Lipase-catalyzed transesterification of ethyl ferulate with triolein in solvent-free medium

[1]  Yuanfa Liu,et al.  Solvent-free enzymatic synthesis of feruloylated diacylglycerols and kinetic study , 2009 .

[2]  J. A. Laszlo,et al.  1,3-Diferuloyl-sn-glycerol from the biocatalytic transesterification of ethyl 4-hydroxy-3-methoxy cinnamic acid (ethyl ferulate) and soybean oil , 2009, Biotechnology Letters.

[3]  Gang Xu,et al.  Kinetic study of lipase catalyzed asymmetric transesterification of mandelonitrile in solvent-free system , 2008 .

[4]  Yuanfa Liu,et al.  Solvent-free enzymatic preparation of feruloylated monoacylglycerols optimized by response surface methodology. , 2008, Journal of agricultural and food chemistry.

[5]  J. A. Laszlo,et al.  Identification and quantification of feruloylated mono-, di-, and triacylglycerols from vegetable oils , 2006 .

[6]  Isabelle Benoit,et al.  Feruloyl esterases as a tool for the release of phenolic compounds from agro-industrial by-products. , 2006, Carbohydrate research.

[7]  G. Yadav,et al.  Lipase catalyzed transesterification of methyl acetoacetate with n-butanol , 2005 .

[8]  J. Baratti,et al.  Short chain flavour esters synthesis by microbial lipases , 1990, Biotechnology Letters.

[9]  I. Kubo,et al.  Molecular design of multifunctional food additives: antioxidative antifungal agents. , 2004, Journal of agricultural and food chemistry.

[10]  I. Kubo,et al.  Lipoxygenase inhibitory activity of octyl gallate. , 2004, Journal of agricultural and food chemistry.

[11]  C. Akoh,et al.  Lipase-catalyzed synthesis of terpene esters by transesterification in n-hexane , 1994, Biotechnology Letters.

[12]  J. A. Laszlo,et al.  Packed-bed bioreactor synthesis of feruloylated monoacyl- and diacylglycerols: clean production of a “green” sunscreen , 2003 .

[13]  G. Yadav,et al.  Kinetic modeling of immobilized-lipase catalyzed transesterification of n-octanol with vinyl acetate in non-aqueous media , 2003 .

[14]  Ü. Mehmetoğlu,et al.  The production of isoamyl acetate using immobilized lipases in a solvent-free system , 2002 .

[15]  Ha Won Kim,et al.  FA15, a hydrophobic derivative of ferulic acid, suppresses inflammatory responses and skin tumor promotion: comparison with ferulic acid. , 2002, Cancer letters.

[16]  H. Kikuzaki,et al.  Antioxidant properties of ferulic acid and its related compounds. , 2002, Journal of agricultural and food chemistry.

[17]  D. Combes,et al.  Effect of soluble additives on enzyme thermo- and/or baro-deactivation , 1999 .

[18]  G. Williamson,et al.  Hydroxycinnamates in plants and food: current and future perspectives† , 1999 .

[19]  M. Legoy,et al.  An original transesterification route for fatty acid ester production from vegetable oils in a solvent-free system , 1997 .

[20]  F. Iverson Phenolic antioxidants: Health Protection Branch studies on butylated hydroxyanisole. , 1995, Cancer letters.

[21]  J. Shaw,et al.  Production of propylene glycol fatty acid monoesters by lipase-catalyzed reactions in organic solvents , 1994 .

[22]  B. Mattiasson,et al.  Facile synthesis of fatty acid esters in high yields , 1992 .

[23]  D. Combes,et al.  Kinetics of geranyl acetate synthesis by lipase-catalysed transesterification in n-hexane , 1992 .

[24]  Peter Schuler Natural Antioxidants Exploited Commercially , 1990 .

[25]  M. Iwai,et al.  Synthesis of Terpene Alcohol Esters by Lipase , 1980 .