    Nakazawa, A.3    Kondo, K.4
  • 14
    • 0030910121 scopus 로고    scopus 로고
    • Exploitation of subtilisin BPN' as catalyst for the synthesis of peptides containing noncoded amino acids, peptide mimetics and peptide conjugates
    • Moree W.J., Sears P., Kawashiro K., Witte K., and Wong C.H. Exploitation of subtilisin BPN' as catalyst for the synthesis of peptides containing noncoded amino acids, peptide mimetics and peptide conjugates. J. Am. Chem. Soc. 119 (1997) 3942-3947
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3942-3947
    • Moree, W.J.1    Sears, P.2    Kawashiro, K.3    Witte, K.4    Wong, C.H.5
  • 15
    • 0037071912 scopus 로고    scopus 로고
    • Lipases and (R)-oxynitrilases: useful tools in organic synthesis
    • Gotor V. Lipases and (R)-oxynitrilases: useful tools in organic synthesis. J. Biotechnol. 96 (2002) 35-42
    • (2002) J. Biotechnol. , vol.96 , pp. 35-42
    • Gotor, V.1
  • 16
    • 0034697072 scopus 로고    scopus 로고
    • Customizing lipases for biocatalysis: a survey of chemical, physical and molecular approaches
    • Villeneuve P., Muderhwa J., Graille J., and Haas M.J. Customizing lipases for biocatalysis: a survey of chemical, physical and molecular approaches. J. Mol. Catal. B: Enzym. 9 (2000) 113-148
    • (2000) J. Mol. Catal. B: Enzym. , vol.9 , pp. 113-148
    • Villeneuve, P.1    Muderhwa, J.2    Graille, J.3    Haas, M.J.4
  • 17
    • 0032825993 scopus 로고    scopus 로고
    • Non-conventional hydrolase chemistry: amide and carbamate bond formation catalysed by lipases
    • Gotor V. Non-conventional hydrolase chemistry: amide and carbamate bond formation catalysed by lipases. Bioorg. Med. Chem. 7 (1999) 2189-2197
    • (1999) Bioorg. Med. Chem. , vol.7 , pp. 2189-2197
    • Gotor, V.1
  • 18
    • 0035931359 scopus 로고    scopus 로고
    • One pot biocatalysed preparation of substituted amides as intermediates of pharmaceuticals
    • Baldessari A., and Mangone C.P. One pot biocatalysed preparation of substituted amides as intermediates of pharmaceuticals. J. Mol. Catal. B: Enzym. 11 (2001) 335-341
    • (2001) J. Mol. Catal. B: Enzym. , vol.11 , pp. 335-341
    • Baldessari, A.1    Mangone, C.P.2
  • 19
    • 0011440725 scopus 로고
    • An enzymatic method for the preparation of chiral diamides
    • Gotor V., Garcia M.J., and Rebolledo F. An enzymatic method for the preparation of chiral diamides. Tetrahedron: Asymmetry 1 (1990) 277-278
    • (1990) Tetrahedron: Asymmetry , vol.1 , pp. 277-278
    • Gotor, V.1    Garcia, M.J.2    Rebolledo, F.3
  • 20
    • 0025879928 scopus 로고
    • Enzyme-mediated enantioselective acylation of secondary amines in organic solvents
    • Asensio G., Andreu C., and Marco J.A. Enzyme-mediated enantioselective acylation of secondary amines in organic solvents. Tetrahedron Lett. 32 (1991) 4197-4198
    • (1991) Tetrahedron Lett. , vol.32 , pp. 4197-4198
    • Asensio, G.1    Andreu, C.2    Marco, J.A.3
  • 21
    • 0032530944 scopus 로고    scopus 로고
    • Enzymatic amidation for the synthesis of biodegradable surfactants: synthesis of n-acylated hdroxylated amides
    • Maugard T., Remaud-Simeon M., Petre D., and Manson P. Enzymatic amidation for the synthesis of biodegradable surfactants: synthesis of n-acylated hdroxylated amides. J. Mol. Catal. B: Enzym. 5 (1998) 13-17
    • (1998) J. Mol. Catal. B: Enzym. , vol.5 , pp. 13-17
    • Maugard, T.1    Remaud-Simeon, M.2    Petre, D.3    Manson, P.4
  • 22
    • 84907037923 scopus 로고
    • Chemoselectivity of enzymes in anhydrous media is strongly solvent dependent
    • Tawaki S., and Klibanov A.M. Chemoselectivity of enzymes in anhydrous media is strongly solvent dependent. Biocatalysis 8 (1993) 3-19
    • (1993) Biocatalysis , vol.8 , pp. 3-19
    • Tawaki, S.1    Klibanov, A.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.