2011
DOI: 10.1016/j.molcatb.2011.07.002
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Lipase-catalyzed synthesis of 4-methoxy cinnamoyl glycerol

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Cited by 11 publications
(13 citation statements)
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“…4 Until now, only feruloyl glycerol, caffeate glycerol and 4-methoxy cinnamoyl glycerol have been synthesized in the enzymatic method but other kinds of PAGs with different PAs have rarely been reported. 3,8,9 Among the reported references, the studies only focused on the synthesis technology of PAGs and much less attention on their structural identication and their functional properties. [10][11][12] Apart from antioxidant and anti-UV, PAs have also been reported to have remarkable antibacterial effects against Gram-positive and Gram-negative bacteria.…”
Section: Introductionmentioning
confidence: 99%
“…4 Until now, only feruloyl glycerol, caffeate glycerol and 4-methoxy cinnamoyl glycerol have been synthesized in the enzymatic method but other kinds of PAGs with different PAs have rarely been reported. 3,8,9 Among the reported references, the studies only focused on the synthesis technology of PAGs and much less attention on their structural identication and their functional properties. [10][11][12] Apart from antioxidant and anti-UV, PAs have also been reported to have remarkable antibacterial effects against Gram-positive and Gram-negative bacteria.…”
Section: Introductionmentioning
confidence: 99%
“…The 4-methoxycinnamoylglycerol (4-MCG) is in form of mono-and di-esters when the esterification reaction is carried out in the presence of p-toluenesulfonic acid (p-TSA) (Holser, 2008;Holser et al 2008). An improved conversion yield was reported by enzymatic synthesis using lipase, in addition to the prevalence of the monoester at short reaction times and less harmful side effects compared with the chemical route (Patil et al 2011). It is well-know that lipases act as estearases in non-aqueous reaction media (Bernal et al 2018; Fernandez-Lafuente, 2010), including the esterification of cinnamic acid (Patil et al 2011) and/or glycerol (Yesiloglu & Kilic, 2004) and the obtained products have different industrial applications (Naik et al 2010).…”
Section: Introductionmentioning
confidence: 99%
“…An improved conversion yield was reported by enzymatic synthesis using lipase, in addition to the prevalence of the monoester at short reaction times and less harmful side effects compared with the chemical route (Patil et al 2011). It is well-know that lipases act as estearases in non-aqueous reaction media (Bernal et al 2018; Fernandez-Lafuente, 2010), including the esterification of cinnamic acid (Patil et al 2011) and/or glycerol (Yesiloglu & Kilic, 2004) and the obtained products have different industrial applications (Naik et al 2010). The lipase activity and selectivity depend on water activity (Lee & Parkin, 2001) and solvent polarity (Kuo & Parkin, 1996) of the reaction media.…”
Section: Introductionmentioning
confidence: 99%
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“…Immobilized CALB is a highly thermostable lipase with high non-specific acylglycerol positional selectivity and a high promiscuity towards substrates, ranging from linear, saturated, fatty acids to cyclic, heteroatom, aromatic carboxylic acids (Hayes, 2004;Patil et al, 2011). Immobilzed CALB also demonstrates robust activity in non-aqueous media (Secundo and Carrea, 2002;Sharma and Kanwar, 2014).…”
Section: Introductionmentioning
confidence: 99%