
Bioorganic and Medicinal Chemistry Letters p. 633 - 636 (1999)
Update date:2022-08-17
Topics:
Bastida, Agatha
Fernandez-Lafuente, Roberto
Fernandez-Lorente, Gloria
Guisan, Jose M.
Pagani, Giuseppe
Terreni, Marco
Penta-O-acetyl-α-D-Glucopyranose was selectively deacetylated in aqueous media by lipases from Candida cilindracea (CCL) adsorbed on octyl- agarose support. Enzymatic hydrolyses was regioselective at the 4-position under neutral pH and towards the 6 position under acidic conditions. This enzymatic approach allows the one step synthesis of 1,2,3,6-tetra-O-acetyl- α-D-glucopyranoses 1, a useful intermediate in oligosaccharide synthesis.
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