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A Simple Procedure for the Regioselective Synthesis of Fatty Acid Esters of Maltose, Leucrose, Maltotriose and n-Dodecyl Maltosides

✍ Scribed by Manuel Ferrer; M Angeles Cruces; Francisco J Plou; Manuel Bernabé; Antonio Ballesteros


Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
150 KB
Volume
56
Category
Article
ISSN
0040-4020

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✦ Synopsis


AbstractÐThe enzymatic acylation of several di-and trisaccharides with acyl donors ranging from 8 to 18 carbon atoms was carried out by transesteri®cation with the corresponding vinyl esters. The reaction was performed in 2-methyl-2-butanol/dimethylsulfoxide mixtures using the lipase from Humicola lanuginosa (immobilized on Celite). Maltose, maltotriose and n-dodecyl maltosides were speci®cally acylated in the primary hydroxyl of the non-reducing-end glucose moiety; the acylation of leucrose occurred preferentially in the primary hydroxyl of the glucose ring.


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