2021
DOI: 10.1080/10242422.2021.1952192
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Regioselective synthesis of 6’’-O-lauroyl-1-kestose and 6’’’-O-lauroylnystose by sequential enzymatic reactions of transfructosylation and acylation

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Cited by 4 publications
(2 citation statements)
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“…The mobile phase was methanol–water 90:10 at 0.6 mL/min. FOS are not completely soluble in the reactional system; however, once converted to bioconjugates, their solubility increased as the acylation reaction proceeded, as that kind of compound also has emulsification properties [ 21 , 25 , 43 ]. At the end of reaction, the immobilized lipase was filtered and the reaction solvent was eliminated in a Buchi TM rotary evaporator.…”
Section: Methodsmentioning
confidence: 99%
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“…The mobile phase was methanol–water 90:10 at 0.6 mL/min. FOS are not completely soluble in the reactional system; however, once converted to bioconjugates, their solubility increased as the acylation reaction proceeded, as that kind of compound also has emulsification properties [ 21 , 25 , 43 ]. At the end of reaction, the immobilized lipase was filtered and the reaction solvent was eliminated in a Buchi TM rotary evaporator.…”
Section: Methodsmentioning
confidence: 99%
“…Then, 1 mL of this mixture was deposited on the target plate and dried at room temperature. The equipment was calibrated from 380 to 3000 m / z with 1-kestose as the standard [ 43 , 44 ].…”
Section: Methodsmentioning
confidence: 99%