Kobayashi_2010_Biotechnol.Lett_32_1679

Reference

Title : Efficient synthesis of 6-O-palmitoyl-1,2-O-isopropylidene-alpha-D-glucofuranose in an organic solvent system by lipase-catalyzed esterification - Kobayashi_2010_Biotechnol.Lett_32_1679
Author(s) : Kobayashi T , Ehara T , Mizuoka T , Adachi S
Ref : Biotechnol Lett , 32 :1679 , 2010
Abstract :

In order to synthesize a sugar ester at high concentration, 1,2-O-isopropylidene-alpha-D-glucofuranose (IpGlc), which is one of the sugar acetals and is more hydrophobic than unmodified glucose, was esterified with palmitic acid at 40 degrees C using immobilized lipase from Candida antarctica in some organic solvents or their mixtures. Acetone + t-butyl alcohol (3:1 v/v) improved both the initial reaction rate and yield after 80 h: the product reached its maximum value (240 mmol/kg solvent; ca. 110 g/kg solvent) when 400 mmol IpGlc/kg solvent and 1,200 mmol palmitic acid/kg solvent were used in this solvent mixture.

PubMedSearch : Kobayashi_2010_Biotechnol.Lett_32_1679
PubMedID: 20574832

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Citations formats

Kobayashi T, Ehara T, Mizuoka T, Adachi S (2010)
Efficient synthesis of 6-O-palmitoyl-1,2-O-isopropylidene-alpha-D-glucofuranose in an organic solvent system by lipase-catalyzed esterification
Biotechnol Lett 32 :1679

Kobayashi T, Ehara T, Mizuoka T, Adachi S (2010)
Biotechnol Lett 32 :1679