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
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 ◽  
...  

2011 ◽  
Vol 396-398 ◽  
pp. 1318-1324 ◽  
Author(s):  
Yin Zhen Wang ◽  
Qun Liang Li ◽  
Wu Yue ◽  
Ping Jia Yao ◽  
Yua Nan Wei

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.


2015 ◽  
Author(s):  
Jaquelinne de Jorge Bassi ◽  
Larissa Midiane Todero ◽  
Flávia Arantes Pires Lage ◽  
Maria Carolina Cucatti Corradini ◽  
DANIELA B. HIRATA ◽  
...  

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