Immobilized Lipase Based on Hollow Mesoporous Silicon Spheres for Efficient Enzymatic Synthesis of Resveratrol Ester Derivatives

2021 ◽  
Author(s):  
Liu-Jia Xu ◽  
Tao Yang ◽  
Jing Wang ◽  
Feng-Hong Huang ◽  
Ming-Ming Zheng
Keyword(s):  
Enzymatic Synthesis ◽  
Immobilized Lipase ◽  
Mesoporous Silicon ◽  
Silicon Spheres

Enzymatic synthesis of esters using an immobilized lipase

1991 ◽  
Vol 37 (11) ◽  
pp. 1004-1009 ◽  
Author(s):  
Giorgio Carta ◽  
John L. Gainer ◽  
Alan H. Benton
Keyword(s):  
Enzymatic Synthesis ◽  
Immobilized Lipase

Enzymatic synthesis of isoamyl butyrate catalyzed by immobilized lipase on poly-methacrylate particles: optimization, reusability and mass transfer studies

2015 ◽  
Vol 38 (8) ◽  
pp. 1601-1613 ◽  
Author(s):  
Larissa M. Todero ◽  
Jaquelinne J. Bassi ◽  
Flávia A. P. Lage ◽  
Maria Carolina C. Corradini ◽  
Jayne C. S. Barboza ◽  
...  
Keyword(s):  
Mass Transfer ◽  
Enzymatic Synthesis ◽  
Immobilized Lipase ◽  
Mass Transfer Studies

scholarly journals Cover Picture: Highly Crystalline Mesoporous Silicon Spheres for Efficient Visible Photocatalytic Hydrogen Evolution (ChemNanoMat 1/2017)

ChemNanoMat ◽  
2016 ◽  
Vol 3 (1) ◽  
pp. 1-1
Author(s):  
Hongguang Song ◽  
Dong Liu ◽  
Jia Yang ◽  
Lei Wang ◽  
Hangxun Xu ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Mesoporous Silicon ◽  
Photocatalytic Hydrogen Evolution ◽  
Silicon Spheres

6-O-(10-Undecylenoyl)-D-Glucose: Controlled Enzymatic Synthesis and Structure Elucidation by 1H and 13C NMR

2011 ◽  
Vol 396-398 ◽  
pp. 1318-1324 ◽  
Author(s):  
Yin Zhen Wang ◽  
Qun Liang Li ◽  
Wu Yue ◽  
Ping Jia Yao ◽  
Yua Nan Wei
Keyword(s):  
Enzymatic Synthesis ◽  
Methyl Ketone ◽  
Immobilized Lipase ◽  
Methanol Solution ◽  
Undecylenic Acid ◽  
Ethyl Methyl ◽  
Lipase Enzyme ◽  
Ethyl Methyl Ketone ◽  
O 10 ◽  
C Nmr

A direct esterification synthesis of glucose undecylenic acid sugar monoester is described, using the immobilized lipase enzyme NOVO-435 in 2-methyl-2-butonal and in ethyl methyl ketone (EMK). conditions were optimized in order to produce the monoester more rapidly and in higher yield. After the reaction product was purified, mass spectroscopy revealed that it had a molecular weight of 346.2 AMU. Further characterization by 1H and 13C NMR spectroscopy was carried out, including two-dimensional (2D) 1H-1H COSY and heteronuclear 1H-13C HSQC experiments. These data enabled identification of the monoester product to be 6-O-(10-undercylenoyl)α-D-glucose (74%), and 6-O-(10-undercylenoyl)β-D-glucose (26%) in methanol solution.

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